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C123
                  MANAGING THE GERIATRIC PATIENT
                  ANN ESHENAUR SPOLARICH, RDH, PHD
                  THURSDAY, FEBRUARY 21




DISCLAIMER: This work, audio recordings and the accompanying handout, are the intellectual property of the clinician, and permission has
been granted to the Chicago Dental Society, its members, successors and assigns, for the unrestricted, absolute, perpetual, worldwide right
to distribute solely as an educational material at the scientific program being presented at the 2011 Midwinter Meeting. Permission has been
granted for this work to be shared for non-commercial education purposes only. No other use, including reproduction, retransmission in any
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does not assume any responsibility or liability for the content, accuracy, or compliance with applicable laws, and the Chicago Dental Society
shall not be sued for any claim involving the distribution of this work.
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RETURN EVALUATION CARD TO:                                                                      DO NOT FOLD CARD. FOR CDS PERMANENT FILES.
Chicago Dental Society
Aloysius F. Kleszynski, DDS
401 N. Michigan Ave., Suite 200, Chicago, IL 60611-5585
COURSE TITLE:                        Pharmacologic Management of the Geriatric Patient: Oral
                                     Health Care Considerations

COURSE INSTRUCTOR:                   Ann Eshenaur Spolarich, RDH, PhD

COURSE CREDITS:                      3 CEUs

COURSE DATE:                         February 22, 2013
_____________________________________________________________________________
COURSE DESCRIPTION: The purpose of this course is to review characteristics and disease
trends among the aging population, and oral disease risks associated with medications and
common systemic diseases. Most patients take multiple medications, many of which have oral
complications and drug interactions of significance to dentistry. Medication therapies, oral drug
and disease complications, drug interactions and dental practice management considerations will
be discussed. Recommendations for treatment modifications and oral hygiene self-care programs
will be provided.

LEARNING OBJECTIVES:

Upon completion of this continuing education program, course participants will be able to:

1.     Describe common oral disorders observed in the elderly population, including
       xerostomia, taste and smell disorders, orofacial muscular disorders, and lichenoid drug
       reactions.

2.     Discuss the pathophysiology of common diseases associated with aging, including
       cardiovascular disease, gastrointestinal problems, and depression.

2.     Identify the major classes of medications associated with and/or used to treat these
       conditions.

4.     Discuss the oral side effects and other adverse events associated with each of these
       disease states and related medication therapies.

5.     Identify modifications necessary to safely treat patients who present with these medical
       conditions.

6.     Recommend appropriate oral hygiene strategies for each of these patient populations.




*These course materials may not be duplicated without the written consent of the course
instructor.




                                                                                                  1
I.   Selected Agents for the Treatment of Depression

     -dopamine-reuptake inhibitor - bupropion (Wellbutrin, Zyban)
     -depression, smoking cessation
     -increased risk for seizures; alcohol lowers seizure threshold
     -risk for emergent hypertension *take BP on patients using this drug

     -monoamine oxidase inhibitors (MAOIs)
              -isocarboxazid (Marplan)
              -phenelzine (Nardil)
              -selegiline (Atapryl, Eldepryl, Selpak)
              -tranylcypromine (Parnate)
     -atypical, non-endogenous or neurotic depression
     -depression associated with Parkinson’s disease
     -investigational for ADHD, Alzheimer’s, Schizophrenia
     -post-traumatic stress disorder *take BP on patients using these drugs

     -selective serotonin reuptake inhibitors (SSRIs)
              -citalopram (Celexa)
              -escitalopram oxalate (Lexapro)
              -fluoxetine (Prozac, Sarafem)
              -paroxetine (Paxil)
              -sertraline (Zoloft)
     -over 15 approved indications
     -depression, geriatric depression, generalized anxiety disorder, social phobias, social anxiety
     disorders, diabetic neuropathies, anorexia, bulimia, premenstrual syndrome, obsessive
     compulsive disorder (OCD), panic attacks/disorders
     *biggest US market sellers: Paxil and Zoloft
     -sertraline (Zoloft) is only drug approved for use in children for OCD

     -recent concerns over whether use of SSRIs in adolescents increases risk for suicide: increased
     number of cases of suicide attempts prompted FDA to require relabeling of these drugs
     -agitation, anxiety, hostility, aggression = known side effects
     -watch for signs of change in depression and related behaviors or any of the above side effects
     during first 6 weeks of therapy: highest risk time period for suicide attempt

             -venlafaxine (Effexor)
             -selective serotonin/norepinephrine reuptake inhibitor
             -depression, anxiety, panic disorder; investigational for OCD, hot flashes, neuropathic
             pain, ADHD
             -raises BP (diastolic) and heart rate *take BP on patients using this drug

     -tetracyclic - maprotiline (Ludiomil)
     -depression, anxiety with depression
     -investigational:bulimia, enuresis, pain, panic attacks, tension headaches, cocaine withdrawal

     -tricyclics (secondary amines)
              -amoxapine (Ascendin)
              -desipramine (Norpramin)
              -nortriptyline (Aventyl, Pamelor)
              -protriptyline (Vivactil)


                                                                                                       2
-treatment of depression in conjunction with psychotherapy
              -adjunctive therapy for chronic pain, peripheral neuropathies
              -investigational for substance-related disorders, ADHD

      -tricyclics (tertiary amines)
               -amitriptyline (Elavil, Vanatrip)
               -clomipramine (Anafranil)
               -doxepin (Sinequan)
               -imipramine (Tofranil)
               -trimipramine (Surmontil)
               -treatment of depression with psychotherapy
               -chronic pain, neuropathic pain, migraines, depression with anxiety
               *take BP on patients using these drugs

      General Adverse Effects
            - orthostatic hypotension
            - sedation
            - dizziness, light-headedness


II.   MAJOR TRANQUILIZERS/ANTIPSYCHOTICS

A.    Pharmacology and Use

      -Older term: neuroleptic drugs
      -A chemically diverse but pharmacologically similar class of drugs used to treat a variety of
      conditions
      -Used in the treatment of:
          -Psychotic disorders – Schizophrenia, paranoia
          -Acute delirium and dementia
          -Manic episodes during induction of lithium
          -Movement disorders – Huntington’ disease, Tourette’s syndrome, ballismus
          -Intractable hiccups
          -Severe nausea and vomiting

      -Individual drugs bind to a variety of receptors and act as antagonists:
          -dopaminergic, alpha1 and alpha2 adrenergic, serotonergic (5-HT), muscarinic,
          H1 histamine, sigma opioid

      -Blockade of dopaminergic transmission in various areas of brain is thought to be responsible for
      their major effects
          -Antipsychotic action = blockage in prefrontal cortex and limbic areas
          -Extrapyramidal side effects = blockade in basal ganglia
          -Antiemetic effects = blockade in chemoreceptor trigger zone of the medulla

      -All antipsychotics have high therapeutic index
      -Not addictive




                                                                                                      3
B.     Side Effects

       -Extrapyramidal side effects:
           Parkinsonism – akinesia (difficulties in initiating movement), tremor, rigidity
           Caused by blockade of D2 receptors in basal ganglia
       -Akathisia = restless legs syndrome; Caused by D2 receptor blockage in basal ganglia
       -Dystonia – sustained muscular contraction
       -Tardive Dyskinesia – abnormal movements, particularly of face and tongue, but may also be of
       trunk and limbs
           -Noticeable after at least 6 months of chronic treatment
           - begins with spastic, thrusting tongue movement, body restlessness, changes in HR &
           respiration
       *Most extrapyramidal side effects are treatable with anticholinergic drugs

       Sedation and autonomic side effects are caused by blockade of histamine, cholinergic and
       adrenergic receptors
           -orthostatic hypotension
           -blurred vision
           -dry mouth
           -nasal congestion
           -constipation
           -urinary retention

C.     Drug Interactions of Significance to Dentistry

       -Antipsychotics potentiate the actions of
          -sedatives
          -analgesics
          -antihistamines
       -Antipsychotics potentiate the respiratory depression caused by opioids
       -Antacids = decrease absorption of antipsychotics
       -Anticonvulsants = decrease plasma levels of antipsychotics
       -Antipsychotics may alter efficacy of antihypertensive medications
               *monitor vital signs



TYPICAL ANTIPSYCHOTICS                              ATYPICAL ANTIPSYCHOTICS
chlorpromazine (Thorazine) = Schizophrenia,         aripiprazole (Abilify) = Commonly used agent in
nausea/vomiting, intractable hiccups,               schizophrenia, treatment and stabilization of
combativeness                                       bipolar disorder
                                                    -Low risk of EPS
                                                    -Does not cause as much weight gain as other
                                                    antipsychotics, but may be less effective than
                                                    others
fluphenazine (Prolixin) = management of             clozapine (Clozaril) = Schizophrenia; severe OCD,
psychotic disorders and schizophrenia; improves     childhood psychosis, attempted suicide, substance
outcomes in patients with psychoses who are         abuse recovery
nonadherent with oral antipsychotics                Side effect: agranulocytosis – susceptibility to
                                                    infection, hypersalivation (others cause
                                                    xerostomia), weight gain, reduced risk of EPS


                                                                                                       4
haloperidol (Haldol)                                 olanzapine (Zyprexa) = Schizophrenia, bipolar
RX for schizophrenia and Tourette’s; severe          disorder, acute agitation
behavioral problems in children
-EPS of TMJ
pimozide (Orap) = suppression of severe motor and    olanzapine and fluoxetine (Symbyax) = treatment
phonic tics with Tourette’s                          of depressive episodes associated with bipolar
-prolongs QT interval: consult physician prior to    disorder
administering vasoconstrictor
prochlorperazine (Compro, Compazine) =               paliperidone (Invega) = Schizophrenia
antiemetic; psychosis, anxiety
-EPS side effect: torticollis (neck muscle spasm)
promethazine (Phenadoz, Phenergan,                   quetiapine (Seroquel) = Schizophrenia, acute
Promethegan) = antiemetic, antihistamine,            manic episodes and/or depressive episodes with
sedative, motion sickness, post-operative pain,      bipolar disorder (monotherapy or with lithium)
anesthetic
-EPS side effect: tardive dyskinesia, Parkinson’s
syndrome, akathisia is most common in elderly
patients
thiothixene (Navane) = psychotic disorders in        risperdone (Risperdal) = Commonly used agent in
children, rapid tranquilization of agitated child;   schizophrenia, acute mania and/or
patients with dementia                               irritability/aggression with bipolar disorder,
-prolongs QT interval: consult physician prior to    behavioral problems with dementia, Tourette’s
administering vasoconstrictor
                                                     ziprasidone (Geodon) = schizophrenia, acute manic
                                                     or mixed episodes with bipolar disorder with or
                                                     without psychosis, acute agitation with
                                                     schizophrenia
                                                     -prolongs QT interval: consult physician prior to
                                                     administering vasoconstrictor


Why are Cholinesterase Inhibitors typically used?

   •   Indirect-Acting Cholinergic Drugs
   •   Also known as “cholinesterase inhibitors”
   •   These drugs stop the breakdown of acetylcholine (via cholinesterase), which allows for the
       concentration of acetylcholine to build up = acetylcholine remains active and stimulates the
       PANS
   •   These drugs produce PANS stimulation
   •   Dementia with Alzheimer’s disease
   •   Investigational for mild to moderate dementia with Parkinson’s disease
   •   Examples:
           o donepezil (Aricept)
           o rivastigmine (Exelon)
           o galantamine (Razadyne)

Side Effects of Direct-Acting and Indirect-Acting Cholinergic Drugs
    • nausea, vomiting, diarrhea (by increasing GI activity)
    • salivation, sweating (increased gland secretions)
    • bronchoconstriction


                                                                                                       5
•   constricted pupils
       •   Paralysis at high doses (effect at neuromuscular junction)
       •   CNS = confusion

Anticholinergic Drugs for Parkinson’s Disease

       •   benztropine (Cogentin)
       •   trihexyhenidyl (not in U.S.; Canadian drug)

Anticholinergic Drugs (Parasympatholytics)

       •   Prevent the action of acetylcholine at the postganglionic PANS nerve endings
       •   “blocker” drugs or antagonists
       •   Block the receptor site for acetylcholine
       •   Do not prevent release of ACH
       •   Acetylcholine cannot act on receptors in smooth muscle, glands or the heart
       •   Also called antimuscarinic drugs (block muscarinic receptors but not nicotinic receptors)

Pharmacologic Effects of Anticholinergic Drugs

       •   Reduce PANS activity
              o Skin = decrease sweating
              o GI = decrease salivation, decreased gut motility
              o Urinary tract = urine retention
              o Respiratory = bronchodilation
              o CNS = decreased concentration/memory; sedation; possible hallucinations and coma

Adverse Reactions to Anticholinergic Drugs

       •   Frequently are extensions of their pharmacologic effects
       •   Xerostomia
       •   Blurred vision, photophobia
       •   Tachycardia
       •   Fever
       •   Urinary and GI stasis
       •   Hyperpyrexia (elevated temperature)
       •   Hot, dry flushed skin (lack of sweating)
       •   Toxicity = CNS excitation = delirium, hallucinations, convulsions, respiratory depression


III.       ORAL HEALTH CONSIDERATIONS FOR NEUROPSYCHIATRIC CONDITIONS

           - most neuropsychiatric medications cause xerostomia
                    -watch for opportunistic infections
                    -loss of protective effects: viral, fungal, bacterial infections
                    -traumatic aphthous ulcers
           - lack of interest in performing daily self-care
           - increased demineralization, caries and gingival disease
           - lack of interest/motivation to seek treatment



                                                                                                       6
- caution with epinephrine = Monitor vital signs!
              -use vasoconstrictors cautiously with all classes of antidepressants except SSRIs
              -tricyclics and monoamine oxidase inhibitors
              -venlafaxine (Effexor) – depression, anxiety, OCD, ADHD
              --all drugs for ADHD
              -some antipsychotics = consult drug reference guide
      -SSRIs = bruxism: increased extrapyramidal effects
                       -burning mouth syndrome = observed in depression and anxiety; tricyclics

IV.   PEPTIC ULCER DISEASE

1.    Incidence and Prevalence
      -among most common human ailments
      -peak prevalence occurs in young adulthood (age 30 to 50 years)
              -first degree relatives have threefold higher risk
              -higher prevalence seen among:
                       -smokers
                       -heavy drinkers
                       -hyperparathyroidism
                       -renal dialysis patients
                       -use of NSAIDS for longer than 1 month
              -death (from complications) of disease occur in elderly
2.    Etiology
      -primary aggressive factor: Helicobacter pylori infection
      -present in more than 90% of cases
      -contributing factors:
              -acid hypersecretion
              -cigarette smoking
              -psychological and physical stress – increases acid secretion
              -use of NSAIDS for longer than 1 month
              -NSAID-induced ulcers occur more often in stomach than duodenum
              -concomitant use of aspirin, alcohol, corticosteroids and anticoagulants increases
              risk
                       -obsessive compulsive disorder – increases acid secretion
                       -caffeine – increases acid secretion
                       -alcohol – alters cell permeability, leads to cell death = injures mucosa
3.    Treatment
             -if ulcer is confined and uncomplicated: antisecretory drugs
             -if H pylori is present: antisecretory drugs with antimicrobials
             -combination therapy is used:
                      -tetracycline and metronidazole or amoxicillin and clarithromycin
                      with proton-pump inhibitor or bismuth subsalicylate (Pepto-Bismol)
             -treatment lasts for 2 weeks
             -modification of factors that contribute to ulceration




                                                                                                   7
Medications

     - OTC antacids
     - weak bases that interact with stomach acid to form water and salt; raise gastric pH
     - composition: aluminum hydroxide, magnesium hydroxide, calcium carbonate

     - Histamine H2 receptor antagonists
     - OTC meds used to manage symptoms of heartburn, acid indigestion, benign gastric and
      duodenal ulcers, GERD, hypersecretory conditions and erosive esophagitis
     - cimetidine (Tagamet), famotidine (Pepcid), nizatidine (Axid) and ranitidine
       hydrochloride (Zantac)

     - Proton pump inhibitors
     - bind to H+/K+-ATPase enzyme system (proton pump) in parietal cells which reduces
       acid secretion
     - reduce gastric secretions, neutralize gastric acid after release, protect gastric mucosa
       from damage
     -chronic use is linked to stomach cancer
     -associated with osteoporosis and risk for hip fracture
     - esomeprazole (Nexium), lansoprazole (Prevacid), omeprazole (Prilosec),
       pantoprazole (Protonix), esomeprazole (Nexium), rabeprazole (Aciphex)

4.   Dental Considerations
              -thorough medical history review for risk factors and symptoms
              -avoid prescribing: aspirin, aspirin-containing products, NSAIDS
                       -use acetaminophen (Tylenol)
                       -Cox-2 inhibitors (Celebrex)
              -H2 receptor blockers like cimetidine (Tagament) decrease the metabolism of
               many drugs:
                       -diazepam, lidocaine (adjust dosage)
              -H pylori is found in dental plaque = reservoir for infection/reinfection
                       -good oral hygiene; frequent scaling and root planing
              -use of antibiotics = Candidiasis will require antifungal therapy
              -oral manifestations of peptic ulcer disease:
                       -vascular malformations of lip (macules, venous pool)
                       -enamel erosion
              -GI medications:
                       -taste alteration
                       -blood dyscrasias = increased risk for infections, bleeding
                       -xerostomia
     - OTC antacids bind to other meds in the stomach = antacids and tetracycline
     - OTC antacids alter absorption, bioavailability and elimination of many drugs
              - wait 2 hours before/after taking antacids before taking other meds
     - histamine H2 receptor antagonists and proton pump inhibitors decrease the availability
       of azole antifungals
     - Tagamet and Zantac alter effects of warfarin
     - Tagamet increases serum concentrations of some benzodiazepines, lidocaine and the
        quinolone antibiotics




                                                                                                  8
DRUG                                      ORAL SIDE EFFECTS
 omeprazole (Prilosec®)                    xerostomia, taste alteration, esophageal
                                           candidiasis, pharyngeal pain
 pantoprazole (Protonix®)                  xerostomia, taste alteration, pharyngitis, increased
                                           cough, aphthous stomatitis, gingivitis, glossitis,
                                           halitosis, oral moniliasis, tongue discoloration,
                                           herpes simplex, erythema multiforme
 nizatidine (Axid®)                        xerostomia, laryngeal edema
 ranitidine bismuth citrate (Tritec®)      taste alteration, darkening of tongue
 ranitidine hydrochloride (Zantac®)        erythema multiforme
 rabeprazole (Aciphex™)                    xerostomia, mouth ulcerations
 esomeprazole (Nexium™)                    xerostomia, ulcerative stomatitis, taste loss
Oral side effects associated with gastrointestinal medications

V.        CARDIOVASCULAR DISEASE

DRUGS THAT ALTER BLEEDING

ANTIPLATELET MEDICATIONS

          -aspirin = antiplatelet drug
          -blocks cyclo-oxygenase, an enzyme associated with clot formation
          -inhibits platelet aggregation
          -prevents thrombus formation on atherosclerotic plaques
          -lowers risk of MI in those with increased risk for atherosclerosis/thrombogenesis
          -lowers risk of MI and stroke in those with previous history of MI and stroke, unstable angina,
          post-coronary artery bypass grafting
          -one enteric coated 325 mg tablet of aspirin daily or 81 mg low dose aspirin

Sudden Discontinuation of Aspirin

     Discontinuing the use of aspirin increases mortality risk 1
     Large clinical trial (n=1358) with hospitalized patients with an acute coronary syndrome 2
             3 groups: never taken an oral antiplatelet agent (n=930), Hx of prior use (n=355), recently
             discontinued use (n=73)
             Among recently discontinued aspirin group, mostly due to physician recommendation prior to
             surgery, there was a higher 30 day rate of death or MI and adverse bleedings than among
             prior users
             No difference in the incidence of death or MI at 30 days between nonusers and prior users.
             Recent withdrawal displayed worse clinical outcomes than nonusers.

     1.   Ho PM, Spertus JA, Masoudi FA, et al. Impact of medication therapy discontinuation on mortality after myocardial
          infarction. Arch Intern Med. 2006 Sep 25;166(17):1842-7.
     2.   Collet JP, Montalscot G, Blanchet B, et al. Impact of prior use or recent withdrawal of oral antiplatelet agents on acute
          coronary syndromes. Circulation. 2004 Oct 19;110(16):2361-7. Epub 2004 Oct 11.



     A meta-analysis reviewing data from over 50,000 patients showed that aspirin non-
     adherence/withdrawal was associated with a three-fold higher risk for major adverse cardiac events. 3
     Risk was even greater among patients with coronary stents.
            Risk was amplified by a factor of 89 in patient who had undergone stenting.


                                                                                                                                 9
3. Biondi-Zoccai GG, Lotrionte M, Agostoni P, et al. A systematic review and meta-analysis on the hazards of discontinuing or
not adhering to aspirin among 50,279 patients at risk for coronary artery disease. Eur Heart J. 2006 Nov;27(22):2667-74. Epub
2006 Oct 19.



other anti-platelet medications:

         aspirin and dipyridamole (Aggrenox)
         cilostazole (Pletal)

    ticlopidine (Ticlid) – used for those who are intolerant to aspirin, when aspirin therapy has failed,
    and coronary stent implantation
         Lowers risk of stent thrombosis
         Low risk of bleeding complications compared to other strategies

    clopidogrel (Plavix)
        Replaced use of ticlopidine
        Lower rates of major adverse cardiac events and mortality compared with ticlopidine
        Better safety-tolerability profile
            Lower risk of neutropenia
        Indications: reduce rate of TE (MI, stroke, vascular death) in patients with recent MI or stroke;
        reduce rate of TE in patients with unstable angina managed medically or with PCI (with or
        without stents); reduces rate of death and TE in patients with ST-Sement elevation MI managed
        medically
        Dosing: 300 mg loading dose; 75 mg daily (with aspirin 81-325 mg daily)
        Problems:
            Drug interactions
            Slow onset of action
            Wide variability in patient response
                     Includes “no” response

    prasugrel (Effient) *new drug approved in July 2009
       Approved for patients with acute coronary syndromes undergoing PCI
       Indications: Reduces rate of thrombotic cardiovascular events (eg, stent thrombosis) in patients
       with unstable angina, non-ST-segment elevation MI, or ST-elevation MI (STEMI) managed with
       percutaneous coronary intervention
       Loading dose of 60 mg followed by maintenance dose of 10 mg
       Manufacturer labeling states to also take 75-325 mg aspirin once daily upon recommendation of
       provider

    clopidogrel (Plavix) and prasugrel (Effient)
        Prodrugs
        Noncompetitive antagonists of P2Y12 receptor
        Inhibit ability of adenosine diphosphate (ADP) to induce platelet aggregation and decreases
        subsequent platelet aggregation
        Block receptor for the life of the platelet = irreversible effect
        action is independent of and additive to aspirin

Prevention of premature discontinuation of dual antiplatelet therapy
in patients with coronary artery stents: a science advisory from the
American Heart Association, American College of Cardiology, Society

                                                                                                                           10
for Cardiovascular Angiography and Interventions, American College
of Surgeons, and American Dental Association, with representation
from the American College of Physicians.
Grines CL, Bonow RO, Casey DE Jr, Gardner TJ, Lockhart PB, Moliterno DJ, O'Gara P, Whitlow P; American
Heart Association; American College of Cardiology; Society for Cardiovascular Angiography and Interventions;
American College of Surgeons; American Dental Association; American College of Physicians. William Beaumont
Hospital, Royal Oak, Michigan, USA. J Am Dent Assoc. 2007 May;138(5):652-5.


Abstract
BACKGROUND: and Overview. Dual antiplatelet therapy with aspirin and a thienopyridine has been
shown to reduce cardiac events after coronary stenting. However, many patients and health care providers
prematurely discontinue dual antiplatelet therapy, which greatly increases the risk of stent thrombosis,
myocardial infarction and death. CONCLUSIONS AND CLINICAL IMPLICATIONS: This advisory
stresses the importance of 12 months of dual antiplatelet therapy after placement of a drug-eluting stent
and educating patients and health care providers about hazards of premature discontinuation. It also
recommends postponing elective surgery for one year, and if surgery cannot be deferred, considering the
continuation of aspirin during the perioperative period in high-risk patients with drug-eluting stents.
PMID: 17473044
*Link to download free full text copy: http://jada.ada.org/cgi/content/full/138/5/652
3 Recommendations from Advisory Statement (listed above):

    Those concerned about peri/postprocedural bleeding must be aware of catastrophic risks of premature
    discontinuation
        -Consult cardiologist to discuss optimal patient management strategies

    Elective procedures with significant risk of peri/postoperative bleeding should be deferred until
    patient has completed an appropriate course of thienopyridine therapy:
        -12 months after DES implantation if they are not at high risk of bleeding
        -Minimum of one month for bare-metal stent implantation

    Patients with DES who are to undergo subsequent procedures that mandate discontinuation of drug
    therapy, aspirin should be continued if at all possible
        -Restart thienopyridine as soon as possible after the procedure because of concerns of late stent
        thrombosis

platelet glycoprotein IIb/IIIa receptor antagonists (fibrinogen receptor inhibitors):

        -used in combination with aspirin and heparin to treat unstable angina
        -decrease the incidence of death and MI
        -inhibit final common pathway involved in adhesion, activation, aggregation
        abciximab (ReoPro)
        eptifibatide (Integrilin)
        tirofiban (Aggrastat)




                                                                                                            11
NSAIDS

Ibuprofen has a very short half-life (2-4 hours)

    Withhold for 4-6 half-lives prior to invasive dental surgical procedures (about 1 day prior to
    treatment)

Cause bleeding as a side effect, especially GI bleeding

FDA Black Box Warning: NSAIDs are associated with an increased risk of adverse
cardiovascular thrombotic events, including fatal MI and stroke.


   In 2006, the FDA issued an informational statement to healthcare professionals stating
that “ibuprofen can interfere with the anti-platelet effect of low dose aspirin (81 mg per
day), potentially rendering aspirin less effective when used for cardioprotection and
stroke prevention. Healthcare professionals should advise consumers and patients
regarding the appropriate concomitant use of ibuprofen and aspirin.” 1 The concern is
that concurrent use of these medications can increase risk for adverse cardiac events,
and thus, the FDA issued the following considerations:

    •    “Counseling patients about the appropriate timing of ibuprofen dosing if they are also taking
         aspirin for cardioprotective effects.
    •    With occasional use of ibuprofen, there is likely to be minimal risk from any attenuation of the
         antiplatelet effect of low dose aspirin, because of the long-lasting effect of aspirin on platelets.
    •    Patients who use immediate release aspirin (not enteric coated) and take a single dose of
         ibuprofen 400 mg should dose the ibuprofen at least 30 minutes or longer after aspirin ingestion,
         or more than 8 hours before aspirin ingestion to avoid attenuation of aspirin’s effect.
    •    Recommendations about the timing of concomitant use of ibuprofen and enteric-coated low dose
         aspirin cannot be made based upon available data.
    •    Other nonselective OTC NSAIDs should be viewed as having the potential to interfere with the
         antiplatelet effect of low-dose aspirin unless proven otherwise.
    •    Prescribing analgesics that do not interfere with the antiplatelet effect of low dose aspirin for high
         risk populations.” 1

1. U.S. Food and Drug Administration. U. S. Department of Health and Human Services. Information for Healthcare
Professionals: Concomitant Use of Ibuprofen and Aspirin. New Information [9/2006] - Concomitant Use of Ibuprofen and
Aspirin. Available at:
http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm125222.htm

ANTICOAGULANT MEDICATIONS

    •    Antithrombins
            o antithrombin
            o heparin
    •    Coumarin derivatives
            o warfarin (Coumadin, Jantoven)
    •    Thrombin inhibitors
            o argatroban – px/tx of thrombosis with heparin-induced thrombocytopenia (HIT); adjunct
                to PCI if at risk for HIT



                                                                                                                       12
o   bivalirudin (Angiomax) – with ASA for unstable angina receiving PCI; undergoing PCI
            with risk for HIT
        o   dabigatran etexilate (Pradaxa) – thromboprophylaxis for hip/knee replacement
        o   desirudin (Iprivask) – prophylaxis of DVT for hip replacement
        o   fondaparinux (Arixtra) – thromboprophylaxis for hip/knee replacement
        o   lepirudin (Refludan) – anticoagulation with HIT
        o   rivaroxaban (Xarelto) – thromboprophylaxis for hip/knee replacement


ANTITHROMBINS

•   Antithrombin III (Atryn, Thrombate III)
        o given to those with an antithrombin III deficiency
•   Heparin - enhances the inhibition rate of clotting proteases by antithrombin III impairing normal
    hemostasis and inhibition of factor Xa.
•   Low molecular weight heparins - strongly inhibit factor Xa; higher ratio of antifactor Xa to
    antifactor IIa activity than unfractionated heparin.

Heparin
• Naturally-produced anticoagulant (anti-thrombin)
• Synthetic version given by IV
• Indications: prevention and treatment of thromboembolic disorders
• Anticoagulant for dialysis procedures
• Heparin Lock flush used to clear IV lines
• Produces immediate anticoagulation effect
• Patient admitted to hospital is started on heparin and warfarin: heparin produces initial effect

Low Molecular Weight Heparins
• Use: prevention of DVT with or without PE; reduce risk for PE; acute unstable angina; non-Q-
   wave MI
• Mechanism: Inhibit factor Xa and IIa (thrombin)
      o dalteparin (Fragmin)
      o enoxaparin (Lovenox)
      o tinzaparin (Innohep)

Indications for enoxaparin (Lovenox)
• Acute coronary syndromes: Unstable angina, non-ST-elevation, and ST-elevation MI
• DVT prophylaxis: Following hip or knee replacement surgery, abdominal surgery, or in medical
    patients with severely-restricted mobility during acute illness who are at risk for TE
    complications
• DVT treatment (acute): Inpatient treatment (patients with and without PE and outpatient
    treatment (patients without PE)
        o Note: High-risk patients include those with one or more of the following risk factors: >40
             years of age, obesity, general anesthesia lasting >30 minutes, malignancy, history of deep
             vein thrombosis or pulmonary embolism
• Used following hip and knee replacement – at least 10 days and
        o until risk for DVT has subsided or
        o patient is adequately anticoagulated on warfarin




                                                                                                     13
COUMARIN DERIVATIVES

•   warfarin (Coumadin, Jantoven)
•   interferes with liver synthesis of vitamin-K dependent clotting factors
•   effects occurs in 4 to 5 days
•   when patient is admitted to hospital with stroke, there is a 1 to 2 day overlap period with heparin
    following warfarin administration to prevent hypercoagulable state
        o Heparin produces immediate effect
        o Takes 4-5 days for effects of warfarin to occur
•   Indications for warfarin:
        o Prophylaxis and treatment of TE disorders (venous and pulmonary) and embolic
             complications that arise from atrial fibrillation or cardiac valve replacement
        o Adjunct to reduce risk of systemic embolism (recurrent MI, stroke) after MI
•   Investigational: prevention of recurrent TIA
•   Many things can upset a patient’s level of anticoagulation from warfarin:
        o Fever
        o Flu
        o Diarrhea or vomiting
        o Use of many drugs, including antibiotics
        o Change in diet (consumption of green leafy vegetables increases vitamin K intake =
             promotes clotting)
                     Need vitamin K to synthesize clotting factors in liver
                     Warfarin shuts off production of these clotting factors


**Key messages: warfarin causes the greatest number of drug interactions
      o Always check compatibility prior to issuing a prescription
      o Always ask about the INR and monitor INR status across time to examine trends in
          anticoagulation control

THROMBIN INHIBITORS

dabigatran (Pradaxa)
• FDA approved October 2010
• Thrombin inhibitor
• Prodrug = lacks anticoagulant activity
         o converted in vivo to active dabigatran
• specific, reversible, direct thrombin inhibitor that inhibits both free and fibrin-bound thrombin
• prevents thrombin-mediated effects, and by inhibiting thrombin-induced platelet aggregation
• Dabigatran inhibits coagulation by preventing thrombin-mediated effects, including cleavage of
    fibrinogen to fibrin monomers, activation of factors V, VIII, XI, and XIII
• Indications:
• Prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation
• Postoperative thromboprophylaxis after total hip or knee replacement
         o Knee replacement – up to 10 days
         o Hip replacement – up to 35 days
• compared to warfarin (Coumadin)
• advantages: no monthly monitoring; fewer drug-drug and drug-diet interactions
• disadvantages: very expensive; twice daily dosing



                                                                                                      14
•   in studies, patients who took Pradaxa had fewer strokes than those taking warfarin
         o RE-LY trial = Randomized Evaluation of Long-Term Anticoagulation Therapy
•   adverse effects: bleeding, GI effects


Indications for Direct Antithrombins (Thrombin Inhibitors)
• Prevent/reduce ischemia with unstable angina
• Prevent DVT following hip replacement
• Prevent/treat thromboembolism
• Treatment of heparin-induced thrombocytopenia (HIT)

rivaroxaban (Xarelto) (riv a ROX a ban)
• New drug – FDA approval announced July 1, 2011
• First and only oral anticoagulant approved in US for orthopedic surgery
• Factor Xa inhibitor
• Mechanism: inhibits platelet activation and fibrin clot formation via direct, selective, and
    reversible inhibition of factor Xa in both the intrinsic and extrinsic coagulation pathways
• Indications:
        o Postoperative thromboprophylaxis in patients who have undergone hip or knee
            replacement surgery
• Adults: Postoperative thromboprophylaxis:
        o Knee replacement: 10 mg once daily; recommended total duration of therapy: 12-14 days
        o Hip replacement: 10 mg once daily; total duration of therapy: 35 days


fondaparinux (Arixtra) (fon da PARE i nuks)
• Factor Xa inhibitor
       o causes an antithrombin III-mediated selective inhibition of factor Xa
• Interrupts the blood coagulation cascade and inhibits thrombin formation and thrombus
    development
• Indications:
• Prophylaxis of deep vein thrombosis (DVT) in patients undergoing surgery for hip replacement
    and knee replacement
• hip fracture (including extended prophylaxis following hip fracture surgery)
• abdominal surgery (in patients at risk for thromboembolic complications)
• treatment of acute pulmonary embolism (PE)
• treatment of acute DVT without PE
• Usual duration: 5-9 days
       o up to 10 days following abdominal surgery
       o up to 11 days following hip replacement or knee replacement
• Extended prophylaxis is recommended following hip fracture surgery
       o has been tolerated for up to 32 days total
• Acute DVT/PE treatment:
       o Note: Start warfarin on the first treatment day and continue fondaparinux until INR is
           between 2 and 3 (usually 5-7 days) (Hirsh, 2008)




                                                                                              15
COMMON ORAL PROBLEMS IN ELDERLY PATIENTS

Disease or Drug Induced Xerostomia

         Caries and Demineralization           Tooth Sensitivity
         Periodontal Disease                   Fungal Infections
         Viral Infections                      Pain and Ulcerations
         Food Packing/Decreased Oral Clearance

Oral signs and symptoms associated with drug-induced xerostomia

Caries                                        Enamel demineralization
Enamel erosion                                Cemental abrasion on exposed root surfaces
Dentinal hypersensitivity                     Increased gingivitis and periodontal infection
Opportunistic infections                      Increased viral infections
Oral ulcerations/stomatitis                   Taste alteration
Dry, cracked, bleeding lips                   Fissured, sore tongue
Angular cheilitis                             Friable oral mucosa
Difficulty speaking, chewing,                 Difficulty wearing dentures or appliances
swallowing


Drug classes that produce neural effects on the salivary glands

The following are examples of anticholinergic drugs that reduce the volume of serous saliva:


Antidepressants            Antiemetics        Antihistamines              Antihypertensives
Anti-parkinsonian drugs              Antipsychotics              Antispasmodics


The following are examples of sympathomimetic drugs that produce a viscous, mucinous saliva:


Amphetamines               Appetite suppressants
Bronchodilators            Decongestants


Sources: Sreeby LM, Schwartz SS: A reference guide to drugs and dry mouth, 2nd ed, Gerodontol 14:33-47, 1997;Porter SR,
Scully C, Hegarty AM: An update of the etiology and management of xerostomia, Oral Surg Oral Med Oral Pathol Pral Radiol
Endod 97:28-46, 2004; Nähri TO, Meurman JH, Ainamo A: Xerostomia and hyposalivation: causes, consequences and
treatment in the elderly, Drugs & Aging 15:103-116, 1999.



Drug classes associated with causing xerostomia
Antiacne agents                      Antianxiety agents          Anticholinergics/Antispasmodics
Anticonvulsants                      Antidepressants             Antidiarrheals
Antiemetics                          Antihistamines              Antihypertensives
Anti-inflammatory analgesics         Antinauseants               Anti-parkinsonian agents



                                                                                                                      16
Antipsychotics                        Anorexiants                 Bronchodilators
Decongestants                         Diuretics                   Muscle Relaxants
Narcotic Analgesics                   Sedatives


Source: USP DI® Drug Information for the Healthcare Professional, vol 1, ed. 24, Englewood, CO, Micromedix, Inc., 2004.


Taste and Smell Disorders

Drugs that alter taste
Alcohol detoxification agents                            Alzheimer’s medications
Analgesics (NSAIDS)                                      Anesthetics (general and local)
Anorexiants                                              Antacids
Antianxiety agents                                       Antiarthritics
Anticholinergics                                         Anticonvulsants
Antidepressants                                          Antidiabetics (oral hypoglycemics)
Antidiarrheals                                           Antiemetics
Antifungals                                              Antigout medications
Antihistamine (H1) antagonists                           Antihistamine (H2) antagonists
Antihyperlipidemics                                      Antiinfectives
Anti-inflammatory/antiarthritics                         Antimigraine agents
Antiparkinson agents                                     Antipsychotics
Antithyroid medications                                  Antivirals
Anxiolytics/sedatives                                    Asthma preventives
Bronchodilators                                          Calcium-affecting drugs
Cancer chemotherapeutics                                 Cardiovascular medications
CNS stimulants                                           Decongestants
Diuretics                                                Glucocorticoids
Gallstone solubilization agents                          Hemorheologics
Immunomodulators                                         Immunosuppressants
Irritable bowel syndrome medications                     Methylxanthines
Nicotine replacement drugs                               Ophthalmics
Proton pump inhibitors                                   Retinoids, systemic
Salivary stimulants                                      Skeletal muscle relaxants
Vitamins


Source: Gage TW, Pickett FA: Mosby’s dental drug reference, ed. 7, St. Louis, 2005, Elsevier Mosby.




                                                                                                                          17
Systemic drugs associated with lichenoid drug reactions
Category                                 Agents
Analgesic agents                         NSAIDs, propoxyphene/acetaminophen, acetaminophen/codeine
Antianxiety drugs                        benzodiazepines
Antiarrhythmics                          quinidine
Anticonvulsant drugs                     Depakote
Antineoplastic drugs                     levamisole
Cardiovascular agents                    Beta-adrenergic blockers, angiotensin II antagonist, calcium
                                         channel blockers, cardiac glycoside, methyldopa, thiazide
                                         diuretics, potassium supplements
Gastric acid secretion inhibitors H2-antagonists
Hormone replacement                      Thyroid hormone, insulin, sulfonylureas, metformin, oral
                                         contraceptives, estrogen, progesterone
Photographic Dyes
Uricosuric agent                         Allopurinol




                                                                                                        18
COURSE TITLE:                 Commonly Prescribed Medications and
                              Managing the Oral Side Effects of Medication Use

COURSE INSTRUCTOR: Ann Eshenaur Spolarich, RDH, PhD

COURSE CREDITS:               3 Hours

COURSE DATE:            February 21, 2013
________________________________________________________________________
COURSE DESCRIPTION:

The purpose of this course is to review the 20 most commonly prescribed medications taken by
clients treated in the oral health care environment. In addition, drug interactions, popular drugs
in the media and new drugs in dentistry will be discussed. A comprehensive review of drugs and
dental care products used to manage the oral side effects of medications will be presented.


LEARNING OBJECTIVES:

Upon completion of this continuing education course, the participant will be able to:

1.     Identify and discuss commonly prescribed medications taken by clients treated in the oral
       health care setting.

2.     Identify common drug interactions of significance to dental professionals.

3.     List several new dental drugs and discuss their indications for use in practice.

4.     Discuss the management of oral side effects caused by medications.




*This material may not be reproduced without the written permission of the author.




                                                                                                 1
TOP 20 MOST COMMONLY PRESCRIBED MEDS
                                  2011
                    (Total Prescriptions Dispensed)
1. hydrocodone and acetaminophen                 2. hydrocodone and acetaminophen
3. levothyroxine sodium                          4. lisinopril
5. Lipitor                                       6. simvastatin
7. Plavix                                        8. Singulair
9. azithromycin                                  10. Crestor
11. Nexium                                       12. levothyroxine sodium
13. metoprolol tartrate                          14. hydrocodone and acetaminophen
15. Synthroid                                    16. Lexapro
17. Proair HFA                                   18. ibuprofen
19. trazodone HCl                                20. amoxicillin


INDICATIONS                                       DRUGS
pain relievers                                    hydrocodone and acetaminophen,
                                                  ibuprofen
hypercholesterolemia                              Lipitor, simvastatin, Crestor
hypertension                                      lisinopril, metoprolol
adverse thromboembolic events                     Plavix
endocrine disorders                               levothyroxine, Synthroid
antibiotics                                       amoxicillin, azithromycin
antidepressants                                   Lexapro, trazodone
GERD, reflux or hypersecretory disease            Nexium
respiratory disease                               Singulair, ProAir HFA


PAIN RELIEVERS

BRAND NAME: Co-Gesic, hycet, Lorcet, Lortab, Margesic, Maxidone, Norco, Stagesic, Vicodin, Xodol,
Zamicet, Zydone
GENERIC NAME: HYCD/APAP (hydrocodone with acetaminophen)
THERAPEUTIC CATEGORY: opioid analgesic
USE: post-operative pain control
ORAL COMPLICATIONS: xerostomia (rare)
DRUG INTERACTIONS: Concurrent use of hydrocodone with MAO inhibitors (Nardil, Parnate,
Marplan), tricyclic antidepressants (Elavil) and general anesthetics potentiates the effects of the
hydrocodone, and increases the risk for toxicity. Dextroamphetamine enhances the analgesic effect of the
hydrocodone. Additive CNS effects may occur when taking hydrocodone with other narcotics,
antipsychotics, antianxiety agents, general anesthetics and other CNS depressants (eg. alcohol).
Phenothiazines (eg. Thorazine) may decrease the analgesic effect of hydrocodone. Acetaminophen taken
with alcohol, barbituates or carbamazepine (Tegretol) increases the risk for liver toxicity. Chronic use of
acetaminophen may significantly enhance the anticoagulation effects of warfarin (Coumadin).




                                                                                                         2
BRAND NAME: Caldolor, Ibu, Motrin
GENERIC NAME: ibuprofen
THERAPEUTIC CATEGORY: NSAID
USE: management of mild to moderate pain; inflammatory diseases and rheumatoid disorders, fever,
dysmenorrhea
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: Ibuprofen and other non-selective NSAIDS can interfere with the antiplatelet
and cardioprotective effects of aspirin: follow appropriate timing of dosing. Avoid use in aspirin-allergic
patients. Ibuprofen may increase the levels of anticoagulants, antiplatelet drugs, bisphosphonates,
cyclosporine, digoxin, haloperidol, lithium, methotrexate, NSAIDS, potassium-sparing diuretics,
quinolone antibiotics, salicylates, thrombolytic agents, vancomycin and vitamin K antagonists. Levels of
ibuprofen may be increased by ACE inhibitors, angiotensin II receptor blockers, antidepressants
(tricyclic, teriary amine), systemic corticosteroids, glucosamine, herbs that have anticoagulant or
antiplatelet properties, NSAIDS, probenecid, SSRIs, serotonin/norepinephrine reuptake inhibitors.
Ibuprofen may decrease the levels of ACE inhibitors, angiotensin II receptor blockers, antiplatelet agents,
beta blockers, loop diuretics, potassium-sparing diuretics, salicylates and thiazide diuretics. Levels of
ibuprofen may be decreased by bile acid sequestrants, NSAIDS and salicylates. Avoid alcohol.

HYPERCHOLESTEROLEMIA

BRAND NAME: Lipitor
GENERIC NAME: atorvastatin
THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor
USE: hypercholesterolemia
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: The risk for myopathy/rhabdomyolysis is increased with concurrent use of the
macrolide antibiotics clarithromycin and erythromycin, and the azole antifungal agents fluconazole
(Diflucan), itraconazole (Sporanox) and ketoconazole (Nizoral). Risk for rhabdomyolysis also may be
increased with concurrent use of other lipid lowering agents, cyclosporoine, certain calcium channel
blockers (diltiazem (Cardizem), verapamil (Calan)) and protease inhibitors. Atorvastatin may also
increase the effect of levothyroxine (Synthroid).

BRAND NAME: Zocor
GENERIC NAME: simvastatin
THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor
USE: hypercholesterolemia
ORAL COMPLICATIONS: taste alteration
DRUG INTERACTIONS: The risk for myopathy/rhabdomyolysis is increased with concurrent use of the
macrolide antibiotics clarithromycin and erythromycin, and the azole antifungal agents fluconazole,
itraconazole and ketoconazole. Risk for rhabdomyolysis also may be increased with concurrent use of
other lipid lowering agents, cyclosporoine, certain calcium channel blockers and protease inhibitors. The
anticoagulant effect of warfarin may be increased by simvastatin.

BRAND NAME: Crestor
GENERIC NAME: rosuvastatin calcium
THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor
USE: used with dietary therapy for hyperlipidemias to reduce elevated total cholesterol, LDL-C,
apolipoprotein B and triglycerides in patients with hypercholesterolemia and for treatment of familial
hypercholesterolemia
ORAL COMPLICATIONS: none



                                                                                                          3
DRUG INTERACTIONS: The anticoagulant effects of warfarin may be increased by rosuvastatin:
monitor carefully. Rosuvastatin increases the serum concentrations of the hormonal contraceptives
ethinyl estradiol and norgestrel. Concurrent administration of other cholesterol lowering medications
(gemfibrozil, clofibrate, fenofibrate or niacin) may increase the risk for myopathy and rhabdomyolysis.
Metal containing antacids may decrease the plasma concentratins of rosuvastatin: administer antacids at
least 2 hours after dosing. Bile acid sequestrants may reduce the absorption of rosuvastatin.

HYPERTENSION

BRAND NAME: Prinivil, Zestril
GENERIC NAME: lisinopril
THERAPEUTIC CATEGORY: ACE inhibitor
USE: hypertension, adjunctive therapy for congestive heart failure, post-MI if hemodynamically stable
ORAL COMPLICATIONS: xerostomia, dry cough, angioedema
DRUG INTERACTIONS: Increased risk for hypotension with alcohol, phenothiazines
(antipsychotics)and probenecid. ACE inhibitors increase serum concentrations of digoxin, lithium and
sulfonylureas (oral hypoglycemics). Increased risk for toxicity with potassium or potassium-sparing
diuretics. Diuretics have additive hypotensive effects when used with ACE inhibitors. Caution when
using NSAIDS in patients with compromised renal function who are taking ACE inhibitors. NSAIDS,
including high dose aspirin, may decrease the antihypertensive effects of ACE inhibitors. Antacids
decrease the bioavailability of ACE inhibitors.

BRAND NAME: Toprol-XL
GENERIC NAME: metoprolol succinate
THERAPEUTIC CATEGORY: cardioselective beta blocker
USE: hypertension, angina, prevention of MI, atrial fibrillation; investigational for ventricular
arrhythmias, migraines, essential tremors, aggressive behavior
ORAL COMPLICATIONS: xerostomia
DRUG INTERACTIONS: Metoprolol may increase the effects of other drugs that slow AV conduction,
alpha-blockers and alpha-adrenergic stimulants (eg. epinephrine). Epinephrine is safe to use in patients
taking cardioselective beta blockers (lowest dose, least concentration). NSAIDS (ibuprofen,
indomethacin) used for greater than 3 weeks can decrease the antihypertensive effects of the drug. The
effects of beta blockers are decreased with aluminum salts, calcium salts, barbituates, bile acid
sequestrants (cholesterol-lowering drugs), NSAIDS, penicillins, rifampin and salicylates. Beta blockers
may decrease the effects of sulfonylureas (oral hypoglycemics), and may slow the metabolism of
lidocaine. Increased hypotension and bradycardia may be observed with concurrent use of inhaled
anesthetics and fentanyl derivatives.

ADVERSE THROMBOEMBOLIC EVENTS

BRAND NAME: Plavix
GENERIC NAME: clopidogrel
THERAPEUTIC CATEGORY: antiplatelet agent
USE: reduce risk of atherosclerotic events in patients with history of recent MI, stroke, or established
peripheral arterial disease; acute coronary syndrome (unstable angina)
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: Clopidogrel interfere with the metabolism of many medications, including
oral hypoglycemics, phenytoin and some NSAIDS, increasing risk for toxicity. Concurrent use of
clopidogrel with naproxen increases risk for GI bleeding. Anticoagulant medications taken with
antiplatelet medications increases risk for bleeding. Atorvastatin (Lipitor) and macrolide antibiotics



                                                                                                           4
(clarithromycin, erythromycin) decrease the effects of clopidogrel. Many herbs interact with Plavix and
increase risk for bleeding: discontinue 14 days prior to surgery.

ENDOCRINE DISORDERS

BRAND NAME: Synthroid
GENERIC NAME: levothyroxine
THERAPEUTIC CATEGORY: hormone
USE: hypothyroidism
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: Levothyroxine increases the effects of oral anticoagulants (Coumadin),
causing an increased risk of bleeding. When taken together, toxicity may occur for both levothyroxine
and tricyclic antidepressants (Elavil). Antacids containing aluminum and magnesium, iron, bile acid
sequestrants (colestipol, cholestyramine), and the ulcer medication sucralfate (Carafate) decrease the
absorption of levothyroxine. Certain seizure medications (phenytoin, phenobarbitol and carbamazepine)
and the TB medication rifampin (Rifadin) decrease levothyroxine levels. Levothyroxine may decrease
the effect of oral sulfonylureas.


ANTIBIOTICS

BRAND NAME: Amoxil, Moxatag
GENERIC NAME: amoxicillin
THERAPEUTIC CATEGORY: antibiotic
USE: infections of ear, skin, respiratory and urinary tracts; premedication
ORAL COMPLICATIONS: oral candidiasis and black hairy tongue
DRUG INTERACTIONS: Concomitant use of amoxicillin and erythromycin or amoxicillin and
tetracycline is contraindicated. Amoxicillin may decrease the efficacy of oral contraceptives; therefore,
patients should be instructed to use an alternative form of birth control while taking this antibiotic.
Disulfiram (Antabuse), used to treat alcoholism, and the uric acid lowering agent probenecid (Benemid)
cause increased levels of amoxicillin The effects of warfarin may be increased.


BRAND NAME: AzaSite, Zithromax, Zmax
GENERIC NAME: azithromycin
THERAPEUTIC CATEGORY: macrolide antibiotic
USE: orofacial and respiratory tract infections; middle ear infections, pharyngitis, strep throat, tonsillitis,
pneumonia; premedication
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: Antacids containing aluminum or magnesium (Maalox, Mylanta) should not
be taken with azithromycin, as antacids decrease serum levels of the drug. Two hours should lapse prior
to taking azithromycin following the use of an antacid. As with erythromycin, azithromycin interacts
with many drugs, and may increase the levels of some antihistamines (Hismanal), cyclosporine
(Sandimmune), carbamazepine (Tegretol), digoxin (Lanoxin), phenytoin (Dilantin), triazolam (Halcion),
warfarin (Coumadin) and antiasthmatic drugs containing theophylline. Concomitant use of the macrolide
antibiotics with the HMG Co-A reductase inhibitors increases the risk for rhabdomyolysis. Antibiotics
decrease the effectiveness of oral contraceptives.




                                                                                                              5
ANTIDEPRESSANTS

BRAND NAME: Lexapro
GENERIC NAME: escitalopram
THERAPEUTIC CATEGORY: selective serotonin reuptake inhibitor
USE: major depressive disorder; generalized anxiety disorders (GAD)
ORAL COMPLICATIONS: xerostomia, toothache, vomiting
DRUG INTERACTIONS: Do not take this drug with MAOIs: fatal reactions have been reported.
Combined use of this drug with other SSRIs and/or other classes of antidepressants increases risk for
serotonin syndrome. Use of this drug with aspirin, NSAIDS and other drugs that alter coagulation
increases risk for bleeding. Systemic azole antifungals, ciprofloxacin, clarithromycin, diclofenac,
doxycycline, erythromycin, and other CYP3A4 inhibitors may increase the levels and/or effects of
escitalopram. Avoid drinking alcohol with this medication. Combined use of SSRIs with sumatriptan
(Imitrex) or other serotonin agonists may result in toxicity. CYP3A4 inducers may decrease the
levels/effects of escitalopram, including cabamazepine nafcillin, phenobarbital and phenytoin.

BRAND NAME: Oleptro
GENERIC NAME: trazodone
THERAPEUTIC CATEGORY: serotonin reuptake inhibitor/antagonist
USE: major depressive disorder
ORAL COMPLICATIONS: xerostomia, taste alteration
DRUG INTERACTIONS: Sedative effects may be increased with alcohol and other CNS depressants;
levels of trazodone may be increased by buspirone, SSRIs and venlafaxine. Trazodone may decrease
levels/effects of dabigatran. Avoid use of methylene blue (used to treat methemoglobinemia and UTI).


GERD OR HYPERSECRETORY DISEASE

BRAND NAME: Nexium
GENERIC NAME: esomeprazole
THERAPEUTIC CATEGORY: proton pump inhibitor
USE: short-term treatment of erosive esophagitis; symptomatic gastroesophageal reflux disease (GERD)
ORAL COMPLICATIONS: xerostomia
DRUG INTERACTIONS: Esomeprazole may increase the levels of carbamazepine, statin drugs, and
some benzodiazepines (diazepam, midazolam, triazolam). Drugs in this class may decrease the
absorption of antiretroviral medications, iron, and systemic antifungal medications (itraconazole,
ketoconazole). Esomeprazole may decrease the levels of phenytoin. Drug absorption is significantly
decreased (43%-53%) when taken with food; take at least 1 hour before meals.

RESPIRATORY DISEASE

BRAND NAME: Singulair
GENERIC NAME: montelukast
THERAPEUTIC CATEGORY: leukotriene-receptor antagonist
USE: prophylaxis and chronic treatment of asthma; seasonal allergies; perennial allergic rhinitis
ORAL COMPLICATIONS: none
DRUG INTERACTIONS: Phenylketonuric patients should be informed that the chewable tablets contain
phenylalanine. Carbamazepine, phenobarbital, phenytoin, rifampin, and nafcillin may decrease the levels
of montelukast. St. John’s wort may also decrease the levels of montelukast.




                                                                                                        6
BRAND NAME: ProAir HFA
GENERIC NAME: albuterol
THERAPEUTIC CATEGORY: beta 2-adrenergic agonist
USE: asthma, chronic obstructive pulmonary disorder (COPD)
ORAL COMPLICATIONS: xerostomia, altered taste, vomiting, tooth discoloration
DRUG INTERACTIONS: Increased toxicity (cardiovascular effects) is noted when albuterol is
used with any of the following drugs: MAO inhibitors (Marplan, Nardil, Parnate), tricyclic
antidepressants (Elavil), sympathomimetic agents (amphetamines, dopamine) and inhaled
anesthetics(malignant arrhythmias). The effect of albuterol is decreased when used with
nonselective beta blockers. When used with inhaled ipratropium (Atrovent), an increase in the
duration of bronchodilation may occur.


REFERENCES FOR TOP 20 MEDICATIONS

Top 200 Medications for 2011. Source: IMS Health. Available at:
http://www.pharmacytimes.com/publications/issue/2012/July2012/Top-200-Drugs-of-2011

Physicians’ Desk Reference, ed. 65. Montvale, Medical Economics Co, Inc., 2011.

Mycek MJ, Harvey RA, Champe PC: Lippincott’s Illustrated Reviews: Pharmacology. ed. 3.
Philadelphia, Lippincott-Raven, 2006.

Wynn RL, Meiller TF, Crossley HL. Drug Information Handbook in Dentistry. 18th ed. Hudson, Lexi-
Comp Inc., 2012.

Gage TW, Pickett FA. Mosby’s Dental Drug Reference. 7th ed. St. Louis, Mosby, Inc., 2005.

Pickett FA, Terezhalmy GT. Dental Drug Reference with Clinical Implications. 2nd ed. Baltimore,
Lippincott Williams & Wilkens, 2008.


FDA WATCHES AND WARNINGS

varenicline (Chantix)
   FDA Safety Alert and Public Health Advisory Statement
   Patients should be provided with a medication guide highlighting neuropsychiatric symptoms
   receiving this medication
   Angioedema, serious skin reactions, visual impairment, accidental injury
   July 2011 – relabeling changes due to cardiovascular concerns; FDA is requiring
   manufacturer to conduct meta-analysis of clinical trials to examine risks:
   http://www.fda.gov/Drugs/DrugSafety/ucm259161.htm#safety

azithromycin, clarithromycin
    May be associated with liver failure




                                                                                                   7
tramadol (Ultram, Ultracet)
   FDA safety labeling revision
   Potential risk for potentially life-threatening serotonin syndrome
   Serotonin syndrome may occur with use of tramadol alone or with concurrent use of SSRIs,
   tricyclic antidepressants, MAOIs
   Adverse events may occur at recommended tramadol dose
   tramadol is indicated for moderate to moderately severe pain in adults for short-term use (≤5
   days) for acute pain



       MANAGEMENT OF ORAL SIDE EFFECTS CAUSED BY MEDICATIONS

FLUORIDE THERAPY

For caries control:

Prescription fluorides for supplemental home use:
 1.1% neutral sodium     5000 ppm     Clinpro 5000 Anti-Cavity Toothpaste (3M ESPE),
 gel or dentifrice       Prescription Control Rx (Discus Dental), Fluoridex Daily Defense
                                      Dentifrice and Gel (Discus Dental), NUPRO
                                      NuSolutions Toothpaste (Dentsply), Oral B Neutracare
                                      (P&G), PreviDent 5000 Booster toothpaste, PreviDent
                                      Gel, PreviDent 5000 Plus (Colgate), ProDenRx
                                      Dentifrice and Gel (Zila), Topex Take Home Care
                                      (Sultan Healthcare)
 0.2% neutral sodium     920 ppm      CaviRinse (3M ESPE), NaFrinse (Medical Products
 rinse                   Prescription Laboratory), Oral B Fluorinse (P&G), PreviDent
                                      Dental Rinse (Colgate), ProDenRx Rinse (Zila)
 1.1% sodium and         5000 ppm     Phos-Flur (Colgate)
 acidulated              Prescription
 phosphate gel
 0.4% stannous           1000 ppm     Fluoridex Daily Defense Sensitivity Relief (Discus
 fluoride gel                         Dental); Gel-Kam Oral Rinse (Colgate), Kid Kare Plus
                                      0.4% Stannous Fluoride Brush-on Dentifrice, Kids
                                      Kare 0.4% Stannous Fluoride Brush-on Gel (Zila),
                                      ProDenRx 0.4% Stannous Fluoride Brush-on Gel
                                      (Zila), Topex Take Home Care (Sultan Healthcare)
 0.63% stannous          30 ml dose PerioMed (3M ESPE), Fluoridex Daily Renewal
 fluoride rinse          dilution = 7 (Discus Dental)
                         mg fl- ion
                         and 22 mg
                         stannous
                         ion




                                                                                                   8
Over-the-counter supplemental fluorides for home use:
 0.05% neutral sodium rinse 230 ppm Reach Act, Fluorigard, NaF rinse acidulated, NaF
                                      rinse neutral
 0.044% sodium and          200 ppm Phos-Flur (Colgate); OrthoWash (3M ESPE)
 acidulated phosphate rinse
 0.4% stannous fluoride gel 1000      Gel-Kam Treatment Gel (Colgate), Just For Kids
                            ppm       (3M ESPE), Omni Gel (3M ESPE), Oral B Stop
                                      (P&G)
 0.0221% sodium fluoride              Listerine Total Care, Listerine Smart Rinse (J&J)


Fluoride Varnishes: 22,600 PPM sodium fluoride
5% sodium fluoride varnish   varnish in AllSolutions (Dentsply)
(in-office use only)         a tube or   Duraphat (Colgate)
                             single-     Duraflor (A.R. Medicom)
                             unit dose   Enamel Pro Varnish with ACP (Premier)
                             dispensers FluoroDose (Centrix)
                                         Fluoridex Lasting Defense (Discus Dental)
                                         Prevident (Colgate)
                                         Profluorid Varnish (VOCO)
                                         Vanish (Omni/3M EPSE)
                                         VarnishAmerica with xylitol (Medical Products Laboratories)
                                         Vella with xylitol (Preventech)
                                         Waterpik UltraThin (Teledyne)

SALIVARY REPLACEMENT THERAPY

1. OTC Artificial Saliva Preparations:
 PRODUCT
 Entertainer’s Secret®
 Moi-Stir®
 Mouthkote®
 Salivart®
 Salix®

       -carboxymethylcellulose = gives feeling of viscosity
       -relief while product is in contact with the tissues; convenience
       -some contain preservatives: parabens (PABA) = allergy potential

2. Biotene product line (GlaxoSmithKline): toothpaste, oral gel, mouthrinse, chewing gum
        -contain 3 key salivary enzymes found in natural saliva; sodium fluoride, xylitol

3. Orajel product line (Del Pharmaceuticals, Inc.): dry mouth moisturizing gel and spray
       - moisturizing gel and spray
               -18% glycerin; -sorbitol (gel); xylitol (spray)
       -moisturizing toothpaste
               -thione antioxidant complex; sodium monofluorophosphate (0.18% w/v fluoride ion)
               -sugar-free; sorbitol, xylitol; no sodium lauryl sulfate


                                                                                                   9
4. Oasis (Oasis Consumer Healthcare)
      -mouthwash or mouth spray
      -“TriHydra” technology: hydrophilic polymers, xanthum gum, glycerine and
      carboxymethylcellulose; relieves symptoms for up to 2 hours

5. GC Dry Mouth Gel (GC America)
      -alcohol free, sugar free, neutral pH, applied as needed

6. Salese (Nuvora)
        -lozenge with water absorbing polymer plus xylitol; raises pH; Dentiva: antimicrobial
7. Colgate Dry Mouth Relief Mouthrinse (Colgate Oral Pharmaceuticals)
        -fluoride mouthrinse (0.02% sodium fluoride = 90 ppm); tri-polymer system to help coat soft
        tissues; moisture retention; alcohol free; soothing, mild flavor

8. Two prescription drugs now available to stimulate salivary flow:
       Salagen (5 mg pilocarpine hydrochloride)
       -cholinergic agonist that stimulates muscarinic acetylcholine receptors in the salivary glands to
       increase serous salivary flow.
       -need to take the drug for a minimum of 90 days to see optimum effects
       -contraindicated if known hypersensitivity to the drug, uncontrolled asthma or narrow-angle
       glaucoma
       -drug interactions associated with pilocarpine include anticholinergic medications (eg.
       antiparkinsonion drugs, carbamazepine, digoxin, sedative antihistamines, tricyclic
       antidepressants), cholinergic medications (eg. antiglaucoma drugs) and beta-adrenergic blocking
       drugs
       -indicated for radiation therapy patients and Sjogren’s syndrome
               - dosage: for radiation therapy patients:
                           - 5 mg tid (15-30 mg per day); 12 weeks of therapy
               - dosage: for Sjogren’s patients:
                           - 5 mg qid; efficacy has been established after 6 weeks of use

        Evoxac (cevimeline)
        -cholinergic agonist used to treat xerostomia in patients with Sjogren’s syndrome
                 - dosage: 30 mg tid
        -contraindications: hypersensitivity to drug or any of its components, uncontrolled
         asthma, narrow-angle glaucoma, acute iritis, conditions where miosis is undesirable
        -use with caution in patients with CV disease, asthma, COPD, decreased visual acuity, the
        elderly, or in those with kidney problems

ANTIMICROBIALS
     -an important adjunct in managing the oral complications of xerostomia
     -reduce plaque formation, and to prevent or reduce the severity of gingivitis
     -promotes a healthy oral ecosystem
     -OTC and prescription antimicrobials available on the market from which to choose
     -3 FDA and ADA approved antimicrobials: chlorhexidine, Listerine® and triclosan
     (Colgate® Total)
     - Other agents available as mouthrinses exhibit antibacterial properties, but do not
         possess good substantivity:
            -stannous fluoride = antibacterial. carioprotective and desensitizing effects



                                                                                                       10
-cetylpyridinium chloride = rupture bacterial cell walls and alter cytoplasmic
              contents; bind strongly to plaque and tooth surfaces (Cepacol®, Scope®,
              Advanced Formula Viadent®; alcohol free: Crest® Pro Health Rinse, BreathRx)
              -Crest Pro Health Rinse with CPC has data to support 12 hour substantivity =
              vehicle improves bioavailability
              -oxygenating agents = damage bacteria by altering cell membrane permeability

        -Natural Dentist® Health Gums Moisturizing Antigingivitis Mouthrinse
             -contains all natural formulation
             -germ kill of 40 oral pathogens, including Strep mutans and some red complex
             -comparable to Listerine® in terms of pathogen reduction
             -4 published clinical trials and MIC laboratory data to support efficacy

       -Triclosan (Colgate® Total toothpaste)
              -antimicrobial agent in dentifrice form = decreases plaque viability
              -both antimicrobial and anti-inflammatory properties
              -unique technology of delivery mode: PVM/MA copolymer = GANTREZ
              -copolymer allows binding to surfaces with slow release; promotes
              adhesion/uptake of triclosan on enamel, plaque and soft tissue
              -triclosan: broad spectrum, substantive to 12 hours
              -over 75 clinical trials to support safety and efficacy of Colgate® Total
              -anti-inflammatory effect: dampens stimulation of the production of IL1-
                beta and TNF alpha = inflammatory mediators (cytokines) that destroy
                tissue and bone = local host modulation

       -Crest® Pro Health dentifrice
             -stannous fluoride multi-care dentifrice
             -older formulations: adverse taste and staining effects; instable in aqueous
              solutions
             -0.454% stabilized stannous fluoride with sodium hexametaphosphate
             -sodium hexametaphosphate = pyrophosphonate (anti-calculus/anti-
               staining)
                      -polymer of repeated pyrophosphate subunits
                      -stronger affinity to calcium hydroxyapatite in enamel and dentin
                      -greater prevention of crystallization at enamel surface (calculus
                       prevention) and adsorption of stains from chromogens (staining)
             - silica-based low-water dentifrice to reduce hydrolysis of sodium
             hexametaphosphate and to maintain effective pyrophosphate levels
             -12 hour substantivitiy

Important take home messages with antimicrobials:

- chlorhexidine and CPC are cations: drug reactions with SLS and fluoride = wait 30 minutes
after brushing or vigorously remove all toothpaste residue before rinsing
- chlorhexidine and Listerine have been shown to kill 7 species of Candida
- chlorhexidine and Listerine kill multiple species of Strep: Strep mutans



                                                                                              11
- chlorhexidine and Listerine have been shown to reduce incidence and severity of aphthous
ulcers


ANTIFUNGALS

        -    fungal infections occur as a result of alterations in oral flora, immunosuppression and
             underlying systemic disease (diabetes, xerostomia, anemia, chemo, inhaled steroids)
        - opportunistic infections
        - clinical presentation:
                 - pseudomembranous appearance (bright red with overlying white pseudomembrane);
                 atrophic appearance (tongue); hyperkeratotic appearance (denture stomatitis);
                 symptomatic geographic tongue; angular cheilitis

        -drug therapy includes topical and systemic medications depending upon the extent and severity
        of the infection.
        -azole antifungals are used to treat chronic, extensive mucocutaneous candidiasis
        -polyenes are used to treat local candidiasis (topicals)

        -antifungals are being used in combination with corticosteroids, such as nystatin and
        triamcinolone, to treat both the fungal infection and the inflammation of angular cheilitis
        - medications must be used for a minimum of 48 hours after the disappearance of clinical
        signs and symptoms; re-evaluate condition 14 days after therapy has been completed
        - efficacy of topical drugs is dependent upon contact with the lesions
        - some topical preparations contain sugar - may choose to prescribe vaginal preparation
        - in addition to antifungals, consider chlorhexidine or essential oil mouthrinses
          for long term prevention
        - prescription antifungals for systemic use if patient is refractory to topicals:
                 *cautions: liver function and multiple drug interactions

Topical Antifungal Medications:
 nystatin ointment              apply thin coat to affected area (or inner surface of denture) 4-5
                                times per day
 Mycelex ® 10 mg troches        disp: 70 troches; dissolve 1 troche in mouth 5 times per day until
 (clotrimazole)                 gone; leave any prosthesis out during treatment and soak prosthesis
                                in nystatin liquid suspension overnight
 Nizoral® 2% cream              apply thin coat to affect areas (or to inner surface of denture) after
 (ketoconazole)                 meals
 iodoquinol and hydrocortisone  apply locally to affected area 3-4 times per day for 10 days to 2
 cream                          weeks, then re-evaluate
 nystatin and triamcinolone     apply locally to affected area 4 times per day for 10 days to 3 weeks
 acetonide ointment             and then re-evaluate

Topical nystatin:
       - is well-tolerated, non-sensitizing
       - soak dentures in nystatin suspension overnight
       - nystatin ointment can be placed in denture and worn during day (like an adhesive)




                                                                                                       12
Systemic Azole Antifungal Medications:
 Diflucan®      fluconazole    Take 2 tablets on day 1, then 1 tablet daily for 14 days until gone
 100 mg tablets                *a shorter course may be adequate; extensive infection may require
                               second course of treatment
 Nizoral®       ketoconazole   Take 1 tablet daily with a meal for 14 days
 200 mg                        *may cause irreversible liver damage with long-term use (greater
                               than 3 weeks)

ANTIVIRALS

       - viral infections: acute onset of symptoms
       - vesicular eruption of soft tissues
       - rupture of vesicles leaves ulcerations
       - ulcerations are generally small in size
       - if left untreated, ulcerations coalesce to form large lesions
       - primary infection can present as: gingivostomatitis, recurrent lip lesions (herpes labialis),
       intraoral ulcers (recurrent intraoral herpes) that involve oral/perioral tissues
       - primary infection is systemic that leads to acute gingivostomatitis involving multiple tissues:
       buccal mucosa, lips, tongue, floor of mouth, gingiva
       - management of viral infections is generally palliative (although acyclovir is now used for
       prevention of primary infections)
       - treatment of primary infections includes combination therapy:
                          - acyclovir
                          - topical anesthetic rinses (eg. Benadryl, Xylocaine viscous, OTC
                             benzocaine products )
                          - fluids, vitamins and mineral supplements and rest

Antiviral Medications for Herpes Simplex:
 Zovirax® 200 mg tablets acyclovir                   take 1 capsule 5 times per day for 10 days or 2
                                                     capsules 3 times per day for 10 days
 Zovirax® ointment 5%       acyclovir                apply q 3 hours (6 times/day) for 7 days
 Denavir® cream 10mg/g      penciclovir              apply every 2 hours (lips and face only) for 4 days
 (1%)
 Valtrex® 500 mg            valacyclovir         2 grams twice daily for 1 day at prodrome
                                                 (separate doses by 12 hours)
 Abreva (OTC)               docosanol 10%        apply locally as directed 5 times per day; start at
                                                 prodrome and continue for 4 days; do not apply
                                                 directly to inside of mouth or around eyes
 Viroxyn® (OTC)             alcohol/benzalkonium single dose applicator/vial; at prodrome, rub
                            chloride             medication into lesion until medication is gone
                                                 (10 seconds)

ORAL ULCERATIONS (NON-VIRAL) AND PAIN CONTROL

       -Recurrent Aphthous Stomatitis:
              - patients with recurrent aphthous should be evaluated for iron, folic acid and/or vitamin
              B12 deficiency
              - severe recurrent aphthous may be treated with an oral suspension of
              tetracycline




                                                                                                       13
- regular use of Listerine has been shown to reduce the frequency, duration and severity
                of lesions; chlorhexidine has been shown to reduce duration of lesions

        -localized ulcerations:
                 - OTC topical anesthetic agents containing benzocaine in protective preparations
                 - Benzocaine and tetracaine (Viractin) are esther anesthetics; therefore, caution must be
                 used when recommending these OTC products to clients with reported allergies to
                 anesthetics or to PABA
                 - Debacterol (sulfonated phenolics in aqueous solution) – therapeutic
                cauterization
                         - dry ulcer, apply directly to lesion, keep in contact for 5-10 seconds; (larger
                         lesions may need up to 2 minutes); rinse immediately, and expectorate with water

        -generalized oral pain:
               - OTC agent such as Chloraseptic® spray
               - prescription mouthrinse Xylocaine ® 2% (viscous lidocaine)
               - Benadryl® elixir and Benylin® cough syrup

        -severe pain, such as that associated with mucositis:
                - anesthetic agents may be mixed with OTC coating agents to provide lubrication and
                relief from pain
                - Benadryl® elixir added in equal amounts to Maalox®, Mylanta® or Kaopectate®
                - sucralfate (Carafate®), the prescription medication used to treat duodenal ulcers, may
                be prepared as a 1 gm/15 mL suspension for use in this population as well. (A
                pharmacist should be consulted to assist with the preparation of oral suspensions.)

        -dry, cracked lips: topical water-based product; Oral Balance®

Topical prescription agents for aphthous lesions:
 amlexanox oral paste 5%          Apthasol®                             apply 4 times per day (after
                                                                        meals and at bedtime) until area
                                                                        heals
 triamcinolone acetonide            Oralone®0.1%; Kenalog in            apply after each meal and at
 Dental Paste                       Orabase® 0.1%                       bedtime
 chlorhexidine oral rinse           Peridex®, PerioGard®                rinse with 20 ml for 30 sec tid
 fluocinonide 0.05%                 Lidex® ointment mixed 50/50         apply thin layer to oral lesions 4
 (used for oral inflammatory        with Orabase (30 grams total)       times per day
 lesions that do not respond to
 Kenalog in Orabase®)
 clobetasol propionate 0.05%        Temovate®                           apply small quantity with a
                                                                        cotton tip applicator to affected
                                                                        area 3-4 times daily
 betamethasone 0.1% ointment                                            apply small quantity with a
                                                                        cotton tip applicator to affected
                                                                        area 3-4 times daily
 dexamethasone elixir               Decadron®                           rinse with 1 teaspoon for 2
 0.5 mg/5 mL                                                            minutes 4 times per day and
                                                                        expectorate




                                                                                                            14
Topical OTC agents for aphthous/pain control:
 Benzyl alcohol                 Zilactin® Gel                 apply q 3-4 hours
 Benzocaine 10%                 Zilactin® B                   apply q 3-4 hours
 Lidocaine 2.5%                 Zilactin L                    apply q 3-4 hours
 Diphenhydramine                Benadryl® Elixir              swish with 1 tsp for 2 min before
                                                              each meal (can be used as a
                                                              swish and swallow)
 Benzocaine, gelatin, pectin and   Orabase® with Benzocaine   apply 3-4 times/day
 sodium carboxymethylcellulose
 Tetracaine Hydrochloride 1%       Viractin®                  apply 3-4 times/day up to 7 days




                                                                                             15

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C123 managing the geriatric patientmanaging the geriatric patient

  • 1. C123 MANAGING THE GERIATRIC PATIENT ANN ESHENAUR SPOLARICH, RDH, PHD THURSDAY, FEBRUARY 21 DISCLAIMER: This work, audio recordings and the accompanying handout, are the intellectual property of the clinician, and permission has been granted to the Chicago Dental Society, its members, successors and assigns, for the unrestricted, absolute, perpetual, worldwide right to distribute solely as an educational material at the scientific program being presented at the 2011 Midwinter Meeting. Permission has been granted for this work to be shared for non-commercial education purposes only. No other use, including reproduction, retransmission in any form or by any means or editing of the information may be made without the written permission of the author. The Chicago Dental Society does not assume any responsibility or liability for the content, accuracy, or compliance with applicable laws, and the Chicago Dental Society shall not be sued for any claim involving the distribution of this work.
  • 2. Chicago Dental Society MWM & REGIONAL MEETING COURSE EVALUATION Speaker: Date: Subject: Number of attendees: PLEASE RATE YOUR SPEAKER AS TO: Excellent Good Fair Poor N/A • Subject selected................................. 4 3 2 1 0 • Timeliness of subject ......................... 4 3 2 1 0 • Comprehensiveness........................... 4 3 2 1 0 • Meeting your expectations ................ 4 3 2 1 0 • Content level...................................... 4 3 2 1 0 • Delivery .............................................. 4 3 2 1 0 • Voice quality....................................... 4 3 2 1 0 • Holding your interest ......................... 4 3 2 1 0 • Appropriate audiovisuals ................... 4 3 2 1 0 • Effective audiovisuals ........................ 4 3 2 1 0 • Overall evaluation of speaker ............ 4 3 2 1 0 • Overall evaluation of program........... 4 3 2 1 0 Should this speaker be invited for future meetings? Yes q No q What topics of interest would you like to see covered in the future? Comments (use reverse if you need additional space): Name (requested but not required—please print): RETURN EVALUATION CARD TO: DO NOT FOLD CARD. FOR CDS PERMANENT FILES. Chicago Dental Society Aloysius F. Kleszynski, DDS 401 N. Michigan Ave., Suite 200, Chicago, IL 60611-5585
  • 3. COURSE TITLE: Pharmacologic Management of the Geriatric Patient: Oral Health Care Considerations COURSE INSTRUCTOR: Ann Eshenaur Spolarich, RDH, PhD COURSE CREDITS: 3 CEUs COURSE DATE: February 22, 2013 _____________________________________________________________________________ COURSE DESCRIPTION: The purpose of this course is to review characteristics and disease trends among the aging population, and oral disease risks associated with medications and common systemic diseases. Most patients take multiple medications, many of which have oral complications and drug interactions of significance to dentistry. Medication therapies, oral drug and disease complications, drug interactions and dental practice management considerations will be discussed. Recommendations for treatment modifications and oral hygiene self-care programs will be provided. LEARNING OBJECTIVES: Upon completion of this continuing education program, course participants will be able to: 1. Describe common oral disorders observed in the elderly population, including xerostomia, taste and smell disorders, orofacial muscular disorders, and lichenoid drug reactions. 2. Discuss the pathophysiology of common diseases associated with aging, including cardiovascular disease, gastrointestinal problems, and depression. 2. Identify the major classes of medications associated with and/or used to treat these conditions. 4. Discuss the oral side effects and other adverse events associated with each of these disease states and related medication therapies. 5. Identify modifications necessary to safely treat patients who present with these medical conditions. 6. Recommend appropriate oral hygiene strategies for each of these patient populations. *These course materials may not be duplicated without the written consent of the course instructor. 1
  • 4. I. Selected Agents for the Treatment of Depression -dopamine-reuptake inhibitor - bupropion (Wellbutrin, Zyban) -depression, smoking cessation -increased risk for seizures; alcohol lowers seizure threshold -risk for emergent hypertension *take BP on patients using this drug -monoamine oxidase inhibitors (MAOIs) -isocarboxazid (Marplan) -phenelzine (Nardil) -selegiline (Atapryl, Eldepryl, Selpak) -tranylcypromine (Parnate) -atypical, non-endogenous or neurotic depression -depression associated with Parkinson’s disease -investigational for ADHD, Alzheimer’s, Schizophrenia -post-traumatic stress disorder *take BP on patients using these drugs -selective serotonin reuptake inhibitors (SSRIs) -citalopram (Celexa) -escitalopram oxalate (Lexapro) -fluoxetine (Prozac, Sarafem) -paroxetine (Paxil) -sertraline (Zoloft) -over 15 approved indications -depression, geriatric depression, generalized anxiety disorder, social phobias, social anxiety disorders, diabetic neuropathies, anorexia, bulimia, premenstrual syndrome, obsessive compulsive disorder (OCD), panic attacks/disorders *biggest US market sellers: Paxil and Zoloft -sertraline (Zoloft) is only drug approved for use in children for OCD -recent concerns over whether use of SSRIs in adolescents increases risk for suicide: increased number of cases of suicide attempts prompted FDA to require relabeling of these drugs -agitation, anxiety, hostility, aggression = known side effects -watch for signs of change in depression and related behaviors or any of the above side effects during first 6 weeks of therapy: highest risk time period for suicide attempt -venlafaxine (Effexor) -selective serotonin/norepinephrine reuptake inhibitor -depression, anxiety, panic disorder; investigational for OCD, hot flashes, neuropathic pain, ADHD -raises BP (diastolic) and heart rate *take BP on patients using this drug -tetracyclic - maprotiline (Ludiomil) -depression, anxiety with depression -investigational:bulimia, enuresis, pain, panic attacks, tension headaches, cocaine withdrawal -tricyclics (secondary amines) -amoxapine (Ascendin) -desipramine (Norpramin) -nortriptyline (Aventyl, Pamelor) -protriptyline (Vivactil) 2
  • 5. -treatment of depression in conjunction with psychotherapy -adjunctive therapy for chronic pain, peripheral neuropathies -investigational for substance-related disorders, ADHD -tricyclics (tertiary amines) -amitriptyline (Elavil, Vanatrip) -clomipramine (Anafranil) -doxepin (Sinequan) -imipramine (Tofranil) -trimipramine (Surmontil) -treatment of depression with psychotherapy -chronic pain, neuropathic pain, migraines, depression with anxiety *take BP on patients using these drugs General Adverse Effects - orthostatic hypotension - sedation - dizziness, light-headedness II. MAJOR TRANQUILIZERS/ANTIPSYCHOTICS A. Pharmacology and Use -Older term: neuroleptic drugs -A chemically diverse but pharmacologically similar class of drugs used to treat a variety of conditions -Used in the treatment of: -Psychotic disorders – Schizophrenia, paranoia -Acute delirium and dementia -Manic episodes during induction of lithium -Movement disorders – Huntington’ disease, Tourette’s syndrome, ballismus -Intractable hiccups -Severe nausea and vomiting -Individual drugs bind to a variety of receptors and act as antagonists: -dopaminergic, alpha1 and alpha2 adrenergic, serotonergic (5-HT), muscarinic, H1 histamine, sigma opioid -Blockade of dopaminergic transmission in various areas of brain is thought to be responsible for their major effects -Antipsychotic action = blockage in prefrontal cortex and limbic areas -Extrapyramidal side effects = blockade in basal ganglia -Antiemetic effects = blockade in chemoreceptor trigger zone of the medulla -All antipsychotics have high therapeutic index -Not addictive 3
  • 6. B. Side Effects -Extrapyramidal side effects: Parkinsonism – akinesia (difficulties in initiating movement), tremor, rigidity Caused by blockade of D2 receptors in basal ganglia -Akathisia = restless legs syndrome; Caused by D2 receptor blockage in basal ganglia -Dystonia – sustained muscular contraction -Tardive Dyskinesia – abnormal movements, particularly of face and tongue, but may also be of trunk and limbs -Noticeable after at least 6 months of chronic treatment - begins with spastic, thrusting tongue movement, body restlessness, changes in HR & respiration *Most extrapyramidal side effects are treatable with anticholinergic drugs Sedation and autonomic side effects are caused by blockade of histamine, cholinergic and adrenergic receptors -orthostatic hypotension -blurred vision -dry mouth -nasal congestion -constipation -urinary retention C. Drug Interactions of Significance to Dentistry -Antipsychotics potentiate the actions of -sedatives -analgesics -antihistamines -Antipsychotics potentiate the respiratory depression caused by opioids -Antacids = decrease absorption of antipsychotics -Anticonvulsants = decrease plasma levels of antipsychotics -Antipsychotics may alter efficacy of antihypertensive medications *monitor vital signs TYPICAL ANTIPSYCHOTICS ATYPICAL ANTIPSYCHOTICS chlorpromazine (Thorazine) = Schizophrenia, aripiprazole (Abilify) = Commonly used agent in nausea/vomiting, intractable hiccups, schizophrenia, treatment and stabilization of combativeness bipolar disorder -Low risk of EPS -Does not cause as much weight gain as other antipsychotics, but may be less effective than others fluphenazine (Prolixin) = management of clozapine (Clozaril) = Schizophrenia; severe OCD, psychotic disorders and schizophrenia; improves childhood psychosis, attempted suicide, substance outcomes in patients with psychoses who are abuse recovery nonadherent with oral antipsychotics Side effect: agranulocytosis – susceptibility to infection, hypersalivation (others cause xerostomia), weight gain, reduced risk of EPS 4
  • 7. haloperidol (Haldol) olanzapine (Zyprexa) = Schizophrenia, bipolar RX for schizophrenia and Tourette’s; severe disorder, acute agitation behavioral problems in children -EPS of TMJ pimozide (Orap) = suppression of severe motor and olanzapine and fluoxetine (Symbyax) = treatment phonic tics with Tourette’s of depressive episodes associated with bipolar -prolongs QT interval: consult physician prior to disorder administering vasoconstrictor prochlorperazine (Compro, Compazine) = paliperidone (Invega) = Schizophrenia antiemetic; psychosis, anxiety -EPS side effect: torticollis (neck muscle spasm) promethazine (Phenadoz, Phenergan, quetiapine (Seroquel) = Schizophrenia, acute Promethegan) = antiemetic, antihistamine, manic episodes and/or depressive episodes with sedative, motion sickness, post-operative pain, bipolar disorder (monotherapy or with lithium) anesthetic -EPS side effect: tardive dyskinesia, Parkinson’s syndrome, akathisia is most common in elderly patients thiothixene (Navane) = psychotic disorders in risperdone (Risperdal) = Commonly used agent in children, rapid tranquilization of agitated child; schizophrenia, acute mania and/or patients with dementia irritability/aggression with bipolar disorder, -prolongs QT interval: consult physician prior to behavioral problems with dementia, Tourette’s administering vasoconstrictor ziprasidone (Geodon) = schizophrenia, acute manic or mixed episodes with bipolar disorder with or without psychosis, acute agitation with schizophrenia -prolongs QT interval: consult physician prior to administering vasoconstrictor Why are Cholinesterase Inhibitors typically used? • Indirect-Acting Cholinergic Drugs • Also known as “cholinesterase inhibitors” • These drugs stop the breakdown of acetylcholine (via cholinesterase), which allows for the concentration of acetylcholine to build up = acetylcholine remains active and stimulates the PANS • These drugs produce PANS stimulation • Dementia with Alzheimer’s disease • Investigational for mild to moderate dementia with Parkinson’s disease • Examples: o donepezil (Aricept) o rivastigmine (Exelon) o galantamine (Razadyne) Side Effects of Direct-Acting and Indirect-Acting Cholinergic Drugs • nausea, vomiting, diarrhea (by increasing GI activity) • salivation, sweating (increased gland secretions) • bronchoconstriction 5
  • 8. constricted pupils • Paralysis at high doses (effect at neuromuscular junction) • CNS = confusion Anticholinergic Drugs for Parkinson’s Disease • benztropine (Cogentin) • trihexyhenidyl (not in U.S.; Canadian drug) Anticholinergic Drugs (Parasympatholytics) • Prevent the action of acetylcholine at the postganglionic PANS nerve endings • “blocker” drugs or antagonists • Block the receptor site for acetylcholine • Do not prevent release of ACH • Acetylcholine cannot act on receptors in smooth muscle, glands or the heart • Also called antimuscarinic drugs (block muscarinic receptors but not nicotinic receptors) Pharmacologic Effects of Anticholinergic Drugs • Reduce PANS activity o Skin = decrease sweating o GI = decrease salivation, decreased gut motility o Urinary tract = urine retention o Respiratory = bronchodilation o CNS = decreased concentration/memory; sedation; possible hallucinations and coma Adverse Reactions to Anticholinergic Drugs • Frequently are extensions of their pharmacologic effects • Xerostomia • Blurred vision, photophobia • Tachycardia • Fever • Urinary and GI stasis • Hyperpyrexia (elevated temperature) • Hot, dry flushed skin (lack of sweating) • Toxicity = CNS excitation = delirium, hallucinations, convulsions, respiratory depression III. ORAL HEALTH CONSIDERATIONS FOR NEUROPSYCHIATRIC CONDITIONS - most neuropsychiatric medications cause xerostomia -watch for opportunistic infections -loss of protective effects: viral, fungal, bacterial infections -traumatic aphthous ulcers - lack of interest in performing daily self-care - increased demineralization, caries and gingival disease - lack of interest/motivation to seek treatment 6
  • 9. - caution with epinephrine = Monitor vital signs! -use vasoconstrictors cautiously with all classes of antidepressants except SSRIs -tricyclics and monoamine oxidase inhibitors -venlafaxine (Effexor) – depression, anxiety, OCD, ADHD --all drugs for ADHD -some antipsychotics = consult drug reference guide -SSRIs = bruxism: increased extrapyramidal effects -burning mouth syndrome = observed in depression and anxiety; tricyclics IV. PEPTIC ULCER DISEASE 1. Incidence and Prevalence -among most common human ailments -peak prevalence occurs in young adulthood (age 30 to 50 years) -first degree relatives have threefold higher risk -higher prevalence seen among: -smokers -heavy drinkers -hyperparathyroidism -renal dialysis patients -use of NSAIDS for longer than 1 month -death (from complications) of disease occur in elderly 2. Etiology -primary aggressive factor: Helicobacter pylori infection -present in more than 90% of cases -contributing factors: -acid hypersecretion -cigarette smoking -psychological and physical stress – increases acid secretion -use of NSAIDS for longer than 1 month -NSAID-induced ulcers occur more often in stomach than duodenum -concomitant use of aspirin, alcohol, corticosteroids and anticoagulants increases risk -obsessive compulsive disorder – increases acid secretion -caffeine – increases acid secretion -alcohol – alters cell permeability, leads to cell death = injures mucosa 3. Treatment -if ulcer is confined and uncomplicated: antisecretory drugs -if H pylori is present: antisecretory drugs with antimicrobials -combination therapy is used: -tetracycline and metronidazole or amoxicillin and clarithromycin with proton-pump inhibitor or bismuth subsalicylate (Pepto-Bismol) -treatment lasts for 2 weeks -modification of factors that contribute to ulceration 7
  • 10. Medications - OTC antacids - weak bases that interact with stomach acid to form water and salt; raise gastric pH - composition: aluminum hydroxide, magnesium hydroxide, calcium carbonate - Histamine H2 receptor antagonists - OTC meds used to manage symptoms of heartburn, acid indigestion, benign gastric and duodenal ulcers, GERD, hypersecretory conditions and erosive esophagitis - cimetidine (Tagamet), famotidine (Pepcid), nizatidine (Axid) and ranitidine hydrochloride (Zantac) - Proton pump inhibitors - bind to H+/K+-ATPase enzyme system (proton pump) in parietal cells which reduces acid secretion - reduce gastric secretions, neutralize gastric acid after release, protect gastric mucosa from damage -chronic use is linked to stomach cancer -associated with osteoporosis and risk for hip fracture - esomeprazole (Nexium), lansoprazole (Prevacid), omeprazole (Prilosec), pantoprazole (Protonix), esomeprazole (Nexium), rabeprazole (Aciphex) 4. Dental Considerations -thorough medical history review for risk factors and symptoms -avoid prescribing: aspirin, aspirin-containing products, NSAIDS -use acetaminophen (Tylenol) -Cox-2 inhibitors (Celebrex) -H2 receptor blockers like cimetidine (Tagament) decrease the metabolism of many drugs: -diazepam, lidocaine (adjust dosage) -H pylori is found in dental plaque = reservoir for infection/reinfection -good oral hygiene; frequent scaling and root planing -use of antibiotics = Candidiasis will require antifungal therapy -oral manifestations of peptic ulcer disease: -vascular malformations of lip (macules, venous pool) -enamel erosion -GI medications: -taste alteration -blood dyscrasias = increased risk for infections, bleeding -xerostomia - OTC antacids bind to other meds in the stomach = antacids and tetracycline - OTC antacids alter absorption, bioavailability and elimination of many drugs - wait 2 hours before/after taking antacids before taking other meds - histamine H2 receptor antagonists and proton pump inhibitors decrease the availability of azole antifungals - Tagamet and Zantac alter effects of warfarin - Tagamet increases serum concentrations of some benzodiazepines, lidocaine and the quinolone antibiotics 8
  • 11. DRUG ORAL SIDE EFFECTS omeprazole (Prilosec®) xerostomia, taste alteration, esophageal candidiasis, pharyngeal pain pantoprazole (Protonix®) xerostomia, taste alteration, pharyngitis, increased cough, aphthous stomatitis, gingivitis, glossitis, halitosis, oral moniliasis, tongue discoloration, herpes simplex, erythema multiforme nizatidine (Axid®) xerostomia, laryngeal edema ranitidine bismuth citrate (Tritec®) taste alteration, darkening of tongue ranitidine hydrochloride (Zantac®) erythema multiforme rabeprazole (Aciphex™) xerostomia, mouth ulcerations esomeprazole (Nexium™) xerostomia, ulcerative stomatitis, taste loss Oral side effects associated with gastrointestinal medications V. CARDIOVASCULAR DISEASE DRUGS THAT ALTER BLEEDING ANTIPLATELET MEDICATIONS -aspirin = antiplatelet drug -blocks cyclo-oxygenase, an enzyme associated with clot formation -inhibits platelet aggregation -prevents thrombus formation on atherosclerotic plaques -lowers risk of MI in those with increased risk for atherosclerosis/thrombogenesis -lowers risk of MI and stroke in those with previous history of MI and stroke, unstable angina, post-coronary artery bypass grafting -one enteric coated 325 mg tablet of aspirin daily or 81 mg low dose aspirin Sudden Discontinuation of Aspirin Discontinuing the use of aspirin increases mortality risk 1 Large clinical trial (n=1358) with hospitalized patients with an acute coronary syndrome 2 3 groups: never taken an oral antiplatelet agent (n=930), Hx of prior use (n=355), recently discontinued use (n=73) Among recently discontinued aspirin group, mostly due to physician recommendation prior to surgery, there was a higher 30 day rate of death or MI and adverse bleedings than among prior users No difference in the incidence of death or MI at 30 days between nonusers and prior users. Recent withdrawal displayed worse clinical outcomes than nonusers. 1. Ho PM, Spertus JA, Masoudi FA, et al. Impact of medication therapy discontinuation on mortality after myocardial infarction. Arch Intern Med. 2006 Sep 25;166(17):1842-7. 2. Collet JP, Montalscot G, Blanchet B, et al. Impact of prior use or recent withdrawal of oral antiplatelet agents on acute coronary syndromes. Circulation. 2004 Oct 19;110(16):2361-7. Epub 2004 Oct 11. A meta-analysis reviewing data from over 50,000 patients showed that aspirin non- adherence/withdrawal was associated with a three-fold higher risk for major adverse cardiac events. 3 Risk was even greater among patients with coronary stents. Risk was amplified by a factor of 89 in patient who had undergone stenting. 9
  • 12. 3. Biondi-Zoccai GG, Lotrionte M, Agostoni P, et al. A systematic review and meta-analysis on the hazards of discontinuing or not adhering to aspirin among 50,279 patients at risk for coronary artery disease. Eur Heart J. 2006 Nov;27(22):2667-74. Epub 2006 Oct 19. other anti-platelet medications: aspirin and dipyridamole (Aggrenox) cilostazole (Pletal) ticlopidine (Ticlid) – used for those who are intolerant to aspirin, when aspirin therapy has failed, and coronary stent implantation Lowers risk of stent thrombosis Low risk of bleeding complications compared to other strategies clopidogrel (Plavix) Replaced use of ticlopidine Lower rates of major adverse cardiac events and mortality compared with ticlopidine Better safety-tolerability profile Lower risk of neutropenia Indications: reduce rate of TE (MI, stroke, vascular death) in patients with recent MI or stroke; reduce rate of TE in patients with unstable angina managed medically or with PCI (with or without stents); reduces rate of death and TE in patients with ST-Sement elevation MI managed medically Dosing: 300 mg loading dose; 75 mg daily (with aspirin 81-325 mg daily) Problems: Drug interactions Slow onset of action Wide variability in patient response Includes “no” response prasugrel (Effient) *new drug approved in July 2009 Approved for patients with acute coronary syndromes undergoing PCI Indications: Reduces rate of thrombotic cardiovascular events (eg, stent thrombosis) in patients with unstable angina, non-ST-segment elevation MI, or ST-elevation MI (STEMI) managed with percutaneous coronary intervention Loading dose of 60 mg followed by maintenance dose of 10 mg Manufacturer labeling states to also take 75-325 mg aspirin once daily upon recommendation of provider clopidogrel (Plavix) and prasugrel (Effient) Prodrugs Noncompetitive antagonists of P2Y12 receptor Inhibit ability of adenosine diphosphate (ADP) to induce platelet aggregation and decreases subsequent platelet aggregation Block receptor for the life of the platelet = irreversible effect action is independent of and additive to aspirin Prevention of premature discontinuation of dual antiplatelet therapy in patients with coronary artery stents: a science advisory from the American Heart Association, American College of Cardiology, Society 10
  • 13. for Cardiovascular Angiography and Interventions, American College of Surgeons, and American Dental Association, with representation from the American College of Physicians. Grines CL, Bonow RO, Casey DE Jr, Gardner TJ, Lockhart PB, Moliterno DJ, O'Gara P, Whitlow P; American Heart Association; American College of Cardiology; Society for Cardiovascular Angiography and Interventions; American College of Surgeons; American Dental Association; American College of Physicians. William Beaumont Hospital, Royal Oak, Michigan, USA. J Am Dent Assoc. 2007 May;138(5):652-5. Abstract BACKGROUND: and Overview. Dual antiplatelet therapy with aspirin and a thienopyridine has been shown to reduce cardiac events after coronary stenting. However, many patients and health care providers prematurely discontinue dual antiplatelet therapy, which greatly increases the risk of stent thrombosis, myocardial infarction and death. CONCLUSIONS AND CLINICAL IMPLICATIONS: This advisory stresses the importance of 12 months of dual antiplatelet therapy after placement of a drug-eluting stent and educating patients and health care providers about hazards of premature discontinuation. It also recommends postponing elective surgery for one year, and if surgery cannot be deferred, considering the continuation of aspirin during the perioperative period in high-risk patients with drug-eluting stents. PMID: 17473044 *Link to download free full text copy: http://jada.ada.org/cgi/content/full/138/5/652 3 Recommendations from Advisory Statement (listed above): Those concerned about peri/postprocedural bleeding must be aware of catastrophic risks of premature discontinuation -Consult cardiologist to discuss optimal patient management strategies Elective procedures with significant risk of peri/postoperative bleeding should be deferred until patient has completed an appropriate course of thienopyridine therapy: -12 months after DES implantation if they are not at high risk of bleeding -Minimum of one month for bare-metal stent implantation Patients with DES who are to undergo subsequent procedures that mandate discontinuation of drug therapy, aspirin should be continued if at all possible -Restart thienopyridine as soon as possible after the procedure because of concerns of late stent thrombosis platelet glycoprotein IIb/IIIa receptor antagonists (fibrinogen receptor inhibitors): -used in combination with aspirin and heparin to treat unstable angina -decrease the incidence of death and MI -inhibit final common pathway involved in adhesion, activation, aggregation abciximab (ReoPro) eptifibatide (Integrilin) tirofiban (Aggrastat) 11
  • 14. NSAIDS Ibuprofen has a very short half-life (2-4 hours) Withhold for 4-6 half-lives prior to invasive dental surgical procedures (about 1 day prior to treatment) Cause bleeding as a side effect, especially GI bleeding FDA Black Box Warning: NSAIDs are associated with an increased risk of adverse cardiovascular thrombotic events, including fatal MI and stroke. In 2006, the FDA issued an informational statement to healthcare professionals stating that “ibuprofen can interfere with the anti-platelet effect of low dose aspirin (81 mg per day), potentially rendering aspirin less effective when used for cardioprotection and stroke prevention. Healthcare professionals should advise consumers and patients regarding the appropriate concomitant use of ibuprofen and aspirin.” 1 The concern is that concurrent use of these medications can increase risk for adverse cardiac events, and thus, the FDA issued the following considerations: • “Counseling patients about the appropriate timing of ibuprofen dosing if they are also taking aspirin for cardioprotective effects. • With occasional use of ibuprofen, there is likely to be minimal risk from any attenuation of the antiplatelet effect of low dose aspirin, because of the long-lasting effect of aspirin on platelets. • Patients who use immediate release aspirin (not enteric coated) and take a single dose of ibuprofen 400 mg should dose the ibuprofen at least 30 minutes or longer after aspirin ingestion, or more than 8 hours before aspirin ingestion to avoid attenuation of aspirin’s effect. • Recommendations about the timing of concomitant use of ibuprofen and enteric-coated low dose aspirin cannot be made based upon available data. • Other nonselective OTC NSAIDs should be viewed as having the potential to interfere with the antiplatelet effect of low-dose aspirin unless proven otherwise. • Prescribing analgesics that do not interfere with the antiplatelet effect of low dose aspirin for high risk populations.” 1 1. U.S. Food and Drug Administration. U. S. Department of Health and Human Services. Information for Healthcare Professionals: Concomitant Use of Ibuprofen and Aspirin. New Information [9/2006] - Concomitant Use of Ibuprofen and Aspirin. Available at: http://www.fda.gov/Drugs/DrugSafety/PostmarketDrugSafetyInformationforPatientsandProviders/ucm125222.htm ANTICOAGULANT MEDICATIONS • Antithrombins o antithrombin o heparin • Coumarin derivatives o warfarin (Coumadin, Jantoven) • Thrombin inhibitors o argatroban – px/tx of thrombosis with heparin-induced thrombocytopenia (HIT); adjunct to PCI if at risk for HIT 12
  • 15. o bivalirudin (Angiomax) – with ASA for unstable angina receiving PCI; undergoing PCI with risk for HIT o dabigatran etexilate (Pradaxa) – thromboprophylaxis for hip/knee replacement o desirudin (Iprivask) – prophylaxis of DVT for hip replacement o fondaparinux (Arixtra) – thromboprophylaxis for hip/knee replacement o lepirudin (Refludan) – anticoagulation with HIT o rivaroxaban (Xarelto) – thromboprophylaxis for hip/knee replacement ANTITHROMBINS • Antithrombin III (Atryn, Thrombate III) o given to those with an antithrombin III deficiency • Heparin - enhances the inhibition rate of clotting proteases by antithrombin III impairing normal hemostasis and inhibition of factor Xa. • Low molecular weight heparins - strongly inhibit factor Xa; higher ratio of antifactor Xa to antifactor IIa activity than unfractionated heparin. Heparin • Naturally-produced anticoagulant (anti-thrombin) • Synthetic version given by IV • Indications: prevention and treatment of thromboembolic disorders • Anticoagulant for dialysis procedures • Heparin Lock flush used to clear IV lines • Produces immediate anticoagulation effect • Patient admitted to hospital is started on heparin and warfarin: heparin produces initial effect Low Molecular Weight Heparins • Use: prevention of DVT with or without PE; reduce risk for PE; acute unstable angina; non-Q- wave MI • Mechanism: Inhibit factor Xa and IIa (thrombin) o dalteparin (Fragmin) o enoxaparin (Lovenox) o tinzaparin (Innohep) Indications for enoxaparin (Lovenox) • Acute coronary syndromes: Unstable angina, non-ST-elevation, and ST-elevation MI • DVT prophylaxis: Following hip or knee replacement surgery, abdominal surgery, or in medical patients with severely-restricted mobility during acute illness who are at risk for TE complications • DVT treatment (acute): Inpatient treatment (patients with and without PE and outpatient treatment (patients without PE) o Note: High-risk patients include those with one or more of the following risk factors: >40 years of age, obesity, general anesthesia lasting >30 minutes, malignancy, history of deep vein thrombosis or pulmonary embolism • Used following hip and knee replacement – at least 10 days and o until risk for DVT has subsided or o patient is adequately anticoagulated on warfarin 13
  • 16. COUMARIN DERIVATIVES • warfarin (Coumadin, Jantoven) • interferes with liver synthesis of vitamin-K dependent clotting factors • effects occurs in 4 to 5 days • when patient is admitted to hospital with stroke, there is a 1 to 2 day overlap period with heparin following warfarin administration to prevent hypercoagulable state o Heparin produces immediate effect o Takes 4-5 days for effects of warfarin to occur • Indications for warfarin: o Prophylaxis and treatment of TE disorders (venous and pulmonary) and embolic complications that arise from atrial fibrillation or cardiac valve replacement o Adjunct to reduce risk of systemic embolism (recurrent MI, stroke) after MI • Investigational: prevention of recurrent TIA • Many things can upset a patient’s level of anticoagulation from warfarin: o Fever o Flu o Diarrhea or vomiting o Use of many drugs, including antibiotics o Change in diet (consumption of green leafy vegetables increases vitamin K intake = promotes clotting) Need vitamin K to synthesize clotting factors in liver Warfarin shuts off production of these clotting factors **Key messages: warfarin causes the greatest number of drug interactions o Always check compatibility prior to issuing a prescription o Always ask about the INR and monitor INR status across time to examine trends in anticoagulation control THROMBIN INHIBITORS dabigatran (Pradaxa) • FDA approved October 2010 • Thrombin inhibitor • Prodrug = lacks anticoagulant activity o converted in vivo to active dabigatran • specific, reversible, direct thrombin inhibitor that inhibits both free and fibrin-bound thrombin • prevents thrombin-mediated effects, and by inhibiting thrombin-induced platelet aggregation • Dabigatran inhibits coagulation by preventing thrombin-mediated effects, including cleavage of fibrinogen to fibrin monomers, activation of factors V, VIII, XI, and XIII • Indications: • Prevention of stroke and systemic embolism in patients with non-valvular atrial fibrillation • Postoperative thromboprophylaxis after total hip or knee replacement o Knee replacement – up to 10 days o Hip replacement – up to 35 days • compared to warfarin (Coumadin) • advantages: no monthly monitoring; fewer drug-drug and drug-diet interactions • disadvantages: very expensive; twice daily dosing 14
  • 17. in studies, patients who took Pradaxa had fewer strokes than those taking warfarin o RE-LY trial = Randomized Evaluation of Long-Term Anticoagulation Therapy • adverse effects: bleeding, GI effects Indications for Direct Antithrombins (Thrombin Inhibitors) • Prevent/reduce ischemia with unstable angina • Prevent DVT following hip replacement • Prevent/treat thromboembolism • Treatment of heparin-induced thrombocytopenia (HIT) rivaroxaban (Xarelto) (riv a ROX a ban) • New drug – FDA approval announced July 1, 2011 • First and only oral anticoagulant approved in US for orthopedic surgery • Factor Xa inhibitor • Mechanism: inhibits platelet activation and fibrin clot formation via direct, selective, and reversible inhibition of factor Xa in both the intrinsic and extrinsic coagulation pathways • Indications: o Postoperative thromboprophylaxis in patients who have undergone hip or knee replacement surgery • Adults: Postoperative thromboprophylaxis: o Knee replacement: 10 mg once daily; recommended total duration of therapy: 12-14 days o Hip replacement: 10 mg once daily; total duration of therapy: 35 days fondaparinux (Arixtra) (fon da PARE i nuks) • Factor Xa inhibitor o causes an antithrombin III-mediated selective inhibition of factor Xa • Interrupts the blood coagulation cascade and inhibits thrombin formation and thrombus development • Indications: • Prophylaxis of deep vein thrombosis (DVT) in patients undergoing surgery for hip replacement and knee replacement • hip fracture (including extended prophylaxis following hip fracture surgery) • abdominal surgery (in patients at risk for thromboembolic complications) • treatment of acute pulmonary embolism (PE) • treatment of acute DVT without PE • Usual duration: 5-9 days o up to 10 days following abdominal surgery o up to 11 days following hip replacement or knee replacement • Extended prophylaxis is recommended following hip fracture surgery o has been tolerated for up to 32 days total • Acute DVT/PE treatment: o Note: Start warfarin on the first treatment day and continue fondaparinux until INR is between 2 and 3 (usually 5-7 days) (Hirsh, 2008) 15
  • 18. COMMON ORAL PROBLEMS IN ELDERLY PATIENTS Disease or Drug Induced Xerostomia Caries and Demineralization Tooth Sensitivity Periodontal Disease Fungal Infections Viral Infections Pain and Ulcerations Food Packing/Decreased Oral Clearance Oral signs and symptoms associated with drug-induced xerostomia Caries Enamel demineralization Enamel erosion Cemental abrasion on exposed root surfaces Dentinal hypersensitivity Increased gingivitis and periodontal infection Opportunistic infections Increased viral infections Oral ulcerations/stomatitis Taste alteration Dry, cracked, bleeding lips Fissured, sore tongue Angular cheilitis Friable oral mucosa Difficulty speaking, chewing, Difficulty wearing dentures or appliances swallowing Drug classes that produce neural effects on the salivary glands The following are examples of anticholinergic drugs that reduce the volume of serous saliva: Antidepressants Antiemetics Antihistamines Antihypertensives Anti-parkinsonian drugs Antipsychotics Antispasmodics The following are examples of sympathomimetic drugs that produce a viscous, mucinous saliva: Amphetamines Appetite suppressants Bronchodilators Decongestants Sources: Sreeby LM, Schwartz SS: A reference guide to drugs and dry mouth, 2nd ed, Gerodontol 14:33-47, 1997;Porter SR, Scully C, Hegarty AM: An update of the etiology and management of xerostomia, Oral Surg Oral Med Oral Pathol Pral Radiol Endod 97:28-46, 2004; Nähri TO, Meurman JH, Ainamo A: Xerostomia and hyposalivation: causes, consequences and treatment in the elderly, Drugs & Aging 15:103-116, 1999. Drug classes associated with causing xerostomia Antiacne agents Antianxiety agents Anticholinergics/Antispasmodics Anticonvulsants Antidepressants Antidiarrheals Antiemetics Antihistamines Antihypertensives Anti-inflammatory analgesics Antinauseants Anti-parkinsonian agents 16
  • 19. Antipsychotics Anorexiants Bronchodilators Decongestants Diuretics Muscle Relaxants Narcotic Analgesics Sedatives Source: USP DI® Drug Information for the Healthcare Professional, vol 1, ed. 24, Englewood, CO, Micromedix, Inc., 2004. Taste and Smell Disorders Drugs that alter taste Alcohol detoxification agents Alzheimer’s medications Analgesics (NSAIDS) Anesthetics (general and local) Anorexiants Antacids Antianxiety agents Antiarthritics Anticholinergics Anticonvulsants Antidepressants Antidiabetics (oral hypoglycemics) Antidiarrheals Antiemetics Antifungals Antigout medications Antihistamine (H1) antagonists Antihistamine (H2) antagonists Antihyperlipidemics Antiinfectives Anti-inflammatory/antiarthritics Antimigraine agents Antiparkinson agents Antipsychotics Antithyroid medications Antivirals Anxiolytics/sedatives Asthma preventives Bronchodilators Calcium-affecting drugs Cancer chemotherapeutics Cardiovascular medications CNS stimulants Decongestants Diuretics Glucocorticoids Gallstone solubilization agents Hemorheologics Immunomodulators Immunosuppressants Irritable bowel syndrome medications Methylxanthines Nicotine replacement drugs Ophthalmics Proton pump inhibitors Retinoids, systemic Salivary stimulants Skeletal muscle relaxants Vitamins Source: Gage TW, Pickett FA: Mosby’s dental drug reference, ed. 7, St. Louis, 2005, Elsevier Mosby. 17
  • 20. Systemic drugs associated with lichenoid drug reactions Category Agents Analgesic agents NSAIDs, propoxyphene/acetaminophen, acetaminophen/codeine Antianxiety drugs benzodiazepines Antiarrhythmics quinidine Anticonvulsant drugs Depakote Antineoplastic drugs levamisole Cardiovascular agents Beta-adrenergic blockers, angiotensin II antagonist, calcium channel blockers, cardiac glycoside, methyldopa, thiazide diuretics, potassium supplements Gastric acid secretion inhibitors H2-antagonists Hormone replacement Thyroid hormone, insulin, sulfonylureas, metformin, oral contraceptives, estrogen, progesterone Photographic Dyes Uricosuric agent Allopurinol 18
  • 21. COURSE TITLE: Commonly Prescribed Medications and Managing the Oral Side Effects of Medication Use COURSE INSTRUCTOR: Ann Eshenaur Spolarich, RDH, PhD COURSE CREDITS: 3 Hours COURSE DATE: February 21, 2013 ________________________________________________________________________ COURSE DESCRIPTION: The purpose of this course is to review the 20 most commonly prescribed medications taken by clients treated in the oral health care environment. In addition, drug interactions, popular drugs in the media and new drugs in dentistry will be discussed. A comprehensive review of drugs and dental care products used to manage the oral side effects of medications will be presented. LEARNING OBJECTIVES: Upon completion of this continuing education course, the participant will be able to: 1. Identify and discuss commonly prescribed medications taken by clients treated in the oral health care setting. 2. Identify common drug interactions of significance to dental professionals. 3. List several new dental drugs and discuss their indications for use in practice. 4. Discuss the management of oral side effects caused by medications. *This material may not be reproduced without the written permission of the author. 1
  • 22. TOP 20 MOST COMMONLY PRESCRIBED MEDS 2011 (Total Prescriptions Dispensed) 1. hydrocodone and acetaminophen 2. hydrocodone and acetaminophen 3. levothyroxine sodium 4. lisinopril 5. Lipitor 6. simvastatin 7. Plavix 8. Singulair 9. azithromycin 10. Crestor 11. Nexium 12. levothyroxine sodium 13. metoprolol tartrate 14. hydrocodone and acetaminophen 15. Synthroid 16. Lexapro 17. Proair HFA 18. ibuprofen 19. trazodone HCl 20. amoxicillin INDICATIONS DRUGS pain relievers hydrocodone and acetaminophen, ibuprofen hypercholesterolemia Lipitor, simvastatin, Crestor hypertension lisinopril, metoprolol adverse thromboembolic events Plavix endocrine disorders levothyroxine, Synthroid antibiotics amoxicillin, azithromycin antidepressants Lexapro, trazodone GERD, reflux or hypersecretory disease Nexium respiratory disease Singulair, ProAir HFA PAIN RELIEVERS BRAND NAME: Co-Gesic, hycet, Lorcet, Lortab, Margesic, Maxidone, Norco, Stagesic, Vicodin, Xodol, Zamicet, Zydone GENERIC NAME: HYCD/APAP (hydrocodone with acetaminophen) THERAPEUTIC CATEGORY: opioid analgesic USE: post-operative pain control ORAL COMPLICATIONS: xerostomia (rare) DRUG INTERACTIONS: Concurrent use of hydrocodone with MAO inhibitors (Nardil, Parnate, Marplan), tricyclic antidepressants (Elavil) and general anesthetics potentiates the effects of the hydrocodone, and increases the risk for toxicity. Dextroamphetamine enhances the analgesic effect of the hydrocodone. Additive CNS effects may occur when taking hydrocodone with other narcotics, antipsychotics, antianxiety agents, general anesthetics and other CNS depressants (eg. alcohol). Phenothiazines (eg. Thorazine) may decrease the analgesic effect of hydrocodone. Acetaminophen taken with alcohol, barbituates or carbamazepine (Tegretol) increases the risk for liver toxicity. Chronic use of acetaminophen may significantly enhance the anticoagulation effects of warfarin (Coumadin). 2
  • 23. BRAND NAME: Caldolor, Ibu, Motrin GENERIC NAME: ibuprofen THERAPEUTIC CATEGORY: NSAID USE: management of mild to moderate pain; inflammatory diseases and rheumatoid disorders, fever, dysmenorrhea ORAL COMPLICATIONS: none DRUG INTERACTIONS: Ibuprofen and other non-selective NSAIDS can interfere with the antiplatelet and cardioprotective effects of aspirin: follow appropriate timing of dosing. Avoid use in aspirin-allergic patients. Ibuprofen may increase the levels of anticoagulants, antiplatelet drugs, bisphosphonates, cyclosporine, digoxin, haloperidol, lithium, methotrexate, NSAIDS, potassium-sparing diuretics, quinolone antibiotics, salicylates, thrombolytic agents, vancomycin and vitamin K antagonists. Levels of ibuprofen may be increased by ACE inhibitors, angiotensin II receptor blockers, antidepressants (tricyclic, teriary amine), systemic corticosteroids, glucosamine, herbs that have anticoagulant or antiplatelet properties, NSAIDS, probenecid, SSRIs, serotonin/norepinephrine reuptake inhibitors. Ibuprofen may decrease the levels of ACE inhibitors, angiotensin II receptor blockers, antiplatelet agents, beta blockers, loop diuretics, potassium-sparing diuretics, salicylates and thiazide diuretics. Levels of ibuprofen may be decreased by bile acid sequestrants, NSAIDS and salicylates. Avoid alcohol. HYPERCHOLESTEROLEMIA BRAND NAME: Lipitor GENERIC NAME: atorvastatin THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor USE: hypercholesterolemia ORAL COMPLICATIONS: none DRUG INTERACTIONS: The risk for myopathy/rhabdomyolysis is increased with concurrent use of the macrolide antibiotics clarithromycin and erythromycin, and the azole antifungal agents fluconazole (Diflucan), itraconazole (Sporanox) and ketoconazole (Nizoral). Risk for rhabdomyolysis also may be increased with concurrent use of other lipid lowering agents, cyclosporoine, certain calcium channel blockers (diltiazem (Cardizem), verapamil (Calan)) and protease inhibitors. Atorvastatin may also increase the effect of levothyroxine (Synthroid). BRAND NAME: Zocor GENERIC NAME: simvastatin THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor USE: hypercholesterolemia ORAL COMPLICATIONS: taste alteration DRUG INTERACTIONS: The risk for myopathy/rhabdomyolysis is increased with concurrent use of the macrolide antibiotics clarithromycin and erythromycin, and the azole antifungal agents fluconazole, itraconazole and ketoconazole. Risk for rhabdomyolysis also may be increased with concurrent use of other lipid lowering agents, cyclosporoine, certain calcium channel blockers and protease inhibitors. The anticoagulant effect of warfarin may be increased by simvastatin. BRAND NAME: Crestor GENERIC NAME: rosuvastatin calcium THERAPEUTIC CATEGORY: HMG-CoA reductase inhibitor USE: used with dietary therapy for hyperlipidemias to reduce elevated total cholesterol, LDL-C, apolipoprotein B and triglycerides in patients with hypercholesterolemia and for treatment of familial hypercholesterolemia ORAL COMPLICATIONS: none 3
  • 24. DRUG INTERACTIONS: The anticoagulant effects of warfarin may be increased by rosuvastatin: monitor carefully. Rosuvastatin increases the serum concentrations of the hormonal contraceptives ethinyl estradiol and norgestrel. Concurrent administration of other cholesterol lowering medications (gemfibrozil, clofibrate, fenofibrate or niacin) may increase the risk for myopathy and rhabdomyolysis. Metal containing antacids may decrease the plasma concentratins of rosuvastatin: administer antacids at least 2 hours after dosing. Bile acid sequestrants may reduce the absorption of rosuvastatin. HYPERTENSION BRAND NAME: Prinivil, Zestril GENERIC NAME: lisinopril THERAPEUTIC CATEGORY: ACE inhibitor USE: hypertension, adjunctive therapy for congestive heart failure, post-MI if hemodynamically stable ORAL COMPLICATIONS: xerostomia, dry cough, angioedema DRUG INTERACTIONS: Increased risk for hypotension with alcohol, phenothiazines (antipsychotics)and probenecid. ACE inhibitors increase serum concentrations of digoxin, lithium and sulfonylureas (oral hypoglycemics). Increased risk for toxicity with potassium or potassium-sparing diuretics. Diuretics have additive hypotensive effects when used with ACE inhibitors. Caution when using NSAIDS in patients with compromised renal function who are taking ACE inhibitors. NSAIDS, including high dose aspirin, may decrease the antihypertensive effects of ACE inhibitors. Antacids decrease the bioavailability of ACE inhibitors. BRAND NAME: Toprol-XL GENERIC NAME: metoprolol succinate THERAPEUTIC CATEGORY: cardioselective beta blocker USE: hypertension, angina, prevention of MI, atrial fibrillation; investigational for ventricular arrhythmias, migraines, essential tremors, aggressive behavior ORAL COMPLICATIONS: xerostomia DRUG INTERACTIONS: Metoprolol may increase the effects of other drugs that slow AV conduction, alpha-blockers and alpha-adrenergic stimulants (eg. epinephrine). Epinephrine is safe to use in patients taking cardioselective beta blockers (lowest dose, least concentration). NSAIDS (ibuprofen, indomethacin) used for greater than 3 weeks can decrease the antihypertensive effects of the drug. The effects of beta blockers are decreased with aluminum salts, calcium salts, barbituates, bile acid sequestrants (cholesterol-lowering drugs), NSAIDS, penicillins, rifampin and salicylates. Beta blockers may decrease the effects of sulfonylureas (oral hypoglycemics), and may slow the metabolism of lidocaine. Increased hypotension and bradycardia may be observed with concurrent use of inhaled anesthetics and fentanyl derivatives. ADVERSE THROMBOEMBOLIC EVENTS BRAND NAME: Plavix GENERIC NAME: clopidogrel THERAPEUTIC CATEGORY: antiplatelet agent USE: reduce risk of atherosclerotic events in patients with history of recent MI, stroke, or established peripheral arterial disease; acute coronary syndrome (unstable angina) ORAL COMPLICATIONS: none DRUG INTERACTIONS: Clopidogrel interfere with the metabolism of many medications, including oral hypoglycemics, phenytoin and some NSAIDS, increasing risk for toxicity. Concurrent use of clopidogrel with naproxen increases risk for GI bleeding. Anticoagulant medications taken with antiplatelet medications increases risk for bleeding. Atorvastatin (Lipitor) and macrolide antibiotics 4
  • 25. (clarithromycin, erythromycin) decrease the effects of clopidogrel. Many herbs interact with Plavix and increase risk for bleeding: discontinue 14 days prior to surgery. ENDOCRINE DISORDERS BRAND NAME: Synthroid GENERIC NAME: levothyroxine THERAPEUTIC CATEGORY: hormone USE: hypothyroidism ORAL COMPLICATIONS: none DRUG INTERACTIONS: Levothyroxine increases the effects of oral anticoagulants (Coumadin), causing an increased risk of bleeding. When taken together, toxicity may occur for both levothyroxine and tricyclic antidepressants (Elavil). Antacids containing aluminum and magnesium, iron, bile acid sequestrants (colestipol, cholestyramine), and the ulcer medication sucralfate (Carafate) decrease the absorption of levothyroxine. Certain seizure medications (phenytoin, phenobarbitol and carbamazepine) and the TB medication rifampin (Rifadin) decrease levothyroxine levels. Levothyroxine may decrease the effect of oral sulfonylureas. ANTIBIOTICS BRAND NAME: Amoxil, Moxatag GENERIC NAME: amoxicillin THERAPEUTIC CATEGORY: antibiotic USE: infections of ear, skin, respiratory and urinary tracts; premedication ORAL COMPLICATIONS: oral candidiasis and black hairy tongue DRUG INTERACTIONS: Concomitant use of amoxicillin and erythromycin or amoxicillin and tetracycline is contraindicated. Amoxicillin may decrease the efficacy of oral contraceptives; therefore, patients should be instructed to use an alternative form of birth control while taking this antibiotic. Disulfiram (Antabuse), used to treat alcoholism, and the uric acid lowering agent probenecid (Benemid) cause increased levels of amoxicillin The effects of warfarin may be increased. BRAND NAME: AzaSite, Zithromax, Zmax GENERIC NAME: azithromycin THERAPEUTIC CATEGORY: macrolide antibiotic USE: orofacial and respiratory tract infections; middle ear infections, pharyngitis, strep throat, tonsillitis, pneumonia; premedication ORAL COMPLICATIONS: none DRUG INTERACTIONS: Antacids containing aluminum or magnesium (Maalox, Mylanta) should not be taken with azithromycin, as antacids decrease serum levels of the drug. Two hours should lapse prior to taking azithromycin following the use of an antacid. As with erythromycin, azithromycin interacts with many drugs, and may increase the levels of some antihistamines (Hismanal), cyclosporine (Sandimmune), carbamazepine (Tegretol), digoxin (Lanoxin), phenytoin (Dilantin), triazolam (Halcion), warfarin (Coumadin) and antiasthmatic drugs containing theophylline. Concomitant use of the macrolide antibiotics with the HMG Co-A reductase inhibitors increases the risk for rhabdomyolysis. Antibiotics decrease the effectiveness of oral contraceptives. 5
  • 26. ANTIDEPRESSANTS BRAND NAME: Lexapro GENERIC NAME: escitalopram THERAPEUTIC CATEGORY: selective serotonin reuptake inhibitor USE: major depressive disorder; generalized anxiety disorders (GAD) ORAL COMPLICATIONS: xerostomia, toothache, vomiting DRUG INTERACTIONS: Do not take this drug with MAOIs: fatal reactions have been reported. Combined use of this drug with other SSRIs and/or other classes of antidepressants increases risk for serotonin syndrome. Use of this drug with aspirin, NSAIDS and other drugs that alter coagulation increases risk for bleeding. Systemic azole antifungals, ciprofloxacin, clarithromycin, diclofenac, doxycycline, erythromycin, and other CYP3A4 inhibitors may increase the levels and/or effects of escitalopram. Avoid drinking alcohol with this medication. Combined use of SSRIs with sumatriptan (Imitrex) or other serotonin agonists may result in toxicity. CYP3A4 inducers may decrease the levels/effects of escitalopram, including cabamazepine nafcillin, phenobarbital and phenytoin. BRAND NAME: Oleptro GENERIC NAME: trazodone THERAPEUTIC CATEGORY: serotonin reuptake inhibitor/antagonist USE: major depressive disorder ORAL COMPLICATIONS: xerostomia, taste alteration DRUG INTERACTIONS: Sedative effects may be increased with alcohol and other CNS depressants; levels of trazodone may be increased by buspirone, SSRIs and venlafaxine. Trazodone may decrease levels/effects of dabigatran. Avoid use of methylene blue (used to treat methemoglobinemia and UTI). GERD OR HYPERSECRETORY DISEASE BRAND NAME: Nexium GENERIC NAME: esomeprazole THERAPEUTIC CATEGORY: proton pump inhibitor USE: short-term treatment of erosive esophagitis; symptomatic gastroesophageal reflux disease (GERD) ORAL COMPLICATIONS: xerostomia DRUG INTERACTIONS: Esomeprazole may increase the levels of carbamazepine, statin drugs, and some benzodiazepines (diazepam, midazolam, triazolam). Drugs in this class may decrease the absorption of antiretroviral medications, iron, and systemic antifungal medications (itraconazole, ketoconazole). Esomeprazole may decrease the levels of phenytoin. Drug absorption is significantly decreased (43%-53%) when taken with food; take at least 1 hour before meals. RESPIRATORY DISEASE BRAND NAME: Singulair GENERIC NAME: montelukast THERAPEUTIC CATEGORY: leukotriene-receptor antagonist USE: prophylaxis and chronic treatment of asthma; seasonal allergies; perennial allergic rhinitis ORAL COMPLICATIONS: none DRUG INTERACTIONS: Phenylketonuric patients should be informed that the chewable tablets contain phenylalanine. Carbamazepine, phenobarbital, phenytoin, rifampin, and nafcillin may decrease the levels of montelukast. St. John’s wort may also decrease the levels of montelukast. 6
  • 27. BRAND NAME: ProAir HFA GENERIC NAME: albuterol THERAPEUTIC CATEGORY: beta 2-adrenergic agonist USE: asthma, chronic obstructive pulmonary disorder (COPD) ORAL COMPLICATIONS: xerostomia, altered taste, vomiting, tooth discoloration DRUG INTERACTIONS: Increased toxicity (cardiovascular effects) is noted when albuterol is used with any of the following drugs: MAO inhibitors (Marplan, Nardil, Parnate), tricyclic antidepressants (Elavil), sympathomimetic agents (amphetamines, dopamine) and inhaled anesthetics(malignant arrhythmias). The effect of albuterol is decreased when used with nonselective beta blockers. When used with inhaled ipratropium (Atrovent), an increase in the duration of bronchodilation may occur. REFERENCES FOR TOP 20 MEDICATIONS Top 200 Medications for 2011. Source: IMS Health. Available at: http://www.pharmacytimes.com/publications/issue/2012/July2012/Top-200-Drugs-of-2011 Physicians’ Desk Reference, ed. 65. Montvale, Medical Economics Co, Inc., 2011. Mycek MJ, Harvey RA, Champe PC: Lippincott’s Illustrated Reviews: Pharmacology. ed. 3. Philadelphia, Lippincott-Raven, 2006. Wynn RL, Meiller TF, Crossley HL. Drug Information Handbook in Dentistry. 18th ed. Hudson, Lexi- Comp Inc., 2012. Gage TW, Pickett FA. Mosby’s Dental Drug Reference. 7th ed. St. Louis, Mosby, Inc., 2005. Pickett FA, Terezhalmy GT. Dental Drug Reference with Clinical Implications. 2nd ed. Baltimore, Lippincott Williams & Wilkens, 2008. FDA WATCHES AND WARNINGS varenicline (Chantix) FDA Safety Alert and Public Health Advisory Statement Patients should be provided with a medication guide highlighting neuropsychiatric symptoms receiving this medication Angioedema, serious skin reactions, visual impairment, accidental injury July 2011 – relabeling changes due to cardiovascular concerns; FDA is requiring manufacturer to conduct meta-analysis of clinical trials to examine risks: http://www.fda.gov/Drugs/DrugSafety/ucm259161.htm#safety azithromycin, clarithromycin May be associated with liver failure 7
  • 28. tramadol (Ultram, Ultracet) FDA safety labeling revision Potential risk for potentially life-threatening serotonin syndrome Serotonin syndrome may occur with use of tramadol alone or with concurrent use of SSRIs, tricyclic antidepressants, MAOIs Adverse events may occur at recommended tramadol dose tramadol is indicated for moderate to moderately severe pain in adults for short-term use (≤5 days) for acute pain MANAGEMENT OF ORAL SIDE EFFECTS CAUSED BY MEDICATIONS FLUORIDE THERAPY For caries control: Prescription fluorides for supplemental home use: 1.1% neutral sodium 5000 ppm Clinpro 5000 Anti-Cavity Toothpaste (3M ESPE), gel or dentifrice Prescription Control Rx (Discus Dental), Fluoridex Daily Defense Dentifrice and Gel (Discus Dental), NUPRO NuSolutions Toothpaste (Dentsply), Oral B Neutracare (P&G), PreviDent 5000 Booster toothpaste, PreviDent Gel, PreviDent 5000 Plus (Colgate), ProDenRx Dentifrice and Gel (Zila), Topex Take Home Care (Sultan Healthcare) 0.2% neutral sodium 920 ppm CaviRinse (3M ESPE), NaFrinse (Medical Products rinse Prescription Laboratory), Oral B Fluorinse (P&G), PreviDent Dental Rinse (Colgate), ProDenRx Rinse (Zila) 1.1% sodium and 5000 ppm Phos-Flur (Colgate) acidulated Prescription phosphate gel 0.4% stannous 1000 ppm Fluoridex Daily Defense Sensitivity Relief (Discus fluoride gel Dental); Gel-Kam Oral Rinse (Colgate), Kid Kare Plus 0.4% Stannous Fluoride Brush-on Dentifrice, Kids Kare 0.4% Stannous Fluoride Brush-on Gel (Zila), ProDenRx 0.4% Stannous Fluoride Brush-on Gel (Zila), Topex Take Home Care (Sultan Healthcare) 0.63% stannous 30 ml dose PerioMed (3M ESPE), Fluoridex Daily Renewal fluoride rinse dilution = 7 (Discus Dental) mg fl- ion and 22 mg stannous ion 8
  • 29. Over-the-counter supplemental fluorides for home use: 0.05% neutral sodium rinse 230 ppm Reach Act, Fluorigard, NaF rinse acidulated, NaF rinse neutral 0.044% sodium and 200 ppm Phos-Flur (Colgate); OrthoWash (3M ESPE) acidulated phosphate rinse 0.4% stannous fluoride gel 1000 Gel-Kam Treatment Gel (Colgate), Just For Kids ppm (3M ESPE), Omni Gel (3M ESPE), Oral B Stop (P&G) 0.0221% sodium fluoride Listerine Total Care, Listerine Smart Rinse (J&J) Fluoride Varnishes: 22,600 PPM sodium fluoride 5% sodium fluoride varnish varnish in AllSolutions (Dentsply) (in-office use only) a tube or Duraphat (Colgate) single- Duraflor (A.R. Medicom) unit dose Enamel Pro Varnish with ACP (Premier) dispensers FluoroDose (Centrix) Fluoridex Lasting Defense (Discus Dental) Prevident (Colgate) Profluorid Varnish (VOCO) Vanish (Omni/3M EPSE) VarnishAmerica with xylitol (Medical Products Laboratories) Vella with xylitol (Preventech) Waterpik UltraThin (Teledyne) SALIVARY REPLACEMENT THERAPY 1. OTC Artificial Saliva Preparations: PRODUCT Entertainer’s Secret® Moi-Stir® Mouthkote® Salivart® Salix® -carboxymethylcellulose = gives feeling of viscosity -relief while product is in contact with the tissues; convenience -some contain preservatives: parabens (PABA) = allergy potential 2. Biotene product line (GlaxoSmithKline): toothpaste, oral gel, mouthrinse, chewing gum -contain 3 key salivary enzymes found in natural saliva; sodium fluoride, xylitol 3. Orajel product line (Del Pharmaceuticals, Inc.): dry mouth moisturizing gel and spray - moisturizing gel and spray -18% glycerin; -sorbitol (gel); xylitol (spray) -moisturizing toothpaste -thione antioxidant complex; sodium monofluorophosphate (0.18% w/v fluoride ion) -sugar-free; sorbitol, xylitol; no sodium lauryl sulfate 9
  • 30. 4. Oasis (Oasis Consumer Healthcare) -mouthwash or mouth spray -“TriHydra” technology: hydrophilic polymers, xanthum gum, glycerine and carboxymethylcellulose; relieves symptoms for up to 2 hours 5. GC Dry Mouth Gel (GC America) -alcohol free, sugar free, neutral pH, applied as needed 6. Salese (Nuvora) -lozenge with water absorbing polymer plus xylitol; raises pH; Dentiva: antimicrobial 7. Colgate Dry Mouth Relief Mouthrinse (Colgate Oral Pharmaceuticals) -fluoride mouthrinse (0.02% sodium fluoride = 90 ppm); tri-polymer system to help coat soft tissues; moisture retention; alcohol free; soothing, mild flavor 8. Two prescription drugs now available to stimulate salivary flow: Salagen (5 mg pilocarpine hydrochloride) -cholinergic agonist that stimulates muscarinic acetylcholine receptors in the salivary glands to increase serous salivary flow. -need to take the drug for a minimum of 90 days to see optimum effects -contraindicated if known hypersensitivity to the drug, uncontrolled asthma or narrow-angle glaucoma -drug interactions associated with pilocarpine include anticholinergic medications (eg. antiparkinsonion drugs, carbamazepine, digoxin, sedative antihistamines, tricyclic antidepressants), cholinergic medications (eg. antiglaucoma drugs) and beta-adrenergic blocking drugs -indicated for radiation therapy patients and Sjogren’s syndrome - dosage: for radiation therapy patients: - 5 mg tid (15-30 mg per day); 12 weeks of therapy - dosage: for Sjogren’s patients: - 5 mg qid; efficacy has been established after 6 weeks of use Evoxac (cevimeline) -cholinergic agonist used to treat xerostomia in patients with Sjogren’s syndrome - dosage: 30 mg tid -contraindications: hypersensitivity to drug or any of its components, uncontrolled asthma, narrow-angle glaucoma, acute iritis, conditions where miosis is undesirable -use with caution in patients with CV disease, asthma, COPD, decreased visual acuity, the elderly, or in those with kidney problems ANTIMICROBIALS -an important adjunct in managing the oral complications of xerostomia -reduce plaque formation, and to prevent or reduce the severity of gingivitis -promotes a healthy oral ecosystem -OTC and prescription antimicrobials available on the market from which to choose -3 FDA and ADA approved antimicrobials: chlorhexidine, Listerine® and triclosan (Colgate® Total) - Other agents available as mouthrinses exhibit antibacterial properties, but do not possess good substantivity: -stannous fluoride = antibacterial. carioprotective and desensitizing effects 10
  • 31. -cetylpyridinium chloride = rupture bacterial cell walls and alter cytoplasmic contents; bind strongly to plaque and tooth surfaces (Cepacol®, Scope®, Advanced Formula Viadent®; alcohol free: Crest® Pro Health Rinse, BreathRx) -Crest Pro Health Rinse with CPC has data to support 12 hour substantivity = vehicle improves bioavailability -oxygenating agents = damage bacteria by altering cell membrane permeability -Natural Dentist® Health Gums Moisturizing Antigingivitis Mouthrinse -contains all natural formulation -germ kill of 40 oral pathogens, including Strep mutans and some red complex -comparable to Listerine® in terms of pathogen reduction -4 published clinical trials and MIC laboratory data to support efficacy -Triclosan (Colgate® Total toothpaste) -antimicrobial agent in dentifrice form = decreases plaque viability -both antimicrobial and anti-inflammatory properties -unique technology of delivery mode: PVM/MA copolymer = GANTREZ -copolymer allows binding to surfaces with slow release; promotes adhesion/uptake of triclosan on enamel, plaque and soft tissue -triclosan: broad spectrum, substantive to 12 hours -over 75 clinical trials to support safety and efficacy of Colgate® Total -anti-inflammatory effect: dampens stimulation of the production of IL1- beta and TNF alpha = inflammatory mediators (cytokines) that destroy tissue and bone = local host modulation -Crest® Pro Health dentifrice -stannous fluoride multi-care dentifrice -older formulations: adverse taste and staining effects; instable in aqueous solutions -0.454% stabilized stannous fluoride with sodium hexametaphosphate -sodium hexametaphosphate = pyrophosphonate (anti-calculus/anti- staining) -polymer of repeated pyrophosphate subunits -stronger affinity to calcium hydroxyapatite in enamel and dentin -greater prevention of crystallization at enamel surface (calculus prevention) and adsorption of stains from chromogens (staining) - silica-based low-water dentifrice to reduce hydrolysis of sodium hexametaphosphate and to maintain effective pyrophosphate levels -12 hour substantivitiy Important take home messages with antimicrobials: - chlorhexidine and CPC are cations: drug reactions with SLS and fluoride = wait 30 minutes after brushing or vigorously remove all toothpaste residue before rinsing - chlorhexidine and Listerine have been shown to kill 7 species of Candida - chlorhexidine and Listerine kill multiple species of Strep: Strep mutans 11
  • 32. - chlorhexidine and Listerine have been shown to reduce incidence and severity of aphthous ulcers ANTIFUNGALS - fungal infections occur as a result of alterations in oral flora, immunosuppression and underlying systemic disease (diabetes, xerostomia, anemia, chemo, inhaled steroids) - opportunistic infections - clinical presentation: - pseudomembranous appearance (bright red with overlying white pseudomembrane); atrophic appearance (tongue); hyperkeratotic appearance (denture stomatitis); symptomatic geographic tongue; angular cheilitis -drug therapy includes topical and systemic medications depending upon the extent and severity of the infection. -azole antifungals are used to treat chronic, extensive mucocutaneous candidiasis -polyenes are used to treat local candidiasis (topicals) -antifungals are being used in combination with corticosteroids, such as nystatin and triamcinolone, to treat both the fungal infection and the inflammation of angular cheilitis - medications must be used for a minimum of 48 hours after the disappearance of clinical signs and symptoms; re-evaluate condition 14 days after therapy has been completed - efficacy of topical drugs is dependent upon contact with the lesions - some topical preparations contain sugar - may choose to prescribe vaginal preparation - in addition to antifungals, consider chlorhexidine or essential oil mouthrinses for long term prevention - prescription antifungals for systemic use if patient is refractory to topicals: *cautions: liver function and multiple drug interactions Topical Antifungal Medications: nystatin ointment apply thin coat to affected area (or inner surface of denture) 4-5 times per day Mycelex ® 10 mg troches disp: 70 troches; dissolve 1 troche in mouth 5 times per day until (clotrimazole) gone; leave any prosthesis out during treatment and soak prosthesis in nystatin liquid suspension overnight Nizoral® 2% cream apply thin coat to affect areas (or to inner surface of denture) after (ketoconazole) meals iodoquinol and hydrocortisone apply locally to affected area 3-4 times per day for 10 days to 2 cream weeks, then re-evaluate nystatin and triamcinolone apply locally to affected area 4 times per day for 10 days to 3 weeks acetonide ointment and then re-evaluate Topical nystatin: - is well-tolerated, non-sensitizing - soak dentures in nystatin suspension overnight - nystatin ointment can be placed in denture and worn during day (like an adhesive) 12
  • 33. Systemic Azole Antifungal Medications: Diflucan® fluconazole Take 2 tablets on day 1, then 1 tablet daily for 14 days until gone 100 mg tablets *a shorter course may be adequate; extensive infection may require second course of treatment Nizoral® ketoconazole Take 1 tablet daily with a meal for 14 days 200 mg *may cause irreversible liver damage with long-term use (greater than 3 weeks) ANTIVIRALS - viral infections: acute onset of symptoms - vesicular eruption of soft tissues - rupture of vesicles leaves ulcerations - ulcerations are generally small in size - if left untreated, ulcerations coalesce to form large lesions - primary infection can present as: gingivostomatitis, recurrent lip lesions (herpes labialis), intraoral ulcers (recurrent intraoral herpes) that involve oral/perioral tissues - primary infection is systemic that leads to acute gingivostomatitis involving multiple tissues: buccal mucosa, lips, tongue, floor of mouth, gingiva - management of viral infections is generally palliative (although acyclovir is now used for prevention of primary infections) - treatment of primary infections includes combination therapy: - acyclovir - topical anesthetic rinses (eg. Benadryl, Xylocaine viscous, OTC benzocaine products ) - fluids, vitamins and mineral supplements and rest Antiviral Medications for Herpes Simplex: Zovirax® 200 mg tablets acyclovir take 1 capsule 5 times per day for 10 days or 2 capsules 3 times per day for 10 days Zovirax® ointment 5% acyclovir apply q 3 hours (6 times/day) for 7 days Denavir® cream 10mg/g penciclovir apply every 2 hours (lips and face only) for 4 days (1%) Valtrex® 500 mg valacyclovir 2 grams twice daily for 1 day at prodrome (separate doses by 12 hours) Abreva (OTC) docosanol 10% apply locally as directed 5 times per day; start at prodrome and continue for 4 days; do not apply directly to inside of mouth or around eyes Viroxyn® (OTC) alcohol/benzalkonium single dose applicator/vial; at prodrome, rub chloride medication into lesion until medication is gone (10 seconds) ORAL ULCERATIONS (NON-VIRAL) AND PAIN CONTROL -Recurrent Aphthous Stomatitis: - patients with recurrent aphthous should be evaluated for iron, folic acid and/or vitamin B12 deficiency - severe recurrent aphthous may be treated with an oral suspension of tetracycline 13
  • 34. - regular use of Listerine has been shown to reduce the frequency, duration and severity of lesions; chlorhexidine has been shown to reduce duration of lesions -localized ulcerations: - OTC topical anesthetic agents containing benzocaine in protective preparations - Benzocaine and tetracaine (Viractin) are esther anesthetics; therefore, caution must be used when recommending these OTC products to clients with reported allergies to anesthetics or to PABA - Debacterol (sulfonated phenolics in aqueous solution) – therapeutic cauterization - dry ulcer, apply directly to lesion, keep in contact for 5-10 seconds; (larger lesions may need up to 2 minutes); rinse immediately, and expectorate with water -generalized oral pain: - OTC agent such as Chloraseptic® spray - prescription mouthrinse Xylocaine ® 2% (viscous lidocaine) - Benadryl® elixir and Benylin® cough syrup -severe pain, such as that associated with mucositis: - anesthetic agents may be mixed with OTC coating agents to provide lubrication and relief from pain - Benadryl® elixir added in equal amounts to Maalox®, Mylanta® or Kaopectate® - sucralfate (Carafate®), the prescription medication used to treat duodenal ulcers, may be prepared as a 1 gm/15 mL suspension for use in this population as well. (A pharmacist should be consulted to assist with the preparation of oral suspensions.) -dry, cracked lips: topical water-based product; Oral Balance® Topical prescription agents for aphthous lesions: amlexanox oral paste 5% Apthasol® apply 4 times per day (after meals and at bedtime) until area heals triamcinolone acetonide Oralone®0.1%; Kenalog in apply after each meal and at Dental Paste Orabase® 0.1% bedtime chlorhexidine oral rinse Peridex®, PerioGard® rinse with 20 ml for 30 sec tid fluocinonide 0.05% Lidex® ointment mixed 50/50 apply thin layer to oral lesions 4 (used for oral inflammatory with Orabase (30 grams total) times per day lesions that do not respond to Kenalog in Orabase®) clobetasol propionate 0.05% Temovate® apply small quantity with a cotton tip applicator to affected area 3-4 times daily betamethasone 0.1% ointment apply small quantity with a cotton tip applicator to affected area 3-4 times daily dexamethasone elixir Decadron® rinse with 1 teaspoon for 2 0.5 mg/5 mL minutes 4 times per day and expectorate 14
  • 35. Topical OTC agents for aphthous/pain control: Benzyl alcohol Zilactin® Gel apply q 3-4 hours Benzocaine 10% Zilactin® B apply q 3-4 hours Lidocaine 2.5% Zilactin L apply q 3-4 hours Diphenhydramine Benadryl® Elixir swish with 1 tsp for 2 min before each meal (can be used as a swish and swallow) Benzocaine, gelatin, pectin and Orabase® with Benzocaine apply 3-4 times/day sodium carboxymethylcellulose Tetracaine Hydrochloride 1% Viractin® apply 3-4 times/day up to 7 days 15