SlideShare une entreprise Scribd logo
1  sur  76
The LaMonica Family:
Joint Pain
Molly Bruce, RN, BSN, FNP-Student
NURO 752
Mrs. Sofia LaMonica is a 78-yr-female who presents
with c/o shoulder pain, hip pain, fatigue, and weakness
that began about one month ago. She was diagnosed
with mild iron deficiency anemia (improved with
treatment), depression, Vitamin D deficiency (corrected
on replacement), and fibromyalgia by her previous PCP.
She has not noted improvement in sxs on current
regimen of cyclobenzaprine 10 mg at bedtime and
duloxetine 60 mg daily. Her daughter is with her and
reports that her mother has difficulty dressing herself,
needs help to stand from a chair, and has difficulty lifting
her arms. She denies headaches or changes in vision
or hearing.
Social History
Moved from Sicily 7 years ago to live with her daughter
and her son-in-law. Her primary language is Italian and
she speaks little English. Never smoker. Occasional
glass of wine. Former elementary school teacher. Four
children, 3 of whom live in the US, one is deceased.
Widowed x 25 yrs, not sexually active since her
husband died.
Past Medical History: HTN controlled on meds x 6
years, OA for which she takes occasional ibuprofen.
Hysterectomy age 38, no HRT, DEXA 4 years ago
normal BMD.
Family Medical Hx: Adopted, knows no biologic family
hx. Oldest daughter died age 24 from Lupus Nephritis
complications. All other children are well.
Medications
• Duloxetine 60 mg daily
• Cyclobenzaprine 10 mg at bedtime
• Valsartan 160 mg daily
• HCTZ 25 mg each morning
• Calcium 600 mg twice daily
• Vitamin D 2000 mg daily
• Ibuprofen 400-600 mg up to three times daily PRN
Considerations
• What are some socio-cultural considerations that should
be implemented for this patient?
• Consider the patient’s religious beliefs, family structure,
ethnic value, and cultural identity.
• Would it be appropriate to use her daughter as a
translator?
• No!
• What are the legal implications for using her daughter as a
translator?
• Misinterpretation of information could lead to mistakes or
misdiagnosis.
ROS: Pertinent Findings
• General: positive for – fatigue, weakness
• Psychological: negative for anxiety,
depression, memory loss
• Ophthalmic: positive for dry eyes. Negative for
blurry vision, vision loss other than r/t age
• ENT: Positive for decreased hearing r/t age.
Negative for - earache, sore throat, hoarseness,
dysphagia, facial pain, and dry mouth, jaw
claudication
• Allergy and Immunology: negative for hx of
allergies or frequent infections
• Hematological and Lymphatic: negative for
excessive bruising, swollen or painful nodes
• Endocrine: negative for hx of diabetes, thyroid
problems
• Respiratory: negative, denies SOB, wheezing,
cough
• Cardiovascular: positive for peripheral edema
in the evenings, resolves by morning; negative
for Chest pain, palpitations
• Gastrointestinal: positive for occasional
indigestion; negative for reflux, black or bloody
stools
• Genitourinary: positive for hx of UTI, otherwise
negative
• Musculoskeletal: Positive for - Joint pain,
Stiffness and Morning stiffness; negative for
joint swelling or redness
• Neurological: negative for - headaches and
numbness/tingling; positive for occasional
vertigo
• Skin/Hair/Nails: Negative for rash, itch,
unusual lesions, dandruff, abnormal nails.
Joints
Physical Exam
• VS: BP 124/62 | Pulse 68 | Temp
97.9 °F (36.6 °C) (Oral) | Resp
16 | Ht 1.626 m (5' 4") | Wt
60.782 kg (134 lb) | BMI 23.00
kg/m2
• General: NAD
• HENT: TM Pearly Gray, no
enlarged or tender nodes, thyroid
normal, PERLA, EOM intact, no
nystagmus
• Mouth: MMM, no lesions noted,
good dentition, uvula midline,
pharynx without erythema or
exudate
• Skin/Nails: warm & dry w/out
rash, no increased warmth or
tenderness
• CV: RRR: Temporal pulse 2+,
equal with no masses or
tenderness; trace edema from
toes to mid calf, cap refill
bilateral great toes <3 secs,
Pedal & PT pulses 1+, Radial
pulse 2+
• Lungs: CTA throughout; Normal
respiratory effort & rate
• Sensation: intact to touch,
position
• Strength: 4/5 UE & LE bilateral,
unable to stand without
assistance
• Neuro: Neg Romberg, finger to
nose & rapid alternating
movements normal
• DIP: no swelling, normal motion,
Heberden’s nodes 2,3 bilaterally
• PIP: no swelling, tenderness;
minor Bouchard’s nodes
throughout
• MCP: no swelling or tenderness
• Grip: mildly decreased strength,
complete, equal
• Wrist: decreased motion, no
swelling or tenderness
• Elbow: normal motion, no
swelling or tenderness
• Shoulder: limited, painful
motion, 5/10 tenderness, no
swelling
• Hip: mildly decreased adduction
and abduction
• Knee: normal motion, no
swelling, mild crepitus
• Ankle: normal motion, no
redness or swelling
• Foot/Toes: + squeeze
• Tender points: Widespread,
18/18 positive 3-4/10
• Other: Normal gait
Osteoarthritis
Osteoarthritis
• Definition: A degenerative disorder of the joints, with a prevalence that
increases with age. Joints affected normally involve the knee, hip,
hands, cervical and lumbar spine. These patients may have stiffness
and joint pain WORSE with activity.
• Pharmacologic Treatment Options
• Hand OA: Topical capsaicin or topical NSAIDs, oral NSAIDs/COX-2
inhibitors, tramadol
• >75 years-old, use topical rather than oral NSAIDs.
• Knee OA: Acetaminophen, oral NSAIDs, topical NSAIDs, tramadol,
intraarticular corticosteroid injections
• Hip OA: Acetaminophen, oral NSAIDs, tramadol, intraarticular corticosteroid
injections
• Risk Factors
• Older age
• Sex (females>males)
• Obesity
• Occupation: repetitive movement of joints
(Hochberg et al, 2012)
Diagnostics
• What studies/labs should be ordered?
CBC, CMP, Vitamin D, Inflammatory Markers, UA
Lab Results: CBC
Lab Results: CMP
Question
• Were there any CMP or CBC values that were significant to
developing differentials?
WBC: 13.0 (H)
Hemoglobin: 11.1 (L)
Seg (neutrophils): 88.9% (H)
Lymphocytes: 9.1% (L)
Monocytes: 1.8% (L)
Absolute neutrophils: 11.6 (H)
Urea Nitrogen: 24 (H)
Glucose: 102 (H)
BUN/Creatinine: 21.6 (H)
• Look at inflammatory markers and urinalysis!
Additional Work-Up
• ESR (Sed Rate): 84 (H)
• CRP: <0.8
• CPK: 189 U/L
• Rheumatoid Factor <30.0 IU/ML
• Vitamin D : 46 (25-Hydroxy)
• Color, UA yellow
• Appearance, Urine clear
• Glucose, Ur neg
• Bilirubin Urine neg
• Ketones, Ua neg
• Specific Gravity, Urine 1.005
• Blood, Urine neg
• pH, Urine 5
• Protein Urine neg
• Urobilinogen, Ua 0.2
• Nitrite, Urine neg
• WBC Esterase/Urine neg
Labs in Inflammatory Disorders
Acute Phase Reactants: Blood proteins that are either increased or decreased
w/in hours of inflammatory response.
CBC w/ diff: blood counts
CMP: liver and kidney functions
ANA: Elevated in SLE, Sjogren’s syndrome, RA, mixed connective tissue
disease, scleroderma, polymyositis/dermatomyositis
Anti-extractable nuclear antigen (ENA): Highly specific for SLE, but only found
in around 25% of SLE patients. Also found in systemic sclerosis and mixed
connective tissue disease
Rheumatoid factor: Sensitive for detecting RA
Anti-cyclic citrullinated peptide antibody (CCP): A newer biomarker for RA. Do
this lab w/ RF for RA dx. CCP can also be found in psoriatic arthritis, lupus,
Sjogren’s syndrome, TB, and inflammatory myopathies.
(Castro & Gourley, 2010)
Differential Diagnosis
Mrs. LaMonica: 78 years-old w/ shoulder and hip pain,
fatigue, morning stiffness and weakness x 1 month in
addition to difficulty dressing herself, lifting her arms, and
standing up from a seated position. Elevated ESR.
• Polymyalgia Rheumatica
• Rheumatoid Arthritis
• Fibromyalgia
• Polymyositis
• Overuse bursitis/tendonitis
Polymyalgia Rheumatica (PMR): An inflammatory
rheumatologic disorder with manifestations of aching and
morning stiffness that could involve the neck, hips, shoulders,
and torso.
Polymyalgia Rheumatica
• Pathophysiology: The cause of PMR is not known, but
inflammation is thought to occur due to an autoimmune
reaction causing the immune system to attack the
synovium. The reason for this is unknown. Environmental
and genetic factors are thought to play a role.
• Risk Factors
• Older age
• Average age of onset is 70 years-old
• Sex
• Females are twice as likely to develop PMR
• Ethnicity
• Caucasian patients are more likely to develop PMR
(Saad, 2014)
Polymyalgia Rheumatica: ACR
Diagnostic Criteria
1: An age of 50 years-old+ at onset
2: Bilateral aching & morning stiffness that lasts 30 minutes
or more that persists for at least 1 month, and involves at
least 2/3 following areas: neck or torso, shoulders or
proximal regions of the arms, and hips or proximal aspects of
the thighs
3: ESR (Westergren) elevated to 40 mm/h or more
4: Normocytic, normochromic anemia in approximately 50%
of patients
Mrs. LaMonica: PMR
Symptoms/RFs
• Shoulder and hip pain
• Morning stiffness
• >50 years-old
• Female
• Difficulty standing from
seated position
• Elevated ESR
• Swelling in lower
extremities
• Depression
• Rapid onset of symptoms;
symptoms for one month
• Decreased ROM in wrists,
shoulders, hips
PMR: Treatment
• PO Steroid and Tapering Regimen
• Prednisone 15mg QD x 3 weeks
• Then 12.5 mg QD x 3 weeks
• Then 10 mg QD x 4-6 weeks
• Then reduce by 1 mg Q 4-8 weeks OR alternate day reductions (7.5
mg/10 mg alternate days)
• IM Methylprednisolone: Used in milder cases. May reduce risk of
steroid-induced complications.
• Initial dose of 120 mg Q 3-4 weeks
• Reduce by 20 mg Q 2-3 months
• Duration of Treatment: Normally, 1-3 years of treatment is needed.
Some require small doses beyond this. Stop steroids when
continued lack of inflammatory symptoms. If needing > 3 years of
treatment, may need to consider alternative dx.
• Additional Therapies: Bone protection needed with LT corticosteroid
therapy.
(Dasgupta, 2010)
PMR: Relapse
Relapse should be treated ONLY under specialist care.
• Relapse includes recurring symptoms of PMR or new
onset of GCA.
• Treating Relapse:
• Onset of GCA
• Follow usual treatment guidelines for GCA.
• Recurring PMR
• Increase prednisone to previous higher dose
• Administer a single dose of IM methylprednisolone 120 mg
• After 2 relapses, need to consider immunosuppressive
therapy.
(Dasgupta, 2010)
PMR and GCA can occur together. We need to assess Mrs.
LaMonica for this, before implementing her treatment plan!
Giant Cell Arteritis: A chronic systemic inflammatory
vasculitis of both medium and large arteries that occurs in
patients >50 years-old. It often affects superficial temporal
arteries, and occurs due to an autoimmune reaction.
• Risk Factors: Etiology and pathogenesis unknown.
• Diagnosis of PMR (15% w/ PMR will develop GCA)
• Age (>50)
• Sex (F>M)
(Dasgupta et al., 2010)
GCA
• Diagnostics
• Temporal Artery Biopsy
• Can be negative in some patients. If they have a typical clinical
picture of GCA and respond to steroids, should be regarded as
having GCA.
• Others: CBC, urea, electrolytes, LFTs, CRP, ESR
• Acute-phase response is characteristic: elevated ESR, CRP,
anemia, abnormal LFTs, thrombocytosis, raised alk phos
(Dasgupta et al., 2010)
American College of Rheumatology
Classification Criteria for Giant Cell
Arteritis
Criterion[∗] Definition
Age at disease onset ≥50 yr Development of symptoms or findings beginning at
age 50 or older
New headache New onset or new type of localized pain in the head
Temporal artery abnormality Temporal artery tenderness to palpation or
decreased pulsation, unrelated to arteriosclerosis of
cervical arteries
Elevated erythrocyte sedimentation rate (ESR) ESR ≥50 mm/hr by the Westergren method
Abnormal artery biopsy Biopsy specimen with artery showing vasculitis
characterized by a predominance of mononuclear
cell infiltration or granulomatous inflammation,
usually with multinucleated giant cells
Symptoms of Giant Cell
Arteritis
Symptom Frequency (%)
Headache 76
Weight loss 43
Fever 42
Fatigue 39
Any visual symptom 37
Anorexia 35
Jaw claudication 34
Polymyalgia rheumatica 34
Arthralgia 30
Unilateral visual loss 24
Bilateral visual loss 15
Vertigo 11
Diplopia 9
Mrs. LaMonica: GCA
Symptoms/RFs
• 15-20% of patients with PMR might also have Giant Cell Arteritis
(GCA).
• Positive findings:
• >50 years-old
• Elevated ESR
• Occasional vertigo
• Negative findings:
• No headache
• No tenderness to temporal artery or decreased pulsation
• No jaw claudication
Is it likely that Mrs. LaMonica could also have GCA?
If we had a strong suspicion for GCA, would a referral be urgent?
GCA: Treatment
If Mrs. LaMonica were to develop GCA it would require a
PROMPT REFERRAL!
• 1/5th of GCA cases result in irreversible blindness.
Preventable with prompt diagnosis and treatment.
• Glucocorticosteroids: Start while awaiting results from
temporal artery biopsy.
• Uncomplicated GCA (NO visual disturbance or jaw
claudication): 40-60 mg prednisone QD
• Complicated GCA (evolving visual loss): 500 mg- 1 g of IV
methylprednisolone for 3 days before PO
glucocorticosteroids
• Visual Loss: 60 mg prednisone QD to protect contralateral
eye
• May require 1-2 years of treatment (Dasgupta et al., 2010)
Plan
• Pharmacologic:
• Prednisone 15mg PO daily x 3 weeks, then 12.5mg PO daily x 3
weeks, then 10mg PO daily x 4-6 weeks, then reduce by 1mg Q
4-8weeks
• Continue calcium and vitamin D. Add a Bisphosphonate
(Alendronate 10mg PO daily).
• D/C Ibuprofen. Start topical capsaicin for OA, 0.025 to 0.075%
TID-QID, as needed. Acetaminophen 650-1000mg up to QID, as
needed (no more than 4000mg/day to avoid liver toxicity).
• D/C Cyclobenzaprine. Increased r/of serotonin syndrome w./
Cymbalta. Also, increased r/of drowsiness and fatigue.
• Nonpharmacologic: Limit ETOH, do not smoke cigarettes, weight-
bearing exercise (as tolerated)
• Education: Educate on prednisone therapy- can weaken immune
system, no live vaccines, take w/ food, side effects; Educate on
S/S of GCA and importance of seeking emergent care if these
develop. Do NOT abruptly stop taking steroids.
(Dasgupta et al., 2009)
Recommendations for
Glucocorticoid Treatment
Falls: Risk Factors
• Polypharmacy: 4+
medications
• Accident, environmental
hazard
• Confusion, cognitive
impairment
• Postural hypotension
• Medications:
corticosteroids,
sedatives, anxiolytic
drugs, antihypertensive
meds
Preventing Falls in the
Elderly
• Elimination of
environmental hazards
• Review and modify
medications
• Provide balance training
• Involve family
• Provide follow-up
PMR: Follow-up & Monitoring
• Follow-up schedule: 24-72 hours; weeks 1-3, 6; months 3,
6, 9, 12 in first year (+ extra visits if relapse of adverse
events)
• Clinical Monitoring: At each follow-up visit, assess for…
• Response to treatment and disease activity
• Disease complications (ex. GCA)
• Atypical features
• Side effects r/t steroid therapy
• Laboratory Monitoring
• CBC, ESR, CRP, urea, electrolytes, glucose
Follow-up
Mrs. LaMonica returns two days later. Her HPI, ROS, and PE
remain unchanged. You review the lab results with her and
her daughter and discuss the likely differentials with patient
as well as your plan of care.
Should we refer Mrs. LaMonica
to a specialist?
Consider referral if…
A) Presentation with atypical
features/features that are
unlikely in PMR:
1. <60 years-old
2. >2 months onset
3. No shoulder involvement
4. No inflammatory stiffness
5. Prominent systemic features,
night pain, wt loss, neuro signs
6. Symptoms of other rheumatic
disease
7. Normal or extremely high
acute-phase response
B) Dilemmas in treatment
including:
1. Unresponsive or incomplete
response to corticosteroids
2. Contraindications to
corticosteroid therapy
3. A need for corticosteroid
therapy that will be prolonged
(>2 years)
Patients with typical clinical
presentations, adequate
response to treatment, and no
adverse events can be managed
in a primary care setting.
(Dasgupta et al., 2009)
Osteoporosis
• Primary
• Postmenopausal: low estrogen
• Senile: occurs > 70 years-old
• Secondary: Caused by other etiologies
• Diseases
• Pharmacological therapy
• Lifestyle behaviors
• Imaging Recommendations
• BMD every two years, in the absence
of new risk factors.
• FRAX
• http://www.shef.ac.uk/FRAX/
Mrs. LaMonica’s FRAX Score
Health Maintenance
What health maintenance does Mrs. LaMonica need, being
that she is a 78 year-old female?
• Bone Mineral Density (every other year): Last done 4
years ago
• Colonoscopy (every 5-10 years after age 50)
• Mammogram (annually after age 40)
• Vaccinations: PNA (>65 years-old), Zostavax (>60 years-
old), Tetanus
Sarah LaMonica
History of Present
Illness
Sarah LaMonica is a 27-yr-old female who presents today with c/o
painful red and swollen fingers, elbows, and knees for the past 3
weeks. She states her joints began to hurt after she returned from a 2
week backpacking trip with her partner along the Appalachian Trail.
She denies injury but did have a tick bite. She c/o feeling fatigued
even though she states she is resting well at night. She has not been
able to do her usual daily workout or runs because of the stiffness
and pain. She states it takes her “all morning to loosen up” and then
she is still stiff, but not as bad. States this “has really messed my life
up”. She denies other health issues other than PTSD. Reports her
LMP was 1 week ago. Her grandmother, Sophia LaMonica is a
patient here, and was recently diagnosed with PMR. Sarah wonders
if she could have that too since she is so tired.
Social History
• Lives with her partner, Diane and 9 month old adopted daughter,
Abbie. She attended college for one year but dropped out and joined
the army. She had two tours in Iraq, one for 6 months followed by a
second tour for 12 months. Manages a food co-op and taking some
education classes.
• Denies smoking. Drinks 1-2 beers each weekend with her friends.
Denies recreational drugs. Sexually active in monogamous relationship
with partner of 5 years. States she has a good family relationship
which has helped her deal with her PTSD since leaving the military.
The food co-op does not provide health insurance and she cannot get
coverage under her partner’s policy.
Family History
• Mother: 49yo- HTN, OA
• Father: 56yo- HTN, COPD, former smoker
• Brother: 18yo- healthy
• Sister: 16yo- asthma
• Paternal Grandmother: deceased 78yo- COPD, CHF
• Paternal Grandfather: deceased 82yo- COPD, MI
• Maternal Grandmother: 76yo- HTN, OA, PMR
• Maternal Grandfather: deceased 53yo- MI, HTN, CVA
• Maternal Aunt: deceased r/t SLE nephritis
Past Medical History
• PTSD
• Anxiety
• Appendectomy, age 9
Current Medications
• No prescription medications
• Takes daily MVI, Benadryl at night for sleep
• Was on Zoloft and Xanax for anxiety but could not afford it
Review of Systems
• General: positive for – fatigue, negative
for weakness
• Psychological: positive anxiety,
depression related to PTSD
• Ophthalmic:. Negative for blurry vision,
vision loss, dry eyes
• ENT: Negative for - earache, sore throat,
hoarseness, dysphagia, facial pain, and
dry mouth
• Allergy and Immunology: negative for
hx of allergies or frequent infections
• Hematological and Lymphatic:
negative for excessive bruising, swollen
or painful nodes
• Endocrine: negative for hx of diabetes,
thyroid problems
• Respiratory: negative, denies SOB,
wheezing, cough
• Cardiovascular: negative for Chest pain,
palpitations, edema
• Gastrointestinal: negative for reflux,
black or bloody stools, indigestion
• Genitourinary: negative for hx of UTI,
menorrhagia, metrorrhagia
• Musculoskeletal: Positive for - Joint
pain, Stiffness and Morning stiffness,
joint swelling
• Neurological: negative for - headaches
and numbness/tingling
• Skin/Hair/Nails: Negative for rash, itch,
unusual lesions, abnormal nails.
Physical Exam
• General: healthy, NAD
• Skin/Nails: no rashes, ulcers;
nails normal
• Lymph: no adenopathy noted
• Scalp/Hair: no scaling, no
alopecia
• Eyes: non injected, PEERLA,
EOMS full
• Mouth: normal mucosa
moisture, no ulcers
• Neck: no masses, thyroid
normal
• CV: RRR, normal S1 & S2, no
murmurs or rubs
• Lungs: clear to auscultation
• Abd: non tender, no
organomegaly
• C-Spine: normal lateral
rotation, lateral bending,
flexion and extension
• T-Spine: normal flexion and
extension, no tenderness,
normal alignment
• L-S Spine: normal flexion and
extension, no tenderness,
normal alignment
• Reflexes: 2+ biceps, triceps,
brachioradialis, knee and
ankle
• Muscles: 5/5 for deltoids,
biceps, triceps, quadriceps,
hamstrings and hip flexors
• Sensation: normal to light
touch, vibration and position
• Shoulders: FROM, no
swelling
• Elbows: 1+ swelling R elbow;
trace L elbow
• Wrists: trace swelling &
tenderness bilateral wrists
• MCPs: 3+ tenderness
throughout with trace
swelling 1, 2 L, 1+ 1,2 R
• PIPs: 2+ swelling & tenderness
2-5 bilaterally
• DIPs: no swelling, no
tenderness
• HIPs: FROM, no swelling
• Knees: L FROM, Tenderness;
R 1 + tenderness, 1-2+
swelling, no redness, mildly
increased warmth
• Ankles: no tenderness or
swelling
• Feet/toes: no swelling or
tenderness
• Bursa: no tenderness or
swelling
Physical Exam
Swollen PIPs
5
4
3
2
1
No swollen DIPs
Swollen MCPs
Physical Exam
Swollen knee
Evaluation
• Differential Diagnosis
• Rheumatoid arthritis
• Lyme disease
• SLE
• Osteoarthritis
• Psoriatic arthritis
Labs and Diagnostics
• CBC w/ differential
• CMP
• Rheumatoid Factor
• Acute Phase Reactants: ESR, CRP
• Anticyclic citrullinated peptide (Anti-CCP) antibodies
• Imaging: Ms. LaMonica is uninsured. Would you obtain
an X-ray on this patient?
Lab Results: CBC
Lab Results: CMP
Lab Results
The 2010 ACR-EULAR Classification Criteria for RA
Score
A) Joint Involvement
1 large joint 0
2-10 large joints 1
1-3 small joints (w/ or w/o involvement of large joints) 2
4-10 small joints (w/ or w/o involvement of large joints) 3
>10 joints (at least 1 small joint) 5
B) Serology (at least 1 test result needed for
classification)
Negative RF and negative anti-CCP 0
Low-positive RF or low-positive anti-CCP 2
High-positive RF or high-positive anti-CCP 3
C) Acute-phase reactants (at least 1 needed for
class.)
Normal CRP and normal ESR 0
Abnormal CRP or abnormal ESR 1
D) Duration of symptoms
<6 weeks 0
Sarah LaMonica
Score
A) Joint Involvement
1 large joint 0
2-10 large joints 1
1-3 small joints (w/ or w/o involvement of large joints) 2
4-10 small joints (w/ or w/o involvement of large joints) 3
>10 joints (at least 1 small joint) 5
B) Serology (at least 1 test result needed for
classification)
Negative RF and negative anti-CCP 0
Low-positive RF or low-positive anti-CCP 2
High-positive RF or high-positive anti-CCP 3
C) Acute-phase reactants (at least 1 needed for
class.)
Normal CRP and normal ESR 0
Abnormal CRP or abnormal ESR 1
D) Duration of symptoms
<6 weeks 0
Rheumatoid Arthritis
• Definition: An inflammatory disease characterized by swelling,
pain, stiffness, and loss of function of joints. Commonly occurs
in wrist and fingers.
• Pathophysiology: Autoimmune. WBCs travel to synovium and
cause synovitis, resulting in warm, red, swollen, and painful
joints. With progression of disease, inflammation of the
synovium results in destruction of cartilage and bone in the joint.
Thought to be caused by environmental and genetic factors.
• Risk Factors:
• Sex: F>M
• Age: middle-age
• Family history
(U.S. National Library of Medicine, 2015)
Rheumatoid Arthritis
(ACR, 2012)
Clinical Practice Guidelines:
Treatment of Early RA
(Singh et al,
2012)
(Singh et al, 2012)
Pharmacological Interventions
for RA
There is NO cure for RA. The goal of treatment is to lessen
symptoms and slow progression of disease.
• Glucocorticoids: May be prescribed at initial presentation of RA
symptoms or for flares. Resolution of joint pain and inflammation
after steroid therapy can help further confirm susceptibility of
RA.
• NSAIDs: Improve mobility. Help with pain.
• DMARDs: Mainstay treatment; methotrexate,
hydroxychloroquine, sulfasalazine, leflunomide
• Biologic agents: abatacept, humira, anakinra, etanercept,
remicaide, rituxan, etc.; normally taken w/ methotrexate
(ACR, 2012)
Non-pharmacological
Interventions for RA
• Diet
• Low cholesterol (at risk for CAD)
• Fish oils, plant oils can improve pain and swelling of joints
• Occupational/physical therapy: Can help preserve joint function
• Splints: Reduce joint pain and improve function of joints
• Exercise
• Increase ROM: preserve/restore joint function
• Increase strength: isotonic, isometric, isokinetic
• Increase endurance: walking, cycling, swimming
• Surgery: End-stage RA; damaged joints
(National Guideline Clearinghouse, 2012)
Sarah LaMonica: Plan
• What medications will you prescribe, if any?
• Prednisone, taper as directed.
• What education will you provide the patient with?
• Take prednisone with food. Discuss side effects: emotional
lability, appetite changes, anxiety, insomnia, headache,
weight gain, etc.
• What are her options for obtaining health insurance?
• Medicaid: see if she meets qualifications
• Medically Indigent Adult Programs
• Veterans Benefits
(Forester, 2009)
Follow-up
Ms. LaMonica returns to the clinic in one week. Her joint
swelling has improved on prednisone and she generally is
feeling much better. She continues on prednisone taper.
PE: Unchanged other than she now has no swelling in her
joints.
What is your diagnosis, based on the findings?
Plan
• Prescriptions: NSAIDs, if still having joint pain. Continue
prednisone taper.
• Referrals: Rheumatology, first available appointment.
Send over copies of her office notes, labs, and current
medications.
• Patient Education: Educate patient on rheumatoid arthritis
and how it can be managed. Educate on importance of
seeing rheumatologist.
• Follow-up: After rheumatology consult, and as needed.
The Uninsured
Resources for PCP:
• GoodRx
• What You Can Do to Help Uninsured Patients:
http://www.aafp.org/fpm/2009/0900/p21.html
• Is the patient really uninsurable?
• Review OOP costs of labs/diagnostics with patients
• Prescribe generic medications
• Be aware of large retail companies offering more affordable
medication prices
• Offer discounts to cash-paying patients
PTSD
Sarah, returns several months later. She has been
diagnosed with RA. The diagnosis seems to have triggered
her nightmares, anxiety and insomnia. She is having a hard
time taking care of Abbie and had to quit her job. Things
were going so well. Now she needs your help. Can you give
her something for sleep? She just wants to be knocked out.
PTSD
• Definition: Occur in patients for >1 month after being exposed to
a traumatic event causing them significant distress or
impairment in occupational, social or other areas of functioning.
• Symptoms: avoidance of stimuli associated w/ traumatizing
event, re-experiencing of the traumatic event, numbing
sensation, increased arousal
• PTSD can appear alone, or more commonly w/ co-occurring
conditions (insomnia, identity problems, mood changes,
difficulties in interpersonal relationships, nightmares, chronic
pain) or with other psychiatric disorders (anxiety, depression,
substance abuse)
May have delayed onset (at least 6 months after the event).
(Department of Veterans Affairs, 2010)
PTSD: Screening
In primary care, the PTSD Screen is used:
In your life, have you ever had any experience that was so frightening, horrible, or
upsetting that, in the past month, you:
1. Have had nightmares about it or thought about it when you did not want to?
YES / NO
2. Tried hard not to think about it or went out of your way to avoid situations that
reminded you of it?
YES / NO
3. Were constantly on guard, watchful, or easily startled?
YES / NO
4. Felt numb or detached from others, activities, or your surroundings?
YES / NO
The results of this test are considered "positive" if a patient answers "yes" to any
three items.
(Department of Veterans Affairs, 2010)
PTSD: Treatment
• First-line treatment for PTSD based on guidelines suggest the
initiation of psychotherapeutic interventions using effective
modalities of trauma-focused therapy or stress management
AND/OR initiating pharmacotherapy (mono-therapy using SSRI or
SNRI)
• Adjunctive therapy might include treatment of symptom-specific
management including insomnia, pain, or anger.
• Ensure the patient has an adequate support system.
(Department of Veterans Affairs, 2010)
PTSD: Resources
• General and mental
health; Refer patient!
• Support groups
• VA Benefits Counselors
• PTSD Association
• Anxiety and Depression
Association of America
• National Alliance for
Mental Illness
References
• American College of Rheumatology. (2012). Rheumatoid arthritis. Retrieved from:
https://www.rheumatology.org/Practice/Clinical/Patients/Diseases_And_Conditions/Rheumatoid_Arthritis/
• American College of Rheumatology. (2010). Rheumatoid arthritis classification. Retrieved from:
https://www.rheumatology.org/practice/clinical/classification/ra/ra_2010.asp
• Castro, C. & Gourley, M. (2010). Diagnostic testing and interpretation of tests for autoimmunity. The Journal
of Allergy and Clinical Immunology, 125(2), 238-247.
• Clauw, D.J. (2014). Fibromyalgia: A clinical review. The Journal of the American Medical Association, 311(15),
1547-1555.
• Dasgupta, B., Borg, F., Hassan, N., Barraclough, K., Bourke, B., Fulcher, J.,… & Hollywood, J. (2009). BSR
and BHPR guidelines for the management of polymyalgia rheumatica. Oxford Journals, 109(10), 1-5.
• Dasguta, B. (2010). Concise guidance: Diagnosis and management of giant cell arteritis. Retrieved from:
https://www.rcplondon.ac.uk/sites/default/files/giant-cell-arteritis-concise-guideline.pdf
• Dasgupta, B., Borg. F., Hassan, N., Alexander, L., Barraclough, K., Bourke, B.,…Fulcher, J. (2010). BSR and
BHPR guidelines for the management of giant cell arteritis. Oxford Journals, 109(10).
• Department of Veterans Affairs. 2010. Clinical practice guidelines for management of post-traumatic stress.
Retrieved from: http://www.healthquality.va.gov/guidelines/MH/ptsd/cpg_PTSD-FULL-201011612.pdf
• Forester, R., & Heck, R. (2009). What you can do to help your uninsured patients. Family Practice
Management, 16(5), 21-24.
• Grossman, J., Gordon, R., Ranganath, V., Deal, C., Caplan, L., Chen, W.,… & Curtis, J. (2010). American
College of Rheumatology recommendations for the prevention and treatment of glucocorticoid-induced
osteoporosis.
References Cont’d
• Hochberg, M., Altman, R., April, K., Benkhalti, M., Guyatt, G., McGowan, J.,… & Towheed, T. (2012). Recommendations for the use of
nonpharmacologic and pharmacologic therapies in osteoarthritis of the hand, hip, and knee. Arthritis Care and Research, 64(4), 465-474.
• National Clinical Guideline Centre. (2014). Osteoarthritis: Care and management in adults. Retrieved from:
http://www.guideline.gov/content.aspx?f=rss&id=47862#Section420
• National Guideline Clearinghousee. Rheumatoid arthritis: Diagnosis, management and monitoring. Retrieved from:
http://www.guideline.gov/content.aspx?id=39244
• National Institute of Arthritis and Musculoskeletal and Skin Diseases. (2012). Polymyalgia rheumatica and giant cell arteritis. Retrieved from:
http://www.niams.nih.gov/health_info/polymyalgia/
• National Osteoporosis Foundation. (2014). Clinician’s guide to prevention and treatment of osteoporosis. Retrieved from:
http://nof.org/files/nof/public/content/file/2791/upload/919.pdf
• Saad, E.R. (2014). Polymyalgia rheumatica. Retried from: http://emedicine.medscape.com/article/330815-overview#a4
• Sinusas, K. (2012). Osteoarthritis: Diagnosis and treatment. American Family Physician, 85(1), 49-56.
• United States National Library of Medicine. (2015). Rheumatoid arthritis. Retrieved from:
http://www.nlm.nih.gov/medlineplus/rheumatoidarthritis.html
• University of Maryland Medical Center. (2013). Osteoporosis. Retrieved from: http://umm.edu/health/medical/reports/articles/osteoporosis
• Veterans Health Initiative. (2002). Post-traumatic stress disorder: Implications for primary care. Retrieved from:
http://www.publichealth.va.gov/docs/vhi/posttraumatic.pdf

Contenu connexe

Tendances

Rheumatoid arthritis diagnosis
Rheumatoid arthritis diagnosisRheumatoid arthritis diagnosis
Rheumatoid arthritis diagnosisAmaal bataiha
 
Rheumatoid arthritis
Rheumatoid arthritisRheumatoid arthritis
Rheumatoid arthritisswathisravani
 
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...Richard Brown
 
Approach to myopathy
Approach to myopathyApproach to myopathy
Approach to myopathyNeurologyKota
 
Critical illness Polyneuropathy & Myopathy
Critical illness Polyneuropathy & MyopathyCritical illness Polyneuropathy & Myopathy
Critical illness Polyneuropathy & MyopathyNeurologyKota
 
Case study-motor system,myopathy,muscular dystrophy
Case study-motor system,myopathy,muscular dystrophyCase study-motor system,myopathy,muscular dystrophy
Case study-motor system,myopathy,muscular dystrophyapoorvaerukulla
 
Myopathies and its ayurvedic perspective
Myopathies and its ayurvedic perspective  Myopathies and its ayurvedic perspective
Myopathies and its ayurvedic perspective Rashmi Ramankutty
 
Myopathy for medical students
Myopathy for medical studentsMyopathy for medical students
Myopathy for medical studentsDr-Ashraf Abdou
 
Rheumatoid arthritis -gihs
Rheumatoid arthritis  -gihsRheumatoid arthritis  -gihs
Rheumatoid arthritis -gihsgangahealth
 
Proximal limb girdle syndromes approach
Proximal limb girdle syndromes approachProximal limb girdle syndromes approach
Proximal limb girdle syndromes approachAshok vp
 
Myasthenia gravis
Myasthenia gravisMyasthenia gravis
Myasthenia gravisSijo A
 
Myopathy undergraduate
Myopathy undergraduateMyopathy undergraduate
Myopathy undergraduateOsama Ragab
 
Rheumatoid arthritis nov 2020
Rheumatoid arthritis nov 2020Rheumatoid arthritis nov 2020
Rheumatoid arthritis nov 2020Mukiza1
 

Tendances (20)

Rheumatoid arthritis diagnosis
Rheumatoid arthritis diagnosisRheumatoid arthritis diagnosis
Rheumatoid arthritis diagnosis
 
Rhumatoid arthritis
Rhumatoid arthritisRhumatoid arthritis
Rhumatoid arthritis
 
Rheumatoid arthritis
Rheumatoid arthritisRheumatoid arthritis
Rheumatoid arthritis
 
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...
Myasthenia Gravis and Guillan Barre Syndrome (Acute Inflammatory Demyelinatin...
 
Approach to myopathy
Approach to myopathyApproach to myopathy
Approach to myopathy
 
Dm msk compl.
Dm msk compl.Dm msk compl.
Dm msk compl.
 
Myasthenia gravis
Myasthenia gravisMyasthenia gravis
Myasthenia gravis
 
Critical illness Polyneuropathy & Myopathy
Critical illness Polyneuropathy & MyopathyCritical illness Polyneuropathy & Myopathy
Critical illness Polyneuropathy & Myopathy
 
Myopathies
MyopathiesMyopathies
Myopathies
 
Case study-motor system,myopathy,muscular dystrophy
Case study-motor system,myopathy,muscular dystrophyCase study-motor system,myopathy,muscular dystrophy
Case study-motor system,myopathy,muscular dystrophy
 
Myopathies and its ayurvedic perspective
Myopathies and its ayurvedic perspective  Myopathies and its ayurvedic perspective
Myopathies and its ayurvedic perspective
 
Myopathy for medical students
Myopathy for medical studentsMyopathy for medical students
Myopathy for medical students
 
Rheumatoid arthritis -gihs
Rheumatoid arthritis  -gihsRheumatoid arthritis  -gihs
Rheumatoid arthritis -gihs
 
Proximal limb girdle syndromes approach
Proximal limb girdle syndromes approachProximal limb girdle syndromes approach
Proximal limb girdle syndromes approach
 
Myasthenia gravis
Myasthenia gravisMyasthenia gravis
Myasthenia gravis
 
Myopathy undergraduate
Myopathy undergraduateMyopathy undergraduate
Myopathy undergraduate
 
Myasthenia gravis
Myasthenia gravisMyasthenia gravis
Myasthenia gravis
 
Rheumatoid arthritis nov 2020
Rheumatoid arthritis nov 2020Rheumatoid arthritis nov 2020
Rheumatoid arthritis nov 2020
 
Rheumatoid Arthritis
Rheumatoid ArthritisRheumatoid Arthritis
Rheumatoid Arthritis
 
Myasthenia gravis
Myasthenia gravisMyasthenia gravis
Myasthenia gravis
 

En vedette

polymyalgia rheumatica
polymyalgia rheumaticapolymyalgia rheumatica
polymyalgia rheumaticadrmomusa
 
Upper Respiratory Infection (URI) Cheat Sheet
Upper Respiratory Infection (URI) Cheat SheetUpper Respiratory Infection (URI) Cheat Sheet
Upper Respiratory Infection (URI) Cheat SheetJustin Berk
 
Rheumatic Disorders Part IV
Rheumatic Disorders Part IVRheumatic Disorders Part IV
Rheumatic Disorders Part IVCarmela Domocmat
 
community acquired pneumonia (CAP)
community acquired pneumonia (CAP) community acquired pneumonia (CAP)
community acquired pneumonia (CAP) Hamdi Turkey
 

En vedette (6)

StephanieWalkerPMR
StephanieWalkerPMRStephanieWalkerPMR
StephanieWalkerPMR
 
polymyalgia rheumatica
polymyalgia rheumaticapolymyalgia rheumatica
polymyalgia rheumatica
 
Upper Respiratory Infection (URI) Cheat Sheet
Upper Respiratory Infection (URI) Cheat SheetUpper Respiratory Infection (URI) Cheat Sheet
Upper Respiratory Infection (URI) Cheat Sheet
 
Rheumatic Disorders Part IV
Rheumatic Disorders Part IVRheumatic Disorders Part IV
Rheumatic Disorders Part IV
 
community acquired pneumonia (CAP)
community acquired pneumonia (CAP) community acquired pneumonia (CAP)
community acquired pneumonia (CAP)
 
congestive heart failure
 congestive heart failure congestive heart failure
congestive heart failure
 

Similaire à LaMonicaFamily_JointPain_Bruce_N752

Neuromyelitis Optica
Neuromyelitis OpticaNeuromyelitis Optica
Neuromyelitis OpticaArka De
 
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and Treatment
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and TreatmentDr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and Treatment
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and TreatmentPeer Support Network
 
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docx
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docxSOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docx
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docxrosemariebrayshaw
 
Myxedema & hypothyroid
Myxedema &  hypothyroidMyxedema &  hypothyroid
Myxedema & hypothyroidAhad Lodhi
 
JIA1.ppt a basic approach to know about JIA
JIA1.ppt a basic approach to know about JIAJIA1.ppt a basic approach to know about JIA
JIA1.ppt a basic approach to know about JIARitasman Baisya
 
hypothyroidism.pdf
hypothyroidism.pdfhypothyroidism.pdf
hypothyroidism.pdfWafa sheikh
 
Tuberculous meningitis
Tuberculous meningitisTuberculous meningitis
Tuberculous meningitisarnab ghosh
 
Cerebral Venous Sinus Thrombosis (CVST) Case Report
Cerebral Venous Sinus Thrombosis (CVST) Case ReportCerebral Venous Sinus Thrombosis (CVST) Case Report
Cerebral Venous Sinus Thrombosis (CVST) Case ReportAHMED TANJIMUL ISLAM
 
an Approach to Dyspepsia
an Approach to Dyspepsiaan Approach to Dyspepsia
an Approach to DyspepsiaAhmed Almumtin
 
Tbm case presentation by dr imtiaz
Tbm case presentation by dr imtiazTbm case presentation by dr imtiaz
Tbm case presentation by dr imtiazWest Medicine Ward
 
A young woman with lupus
A young woman with lupusA young woman with lupus
A young woman with lupusEnida Xhaferi
 
barded bidel syndrome
barded bidel syndromebarded bidel syndrome
barded bidel syndromeJani Mehul
 

Similaire à LaMonicaFamily_JointPain_Bruce_N752 (20)

Neuromyelitis Optica
Neuromyelitis OpticaNeuromyelitis Optica
Neuromyelitis Optica
 
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and Treatment
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and TreatmentDr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and Treatment
Dr Richard Schloeffel - Chronic Fatigue Syndrome Diagnosis and Treatment
 
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docx
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docxSOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docx
SOAP NOTEName  C.M.Date 04082016Time 1055Pt. Encount.docx
 
Ra and oa residents
Ra and oa residentsRa and oa residents
Ra and oa residents
 
Myxedema & hypothyroid
Myxedema &  hypothyroidMyxedema &  hypothyroid
Myxedema & hypothyroid
 
JIA1.ppt a basic approach to know about JIA
JIA1.ppt a basic approach to know about JIAJIA1.ppt a basic approach to know about JIA
JIA1.ppt a basic approach to know about JIA
 
Multiple sclerosis 2015
Multiple sclerosis 2015 Multiple sclerosis 2015
Multiple sclerosis 2015
 
SLE
SLESLE
SLE
 
hypothyroidism.pdf
hypothyroidism.pdfhypothyroidism.pdf
hypothyroidism.pdf
 
Tuberculous meningitis
Tuberculous meningitisTuberculous meningitis
Tuberculous meningitis
 
Evans syndrome
Evans syndromeEvans syndrome
Evans syndrome
 
A case profile of sle
A case profile of sleA case profile of sle
A case profile of sle
 
celiac disease
celiac diseaseceliac disease
celiac disease
 
Cerebral Venous Sinus Thrombosis (CVST) Case Report
Cerebral Venous Sinus Thrombosis (CVST) Case ReportCerebral Venous Sinus Thrombosis (CVST) Case Report
Cerebral Venous Sinus Thrombosis (CVST) Case Report
 
Grand round- SLE- LUPUS NEPHRITIS
Grand round- SLE- LUPUS NEPHRITISGrand round- SLE- LUPUS NEPHRITIS
Grand round- SLE- LUPUS NEPHRITIS
 
an Approach to Dyspepsia
an Approach to Dyspepsiaan Approach to Dyspepsia
an Approach to Dyspepsia
 
Tbm case presentation by dr imtiaz
Tbm case presentation by dr imtiazTbm case presentation by dr imtiaz
Tbm case presentation by dr imtiaz
 
Extern con ortho
Extern con orthoExtern con ortho
Extern con ortho
 
A young woman with lupus
A young woman with lupusA young woman with lupus
A young woman with lupus
 
barded bidel syndrome
barded bidel syndromebarded bidel syndrome
barded bidel syndrome
 

LaMonicaFamily_JointPain_Bruce_N752

  • 1. The LaMonica Family: Joint Pain Molly Bruce, RN, BSN, FNP-Student NURO 752
  • 2. Mrs. Sofia LaMonica is a 78-yr-female who presents with c/o shoulder pain, hip pain, fatigue, and weakness that began about one month ago. She was diagnosed with mild iron deficiency anemia (improved with treatment), depression, Vitamin D deficiency (corrected on replacement), and fibromyalgia by her previous PCP. She has not noted improvement in sxs on current regimen of cyclobenzaprine 10 mg at bedtime and duloxetine 60 mg daily. Her daughter is with her and reports that her mother has difficulty dressing herself, needs help to stand from a chair, and has difficulty lifting her arms. She denies headaches or changes in vision or hearing.
  • 3. Social History Moved from Sicily 7 years ago to live with her daughter and her son-in-law. Her primary language is Italian and she speaks little English. Never smoker. Occasional glass of wine. Former elementary school teacher. Four children, 3 of whom live in the US, one is deceased. Widowed x 25 yrs, not sexually active since her husband died.
  • 4. Past Medical History: HTN controlled on meds x 6 years, OA for which she takes occasional ibuprofen. Hysterectomy age 38, no HRT, DEXA 4 years ago normal BMD. Family Medical Hx: Adopted, knows no biologic family hx. Oldest daughter died age 24 from Lupus Nephritis complications. All other children are well.
  • 5. Medications • Duloxetine 60 mg daily • Cyclobenzaprine 10 mg at bedtime • Valsartan 160 mg daily • HCTZ 25 mg each morning • Calcium 600 mg twice daily • Vitamin D 2000 mg daily • Ibuprofen 400-600 mg up to three times daily PRN
  • 6. Considerations • What are some socio-cultural considerations that should be implemented for this patient? • Consider the patient’s religious beliefs, family structure, ethnic value, and cultural identity. • Would it be appropriate to use her daughter as a translator? • No! • What are the legal implications for using her daughter as a translator? • Misinterpretation of information could lead to mistakes or misdiagnosis.
  • 7. ROS: Pertinent Findings • General: positive for – fatigue, weakness • Psychological: negative for anxiety, depression, memory loss • Ophthalmic: positive for dry eyes. Negative for blurry vision, vision loss other than r/t age • ENT: Positive for decreased hearing r/t age. Negative for - earache, sore throat, hoarseness, dysphagia, facial pain, and dry mouth, jaw claudication • Allergy and Immunology: negative for hx of allergies or frequent infections • Hematological and Lymphatic: negative for excessive bruising, swollen or painful nodes • Endocrine: negative for hx of diabetes, thyroid problems • Respiratory: negative, denies SOB, wheezing, cough • Cardiovascular: positive for peripheral edema in the evenings, resolves by morning; negative for Chest pain, palpitations • Gastrointestinal: positive for occasional indigestion; negative for reflux, black or bloody stools • Genitourinary: positive for hx of UTI, otherwise negative • Musculoskeletal: Positive for - Joint pain, Stiffness and Morning stiffness; negative for joint swelling or redness • Neurological: negative for - headaches and numbness/tingling; positive for occasional vertigo • Skin/Hair/Nails: Negative for rash, itch, unusual lesions, dandruff, abnormal nails.
  • 9. Physical Exam • VS: BP 124/62 | Pulse 68 | Temp 97.9 °F (36.6 °C) (Oral) | Resp 16 | Ht 1.626 m (5' 4") | Wt 60.782 kg (134 lb) | BMI 23.00 kg/m2 • General: NAD • HENT: TM Pearly Gray, no enlarged or tender nodes, thyroid normal, PERLA, EOM intact, no nystagmus • Mouth: MMM, no lesions noted, good dentition, uvula midline, pharynx without erythema or exudate • Skin/Nails: warm & dry w/out rash, no increased warmth or tenderness • CV: RRR: Temporal pulse 2+, equal with no masses or tenderness; trace edema from toes to mid calf, cap refill bilateral great toes <3 secs, Pedal & PT pulses 1+, Radial pulse 2+ • Lungs: CTA throughout; Normal respiratory effort & rate • Sensation: intact to touch, position • Strength: 4/5 UE & LE bilateral, unable to stand without assistance • Neuro: Neg Romberg, finger to nose & rapid alternating movements normal • DIP: no swelling, normal motion, Heberden’s nodes 2,3 bilaterally • PIP: no swelling, tenderness; minor Bouchard’s nodes throughout • MCP: no swelling or tenderness • Grip: mildly decreased strength, complete, equal • Wrist: decreased motion, no swelling or tenderness • Elbow: normal motion, no swelling or tenderness • Shoulder: limited, painful motion, 5/10 tenderness, no swelling • Hip: mildly decreased adduction and abduction • Knee: normal motion, no swelling, mild crepitus • Ankle: normal motion, no redness or swelling • Foot/Toes: + squeeze • Tender points: Widespread, 18/18 positive 3-4/10 • Other: Normal gait
  • 11. Osteoarthritis • Definition: A degenerative disorder of the joints, with a prevalence that increases with age. Joints affected normally involve the knee, hip, hands, cervical and lumbar spine. These patients may have stiffness and joint pain WORSE with activity. • Pharmacologic Treatment Options • Hand OA: Topical capsaicin or topical NSAIDs, oral NSAIDs/COX-2 inhibitors, tramadol • >75 years-old, use topical rather than oral NSAIDs. • Knee OA: Acetaminophen, oral NSAIDs, topical NSAIDs, tramadol, intraarticular corticosteroid injections • Hip OA: Acetaminophen, oral NSAIDs, tramadol, intraarticular corticosteroid injections • Risk Factors • Older age • Sex (females>males) • Obesity • Occupation: repetitive movement of joints (Hochberg et al, 2012)
  • 12. Diagnostics • What studies/labs should be ordered? CBC, CMP, Vitamin D, Inflammatory Markers, UA
  • 15. Question • Were there any CMP or CBC values that were significant to developing differentials? WBC: 13.0 (H) Hemoglobin: 11.1 (L) Seg (neutrophils): 88.9% (H) Lymphocytes: 9.1% (L) Monocytes: 1.8% (L) Absolute neutrophils: 11.6 (H) Urea Nitrogen: 24 (H) Glucose: 102 (H) BUN/Creatinine: 21.6 (H) • Look at inflammatory markers and urinalysis!
  • 16. Additional Work-Up • ESR (Sed Rate): 84 (H) • CRP: <0.8 • CPK: 189 U/L • Rheumatoid Factor <30.0 IU/ML • Vitamin D : 46 (25-Hydroxy) • Color, UA yellow • Appearance, Urine clear • Glucose, Ur neg • Bilirubin Urine neg • Ketones, Ua neg • Specific Gravity, Urine 1.005 • Blood, Urine neg • pH, Urine 5 • Protein Urine neg • Urobilinogen, Ua 0.2 • Nitrite, Urine neg • WBC Esterase/Urine neg
  • 17. Labs in Inflammatory Disorders Acute Phase Reactants: Blood proteins that are either increased or decreased w/in hours of inflammatory response. CBC w/ diff: blood counts CMP: liver and kidney functions ANA: Elevated in SLE, Sjogren’s syndrome, RA, mixed connective tissue disease, scleroderma, polymyositis/dermatomyositis Anti-extractable nuclear antigen (ENA): Highly specific for SLE, but only found in around 25% of SLE patients. Also found in systemic sclerosis and mixed connective tissue disease Rheumatoid factor: Sensitive for detecting RA Anti-cyclic citrullinated peptide antibody (CCP): A newer biomarker for RA. Do this lab w/ RF for RA dx. CCP can also be found in psoriatic arthritis, lupus, Sjogren’s syndrome, TB, and inflammatory myopathies. (Castro & Gourley, 2010)
  • 18. Differential Diagnosis Mrs. LaMonica: 78 years-old w/ shoulder and hip pain, fatigue, morning stiffness and weakness x 1 month in addition to difficulty dressing herself, lifting her arms, and standing up from a seated position. Elevated ESR. • Polymyalgia Rheumatica • Rheumatoid Arthritis • Fibromyalgia • Polymyositis • Overuse bursitis/tendonitis
  • 19. Polymyalgia Rheumatica (PMR): An inflammatory rheumatologic disorder with manifestations of aching and morning stiffness that could involve the neck, hips, shoulders, and torso.
  • 20. Polymyalgia Rheumatica • Pathophysiology: The cause of PMR is not known, but inflammation is thought to occur due to an autoimmune reaction causing the immune system to attack the synovium. The reason for this is unknown. Environmental and genetic factors are thought to play a role. • Risk Factors • Older age • Average age of onset is 70 years-old • Sex • Females are twice as likely to develop PMR • Ethnicity • Caucasian patients are more likely to develop PMR (Saad, 2014)
  • 21. Polymyalgia Rheumatica: ACR Diagnostic Criteria 1: An age of 50 years-old+ at onset 2: Bilateral aching & morning stiffness that lasts 30 minutes or more that persists for at least 1 month, and involves at least 2/3 following areas: neck or torso, shoulders or proximal regions of the arms, and hips or proximal aspects of the thighs 3: ESR (Westergren) elevated to 40 mm/h or more 4: Normocytic, normochromic anemia in approximately 50% of patients
  • 22. Mrs. LaMonica: PMR Symptoms/RFs • Shoulder and hip pain • Morning stiffness • >50 years-old • Female • Difficulty standing from seated position • Elevated ESR • Swelling in lower extremities • Depression • Rapid onset of symptoms; symptoms for one month • Decreased ROM in wrists, shoulders, hips
  • 23. PMR: Treatment • PO Steroid and Tapering Regimen • Prednisone 15mg QD x 3 weeks • Then 12.5 mg QD x 3 weeks • Then 10 mg QD x 4-6 weeks • Then reduce by 1 mg Q 4-8 weeks OR alternate day reductions (7.5 mg/10 mg alternate days) • IM Methylprednisolone: Used in milder cases. May reduce risk of steroid-induced complications. • Initial dose of 120 mg Q 3-4 weeks • Reduce by 20 mg Q 2-3 months • Duration of Treatment: Normally, 1-3 years of treatment is needed. Some require small doses beyond this. Stop steroids when continued lack of inflammatory symptoms. If needing > 3 years of treatment, may need to consider alternative dx. • Additional Therapies: Bone protection needed with LT corticosteroid therapy. (Dasgupta, 2010)
  • 24. PMR: Relapse Relapse should be treated ONLY under specialist care. • Relapse includes recurring symptoms of PMR or new onset of GCA. • Treating Relapse: • Onset of GCA • Follow usual treatment guidelines for GCA. • Recurring PMR • Increase prednisone to previous higher dose • Administer a single dose of IM methylprednisolone 120 mg • After 2 relapses, need to consider immunosuppressive therapy. (Dasgupta, 2010)
  • 25. PMR and GCA can occur together. We need to assess Mrs. LaMonica for this, before implementing her treatment plan! Giant Cell Arteritis: A chronic systemic inflammatory vasculitis of both medium and large arteries that occurs in patients >50 years-old. It often affects superficial temporal arteries, and occurs due to an autoimmune reaction. • Risk Factors: Etiology and pathogenesis unknown. • Diagnosis of PMR (15% w/ PMR will develop GCA) • Age (>50) • Sex (F>M) (Dasgupta et al., 2010)
  • 26. GCA • Diagnostics • Temporal Artery Biopsy • Can be negative in some patients. If they have a typical clinical picture of GCA and respond to steroids, should be regarded as having GCA. • Others: CBC, urea, electrolytes, LFTs, CRP, ESR • Acute-phase response is characteristic: elevated ESR, CRP, anemia, abnormal LFTs, thrombocytosis, raised alk phos (Dasgupta et al., 2010)
  • 27.
  • 28. American College of Rheumatology Classification Criteria for Giant Cell Arteritis Criterion[∗] Definition Age at disease onset ≥50 yr Development of symptoms or findings beginning at age 50 or older New headache New onset or new type of localized pain in the head Temporal artery abnormality Temporal artery tenderness to palpation or decreased pulsation, unrelated to arteriosclerosis of cervical arteries Elevated erythrocyte sedimentation rate (ESR) ESR ≥50 mm/hr by the Westergren method Abnormal artery biopsy Biopsy specimen with artery showing vasculitis characterized by a predominance of mononuclear cell infiltration or granulomatous inflammation, usually with multinucleated giant cells
  • 29. Symptoms of Giant Cell Arteritis Symptom Frequency (%) Headache 76 Weight loss 43 Fever 42 Fatigue 39 Any visual symptom 37 Anorexia 35 Jaw claudication 34 Polymyalgia rheumatica 34 Arthralgia 30 Unilateral visual loss 24 Bilateral visual loss 15 Vertigo 11 Diplopia 9
  • 30. Mrs. LaMonica: GCA Symptoms/RFs • 15-20% of patients with PMR might also have Giant Cell Arteritis (GCA). • Positive findings: • >50 years-old • Elevated ESR • Occasional vertigo • Negative findings: • No headache • No tenderness to temporal artery or decreased pulsation • No jaw claudication Is it likely that Mrs. LaMonica could also have GCA? If we had a strong suspicion for GCA, would a referral be urgent?
  • 31. GCA: Treatment If Mrs. LaMonica were to develop GCA it would require a PROMPT REFERRAL! • 1/5th of GCA cases result in irreversible blindness. Preventable with prompt diagnosis and treatment. • Glucocorticosteroids: Start while awaiting results from temporal artery biopsy. • Uncomplicated GCA (NO visual disturbance or jaw claudication): 40-60 mg prednisone QD • Complicated GCA (evolving visual loss): 500 mg- 1 g of IV methylprednisolone for 3 days before PO glucocorticosteroids • Visual Loss: 60 mg prednisone QD to protect contralateral eye • May require 1-2 years of treatment (Dasgupta et al., 2010)
  • 32. Plan • Pharmacologic: • Prednisone 15mg PO daily x 3 weeks, then 12.5mg PO daily x 3 weeks, then 10mg PO daily x 4-6 weeks, then reduce by 1mg Q 4-8weeks • Continue calcium and vitamin D. Add a Bisphosphonate (Alendronate 10mg PO daily). • D/C Ibuprofen. Start topical capsaicin for OA, 0.025 to 0.075% TID-QID, as needed. Acetaminophen 650-1000mg up to QID, as needed (no more than 4000mg/day to avoid liver toxicity). • D/C Cyclobenzaprine. Increased r/of serotonin syndrome w./ Cymbalta. Also, increased r/of drowsiness and fatigue. • Nonpharmacologic: Limit ETOH, do not smoke cigarettes, weight- bearing exercise (as tolerated) • Education: Educate on prednisone therapy- can weaken immune system, no live vaccines, take w/ food, side effects; Educate on S/S of GCA and importance of seeking emergent care if these develop. Do NOT abruptly stop taking steroids. (Dasgupta et al., 2009)
  • 34. Falls: Risk Factors • Polypharmacy: 4+ medications • Accident, environmental hazard • Confusion, cognitive impairment • Postural hypotension • Medications: corticosteroids, sedatives, anxiolytic drugs, antihypertensive meds Preventing Falls in the Elderly • Elimination of environmental hazards • Review and modify medications • Provide balance training • Involve family • Provide follow-up
  • 35. PMR: Follow-up & Monitoring • Follow-up schedule: 24-72 hours; weeks 1-3, 6; months 3, 6, 9, 12 in first year (+ extra visits if relapse of adverse events) • Clinical Monitoring: At each follow-up visit, assess for… • Response to treatment and disease activity • Disease complications (ex. GCA) • Atypical features • Side effects r/t steroid therapy • Laboratory Monitoring • CBC, ESR, CRP, urea, electrolytes, glucose
  • 36. Follow-up Mrs. LaMonica returns two days later. Her HPI, ROS, and PE remain unchanged. You review the lab results with her and her daughter and discuss the likely differentials with patient as well as your plan of care.
  • 37. Should we refer Mrs. LaMonica to a specialist? Consider referral if… A) Presentation with atypical features/features that are unlikely in PMR: 1. <60 years-old 2. >2 months onset 3. No shoulder involvement 4. No inflammatory stiffness 5. Prominent systemic features, night pain, wt loss, neuro signs 6. Symptoms of other rheumatic disease 7. Normal or extremely high acute-phase response B) Dilemmas in treatment including: 1. Unresponsive or incomplete response to corticosteroids 2. Contraindications to corticosteroid therapy 3. A need for corticosteroid therapy that will be prolonged (>2 years) Patients with typical clinical presentations, adequate response to treatment, and no adverse events can be managed in a primary care setting. (Dasgupta et al., 2009)
  • 38. Osteoporosis • Primary • Postmenopausal: low estrogen • Senile: occurs > 70 years-old • Secondary: Caused by other etiologies • Diseases • Pharmacological therapy • Lifestyle behaviors • Imaging Recommendations • BMD every two years, in the absence of new risk factors. • FRAX • http://www.shef.ac.uk/FRAX/
  • 40. Health Maintenance What health maintenance does Mrs. LaMonica need, being that she is a 78 year-old female? • Bone Mineral Density (every other year): Last done 4 years ago • Colonoscopy (every 5-10 years after age 50) • Mammogram (annually after age 40) • Vaccinations: PNA (>65 years-old), Zostavax (>60 years- old), Tetanus
  • 41.
  • 42.
  • 44. History of Present Illness Sarah LaMonica is a 27-yr-old female who presents today with c/o painful red and swollen fingers, elbows, and knees for the past 3 weeks. She states her joints began to hurt after she returned from a 2 week backpacking trip with her partner along the Appalachian Trail. She denies injury but did have a tick bite. She c/o feeling fatigued even though she states she is resting well at night. She has not been able to do her usual daily workout or runs because of the stiffness and pain. She states it takes her “all morning to loosen up” and then she is still stiff, but not as bad. States this “has really messed my life up”. She denies other health issues other than PTSD. Reports her LMP was 1 week ago. Her grandmother, Sophia LaMonica is a patient here, and was recently diagnosed with PMR. Sarah wonders if she could have that too since she is so tired.
  • 45. Social History • Lives with her partner, Diane and 9 month old adopted daughter, Abbie. She attended college for one year but dropped out and joined the army. She had two tours in Iraq, one for 6 months followed by a second tour for 12 months. Manages a food co-op and taking some education classes. • Denies smoking. Drinks 1-2 beers each weekend with her friends. Denies recreational drugs. Sexually active in monogamous relationship with partner of 5 years. States she has a good family relationship which has helped her deal with her PTSD since leaving the military. The food co-op does not provide health insurance and she cannot get coverage under her partner’s policy.
  • 46. Family History • Mother: 49yo- HTN, OA • Father: 56yo- HTN, COPD, former smoker • Brother: 18yo- healthy • Sister: 16yo- asthma • Paternal Grandmother: deceased 78yo- COPD, CHF • Paternal Grandfather: deceased 82yo- COPD, MI • Maternal Grandmother: 76yo- HTN, OA, PMR • Maternal Grandfather: deceased 53yo- MI, HTN, CVA • Maternal Aunt: deceased r/t SLE nephritis
  • 47. Past Medical History • PTSD • Anxiety • Appendectomy, age 9 Current Medications • No prescription medications • Takes daily MVI, Benadryl at night for sleep • Was on Zoloft and Xanax for anxiety but could not afford it
  • 48. Review of Systems • General: positive for – fatigue, negative for weakness • Psychological: positive anxiety, depression related to PTSD • Ophthalmic:. Negative for blurry vision, vision loss, dry eyes • ENT: Negative for - earache, sore throat, hoarseness, dysphagia, facial pain, and dry mouth • Allergy and Immunology: negative for hx of allergies or frequent infections • Hematological and Lymphatic: negative for excessive bruising, swollen or painful nodes • Endocrine: negative for hx of diabetes, thyroid problems • Respiratory: negative, denies SOB, wheezing, cough • Cardiovascular: negative for Chest pain, palpitations, edema • Gastrointestinal: negative for reflux, black or bloody stools, indigestion • Genitourinary: negative for hx of UTI, menorrhagia, metrorrhagia • Musculoskeletal: Positive for - Joint pain, Stiffness and Morning stiffness, joint swelling • Neurological: negative for - headaches and numbness/tingling • Skin/Hair/Nails: Negative for rash, itch, unusual lesions, abnormal nails.
  • 49. Physical Exam • General: healthy, NAD • Skin/Nails: no rashes, ulcers; nails normal • Lymph: no adenopathy noted • Scalp/Hair: no scaling, no alopecia • Eyes: non injected, PEERLA, EOMS full • Mouth: normal mucosa moisture, no ulcers • Neck: no masses, thyroid normal • CV: RRR, normal S1 & S2, no murmurs or rubs • Lungs: clear to auscultation • Abd: non tender, no organomegaly • C-Spine: normal lateral rotation, lateral bending, flexion and extension • T-Spine: normal flexion and extension, no tenderness, normal alignment • L-S Spine: normal flexion and extension, no tenderness, normal alignment • Reflexes: 2+ biceps, triceps, brachioradialis, knee and ankle • Muscles: 5/5 for deltoids, biceps, triceps, quadriceps, hamstrings and hip flexors • Sensation: normal to light touch, vibration and position • Shoulders: FROM, no swelling • Elbows: 1+ swelling R elbow; trace L elbow • Wrists: trace swelling & tenderness bilateral wrists • MCPs: 3+ tenderness throughout with trace swelling 1, 2 L, 1+ 1,2 R • PIPs: 2+ swelling & tenderness 2-5 bilaterally • DIPs: no swelling, no tenderness • HIPs: FROM, no swelling • Knees: L FROM, Tenderness; R 1 + tenderness, 1-2+ swelling, no redness, mildly increased warmth • Ankles: no tenderness or swelling • Feet/toes: no swelling or tenderness • Bursa: no tenderness or swelling
  • 50. Physical Exam Swollen PIPs 5 4 3 2 1 No swollen DIPs Swollen MCPs
  • 51.
  • 53. Evaluation • Differential Diagnosis • Rheumatoid arthritis • Lyme disease • SLE • Osteoarthritis • Psoriatic arthritis
  • 54. Labs and Diagnostics • CBC w/ differential • CMP • Rheumatoid Factor • Acute Phase Reactants: ESR, CRP • Anticyclic citrullinated peptide (Anti-CCP) antibodies • Imaging: Ms. LaMonica is uninsured. Would you obtain an X-ray on this patient?
  • 58. The 2010 ACR-EULAR Classification Criteria for RA Score A) Joint Involvement 1 large joint 0 2-10 large joints 1 1-3 small joints (w/ or w/o involvement of large joints) 2 4-10 small joints (w/ or w/o involvement of large joints) 3 >10 joints (at least 1 small joint) 5 B) Serology (at least 1 test result needed for classification) Negative RF and negative anti-CCP 0 Low-positive RF or low-positive anti-CCP 2 High-positive RF or high-positive anti-CCP 3 C) Acute-phase reactants (at least 1 needed for class.) Normal CRP and normal ESR 0 Abnormal CRP or abnormal ESR 1 D) Duration of symptoms <6 weeks 0
  • 59. Sarah LaMonica Score A) Joint Involvement 1 large joint 0 2-10 large joints 1 1-3 small joints (w/ or w/o involvement of large joints) 2 4-10 small joints (w/ or w/o involvement of large joints) 3 >10 joints (at least 1 small joint) 5 B) Serology (at least 1 test result needed for classification) Negative RF and negative anti-CCP 0 Low-positive RF or low-positive anti-CCP 2 High-positive RF or high-positive anti-CCP 3 C) Acute-phase reactants (at least 1 needed for class.) Normal CRP and normal ESR 0 Abnormal CRP or abnormal ESR 1 D) Duration of symptoms <6 weeks 0
  • 60. Rheumatoid Arthritis • Definition: An inflammatory disease characterized by swelling, pain, stiffness, and loss of function of joints. Commonly occurs in wrist and fingers. • Pathophysiology: Autoimmune. WBCs travel to synovium and cause synovitis, resulting in warm, red, swollen, and painful joints. With progression of disease, inflammation of the synovium results in destruction of cartilage and bone in the joint. Thought to be caused by environmental and genetic factors. • Risk Factors: • Sex: F>M • Age: middle-age • Family history (U.S. National Library of Medicine, 2015)
  • 62. Clinical Practice Guidelines: Treatment of Early RA (Singh et al, 2012)
  • 63. (Singh et al, 2012)
  • 64. Pharmacological Interventions for RA There is NO cure for RA. The goal of treatment is to lessen symptoms and slow progression of disease. • Glucocorticoids: May be prescribed at initial presentation of RA symptoms or for flares. Resolution of joint pain and inflammation after steroid therapy can help further confirm susceptibility of RA. • NSAIDs: Improve mobility. Help with pain. • DMARDs: Mainstay treatment; methotrexate, hydroxychloroquine, sulfasalazine, leflunomide • Biologic agents: abatacept, humira, anakinra, etanercept, remicaide, rituxan, etc.; normally taken w/ methotrexate (ACR, 2012)
  • 65. Non-pharmacological Interventions for RA • Diet • Low cholesterol (at risk for CAD) • Fish oils, plant oils can improve pain and swelling of joints • Occupational/physical therapy: Can help preserve joint function • Splints: Reduce joint pain and improve function of joints • Exercise • Increase ROM: preserve/restore joint function • Increase strength: isotonic, isometric, isokinetic • Increase endurance: walking, cycling, swimming • Surgery: End-stage RA; damaged joints (National Guideline Clearinghouse, 2012)
  • 66. Sarah LaMonica: Plan • What medications will you prescribe, if any? • Prednisone, taper as directed. • What education will you provide the patient with? • Take prednisone with food. Discuss side effects: emotional lability, appetite changes, anxiety, insomnia, headache, weight gain, etc. • What are her options for obtaining health insurance? • Medicaid: see if she meets qualifications • Medically Indigent Adult Programs • Veterans Benefits (Forester, 2009)
  • 67. Follow-up Ms. LaMonica returns to the clinic in one week. Her joint swelling has improved on prednisone and she generally is feeling much better. She continues on prednisone taper. PE: Unchanged other than she now has no swelling in her joints. What is your diagnosis, based on the findings?
  • 68. Plan • Prescriptions: NSAIDs, if still having joint pain. Continue prednisone taper. • Referrals: Rheumatology, first available appointment. Send over copies of her office notes, labs, and current medications. • Patient Education: Educate patient on rheumatoid arthritis and how it can be managed. Educate on importance of seeing rheumatologist. • Follow-up: After rheumatology consult, and as needed.
  • 69. The Uninsured Resources for PCP: • GoodRx • What You Can Do to Help Uninsured Patients: http://www.aafp.org/fpm/2009/0900/p21.html • Is the patient really uninsurable? • Review OOP costs of labs/diagnostics with patients • Prescribe generic medications • Be aware of large retail companies offering more affordable medication prices • Offer discounts to cash-paying patients
  • 70. PTSD Sarah, returns several months later. She has been diagnosed with RA. The diagnosis seems to have triggered her nightmares, anxiety and insomnia. She is having a hard time taking care of Abbie and had to quit her job. Things were going so well. Now she needs your help. Can you give her something for sleep? She just wants to be knocked out.
  • 71. PTSD • Definition: Occur in patients for >1 month after being exposed to a traumatic event causing them significant distress or impairment in occupational, social or other areas of functioning. • Symptoms: avoidance of stimuli associated w/ traumatizing event, re-experiencing of the traumatic event, numbing sensation, increased arousal • PTSD can appear alone, or more commonly w/ co-occurring conditions (insomnia, identity problems, mood changes, difficulties in interpersonal relationships, nightmares, chronic pain) or with other psychiatric disorders (anxiety, depression, substance abuse) May have delayed onset (at least 6 months after the event). (Department of Veterans Affairs, 2010)
  • 72. PTSD: Screening In primary care, the PTSD Screen is used: In your life, have you ever had any experience that was so frightening, horrible, or upsetting that, in the past month, you: 1. Have had nightmares about it or thought about it when you did not want to? YES / NO 2. Tried hard not to think about it or went out of your way to avoid situations that reminded you of it? YES / NO 3. Were constantly on guard, watchful, or easily startled? YES / NO 4. Felt numb or detached from others, activities, or your surroundings? YES / NO The results of this test are considered "positive" if a patient answers "yes" to any three items. (Department of Veterans Affairs, 2010)
  • 73. PTSD: Treatment • First-line treatment for PTSD based on guidelines suggest the initiation of psychotherapeutic interventions using effective modalities of trauma-focused therapy or stress management AND/OR initiating pharmacotherapy (mono-therapy using SSRI or SNRI) • Adjunctive therapy might include treatment of symptom-specific management including insomnia, pain, or anger. • Ensure the patient has an adequate support system. (Department of Veterans Affairs, 2010)
  • 74. PTSD: Resources • General and mental health; Refer patient! • Support groups • VA Benefits Counselors • PTSD Association • Anxiety and Depression Association of America • National Alliance for Mental Illness
  • 75. References • American College of Rheumatology. (2012). Rheumatoid arthritis. Retrieved from: https://www.rheumatology.org/Practice/Clinical/Patients/Diseases_And_Conditions/Rheumatoid_Arthritis/ • American College of Rheumatology. (2010). Rheumatoid arthritis classification. Retrieved from: https://www.rheumatology.org/practice/clinical/classification/ra/ra_2010.asp • Castro, C. & Gourley, M. (2010). Diagnostic testing and interpretation of tests for autoimmunity. The Journal of Allergy and Clinical Immunology, 125(2), 238-247. • Clauw, D.J. (2014). Fibromyalgia: A clinical review. The Journal of the American Medical Association, 311(15), 1547-1555. • Dasgupta, B., Borg, F., Hassan, N., Barraclough, K., Bourke, B., Fulcher, J.,… & Hollywood, J. (2009). BSR and BHPR guidelines for the management of polymyalgia rheumatica. Oxford Journals, 109(10), 1-5. • Dasguta, B. (2010). Concise guidance: Diagnosis and management of giant cell arteritis. Retrieved from: https://www.rcplondon.ac.uk/sites/default/files/giant-cell-arteritis-concise-guideline.pdf • Dasgupta, B., Borg. F., Hassan, N., Alexander, L., Barraclough, K., Bourke, B.,…Fulcher, J. (2010). BSR and BHPR guidelines for the management of giant cell arteritis. Oxford Journals, 109(10). • Department of Veterans Affairs. 2010. Clinical practice guidelines for management of post-traumatic stress. Retrieved from: http://www.healthquality.va.gov/guidelines/MH/ptsd/cpg_PTSD-FULL-201011612.pdf • Forester, R., & Heck, R. (2009). What you can do to help your uninsured patients. Family Practice Management, 16(5), 21-24. • Grossman, J., Gordon, R., Ranganath, V., Deal, C., Caplan, L., Chen, W.,… & Curtis, J. (2010). American College of Rheumatology recommendations for the prevention and treatment of glucocorticoid-induced osteoporosis.
  • 76. References Cont’d • Hochberg, M., Altman, R., April, K., Benkhalti, M., Guyatt, G., McGowan, J.,… & Towheed, T. (2012). Recommendations for the use of nonpharmacologic and pharmacologic therapies in osteoarthritis of the hand, hip, and knee. Arthritis Care and Research, 64(4), 465-474. • National Clinical Guideline Centre. (2014). Osteoarthritis: Care and management in adults. Retrieved from: http://www.guideline.gov/content.aspx?f=rss&id=47862#Section420 • National Guideline Clearinghousee. Rheumatoid arthritis: Diagnosis, management and monitoring. Retrieved from: http://www.guideline.gov/content.aspx?id=39244 • National Institute of Arthritis and Musculoskeletal and Skin Diseases. (2012). Polymyalgia rheumatica and giant cell arteritis. Retrieved from: http://www.niams.nih.gov/health_info/polymyalgia/ • National Osteoporosis Foundation. (2014). Clinician’s guide to prevention and treatment of osteoporosis. Retrieved from: http://nof.org/files/nof/public/content/file/2791/upload/919.pdf • Saad, E.R. (2014). Polymyalgia rheumatica. Retried from: http://emedicine.medscape.com/article/330815-overview#a4 • Sinusas, K. (2012). Osteoarthritis: Diagnosis and treatment. American Family Physician, 85(1), 49-56. • United States National Library of Medicine. (2015). Rheumatoid arthritis. Retrieved from: http://www.nlm.nih.gov/medlineplus/rheumatoidarthritis.html • University of Maryland Medical Center. (2013). Osteoporosis. Retrieved from: http://umm.edu/health/medical/reports/articles/osteoporosis • Veterans Health Initiative. (2002). Post-traumatic stress disorder: Implications for primary care. Retrieved from: http://www.publichealth.va.gov/docs/vhi/posttraumatic.pdf

Notes de l'éditeur

  1. Mrs. LaMonica’s chief complaint is shoulder and hip pain, fatigue, and weakness x 1 month in addition to difficulty dressing herself, lifting her arms, and standing up from a seated position. It seems that she was seen for similar symptoms in the past, and was given prescriptions for cyclobenzaprine and Cymbalta for a dx of fibromylagia w/ co-existing depression and fatigue. The guidelines state that 1st line treatment for fibromyalgia are TCAs also cyclobenzaprine (flexeril) which is structurally similar to TCAs, SNRIS (Cymbalta), and gabapentinoids (gabapentin, pregabalin). And it states that patients often benefit from 2-3 of these classes together (Clauw, 2014). It seems that Mrs. LaMonica was put on appropriate medications for fibromyalgia based on the literature, so the fact that she has not seen any improvements makes it questionable as to if this was an appropriate diagnosis for her. H/e, we would also want to inquire further about how long she has been on these medications for. Is there anything else here we would like to further inquire about? -More about depression- what symptoms has she been having exactly? -More about shoulder and hip pain- bilateral? Any injury? Has she taken anything for her pain? -More about her fatigue- how many hrs of sleep is she getting/night? Meds? -More about weakness- given her age, any falls? -How long ago did her PCP diagnose her with fibromyalgia/depression? Clauw, D.J. (2014). Fibromyalgia: A clinical review. The Journal of the American Medical Association, 311(15), 1547-1555. Cyclobenzaprine: Muscle spasm- improves sleep, visceral motility, and pain. But the evidence shows it may not persist past 8 weeks. Cymbalta: good for comorbid depression and fatigue w/ fibromyalgia. ---[[[But, these together increase risk of SEROTONIN SYNDROME.]]] Microcytic hypochromic- Fe def.
  2. What are some things we could take into consideration involving her social hx? -Language barrier. What does she do in her free time, since she’s retired? How is her support system? Does she have friends she sees regularly, or only her family?
  3. Any red flags here? Adopted- doesn’t know her family history. Last DEXA 4 years ago Daughter- Lupus HRT- hormone replacement therapy
  4. QUESTIONS: Do any of the meds have side effects that may be responsible for her symptoms? If so, should you stop any of them at this point? ---valsartan- may cause arthralgia –I feel like, at this point we need to know more about her condition before stopping this med. ---HCTZ: weakness, muscle cramps ---Cymbalta/flexeril: Fatigue ---May stop cyclobenzaprine to decrease r/of serotonin syndrome and drowsiness/fatigue d/t her age. Dependent on how long she’s been trying this therapy. Since she has depressive symptoms, could keep her on Cymbalta for now, if it’s working for her, and again depending on how long she’s been trying it for. Any of these meds of concern, given her age of 78 years-old? What are those concerns? ---cyclobenzaprine: drowsiness, fatigue (+ Cymbalta) –also risk for serotonin syndrome.
  5. Taking into consideration that Mrs. LaMonica moved from Italy 7 years ago and primarily speaks Italian, what are some socio-cultural considerations that we should implement for her? 2 & 3: Using a family member as a translator is not a good idea for many reasons. One of those being that family members or friends have a personal and emotional attachment to the patient, so they could add their own opinion or withhold important parts of the message about the patient. Also, family members usually lack the medical understanding that qualified medical interpreters have, ensuring that medical information is properly relayed and mistakes or misdiagnoses are not made. TITLE VI OF THE CIVIL RIGHTS ACT OF 1964- Prohibition against national origin discrimination affecting limited English proficient persons. Addresses need for interpreter.
  6. Next Question: Based on these findings from the review of systems, and from her HPI, what systems should we focus on during the physical? -Focus in on musculoskeletal and neuro (vertigo) and CV PERTINENTS ARE IN BLUE
  7. Just as a review before we look further at her physical exam findings.. This slide shows where the DIP joint, or distal interphalangeal joints… PIP joints, or proximal interphalangeal joints… AND… MCP joints, or metacarpophalangeal joints are located.
  8. VSS. PT= posterior tibial Foot/toes: + squeeze: Squeeze test is a method of identifying inflammation in the absence of obvious swelling or tenderness of metacarpophalangeal joints, or in this case, metatarsophalangeal joints. To test the fingers/hand, the 2nd through 4th metacarpo-phalangeal joints are squeezed together, and to test the toes/foot, all of the metatarsophalangeal joints are squeezed together. If the squeeze causes pain, it raises the possibility of underlying joint inflammation. Tender points in 11-18 areas could indicate fibromyalgia. But, a lot of the tender point areas are already where she is experiencing some of her pain, like her shoulders and hips. Heberden’s and Bouchard’s nodes are found in OA, which the patient has already been dxed with. Which of the findings on PE are pertinent to her complaints? WHY? Decreased ROM, decreased strength Which findings direct the testing you will order? Inflammatory markers
  9. Mrs. LaMonica has OA. So this shows that the Heberden nodes are located at the DIP joints, and Bouchard’s nodes at the PIP joints. Mnemonic: Heberden’s nodes are Higher up on the finger. Bouchard’s nodes are closer to the Body. HD: High Definition (Heberden=DIP) BP: Blood Pressure (Bouchard=PIP)
  10. 2: TX…Mrs. LaMonica is taking Ibuprofen PO PRN. We should inquire further about her OA to see if this is controlling her symptoms, and especially given her age. ACR guidelines recommend patient’s over 75 to use topical preparations instead of oral NSAIDs, so this could be used for her OA in her hand, to see if this controls her symptoms. -Aes of NSAIDS: GIB, increase BP– NSAIDs in the elderly can increase risk of drug-drug interactions. Can increase BP, can cause hypoglycemia if used with insulin or oral hypoglycemics. Nephrotoxic and hepatotoxic. CAP-SAY-UH-SIN It’s also important to note that first, for mild OA, recommendations are to encourage regular exercise and weight loss if overweight for management of OA. Consider PT for supervised exercise.
  11. So going back to her current complaints and findings of shoulder and hip pain, fatigue, decreased ROM, difficult standing from seated position, and weakness what diagnostics should we order for her? CBC: We want to look at her blood counts. Any anemia? Infection? CMP: Kidney and liver function Vitamin D: --she was just given replacement for this. Inflammatory markers: Our physical exam revealed the possibility of inflammation UA: assess renal injury– glomerulonephritis or interstitial nephritis/ kidney problems or signs of infection
  12. The CBC reveals that… WBC= elevated to 13- could be elevated d/t inflammation Hemoglobin: 11.1 (L) Seg (neutrophils)= elevated to 88.9%-- could be elevated d/t inflammation, infection, stresors Lymphocytes= low at 9.1%--Autoimmune disorders can l/t low lymphocyte count; immunosuppression Monocytes= low at 1.8%-- low monocytes can indicate– immunosuppression Absolute neutrophils: elevated to 11.6
  13. Urea Nitrogen: Elevated at 24 –can increase w/ age. Glucose: Slightly elevated at 102 BUN/Creatinine: Elevated to 21.6 ---all else looks OK. –dehydration?
  14. 1: Not really? Could have some type of inflammatory process going on based on interpretation of CBC 3: Any other diagnostic studies? Not at this point. How can we interpret these lab results? Normal in PMR for WBC to be mildly elevated. Normocytic normochromic anemia is found in 50% of patients.
  15. What are the implications of these results? ESR: <17 in males, <25 in females CRP: <1 ; systemic inflammation will be >10 CPK: 22-198 RF: <40-60 Vitamin D: >30 UA: NEGATIVE So, going back to the first PCP’s diagnosis of fibromyalgia, with fibromyalgia, the ESR, CRP, Vitamin D… all of these labs would be normal, since it’s more of a neuropathic disorder than inflammatory. And this is not the case with Mrs. LaMonica, as all is normal except for the ESR, which is elevated. So this is something to take into consideration. PMR: ESR and CRP are likely elevated with a variable CBC.
  16. 1: + vs. -; examples of these include ESR, C-reactive protein, which are the most widely used. Others include fibrinogen, ferritin, which are rarely used for clinical use. 2: CBC: normochromic, normocytic anemia which could indicate a chronic or severe disease. Platelets and WBCs could be helpful for diagnosing various disorders. For example, in SLE, leuokpenia and thromboytopenia are common, which wasn’t the case for Mrs. LaMonica. 3: CMP: autoimmune hepatitis? Liver/kidney functions 6: RF: Absent in 15% of patients w/ RA. Sjorgen’s Syndrome: showgrenz syndrome ANA- Antinuclear antibodies (ANAs, also known as antinuclear factor or ANF) are autoantibodies that bind to contents of the cell nucleus. In normal individuals, the immune system produces antibodies to foreign proteins (antigens) but not to human proteins (autoantigens).
  17. What are some differentials we could think of for Mrs. LaMonica? Of these differentials, which do you think is the best fit based on Mrs. LaMonica’s complaints, physical exam findings, and lab results? RA: + RF, which Mrs. LaMonica did not have. H/e, some patients with RA may have a negative RF. Also, something else to consider is that with RA, the patient normally presents with symmetric arthritis of the small joints of the hands and feet, which was not similar to Mrs. LaMonica’s presentation. Fibromylalgia: The ESR and CRP are usually normal. Polymyositis: Presents as weakness of shoulder and pelvic girdles; but with this, there will likely be an elevated muscle enzymes with a + ANA. Overuse bursitis/tendonitis: The patient will have a normal ESR.
  18. http://www.uptodate.com/contents/clinical-manifestations-and-diagnosis-of-polymyalgia-rheumatica
  19. Synovium: lining of joint http://www.niams.nih.gov/health_info/polymyalgia/
  20. ACR: American College of Rheum? 1: Mrs. LaMonica is 78. 2: shoulder pain, hip pain and has been occurring for about 1 month. She also has morning stiffness. 3: Mrs. LaMonica’s ESR was elevated at 84
  21. All of these could be associated with PMR.
  22. ***In PMR, a clinical response of >70% is expected at 1 week, w/ normalization of lab inflammatory markers at 4 weeks. W/ failure of steroid response, need to consider alternative pathology and refer pt to see a specialist. I also found in the research that no solid evidence exists for an ideal steroid regimen that is suitable for all patients, so dosage and tapering of Prednisone should be tailored based on the patient. Steroids: N/V, dyspepsia, Gi perforation
  23. The average age at diagnosis is 72 years-old. GCA affects arteries of the head and neck, in addition to the 3 arteries that branch out from the arch of the ascending aorta, and their branches—the thoracic aorta, the axillary arteries, the vertebral arteries, and further on in the head in the ophthalmic and external carotid arteries (the temporal and occipital arteries). It can cause occlusion of the arteries and ischemia (tissue death). Inflammation of lining of arteries.
  24. “Giant cell arteritis” is a term often used to characterize the disease because when one looks at biopsies of inflamed temporal arteries under a microscope, you can often see large or “giant” cells.
  25. So of these symptoms, Mrs. LaMonica DID complain of occasional vertigo, dry eyes, fatigue, arthralgia, and she likely has PMR. H/e, she doesn’t have a lot of the main symptoms like headache, temporal tenderness, or jaw claudication, so at this point, we’re thinking it’s unlikely that she has GCA, but d/t the 15-20% risk of associated GCA w/ PMR, this is something that we certainly need to educate Mrs. LaMonica on so that we can keep it on the radar and she’ll know when to seek treatment if it does arise.
  26. We’ve already determined that she likely does not have GCA at this time. Her + findings are her age, elevated ESR, and occasional vertigo… but her age and elevated ESR could also be linked back to her PMR. She had major negative findings here. If we DID have a strong suspicion for GCA, would a referral be urgent? GO TO NEXT SLIDE….
  27. 1: Irreversible blindness results from necrosis of the posterior ciliary branch of the opthalmic artery and is usually preventable by early dx and corticosteroid tx. Sxs of GCA should rapidly respond to glucocorticoid treatment. If doesn’t, think of alt. dx. Follow-up, similar to PMR: Weeks 0, 1, 3, 6 then months 3, 6, 9, 12 in 1st year Labs at follow-up: CBC, ESR/CRP, urea and electrolytes, glucose Q 2 years: CXR- monitor for aortic aneurysm Low- dose aspirin if no CI. Suggested tapering regimen: 40–60 mg prednisolone continued until symptoms and laboratory abnormalities resolve (at least 3–4 weeks); then dose is reduced by 10 mg every 2 weeks to 20 mg; then by 2.5 mg every 2–4 weeks to 10 mg; and then by 1 mg every 1–2 months provided there is no relapse.
  28. We now know that Mrs. LaMonica has polymyalgia rheumatica without giant cell arteritis, so we can come up with an adequate treatment plan now. BIPHOSPH: So for her, given her age and history and because she’ll be using steroids, the guidelines suggest Vitd, calcium, and bisphosphonates. This is because with corticosteroid treatment in large doses of prednisone exceeding 5-7.5mg/day OR steroid usage beyond 1 month’s duration, corticosteroid-induced osteoporosis prophylaxis is recommended with these medications. (Bisphosphonates- Alendronate 10mg PO QD, Risedronate); ADDITIONALLY: Mrs. LaMonica needs to come OFF of her NSAIDs to minimize GIB, because biphosphonate + NSAIDs + prednisone can increase the risk of upper GI Aes. Maybe try the topical capsaicin for her. CAP-SAY-UH-SIN NONPHARM: To help decrease further risks of osteoporosis. EDUCATE: side effects will be discussed with her. Also she’ll need to be educated on when to call her provider– if she experiences blurred vision/eye pain/seeing halos around lights (GLAUCOMA/CATARACTS); severe depression or changes in personality or behavior; S/S pancreatitis (severe pain in her upper stomach, N/V, tachycardia); severe HA, blurred vision, tinnitus, anxiety, chest pain, SOB (High BP)
  29. As we mentioned in our pharmacologic plan, Mrs. LaMonica is at risk for osteoporosis d/t long-term steroid usage. Steroids can cause reduced calcium absorption from the intestine, increased renal calcium excretion, inhibition of bone formation, increased bone resorption. All of these can lead to bone loss and will increase Mrs. LaMonica’s risk for falls and fractures, which will also need to be an education point during this encounter. So, as the guidelines suggest, we started Mrs. LaMonica on Alendronate, since she is postmenopausal, >50 years-old, and is anticipated to be on steroids for >3 months. She’ll also need to be counseled on lifestyle modifications– she’ll need a baseline BMD, weight-bearing exercises, smoking cessation, avoid excessive ETOH usage, etc.
  30. While we’re on the topic of falls, these are some common RFs for falls in the elderly, in addition to tips for preventing falls. RFs: POLYPHARMACY: Mrs. LaMonica is on more than 4 meds, so she could be at risk for this. ENVIRONMENTAL HAZARDS: poor lighting, unsafe stairways, irregular floor surfaces– need to educate Mrs. LaMonica on this. MEDICATIONS: Mrs. LaMonica is on corticosteroids and antihypertensives (decr. BP). We took her off of her Flexeril, which could cause some sedation in her. Prevention: An important portion of visits with the elderly is reviewing medications including Rxs, OTCs, herbal and illicit drugs. We also need to make sure environmental hazards have been removed. We can provide the patient with balance training if needed. We should always involve the family, and provide follow-up. http://www.merckmanuals.com/professional/geriatrics/falls-in-the-elderly/falls-in-the-elderly
  31. FOLLOW-UP: Part of confirming the diagnosis of PMR involves evidence of an adequate response to steroid therapy. So, we want her to return within 24-72 hours. The prednisone should improve her symptoms. As we discussed earlier, a study I found showed that >70% of patients will improve on steroids within the 1st week of steroid therapy, and their inflammatory markers will be normalized at 4 weeks. If there is a lesser response to this, an alternative condition should be assessed. CBC: Anemia? ESR/CRP: Inflammation? Urea: kidney function Electrolytes: --prednisone can lower her K. NA retention Glucose: On steroid therapy. –could increase. -We’ll also want to assess her BP at each visit, since this can be increased. And we may also check her weight.
  32. Remain unchanged?! Refer to Rheumatology!
  33. Answer: Yes, dilemmas in treatment—unresponsive or incomplete response to corticosteroids. So, we ARE going to refer Mrs. LaMonica to Rheumatology, and we will request the next available appt w/in 1-2 weeks. We’ll send copies of her office notes, labs, and current medications in addition to notifying them on the need for a translator.
  34. Mrs. LaMonica is at risk for both primary and secondary causes of osteoporosis. She’s at risk for primary d/t being postmenopausal and d/t her age. She’s at risk for secondary osteoporosis d/t her corticosteroid therapy. Other overall RFs: White/Asian race, older age (thinning bones), female (men start out with more bone density and lose Ca at a slower rate than F), thin build (BMI <21_, low vitamin d or calcium, family hx IMAGING RECOMMENDATIONS: BMD testing is recommended for all postmenopausal women <65 years-old w/ 1+ RF for osteoporosis AND all postmenopausal women >65 years-old. W/out new risk factors, screening shouldn’t be performed more frequently than Q 2 years. http://umm.edu/health/medical/reports/articles/osteoporosis Diseases- Cushing's syndrome, cancer Drugs causing osteoporosis- corticosteroids, loop diuretics, methotrexate, heparin, cyclosporine. Lifestyle behaviors: ETOH abuse, smoking, immobilization ETOH: Interferes with absorption of Ca and VitD by pancreas; some studies show can decrease estrogen Corticosteroids: Increased bone resorption, decrease bone formation; Affect Ca and bone metabolism; increase ca excretion thru kidneys Low Estrogen: postmenopausal women- Osteoclast apoptosis is regulated by estrogens. With estrogen deficiency, the osteoclasts live longer and are therefore able to resorb more bone. Also w/ an estrogen deficiency, the skeleton is more sensitive to PTH resulting in an increased resorption of Ca from the bone and in turn decreases TPH secrection, Vitamin D production, and Ca absorption leading to loss of bone. Smoking: Toxins can decrease estrogen; increase cortisol—bone breakdown
  35. FRAX was developed by the World Health Organizations as a way to evaluate the risk of fractures for patients. So here it shows the probability of hip fracture in 10-years, and the probability of a major osteoporotic fracture (spine, forearm, hip, or shoulder fracture) over 10-years. Last BMD was 4 years ago, and was normal. I put in a normal T-score for the BMD, though this info is kind of out-of date. So this is just an example of what Mrs. LaMonica’s FRAX score might be.
  36. 1: BMD: Mrs. LaMonica will definitely need a BMD, since she is overdue and also because of her current condition and being started on LT steroids. We’ll want a baseline here. 2: We also need to ask her when her last colonoscopy was done and if there were any polyps found, in addition to her GI specialist’s recommendations for her next colonoscopy. (National Osteoporosis Foundation, 2014)
  37. This scenario is similar to Mrs. LaMonica’s. This is just a good reminder that we should always be sure that we don’t just look at our elderly patients and think it’s just due to old age. Still make your differential diagnoses list and order labs and diagnostics based on presenting symptoms. If Mrs. LaMonica’s previous PCP would have at least drawn a CBC, they likely would have been able to see that something greater than fibromyalgia was going on with her. Also, it’s important to realize that w/out proper treatment, this could really impact the patient’s home life and overall quality of life, so it’s important to take all complaints seriously.
  38. Comparison of PMR to fibromyalgia http://www.obgyn.net/sites/default/files/figures_diagrams/polymyalgia_rheumatica_table.jpg
  39. Is there anything else here we would like to further inquire about? Is pain and swelling symmetrical? Any rashes? How long was the tick on her for? Did she remove the tick completely? Any redness/swelling at site? Fevers/chills? Has she ever had episodes of joint pain before? How is her PTSD being managed? Fingers, elbows, knees; tick bite Does she have a hx of lupus, IDA, Vitamin B12 deficiency, thyroid problems?
  40. Red flags? -NO INSURANCE, served two tours in Iraq, hx of PTSD
  41. Red flags here? A lot of rheumatology issues and arthritis. Also, a lot of cardiac hx.
  42. What other questions would you want to inquire about here and what are some red flags? How long has she had PTSD- did she take meds for this? Benadryl for sleep?!?!?!?! How often does she do this?! Is she still having issues with anxiety? How is she controlling nonpharmacologically if so, and is this helping? Allergies? Immunizations? Why is she getting daily MVI? Hx of vitamin deficiency? MVI: Multi-vitamin infusions
  43. Initial manifestations of Rheumatoid arthritis: inflammation, weakness, weight loss, malaise, fatigue, anorexia, aching and stiffness. Painful, tender, swollen joints. Morning stiffness lasts for as long as 1-2 hours.
  44. PE of the peripheral joints and the axial skeleton is central to the eval of a patient with RA. On palpation, the inflamed joint feels warm and tender and the synovial membrane feels thickened and boggy.
  45. PIP – proximal intraphalangeal MCP – Metacaropophalangeal joint So she is having some symmetrical swelling in the joints of her hands here. -Early rheumatoid arthritis tends to affects your smaller joints first – particularly the joints that attach your fingers to your hands and your toes to your feet. As the disease progresses, symptoms often spread to wrist, knees, ankles, elbows, hips, and shoulders. Our patient has swollen/painful fingers, elbows, and knees. -Periods of increased disease activity, called flares, alternate with periods of relative remission — when the swelling and pain fade or disappear.
  46. Sites of hand or wrist involvement and their potential disease associations. So our patient has swelling at her PIP and MCP joints, as well as her wrist, which are all associated with RA.
  47. She also has swelling and warmth in her knee, which could be associated with RA.
  48. Based on the HPI and PE, what are some ddx we could come up with so far for this patient? 1) So, we definitely will have RA on our radar due to her presentation. She has swelling in her PIP, MCP, and wrist joints in addition to her knee, just as RA can present. 2) Lyme disease will be on our radar, too, since she admits to having a tick bite. With lyme disase, you can experience joint pain. However, with her, she had no rash. Which with lyme, you don’t necessarily have to have a bulls eye rash, but in many cases you will. 3) Lupus will also be on our radar. Lupus can present with polyarthritis in the small joints of hands/feet as a presenting manifestation. To differentiate, an ANA could be drawn, which is usually elevated in Lupus, and not in RA. 4) I added OA, too, but given her age, this is a more unlikely diagnosis for her. Also w/ OA, pain and stiffness usually is worse with activity, unlike her presenting symptoms of stiffness mostly in the morning. 5) Psoriatic arthritis involves small joints of hands/feet but is usually not symmetric, like RA is. Also, normally fewer than 5 joints are affected.
  49. Before we come up with a plan, we need to confirm our diagnosis with labs and diagnostics. Ms. LaMonica does NOT have health insurance. Because of this, what labs should we order for her, taking her lack of insurance into consideration? What other testing? Why? Are these essential for a patient without insurance? So, at the clinic I’ve done a lot of my clinical hours at, I was given a sheet with the costs of each lab for a patient paying out of pocket that the clinic had come up with. On their list for that particular clinic, if she were to pay on the date of service, a CBC would cost $15, a CMP $16, an ESR $10, anti-CCP would cost $30, CRP $10, RF $12- so these labs alone would cost her around $93 OOP. But, they all seem necessary to be drawn. ---RF: RF is NOT specific, it can be positive in other diseases, but this can be useful still in a patient with sxs of RA because if they are presenting as if they have the disease, and these levels are positive, it is likely they probably have the dz. And I also found that RF is found in about 80% of patients with RA in time, but as few as 30% of patients have a + RF at the start of the disease- so that’s something to keep in mind., that it may not show up + initially. ---Anti-CCP antibodies: This is important to be drawn because it can confirm a diagnosis of RA, since it is + in most patients with the dz. In fact, in can be + years before the disease presents itself. It’s found in 60-70% of patients with RA. ---ESR, CRP: Both will show if there is any inflammation, and are therefore important for determining what is going on with the patient. ---CBC: We definitely want to know blood counts for this patient- do they have anemia? Which could be common with RA.—normocytic normochromic anemia ---CMP: We’ll also want to know how her electrolytes are doing, what her kidney/liver function are like—especially if we’re going to start her on a medication. Many antirheumatic agents have renal and hepatic toxicity and may be contraindicated if these organs are severely impaired. X-RAY: More pricey OOP, and the evidence also shows that they are not very useful in early stages of RA, because bone damage will probably not be evident yet. H/e, if you were to suspect another cause of the joint pain, this could be useful. Later on, an x-ray will be a helpful tool to determine joint destruction and to monitor progression of the disease. But for this patient, presenting early and not having an established dx of RA, and no known injury as well as being uninsured, this is something we can skip for now.
  50. RDW: 14.7%- slightly elevated. Common in RA patients w/ anemia of chronic dz. Indicates RBCs are more variable in V than normal. Lymphocytes: 16.6% (Low). D/t inflammatory process of RA. Autoimmune disorders can l/t low lymphocyte count. Steroids can further decrease lymph count.
  51. Glucose: 105 (H) Globulin: 4.6 (H)– d/t chronic inflammatory dzs- Can be elevated in RA, lupus and other autoimmune disorders BUN/Creatinine: 22.2 (H) Globulins are a group of proteins w/in the blod that are produced by the liver and the immune system.
  52. This is a chart used for newly presenting patients w/ symptoms similar to RA. And it was created by the American College of Rheumatology and European League Against Rheumatism. Large joints: shoulders, elbows, hips, knees, ankles Small joints: MCP, PIP joints, 2nd-5th metatarsophalangeal joints, thumb interphalangeal joints, and wrists >6/10: indicates RA; but if <6/10, doesn’t mean their status might not change over time.
  53. PATIENT: Two Large joints involved: elbows, knees (1 pt) Small joints: wrists, MCP joints, PIP joints (2 pts) Serology: high + RF and CPP (3 pts) Acute-phase reactants: abnormal CRP and ESR (1 pt) Duration of sxs: < 6 weeks (0 pts) ----TOTAL: 7/10 pts- Classified as having RA.
  54. http://www.nlm.nih.gov/medlineplus/rheumatoidarthritis.html RA can be mild or severe. In most cases patients will have a chronic, lifelong course. Patients can have waxing and waning of the disease.
  55. The normal joint structure appears on the left. On the right is the joint with rheumatoid arthritis. RA causes synovitis, pain and swelling of the synovium (the tissue that lines the joint). This can make cartilage (the tissue that cushions between joints) and bone erode, or wear away.
  56. Early RA (<6 months) Low, moderate, and high disease activity w/ absence of poor prognostic features: DMARD mono-therapy Moderate, high disease activity w/ poor prognostic features: DMARD combination therapy (double & triple therapy) High disease activity w/ poor prognostic features: anti-TNF biologic w/ or w/o methotrexate
  57. Pharmacological Management for established RA: >6 months. More complicated- involves intitiating/switching among DMARDs, switching from DMARDs to biological agents, swithcing among bilogic agents, etc.
  58. DMARDs: Used in early treatment. Biologic agents: Used for more serious disease. With the right pharmacolgical therapy, patients can go into remission. Before starting drug therapy, patients should get vaccinated for bacterial infections such as pneumonia, and viruses such as influenza, hepatitis B, human papillomavirus, and varicella zoster. They should also have a PPD done. Also patients should be monitored Q1-3 months to achieve low disease activity or remission. Additionally, pregnancy should be avoided while on DMARDs or biologic agents. –bio agent- more sussceptible to infection Methotrexate- take folic acid with.
  59. 1) The chronic inflammation with RA puts patients at risk for coronary artery disease. 5) Inactivity can l/t loss of joint motion, contractions, and loss of muscle strength.
  60. 1) So, if Ms. LaMonica DID have insurance, we might just give her a Medrol dose pack. H/e, these are costly, so given her circumstances, we’re going to prescribe her with Prednisone today and giver her instructions on tapering it, since prednisone is cheaper. Prednisone is about $4-5, versus a Medrol Dose Pack which could cost $20 and up.
  61. The diagnosis of RA is based on lab tests and clinical manifestations, in addition to her adequate response to her steroids. However, patients should be seen by rheumatology for a confirmation of the diagnosis before being started on any medications, such as DMARDs.
  62. Sarah LaMonica will likely get insurance, if not through Medicaid, then through her Veterans Benefits. But for patients who cannot get insured, we really need to learn how to best care for these patients. GOODRX: App on smartphone or on internet; gives access to free coupons and offers a price comparison of different medications. I’ve seen this used A LOT during my clinicals. One of my rotations served individuals of lower economic status and many were uninsured, so the NP I was with would always print coupons out for patients and find where they could obtain their medications for the cheapest price. SO that was very helpful for that population. I found this website to be really helpful. It discusses how you can better assist uninsured patients. --And the first tip they include involves confirming that the patient is actually uninsurable. Many patients are not aware of programs they might be eligible for, such as Medicaid or programs for Medically Indigent Adults. Also, like our patient, she likely will qualify for veterans benefits and may have not realized it. --It’s also important for the PCP to go over costs of labs and services so they’ll know what to expect and will be given options on what they would like to have done based on cost. Another tip on the website is to choose generic drugs whenever possible, since these can save patients a lot of money. Also, PCPs should be aware of low-cost medications offered by large retailers. We have Publix here in GA and they have a medication list where many meds are either free or $4. There are other tips on the site that I found very helpful too. Medicare patients generally have good access to providers– about 96% of offices.
  63. What else do we need to inquire about here? Any income? Is she still with her partner? Does she have money saved up? Living arrangements? Diet? Any support? Who is caring for her daughter?
  64. It’s also important to note that PTSD does not JUST occur in the military community. It can also occur in entire communities for example after a natural disaster. It also can affect individual people. I once cared for a man who had a diagnosis of PTSD due to fear of his implanted-cardioverter-defibrillator (ICD) firing, because he had experienced that before and it was very traumatic to him. PTSD can also interfere with home life and work, just like how Sarah is having problems caring for her daughter and had to quit her job. It could also cause tension between significant other. So it’s important to inquire about this. Is she getting support from her significant other? Or is there tension between them because of her issues that is further impacting her symptoms.
  65. In there primary care setting, there are a few points that need to be considered… 1) Need to screen the patient. I read somewhere that it was recommended for PCPs to screen military patients at least once a year for PTSD, to ensure that prompt referrals and treatment can be given to the patient. Is the patient suicidal or homicidal? Safety is a major issue that needs to be considered here. Need to skillfully inquire about trauma history and traumatic events that have occurred in the patient’s life Educate the patient on PTSD and psychological treatment options Make recommendations for further evaluation and referral It’s also important to educate staff on how to recognize PTSD… many times the patient may not admit to having PTSD. They may present as angry, confused, depressed, and may be abusers of ETOH or drugs. Know that a PCP will not diagnose PTSD, but we should be able to recognize symptoms of PTSD so we can appropriately refer these patients to mental health. I read that some PCPs will actually treat PTSD with medications. But from the research I’ve done, it seems like these patients would really benefit from seeing a mental health provider since sometimes these patients can be treated w/o medications and instead just psychotherapy to actually help them work through their problems instead of just taking a pill. Also, for our patient, given that she was in the military, there are many mental health services offered w/in the VA HC system, that should be considered. Lastly, if the patient refuses treatment by mental health, try using the term “evaluation” by a mental health provider instead. Tell them they can ask them questions and decide from there if it’ll be helpful to them. Also give them education materials and normalize the idea of treatment. If they are still resistant, bring it up again at the next follow-up appointment. Give them some time to think it over.
  66. PTSD Association: ongoing education about PTSD, linkage with appropriate services, and helps you locate care/support for individuals and family members. Anxiety and Depression Association of America: offers a list of support groups across the country for a number of mental health conditions. National Alliance for Mental Illness: Information HelpLine provides support, referral and information on mental illness care. You may also find family support groups in a NAMI state or local affiliate online or by calling 1(800)950-NAMI (6264).