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Chapter 40 
Antibiotics Affecting Protein 
Synthesis 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Physiology 
• In all cells, the process of protein synthesis is divided 
into two sections: transcription and translation. 
• Initially, transcription occurs within the nucleus, 
producing messenger ribonucleic acid (mRNA). 
• This mRNA migrates from the nucleus to the cytoplasm. 
During this step, mRNA goes through different types of 
maturation, including one called splicing, during which 
the noncoding sequences are eliminated. 
• Translation occurs in the cytoplasm. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Protein Synthesis 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Aminoglycosides 
• The aminoglycosides have been in use since 1944. 
• They are extremely effective antibiotics for treating 
severe infections. 
• However, their general use is limited because of the 
potential for serious adverse effects. 
• Prototype drug: gentamicin 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Core Drug Knowledge 
• Pharmacotherapeutics 
– Serious infections 
• Pharmacokinetics 
– Distribution: throughout the body except CS; higher 
concentration in kidneys than serum 
• Pharmacodynamics 
– Entering the bacterial cell and binding to the 30S 
ribosomal subunit 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Core Drug Knowledge (cont.) 
• Contraindications and precautions 
– Hypersensitivity, pregnancy and lactation 
• Adverse effects 
– Neurotoxicity, nephrotoxicity, ototoxicity, and 
neuromuscular blockade 
• Drug interactions 
– Acyclovir, amphotericin B, cephalothin, cisplatin, 
cyclosporine, loop diuretics, prostaglandin synthetase 
inhibitors, and vancomycin 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Core Patient Variables 
• Health status 
– Past medical and any kidney problems 
• Life span and gender 
– Ototoxic to the fetus, assess pregnancy status. 
• Lifestyle, diet, and habits 
– Assess the nutritional status of the patient. 
• Environment 
– Assess the environment where the drug will be 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
given.
Gentamicin: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to potential drug-related allergic 
reactions or neuromuscular blockade or suppression of 
bone marrow function 
– Desired outcome: The patient will remain free of 
injury and will contact the prescriber if unusual 
adverse effects occur. 
• Diarrhea related to drug effects 
– Desired outcome: The patient will avoid 
dehydration, maintain fluid intake, and contact the 
prescriber if diarrhea persists. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Nursing Diagnoses and 
Outcomes (cont.) 
• Imbalanced Nutrition: Less than Body Requirements, 
related to drug-induced GI effects or superinfection 
– Desired outcome: The patient will maintain body 
weight and report any persistent adverse effect. 
• Risk for Injury related to CNS effects 
– Desired outcome: The patient will remain free of 
injury and contact the provider if confusion, 
disorientation, or depression occurs. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Nursing Diagnoses and 
Outcomes (cont.) 
• Disturbed Sensory Perception related to potential 
ototoxicity 
– Desired outcome: The patient will report sensory or 
perceptual changes to the prescriber. 
• Excess Fluid Volume related to potential nephrotoxicity 
– Desired outcome: The patient will report any 
weight gain exceeding 3 lb to the health care 
prescriber. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Planning and Interventions 
• Maximizing therapeutic effects 
– Make sure that patients receive the full course as 
prescribed at around-the-clock intervals. 
– Do not give at the same time as extended penicillin. 
• Minimizing adverse effects 
– Maintain blood levels of gentamicin within a 
therapeutic margin that is very narrow. 
– Monitor for signs of ototoxicity and nephrotoxicity. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Gentamicin: Teaching, Assessment, and 
Evaluations 
• Patient and family education 
– Patients should not take the drug if pregnant or 
breast-feeding. 
– Teach patients how to identify, report, and manage 
signs and symptoms of allergic reaction and adverse 
effects. 
• Ongoing assessment and evaluation 
– Coordinate the care of the patient to ensure that 
other potentially nephrotoxic or ototoxic drugs are 
not added to the treatment plan. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Gentamicin is effective against which of the following 
organism(s)? 
– A. Pseudomonas aeruginosa 
– B. Proteus mirabilis 
– C. Klebsiella 
– D. Enterobacter 
– E. All of the above
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• E. All of the above 
• Rationale: Gentamicin is effective in managing 
infections caused by gram-negative bacilli. 
• Susceptible organisms include Pseudomonas 
aeruginosa, Proteus mirabilis, Escherichia coli; 
Klebsiella, Enterobacter, Serratia, and Citrobacter 
species; and staphylococci.
Lincosamides 
• They are very toxic drugs. 
• Their use must be monitored and limited to situations 
with infections by bacteria with known sensitivity. 
• Prototype drug: clindamycin (Cleocin) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Core Drug Knowledge 
• Pharmacotherapeutics 
– Aerobic gram-positive cocci and several anaerobic 
gram-negative and gram-positive organisms 
• Pharmacokinetics 
– Varies with route of administration. Metabolized: 
liver. Excreted: bile and urine. 
• Pharmacodynamics 
– Enters the bacterial cell and binds to bacterial 
ribosomes, suppressing protein synthesis 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Hypersensitivity, pregnancy, and lactation 
• Adverse effects 
– Pseudomembranous colitis, maculopapular rash, 
erythema, and pruritus 
• Drug interactions 
– Neuromuscular blockers, aluminum salts, 
cyclosporine, benzoyl peroxide, tretinoin, and 
salicylic acid 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Core Patient Variables 
• Health status 
– Assess for allergy to medication. 
• Life span and gender 
– Assess the growth and developmental level of the 
child or infant. 
• Lifestyle, diet, and habits 
– Assess lifestyle to ensure that the drug will be given 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
properly. 
• Environment 
– Assess the environment where the drug will be given.
Clindamycin: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to allergic reactions 
– Desired outcome: The patient will stop drug 
therapy and immediately report symptoms of allergic 
reaction to the prescriber. 
• Diarrhea related to drug effects 
– Desired outcome: The patient will avoid 
dehydration and report persistent diarrhea to the 
provider. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Nursing Diagnoses and 
Outcomes (cont.) 
• Imbalanced nutrition: Less than Body Requirements, 
related to drug-related GI effects, alteration in taste, 
superinfections 
– Desired outcome: The patient will maintain body 
weight and report persistent symptoms affecting 
nutritional status. 
• Risk for Injury related to possible blood dyscrasias 
– Desired outcome: The patient will remain injury-free 
throughout drug therapy. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Planning and Interventions 
• Maximizing therapeutic effects 
– Make sure that the patient receives the full course of 
clindamycin as prescribed. 
– Coordinate the administration of drugs to decrease 
potential undesired interactions. 
• Minimizing adverse effects 
– Clindamycin should be administered on an empty 
stomach with a full glass of water. 
– Report diarrhea to the provider immediately. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Clindamycin: Teaching, Assessment, and 
Evaluations 
• Patient and family education 
– Advise patients to contact the prescriber immediately 
if they experience diarrhea. 
– Teach patients to recognize and report symptoms of 
allergic reaction and superinfection. 
• Ongoing assessment and evaluation 
– Monitor the patient for the onset of diarrhea. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• What is the most serious adverse reaction of clindamycin 
administration? 
– A. Respiratory arrest 
– B. Pseudomembranous colitis 
– C. Ventricular tachycardia 
– D. Ototoxicity
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. Pseudomembranous colitis 
• Rationale: Pseudomembranous colitis is the most 
serious side effect of clindamycin and carries a Black 
Box warning because of this side effect.
Macrolide Antibiotics 
• The macrolide antibiotics have been in use since 1952. 
• They are characterized by molecules made up of large-ring 
lactones. 
• Macrolides are bacteriostatic or bactericidal in susceptible 
bacteria. 
• Prototype drug: erythromycin 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Core Drug Knowledge 
• Pharmacotherapeutics 
– Treating Legionnaire disease, Mycoplasma 
pneumoniae pneumonia, diphtheria, chlamydial 
infections, and chancroid 
• Pharmacokinetics 
– The drug is easily inactivated by gastric acid. Peak 1 
to 4 hours. Metabolized: liver. Excreted: urine and 
bile. 
• Pharmacodynamics 
– Inhibiting RNA-dependent protein synthesis at the 
chain elongation step 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Allergy to medication 
• Adverse effects 
– GI symptoms, urticaria, maculopapular rash, 
erythema, and interstitial nephritis 
• Drug interactions 
– Astemizole and terfenadine 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Core Patient Variables 
• Health status 
– Assess medical history and allergies. 
• Life span and gender 
– Assess pregnancy and lactation status. 
• Lifestyle, diet, and habits 
– Instruct how to take the medication to avoid toxicity. 
• Environment 
– Assess the environment where the drug will be given. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to possible allergic reactions 
– Desired outcome: The patient will stop drug therapy and 
report any signs of allergic reaction immediately to the 
prescriber. 
• Diarrhea related to drug-induced GI upset 
– Desired outcome: The patient will avoid dehydration, 
maintain fluid intake, and contact the prescriber if 
diarrhea persists. 
• Risk for Infection related to potential for superinfection 
following drug therapy 
– Desired outcome: The patient will contact the provider if 
any signs of superinfection occur, for example, sore throat 
or fever. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Planning and Interventions 
• Maximizing therapeutic effects 
– Reconstitute erythromycin with sterile water only. 
– Prepared infusion solutions that are stored at room 
temperature must be used within 8 hours. 
• Minimizing adverse effects 
– Because erythromycin can be very irritating to veins, 
it is important to administer IV infusions over 30 to 
60 minutes. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Erythromycin: Teaching, Assessment, and 
Evaluations 
• Patient and family education 
– Encourage patients to take the complete course of 
antibiotics. 
– Advise patients to take erythromycin on an empty 
stomach, unless GI distress is unbearable. 
• Ongoing assessment and evaluation 
– Monitor for signs of allergic reactions, resolution of 
presenting signs and symptoms of infection, and 
signs of superinfection. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Grapefruit juice will decrease the serum concentration of 
erythromycin. 
– A. True 
– B. False
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. False 
• Rationale: Instruct the patient to avoid grapefruit or 
grapefruit juice because it increases the serum 
concentration of erythromycin and may cause adverse 
effects or toxicity.
Oxazolidinones 
• Oxazolidinones are the first new class of antibiotics 
developed specifically for treating methicillin-resistant 
Staphylococcus aureus (MRSA) infections. 
• Prototype drug: linezolid (Zyvox) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Core Drug Knowledge 
• Pharmacotherapeutics 
– Treatment of VRE and MRSA 
• Pharmacokinetics 
– Administered: oral or IV. Metabolism: liver. Excreted: 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
kidneys. 
• Pharmacodynamics 
– Blocking the early stages of the process bacteria use 
to make proteins
Linezolid: Core Drug Knowledge (cont.) 
• Contraindications and precautions 
– Hypersensitivity 
• Adverse effects 
– Diarrhea, headache, nausea, and vomiting 
• Drug interactions 
– Adrenergic and serotonergic agents 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Core Patient Variables 
• Health status 
– Assess medical history. 
• Life span and gender 
– Pregnancy Category C drug 
• Lifestyle, diet, and habits 
– Evaluate diet and alcohol use. 
• Environment 
– Assess the environment where the drug will be given. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Nursing Diagnoses and 
Outcomes 
• Deficient Fluid Volume related to nausea, vomiting, and 
diarrhea from linezolid therapy 
– Desired outcome: The patient will remain well 
hydrated throughout therapy. 
• Risk for Injury related to thrombocytopenia and 
pseudomembranous colitis 
– Desired outcome: The patient will remain free 
from injury and contact the health care provider 
immediately if any signs of bleeding or abdominal 
pain occur. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Nursing Diagnoses and 
Outcomes (cont.) 
• Risk for Injury related to hypertensive crisis 
– Desired outcome: The patient will remain 
normotensive by adhering to antihypertensive 
therapy and limiting foods or beverages with 
tyramine, caffeine, or alcohol. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Planning and Interventions 
• Maximizing therapeutic effects 
– Administer at evenly spaced intervals. 
• Minimizing adverse effects 
– To avoid hypertensive crisis, monitor the patient’s 
intake of food or beverages containing tyramine, 
caffeine, or alcohol. 
– Serial blood pressure readings should be obtained 
throughout therapy. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Linezolid: Teaching, Assessment, and 
Evaluations 
• Patient and family education 
– Explain dietary restrictions, focusing on food or 
beverages containing tyramine, caffeine, or alcohol. 
– Teach patients the signs and symptoms of 
thrombocytopenia and pseudomembranous colitis. 
• Ongoing assessment and evaluation 
– Monitor for efficacy of treatment and resolution of 
the presenting infection. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Linezolid is classified as a Pregnancy Category ___ drug. 
– A. A 
– B. B 
– C. C 
– D. D 
– E. X
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• C. C 
• Rationale: Linezolid is classified as a pregnancy category 
C drug.
Streptogramins 
• Streptogramins are the newest class of antibiotics. 
• Designed to eradicate “superbugs” resistant to other 
antibiotics. 
• Prototype drug: quinupristin/dalfopristin (Synercid) 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Quinupristin/Dalfopristin: Core Drug 
Knowledge 
• Pharmacotherapeutics 
– Serious or life-threatening infections associated with 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
VRE 
• Pharmacokinetics 
– Administered: IV. T½: 1 hour. 
• Pharmacodynamics 
– Inhibits bacterial protein synthesis by irreversibly 
blocking ribosome functioning
Quinupristin/Dalfopristin: Core Drug 
Knowledge (cont.) 
• Contraindications and precautions 
– Hypersensitivity 
• Adverse effects 
– Pseudomembranous colitis, superinfection, and 
hepatotoxicity 
• Drug interactions 
– Drugs that are metabolized by CYP3A4, a cytochrome 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
of P-450
Quinupristin/Dalfopristin: Core Patient 
Variables 
• Health status 
– Assess health history and contraindications to 
medication use. 
• Life span and gender 
– Pregnancy Category B drug 
• Environment 
– Assess the environment where the drug will be given. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Quinupristin/Dalfopristin: Nursing 
Diagnoses and Outcomes 
• Pain related to IV administration 
– Desired outcome: The patient will inform you 
immediately should pain at the injection site occur. 
• Diarrhea related to potential pseudomembranous colitis 
– Desired outcome: The patient will remain well 
hydrated throughout therapy and report any diarrhea 
immediately. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Quinupristin/Dalfopristin: Nursing 
Diagnoses and Outcomes (cont.) 
• Risk for Injury related to potential superinfection or 
hepatotoxicity 
– Desired outcome: The patient will remain free of 
injury throughout therapy. 
• Risk for Impaired Skin Integrity related to rash or 
pruritus. 
– Desired outcome: The patient will report itching or 
rash immediately to minimize potential for infection. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Quinupristin/Dalfopristin: Planning and 
Interventions 
• Maximizing therapeutic effects 
– The medication should not be administered with any 
other medications through a Y-site infusion. 
– Flush the line before and after administration with 
5% dextrose and water. 
• Minimizing adverse effects 
– Administer these drugs in a peripherally inserted 
central catheter (PICC) or a central line whenever 
possible. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Quinupristin/Dalfopristin: Teaching, 
Assessment, and Evaluations 
• Patient and family education 
– Teach patients the potential adverse effects. 
– Advise patients to report any diarrhea immediately. 
• Ongoing assessment and evaluation 
– During infusion, monitor the IV site for signs of 
infiltration, edema, or phlebitis. 
– Question the patient regarding pain at the injection 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
site.
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Quinupristin/dalfopristin is best administrated via 
– A. Oral route 
– B. PICC line 
– C. Peripheral IV 
– D. Z-track IM
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• B. PICC line 
• Rationale: Because injection site problems are very 
common with the administration of 
quinupristin/dalfopristin, administer these drugs in a 
peripherally inserted central catheter (PICC) line 
whenever possible.
Tetracyclines 
• The tetracyclines were developed as semisynthetic 
antibiotics based on the structure of a common soil mold. 
• They are broad-spectrum antibiotics that affect both 
gram-positive and gram-negative bacteria. 
• Over the years, major resistance has developed to 
tetracyclines. 
• Prototype drug: tetracycline 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Core Drug Knowledge 
• Pharmacotherapeutics 
– Rickettsia species, Mycoplasma pneumoniae, and 
Chlamydia trachomatis 
• Pharmacokinetics 
– Administered: oral. Excreted: kidneys. 
• Pharmacodynamics 
– Inhibits or retards the growth of bacteria but does 
not kill them 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Allergy, pregnancy, or lactation 
• Adverse effects 
– GI upset, photosensitivity, and rash 
• Drug interactions 
– Penicillin G, aluminum, bismuth, calcium, iron, 
magnesium, and zinc salts 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Core Patient Variables 
• Health status 
– Assess medical status. 
• Life span and gender 
– Pregnancy Category D drug 
• Lifestyle, diet, and habits 
– Assess dietary intake. 
• Environment 
– Assess for exposure to sun. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to potential superinfection or 
allergic drug reaction 
– Desired outcome: The patient will experience no 
new infection and no preventable allergic reaction 
related to tetracycline. 
• Diarrhea related to drug-induced GI effects 
– Desired outcome: The patient will report any 
incidence of diarrhea and follow the prescriber’s 
recommendation. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Nursing Diagnoses and 
Outcomes (cont.) 
• Imbalanced nutrition: Less than Body Requirements, 
related to adverse GI effects of nausea, vomiting, 
diarrhea, and altered taste 
– Desired outcome: The patient will maintain dietary 
intake to provide adequate nutrition. 
• Risk for Impaired Skin Integrity related to drug-induced 
photosensitivity 
– Desired outcome: The patient will dress 
appropriately and take adequate precautionary 
measures while outdoors to avoid unnecessary 
sunburn. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Planning and Interventions 
• Maximizing therapeutic effects 
– To maximize absorption, oral preparations should be 
administered on an empty stomach either 1 hour 
before or 2 hours after any meals or other drugs. 
• Minimizing adverse effects 
– Monitor the patient to ensure that adequate fluids are 
given to replace fluid lost with diarrhea. 
– Wear protective clothing and sunscreen when 
outdoors. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Tetracycline: Teaching, Assessment, and 
Evaluations 
• Patient and family education 
– Advise women of childbearing age that tetracycline 
should not be taken during pregnancy or breast-feeding. 
– Advise patients to take tetracycline on an empty 
stomach. 
• Ongoing assessment and evaluation 
– Monitor renal status to detect and prevent 
hepatotoxicity and to observe for any signs of 
superinfection. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• Tetracycline should not be administered with antacids. 
– A. True 
– B. False
Answer 
• A. True 
• Rationale: Tetracycline forms an insoluble chelate with 
aluminum, bismuth, calcium, iron, magnesium, and zinc 
salts, which are frequently an ingredient in antacids. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Miscellaneous Antibiotics that Affect 
Protein Synthesis 
• Miscellaneous antibiotics include chloramphenicol and 
spectinomycin. 
• Used to treat large outbreaks of typhus 
• Prototype: chloramphenicol 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Core Drug Knowledge 
• Pharmacotherapeutics 
– True broad-spectrum antibiotic 
• Pharmacokinetics 
– Administered: oral and IV. Peak 1 to 3 hours. 
• Pharmacodynamics 
– Inhibiting the protein synthesis of bacterial cells 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Core Drug Knowledge 
(cont.) 
• Contraindications and precautions 
– Toxic reaction to the medication 
• Adverse effects 
– Aplastic anemia, hypoplastic anemia, 
thrombocytopenia, pancytopenia, and 
granulocytopenia 
• Drug interactions 
– Many different types of drugs 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Core Patient Variables 
• Health status 
– Assess medical history. 
• Life span and gender 
– Assess pregnancy status. 
• Environment 
– Assess the environment where the drug will be given. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Nursing Diagnoses and 
Outcomes 
• Risk for Injury related to drug-induced adverse effects, 
such as blood dyscrasias, gray baby syndrome, and CNS 
effects, including optic or peripheral neuritis, headache, 
depression, confusion, or delirium 
– Desired outcome: Regular and careful monitoring 
will protect the patient from permanent drug-related 
adverse effects. 
• Risk for Impaired Skin Integrity, rash and pruritus, 
related to topical drug use 
– Desired outcome: The nurse and patient will 
observe for and report signs of unusual skin reaction 
and contact the prescriber. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Planning and 
Interventions 
• Maximizing therapeutic effects 
– Oral chloramphenicol should be administered on an 
empty stomach 1 hour before or 2 hours after meals. 
• Minimizing adverse effects 
– Monitor plasma concentrations at least weekly or 
more often in patients with hepatic or renal 
impairment. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Chloramphenicol: Teaching, Assessment, 
and Evaluations 
• Patient and family education 
– Explain the importance of completing therapy. 
– Teach patients the importance of measuring fluid 
intake and output accurately. 
• Ongoing assessment and evaluation 
– For patients receiving systemic therapy, coordinate 
serial monitoring of chloramphenicol plasma 
concentrations. 
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Question 
• A serious and potentially life-threatening adverse effect 
of chloramphenicol is “gray baby” syndrome. 
– A. True 
– B. False
Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins 
Answer 
• A. True 
• Rationale: “Gray baby” syndrome is most common in 
premature infants or newborns receiving 
chloramphenicol, whose hepatic systems have 
difficulty conjugating or excreting chloramphenicol.

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Ppt chapter 40

  • 1. Chapter 40 Antibiotics Affecting Protein Synthesis Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 2. Physiology • In all cells, the process of protein synthesis is divided into two sections: transcription and translation. • Initially, transcription occurs within the nucleus, producing messenger ribonucleic acid (mRNA). • This mRNA migrates from the nucleus to the cytoplasm. During this step, mRNA goes through different types of maturation, including one called splicing, during which the noncoding sequences are eliminated. • Translation occurs in the cytoplasm. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 3. Protein Synthesis Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 4. Aminoglycosides • The aminoglycosides have been in use since 1944. • They are extremely effective antibiotics for treating severe infections. • However, their general use is limited because of the potential for serious adverse effects. • Prototype drug: gentamicin Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 5. Gentamicin: Core Drug Knowledge • Pharmacotherapeutics – Serious infections • Pharmacokinetics – Distribution: throughout the body except CS; higher concentration in kidneys than serum • Pharmacodynamics – Entering the bacterial cell and binding to the 30S ribosomal subunit Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 6. Gentamicin: Core Drug Knowledge (cont.) • Contraindications and precautions – Hypersensitivity, pregnancy and lactation • Adverse effects – Neurotoxicity, nephrotoxicity, ototoxicity, and neuromuscular blockade • Drug interactions – Acyclovir, amphotericin B, cephalothin, cisplatin, cyclosporine, loop diuretics, prostaglandin synthetase inhibitors, and vancomycin Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 7. Gentamicin: Core Patient Variables • Health status – Past medical and any kidney problems • Life span and gender – Ototoxic to the fetus, assess pregnancy status. • Lifestyle, diet, and habits – Assess the nutritional status of the patient. • Environment – Assess the environment where the drug will be Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins given.
  • 8. Gentamicin: Nursing Diagnoses and Outcomes • Risk for Injury related to potential drug-related allergic reactions or neuromuscular blockade or suppression of bone marrow function – Desired outcome: The patient will remain free of injury and will contact the prescriber if unusual adverse effects occur. • Diarrhea related to drug effects – Desired outcome: The patient will avoid dehydration, maintain fluid intake, and contact the prescriber if diarrhea persists. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 9. Gentamicin: Nursing Diagnoses and Outcomes (cont.) • Imbalanced Nutrition: Less than Body Requirements, related to drug-induced GI effects or superinfection – Desired outcome: The patient will maintain body weight and report any persistent adverse effect. • Risk for Injury related to CNS effects – Desired outcome: The patient will remain free of injury and contact the provider if confusion, disorientation, or depression occurs. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 10. Gentamicin: Nursing Diagnoses and Outcomes (cont.) • Disturbed Sensory Perception related to potential ototoxicity – Desired outcome: The patient will report sensory or perceptual changes to the prescriber. • Excess Fluid Volume related to potential nephrotoxicity – Desired outcome: The patient will report any weight gain exceeding 3 lb to the health care prescriber. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 11. Gentamicin: Planning and Interventions • Maximizing therapeutic effects – Make sure that patients receive the full course as prescribed at around-the-clock intervals. – Do not give at the same time as extended penicillin. • Minimizing adverse effects – Maintain blood levels of gentamicin within a therapeutic margin that is very narrow. – Monitor for signs of ototoxicity and nephrotoxicity. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 12. Gentamicin: Teaching, Assessment, and Evaluations • Patient and family education – Patients should not take the drug if pregnant or breast-feeding. – Teach patients how to identify, report, and manage signs and symptoms of allergic reaction and adverse effects. • Ongoing assessment and evaluation – Coordinate the care of the patient to ensure that other potentially nephrotoxic or ototoxic drugs are not added to the treatment plan. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 13. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Gentamicin is effective against which of the following organism(s)? – A. Pseudomonas aeruginosa – B. Proteus mirabilis – C. Klebsiella – D. Enterobacter – E. All of the above
  • 14. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • E. All of the above • Rationale: Gentamicin is effective in managing infections caused by gram-negative bacilli. • Susceptible organisms include Pseudomonas aeruginosa, Proteus mirabilis, Escherichia coli; Klebsiella, Enterobacter, Serratia, and Citrobacter species; and staphylococci.
  • 15. Lincosamides • They are very toxic drugs. • Their use must be monitored and limited to situations with infections by bacteria with known sensitivity. • Prototype drug: clindamycin (Cleocin) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 16. Clindamycin: Core Drug Knowledge • Pharmacotherapeutics – Aerobic gram-positive cocci and several anaerobic gram-negative and gram-positive organisms • Pharmacokinetics – Varies with route of administration. Metabolized: liver. Excreted: bile and urine. • Pharmacodynamics – Enters the bacterial cell and binds to bacterial ribosomes, suppressing protein synthesis Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 17. Clindamycin: Core Drug Knowledge (cont.) • Contraindications and precautions – Hypersensitivity, pregnancy, and lactation • Adverse effects – Pseudomembranous colitis, maculopapular rash, erythema, and pruritus • Drug interactions – Neuromuscular blockers, aluminum salts, cyclosporine, benzoyl peroxide, tretinoin, and salicylic acid Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 18. Clindamycin: Core Patient Variables • Health status – Assess for allergy to medication. • Life span and gender – Assess the growth and developmental level of the child or infant. • Lifestyle, diet, and habits – Assess lifestyle to ensure that the drug will be given Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins properly. • Environment – Assess the environment where the drug will be given.
  • 19. Clindamycin: Nursing Diagnoses and Outcomes • Risk for Injury related to allergic reactions – Desired outcome: The patient will stop drug therapy and immediately report symptoms of allergic reaction to the prescriber. • Diarrhea related to drug effects – Desired outcome: The patient will avoid dehydration and report persistent diarrhea to the provider. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 20. Clindamycin: Nursing Diagnoses and Outcomes (cont.) • Imbalanced nutrition: Less than Body Requirements, related to drug-related GI effects, alteration in taste, superinfections – Desired outcome: The patient will maintain body weight and report persistent symptoms affecting nutritional status. • Risk for Injury related to possible blood dyscrasias – Desired outcome: The patient will remain injury-free throughout drug therapy. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 21. Clindamycin: Planning and Interventions • Maximizing therapeutic effects – Make sure that the patient receives the full course of clindamycin as prescribed. – Coordinate the administration of drugs to decrease potential undesired interactions. • Minimizing adverse effects – Clindamycin should be administered on an empty stomach with a full glass of water. – Report diarrhea to the provider immediately. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 22. Clindamycin: Teaching, Assessment, and Evaluations • Patient and family education – Advise patients to contact the prescriber immediately if they experience diarrhea. – Teach patients to recognize and report symptoms of allergic reaction and superinfection. • Ongoing assessment and evaluation – Monitor the patient for the onset of diarrhea. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 23. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • What is the most serious adverse reaction of clindamycin administration? – A. Respiratory arrest – B. Pseudomembranous colitis – C. Ventricular tachycardia – D. Ototoxicity
  • 24. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. Pseudomembranous colitis • Rationale: Pseudomembranous colitis is the most serious side effect of clindamycin and carries a Black Box warning because of this side effect.
  • 25. Macrolide Antibiotics • The macrolide antibiotics have been in use since 1952. • They are characterized by molecules made up of large-ring lactones. • Macrolides are bacteriostatic or bactericidal in susceptible bacteria. • Prototype drug: erythromycin Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 26. Erythromycin: Core Drug Knowledge • Pharmacotherapeutics – Treating Legionnaire disease, Mycoplasma pneumoniae pneumonia, diphtheria, chlamydial infections, and chancroid • Pharmacokinetics – The drug is easily inactivated by gastric acid. Peak 1 to 4 hours. Metabolized: liver. Excreted: urine and bile. • Pharmacodynamics – Inhibiting RNA-dependent protein synthesis at the chain elongation step Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 27. Erythromycin: Core Drug Knowledge (cont.) • Contraindications and precautions – Allergy to medication • Adverse effects – GI symptoms, urticaria, maculopapular rash, erythema, and interstitial nephritis • Drug interactions – Astemizole and terfenadine Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 28. Erythromycin: Core Patient Variables • Health status – Assess medical history and allergies. • Life span and gender – Assess pregnancy and lactation status. • Lifestyle, diet, and habits – Instruct how to take the medication to avoid toxicity. • Environment – Assess the environment where the drug will be given. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 29. Erythromycin: Nursing Diagnoses and Outcomes • Risk for Injury related to possible allergic reactions – Desired outcome: The patient will stop drug therapy and report any signs of allergic reaction immediately to the prescriber. • Diarrhea related to drug-induced GI upset – Desired outcome: The patient will avoid dehydration, maintain fluid intake, and contact the prescriber if diarrhea persists. • Risk for Infection related to potential for superinfection following drug therapy – Desired outcome: The patient will contact the provider if any signs of superinfection occur, for example, sore throat or fever. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 30. Erythromycin: Planning and Interventions • Maximizing therapeutic effects – Reconstitute erythromycin with sterile water only. – Prepared infusion solutions that are stored at room temperature must be used within 8 hours. • Minimizing adverse effects – Because erythromycin can be very irritating to veins, it is important to administer IV infusions over 30 to 60 minutes. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 31. Erythromycin: Teaching, Assessment, and Evaluations • Patient and family education – Encourage patients to take the complete course of antibiotics. – Advise patients to take erythromycin on an empty stomach, unless GI distress is unbearable. • Ongoing assessment and evaluation – Monitor for signs of allergic reactions, resolution of presenting signs and symptoms of infection, and signs of superinfection. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 32. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Grapefruit juice will decrease the serum concentration of erythromycin. – A. True – B. False
  • 33. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. False • Rationale: Instruct the patient to avoid grapefruit or grapefruit juice because it increases the serum concentration of erythromycin and may cause adverse effects or toxicity.
  • 34. Oxazolidinones • Oxazolidinones are the first new class of antibiotics developed specifically for treating methicillin-resistant Staphylococcus aureus (MRSA) infections. • Prototype drug: linezolid (Zyvox) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 35. Linezolid: Core Drug Knowledge • Pharmacotherapeutics – Treatment of VRE and MRSA • Pharmacokinetics – Administered: oral or IV. Metabolism: liver. Excreted: Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins kidneys. • Pharmacodynamics – Blocking the early stages of the process bacteria use to make proteins
  • 36. Linezolid: Core Drug Knowledge (cont.) • Contraindications and precautions – Hypersensitivity • Adverse effects – Diarrhea, headache, nausea, and vomiting • Drug interactions – Adrenergic and serotonergic agents Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 37. Linezolid: Core Patient Variables • Health status – Assess medical history. • Life span and gender – Pregnancy Category C drug • Lifestyle, diet, and habits – Evaluate diet and alcohol use. • Environment – Assess the environment where the drug will be given. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 38. Linezolid: Nursing Diagnoses and Outcomes • Deficient Fluid Volume related to nausea, vomiting, and diarrhea from linezolid therapy – Desired outcome: The patient will remain well hydrated throughout therapy. • Risk for Injury related to thrombocytopenia and pseudomembranous colitis – Desired outcome: The patient will remain free from injury and contact the health care provider immediately if any signs of bleeding or abdominal pain occur. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 39. Linezolid: Nursing Diagnoses and Outcomes (cont.) • Risk for Injury related to hypertensive crisis – Desired outcome: The patient will remain normotensive by adhering to antihypertensive therapy and limiting foods or beverages with tyramine, caffeine, or alcohol. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 40. Linezolid: Planning and Interventions • Maximizing therapeutic effects – Administer at evenly spaced intervals. • Minimizing adverse effects – To avoid hypertensive crisis, monitor the patient’s intake of food or beverages containing tyramine, caffeine, or alcohol. – Serial blood pressure readings should be obtained throughout therapy. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 41. Linezolid: Teaching, Assessment, and Evaluations • Patient and family education – Explain dietary restrictions, focusing on food or beverages containing tyramine, caffeine, or alcohol. – Teach patients the signs and symptoms of thrombocytopenia and pseudomembranous colitis. • Ongoing assessment and evaluation – Monitor for efficacy of treatment and resolution of the presenting infection. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 42. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Linezolid is classified as a Pregnancy Category ___ drug. – A. A – B. B – C. C – D. D – E. X
  • 43. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • C. C • Rationale: Linezolid is classified as a pregnancy category C drug.
  • 44. Streptogramins • Streptogramins are the newest class of antibiotics. • Designed to eradicate “superbugs” resistant to other antibiotics. • Prototype drug: quinupristin/dalfopristin (Synercid) Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 45. Quinupristin/Dalfopristin: Core Drug Knowledge • Pharmacotherapeutics – Serious or life-threatening infections associated with Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins VRE • Pharmacokinetics – Administered: IV. T½: 1 hour. • Pharmacodynamics – Inhibits bacterial protein synthesis by irreversibly blocking ribosome functioning
  • 46. Quinupristin/Dalfopristin: Core Drug Knowledge (cont.) • Contraindications and precautions – Hypersensitivity • Adverse effects – Pseudomembranous colitis, superinfection, and hepatotoxicity • Drug interactions – Drugs that are metabolized by CYP3A4, a cytochrome Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins of P-450
  • 47. Quinupristin/Dalfopristin: Core Patient Variables • Health status – Assess health history and contraindications to medication use. • Life span and gender – Pregnancy Category B drug • Environment – Assess the environment where the drug will be given. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 48. Quinupristin/Dalfopristin: Nursing Diagnoses and Outcomes • Pain related to IV administration – Desired outcome: The patient will inform you immediately should pain at the injection site occur. • Diarrhea related to potential pseudomembranous colitis – Desired outcome: The patient will remain well hydrated throughout therapy and report any diarrhea immediately. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 49. Quinupristin/Dalfopristin: Nursing Diagnoses and Outcomes (cont.) • Risk for Injury related to potential superinfection or hepatotoxicity – Desired outcome: The patient will remain free of injury throughout therapy. • Risk for Impaired Skin Integrity related to rash or pruritus. – Desired outcome: The patient will report itching or rash immediately to minimize potential for infection. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 50. Quinupristin/Dalfopristin: Planning and Interventions • Maximizing therapeutic effects – The medication should not be administered with any other medications through a Y-site infusion. – Flush the line before and after administration with 5% dextrose and water. • Minimizing adverse effects – Administer these drugs in a peripherally inserted central catheter (PICC) or a central line whenever possible. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 51. Quinupristin/Dalfopristin: Teaching, Assessment, and Evaluations • Patient and family education – Teach patients the potential adverse effects. – Advise patients to report any diarrhea immediately. • Ongoing assessment and evaluation – During infusion, monitor the IV site for signs of infiltration, edema, or phlebitis. – Question the patient regarding pain at the injection Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins site.
  • 52. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Quinupristin/dalfopristin is best administrated via – A. Oral route – B. PICC line – C. Peripheral IV – D. Z-track IM
  • 53. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • B. PICC line • Rationale: Because injection site problems are very common with the administration of quinupristin/dalfopristin, administer these drugs in a peripherally inserted central catheter (PICC) line whenever possible.
  • 54. Tetracyclines • The tetracyclines were developed as semisynthetic antibiotics based on the structure of a common soil mold. • They are broad-spectrum antibiotics that affect both gram-positive and gram-negative bacteria. • Over the years, major resistance has developed to tetracyclines. • Prototype drug: tetracycline Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 55. Tetracycline: Core Drug Knowledge • Pharmacotherapeutics – Rickettsia species, Mycoplasma pneumoniae, and Chlamydia trachomatis • Pharmacokinetics – Administered: oral. Excreted: kidneys. • Pharmacodynamics – Inhibits or retards the growth of bacteria but does not kill them Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 56. Tetracycline: Core Drug Knowledge (cont.) • Contraindications and precautions – Allergy, pregnancy, or lactation • Adverse effects – GI upset, photosensitivity, and rash • Drug interactions – Penicillin G, aluminum, bismuth, calcium, iron, magnesium, and zinc salts Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 57. Tetracycline: Core Patient Variables • Health status – Assess medical status. • Life span and gender – Pregnancy Category D drug • Lifestyle, diet, and habits – Assess dietary intake. • Environment – Assess for exposure to sun. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 58. Tetracycline: Nursing Diagnoses and Outcomes • Risk for Injury related to potential superinfection or allergic drug reaction – Desired outcome: The patient will experience no new infection and no preventable allergic reaction related to tetracycline. • Diarrhea related to drug-induced GI effects – Desired outcome: The patient will report any incidence of diarrhea and follow the prescriber’s recommendation. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 59. Tetracycline: Nursing Diagnoses and Outcomes (cont.) • Imbalanced nutrition: Less than Body Requirements, related to adverse GI effects of nausea, vomiting, diarrhea, and altered taste – Desired outcome: The patient will maintain dietary intake to provide adequate nutrition. • Risk for Impaired Skin Integrity related to drug-induced photosensitivity – Desired outcome: The patient will dress appropriately and take adequate precautionary measures while outdoors to avoid unnecessary sunburn. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 60. Tetracycline: Planning and Interventions • Maximizing therapeutic effects – To maximize absorption, oral preparations should be administered on an empty stomach either 1 hour before or 2 hours after any meals or other drugs. • Minimizing adverse effects – Monitor the patient to ensure that adequate fluids are given to replace fluid lost with diarrhea. – Wear protective clothing and sunscreen when outdoors. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 61. Tetracycline: Teaching, Assessment, and Evaluations • Patient and family education – Advise women of childbearing age that tetracycline should not be taken during pregnancy or breast-feeding. – Advise patients to take tetracycline on an empty stomach. • Ongoing assessment and evaluation – Monitor renal status to detect and prevent hepatotoxicity and to observe for any signs of superinfection. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 62. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • Tetracycline should not be administered with antacids. – A. True – B. False
  • 63. Answer • A. True • Rationale: Tetracycline forms an insoluble chelate with aluminum, bismuth, calcium, iron, magnesium, and zinc salts, which are frequently an ingredient in antacids. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 64. Miscellaneous Antibiotics that Affect Protein Synthesis • Miscellaneous antibiotics include chloramphenicol and spectinomycin. • Used to treat large outbreaks of typhus • Prototype: chloramphenicol Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 65. Chloramphenicol: Core Drug Knowledge • Pharmacotherapeutics – True broad-spectrum antibiotic • Pharmacokinetics – Administered: oral and IV. Peak 1 to 3 hours. • Pharmacodynamics – Inhibiting the protein synthesis of bacterial cells Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 66. Chloramphenicol: Core Drug Knowledge (cont.) • Contraindications and precautions – Toxic reaction to the medication • Adverse effects – Aplastic anemia, hypoplastic anemia, thrombocytopenia, pancytopenia, and granulocytopenia • Drug interactions – Many different types of drugs Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 67. Chloramphenicol: Core Patient Variables • Health status – Assess medical history. • Life span and gender – Assess pregnancy status. • Environment – Assess the environment where the drug will be given. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 68. Chloramphenicol: Nursing Diagnoses and Outcomes • Risk for Injury related to drug-induced adverse effects, such as blood dyscrasias, gray baby syndrome, and CNS effects, including optic or peripheral neuritis, headache, depression, confusion, or delirium – Desired outcome: Regular and careful monitoring will protect the patient from permanent drug-related adverse effects. • Risk for Impaired Skin Integrity, rash and pruritus, related to topical drug use – Desired outcome: The nurse and patient will observe for and report signs of unusual skin reaction and contact the prescriber. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 69. Chloramphenicol: Planning and Interventions • Maximizing therapeutic effects – Oral chloramphenicol should be administered on an empty stomach 1 hour before or 2 hours after meals. • Minimizing adverse effects – Monitor plasma concentrations at least weekly or more often in patients with hepatic or renal impairment. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 70. Chloramphenicol: Teaching, Assessment, and Evaluations • Patient and family education – Explain the importance of completing therapy. – Teach patients the importance of measuring fluid intake and output accurately. • Ongoing assessment and evaluation – For patients receiving systemic therapy, coordinate serial monitoring of chloramphenicol plasma concentrations. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins
  • 71. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Question • A serious and potentially life-threatening adverse effect of chloramphenicol is “gray baby” syndrome. – A. True – B. False
  • 72. Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Answer • A. True • Rationale: “Gray baby” syndrome is most common in premature infants or newborns receiving chloramphenicol, whose hepatic systems have difficulty conjugating or excreting chloramphenicol.