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Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins Chapter 40 Antibiotics Affecting Protein Synthesis

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Page 1: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Chapter 40

Antibiotics Affecting Protein Synthesis

Chapter 40

Antibiotics Affecting Protein Synthesis

Page 2: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Physiology 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.

Page 3: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Protein SynthesisProtein Synthesis

Page 4: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Aminoglycosides 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

Page 5: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Core Drug Knowledge 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

Page 6: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Core Drug Knowledge (cont.)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

Page 7: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Core Patient Variables 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 given.

Page 8: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Nursing Diagnoses and Outcomes 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.

Page 9: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Nursing Diagnoses and Outcomes (cont.)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.

Page 10: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Nursing Diagnoses and Outcomes (cont.)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.

Page 11: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Planning and InterventionsGentamicin: 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.

Page 12: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Gentamicin: Teaching, Assessment, and EvaluationsGentamicin: 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.

Page 13: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• 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

Page 14: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.

Page 15: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Lincosamides 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)

Page 16: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Core Drug Knowledge 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

Page 17: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Core Drug Knowledge (cont.)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

Page 18: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Core Patient Variables 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 properly.

• Environment

– Assess the environment where the drug will be given.

Page 19: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Nursing Diagnoses and Outcomes 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.

Page 20: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Nursing Diagnoses and Outcomes (cont.)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.

Page 21: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Planning and InterventionsClindamycin: 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.

Page 22: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Clindamycin: Teaching, Assessment, and EvaluationsClindamycin: 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.

Page 23: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• What is the most serious adverse reaction of clindamycin administration?

– A. Respiratory arrest

– B. Pseudomembranous colitis

– C. Ventricular tachycardia

– D. Ototoxicity

Page 24: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.

Page 25: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Macrolide Antibiotics 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

Page 26: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Core Drug Knowledge 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

Page 27: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Core Drug Knowledge (cont.)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

Page 28: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Core Patient Variables 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.

Page 29: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Nursing Diagnoses and Outcomes 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.

Page 30: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Planning and InterventionsErythromycin: 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.

Page 31: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Erythromycin: Teaching, Assessment, and EvaluationsErythromycin: 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.

Page 32: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

QuestionQuestion

• Grapefruit juice will decrease the serum concentration of erythromycin.

– A. True

– B. False

Page 33: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.

Page 34: Ppt chapter 40

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Oxazolidinones Oxazolidinones

• Oxazolidinones are the first new class of antibiotics developed specifically for treating methicillin-resistant Staphylococcus aureus (MRSA) infections.

• Prototype drug: linezolid (Zyvox)

Page 35: Ppt chapter 40

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Linezolid: Core Drug Knowledge Linezolid: Core Drug Knowledge

• Pharmacotherapeutics

– Treatment of VRE and MRSA

• Pharmacokinetics

– Administered: oral or IV. Metabolism: liver. Excreted: kidneys.

• Pharmacodynamics

– Blocking the early stages of the process bacteria use to make proteins

Page 36: Ppt chapter 40

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Linezolid: Core Drug Knowledge (cont.)Linezolid: Core Drug Knowledge (cont.)

• Contraindications and precautions

– Hypersensitivity

• Adverse effects

– Diarrhea, headache, nausea, and vomiting

• Drug interactions

– Adrenergic and serotonergic agents

Page 37: Ppt chapter 40

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Linezolid: Core Patient Variables 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.

Page 38: Ppt chapter 40

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Linezolid: Nursing Diagnoses and Outcomes 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.

Page 39: Ppt chapter 40

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Linezolid: Nursing Diagnoses and Outcomes (cont.)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.

Page 40: Ppt chapter 40

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Linezolid: Planning and InterventionsLinezolid: 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.

Page 41: Ppt chapter 40

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Linezolid: Teaching, Assessment, and EvaluationsLinezolid: 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.

Page 42: Ppt chapter 40

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QuestionQuestion

• Linezolid is classified as a Pregnancy Category ___ drug.

– A. A

– B. B

– C. C

– D. D

– E. X

Page 43: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• C. C

• Rationale: Linezolid is classified as a pregnancy category C drug.

Page 44: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Streptogramins Streptogramins

• Streptogramins are the newest class of antibiotics.

• Designed to eradicate “superbugs” resistant to other antibiotics.

• Prototype drug: quinupristin/dalfopristin (Synercid)

Page 45: Ppt chapter 40

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Quinupristin/Dalfopristin: Core Drug Knowledge Quinupristin/Dalfopristin: Core Drug Knowledge

• Pharmacotherapeutics

– Serious or life-threatening infections associated with VRE

• Pharmacokinetics

– Administered: IV. T½: 1 hour.

• Pharmacodynamics

– Inhibits bacterial protein synthesis by irreversibly blocking ribosome functioning

Page 46: Ppt chapter 40

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Quinupristin/Dalfopristin: Core Drug Knowledge (cont.)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 of P-450

Page 47: Ppt chapter 40

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Quinupristin/Dalfopristin: Core Patient Variables 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.

Page 48: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Quinupristin/Dalfopristin: Nursing Diagnoses and Outcomes 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.

Page 49: Ppt chapter 40

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Quinupristin/Dalfopristin: Nursing Diagnoses and Outcomes (cont.)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.

Page 50: Ppt chapter 40

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Quinupristin/Dalfopristin: Planning and InterventionsQuinupristin/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.

Page 51: Ppt chapter 40

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Quinupristin/Dalfopristin: Teaching, Assessment, and EvaluationsQuinupristin/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 site.

Page 52: Ppt chapter 40

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QuestionQuestion

• Quinupristin/dalfopristin is best administrated via

– A. Oral route

– B. PICC line

– C. Peripheral IV

– D. Z-track IM

Page 53: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.

Page 54: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Tetracyclines 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

Page 55: Ppt chapter 40

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Tetracycline: Core Drug Knowledge 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

Page 56: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Tetracycline: Core Drug Knowledge (cont.)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

Page 57: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Tetracycline: Core Patient Variables 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.

Page 58: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Tetracycline: Nursing Diagnoses and Outcomes 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.

Page 59: Ppt chapter 40

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Tetracycline: Nursing Diagnoses and Outcomes (cont.)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.

Page 60: Ppt chapter 40

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Tetracycline: Planning and InterventionsTetracycline: 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.

Page 61: Ppt chapter 40

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Tetracycline: Teaching, Assessment, and EvaluationsTetracycline: 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.

Page 62: Ppt chapter 40

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QuestionQuestion

• Tetracycline should not be administered with antacids.

– A. True

– B. False

Page 63: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• A. True

• Rationale: Tetracycline forms an insoluble chelate with aluminum, bismuth, calcium, iron, magnesium, and zinc salts, which are frequently an ingredient in antacids.

Page 64: Ppt chapter 40

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Miscellaneous Antibiotics that Affect Protein Synthesis Miscellaneous Antibiotics that Affect Protein Synthesis

• Miscellaneous antibiotics include chloramphenicol and spectinomycin.

• Used to treat large outbreaks of typhus

• Prototype: chloramphenicol

Page 65: Ppt chapter 40

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Chloramphenicol: Core Drug Knowledge 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

Page 66: Ppt chapter 40

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Chloramphenicol: Core Drug Knowledge (cont.)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

Page 67: Ppt chapter 40

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Chloramphenicol: Core Patient Variables 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.

Page 68: Ppt chapter 40

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Chloramphenicol: Nursing Diagnoses and Outcomes 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.

Page 69: Ppt chapter 40

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Chloramphenicol: Planning and InterventionsChloramphenicol: 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.

Page 70: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

Chloramphenicol: Teaching, Assessment, and EvaluationsChloramphenicol: 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.

Page 71: Ppt chapter 40

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QuestionQuestion

• A serious and potentially life-threatening adverse effect of chloramphenicol is “gray baby” syndrome.

– A. True

– B. False

Page 72: Ppt chapter 40

Copyright © 2012 Wolters Kluwer Health | Lippincott Williams & Wilkins

AnswerAnswer

• 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.