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Units 6-8

QuestionAnswer
Mechanism of Action: Penicillins interfere with cell wall synthesis - causing cells to take up water and lyse
Pencillins: Bacteriostatic or Bacteriocidal Bacteriocidal
Side Effects: Penicillins least SEs of all abx classes, allergic reactions, pain at injection site, hyperkalemia, hypernatremia, fluid overload, bleeding disorders
Toxity: Penicillins neurotoxity
Nursing Considerations: Penicillins monitor for reactions, administer Pen G slowly to avoid potassium overload, ticarcillin for fluid overload and bleeding, do not mix in IV with aminoglycosides, reduce in kidney disease
Other info: Penicillins also called beta lactams, primarily renally eliminated, penicillinases, beta lactamases, cross allergenicity in class
Classes: Penicillins Penicillin, Nafcillin, oxacillin, ampicillin, amoxicillin, carbenicillin, ticaricillin, augmentin, timentin, zosyn
Mechanism of Action: Cephalosporins similar to penicillins. disrupt cell wall systhesis and activate autolysins. death by lysis.
Bactericidal or bacteriostatic: cephalosporins Bactericidal
Side Effects: Cephalosporins allergic reaction, bleeding disorders (vitamin K deficiency), alcohol intolerance, thrombophlebitis at IV stie, pain at IM site, pseudomembranous colitis, carnitine deficiency (Spectracef)
Toxity: Cephalosporins neurotoxity in high does
Nursing Considerations: Cephalosporins monitor for allergic reactions, bleeding, diarrhea, use caution in patient on blood thinners, do not give Spectracef if milk allergic, give IM injections deep into large muscle, alter dosages in renal impairment, monitor IV sites
Other info: Cephalosporins also beta-lactamases, active against a broad spectrum of abx, major cause of ceph resistance is production of beta-lactamases, grouped into 4 generations
Cephalosporin Generations progressing from 1-4 generation drugs, there is (1) increasing activity against gram negative bacteria (2) increasing resistance to destruction by beta-lactamases (3) increasing ability to reach the CSF
Impenem aka Primaxin, also a beta-lactam, very broad spectrum, SEs: hypersensitivity, superinfection with fungi, seizures
Ertapenem aka Ivanz, also a beta-lactam, very broad spectrum, SEs: diarrhea, rashes, nausea, seizures
Aztreonam aka Azactam, only gram negatives, only half a ring so safe to give if allergic to other beta-lactams
Mechanism of Action: Macrolides inhibits protein synthesis by binding to the 50S subunit - suppresion of RNA-dependent protein synthesis
Bactericidal vs Bacteriostatic: Macrolides typically bacteriostatic, but may be bactericidal at high concentrations against susceptible organisms
Side Effects: Macrolides nausea, vomitting, hepatitis, thrombophlebitis (IV azithro or clarithro), prolongation of QT interval, pyloric stenosis in infants
Toxicity: Macrolides ototoxic in high doses, hepatotoxic
Nursing considerations: Macrolides food decreases absorption of some oral forms, those oral forms that can should be given with food to minimize GI effects, don't administer with antacids, monitor IV site for redness, administer slowly, educate patient about long half-life of azithromycin
Drug interactions: Macrolides Erthromycin and Clarithromycin ONLY - inhibitors of cytochrome p450 which may increase concentrations of theophylline, digoxin, carbamazepine, valproic acid, cyclosporin, allegra, phenytoin, warfarin, cisapride, ergot alkaloids
Mechanism of Action: Tetracyclines inhibits protein synthesis by binding to the 30S subunit - suppression of RNA-dependent protein synthesis
Bacteriostatic vs. Bactericidal: Tetracyclines Bacteriostatic
Forms of Tetracycline tetracycline, doxycycline (Vibramycin), minocycline
Side Effects: Tetracyclines heartburn, nausea, vomitting, diarrhea, staining of deciduous teeth if given during pregnancy, excessive urination, damage to vestibular system (minocyline), photosensitivity
Toxicity: Tetracyclines Hepatotoxic at high doses, Nephotoxic in patient with renal impairment
Nursing Considerations: Tetracyclines do not admin with Ca+, antacids, FE+ or MOM. patient education regarding protection from sun and food interactions, IV form should only be used when oral cannot due to increased GI side effects, monitor IV sites for redness, avoid in pregnancy
Mechanism of Action: Clindamycin inhibits protein synthesis by binding exclusively to 50S subunit
Bacteriostatic vs. Bactericidal: Clindamycin typically bacteriostatic, but maybe bactericidal in high concentrations against susceptible organisms
Side Effects: Clindamycin PSEUDOMEMBRANOUS COLITIS, nausea, vomiting, rashes, blood dyscrasias, allergic reaction
Toxicity: Clindamycin hepatoxicity (rare)
Nursing Considerations: Clindamycin monitor for diarrhea, instruct patient to report loose stools, monitor LFTs and blood counts, avoid rapid IV admin.
Mechanism of Action: Linezolid inhibitor of protein synthesis
Bactericidal vs. bacteriostatic: Linezolid bacteriostatic
General information: Linezolid trade name Zyvox, new class called oxazolidinones, designed to have activity against MRSA and VRE, FDA approved only for these infections
Mechanism of Action: Fluoroquinolones inhibit bacterial DNA synthesis
Route of Elimination: Fluoroquinolones renal and hepatic
Side Effects: Fluoroquinolones nausea, vomiting, diarrhea, HA, agitation, dizziness, insomnia, hallucinations and seizures (elderly), variable prolongation of QT, achilles tendon rupture, long bones (children), photosensitivity
Toxicity: Fluoroquinolones hepatoxicity
Nursing Considerations: Fluoroquinolones cautionary use in children and pregnant women, monitor for neuro SEs in elderly, do not admin with Zn, Fe, Ca, Al, Mg, antacids, sucralate, or enteral feedings, IV admin over 60 minutes, reduce doses in renal failure
Mechanism of Action: Sulfonamides suppress bacterial growth by inhibiting synthesis of folic acid
Bactericidal vs. bacteriostatic: Sulfonamides bacteriostatic
Other info: Sulfonamides broad spectrum, resistance of many bacteria to sulfonamides, renal excretion
Side Effects: Sulfonamides hypersensitivity (stevens-johnson syndrome), hemolytic anemias (esp in G6PD deficiency), megaloblastic anemias (folate def), kernicterus in infants, photosensitivity
Toxicities: Sulfonamides renal toxicity from crystal formation, contraindicated in pregnancy due to theoretical of folate
Nursing Considerations: Sulfonamides caution in pregnancy, lactation, neonates, alcoholics, malnourished, admin slow IV infusion, allergic reaction, patient teaching avoid sun and maintain fluid intake, monitor for anemias, blood counts
Mechanism of Action: Aminoglycosides multifactorial inhibition of protein synthesis - bind to 30S subunit
Bactericidal vs. bacteriostatic: Aminoglycosides bactericidal
Route of elimination: Aminoglycosides renal excretion
Side Effects: Aminoglycosides allergic reactions, neuromuscular blockade (fatal respiratory distress), blood dyscrasias, neurologic disorders (parasthesias, optic nerve dysfunction)
Toxicity: Aminoglycosides ototoxicity and nephrotoxicity
Nursing Considerations: Aminoglycosides caution in elderly, renal failure, slow IV piggyback, do not mix in solution (esp penicillins), BUN/creatinine levels, monitor for toxicities, peak and trough level 30-60 mins after IV dose, monitor respiratory status, strict I and Os
Mechanism of Action: Vancomycin inhibition of cell wall synthesis. death by lysis. similar to beta lactams. gram positive bacteria only
Bacteriostatic vs. bactericidal: Vancomycin bactericidal (except for enterococcus)
Route of elimination: Vancomycin Renal excretion
Side Effects: Vancomycin Red-Man Syndrome: flushing, pruritis, erthematous rash on face and upper torso, infuse over 60 min, resolves spontaneously. Also, rash, neutropenia, thrombocytopenia, thrombophlebitis
Toxity: Vancomycin Ototoxicity and nephrotoxicity
Nursing Considerations: Vancomycin caution in renal impairment, caution with other ototoxic/nephrotoxic drugs, admin over 60 mins, peak and trough levels, BUN/creatinine/CBC, monitor IV site for redness
Mechanism of Action: Rifampin inhibits RNA synthesis
Bactericidal vs. bacteriostatic: Rifampin Bacteriocidal
Primary Uses: Rifampin TB, leprosy and MRSA
Route of metabolism/elimination: Rifampin primarily hepatic
Toxicity: Rifampin hepatoxic
List pertinent antifungal agents Amphotericin B, azole antifungals, griseofulvin
Mechanism of Action: Amphotericin B increased permeability of fungal cell walls, decreased viability of the microbe
Preferred use: Amphotericin B systemic fungal infections
Drug interactions: Amphotericin B numerous drug interactions and IV incompatibilities (causes precipitates easily)
Metabolism/elimination: Amphotericin B unknown mechanisms - has been found in tissue 1 year after treatment
Side Effects: Amphotericin B infusion reactions, renal toxicities, hypokalemia, bone marrow suppression, phlebitis
Nursing Considerations: Amphotericin B IV admin only, 1st does should be given with caution (most need pre-treatment with benadryl and tylenol), usually give concurrent infusions of IV saline to hydrate kidneys
Mechanism of Action: Azole antifungals inhibits synthesis of ergogesterol in cell membrane
Drug interactions: Azole antifungals potent inhibitor of cytochrome p450 (increases levels of other drugs)
Side Effects: Azole antifungals GI reactions, rash, phlebitis, cardiac suppression and liver failure (itrakonazole), hepatoxicity, visual disturbances, teratogenic (vorikonazole), inhibition of sex hormones (ketokonazole)
Definition of Antibiotic substance produced by a microorganism that in small amounts inhibits the growth of another microbe
Uses of Antibiotics treat active infections, prophylactic use to prevent infections
Improper uses of Antibiotics treatments of infections that cannot be treated, treatment of fever of unknown origin, improper/incomplete dosages/ treatment of abcesses with omission of surgical drainage
Definition of Selective Toxicity ability of a drug to injure a target cell or target organism without injuring other cells or organisms that are in intimate contact with the target
How is Selective Toxicity achieved? differences in cellular chemistry, selectively interfere with microbial processes
Antibiotic Resistance natural resistance, acquired resistance (organism no longer susceptible to drug, serious clinical problem)
Mechanisms of Microbial Drug Resistance microbes increase production of enzymes that inactivate the drug, reduce drug uptake, drug receptor may change and drug cannot bind, microbes synthesize antagonists to drug
Nosocomial Infection infection acquired in the hospital
Suprainfection new infection that appears during the course of treatment for the primary infection
Broad Spectrum effective against many different types of bacteria (both gram negative and gram positive)
Narrow Spectrum effective against a subset of bacteria
List of Gram Positive Cocci staphylococci, S. pneumoniae, viridans streptococci, Enterococcus sp.
List of Gram Positive Bacilli Corynebacterium sp., Listeria monocytogenes, Nocardia sp.
List of Gram Negative Cocci Moraxella catarrhalis, Neisseria gonnorhoeae, Neisseria meningitidis, Haemophilius influenzae
List of Gram Positive Bacilli E. coli, Enterobacter sp., Citrobacter, Klebsiella, Proteus, Serratia, Salmonella, Shigella, Acinetobacter, Helicobacter, pseudomonas aeruginosa
Bacteriocidal lethal to bacteria at clinically achievable serum concentrations
Bacteriostatic slow microbial growth, but do not cause cell death. must work with body defenses (phagocytes) to eliminate bacteria
Host factors that Modify Drug Choice, Route, or Dosage host defenses, site of infection, severity of infection, age, pregnancy, previous allergic reaction, genetic factors, underlying kidney or liver disease
Safety Concerns with the Use of Antimicrobials toxicity, interactions with other medications, hypersensitivity reactions, fetal damage/risk to pregnant women, antibiotic resistance
Bacteriostatic Inhibitors of Protein Synthesis Tetracyclines, Macrolides, Clindamycin, Linezolid
Bactericidal Inhibitors of Protein Synthesis Aminoglycosides (gentamycin, tobramycin, amikacin)
Aging-related organ decline can change: drug absorption, distribution, metabolism, and especially excretion
Factors in the increase of adverse reactions in the elderly polypharmacy, severe illness, multiple pathologies, and treatment with dangerous drugs
Measures to reduce adverse drug reactions in the elderly thorough drug hx, accounting for pharmokinetic/pharmodynamic changes in elderly, initiating with low doses, simplest regimen possible, monitoring for drug-drug interactions and iatrogenic illness, avoiding drugs on Beers list
Reasons for nonadherence in elderly expense, side effects, thinking drug unnecessary, dosage too high
Created by: rjcrompton
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