Bugs and Drugs: Solving the Antibiotic Dilemma Catherine Davis, Pharm.D. Exempla Saint Joseph Hospital.

Slides:



Advertisements
Similar presentations
TREATMENT FOR SUPERIMPOSED PSEUDOMONAS AERUGINOSA INFECTION.
Advertisements

Monotherapy Versus Combination Therapy
PTP 546 Module 8 Pharmacology of Infections Jayne Hansche Lobert, MS, RN, ACNS-BC, NP 1Lobert.
Antimicrobials: Drugs that Weaken the Cell Wall
Copyright © 2013, 2010 by Saunders, an imprint of Elsevier Inc. Chapter 84 Drugs That Weaken the Bacterial Cell Wall I: Penicillins.
Antibiotics.
Choosing Antimicrobials in Special Situations. Additional considerations in making a final antibiotic selection Site of action – (Will the antibiotic.
Glycopeptides Mark Johnson, Pharm.D., BCPS Associate Professor and Director of Postgraduate Education.
Optimizing Antibiotic Use in 2015
Sorting Out Antibiotics: A systematic approach to antibiotic selection Kenneth Alexander, M.D., Ph.D. Associate Professor of Pediatrics and Microbiology.
CEPHALOSPORINS First used clinically in the early 1960’s. First used clinically in the early 1960’s. They have an important role in the modern treatment.
Cephalosporins.
ANTIBIOTICS.
Antibiotics Ch 37. Definition Medications to treat bacterial infections Ideally, culture of suspect area should be done BEFORE starting antibiotic.
Gram Negative Gram Positive
ANTIBIOTICS LauraLe Dyner MD Pediatric Infectious Disease Fellow March 2009.
Antibiotics 101 Puja Van Epps 1/20/14.
Warren S. Joseph, DPM, FIDSA Roxborough Memorial Hospital, Phila., PA
Beta lactam antibiotics & Other cell wall synthesis inhibitors
Antibiotic Pearls in the Emergency Department
DHS/PP Antimicrobial Therapy David H. Spach, MD Professor of Medicine Division of Infectious Diseases University of Washington, Seattle.
Clinical Cases Beta-Lactam Answers. Case 1 What antibiotic would you recommend for intravenous therapy in a 40yo BM with a Staphylococcus aureus (MSSA)
BETA-LACTAM ANTIMICROBIAL AGENTS Alan M. Stamm, M.D. October 23, 2002.
Using Nursing Home Antibiograms To Improve Antibiotic Prescribing and Delivery Training Slides for Prescribing Clinicians Comprehensive Antibiogram Toolkit.
INF 1 ® Life-Threatening Infections INF 1 ®. INF 2 ® Objectives Recognize predisposing conditions for infection Identify clinical manifestations of infection.
Review of Antibiotics Zagorka Popovski, Pharm.D. Clinical Pharmacist, Intensive Care.
Cephalosporins First Generation Cephalosporins
AMINOGLYCOSIDES The different members of this group share many properties in common. The different members of this group share many properties in common.
General Principles of Antimicrobial Therapy. Concept #1: The guiding principle of antibiotic selection Antibiotic coverage should be kept to the narrowest.
Common ID Syndromes March 2014.
Antibiotics 101 A review of common infections and their treatment For others, like me, who have a mental block against all things related to antibiotics.
PENICILLINS -Commonly used, especially penicillin G -end in –cillin -Bactericidal against most gram-positive bacteria -Interfere with cell wall development.
Impetigo The best topical agent is mupirocin; other agents, such as bacitracin and neomycin, are less effective. Patients who have numerous lesions or.
Hospital Acquired Pneumonia(HAP): is defined as a pneumonia which occurs after 48 hours of admission to hospital. Hospital Acquired Pneumonia(HAP): is.
Microbiology Nuts & Bolts Antibiotics Part 1 Dr David Garner Consultant Microbiologist Frimley Park Hospital NHS Foundation.
PRINCIPLES OF ANTIMICROBIAL THERAPY
Antibiotics Affecting the Bacterial Cell Wall
Antibiotic Cases Nathan P. Samsa, Pharm.D., R.Ph..
Impetigo Mupirocin; (bacitracin and neomycin, are less effective.) numerous lesions or not responding to topical agents: oral antimicrobials effective.
Antimicrobials - Quinolones & Fluoroquinolones Antimicrobials - Quinolones & Fluoroquinolones Pharmacology -1 DSX 215 DSX 215 Dr/ Abdulaziz Saeedan Pharmacy.
Treatment Of Respiratory Tract infections. Prof. Azza ELMedany Department of Pharmacology Ext
Dr. Laila M. Matalqah Ph.D. Pharmacology
Antibiotics: Part II.
Guideline for the Diagnosis and Management of Adults in LTC with Urinary Tract Infection (Part 2) This is intended as a guide for evidence-based decision-making.
Cellulitis Darren Wilson Antibiotic Pharmacist Royal Bournemouth Hospital.
Antibiotics (anti-microbials)
PRINCIPLES OF ANTIBIOTIC THERAPY
PROTEIN SYNTHESIS INHIBITORS THEY WORK BY TARGETING BACTERIAL RIBOSOMES AMINOGLYCOSIDES MACROLIDES TETRACYCLINES SPECTINOMYCIN.
Internal Medicine Mini-Lecture. Learning Points  Basics  Choosing antibiotics  Overview.
Therapeutics 3 Tutoring
Cephalosporins Four Generations! Bactericidal & Time-Dependent!
Therapeutics 3: Antibiotics Tutoring
Antibiotics By Alaina Darby.
Therapeutics III Tutoring February 10th, 2016
WCH / Pediatrics Pharmacy Department Pediatric Dosing Recommendations
Use of antibiotics.
Antimicrobial treatments and their mechanisms of action
The Role of the Microbiology Laboratory in AMS programs
Antimicrobial Spectrum of Activity Visual Learning Exercises (“Flower Diagrams”) This work is licensed under the Creative Commons Attribution-NonCommercial-
Cell wall inhibitor Cephalosporins Dr. Naza M. Ali Lec D
Interior Health Pharmacy Resident Kootenay Lake Hospital
Intro to Antibiotics By: Alaina Darby.
Drugs /Agents Inhibitors of cell wall synthesis
به نام خدا.
PENICILLINS -Commonly used, especially penicillin G -end in –cillin
Overview of Antimicrobials
Introduction to Antimicrobial Stewardship: Bugs and Drugs
Empiric antibiotic therapy
Presentation transcript:

Bugs and Drugs: Solving the Antibiotic Dilemma Catherine Davis, Pharm.D. Exempla Saint Joseph Hospital

Presentation Overview l Briefly review sensitivity testing l Review advantages/disadvantages of commonly prescribed antibiotics l Provide recommendations for appropriate indications for various antibiotics

Drug Expenditures

Challenges in Antimicrobial Selection l Changing resistance patterns l New antibiotics from which to select l National Backorders!!! –Piperacillin/tazobactam –Cefotaxime –Cefotetan –Penicillin –Cefazolin

Sensitivity Testing Minimum Inhibitory Concentration l MIC - concentration at which the growth of the organism is inhibited l “breakpoint” is determined based on serum/tissue levels of respective agent l optimum therapy is for peak to achieve > 8 times the MIC l CANNOT compare actual #’s between different classes of antibiotics

MIC Interpretation l If the sensitivity report indicates an MIC less than a specific concentration (i.e. <8), antibiotic in question should achieve adequate concentrations to inhibit growth l Review all agents listed as susceptible and select the most narrow spectrum/cost effective agent that will cover the organism

Antibiotic Selection: The Right Agent for the Right Patient l Infecting organism l Susceptibility data/local resistance patterns l Site of infection l Duration of hospitalization/prior antibiotics l Allergy history l Age l Renal/Hepatic status l Immunologic status l Pregnancy

Antibiotic Classes l Beta-Lactams –penicillins –cephalosporins –carbapenems –monobactams l Quinolones l Aminoglycosides l Glycopeptides l Macrolides l Miscellaneous l VRE Antibiotics

Penicillins: Pen VK, Ampicillin, Amoxicillin Advantages l good oral absorption l good gram + coverage –Enterococcus –Streptococcus l inexpensive Disadvantages l frequent dosing l increasing resistance –gram negatives –Strep pneumo l inactivates aminoglycosides

Penicillin, Ampicillin, Amoxicillin: Indications for Use l Strep infections known to be PCN sensitive l Enterococcus infections (dose 2 Gms q4h for ampicillin + gentamicin synergy dosed) l Necrotizing fasciitis - PCN 24 MU/day + Clinda 600mg q8h l Renal adjust for CrCl <30 mL/min

AntiStaphylococcal PCN’s Nafcillin, Oxacillin, Dicloxacillin Advantages l excellent Staph aureus coverage –best treatment option for serious MSSA infections l narrow spectrum (no gram negative coverage) l Diclox for Staph Disadvantages l frequent dosing (2 Gms q4-6h) l increasing incidence of MRSA (35% at ESJH) l no Enterococcus coverage

Beta-Lactamase Inhibitors l Amoxicillin/Clavulanate (Augmentin®) l Ampicillin/Sulbactam (Unasyn®) l Piperacillin/Tazobactam (Zosyn®) l Ticarcillin/Clavulanate (Timentin®)

Beta-Lactamase Inhibitors Augmentin, Unasyn, Timentin, Zosyn Advantages l stabilization against beta-lactamases l excellent broad coverage, including anaerobes l Zosyn > Timentin for Pseudomonas l Enterococcus coverage (not Timentin) Disadvantages l GI intolerance (Augmentin) l Superinfections l High cost l frequent dosing l E. coli resistance increasing with Unasyn

Unasyn, Zosyn Indications Unasyn Zosyn l Intraabdominal prophylaxis + gentamicin for E. coli l Mixed infection including Enterococcus l Gms q6h l Severe mixed infection –workhorse ICU drug l Ventilator associated pneumonia +/- AG l Severe diabetic foot infection suspected of involving mixed flora l Narrow as soon as possible l Gms q6h

Cephalosporins: General Similarities l excellent penetration to tissues, including BBB (ceftriaxone, cefotaxime) l coverage based on “generation” l NO ENTEROCOCCUS ACTIVITY l wide therapeutic index l wide range of uses l *historically comprises one of the largest portions of antibiotic budget

Cephalosporins: First Generations l most active against gram positives –cellulitis l good coverage against selected gram negatives (E. coli, Proteus, Klebsiella) –Good option for pyelonephritis l excellent for surgical prophylaxis (cefazolin) l Cefazolin (Ancef®) 1 Gm q8h l Cephalexin (Keflex®) higher MIC’s to Staph

Cephalosporins: Second Generations l less gram positive coverage l additional gram negative coverage, respiratory pathogens (Hemophilus, Moraxella) - cefuroxime (Zinacef®, Ceftin®) l anaerobes (anti-anaerobic agents - cefotetan, cefoxitin, cefmetazole) –~ 75% anaerobic coverage –intraabdominal, GYN prophylaxis

Cefotetan (Cefotan®), Cefoxitin (Mefoxin®): Indications for Use l Surgical Prophylaxis for intraabdominal infections (Cefotan 1 Gm q12h) l Intraabdominal infections from community (no Enterococcus coverage) l Diabetic foot infections (E. coli, anaerobes)

Cephalosporins: Third+ Generations l additional gram negative (nosocomial) coverage, some gram positive, anaerobic coverage l Pseudomonas coverage (ceftazidime, cefepime) l excellent BBB penetration (ceftriaxone, cefotaxime and others) l Good coverage against Strep and Staph (except ceftazidime)

Third Generation Ceph’s: Indication for Use l Cefepime (Maxipime®), ceftazidime (Fortaz®) –Neutropenic Fever (cefepime 2 Gms q12h) –Pseudomonas infections l Cefotaxime (Claforan®), ceftriaxone (Rocephin®) –Meningitis (cefotaxime 2 Gms q8h) –CAP (cefotaxime 1 Gm q8-12h) –Endocarditis with HACEK organisms or PCN intermediate Strep (cefotaxime 2 Gms q8h)

Oral Cephalosporins l 1st Generation: cephalexin (Keflex®) –500 mg TID-QID –UTI l 2nd Generation: None Formulary –Ceftin®, Cefzil®, Lorabid® l 3rd Generation: cefpodoxime (Vantin®) –Oral transition for CAP, STD’s – mg BID

Carbapenems l Imipenem/Cilastatin (Primaxin®) –excellent broad spectrum coverage but increasing Pseudomonas resistance –reserve for resistant organisms, seriously ill patients or PCN allergy –potential for seizures - adjust for renal status –beta-lactamase inducer –500 mg q6-8h l Meropenem (Merrem®) –less seizure risk –fewer indications

Carbapenems: Ertapenem (Invanz®) l Recently approved agent for community infections l Intraabdominal or complicated skin and skin structure infections l No Enterococcus or Pseudomonas coverage l 1 Gm IV q24h l Adjust for CrCl <30 mL/min (500 mg qd)

Monobactam: Aztreonam (Azactam®) l ONLY gram-negative coverage l moderate Pseudomonas activity l safe to use in PCN allergic patients l excellent safety profile l 1 -2 Gms q8h l Adjust for CrCl <30 mL/min

Quinolones Another Class with Generations l excellent tissue penetration l excellent bioavailabilty l convenient dosing l some resistance to Pseudomonas developing l potential for overuse due to many factors l avoid with sucralfate, separate from antacids

Quinolones: “First Generations” l Norfloxacin, Ciprofloxacin l primarily gram negative, including Pseudomonas l some atypical l poor gram positive, no anaerobic l Cipro - interactions with theophylline, warfarin, phenytoin

Quinolones: “Second Generations” l Levofloxacin, Lomefloxacin, Gatifloxacin, Moxifloxacin l additional gram positive and atypical coverage, including Strep pneumoniae l moderate gram negative l excellent bioavailability l Levofloxacin - warfarin interactions l Moxifloxacin - no Pseudomonas coverage, good anaerobic coverage (KP formulary)

Levofloxacin (Levaquin®) Indications for Use l CAP, especially patients with comorbidities –Doxycycline for pts with no comorbidities l Complicated UTI infections (resistant to first generation ceph’s, sulfa) l Gram negative infections in patient allergic to PCN (+/- AG or anaerobic coverage) l Not preferred for cellulitis (750 mg dose) l 500 mg IV/PO qd (adjust for CrCl < 50) l Add metronidazole for anaerobes

Aminoglycosides: Gentamicin, Tobramycin, Amikacin l excellent gram negative coverage –amikacin > tobramycin > gentamicin l synergistic activity –low levels for gram positive synergy (1 mg/kg) –therapeutic levels for gram negative synergy l (5-7mg/kg once daily) l NO Anaerobes - requires 0 2 to get into cell l dosing strategies dependent on indication l toxicities well defined

Glycopeptides: Vancomycin l excellent gram positive l reserve for resistant organisms, PCN/Ceph allergic patients l VRE l GISA?? l nephrotoxicity no longer a real concern l only monitor trough’s except for select situations l oral ONLY for Flagyl failures

Macrolides: erythro-, clarithro-, azithromycin l moderate gram positives (Strep developing resistance - now up to 35%) l good atypical l use for lower respiratory tract infections l erythro and clarithro interactions –theophylline, warfarin (+ azithro) l azithromycin - STD coverage (1 Gm x1) –CAP: mg qd x 5-7 days

Antianaerobic Agents l Metronidazole (Flagyl®) –excellent anaerobic, first line C. difficile –500 mg q12h except C. diff and bowel preps l half-life = 8 hours –Excellent bioavailability –warfarin interaction, disulfiram reactions l Clindamycin (Cleocin®) –gram positive, anaerobic (600 mg IV q8h max) –Use with PCN for nec fasciitis (Gp A Strep) –? Pseudomembranous colitic

Miscellaneous l SMX/TMP (Septra®, Bactrim®) –excellent tissue penetration, broad uses –gram positive and “easy” gram negative –warfarin interaction –Some GI intolerance in elderly

Antifungals: Fluconazole l Not effective against non-albicans strains l Indications for use –C. albicans from sterile body site –C. albicans from multiple non-sterile sites (urine, wound, sputum) –Prophylaxis for recurrent intraabdominal rupture or anastomotic leak l Systemic infections: 800 mg load, 400 mg qd l UTI: 100 mg qd x5 days l Excellent bioavailability

Antibiotic Costs

New Agents for VRE: l Quinupristin/Dalfopristin (Synercid®) –Streptogramin antibiotics –Effective against VREF (not E. faecalis), Staph aureus (MRSA and MSSA) –Dosing: 7.5 mg/kg q8h –Infusion related ADR’s - central line preferred –Potential to elevate liver enzymes –Cyt P 450 3A4 interaction l Non-Formulary

New Agents for VRE Linezolid (Zyvox®) l Oxazolidinone antibiotic l Effective against E. faecalis & E. faecium, MRSA, MSSA, Strep pneumo l IV, PO, Suspension - 100% absorption l 600 mg BID l Thrombocytopenia (> 2 weeks duration of therapy), GI intolerance l MAOI - weak inhibitor l Dopamine, epinephrine - adjust dose down

Cost Comparison

Linezolid (Zyvox®): Indications for Use l VREF –likely will be considered preferred therapy in place of Synercid® –need to carefully evaluate for potential colonization l MRSA Infections ONLY for Vanco intolerant patients –after trial of continuous infusion +/- Benadryl if possible l ID Consult

Resistance: A National Concern l Often result of inappropriate or overuse of antibiotics l Significant financial impact on healthcare l Selecting out multi-drug resistance l Narrow coverage as soon as possible l ? Rotation of preferred classes of antibiotics l Don’t treat colonizations or contaminations