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Newer Antibiotics and How We Should Use Them Mahesh C. Patel, M.D. Division of Infectious Diseases February 3, 2010 Antibacterials Timeline Concentration-Dependent vs. TimeDependent Killing • Time-Dependent (or Conc. Independent) – Eliminate bacteria only when time during which drug concentration is greater than MIC • Concentration-Dependent – Eliminate bacteria when their concentrations are above the MIC of the organism – Post-antibiotic effect MIC vs. MBC Bacteriostatic vs. Bactericidal • • • • Bactericidal: Kill bacteria Bacteriostatic: Reversibly inhibit growth Continuum No rigorous studies exist showing superiority of one type over another • However, -cidal agents preferred in endocarditis, meningitis, neutropenic hosts, sepsis • Static: MIC<MBC; Cidal: MIC=MBC -Static vs. -Cidal • Bacteriostatic – – – – – – Tetracyclines Sulphonamides Trimethoprim Chloramphenicol Macrolides Linosamides (clindamycin) • Bactericidal – – – – – – – Beta-Lactams Daptomycin FQs Aminoglycosides Metronidazole TMP/SMX Nitrofurantoin Linezolid (Zyvox) • Oxazolidinone • Inhibits Protein Synthesis • Bacteriostatic • 600mg po/iv • No renal adjustment • Time-Dependent Killing Linezolid Spectrum of Activity • Clinically important Gram + organisms – MSSA/MRSA, Coag – Staph, E. faecium and faecalis, Strep. (bactericidal) – MTb, MAI Linezolid: What to use it for • Complicated skin and soft tissue structure infections (does not include osteomyelitis) • Nosocomial Pneumonia (MRSA) • VRE (including bacteremia) • DO NOT USE for bacteremias • **(Osteomyelitis, endocarditis, meningitis, intraabdominal infections, etc.)—ID consult Linezolid: Side Effects • Relatively well-tolerated with GI symptoms • Serotonin Syndrome – Fever, agitation, MS changes, tremors if on serotonergic agents – Reversible, nonselective monoamine oxidase inhibitor • Reversible myelosuppresion – Thrombocytopenia (47% if >10d or rx) >>anemia>neutropenia – Duration of treatment > 2 weeks • Neuropathy (peripheral, optic, etc.); Lactic Acidosis, … Daptomycin • First in a novel class: cyclic lipopeptides • Side-lined in 1991 as Phase II trials showd skeletal muscle toxicity with Q12H dosing • Binds to cell membranes of Gram + organisms • Bactericidal • Concentration-Dependent • Pregnancy Category B • 4 to 6 mg/kg iv Q24H (Q48H if CrCl<30 mL/min) Daptomycin (Cubicin) Daptomycin: Spectrum of Activity • Like Glycopeptides, though works on organisms where vancomycin is not effective • MSSA/MRSA, E faecalis and faecium, Coag negative Staph, Strep. • Resistance emerging: If decreased sens to vancomycin, greater likelihood of decreased sens to daptomycin. • Development of resistance during treatment of Enterococcal infections Daptomycin: What to use it for • Complicated SSTI (4mg/kg) • S. aureus bacteremia and endocarditis (6mg/kg) • Osteoarticular infections (but would use higher dose of 8-10mg/kg and use another agent given lower bone levels and resistance emergence on therapy • Enterococcal infections • DO NOT USE: Pulmonary infections (inactivated by surfactant) Daptomycin: Side Effects • No increased GI • Paresthesias, dysesthesias, and peripheral neuropathies • No QTc issues • Muscle toxicity – Begin 7 days after therapy – Resolve during therapy or about 3 days after daptomycin is stopped – Monitor CK when used with other “muscle toxic” agents (ie HMG-CoA reductase inhibs) Tigecycline (Tygacil) • Tetracycline class • Inhibit bacterial protein synthesis (30S) • Bacteriostatic • 100mg iv once, then 50mg iv Q12H with no adjustment needed for renal issues • Pregnancy Category D (bone growth and teeth staining) Tigecycline: Spectrum of Activity • Broad range of pathogens – NO Pseudomonas, Proteus, Morganella, or Providencia – Acinetobacter – MRSA/MSSA, VRE – Anaerobes – Resistance by efflux pumps or ribosomal changes Tigecycline: What to use it for • FDA Approved: • Skin and soft tissue infections – Intra-Abdominal infections – Community-acquired pneumonia – NOT indicated for blood stream infections • At NBHN, reserved for patients with resistant GNRod infections (nonbacteremic) Tigecycline: Side Effects • • • • • Nausea (35%) Vomiting (25%) Phlebitis Increased LFTs (6%) Thrombocytopenia, increased PTT and INR, eosinophilia • Headache, somnolence, taste perversion • Remember: No kids under 8yo Ertapenem (Invanz) • • • • • • Beta-Lactam Bind to PCN-binding proteins (PBPs) Concentration-Dependent Killing Bactericidal Long half life of 4h permits QD dosing Renal adjustment required Ertapenem: Spectrum of Activity • Kinda like ceftriaxone and metronidazole • Gram + bacteria, Enterobacteriaceae, MSSA, Anaerobes • NOT: MRSA, Enterococcus; No Pseudomonas, Acinetobacter • Resistance: Alteration in PBPs, Beta Lactamase production, Efflux pumps, decreased permeability Ertapenem: What to use it for • • • • • • Intraabdominal infections Pneumonia Bacteremia Bone and soft tissue infections Complicated UTIs OB/Gyn infections Doripenem (Doribax) • Much greater Enterobacteriaceae activity including Pseudomonas, Acinetobacter • Lower MICs for GNRs than imipenem or meropenem • Resistance to Imipenem does not mean resistance to Doripenem or meropenem, or vice versa • Less beta-lactamase unstable Carbapenem: Side Effects • Rash, urticaria, cross-reaction with PCNs, nausea, immediate hypersensitivity • Less epileptogenic than imipenem Polymyxins • Very old drugs (1947) • Fell into disuse by 1980 due to nephrotoxicity; topical and oral use • Polymyxin B and Polymyxin E (Colistin) – Polymyxin B (colistemethate) iv – Colistin for inhalation therapy • • • • Penetrate into cell membranes and disrupt Bactericidal and Concentration-Dependent Renal adjustment necessary Poor levels in pleura, joint, CSF, biliary tract Polymyxins: Spectrum of Activity • Broad GNR coverage • Gram +, Gram – cocci, and most anaerobes are RESISTANT • Has been used intrathecally and intraventricularly • Colistimethate as efficacious as piperacillin, imipenem, and ciprofloxacin for treatment of Pseudomonas Polymyxins: Side Effects • Dose-Related Reversible Nephrotoxicity • Dose-Related Reversible Neurotoxicity manifest as neuromuscular blockade Telavancin (Vibativ) • • • • • FDA-approved on Sept 11, 2009 Lipoglycopeptide Synthetic derivative of vancomycin Bactericidal Inhibits cell wall synthesis; bacterial membrane depolarizer • Once daily iv (10mg/kg) • Renal adjustment needed Telavancin: Spectrum of Activity and Uses • MRSA • Gram positives (but not VRE) • Uses – cSSSI – Nosocomial Pneumonia (with Gram negative coverage; non-FDA approved) Telavancin: Side Effects • • • • Mild taste disturbance (33%) Nausea (27%) and Vomiting (14%) Insomnia Coagulation test interference: PT/INR, PTT, Factor Xa; BUT NO increased risk of bleeding • Less common: Headache, Red-man Syndrome, Nephrotoxicity, Diarrhea, Foamy Urine (13%) • QTc prolongation in 1.5% (vs. 0.6% in vancomycin) Anti-Fungals Echinocandins • Caspofungin (Cancidas), Micafungin (Mycamine), Anidulafungin (Eraxis) • Inhibit glucan synthesis (in cell wall); like “PCN of antifungals” • Pregnancy category C • No renal adjustment required Echinocandins: Spectrum of Activity • Candida spp of all types (fungicidal) • Aspergillus spp (fungistatic) • Anidalufungin likley with fewer drug-drug interactions • Micafungin has most data in kids • Caspofungin was 1st • Caspofungin vs. Micafungin for invasive Candidiasis similar results Echinocandins: Uses • Invasive and esophageal candidiasis – Caspo, Anidal., Mica. • Prophylaxis in HSCT patients – Mica. • Invasive aspergillosis in refractory or intolerant patients – Caspo • Fever and neutropenia – Caspo Echinocandins: Side Effects • Not cytochrome P450 metabolized • NOT nephrotoxic or hepatotoxic • Relatively few/minor side effects Newer Azoles • Voriconazole (VFend), Posaconazole (Noxafil) • Many clinically relevant drug-drug interactions (P450) • Voriconazole is available in both iv and po formulations • Posaconzole available in suspension • Both with extensive distribution and penetration into tissues. Voriconazole • Invasive aspergillosis (superior to Ampho B deoxycholate) • Invasive fusarium and scedosporum • Esophageal candidiasis (not licensed) • NOT FDA approved for fever and neutropenia and possibly inferior to liposomal Ampho B Voriconazole: Side Effects • Similar to other triazoles, EXCEPT: • Visual disturbance unique – 30% reported altered or enhanced light perception for ½ hour 30 mins after dose – Blurred vision, color vision changes, photophobia – Rarely results in discontinuation – Mechanism unknown • Hallucinations (12 of 72 in one study) within 24hrs • Photosensitivity, QTc prolongation (rare) Posaconazole (Noxafil) • Only available orally and bioavailability affected by food (fat increases absorption) • No dose adjustment for renal issues • “Moderate” number of drug-drug interactions • Indications: – Prophylaxis of Invasive fungal infections in high risk patients – Oropharyngeal candidiasis – Molds (Aspergillosis, fusariosis, Coccidi., eumycetoma, chromoblastomycosis) • Side Effects: GI and headache