Ticarcillin* Class

Total Page:16

File Type:pdf, Size:1020Kb

Ticarcillin* Class Ticarcillin* Class: β-lactam Overview Ticarcillin is one of the carboxypenicillins, a semisynthetic group of β-lactams. These carboxypenicillins, like ureidopenicillins, were developed for effectiveness against enterobacteriaceae (Klebsiella species, Proteus species, Enterobacter species and Pseudomonas aeruginosa). Carbenicillin was developed by adding a carboxyl group to the penicillin molecule. Ticarcillin was developed by adding additional substitutions to the carbenicillin carboxyl group. Ticarcillin exhibits greater antipseudomonal activity than carbenicillin. Ticarcillin is not acid-stable, therefore the drug is administered parenterally. Resistance Primary mechanisms of resistance against ticarcillin and other β-lactams are production of β-lactamases and alteration of penicillin binding proteins. Decreased permeability through the bacterial cell wall is another mechanism of resistance. Recent epidemiologic surveillance indicates that up to 50% of Pseudomonas aeruginosa isolates are resistant to ticarcillin. Effectiveness Ticarcillin was developed for increased effectiveness against Gram-negative bacteria, like Klebsiella species, Proteus species, Enterobacter species and especially Pseudomonas aeruginos. In fact, ticarcillin is often referred to as an anti-pseudomonal penicillin. This increased effectiveness against Gram-negative organisms is balanced by decreased effectiveness against Gram-positive organisms. These antibacterials can be combined with β-lactamase inhibitors to increase the spectrum of effectiveness against β- lactamase–producing bacteria, such as H influenzae, M catarrhalis, Staphylococcus species, Neisseria gonorrhoeae, Escherichia coli, Klebsiella pneumoniae, Proteus species, Bacteroides fragilis group, Fusobacterium species, Prevotella species and Porphyromonas species. In human medicine, ticarcillin/clavulanate combinations are used in the treatment of infected animal bite wounds and aspiration pneumonia. Ticarcillin is also used in infections caused by Pseudomonas aeruginosa, including osteomyelitis, and abdominal infections. See the penicillin section for an explanation of uptake in body fluids and CSF. *References available by request. Call the Infectious Disease Epidemiology Section, Office of Public Health, Louisiana Department of Health and Hospitals (504-219-4563) .
Recommended publications
  • Medical Review(S) Clinical Review
    CENTER FOR DRUG EVALUATION AND RESEARCH APPLICATION NUMBER: 200327 MEDICAL REVIEW(S) CLINICAL REVIEW Application Type NDA Application Number(s) 200327 Priority or Standard Standard Submit Date(s) December 29, 2009 Received Date(s) December 30, 2009 PDUFA Goal Date October 30, 2010 Division / Office Division of Anti-Infective and Ophthalmology Products Office of Antimicrobial Products Reviewer Name(s) Ariel Ramirez Porcalla, MD, MPH Neil Rellosa, MD Review Completion October 29, 2010 Date Established Name Ceftaroline fosamil for injection (Proposed) Trade Name Teflaro Therapeutic Class Cephalosporin; ß-lactams Applicant Cerexa, Inc. Forest Laboratories, Inc. Formulation(s) 400 mg/vial and 600 mg/vial Intravenous Dosing Regimen 600 mg every 12 hours by IV infusion Indication(s) Acute Bacterial Skin and Skin Structure Infection (ABSSSI); Community-acquired Bacterial Pneumonia (CABP) Intended Population(s) Adults ≥ 18 years of age Template Version: March 6, 2009 Reference ID: 2857265 Clinical Review Ariel Ramirez Porcalla, MD, MPH Neil Rellosa, MD NDA 200327: Teflaro (ceftaroline fosamil) Table of Contents 1 RECOMMENDATIONS/RISK BENEFIT ASSESSMENT ......................................... 9 1.1 Recommendation on Regulatory Action ........................................................... 10 1.2 Risk Benefit Assessment.................................................................................. 10 1.3 Recommendations for Postmarketing Risk Evaluation and Mitigation Strategies ........................................................................................................................
    [Show full text]
  • Severe Sepsis Tipsheet
    Severe Sepsis Tipsheet SEVERE SEPSIS A, B, and C of the following must be met within 6 hours of each other. A. Documentation of a suspected infection. There may be reference to “possible infection,” “suspect infection,” “rule out infection,” or similar documentation. B. TWO or more manifestations of systemic infection according to the Systemic Inflammatory Response Syndrome (SIRS) criteria, which are: • Temperature > 38.3 C or < 36.0 C (> 100.9 F or < 96.8 F) • Heart rate (pulse) > 90 • Respiration > 20 per minute • White blood cell count > 12,000 or < 4,000 or > 10% bands C. Organ dysfunction, evidenced by any one of the following: • Systolic blood pressure (SBP) < 90 mmHg, or mean arterial pressure < 65 mmHg, or a systolic blood pressure decrease of more than 40 mmHg. Physician/APN/PA documentation must be present in the medical record indicating a > 40 mmHg decrease in SBP has occurred and is related to infection, severe sepsis or septic shock and not other causes. • Acute respiratory failure as evidenced by a new need for invasive or non-invasive mechanical ventilation. To use acute respiratory failure as a sign of organ dysfunction there must be: • Documentation of acute respiratory failure AND • Documentation the patient is on mechanical ventilation • Invasive mechanical ventilation requires an endotracheal or tracheostomy tube. Non-invasive mechanical ventilation may be referred to as BiPAP or CPAP. • New need for mechanical ventilation indicates the patient was not using the same type of mechanical ventilation prior to the current acute respiratory failure. • Use the time at which there is documentation the patient has both acute respiratory failure and is on mechanical ventilation.
    [Show full text]
  • Below Are the CLSI Breakpoints for Selected Bacteria. Please Use Your Clinical Judgement When Assessing Breakpoints
    Below are the CLSI breakpoints for selected bacteria. Please use your clinical judgement when assessing breakpoints. The lowest number does NOT equal most potent antimicrobial. Contact Antimicrobial Stewardship for drug selection and dosing questions. Table 1: 2014 MIC Interpretive Standards for Enterobacteriaceae (includes E.coli, Klebsiella, Enterobacter, Citrobacter, Serratia and Proteus spp) Antimicrobial Agent MIC Interpretive Criteria (g/mL) Enterobacteriaceae S I R Ampicillin ≤ 8 16 ≥ 32 Ampicillin-sulbactam ≤ 8/4 16/8 ≥ 32/16 Aztreonam ≤ 4 8 ≥ 16 Cefazolin (blood) ≤ 2 4 ≥ 8 Cefazolin** (uncomplicated UTI only) ≤ 16 ≥ 32 Cefepime* ≤ 2 4-8* ≥ 16 Cefotetan ≤ 16 32 ≥ 64 Ceftaroline ≤ 0.5 1 ≥ 2 Ceftazidime ≤ 4 8 ≥ 16 Ceftriaxone ≤ 1 2 ≥ 4 Cefpodoxime ≤ 2 4 ≥ 8 Ciprofloxacin ≤ 1 2 ≥ 4 Ertapenem ≤ 0.5 1 ≥ 2 Fosfomycin ≤ 64 128 ≥256 Gentamicin ≤ 4 8 ≥ 16 Imipenem ≤ 1 2 ≥ 4 Levofloxacin ≤ 2 4 ≥ 8 Meropenem ≤ 1 2 ≥ 4 Piperacillin-tazobactam ≤ 16/4 32/4 – 64/4 ≥ 128/4 Trimethoprim-sulfamethoxazole ≤ 2/38 --- ≥ 4/76 *Susceptibile dose-dependent – see chart below **Cefazolin can predict results for cefaclor, cefdinir, cefpodoxime, cefprozil, cefuroxime axetil, cephalexin and loracarbef for uncomplicated UTIs due to E.coli, K.pneumoniae, and P.mirabilis. Cefpodoxime, cefinidir, and cefuroxime axetil may be tested individually because some isolated may be susceptible to these agents while testing resistant to cefazolin. Cefepime dosing for Enterobacteriaceae ( E.coli, Klebsiella, Enterobacter, Citrobacter, Serratia & Proteus spp) Susceptible Susceptible –dose-dependent (SDD) Resistant MIC </= 2 4 8 >/= 16 Based on dose of: 1g q12h 1g every 8h or 2g every 8 h Do not give 2g q12 Total dose 2g 3-4g 6g NA Table 2: 2014 MIC Interpretive Standards for Pseudomonas aeruginosa and Acinetobacter spp.
    [Show full text]
  • Management of Penicillin and Beta-Lactam Allergy
    Management of Penicillin and Beta-Lactam Allergy (NB Provincial Health Authorities Anti-Infective Stewardship Committee, September 2017) Key Points • Beta-lactams are generally safe; allergic and adverse drug reactions are over diagnosed and over reported • Nonpruritic, nonurticarial rashes occur in up to 10% of patients receiving penicillins. These rashes are usually not allergic and are not a contraindication to the use of a different beta-lactam • The frequently cited risk of 8 to 10% cross-reactivity between penicillins and cephalosporins is an overestimate based on studies from the 1970’s that are now considered flawed • Expect new intolerances (i.e. any allergy or adverse reaction reported in a drug allergy field) to be reported after 0.5 to 4% of all antimicrobial courses depending on the gender and specific antimicrobial. Expect a higher incidence of new intolerances in patients with three or more prior medication intolerances1 • For type-1 immediate hypersensitivity reactions (IgE-mediated), cross-reactivity among penicillins (table 1) is expected due to similar core structure and/or major/minor antigenic determinants, use not recommended without desensitization • For type-1 immediate hypersensitivity reactions, cross-reactivity between penicillins (table 1) and cephalosporins is due to similarities in the side chains; risk of cross-reactivity will only be significant between penicillins and cephalosporins with similar side chains • Only type-1 immediate hypersensitivity to a penicillin manifesting as anaphylaxis, bronchospasm,
    [Show full text]
  • Antibiotic Use for Sepsis in Neonates and Children: 2016 Evidence Update
    Antibiotic Use for Sepsis in Neonates and Children: 2016 Evidence Update Aline Fuchsa, Julia Bielickia,b, Shrey Mathurb, Mike Sharlandb, Johannes N. Van Den Ankera,c a Paediatric Pharmacology and Pharmacometrics, University Children's Hospital Basel, Basel, Switzerland b Paediatric Infectious Disease Research Group, Institute for Infection and Immunity, St George's University of London, London, United Kingdom c Division of Clinical Pharmacology, Children’s National Health System, Washington, DC, USA WHO-Reviews 1 TABLE OF CONTENTS 1. INTRODUCTION ............................................................................................................................... 3 1.1. Aims ......................................................................................................................................... 3 1.2. Background ............................................................................................................................. 3 1.2.1. Definition and diagnosis ................................................................................................. 3 Neonatal Sepsis ............................................................................................................................... 3 Paediatric Sepsis ............................................................................................................................. 4 Community versus hospital acquired sepsis .................................................................................. 5 1.2.2. Microbiology ..................................................................................................................
    [Show full text]
  • Comparative Activity of Newer Antibiotics Against Gram-Negative Bacilli
    CONTRIBUTION • Comparative activity of newer antibiotics against gram-negative bacilli CYNTHIA C. KNAPP, MS AND JOHN A. WASHINGTON, MD • The in vitro activities of cefoperazone, cefotaxime, ceftriaxone, ceftazidime, azlocillin, mezlocillin, piperacillin, ticarcillin/clavulanate, aztreonam, imipenem, and ciprofloxacin were concurrently deter- mined against over 1,000 isolates of gram-negative bacilli from clinical specimens of patients at the Cleve- land Clinic. Cephalosporins, penicillins, and aztreonam were active against species of Enterobacteriaceae other than Citrobacter freundii, Enterobacter aerogenes, and Enterobacter cloacae. Ceftazidime was the most active cephalosporin against Pseudomonas aeruginosa. Against the Enterobacteriaceae, the rank order of activity of penicillins was ticarcillin/clavulanate > piperacillin > mezlocillin > azlocillin. Against P. aer- uginosa, the rank order of activity of penicillins was piperacillin > ticarcillin/clavulanate > azlocillin > mezlocillin. Aztreonam was less active v P. aeruginosa than ceftazidime, cefoperazone, or piperacillin. The most active antimicrobials against all isolates tested were imipenem and ciprofloxacin. • INDEX TERMS: ANTIBIOTICS, LACTAM; GRAM-NEGATIVE BACTERIA • CLEVE CLIN J MED 1989; 56:161-166 HE RECENT introduction of ciprofloxacin for and penicillins, as well as the monobactam, aztreonam, clinical use follows closely a period of active re- and the carbapenem, imipenem.1-3 search in and development of expanded spec- We compared the susceptibility of more than 1,000 trum p-lactam antibiotics, including cephalo- clinical bacterial isolates to four expanded spectrum Tsporins, penicillins, monobactams, and carbapenems. cephalosporins (cefoperazone, cefotaxime, ceftriaxone, Although numerous published studies compare the ac- and ceftazidime), four expanded spectrum penicillins tivity of ciprofloxacin with other quinolones, only a (azlocillin, mezlocillin, piperacillin, and ticarcil- limited number of studies compare the activity of ci- lin/clavulanate), aztreonam, imipenem, and ciproflox- acin.
    [Show full text]
  • Ertapenem Or Ticarcillin/Clavulanate for the Treatment of Intra-Abdominal Infections Or Acute Pelvic Infections in Pediatric Patients
    The American Journal of Surgery 194 (2007) 367–374 Clinical surgery–American Ertapenem or ticarcillin/clavulanate for the treatment of intra-abdominal infections or acute pelvic infections in pediatric patients Albert E. Yellin, M.D.a,*, Jeffrey Johnson, M.D.b, Iliana Higareda, M.D.c, Blaise L. Congeni, M.D.d, Antonio C. Arrieta, M.D.e, Doreen Fernsler, B.S.f, Joseph West, Ph.D.f, Richard Gesser, M.D.f aDepartment of Surgery, Keck School of Medicine of the University of Southern California, 1200 N State St, Rm 9610, Los Angeles, CA 90033, USA bDepartment of Pediatrics, Keck School of Medicine of the University of Southern California, 1240 N Mission Rd, L902, Los Angeles, CA 90089-9300, USA cHospital Civil de Guadalajara, Hospital 278, 4420 El Retiro St, Guadalajara, Jalisco Mexico dAkron Children’s Hospital, Division of Infectious Diseases, Locust Professional Bldg, 300 Locust St, Ste 4, Akron, OH 44308-1062, USA eChildren’s Hospital of Orange County, Pediatric Infectious Diseases, 455 South Main Street, Orange, CA 92868, USA fMerck Research Laboratories, Merck & Co., Inc., 126 East Lincoln Avenue, Rahway, NJ 07065, USA Manuscript received June 20, 2006; revised manuscript January 20, 2007 Abstract Background: Ertapenem, a group I carbapenem antibiotic, has been shown to be safe and effective in treating adults with complicated intra-abdominal (cIAI) or acute pelvic infection (API). This study evaluated ertapenem for treating these infections in children. Methods: In an open-label study, children aged 2 to 17 years with cIAI or API were randomized 3:1 to receive ertapenem or ticarcillin/clavulanate.
    [Show full text]
  • Effective Reporting of Antimicrobial Susceptibility Test Results
    Laboratory Detection and Reporting of Carbapenem-Resistant Enterobacteriaceae (CRE) CLSI Outreach Working Group Spring, 2016 1 After review of this program, you will be able to: List current CLSI recommendations for antimicrobial susceptibility testing (AST) and reporting of CRE. Describe the differences between CRE (Carbapenem-resistant Enterobacteriaceae) and CPE (Carbapenemase-producing Enterobacteriaceae). Explain the significance of CRE and CPE from clinical and epidemiological perspectives. Describe when and where to go for help when physicians need more information than your laboratory can provide for a potential CRE isolate. 2 Acronyms Used in this Presentation CRE = Carbapenem-R Enterobacteriaceae CPE = Carbapenemase-Producing Enterobacteriaceae Also CRO, CRKP, CPKP, CPO – “O” = organism – “KP”= Klebsiella pneumoniae 3 β-Lactams and GNRs Basic Concepts 4 Common β-Lactam Agents Active Against Gram-Negative Rods (GNR) β-lactam Penicillins Inhibitor Combos Cephalosporins Cephamycin Carbapenems Amoxicillin Amoxicillin-clav Cefazolin (1) Cefoxitin Doripenem Ampicillin Ampicillin- sulb Cefuroxime (2) Cefotetan Ertapenem Piperacillin Piperacillin-tazo Cefotaxime (3) Monobactam Imipenem Ticarcillin Ticarcillin-clav Ceftazidime (3) Aztreonam Meropenem Ceftolozane-tazo Ceftriaxone (3) Ceftaz-avibactam Cefepime (4) 5 β-Lactams β-Lactam β-Lactam (Penicillin) (Penicillin) All β-lactams contain a 4-membered β-lactam ring that is essential for activity 6 Different β-Lactams Penicillins Cephalosporins Cephamycins Carbapenems Monobactam 7 Gram-Negative Bacterial Cell Outer membrane Chromosomal DNA Plasmid DNA Periplasmic space Ribosomes Cell wall 50S 50S 50S (peptidoglycan) 30S 30S 30S Cell membrane Cartoon courtesy of L. Westblade 8 β-Lactam Activity Against Gram-Negatives β-lactam Porin Channel or Efflux Pump Outer membrane Periplasmic space Penicillin-Binding Proteins (PBPs) Cell wall Cartoon courtesy of L.
    [Show full text]
  • TIMENTIN® (Sterile Ticarcillin Disodium and Clavulanate Potassium) for Intravenous Administration
    NDA 50-658/S-023 NDA 50-590/S-058 NDA 50-590/S-059 Page 3 PRESCRIBING INFORMATION TIMENTIN® (sterile ticarcillin disodium and clavulanate potassium) for Intravenous Administration To reduce the development of drug-resistant bacteria and maintain the effectiveness of TIMENTIN (ticarcillin disodium and clavulanate potassium) and other antibacterial drugs, TIMENTIN should be used only to treat or prevent infections that are proven or strongly suspected to be caused by bacteria. DESCRIPTION TIMENTIN is a sterile injectable antibacterial combination consisting of the semisynthetic antibiotic ticarcillin disodium and the β-lactamase inhibitor clavulanate potassium (the potassium salt of clavulanic acid) for intravenous administration. Ticarcillin is derived from the basic penicillin nucleus, 6-amino-penicillanic acid. Chemically, ticarcillin disodium is N-(2-Carboxy-3,3-dimethyl-7-oxo-4-thia-1­ azabicyclo[3.2.0]hept-6-yl)-3-thiophenemalonamic acid disodium salt and may be represented as: Clavulanic acid is produced by the fermentation of Streptomyces clavuligerus. It is a β-lactam structurally related to the penicillins and possesses the ability to inactivate a wide variety of β-lactamases by blocking the active sites of these enzymes. Clavulanic acid is particularly active against the clinically important plasmid-mediated β−lactamases frequently responsible for transferred drug resistance to penicillins and cephalosporins. Chemically, clavulanate potassium is potassium (Z)-(2R,5R)-3-(2-hydroxyethylidene)-7­ oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylate and may be represented structurally as: TIMENTIN is supplied as a white to pale yellow powder for reconstitution. TIMENTIN is very soluble in water, its solubility being greater than 600 mg/mL.
    [Show full text]
  • Cephalosporins and Related Antibiotics Therapeutic Class Review (TCR) November 1, 2017 Please Note: This Clinical Document Has Been Retired
    Cephalosporins and Related Antibiotics Therapeutic Class Review (TCR) November 1, 2017 Please Note: This clinical document has been retired. It can be used as a historical reference. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, digital scanning, or via any information storage or retrieval system without the express written consent of Magellan Rx Management. All requests for permission should be mailed to: Magellan Rx Management Attention: Legal Department 6950 Columbia Gateway Drive Columbia, Maryland 21046 The materials contained herein represent the opinions of the collective authors and editors and should not be construed to be the official representation of any professional organization or group, any state Pharmacy and Therapeutics committee, any state Medicaid Agency, or any other clinical committee. This material is not intended to be relied upon as medical advice for specific medical cases and nothing contained herein should be relied upon by any patient, medical professional or layperson seeking information about a specific course of treatment for a specific medical condition. All readers of this material are responsible for independently obtaining medical advice and guidance from their own physician and/or other medical professional in regard to the best course of treatment for their specific medical condition. This publication, inclusive of all forms contained herein, is intended to be educational in nature and is intended to be used for informational purposes only. Send comments and suggestions to [email protected]. November 2017 Proprietary Information. Restricted Access – Do not disseminate or copy without approval.
    [Show full text]
  • Educational Workshop
    Educational Workshop EW01: Antimicrobial susceptibility testing with EUCAST breakpoints and methods Arranged with the European Committee on Antimicrobial Susceptibility Testing (EUCAST) Convenors: Gunnar Kahlmeter (Växjö, SE) Derek F.J. Brown (Peterborough, UK) Faculty: Rafael Canton Moreno (Madrid, ES) Derek F.J. Brown (Peterborough, UK) Gunnar Kahlmeter (Växjö, SE) Christian G. Giske (Stockholm, SE) Johan Willem Mouton (Nijmegen, NL) Alasdair P. MacGowan (Bristol, UK) Maiken Cavling Arendrup (Copenhagen, DK) 1 2 Canton - What is new in 2013: update on EUCAST breakpoints www.EUCAST.org WHAT IS NEW IN 2013: UPDATE ON EUCAST BREAKPOINTS Departamento de Microbiología II Universidad Complutense. Madrid 2013 www.eucast.org National Breakpoint Committees F, N, NL, S, UK Contract 2011-14 NACs = National Antimicrobial Susceptibility Testing Committees EUCAST General Committee (GC) All European Countries + Countries from outside EUCAST Steering Committee BSAC, CA‐SFM, CRG, NWGA, SRGA + 3 reps from the GC ±2 “visiting” members from the GC Subcommittees Experts Antifungals (ECDC Networks, Expert Rules ESCMID Study Groups) Anaerobes Industry Resistance mechanisms EUCAST implementation Q1 3 Canton - What is new in 2013: update on EUCAST breakpoints . EUCAST General Committee - 35 countries, including Russia and Australia - New countries with interest of being represented (Brazil, US, Japan…) . National breakpoint committees and NACs - Continuous consultation on breakpoints - New countries already represented in the General Committee formed a NAC (Portugal,
    [Show full text]
  • In Vitro Efficacy of Flomoxef Against Extended-Spectrum Beta
    antibiotics Article In Vitro Efficacy of Flomoxef against Extended-Spectrum Beta-Lactamase-Producing Escherichia coli and Klebsiella pneumoniae Associated with Urinary Tract Infections in Malaysia Soo Tein Ngoi 1 , Cindy Shuan Ju Teh 1,*, Chun Wie Chong 2, Kartini Abdul Jabar 1 , Shiang Chiet Tan 1, Lean Huat Yu 1, Kin Chong Leong 3, Loong Hua Tee 3 and Sazaly AbuBakar 1,4 1 Department of Medical Microbiology, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysia; [email protected] (S.T.N.); [email protected] (K.A.J.); [email protected] (S.C.T.); [email protected] (L.H.Y.); [email protected] (S.A.) 2 School of Pharmacy, Monash University Malaysia, Bandar Sunway 47500, Selangor, Malaysia; [email protected] 3 Shionogi Singapore Pte Ltd., 10, Anson Road, #34-14 International Plaza, Singapore 079903, Singapore; [email protected] (K.C.L.); [email protected] (L.H.T.) 4 Tropical Infectious Diseases Research and Education Centre (TIDREC), University of Malaya, Kuala Lumpur 50603, Malaysia * Correspondence: [email protected]; Tel.: +60-379676674 Abstract: The increasing prevalence of extended-spectrum β-lactamase (ESBL)-producing Enter- Citation: Ngoi, S.T.; Teh, C.S.J.; Chong, C.W.; Abdul Jabar, K.; Tan, obacteriaceae has greatly affected the clinical efficacy of β-lactam antibiotics in the management of S.C.; Yu, L.H.; Leong, K.C.; Tee, L.H.; urinary tract infections (UTIs). The limited treatment options have resulted in the increased use of AbuBakar, S. In Vitro Efficacy of carbapenem. However, flomoxef could be a potential carbapenem-sparing strategy for UTIs caused Flomoxef against Extended-Spectrum by ESBL-producers.
    [Show full text]