Literature DB >> 24041466

Ampicillin/sulbactam: its potential use in treating infections in critically ill patients.

Syamhanin Adnan1, David L Paterson, Jeffrey Lipman, Jason A Roberts.   

Abstract

The purpose of this paper was to review the potential utility of ampicillin/sulbactam (SAM) as a therapy for serious infections in critically ill patients. Data for this review were identified by searches of PubMed and of the reference lists of the included articles. We found that SAM appears to have a number of characteristics that support its use in the treatment of serious infections in critically ill patients. SAM demonstrates extensive penetration into many infection sites, supporting its use in a wide range of infection types. Microbiologically, sulbactam has strong intrinsic antibiotic activity against multidrug-resistant (MDR) bacteria, including Acinetobacter baumannii, which supports its use for the treatment of infections mediated by this pathogen. Of some concern, there have been reports showing a decline in susceptibility of some bacteria to SAM. As such, use of lower doses (4/2g/day), particularly for MDR A. baumannii, has been linked with a 30% reduced success rate in critically ill patients. The therapeutic challenges for ensuring achievement of optimal dosing of SAM result partly from bacterial susceptibility but also from the pharmacokinetic (PK) alterations common to β-lactam agents in critical illness. These PK changes are likely to reduce the ability of standard dosing to achieve the concentrations observed in non-critically ill patients. Optimisation of therapy may be more likely with the use of higher doses, administration by 4h infusion or by combination therapy, particularly for the treatment of infections caused by MDR pathogens.
Copyright © 2013 Elsevier B.V. and the International Society of Chemotherapy. All rights reserved.

Entities:  

Keywords:  Ampicillin/sulbactam; Critically ill; Multidrug-resistant; Pharmacodynamics; Pharmacokinetics

Mesh:

Substances:

Year:  2013        PMID: 24041466     DOI: 10.1016/j.ijantimicag.2013.07.012

Source DB:  PubMed          Journal:  Int J Antimicrob Agents        ISSN: 0924-8579            Impact factor:   5.283


  12 in total

1.  Fulminant endocarditis and disseminated infection caused by carbapenem-resistant Acinetobacter baumannii in a renal-pancreas transplant recipient.

Authors:  G Patel; F Perez; A M Hujer; S D Rudin; J J Augustine; G H Jacobs; M R Jacobs; R A Bonomo
Journal:  Transpl Infect Dis       Date:  2015-02-06       Impact factor: 2.228

2.  Molecular mechanisms of sulbactam antibacterial activity and resistance determinants in Acinetobacter baumannii.

Authors:  William F Penwell; Adam B Shapiro; Robert A Giacobbe; Rong-Fang Gu; Ning Gao; Jason Thresher; Robert E McLaughlin; Michael D Huband; Boudewijn L M DeJonge; David E Ehmann; Alita A Miller
Journal:  Antimicrob Agents Chemother       Date:  2015-01-05       Impact factor: 5.191

3.  A Real-World Study Comparing Various Antimicrobial Regimens for Bloodstream Infections Caused by Carbapenem-Resistant Gram-Negative Bacilli in a Tertiary Hospital, Shanghai, China, from 2010 to 2017.

Authors:  Jiaying Tan; Wenjin Yu; Gang Wu; Jun Shen; Yong Fang; Hechen Zhu; Qianyi Xiao; Weixia Peng; Yukun Lan; Ye Gong
Journal:  Infect Drug Resist       Date:  2020-07-21       Impact factor: 4.003

4.  Raf-kinase inhibitor GW5074 shows antibacterial activity against methicillin-resistant Staphylococcus aureus and potentiates the activity of gentamicin.

Authors:  Tatiana Johnston; Gabriel Lambert Hendricks; Steven Shen; Roy Fangxing Chen; Bumsup Kwon; Michael John Kelso; Wooseong Kim; Beth Burgwyn Fuchs; Eleftherios Mylonakis
Journal:  Future Med Chem       Date:  2016-09-21       Impact factor: 3.808

Review 5.  Antimicrobials for the treatment of drug-resistant Acinetobacter baumannii pneumonia in critically ill patients: a systemic review and Bayesian network meta-analysis.

Authors:  Su Young Jung; Seung Hee Lee; Soo Young Lee; Seungwon Yang; Hayeon Noh; Eun Kyoung Chung; Jangik I Lee
Journal:  Crit Care       Date:  2017-12-20       Impact factor: 9.097

6.  Preparation and Evaluation of the ZnO NP-Ampicillin/Sulbactam Nanoantibiotic: Optimization of Formulation Variables Using RSM Coupled GA Method and Antibacterial Activities.

Authors:  Nidhi Sharma; Vineeta Singh; Asheesh Kumar Pandey; Bhartendu Nath Mishra; Maria Kulsoom; Nandita Dasgupta; Saif Khan; Hesham A El-Enshasy; Shafiul Haque
Journal:  Biomolecules       Date:  2019-11-21

7.  Contribution of Acinetobacter-derived cephalosporinase-30 to sulbactam resistance in Acinetobacter baumannii.

Authors:  Shu-Chen Kuo; Yi-Tzu Lee; Tsai-Ling Yang Lauderdale; Wei-Cheng Huang; Ming-Fen Chuang; Chien-Pei Chen; Shey-Chiang Su; Kuan-Rong Lee; Te-Li Chen
Journal:  Front Microbiol       Date:  2015-03-25       Impact factor: 5.640

Review 8.  Multidrug Resistance (MDR) and Collateral Sensitivity in Bacteria, with Special Attention to Genetic and Evolutionary Aspects and to the Perspectives of Antimicrobial Peptides-A Review.

Authors:  András Fodor; Birhan Addisie Abate; Péter Deák; László Fodor; Ervin Gyenge; Michael G Klein; Zsuzsanna Koncz; Josephat Muvevi; László Ötvös; Gyöngyi Székely; Dávid Vozik; László Makrai
Journal:  Pathogens       Date:  2020-06-29

9.  Sulbactam-enhanced cytotoxicity of doxorubicin in breast cancer cells.

Authors:  Shao-Hsuan Wen; Shey-Chiang Su; Bo-Huang Liou; Cheng-Hao Lin; Kuan-Rong Lee
Journal:  Cancer Cell Int       Date:  2018-09-04       Impact factor: 5.722

Review 10.  Durlobactam, a New Diazabicyclooctane β-Lactamase Inhibitor for the Treatment of Acinetobacter Infections in Combination With Sulbactam.

Authors:  Adam B Shapiro; Samir H Moussa; Sarah M McLeod; Thomas Durand-Réville; Alita A Miller
Journal:  Front Microbiol       Date:  2021-07-19       Impact factor: 5.640

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