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Cefepime Versus Piperacillin-Tazobactam for the Treatment of Intra-Abdominal Infections Secondary to Potential AmpC Beta-Lactamase-Producing Organisms.
Gamble, Kelly C; Rose, Dusten T; Chang, Stephanie Y; Hodge, Emily K; Jaso, Theresa C; Trust, Marc D; Daley, Mitchell J.
Afiliação
  • Gamble KC; McLeod Regional Medical Center, Florence, SC, USA.
  • Rose DT; Dell Seton Medical Center at the University of Austin, Austin, TX, USA.
  • Chang SY; Northwestern Medicine Huntley Hospital, Huntley, IL, USA.
  • Hodge EK; Dell Seton Medical Center at the University of Austin, Austin, TX, USA.
  • Jaso TC; Ascension Seton Medical Center Austin, Austin, TX, USA.
  • Trust MD; University of Texas at Austin Dell Medical School, Austin, TX, USA.
  • Daley MJ; Dell Seton Medical Center at the University of Austin, Austin, TX, USA.
Hosp Pharm ; 58(6): 575-583, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38560541
ABSTRACT

Background:

Recent studies have established cefepime as an effective treatment option for AmpC beta-lactamase (AmpC) Enterobacterales; however, the efficacy of beta-lactam/beta-lactamase inhibitors is unclear.

Objective:

The objective of this study was to determine if piperacillintazobactamis an appropriate alternative to cefepime for the treatment of intra-abdominal infections (IAIs) secondary to AmpC-producing organisms.

Methods:

This multicenter, retrospective cohort study was conducted in hospitalized adults with an IAI caused by an AmpC-producing organism and received either cefepime or piperacillin-tazobactam for definitive treatment after a source control procedure. The primary outcome was a composite of surgical site infections, recurrent IAIs, or in-hospital mortality. Secondary outcomes included the individual components of the composite outcome, hospital length of stay (LOS), microbiologic failure, study antibiotic duration, time to clinical resolution, and incidence of Clostridioides difficile infection (CDI).

Results:

This study included 119 patients. There was no difference in the primary outcome between the cefepime and piperacillin-tazobactam groups (35% vs 27%, P = 0.14). Microbiological failure was the only secondary outcome with an observed difference between groups (17% vs 0%, P = 0.01) hospital LOS (15 vs 13 days, P = 0.09), days of therapy (7 vs 7 days, P = 0.87), time to clinical resolution (7 vs 4 days, P = 0.30), and CDI (1% vs 2%, P = 0.58) were all similar.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hosp Pharm Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hosp Pharm Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Estados Unidos