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Assessing clinical cure of empirical piperacillin/tazobactam for ESBL urinary tract infections (ACCEPT-UTI).
Stefanos, Sylvia S; Sakaan, Sami; Samarin, Michael; Gelfand, Michael S; Cleveland, Kerry O; Gant, Jessie; Kermeen, Sydney; Hobbs, Diana A; Hobbs, Athena L V.
Afiliação
  • Stefanos SS; Department of Pharmacy, Methodist University Hospital, 1265 Union Avenue, Memphis, TN 38104, USA.
  • Sakaan S; Department of Pharmacy, Methodist University Hospital, 1265 Union Avenue, Memphis, TN 38104, USA.
  • Samarin M; Department of Pharmacy, Methodist University Hospital, 1265 Union Avenue, Memphis, TN 38104, USA.
  • Gelfand MS; Infectious Diseases, Methodist University Hospital, 1265 Union Avenue, Memphis, TN 38104, USA.
  • Cleveland KO; Division of Infectious Diseases, University of Tennessee Health Science Center, 875 Monroe Avenue, Memphis, TN 38163, USA.
  • Gant J; Infectious Diseases, Methodist University Hospital, 1265 Union Avenue, Memphis, TN 38104, USA.
  • Kermeen S; Division of Infectious Diseases, University of Tennessee Health Science Center, 875 Monroe Avenue, Memphis, TN 38163, USA.
  • Hobbs DA; College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Ave., Memphis, TN 38163, USA.
  • Hobbs ALV; College of Pharmacy, University of Tennessee Health Science Center, 881 Madison Ave., Memphis, TN 38163, USA.
JAC Antimicrob Resist ; 5(3): dlad055, 2023 Jun.
Article em En | MEDLINE | ID: mdl-37180353
ABSTRACT

Background:

Data are limited regarding use of piperacillin/tazobactam for ESBL urinary tract infections (UTIs). The objective of this study was to compare clinical outcomes of patients treated empirically with piperacillin/tazobactam versus carbapenems for ESBL UTIs.

Methods:

This retrospective, observational, propensity score-matched study evaluated adults with an ESBL on urine culture. Patients who had UTI symptoms or leukocytosis, and who received a carbapenem or piperacillin/tazobactam empirically for at least 48 h were included. The primary outcome was clinical success within 48 h, defined as resolution of temperature (36-38°C), resolution of symptoms or leukocytosis (WBC <12 × 103/µL) in the absence of documented symptoms, and the absence of readmission for an ESBL UTI within 6 months. Secondary outcomes included time to clinical resolution, hospital length of stay, and in-hospital and 30 day all-cause mortality.

Results:

Overall, 223 patients were included in the full cohort and 200 patients in the matched cohort (piperacillin/tazobactam = 100, carbapenem = 100). Baseline characteristics were similar between the groups. There was no difference in the primary outcome of clinical success between the carbapenem and piperacillin/tazobactam groups (58% versus 56%, respectively; P = 0.76). Additionally, there was no difference in median (IQR) time to clinical resolution [38.9 h (21.5, 50.9 h) versus 40.3 h (27.4, 57.5 h); P = 0.37], in-hospital all-cause mortality (3% versus 3%; P = 1.00), or 30 day all-cause mortality (4% versus 2%; P = 0.68) between the carbapenem and piperacillin/tazobactam groups, respectively.

Conclusions:

There was no significant difference in clinical success for patients treated empirically with piperacillin/tazobactam compared with carbapenems for ESBL UTIs.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article