Your browser doesn't support javascript.
loading
Clinical characteristics, microbiology and outcomes of a cohort of patients treated with ceftolozane/tazobactam in acute care inpatient facilities, Houston, Texas, USA.
Tran, Truc T; Cabrera, Nicolo L; Gonzales-Luna, Anne J; Carlson, Travis J; Alnezary, Faris; Miller, William R; Sakurai, Aki; Dinh, An Q; Rydell, Kirsten; Rios, Rafael; Diaz, Lorena; Hanson, Blake M; Munita, Jose M; Pedroza, Claudia; Shelburne, Samuel A; Aitken, Samuel L; Garey, Kevin W; Dillon, Ryan; Puzniak, Laura; Arias, Cesar A.
Afiliación
  • Tran TT; Center for Infectious Diseases Research, Houston Methodist Research Institute, Houston, TX, USA.
  • Cabrera NL; Division of Infectious Diseases, Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.
  • Gonzales-Luna AJ; Division of Infectious Diseases, John T. Milliken Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO, USA.
  • Carlson TJ; Department of Pharmacy, Baylor St. Luke's Medical Center, CHI St. Luke's Health, Houston, TX, USA.
  • Alnezary F; Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, TX, USA.
  • Miller WR; Department of Clinical Sciences, Fred Wilson School of Pharmacy, High Point University, High Point, NC, USA.
  • Sakurai A; Department of Pharmacy Practice and Translational Research, University of Houston College of Pharmacy, Houston, TX, USA.
  • Dinh AQ; Department of Clinical and Hospital Pharmacy, College of Pharmacy, Taibah University, Medina, Saudi Arabia.
  • Rydell K; Center for Infectious Diseases Research, Houston Methodist Research Institute, Houston, TX, USA.
  • Rios R; Division of Infectious Diseases, Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.
  • Diaz L; Department of Infectious Diseases and Microbiology, Fujita Health University School of Medicine, Aichi, Japan.
  • Hanson BM; Division of Infectious Diseases, Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.
  • Munita JM; Division of Infectious Diseases, Department of Medicine, Houston Methodist Hospital, Houston, TX, USA.
  • Pedroza C; Molecular Genetics and Antimicrobial Resistance Unit, International Center for Microbial Genomics, Universidad El Bosque, Bogota, Colombia.
  • Shelburne SA; Molecular Genetics and Antimicrobial Resistance Unit, International Center for Microbial Genomics, Universidad El Bosque, Bogota, Colombia.
  • Aitken SL; Genomics and Resistant Microbes Group, Facultad de Medicina Clinica Alemana, Universidad del Desarrollo and Millennium Initiative for Collaborative Research On Bacterial Resistance (MICROB-R), Santiago, Chile.
  • Garey KW; Center for Infectious Diseases, University of Texas Health Science Center School of Public Health, Houston, TX, USA.
  • Dillon R; Genomics and Resistant Microbes Group, Facultad de Medicina Clinica Alemana, Universidad del Desarrollo and Millennium Initiative for Collaborative Research On Bacterial Resistance (MICROB-R), Santiago, Chile.
  • Puzniak L; Center for Clinical Research and Evidence-Based Medicine, The University of Texas Health Science Center at Houston, Houston, TX, USA.
  • Arias CA; Department of Infectious Diseases, Infection Control & Employee Health, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
JAC Antimicrob Resist ; 5(1): dlac131, 2023 Feb.
Article en En | MEDLINE | ID: mdl-36601551
ABSTRACT

Background:

Ceftolozane/tazobactam is a ß-lactam/ß-lactamase inhibitor combination with activity against a variety of Gram-negative bacteria, including MDR Pseudomonas aeruginosa. This agent is approved for hospital-acquired and ventilator-associated bacterial pneumonia. However, most real-world outcome data come from small observational cohorts. Thus, we sought to evaluate the utilization of ceftolozane/tazobactam at multiple tertiary hospitals in Houston, TX, USA.

Methods:

We conducted a multicentre retrospective study of patients receiving at least 48 h of ceftolozane/tazobactam therapy from January 2016 through to September 2019 at two hospital systems in Houston. Demographic, clinical and microbiological data were collected, including the infecting bacterial isolate, when available. The primary outcome was composite clinical success at hospital discharge. Secondary outcomes included in-hospital mortality and clinical disposition at 14 and 30 days post ceftolozane/tazobactam initiation. Multivariable logistic regression analysis was used to identify predictors of the primary outcome and mortality. Recovered isolates were tested for susceptibility to ceftolozane/tazobactam and underwent WGS.

Results:

A total of 263 patients were enrolled, and composite clinical success was achieved in 185 patients (70.3%). Severity of illness was the most consistent predictor of clinical success. Combination therapy with ceftolozane/tazobactam and another Gram-negative-active agent was associated with reduced odds of clinical success (OR 0.32, 95% CI 0.16-0.63). Resistance to ceftolozane/tazobactam was noted in 15.4% of isolates available for WGS; mutations in ampC and ftsI were common but did not cluster with a particular ST.

Conclusions:

Clinical success rate among this patient cohort treated with ceftolozane/tazobactam was similar compared with previous experiences. Ceftolozane/tazobactam remains an alternative agent for treatment of susceptible isolates of P. aeruginosa.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JAC Antimicrob Resist Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JAC Antimicrob Resist Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos