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Efficacy of Continuous vs. Intermittent Administration of Cefepime in Adult ICU Patients with Gram-Negative Bacilli Bacteremia: A Randomized Double-Blind Clinical Study.
Álvarez-Moreno, Carlos Arturo; Nocua-Báez, Laura Cristina; Ortiz, Guillermo; Torres, Juan Carlos; Montenegro, Gabriel; Cervera, Williams; Zuluaga, Luis Fernando; Gómez, Alonso.
Afiliación
  • Álvarez-Moreno CA; Department of Internal Medicine, Infectious Diseases, Universidad Nacional de Colombia, Bogotá 111321, Colombia.
  • Nocua-Báez LC; Department of Internal Medicine, Infectious Diseases, Universidad Nacional de Colombia, Bogotá 111321, Colombia.
  • Ortiz G; Santa Clara Hospital, Bogotá 111711, Colombia.
  • Torres JC; Pablo Tobón Uribe Hospital, Medellín 050034, Colombia.
  • Montenegro G; Palermo Clinic, Bogotá 111311, Colombia.
  • Cervera W; San Ignacio University Hospital, Bogotá 110231, Colombia.
  • Zuluaga LF; Clínica Nueva El Lago, Bogotá 110221, Colombia.
  • Gómez A; Palermo Clinic, Bogotá 111311, Colombia.
Antibiotics (Basel) ; 13(3)2024 Feb 29.
Article en En | MEDLINE | ID: mdl-38534664
ABSTRACT

INTRODUCTION:

The objective of this study was to compare the continuous infusion of cefepime with the intermittent infusion in patients with sepsis caused by Gram-negative bacilli (GNB).

METHODS:

Randomized 11 multicenter double-blinded placebo-controlled study with allocation concealment; multicenter study in the intensive care units of Colombia. Patients with sepsis, severe sepsis or septic shock, and GNB-suspected bacteremia. Cefepime was administered for 7 to 14 days over 30 m intermittently every 8 h over 24 h plus continuous saline solution (0.9%) (G1) or 3 g administered continuously plus saline solution every 8 h (0.9%) (G2). The percentage of clinical response at 3, 7, and 14 days, relapse at 28 days, and mortality at discharge were measured.

RESULTS:

The recruitment was stopped at the suggestion of the Institutional Review Board (IRB) following an FDA alert about cefepime. Thirty-two patients were randomized; 25 received the intervention, and GNB bacteremia was confirmed in 16 (9 G1 and 7 G2). Favorable clinical response in days 3, 7, and 14 was 88.8%, 88.8%, and 77.8% (G1) and was similar for G2 (85.7%). There were no relapses or deaths in G2, while in G1, one relapse and two deaths were observed.

CONCLUSIONS:

The results of this study support the use of cefepime for the treatment of Gram-negative infections in critically ill patients, but we could not demonstrate differences between continuous or intermittent administration because of the small sample size, given the early suspension of the study.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antibiotics (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Colombia Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Antibiotics (Basel) Año: 2024 Tipo del documento: Article País de afiliación: Colombia Pais de publicación: Suiza