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PIPERACILLIN/TAZOBACTAM IN CONTINUOUS INFUSION VERSUS INTERMITTENT INFUSION IN CHILDREN WITH FEBRILE NEUTROPENIA.
Solórzano-Santos, Fortino; Quezada-Herrera, Anai; Fuentes-Pacheco, Yazmín; Rodríguez-Coello, Genoveva; Aguirre-Morales, Carlos E; Izelo-Flores, Dassaev; Muñoz-Hernández, Onofre; Miranda-Novales, María G; Labra-Zamora, María G.
Affiliation
  • Solórzano-Santos F; Research Unit in Evidence-Based Medicine, Hospital Infantil De Mexico "Federico Gómez", Mexico City.
  • Quezada-Herrera A; Hospital del Niño y del Adolescente Morelense, Morelos.
  • Fuentes-Pacheco Y; High Specialty Medical Unit, Hospital de Pediatría, CMN SXXI, Instituto Mexicano del Seguro Social, Mexico City.
  • Rodríguez-Coello G; Hospital para el Niño Poblano, Secretaría de Salud, Puebla de Zaragoza, Puebla.
  • Aguirre-Morales CE; Centro Médico ABC, Mexico City.
  • Izelo-Flores D; Hospital General de Zona No. 20, Instituto Mexicano del Seguro Social, Puebla.
  • Muñoz-Hernández O; Research Directorate, Hospital Infantil de México "Federico Gómez", SSA, Mexico City.
  • Miranda-Novales MG; Analysis and Synthesis of Evidence Research Unit, Coordinación de Investigación en Salud, Instituto Mexicano del Seguro Social, Mexico City, Mexico.
  • Labra-Zamora MG; High Specialty Medical Unit, Hospital de Pediatría, CMN SXXI, Instituto Mexicano del Seguro Social, Mexico City.
Rev Invest Clin ; 71(4): 283-290, 2019.
Article in En | MEDLINE | ID: mdl-31448789
ABSTRACT

Background:

Febrile neutropenia (FN) is a common complication in children who receive chemotherapy for cancer.

Objective:

The objective of this study was to evaluate the clinical efficacy of the continuous versus intermittent infusion of piperacillin/tazobactam (TZP) in febrile neutropenic pediatric patients.

Methods:

This is a non-blinded randomized controlled clinical trial. Eligible group consisted of hemato-oncological patients with FN who were candidates to receive TZP. Patients were randomized to one of two groups Group 1 received antibiotic treatment through intravenous intermittent infusion of TZP 300 mg/kg/day based on piperacillin, divided into four doses, not exceeding 16 g/day; Group 2 received an initial TZP loading dose of 75 mg/kg infusion over 30 min, and then a continuous infusion of TZP 300 mg/kg/day through central line with pump over 24 h.

Results:

There were 176 episodes that could be assessed, 100 in Group 1 and 76 in Group 2. There was no statistically significant difference in treatment failure in the experimental group (continuous infusion) compared with the intermittent group, 21% versus 13% (p = 0.15). The increase in the absolute risk reduction was 0.08% (95% confidence interval 0.12-0.30), and the number needed to treat was 12.4. One patient in each group died.

Conclusions:

There were no differences in fever resolution, clinical cure rate, or mortality when comparing the continuous with the intermittent TZP infusion.
Subject(s)
Key words

Full text: 1 Database: MEDLINE Main subject: Febrile Neutropenia / Piperacillin, Tazobactam Drug Combination / Anti-Bacterial Agents / Neoplasms / Antineoplastic Agents Type of study: Clinical_trials Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Rev Invest Clin Journal subject: MEDICINA Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Main subject: Febrile Neutropenia / Piperacillin, Tazobactam Drug Combination / Anti-Bacterial Agents / Neoplasms / Antineoplastic Agents Type of study: Clinical_trials Limits: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Rev Invest Clin Journal subject: MEDICINA Year: 2019 Type: Article