Antipyretic effect of parenteral paracetamol (propacetamol) in pediatric oncologic patients: a randomized trial

Details

Serval ID
serval:BIB_ACCAFD1E3188
Type
Article: article from journal or magazin.
Collection
Publications
Title
Antipyretic effect of parenteral paracetamol (propacetamol) in pediatric oncologic patients: a randomized trial
Journal
Pediatric Hematology and Oncology
Author(s)
Reymond  D., Birrer  P., Luthy  A. R., Rimensberger  P. C., Beck  M. N.
ISSN
0888-0018
Publication state
Published
Issued date
02/1997
Peer-reviewed
Oui
Volume
14
Number
1
Pages
51-7
Notes
Clinical Trial
Journal Article
Randomized Controlled Trial --- Old month value: Jan-Feb
Abstract
The antipyretic efficacy of propacetamol, an intravenous prodrug of paracetamol, was evaluated in two pediatric prospective randomized studies. In the first, we-compared one standard intravenous dose of propacetamol (30 mg/kg) to one standard intravenous dose of acetylsalicylic acid (ASA, 15 mg/kg) in 10 nononcologic patients with bacterial illnesses. In the second study, we compared two intravenous doses of propacetamol (30 mg/kg versus 15 mg/kg) in 24 oncologic patients with fever and neutropenia. No statistically significant differences in antipyretic efficacy were found between standard doses of propacetamol and ASA; even when half-doses of propacetamol (15 mg/kg) were used, good antipyretic efficacy was observed, which was not statistically different from that observed with the full dose. The use of propacetamol seems promising for patients (such as oncologic patients) who cannot receive enteral paracetamol formulas.
Keywords
Acetaminophen/adverse effects/*therapeutic use Analgesics, Non-Narcotic/adverse effects/*therapeutic use Aspirin/adverse effects/*therapeutic use Bacterial Infections/complications Child Child, Preschool Fever/*drug therapy/etiology Humans Infusions, Intravenous Neoplasms/*complications Neutropenia/drug therapy/etiology Prospective Studies
Pubmed
Web of science
Create date
20/03/2008 10:34
Last modification date
20/08/2019 16:16
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