Please use this identifier to cite or link to this item: https://dora.health.qld.gov.au/qldresearchjspui/handle/1/2974
Title: Extended Versus Standard Antibiotic Course Duration in Children <5 Years of Age Hospitalized With Community-acquired Pneumonia in High-risk Settings: Four-week Outcomes of a Multicenter, Double-blind, Parallel, Superiority Randomized Controlled Trial
Authors: McCallum, G. B.
Fong, S. M.
Grimwood, K.
Nathan, A. M.
Byrnes, C. A.
Ooi, M. H.
Nachiappan, N.
Saari, N.
Morris, P. S.
Yeo, T. W.
Ware, R. S.
Elogius, B. W.
Oguoma, V. M.
Yerkovich, S. T.
De Bruyne, J.
Lawrence, K. A.
Lee, B.
Upham, J. W.
Torzillo, P. J.
Chang, Anne 
Issue Date: 2022
Source: 41, (7), 2022, p. 549-555
Pages: 549-555
Journal: Pediatric Infectious Disease Journal
Abstract: Background: High-level evidence is limited for antibiotic duration in children hospitalized with community-acquired pneumonia (CAP) from First Nations and other at-risk populations of chronic respiratory disorders. As part of a larger study, we determined whether an extended antibiotic course is superior to a standard course for achieving clinical cure at 4 weeks in children 3 months to ≤5 years old hospitalized with CAP. Methods: In our multinational (Australia, New Zealand, Malaysia), double-blind, superiority randomized controlled trial, children hospitalized with uncomplicated, radiographic-confirmed, CAP received 1-3 days of intravenous antibiotics followed by 3 days of oral amoxicillin-clavulanate (80 mg/kg, amoxicillin component, divided twice daily) and then randomized to extended (13-14 days duration) or standard (5-6 days) antibiotics. The primary outcome was clinical cure (complete resolution of respiratory symptoms/signs) 4 weeks postenrollment. Secondary outcomes included adverse events, nasopharyngeal bacterial pathogens and antimicrobial resistance at 4 weeks. Results: Of 372 children enrolled, 324 fulfilled the inclusion criteria and were randomized. Using intention-to-treat analysis, between-group clinical cure rates were similar (extended course: n = 127/163, 77.9%; standard course: n = 131/161, 81.3%; relative risk = 0.96, 95% confidence interval = 0.86-1.07). There were no significant between-group differences for adverse events (extended course: n = 43/163, 26.4%; standard course, n = 32/161, 19.9%) or nasopharyngeal carriage of Streptococcus pneumoniae, Haemophilus influenzae, Moraxella catarrhalis and Staphylococcus aureus or antimicrobial resistance. Conclusions: Among children hospitalized with pneumonia and at-risk of chronic respiratory illnesses, an extended antibiotic course was not superior to a standard course at achieving clinical cure at 4 weeks. Additional research will identify if an extended course provides longer-term benefits.L20188099782022-06-28
2022-07-05
DOI: 10.1097/INF.0000000000003558
Resources: https://www.embase.com/search/results?subaction=viewrecord&id=L2018809978&from=exporthttp://dx.doi.org/10.1097/INF.0000000000003558 |
Keywords: Staphylococcus aureus;Streptococcus pneumoniae;Moraxella catarrhalis;vomiting;treatment duration;amoxicillinamoxicillin plus clavulanic acid;ampicillin;antibiotic agent;cefotaxime;ceftriaxone;cefuroxime;cloxacillin;penicillin G;antibiotic resistance;antibiotic therapy;article;child;community acquired pneumonia;controlled study;diarrhea;double blind procedure;female;Haemophilus influenzae;hospital readmission;hospitalization;human;intention to treat analysis;major clinical study;male;multicenter study;nausea;outcome assessment;parallel design;preschool child;randomized controlled trial;rash;risk factor
Type: Article
Appears in Sites:Children's Health Queensland Publications

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