Safety and Efficacy of C-reactive Protein-guided Antibiotic Use to Treat Acute Respiratory Infections in Tanzanian Children: A Planned Subgroup Analysis of a Randomized Controlled Noninferiority Trial Evaluating a Novel Electronic Clinical Decision Algorithm (ePOCT).


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
13 11 2019
Historique:
received: 24 09 2018
accepted: 30 01 2019
pubmed: 5 2 2019
medline: 15 9 2020
entrez: 5 2 2019
Statut: ppublish

Résumé

The safety and efficacy of using C-reactive protein (CRP) to decide on antibiotic prescription among febrile children at risk of pneumonia has not been tested. This was a randomized (1:1) controlled noninferiority trial in 9 primary care centers in Tanzania (substudy of the ePOCT trial evaluating a novel electronic decision algorithm). Children aged 2-59 months with fever and cough and without life-threatening conditions received an antibiotic based on a CRP-informed strategy (combination of CRP ≥80 mg/L plus age/temperature-corrected tachypnea and/or chest indrawing) or current World Health Organization standard (respiratory rate ≥50 breaths/minute). The primary outcome was clinical failure by day (D) 7; the secondary outcomes were antibiotic prescription at D0, secondary hospitalization, or death by D30. A total of 1726 children were included (intervention: 868, control: 858; 0.7% lost to follow-up). The proportion of clinical failure by D7 was 2.9% (25/865) in the intervention arm vs 4.8% (41/854) in the control arm (risk difference, -1.9% [95% confidence interval {CI}, -3.7% to -.1%]; risk ratio [RR], 0.60 [95% CI, .37-.98]). Twenty of 865 (2.3%) children in the intervention arm vs 345 of 854 (40.4%) in the control arm received antibiotics at D0 (RR, 0.06 [95% CI, .04-.09]). There were fewer secondary hospitalizations and deaths in the CRP arm: 0.5% (4/865) vs 1.5% (13/854) (RR, 0.30 [95% CI, .10-.93]). CRP testing using a cutoff of ≥80 mg/L, integrated into an electronic decision algorithm, was able to improve clinical outcome in children with respiratory infections while substantially reducing antibiotic prescription. NCT02225769.

Sections du résumé

BACKGROUND
The safety and efficacy of using C-reactive protein (CRP) to decide on antibiotic prescription among febrile children at risk of pneumonia has not been tested.
METHODS
This was a randomized (1:1) controlled noninferiority trial in 9 primary care centers in Tanzania (substudy of the ePOCT trial evaluating a novel electronic decision algorithm). Children aged 2-59 months with fever and cough and without life-threatening conditions received an antibiotic based on a CRP-informed strategy (combination of CRP ≥80 mg/L plus age/temperature-corrected tachypnea and/or chest indrawing) or current World Health Organization standard (respiratory rate ≥50 breaths/minute). The primary outcome was clinical failure by day (D) 7; the secondary outcomes were antibiotic prescription at D0, secondary hospitalization, or death by D30.
RESULTS
A total of 1726 children were included (intervention: 868, control: 858; 0.7% lost to follow-up). The proportion of clinical failure by D7 was 2.9% (25/865) in the intervention arm vs 4.8% (41/854) in the control arm (risk difference, -1.9% [95% confidence interval {CI}, -3.7% to -.1%]; risk ratio [RR], 0.60 [95% CI, .37-.98]). Twenty of 865 (2.3%) children in the intervention arm vs 345 of 854 (40.4%) in the control arm received antibiotics at D0 (RR, 0.06 [95% CI, .04-.09]). There were fewer secondary hospitalizations and deaths in the CRP arm: 0.5% (4/865) vs 1.5% (13/854) (RR, 0.30 [95% CI, .10-.93]).
CONCLUSIONS
CRP testing using a cutoff of ≥80 mg/L, integrated into an electronic decision algorithm, was able to improve clinical outcome in children with respiratory infections while substantially reducing antibiotic prescription.
CLINICAL TRIALS REGISTRATION
NCT02225769.

Identifiants

pubmed: 30715250
pii: 5305918
doi: 10.1093/cid/ciz080
doi:

Substances chimiques

Anti-Bacterial Agents 0
C-Reactive Protein 9007-41-4
Albuterol QF8SVZ843E

Banques de données

ClinicalTrials.gov
['NCT02225769']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1926-1934

Commentaires et corrections

Type : CommentIn

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Kristina Keitel (K)

Swiss Tropical and Public Health Institute, Basel.
Department of Pediatric Emergency Medicine, University Hospital Bern, Switzerland.

Josephine Samaka (J)

Ifakara Health Institute, Dar es Salaam, Tanzania.
Amana Hospital, Dar es Salaam, Tanzania.

John Masimba (J)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Hosiana Temba (H)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Zamzam Said (Z)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Frank Kagoro (F)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Tarsis Mlaganile (T)

Ifakara Health Institute, Dar es Salaam, Tanzania.

Willy Sangu (W)

City Council, Dar es Salaam, Tanzania.

Blaise Genton (B)

Swiss Tropical and Public Health Institute, Basel.
Infectious Diseases Service, University Hospital Lausanne, Switzerland.

Valerie D'Acremont (V)

Swiss Tropical and Public Health Institute, Basel.
Department of Ambulatory Care and Community Medicine, University Hospital Lausanne, Switzerland.

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