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DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso

BACKGROUND: Since 2006, Burkina Faso has subsidized the cost of caesarean sections to increase their accessibility. Caesareans are performed by obstetricians, general practitioners, and nurses trained in emergency surgery. While the national caesarean rate is still too low (only 2 % in 2010), 12 to...

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Autores principales: Kaboré, Charles, Ridde, Valéry, Kouanda, Séni, Queuille, Ludovic, Somé, Paul-André, Agier, Isabelle, Dumont, Alexandre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073955/
https://www.ncbi.nlm.nih.gov/pubmed/27769190
http://dx.doi.org/10.1186/s12884-016-1112-8
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author Kaboré, Charles
Ridde, Valéry
Kouanda, Séni
Queuille, Ludovic
Somé, Paul-André
Agier, Isabelle
Dumont, Alexandre
author_facet Kaboré, Charles
Ridde, Valéry
Kouanda, Séni
Queuille, Ludovic
Somé, Paul-André
Agier, Isabelle
Dumont, Alexandre
author_sort Kaboré, Charles
collection PubMed
description BACKGROUND: Since 2006, Burkina Faso has subsidized the cost of caesarean sections to increase their accessibility. Caesareans are performed by obstetricians, general practitioners, and nurses trained in emergency surgery. While the national caesarean rate is still too low (only 2 % in 2010), 12 to 24 % of caesareans performed in hospital are, in fact, not medically indicated. The objective of this study is to evaluate the effectiveness and analyze the implementation of a multi-faceted intervention to lower the rate of non-medically indicated caesareans in Burkina Faso. METHODS: This study combines a multicentre cluster randomized controlled trial with an implementation analysis in a mixed-methods approach. The evidence-based intervention will consist of three strategies to improve the competencies of maternity teams: 1) clinical audits based on objective criteria; 2) training of personnel; and 3) decision-support reminders of indications for caesareans via text messages. The unit of randomization and of intervention is the public hospital equipped with a functional operating room. Using stratified randomization on hospital type and staff qualifications, 11 hospitals have been assigned to the intervention group and 11 to the control group. The intervention will cover 1 year. Every patient who delivered by caesarean during a 6-month period in the year preceding the intervention and the 6 months following its end will be included in the trial. The change in the rate of non-medically indicated caesareans is the main criterion by which the intervention’s impact will be assessed. To analyze the intervention process, a longitudinal qualitative study consisting of deliberative workshops and individual in-depth interviews will be conducted. The target outcome is a 50 % reduction in the rate of non-medically indicated caesareans. DISCUSSION: This study will provide evidence regarding the effectiveness of a multi-faceted intervention for reducing non-medically indicated caesareans in a low-income country. By combining qualitative and quantitative methods, the study’s findings will allow understanding the factors that could influence the intervention process and ultimately the intended outcomes. TRIAL REGISTRATION: The DECIDE trial is registered on the Current Controlled Trials website under the number ISRCTN48510263 on January 28, 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12884-016-1112-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-50739552016-10-27 DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso Kaboré, Charles Ridde, Valéry Kouanda, Séni Queuille, Ludovic Somé, Paul-André Agier, Isabelle Dumont, Alexandre BMC Pregnancy Childbirth Study Protocol BACKGROUND: Since 2006, Burkina Faso has subsidized the cost of caesarean sections to increase their accessibility. Caesareans are performed by obstetricians, general practitioners, and nurses trained in emergency surgery. While the national caesarean rate is still too low (only 2 % in 2010), 12 to 24 % of caesareans performed in hospital are, in fact, not medically indicated. The objective of this study is to evaluate the effectiveness and analyze the implementation of a multi-faceted intervention to lower the rate of non-medically indicated caesareans in Burkina Faso. METHODS: This study combines a multicentre cluster randomized controlled trial with an implementation analysis in a mixed-methods approach. The evidence-based intervention will consist of three strategies to improve the competencies of maternity teams: 1) clinical audits based on objective criteria; 2) training of personnel; and 3) decision-support reminders of indications for caesareans via text messages. The unit of randomization and of intervention is the public hospital equipped with a functional operating room. Using stratified randomization on hospital type and staff qualifications, 11 hospitals have been assigned to the intervention group and 11 to the control group. The intervention will cover 1 year. Every patient who delivered by caesarean during a 6-month period in the year preceding the intervention and the 6 months following its end will be included in the trial. The change in the rate of non-medically indicated caesareans is the main criterion by which the intervention’s impact will be assessed. To analyze the intervention process, a longitudinal qualitative study consisting of deliberative workshops and individual in-depth interviews will be conducted. The target outcome is a 50 % reduction in the rate of non-medically indicated caesareans. DISCUSSION: This study will provide evidence regarding the effectiveness of a multi-faceted intervention for reducing non-medically indicated caesareans in a low-income country. By combining qualitative and quantitative methods, the study’s findings will allow understanding the factors that could influence the intervention process and ultimately the intended outcomes. TRIAL REGISTRATION: The DECIDE trial is registered on the Current Controlled Trials website under the number ISRCTN48510263 on January 28, 2014. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12884-016-1112-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-10-21 /pmc/articles/PMC5073955/ /pubmed/27769190 http://dx.doi.org/10.1186/s12884-016-1112-8 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Kaboré, Charles
Ridde, Valéry
Kouanda, Séni
Queuille, Ludovic
Somé, Paul-André
Agier, Isabelle
Dumont, Alexandre
DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title_full DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title_fullStr DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title_full_unstemmed DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title_short DECIDE: a cluster randomized controlled trial to reduce non-medically indicated caesareans in Burkina Faso
title_sort decide: a cluster randomized controlled trial to reduce non-medically indicated caesareans in burkina faso
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5073955/
https://www.ncbi.nlm.nih.gov/pubmed/27769190
http://dx.doi.org/10.1186/s12884-016-1112-8
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