Evidence map›Paper›PMID 28528578›Full record

Trial reportBMC medicine2017

A cluster-randomized trial to reduce caesarean delivery rates in Quebec: cost-effectiveness analysis.

Mira Johri, Edmond S W Ng, Clara Bermudez-Tamayo, Jeffrey S Hoch, Thierry Ducruet, Nils Chaillet

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in BMC medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 11% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Non-clinical interventions for reducing unnecessary caesarean section.The Cochrane database of systematic reviews · 2018
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 6 institutions in 5 countries.

Mira JohriCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Tour Saint-Antoine, Porte S03-910, 850, rue St-Denis, Montréal, Québec, H2X 0A9, Canada. mira.johri@umontreal.ca.ORCID 0000-0001-5642-787X
Edmond S W NgDirector's Office, London School of Hygiene and Tropical Medicine (LSHTM), London, UK.
Clara Bermudez-TamayoDepartment of Obstetrics and Gynecology, Centre Hospitalier Universitaire (CHU) de Sherbrooke, Sherbrooke, Québec, Canada.
Jeffrey S HochInstitute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Thierry DucruetDepartment of Biostatistics, Centre hospitalier universitaire (CHU) Sainte-Justine, Université de Montréal, Montréal, Québec, Canada.
Nils ChailletDépartement Obstétrique et Gynécologie, Centre Hospitalier de l'Université Laval (CHUL), Québec, Québec, Canada.
Centre hospitalier de l'Université Laval · CACentre Hospitalier Universitaire Sainte-Justine · CAInstituto de Salud Carlos III · ESLondon School of Hygiene & Tropical Medicine · GBSt. Michael's Hospital · CAWorld Health Organization · CH

Funding

CIHR 200702MCT-171307-RFA-CFCF-153236CIHR MOP 81275
6 · The paper itself

Abstract

backgroundWidespread increases in caesarean section (CS) rates have sparked concerns about risks to mothers and infants and rising healthcare costs. A multicentre, two-arm, cluster-randomized trial in Quebec, Canada assessed whether an audit and feedback intervention targeting health professionals would reduce CS rates for pregnant women compared to usual care, and concluded that it reduced CS rates without adverse effects on maternal or neonatal health. The effect was statistically significant but clinically small. We assessed cost-effectiveness to inform scale-up decisions.

methodsA prospective economic evaluation was undertaken using individual patient data from the Quality of Care, Obstetrics Risk Management, and Mode of Delivery (QUARISMA) trial (April 2008 to October 2011). Analyses took a healthcare payer perspective. The time horizon captured hospital-based costs and clinical events for mothers and neonates from labour onset to 3 months postpartum. Resource use was identified and measured from patient charts and valued using standardized government sources. We estimated the changes in CS rates and costs for the intervention group (versus controls) between the baseline and post-intervention periods. We examined heterogeneity between clinical subgroups of high-risk versus low-risk pregnancies and estimated the joint uncertainty in cost-effectiveness over 20,000 trial simulations. We decomposed costs to identify drivers of change.

resultsThe intervention group experienced per-patient reductions of 0.005 CS (95% confidence interval (CI): -0.015 to 0.004, P = 0.09) and $180 (95% CI: -$277 to - $83, P < 0.001). Women with low-risk pregnancies experienced statistically significant reductions in CS rates and costs; changes for the high-risk subgroup were not significant. The intervention was "dominant" (effective in reducing CS and less costly than usual care) in 86.08% of simulations. It reduced costs in 99.99% of simulations. Cost reductions were driven by lower rates of neonatal complications in the intervention group (-$190, 95% CI: -$255 to - $125, P < 0.001). Given 88,000 annual provincial births, a similar intervention could save $15.8 million (range: $7.3 to $24.4 million) in Quebec annually.

conclusionsFrom a healthcare payer perspective, a multifaceted intervention involving audits and feedback resulted in a small reduction in caesarean deliveries and important cost savings. Cost reductions are consistent with improved quality of care in intervention group hospitals.

trial registrationInternational Clinical Trials Registry Platform, ISRCTN95086407 . Registered on 23 October 2007.

Indexed as

Commission on Professional and Hospital ActivitiesCesarean SectionCost-Benefit AnalysisFeedbackFemaleHealth Care CostsHumansInfant, NewbornPregnancyPregnancy OutcomeProspective StudiesQuebecRisk AssessmentAdolescentAdultCaesarean section/utilizationCost-benefit analysisFemaleGuideline adherenceInfantMedical auditMultilevel analysisNewbornPregnancy outcomesRandomized controlled trial

Identifiers

PMID28528578
PMCPMC5439122
OpenAlexW2611893844

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.