Effect of a novel vital sign device on maternal mortality and morbidity in low-resource settings: a pragmatic, stepped-wedge, cluster-randomised controlled trial.



Vousden, Nicola, Lawley, Elodie, Nathan, Hannah L, Seed, Paul T ORCID: 0000-0001-7904-7933, Gidiri, Muchabayiwa Francis, Goudar, Shivaprasad ORCID: 0000-0002-8680-7053, Sandall, Jane ORCID: 0000-0003-2000-743X, Chappell, Lucy C ORCID: 0000-0001-6219-3379, Shennan, Andrew H ORCID: 0000-0001-5273-3132 and CRADLE Trial Collaborative Group,
(2019) Effect of a novel vital sign device on maternal mortality and morbidity in low-resource settings: a pragmatic, stepped-wedge, cluster-randomised controlled trial. The Lancet. Global health, 7 (3). e347-e356.

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Abstract

<h4>Background</h4>In 2015, an estimated 303 000 women died in pregnancy and childbirth. Obstetric haemorrhage, sepsis, and hypertensive disorders of pregnancy account for more than 50% of maternal deaths worldwide. There are effective treatments for these pregnancy complications, but they require early detection by measurement of vital signs and timely administration to save lives. The primary aim of this trial was to determine whether implementation of the CRADLE Vital Sign Alert and an education package into community and facility maternity care in low-resource settings could reduce a composite of all-cause maternal mortality or major morbidity (eclampsia and hysterectomy).<h4>Methods</h4>We did a pragmatic, stepped-wedge, cluster-randomised controlled trial in ten clusters across Africa, India, and Haiti, introducing the device into routine maternity care. Each cluster contained at least one secondary or tertiary hospital and their main referral facilities. Clusters crossed over from existing routine care to the CRADLE intervention in one of nine steps at 2-monthly intervals, with CRADLE devices replacing existing equipment at the randomly allocated timepoint. A computer-generated randomly allocated sequence determined the order in which the clusters received the intervention. Because of the nature of the intervention, this trial was not masked. Data were gathered monthly, with 20 time periods of 1 month. The primary composite outcome was at least one of eclampsia, emergency hysterectomy, and maternal death. This study is registered with the ISRCTN registry, number ISRCTN41244132.<h4>Findings</h4>Between April 1, 2016, and Nov 30, 2017, among 536 223 deliveries, the primary outcome occurred in 4067 women, with 998 maternal deaths, 2692 eclampsia cases, and 681 hysterectomies. There was an 8% decrease in the primary outcome from 79·4 per 10 000 deliveries pre-intervention to 72·8 per 10 000 deliveries post-intervention (odds ratio [OR] 0·92, 95% CI 0·86-0·97; p=0·0056). After planned adjustments for variation in event rates between and within clusters over time, the unexpected degree of variability meant we were unable to judge the benefit or harms of the intervention (OR 1·22, 95% CI 0·73-2·06; p=0·45).<h4>Interpretation</h4>There was an absolute 8% reduction in primary outcome during the trial, with no change in resources or staffing, but this reduction could not be directly attributed to the intervention due to variability. We encountered unanticipated methodological challenges with this trial design, which can provide valuable learning for future research and inform the trial design of future international stepped-wedge trials.<h4>Funding</h4>Newton Fund Global Research Programme: UK Medical Research Council; Department of Biotechnology, Ministry of Science & Technology, Government of India; and UK Department of International Development.

Item Type: Article
Uncontrolled Keywords: CRADLE Trial Collaborative Group, Humans, Pregnancy Complications, Infectious, Sepsis, Pregnancy Complications, Hypertension, Pregnancy-Induced, Eclampsia, Postpartum Hemorrhage, Blood Pressure Determination, Early Diagnosis, Hysterectomy, Maternal Mortality, Pregnancy, Health Personnel, Maternal Health Services, Health Resources, Africa, Haiti, India, Female, Vital Signs, Early Medical Intervention, Heart Rate Determination
Depositing User: Symplectic Admin
Date Deposited: 02 Oct 2019 10:41
Last Modified: 17 Mar 2024 03:04
DOI: 10.1016/s2214-109x(18)30526-6
Open Access URL: https://doi.org/10.1016/S2214-109X(18)30526-6
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URI: https://livrepository.liverpool.ac.uk/id/eprint/3056701