Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3415
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dc.contributor.authorWright, N.-
dc.contributor.authorAbantanga, F.-
dc.contributor.authorAmoah, M-
dc.contributor.authorAppeadu-Mensah, W.-
dc.contributor.authorBokhary, Z.-
dc.contributor.authorBvulani, B.-
dc.contributor.authorDavies, J.-
dc.contributor.authorMiti, S.-
dc.contributor.authorNandi, B.-
dc.contributor.authorNimako, B..-
dc.contributor.authorPoenaru, D.-
dc.contributor.authorTabiri, S.-
dc.contributor.authorYifieyeh, A.-
dc.contributor.authorAde-Ajayi, N.-
dc.contributor.authorSevdalis, N.-
dc.contributor.authorLeather, A.-
dc.date.accessioned2022-03-03T10:35:02Z-
dc.date.available2022-03-03T10:35:02Z-
dc.date.issued2019-
dc.identifier.issn2398502X-
dc.identifier.urihttp://hdl.handle.net/123456789/3415-
dc.description.abstractBackground: Gastroschisis is associated with less than 4% mortality in high-income countries and over 90% mortality in many tertiary paediatric surgery centres across sub-Saharan Africa (SSA). The aim of this trial is to develop, implement and prospectively evaluate an interventional bundle to reduce mortality from gastroschisis in seven tertiary paediatric surgery centres across SSA. Methods: A hybrid type-2 effectiveness-implementation, pre-post study design will be utilised. Using current literature an evidence-based, low-technology interventional bundle has been developed. A systematic review, qualitative study and Delphi process will provide further evidence to optimise the interventional bundle and implementation strategy. The interventional bundle has core components, which will remain consistent across all sites, and adaptable components, which will be determined through in-country co-development meetings. Pre- and post-intervention data will be collected on clinical, service delivery and implementation outcomes for 2-years at each site. The primary clinical outcome will be all-cause, in-hospital mortality. Secondary outcomes include the occurrence of a major complication, length of hospital stay and time to full enteral feeds. Service delivery outcomes include time to hospital and primary intervention, and adherence to the pre-hospital and in-hospital protocols. Implementation outcomes are acceptability, adoption, appropriateness, feasibility, fidelity, coverage, cost and sustainability. Pre- and post-intervention clinical outcomes will be compared using Chi-squared analysis, unpaired t-test and/or Mann-Whitney U test. Time-series analysis will be undertaken using Statistical Process Control to identify significant trends and shifts in outcome overtime. Multivariate logistic regression analysis will be used to identify clinical and implementation factors affecting outcome with adjustment for confounders. This will be the first multi-centre interventional study to our outcome: knowledge aimed at reducing mortality from gastroschisis in low-resource settings. If successful, detailed evaluation of both the clinical and implementation components of the study will allow sustainability in the study sites and further scale-up.en_US
dc.language.isoenen_US
dc.publisherWellcome Trusten_US
dc.relation.ispartofseriesVol. 4;Issue 46-
dc.subjectGastroschisisen_US
dc.subjectInterventionen_US
dc.subjectMortalityen_US
dc.subjectLow-Resource Settingen_US
dc.subjectLMICen_US
dc.subjectImplementationen_US
dc.subjectCongenital Anomalyen_US
dc.subjectNeonatal Surgical Careen_US
dc.titleDEVELOPING AND IMPLEMENTING AN INTERVENTIONAL BUNDLE TO REDUCE MORTALITY FROM GASTROSCHISIS IN LOW-RESOURCE SETTINGSen_US
dc.typeArticleen_US
Appears in Collections:School of Medicine and Health Sciences



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