Introduction of the Ellavi uterine balloon tamponade into the Kenyan and Ghanaian maternal healthcare package for improved postpartum haemorrhage management: an implementation research study

Author:

Parker Megan EORCID,Qureshi Zahida,Deganus Sylvia,Soki James,Cofie Patience,Dapaah Patience,Owusu Rosemond,Gwako George,Osoti Alfred,Ogutu Omondi,Opira Jacqueline,Sunkwa-Mills Gifty,Boamah Martin,Srofenyoh Emmanuel,Aboagye Patrick,Fofie Chris,Kaliti Stephen,Morozoff ChloeORCID,Secor Andrew,Metzler Mutsumi,Abu-Haydar Elizabeth

Abstract

ObjectivesUse of intrauterine balloon tamponades for refractory postpartum haemorrhage (PPH) management has triggered recent debate since effectiveness studies have yielded conflicting results. Implementation research is needed to identify factors influencing successful integration into maternal healthcare packages. The Ellavi uterine balloon tamponade (UBT) (Ellavi) is a new low-cost, preassembled device for treating refractory PPH.DesignA mixed-methods, prospective, implementation research study examining the adoption, sustainability, fidelity, acceptability and feasibility of introducing a newly registered UBT. Cross-sectional surveys were administered post-training and post-use over 10 months.SettingThree Ghanaian (district, regional) and three Kenyan (levels 4–6) healthcare facilities.ParticipantsObstetric staff (n=451) working within participating facilities.InterventionPPH management training courses were conducted with obstetric staff.Primary and secondary outcome measuresFacility measures of adoption, sustainability and fidelity and individual measures of acceptability and feasibility.ResultsAll participating hospitals adopted the device during the study period and the majority (52%–62%) of the employed obstetric staff were trained on the Ellavi; sustainability and fidelity to training content were moderate. The Ellavi was suited for this context due to high delivery and PPH burden. Dynamic training curriculums led by local UBT champions and clear instructions on the packaging yielded positive attitudes and perceptions, and high user confidence, resulting in overall high acceptability. Post-training and post-use, ≥79% of the trainees reported that the Ellavi was easy to use. Potential barriers to use included the lack of adjustable drip stands and difficulties calculating bag height according to blood pressure. Overall, the Ellavi can be feasibly integrated into PPH care and was preferred over condom catheters.ConclusionsThe training package and time saving Ellavi design facilitated its adoption, acceptability and feasibility. The Ellavi is appropriate and feasible for use among obstetric staff and can be successfully integrated into the Kenyan and Ghanaian maternal healthcare package.Trial registration numbersNCT04502173;NCT05340777.

Funder

Foreign, Commonwealth and Development Office

Publisher

BMJ

Subject

General Medicine

Reference40 articles.

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2. WHO . Who recommendations: Uterotonics for the prevention of postpartum haemorrhage. Geneva: who, 2018. Available: https://apps.who.int/iris/bitstream/handle/10665/277276/9789241550420-eng.pdf?ua=1 [Accessed 24 June 2022].

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