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. 2024 Sep 23;13(Suppl 1):S15-S27.
doi: 10.25259/IJMA_34_2024. eCollection 2024 Sep.

Integrating Heat-Stable Carbetocin and Tranexamic Acid for Prevention and Management of Postpartum Hemorrhage in Sub-Saharan Africa: A Five-Country Pilot Implementation Study

Affiliations

Integrating Heat-Stable Carbetocin and Tranexamic Acid for Prevention and Management of Postpartum Hemorrhage in Sub-Saharan Africa: A Five-Country Pilot Implementation Study

Sara Rushwan et al. Int J MCH AIDS. .

Abstract

Background and objective: Globally, postpartum hemorrhage (PPH) remains the most common direct cause of maternal mortality. This study evaluated the feasibility and acceptability of introducing heat-stable carbetocin (HSC) for PPH prevention and tranexamic acid (TXA) for PPH treatment in five Sub-Saharan African countries following recent World Health Organization (WHO) recommendations. This study also assessed healthcare providers' (HCPs') favorability toward using these medicines.

Methods: We conducted a mixed methods pilot implementation study in selected facilities across Burkina Faso, Ethiopia, Ghana, Sierra Leone, and Uganda between May and December 2022. We compared baseline data obtained from patient registers with data collected during implementation on the safe and appropriate use of HSC and TXA using descriptive statistics. HCP responses were analyzed qualitatively using a thematic analysis.

Results: Following training, HSC was administered prophylactically in 11,329 (92.4%) of 12,262 deliveries in all study facilities which received a uteorotonic for PPH prevention during implementation and was used safely and appropriately. TXA administration for PPH treatment was done safely, appropriately, and within the WHO-recommended time. No adverse events were reported throughout the study. HCPs overall showed high confidence in, and favorability toward, using both medicines.

Conclusion and global health implications: Our study demonstrated that HSC and TXA can be safely and appropriately implemented in primary and tertiary facilities, and their introduction is feasible and acceptable from the perspective of HCPs. A holistic approach to training and regular supportive supervision is needed to ensure the continued safe use of these new and lesser-utilized PPH medicines. Dedicated training is required to improve the documentation of patient charts on PPH care. Introducing these medicines holds promise for improving PPH care in low- and middle-income countries, including by addressing suboptimal efficacy due to cold chain system challenges.

Keywords: Heat-Stable Carbetocin; Implementation Research; Postpartum Hemorrhage; Sub-Saharan Africa; Tranexamic Acid.

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Conflict of interest statement

The authors declare no competing interests.

Figures

Figure 1*:
Figure 1*:
Uterotonic administration for PPH prevention by country, facility type, and study phase. Data are presented as percentage of prophylactic uterotonic administered at BEmONC and CEmONC facilities in each study country at baseline (pre-intervention) and during implementation (post-intervention). At baseline, the uterotonics administered were either oxytocin, misoprostol, or oxytocin in combination with misoprostol. During implementation, the uterotonics administered were either HSC, oxytocin, misoprostol, oxytocin in combination with misoprostol, HSC in combination with oxytocin or misoprostol, or carboprost. B = Baseline and I = Implementation *HSC was administered in combination with other uterotonics for PPH prevention to 3.1% (55) of women in CEmONCs in Ghana, 0.5% (7) in Burkina Faso, 0.5% (22) in Uganda, and 0.1% (1) in Sierra Leone. Across all BEmONCs, one patient in Ghana received HSC in combination with other uterotonics. In Ghana, 54 cases in CEmONCs and 1 case in BEmONCs were administered HSC in combination with misoprostol for PPH prevention.
Figure 2:
Figure 2:
HSC administration for PPH prevention during study implementation by country and facility type. Data are presented as percentage of HSC administered at BEmONC and CEmONC facilities in each study country during implementation.
Figure 3:
Figure 3:
Additional uterotonic administration by country, facility type, and study phase. Percentage of additional uterotonic administered at the study facilities at baseline (pre-intervention) and implementation (post-intervention). B = Baseline and I = Implementation

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