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Active sepsis prevention program reduces maternal infection-related complications in Malawi and Uganda

Active sepsis prevention program reduces maternal infection-related complications in Malawi and Ugan…
Photo by Günter Valda / Unsplash
Key Takeaway
Consider implementing structured maternal sepsis programs to reduce infection-related complications in low-resource settings.

This cluster-randomized trial evaluated the Active Prevention and Treatment of Maternal Sepsis (APT-Sepsis) program in Malawi and Uganda. The study included 431,394 women who gave birth during the trial period. The intervention was compared with usual care.

The primary outcome was a composite of infection-related maternal death, infection-related near-miss event, or severe infection-related illness. The composite outcome occurred in 1.4% of women in the intervention group versus 1.9% in the usual-care group (risk ratio 0.68; 95% confidence interval 0.55 to 0.83; P<0.001). Absolute numbers were not reported.

Safety data were not reported in the available information. Limitations were not explicitly listed, but as a cluster-randomized trial, potential biases include contamination and lack of blinding. The study was funded by the Joint Global Health Trials scheme and others.

Clinicians should consider that this structured sepsis care program was associated with a significant reduction in maternal infection-related complications in low-resource settings. However, further research may be needed to assess generalizability and safety.

Study Details

Study typeRct
EvidenceLevel 2
PublishedApr 2026
View Original Abstract ↓
BACKGROUND: Maternal infection and sepsis are major causes of maternal death and severe illness worldwide, particularly in low- and middle-income countries. Inconsistent implementation of evidence-based recommendations for infection prevention and management and delays in detection and treatment of maternal sepsis contribute to the number of preventable deaths. METHODS: We conducted a cluster-randomized trial to assess a multicomponent intervention, the Active Prevention and Treatment of Maternal Sepsis (APT-Sepsis) program. This program was designed to support health care providers in achieving three goals: adherence to World Health Organization (WHO) hand-hygiene standards; adoption of evidence-based practices for maternal infection prevention and management; and early detection of sepsis and use of the FAST-M (fluids, antibiotics, source control, transfer if required, and monitoring) treatment bundle. Usual care was provided in the control group, along with dissemination of guidelines. The primary outcome was a composite of infection-related maternal death, infection-related near-miss event (events in which women survived a life-threatening complication), or severe infection-related illness (deep surgical-site, deep perineal, or body-cavity infection) among women who were pregnant or had recently been pregnant. RESULTS: We randomly assigned 59 health facilities (where 431,394 women gave birth during the trial) in Malawi and Uganda to the intervention group (30 clusters) or the usual-care group (29 clusters). A primary-outcome event occurred in 1.4% of the patients in the intervention group and in 1.9% of those in the usual-care group (risk ratio, 0.68; 95% confidence interval, 0.55 to 0.83; P<0.001). This effect was generally consistent between countries and among facilities of difference sizes and was sustained over time. CONCLUSIONS: Implementation of the APT-Sepsis program led to a significantly lower risk of a composite of infection-related maternal death, infection-related near-miss event, or severe infection-related illness than usual care. (Funded by the Joint Global Health Trials scheme and others; APT-Sepsis ISRCTN number, ISRCTN42347014.).
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