Randomized Trial of Early Detection and Treatment of Postpartum Hemorrhage.

Ioannis Gallos, Adam Devall, James Martin, Lee Middleton, Leanne Beeson, Hadiza Galadanci, Fadhlun Alwy Al-Beity, Zahida Qureshi, G. Justus Hofmeyr, Neil Moran, Sue Fawcus, Lumaan Sheikh, George Gwako, Alfred Osoti, Ashraf Aswat, Kristie Marie Mammoliti, Kulandaipalayam N. Sindhu, Marcelina Podesek, Isobelle Horne, Rebecca TimmsIdnan Yunas, Jenipher Okore, Mandisa Singata-Madliki, Edna Arends, Aminu A. Wakili, Ard Mwampashi, Sidrah Nausheen, Shah Muhammad, Pallavi Latthe, Cherrie Evans, Shahinoor Akter, Gillian Forbes, David Lissauer, Shireen Meher, Andrew Weeks, Andrew Shennan, Anne Ammerdorffer, Eleanor Williams, Tracy Roberts, Mariana Widmer, Olufemi T. Oladapo, Fabiana Lorencatto, Meghan A. Bohren, Suellen Miller, Fernando Althabe, Metin Gülmezoglu, Jeffrey M. Smith, Karla Hemming, Arri Coomarasamy

Research output: Contribution to journalArticlepeer-review

36 Citations (Scopus)

Abstract

Abstract Background Delays in the detection or treatment of postpartum hemorrhage can result in complications or death. A blood-collection drape can help provide objective, accurate, and early diagnosis of postpartum hemorrhage, and delayed or inconsistent use of effective interventions may be able to be addressed by a treatment bundle. Methods We conducted an international, cluster-randomized trial to assess a multicomponent clinical intervention for postpartum hemorrhage in patients having vaginal delivery. The intervention included a calibrated blood-collection drape for early detection of postpartum hemorrhage and a bundle of first-response treatments (uterine massage, oxytocic drugs, tranexamic acid, intravenous fluids, examination, and escalation), supported by an implementation strategy (intervention group). Hospitals in the control group provided usual care. The primary outcome was a composite of severe postpartum hemorrhage (blood loss, ≥1000 ml), laparotomy for bleeding, or maternal death from bleeding. Key secondary implementation outcomes were the detection of postpartum hemorrhage and adherence to the treatment bundle. Results A total of 80 secondary-level hospitals across Kenya, Nigeria, South Africa, and Tanzania, in which 210,132 patients underwent vaginal delivery, were randomly assigned to the intervention group or the usual-care group. Among hospitals and patients with data, a primary-outcome event occurred in 1.6% of the patients in the intervention group, as compared with 4.3% of those in the usual-care group (risk ratio, 0.40; 95% confidence interval [CI], 0.32 to 0.50; P<0.001). Postpartum hemorrhage was detected in 93.1% of the patients in the intervention group and in 51.1% of those in the usual-care group (rate ratio, 1.58; 95% CI, 1.41 to 1.76), and the treatment bundle was used in 91.2% and 19.4%, respectively (rate ratio, 4.94; 95% CI, 3.88 to 6.28). Conclusions Early detection of postpartum hemorrhage and use of bundled treatment led to a lower risk of the primary outcome, a composite of severe postpartum hemorrhage, laparotomy for bleeding, or death from bleeding, than usual care among patients having vaginal delivery. (Funded by the Bill and Melinda Gates Foundation; E-MOTIVE ClinicalTrials.gov number, NCT04341662.)

Original languageEnglish
Pages (from-to)11-21
Number of pages11
JournalNew England Journal of Medicine
Volume389
Issue number1
DOIs
Publication statusPublished - 2023
Externally publishedYes

Keywords

  • Complications of Pregnancy
  • Obstetrics/Gynecology
  • Obstetrics/Gynecology General

Fingerprint

Dive into the research topics of 'Randomized Trial of Early Detection and Treatment of Postpartum Hemorrhage.'. Together they form a unique fingerprint.

Cite this