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Original Articles

Alalfy modified cervical inversion technique as a tamponade in controlling PPH in placenta previa, a multicentric double blind randomized controlled trial

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Pages 3162-3168 | Received 09 Aug 2019, Accepted 06 Oct 2019, Published online: 21 Oct 2019
 

Abstract

Introduction

Postpartum hemorrhage that occurs frequently with placenta previa is one of the causes of maternal mortality in 14% in developing countries.

Objective

To assess efficacy of cervical inversion as a tamponade in controlling bed of placenta in cases of placenta previa.

Patients and method

A prospective randomized controlled study was conducted among a total of 240 pregnant women with placenta previa (120 subjected to Alalfy modified cervical inversion technique plus hemostatic sutures and 120 was not subjected cervical inversion and only was subjected to hemostatic sutures in Obstetrics and Gynecology Department at Suez Canal University hospital, Helwan University and Algezeerah hospital for a planned cesarean section).

Results

The mean intraoperative blood loss, the intraoperative time, and the postoperative hemoglobin show a statistically significant difference between cases with placenta previa who were exposed to cervical inversion in comparison to cases that had no cervical inversion with a p-value <.001.

Conclusion

Modified cervical inversion (Alalfy technique) as a tamponade when added to hemostatic sutures to the placental bed is an easy, rapid, and efficient procedure that can decrease the amount of blood loss, time needed to stop bleeding per bed, total operative time, also it can decrease the need for blood transfusion.

Correction Statement

This article has been republished with minor changes. These changes do not impact the academic content of the article.

Acknowledgements

We thank the staff members who helped us in this study in Suez Canal University Hospital, Helwan University and Algezeerah Hospitals.

Author contribution

All authors participated and made a substantial contribution to all aspects of the research.

Disclosure statement

No potential conflict of interest was reported by the authors.

Data availability

The study was registered in clinicaltrials.gov with identification ID: NCT03772184

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