Use of Misoprostol in the Prevention of Postpartum Haemorrhage Following Caesarean Section
DOI:
https://doi.org/10.61561/ssbgjms.v7i01.141Keywords:
Postpartum haemorrhage, Rectal misoprostol, Caesarean section, Uterotonic, PPH preventionAbstract
Background: Postpartum haemorrhage (PPH) remains a leading cause of maternal mortality, particularly in low-resource settings. Misoprostol, a synthetic prostaglandin E1 analogue, is inexpensive, thermo-stable, and easy to administer; it is increasingly used off-label in obstetrics for PPH prevention and treatment, but locally generated evidence on its rectal use during caesarean section in Bangladesh remains limited.
Objective: To ascertain the use of rectal misoprostol in the prevention of postpartum haemorrhage following caesarean section.
Methods: This was a cross-sectional comparative study conducted in the Department of Obstetrics and Gynaecology, Institute of Child and Mother Health (ICMH), Matuail, Dhaka, from November 2012 to April 2013. A total of 110 pregnant women at ≥37 weeks of gestation undergoing caesarean section were enrolled by consecutive sampling and assigned to two groups of 55 each: Group A (Trial group) received 400 mcg rectal misoprostol immediately after delivery of the baby in addition to standard oxytocin, while Group B (Control group) received standard oxytocin alone (10 IU IV/IM) as per WHO 2012 active management protocol. Outcomes included intra- and post-operative blood loss, incidence of PPH, and side effects. Data were analysed using SPSS version 16.0; chi-square and Fisher's exact tests were used for categorical variables and independent-samples t-test for continuous variables, with p<0.05 considered significant.
Results: The mean age was 21.90±3.73 years in Group A and 22.83±3.51 years in Group B. The majority were housewives (89.1% in Group A vs 96.4% in Group B) and primigravida (92.7% vs 96.4%). Blood loss <1000 ml was significantly more common in Group A than Group B (61.8% vs 29.1%), while blood loss >1000 ml was more frequent in Group B than Group A (70.9% vs 38.2%; p=0.001). Postpartum haemorrhage occurred in 3.6% of women in each group. Pyrexia was observed in 9.1% of Group A and 7.3% of Group B, and nausea in 1.8% and 3.6% respectively, with no significant difference (p=0.676).
Conclusion: Rectal misoprostol given as an adjunct to standard oxytocin was associated with significantly reduced intra- and post-operative blood loss following caesarean section, with a comparable side-effect profile. Given its low cost, thermal stability, and ease of administration, rectal misoprostol may have an important adjunctive role in PPH prevention in tertiary settings, and its use should continue to be explored in adequately powered randomized trials.
References
1.Streatfield PK, Arifeen SE, Al-Sabir A. Bangladesh Maternal Mortality and Health Care Survey 2010. Dhaka: NIPORT, MEASURE Evaluation, ICDDR, B; 2012:1–11.
2.Zuberi NF, Durocher J, Sikander R, Baber N, Blum J, Walraven G. Misoprostol in addition to routine treatment of postpartum hemorrhage: a hospital-based randomized-controlled trial in Karachi, Pakistan. BMC Pregnancy Childbirth 2008;8:40–45.
3.Dutta DC. Complications of the third stage of labour. In: Textbook of Obstetrics, 6th ed. New Delhi: Jaypee Brothers Medical Publishers; 2006:411–418.
4.World Health Organization. The prevention and management of postpartum haemorrhage: report of a technical working group. Geneva: WHO; 1990. Report No. WHO/MCH/90.7.
5.Arias F. Practical Guide to High-Risk Pregnancy and Delivery, 3rd ed. New Delhi: Elsevier India; 1993:433.
6.Walley RL. A double-blind placebo-controlled trial of oxytocin in the management of the third stage of labour. Br J Obstet Gynaecol 2000;107:111–115.
7.Sanghvi HCG, Rivers J, Stanton C. Prevention of postpartum haemorrhage: from research to practice. JHPIEGO Maternal and Neonatal Health Programme; 2004:1–65.
8.World Health Organization. WHO recommendations for the prevention and treatment of postpartum haemorrhage. Geneva: WHO; 2012.
9.DeCherney AH, Nathan L. Postpartum haemorrhage and the abnormal puerperium. In: Current Obstetric & Gynecologic Diagnosis & Treatment, 9th ed. New York: McGraw-Hill; 2003:533–544.
10.Prendiville W, Elbourne D, Chalmers I. The effects of routine oxytocic administration in the management of the third stage of labour: an overview of the evidence from controlled trials. Br J Obstet Gynaecol 1988;95:3–16.
11.Fletcher H, Mitchell S, Frederick J, Simeon D, Brown D. Intravaginal misoprostol versus dinoprostone as cervical ripening and labour-inducing agents. Obstet Gynecol 1994;83:244–247.
12.Hofmeyr GJ, Gülmezoglu AM. Vaginal misoprostol for cervical ripening and induction of labour. Cochrane Database Syst Rev 2003;(1):CD000941.
13.Caliskan E, Meydanli MM, Dilbaz B, Aykan B, Sonmezer M, Haberal A. Is rectal misoprostol really effective in the treatment of third stage of labour? A randomised controlled trial. Am J Obstet Gynecol 2002;187(4):1038–1045.
14.Ayyad I, Omar AA. Prevention of postpartum haemorrhage by rectal misoprostol: a randomised controlled trial. Middle East J Fam Med 2004;5(5):1–5.
15.Hofmeyr GJ, Ferreira S, Nikodem VC, Mangesi L, Singata M, Jafta Z. Misoprostol for treating postpartum haemorrhage: a randomised controlled trial. BMC Pregnancy Childbirth 2004;4(1):16.
16.Mousa HA, Alfirevic Z. Treatment for primary postpartum haemorrhage. Cochrane Database Syst Rev 2007;(1):CD003249.
17.Hofmeyr GJ, Gülmezoglu AM. Misoprostol for the prevention and treatment of postpartum haemorrhage. Best Pract Res Clin Obstet Gynaecol 2008;22(6):1025–1041.
18.Goudar SS, Chakraborty H, Edlavitch SA, et al. Variation in the postpartum haemorrhage rate in a clinical trial of oral misoprostol. J Matern Fetal Neonatal Med 2008;21(8):559–564.
19.Winikoff B, Dabash R, Durocher J, et al. Treatment of post-partum haemorrhage with sublingual misoprostol versus oxytocin in women not exposed to oxytocin during labour: a double-blind, randomised, non-inferiority trial. Lancet 2010;375(9710):210–216.
20.Quaiyum MA, Holston M, Hossain SAH, Bell S, Prata N. Scaling Up of Misoprostol for Prevention of Postpartum Haemorrhage in 29 Upazilas of Bangladesh. Dhaka: ICDDR,B; 2011. Special Publication No. 133. ISBN 978-984-551-323-4:1–24.
21.World Health Organization. Trends in Maternal Mortality: 1990 to 2008. Geneva: WHO, UNICEF, UNFPA and The World Bank; 2010.
22.Gynuity Health Projects. Postpartum Haemorrhage: Responding to the Challenge. New York: Gynuity; 2006.
23.AbouZahr C. Global burden of maternal death and disability. Br Med Bull 2003;67:1–11.
24.Maslovitz S, Barkai G, Lessing JB, Ziv A, Many A. Improved accuracy of postpartum blood loss estimation as assessed by simulation. Acta Obstet Gynecol Scand 2008;87(9):929–934.
25.Patel A, Goudar SS, Geller SE, et al. Drape estimation versus visual assessment for estimating postpartum haemorrhage. Int J Gynecol Obstet 2006;93:220–224.
26.Alfirevic Z, Blum J, Walraven G. Prevention of postpartum haemorrhage with misoprostol. Int J Gynecol Obstet 2007;99(Suppl 2):S198–S201.
27.International Confederation of Midwives, International Federation of Gynecology and Obstetrics. Prevention and Treatment of Post-partum Haemorrhage: New Advances for Low Resource Settings. ICM–FIGO Joint Statement; 2006.
28.World Health Organization. Unedited Report of the 19th Expert Committee on the Selection and Use of Essential Medicines. Geneva: WHO; 2011.
29.Mobeen N, Durocher J, Zuberi N, et al. Administration of misoprostol by trained traditional birth attendants to prevent postpartum haemorrhage in homebirths in Pakistan: a randomised placebo-controlled trial. BJOG 2011;118(3):353–361.
30.EngenderHealth. Preventing Postpartum Haemorrhage: Community-based Distribution of Misoprostol in Tangail District, Bangladesh. RESPOND Project / Mayer Hashi Project Brief No. 2. New York: EngenderHealth; 2010.
31.Naz H, Sarwar I, Fawad A, Nisa AU. Maternal morbidity and mortality due to primary postpartum haemorrhage — experience at Ayub Teaching Hospital, Abbottabad. J Ayub Med Coll Abbottabad 2008;20(2):59–65.
32.Rasheed N, Nasim N, Malik MA. Primary postpartum haemorrhage: comparison of effectiveness of misoprostol and syntocinon in prophylaxis. Professional Med J 2010;17(2):308–313.
33.Hazra S, Chilaka VN, Rajendran S, Konje JC. Massive postpartum haemorrhage as a cause of maternal morbidity in a large tertiary hospital. J Obstet Gynaecol 2004;24:519–520.
34.Gibbs RS. Clinical risk factors for puerperal infection. Obstet Gynecol 1980;55(5 Suppl):178S–184S.
35.American College of Obstetricians and Gynecologists. Postpartum haemorrhage. ACOG Educational Bulletin 1998;243.
36.Choo WL, Chua S, Chong YS, Yeoh CL. Correlation of change in uterine activity to blood loss in the third stage of labour. Obstet Gynaecol 1998;46:178–180.
37.Hofmeyr GJ, Gülmezoglu AM, Novikova N, Linder V, Ferreira S, Piaggio G. Postpartum haemorrhage after caesarean delivery: an analysis of risk factors. South Med J 2005;98(7):681–685.
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