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Misoprostol for miscarriage management in a woman with previous five cesarean deliveries: a case report and literature review

Authors AlSaad D, Al-Obaidly S, Abdulrouf P, Thomas B, Ahmed A, AlHail M

Received 12 January 2017

Accepted for publication 27 February 2017

Published 9 May 2017 Volume 2017:13 Pages 625—627

DOI https://doi.org/10.2147/TCRM.S132294

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Hoa Le

Peer reviewer comments 2

Editor who approved publication: Professor Garry Walsh


Doua AlSaad,1,2 Sawsan Alobaidly,3 Palli Abdulrouf,1 Binny Thomas,4,5 Afif Ahmed,1 Moza AlHail1

1Department of Pharmacy, Women’s Hospital, Hamad Medical Corporation, Doha, Qatar; 2Public Health Program, London School of Hygiene and Tropical Medicine, University of London, UK; 3Department of Obstetrics and Gynecology, Women’s Hospital, 4Clinical Support Service Unit, Hamad Medical Corporation, Doha, Qatar; 5Pharmacy and Life Sciences Research Institute, Robert Gordon University, Aberdeen, Scotland

Background: Misoprostol is an effective medical method for the management of pregnancy loss. However, data on its efficacy and safety in women with previous cesarean deliveries are limited.
Case presentation: We report a 36-year-old patient, gravida 11 para 6, with a diagnosis of missed miscarriage at 15 weeks of gestation. The patient had a significant obstetric history of previous five cesarean deliveries and uterine rupture. Following patient counseling about the medical and surgical options of managing her miscarriage, the patient opted for medical method. Low-dose misoprostol of 100 µg was inserted vaginally and repeated again after 6 hours. The patient had an uneventful complete miscarriage following the second dose of misoprostol. No uterine rupture, no extra vaginal bleeding, and no blood transfusion were observed.
Conclusion: We conclude that adopting a low-dose misoprostol protocol could be potentially safe and effective in managing second trimester missed miscarriage in women with repeated cesarean deliveries and/or uterine rupture history. Further studies are needed to confirm these results.

Keywords:
cesarean section, uterine rupture, prostaglandin E1, misoprostol, second trimester, miscarriage, abortion

Introduction

Uterine rupture is one of the most catastrophic obstetric events that is associated with a high incidence of morbidity and mortality. Complications of uterine rupture can affect not only the current pregnancy but also future fertility and future pregnancy outcomes. Uterine rupture is more common in grand multiparous women and in those with previous cesarean sections.1,2

The rate of cesarean section is increasing worldwide. Consequently, the rate of women with a previous cesarean section is increasing and the risk of uterine rupture is becoming higher. Although the incidence rate of uterine rupture in women with previously scarred uterus remains low (<1%), it is still considered as a threat for obstetricians.2

Misoprostol, a prostaglandin E1 (PGE1) analog, is widely used for the medical management of pregnancy loss. Misoprostol is inexpensive and stable at room temperature and can be given orally, vaginally, sublingually, buccally, or rectally. However, its use for managing miscarriage cases is still off-label.3

Different protocols are available for the medical management of first and second trimester miscarriages using misoprostol.2,4,5 However, a definite misoprostol protocol with good efficacy and safety for termination of pregnancy in women with more than one previous cesarean delivery is lacking.6,7 This case report presents our experience with the use of misoprostol for the management of second trimester miscarriage in a high-risk patient with previous five cesarean sections and uterine rupture.

Case presentation

A 36-year-old patient, gravida 11 para 6, with an ultrasound diagnosis of “missed miscarriage”, presented to our hospital with lower abdominal pain. She was 18+ gestational weeks by the last menstrual period (LMP) and 15+ gestational weeks by the ultrasound. Her previous obstetric history was significant for five lower segment cesarean sections (LSCS), four miscarriages, and one uterine rupture.

In her fifth pregnancy, she had a fetal demise at ~24 weeks of gestation, which was medically terminated. The patient was induced once; however, details of the medical induction were not available to review. The pregnancy termination was complicated by uterine rupture, which was managed by laparotomy, hysterotomy, and uterine rupture repair. Two of the five LSCS were done electively following the uterine rupture repair. The patient was healthy otherwise.

On physical examination, the patient was vitally stable, and the abdomen was soft with no tenderness on palpation. Pelvic transabdominal ultrasound was requested to rule out scar rupture. The myometrium–bladder interface was preserved, and scar thickness was 5 mm, which was normal for a previous cesarean section.8,9 All laboratory findings were within the normal ranges.

Conservative, medical, and surgical management options and the associated risks and benefits were discussed with the patient. She opted for medical management. Accordingly, a low-dose misoprostol of 100 μg was inserted vaginally in the posterior fornix, and 6 hours later, a repeat dose was given. Two hours after the second dose, the patient started to have pain and contractions. She was vitally stable. Her vaginal examination revealed an opened cervical os, and tissues were felt in the vagina; hence, the patient was shifted to labor and delivery suite for monitoring. After receiving adequate analgesia, a pelvic transabdominal ultrasound was done for scar thickness, which showed a thinning out of the myometrium at a scar site measuring 2 mm. Two hours later, the fetus was aborted that weighed 60 g, and 20 units of oxytocin infusion was started. One hour later, the placenta was delivered completely. The estimated blood loss was 180 mL. The patient was vitally stable all through with no extra bleeding.

The following day, the patient was stable with minimal vaginal bleeding and the repeated complete blood count (CBC) was normal; a prophylactic antibiotic amoxicillin–clavulanate 625 mg every 8 hours orally for 7 days was started. On Day 2 post miscarriage, the patient was discharged home with a follow-up appointment.

Discussion

To our knowledge, there are no published reports describing the outcomes of low-dose misoprostol in managing the second trimester missed miscarriage in women with previous five cesarean deliveries and a history of uterine rupture. Different protocols are available for the medical management of second trimester miscarriage in women with intact uterus.4,5 However, management options for cases with scarred uterus are limited and the potential risk for maternal complications is high.6,7 Hence, it is essential to report outcomes of management.

The optimal dose of misoprostol varies widely from 20 to 600 μg depending on the indication and the gestational age. In women with a scarred uterus, lower doses of misoprostol are recommended due to the risk of uterine rupture.5 In this case report, a low-dose misoprostol of 100 μg every 6 hours was considered to minimize the risk of uterine rupture while maintaining effectiveness.

Two systematic reviews published in 2009 evaluated the risk of uterine rupture in women with previous cesarean delivery who used misoprostol for the management of second trimester abortion.10,11 The risk of uterine rupture for women with or without previous cesarean delivery was similar. Nevertheless, there was insufficient information about uterine rupture risk in women with more than one previous cesarean delivery or with previous classical cesarean section, and information about optimum dosing regimen of misoprostol was missing. Accordingly, findings should be applied with caution.

A more recent systematic review and meta-analysis assessed the efficacy and safety of cervical ripening agents in the second trimester of pregnancy in patients with a previous cesarean delivery.12 The review concluded that PGE1 use was efficacious and was not associated with a significantly increased risk for uterine rupture among women with only one cesarean delivery. However, in women with two or more cesarean deliveries, the risk for uterine rupture increased significantly compared to that in women without a previous cesarean delivery, although the absolute risk appeared to be relatively small. The review results were limited by the variation in hospital protocols, doses, routes of administration, and nonuniform reporting of the number of previous cesarean deliveries (1 or >1), as well as the lack of information regarding the types of previous uterine scar. The use of misoprostol in two women with previous three cesarean deliveries was described by Alsibiani.13 One woman received 800 μg of oral misoprostol for the second trimester termination of pregnancy, while the other woman received 800 μg of vaginal misoprostol for the first trimester missed miscarriage. Favorable results were reported concerning a single high dose of misoprostol use as part of abortion management, but the safety could not be ascertained from that study.

Overall, limited data are available regarding misoprostol safety in women with previous multiple cesarean deliveries, and available evidences are mainly dependent on individual practice and/or underpowered retrospective studies. Furthermore, there are inconsistencies about the optimum regimen of misoprostol, and the optimum dose is yet to be established.

Conclusion

Favorable results were obtained with low-dose misoprostol for the second trimester missed miscarriage management in a woman with previous repeated cesarean deliveries and a history of uterine rupture. Safety concerns such as uterine rupture and excessive bleeding were not encountered. However, the effectiveness and safety cannot be ascertained based on this case report solely.

Acknowledgments

This work was supported by the Hamad Medical Research Center, Hamad Medical Corporation, Qatar. Waiver of informed consent was obtained from the Hamad Medical Research Center (reference number: 16112/16).

Disclosure

The authors report no conflicts of interest in this work.


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