Abstract

Background: Misoprostol is a synthetic prostaglandin E1 that induces cervical effacement and uterine contractions at all gestational ages, thus facilitating uterine evacuation and pregnancy termination. Successful medical evacuation of spontaneous miscarriage with minimal adverse effects can be performed using misoprostol-only regimen if given as indicated and if the administered dose, frequency of the dosage, and number of total doses are appropriate. Aim: To conduct a drug use evaluation by investigating indications, appropriateness of dosing, and clinical outcome of misoprostol-only regimen when used for medical evacuation of spontaneous miscarriage at the Women's Hospital in Doha, Qatar. Materials and methods: A retrospective descriptive drug use evaluation was conducted on women with spontaneous miscarriage who received misoprostol for medical evacuation during August 2013. The current practice at the Women's Hospital was compared with the recommendation from the World Health Organization (WHO). Patients were stratified into three groups based on weeks of amenorrhea. Results: A total of 107 patients received misoprostol during August 2013, of which 33 (31%) were included in the study. In these patients, the main indication for misoprostol use was missed miscarriage (54.5%). In the group of patients at ≤ 9 weeks of gestation, 80% received an initial dose of 800 μg, 80% received frequency within the WHO recommendation, and the majority had surgical evacuation (80%). In the group of patients at 10–12 weeks of gestation, more than 80% received an initial dose of 800 μg, 6% received frequency within the WHO recommendation, and more than 75% had successful medical evacuation. In the group of patients at 13–22 weeks of gestation, more than 80% received an initial dose of 400 μg, more than 80% received frequency within the WHO recommendation, and 54% had successful medical evacuation. Overall, more than 70% of the patients received ≤ 3 total doses of misoprostol and more than 60% had successful medical evacuation as a clinical outcome. Conclusions: Despite the current practice at the Women's Hospital not always being in accordance with the WHO recommendation, successful medical evacuation was achieved in most patients.

Highlights

  • Miscarriage is termination of pregnancy before 20 weeks of gestation with a fetus/embryo weighing # 500 g.1 – 4 Pregnancy termination can be either spontaneous or induced.[1,2] Spontaneous miscarriages are categorized as threatened miscarriage, inevitable miscarriage, incomplete miscarriage, missed miscarriage, septic miscarriage, and complete miscarriage.[2]

  • In the group of patients at 13 –22 weeks of gestation, more than 80% received an initial dose of 400 mg, more than 80% received frequency within the World Health Organization (WHO) recommendation, and 54% had successful medical evacuation

  • In the Women’s Hospital (WH) in Doha, Qatar, misoprostolonly regimen is widely used in the first- and secondtrimester for medical evacuation of spontaneous miscarriage

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Summary

Introduction

Miscarriage is termination of pregnancy before 20 weeks of gestation with a fetus/embryo weighing # 500 g.1 – 4 Pregnancy termination can be either spontaneous or induced.[1,2] Spontaneous miscarriages are categorized as threatened miscarriage, inevitable miscarriage, incomplete miscarriage, missed miscarriage, septic miscarriage, and complete miscarriage.[2]. Aim: To conduct a drug use evaluation by investigating indications, appropriateness of dosing, and clinical outcome of misoprostol-only regimen when used for medical evacuation of spontaneous miscarriage at the Women’s Hospital in Doha, Qatar. Results: A total of 107 patients received misoprostol during August 2013, of which 33 (31%) were included in the study In these patients, the main indication for misoprostol use was missed miscarriage (54.5%). In the group of patients at #9 weeks of gestation, 80% received an initial dose of 800 mg, 80% received frequency within the WHO recommendation, and the majority had surgical evacuation (80%). In the group of patients at 10 –12 weeks of gestation, more than 80% received an initial dose of 800 mg, 6% received frequency within the WHO recommendation, and more than 75% had successful

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