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Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study
BACKGROUND: Oral misoprostol as an induction of labour (IOL) agent is rapidly gaining popularity in resource-limited settings because it is cheap, stable at ambient temperatures, and logistically easier to administer compared to dinoprostone and oxytocin. We aim to investigate the safety and effecti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591556/ https://www.ncbi.nlm.nih.gov/pubmed/28886702 http://dx.doi.org/10.1186/s12884-017-1483-5 |
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author | Morris, Marilyn Bolnga, John W. Verave, Ovoi Aipit, Jimmy Rero, Allanie Laman, Moses |
author_facet | Morris, Marilyn Bolnga, John W. Verave, Ovoi Aipit, Jimmy Rero, Allanie Laman, Moses |
author_sort | Morris, Marilyn |
collection | PubMed |
description | BACKGROUND: Oral misoprostol as an induction of labour (IOL) agent is rapidly gaining popularity in resource-limited settings because it is cheap, stable at ambient temperatures, and logistically easier to administer compared to dinoprostone and oxytocin. We aim to investigate the safety and effectiveness of a regimen of oral misoprostol in Papua New Guinean women undergoing IOL. METHODS: As part of a prospective dose escalation study conducted at Modilon Hospital in Papua New Guinea, women with a singleton pregnancy in cephalic presentation and an unfavourable cervix who gave written informed consent were administered oral misoprostol, commencing at 25mcg once every 2 h for 4 doses and increased to 50mcg once every 2 h for 8 doses within 24 h. The primary outcomes studied were i) the proportion of women delivering within 24 h of oral misoprostol administration, and ii) rates of maternal and perinatal severe adverse events. RESULTS: Of 6167 labour ward screened admissions, 209 women (3%) fulfilled the study inclusion criteria and underwent IOL. Overall, 74% (155/209 [95% confidence interval 67.6–79.9]) delivered within 24 h. Most women (90%; 188/209; 95% CI [84.9–93.5]) delivered vaginally with 86% (180/209) having a good outcome for both the mother and baby. Of the 10% (21/209) who failed IOL and underwent caesarean section, a significant proportion of their babies were admitted to special-care nursery compared to babies delivered vaginally (20/21 [95%] versus 8/188 [4%]; Fisher Exact test P < 0.001), but their perinatal mortality rate was not significantly higher (1/21 [5%] versus 2/188 [1%]; P = 0.30). The only maternal death was not study related and occurred in a patient with post-partum haemorrhage, 15 h post-delivery. CONCLUSION: The oral misoprostol regimen for IOL described in the present study is safe, effective and logistically feasible to administer in a resource-limited setting. |
format | Online Article Text |
id | pubmed-5591556 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55915562017-09-13 Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study Morris, Marilyn Bolnga, John W. Verave, Ovoi Aipit, Jimmy Rero, Allanie Laman, Moses BMC Pregnancy Childbirth Research Article BACKGROUND: Oral misoprostol as an induction of labour (IOL) agent is rapidly gaining popularity in resource-limited settings because it is cheap, stable at ambient temperatures, and logistically easier to administer compared to dinoprostone and oxytocin. We aim to investigate the safety and effectiveness of a regimen of oral misoprostol in Papua New Guinean women undergoing IOL. METHODS: As part of a prospective dose escalation study conducted at Modilon Hospital in Papua New Guinea, women with a singleton pregnancy in cephalic presentation and an unfavourable cervix who gave written informed consent were administered oral misoprostol, commencing at 25mcg once every 2 h for 4 doses and increased to 50mcg once every 2 h for 8 doses within 24 h. The primary outcomes studied were i) the proportion of women delivering within 24 h of oral misoprostol administration, and ii) rates of maternal and perinatal severe adverse events. RESULTS: Of 6167 labour ward screened admissions, 209 women (3%) fulfilled the study inclusion criteria and underwent IOL. Overall, 74% (155/209 [95% confidence interval 67.6–79.9]) delivered within 24 h. Most women (90%; 188/209; 95% CI [84.9–93.5]) delivered vaginally with 86% (180/209) having a good outcome for both the mother and baby. Of the 10% (21/209) who failed IOL and underwent caesarean section, a significant proportion of their babies were admitted to special-care nursery compared to babies delivered vaginally (20/21 [95%] versus 8/188 [4%]; Fisher Exact test P < 0.001), but their perinatal mortality rate was not significantly higher (1/21 [5%] versus 2/188 [1%]; P = 0.30). The only maternal death was not study related and occurred in a patient with post-partum haemorrhage, 15 h post-delivery. CONCLUSION: The oral misoprostol regimen for IOL described in the present study is safe, effective and logistically feasible to administer in a resource-limited setting. BioMed Central 2017-09-08 /pmc/articles/PMC5591556/ /pubmed/28886702 http://dx.doi.org/10.1186/s12884-017-1483-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Morris, Marilyn Bolnga, John W. Verave, Ovoi Aipit, Jimmy Rero, Allanie Laman, Moses Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title | Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title_full | Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title_fullStr | Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title_full_unstemmed | Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title_short | Safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
title_sort | safety and effectiveness of oral misoprostol for induction of labour in a resource-limited setting: a dose escalation study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5591556/ https://www.ncbi.nlm.nih.gov/pubmed/28886702 http://dx.doi.org/10.1186/s12884-017-1483-5 |
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