Publication:
Naproxen suppository for perineal pain after vaginal delivery

dc.contributor.authorSkuntala Wilasrusmeeen_US
dc.contributor.authorApichart Chittachareonen_US
dc.contributor.authorSiriwan Jirasiritumen_US
dc.contributor.authorPrasong Srisangchaien_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherCenters for Disease Control (CDC), Thailand Field Stationen_US
dc.date.accessioned2018-07-12T02:47:49Z
dc.date.available2018-07-12T02:47:49Z
dc.date.issued2008-01-01en_US
dc.description.abstractObjective: To assess the effectiveness of rectal naproxen for reducing perineal pain after vaginal delivery. Methods: A double-blind randomized controlled trial of 142 post partum women randomly allocated to receive either naproxen (71 patients) or placebo (71 patients) suppositories. The first dose was given immediately after complete perineal suturing, while the second dose was given 6 hours post partum. The validated Thai short-form McGill pain questionnaire was used to evaluate perineal pain at 0, 6, and 24 hours post partum. Pain scores were analyzed using the unpaired t test. Results: Pain scores at 6 and 24 hours for women in the naproxen group were significantly lower compared with women in the placebo group (6.4 and 2.3 vs 18.4 and 5.5; P < 0.001). No side effects with naproxen were found. Conclusions: Rectal naproxen is effective and safe for reducing perineal pain after vaginal delivery. © 2008 International Federation of Genecology and Obstetrics.en_US
dc.identifier.citationInternational Journal of Gynecology and Obstetrics. Vol.102, No.1 (2008), 19-22en_US
dc.identifier.doi10.1016/j.ijgo.2008.01.015en_US
dc.identifier.issn00207292en_US
dc.identifier.other2-s2.0-46549083844en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/19809
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=46549083844&origin=inwarden_US
dc.subjectMedicineen_US
dc.titleNaproxen suppository for perineal pain after vaginal deliveryen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=46549083844&origin=inwarden_US

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