The effect of hyoscine butylbromide on the first stage of labour in term pregnancies

Objective  To determine whether hyoscine butylbromide shortens the first stage of labour, without an increase in maternal or neonatal complications. Design  Randomised, double‐blinded, controlled trial. Setting  The Antenatal clinics and Labour and Delivery ward of the University Hospital of the Wes...

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Veröffentlicht in:BJOG : an international journal of obstetrics and gynaecology 2007-12, Vol.114 (12), p.1542-1546
Hauptverfasser: Samuels, LA, Christie, L, Roberts‐Gittens, B, Fletcher, H, Frederick, J
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container_end_page 1546
container_issue 12
container_start_page 1542
container_title BJOG : an international journal of obstetrics and gynaecology
container_volume 114
creator Samuels, LA
Christie, L
Roberts‐Gittens, B
Fletcher, H
Frederick, J
description Objective  To determine whether hyoscine butylbromide shortens the first stage of labour, without an increase in maternal or neonatal complications. Design  Randomised, double‐blinded, controlled trial. Setting  The Antenatal clinics and Labour and Delivery ward of the University Hospital of the West Indies, Kingston, Jamaica. Population  Women in spontaneous labour at term. Methods  Either drug or placebo was given intravenously once the women entered active labour. Main outcome measures  The duration of the first stage of labour. Secondary outcomes included comparisons of the duration of the second and third stages of labour, blood loss at delivery, rate of caesarean section, and APGAR scores in the neonates between the two groups. Results  A total of 129 women yielded data for analysis. Of these, 69 women received the placebo and 60 received hyoscine butylbromide. The mean time for the first stage in the control group was 228 minutes, compared with 156 minutes in the drug group, representing a decrease of 31.7% (P = 0.001). There was no significant change in the duration of the second and third stages of labour, and no difference in blood loss or in APGAR scores. There was a slight (but statistically insignificant) increase in the caesarean section rate. Conclusion  Hyoscine butylbromide is effective in significantly reducing the duration of the first stage of labour, and it is not associated with any obvious adverse outcomes in mother or neonate.
doi_str_mv 10.1111/j.1471-0528.2007.01497.x
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Design  Randomised, double‐blinded, controlled trial. Setting  The Antenatal clinics and Labour and Delivery ward of the University Hospital of the West Indies, Kingston, Jamaica. Population  Women in spontaneous labour at term. Methods  Either drug or placebo was given intravenously once the women entered active labour. Main outcome measures  The duration of the first stage of labour. Secondary outcomes included comparisons of the duration of the second and third stages of labour, blood loss at delivery, rate of caesarean section, and APGAR scores in the neonates between the two groups. Results  A total of 129 women yielded data for analysis. Of these, 69 women received the placebo and 60 received hyoscine butylbromide. The mean time for the first stage in the control group was 228 minutes, compared with 156 minutes in the drug group, representing a decrease of 31.7% (P = 0.001). There was no significant change in the duration of the second and third stages of labour, and no difference in blood loss or in APGAR scores. There was a slight (but statistically insignificant) increase in the caesarean section rate. Conclusion  Hyoscine butylbromide is effective in significantly reducing the duration of the first stage of labour, and it is not associated with any obvious adverse outcomes in mother or neonate.</description><identifier>ISSN: 1470-0328</identifier><identifier>EISSN: 1471-0528</identifier><identifier>DOI: 10.1111/j.1471-0528.2007.01497.x</identifier><identifier>PMID: 17903230</identifier><identifier>CODEN: BIOGFQ</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Apgar Score ; Biological and medical sciences ; Buscopan ; Butylscopolammonium Bromide - therapeutic use ; Cesarean Section - statistics &amp; numerical data ; Childbirth &amp; labor ; Clinical outcomes ; Clinical trials ; Double-Blind Method ; Drug therapy ; Female ; first stage ; Gynecology. Andrology. Obstetrics ; Humans ; Hyoscine ; Labor Stage, First - drug effects ; Labor, Induced - methods ; labour ; Medical sciences ; Obstetrics ; Parasympatholytics - therapeutic use ; Postpartum Hemorrhage - chemically induced ; Pregnancy ; Pregnancy Outcome ; shortens ; Time Factors</subject><ispartof>BJOG : an international journal of obstetrics and gynaecology, 2007-12, Vol.114 (12), p.1542-1546</ispartof><rights>RCOG 2007 BJOG An International Journal of Obstetrics and Gynaecology</rights><rights>2008 INIST-CNRS</rights><rights>2007 The Authors Journal compilation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4247-1a8d85c578d6000a7a07dab9c13362f8ce4de04fdeaa7c8276c5ec5b8031baf73</citedby><cites>FETCH-LOGICAL-c4247-1a8d85c578d6000a7a07dab9c13362f8ce4de04fdeaa7c8276c5ec5b8031baf73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1471-0528.2007.01497.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1471-0528.2007.01497.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19438441$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17903230$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Samuels, LA</creatorcontrib><creatorcontrib>Christie, L</creatorcontrib><creatorcontrib>Roberts‐Gittens, B</creatorcontrib><creatorcontrib>Fletcher, H</creatorcontrib><creatorcontrib>Frederick, J</creatorcontrib><title>The effect of hyoscine butylbromide on the first stage of labour in term pregnancies</title><title>BJOG : an international journal of obstetrics and gynaecology</title><addtitle>BJOG</addtitle><description>Objective  To determine whether hyoscine butylbromide shortens the first stage of labour, without an increase in maternal or neonatal complications. Design  Randomised, double‐blinded, controlled trial. Setting  The Antenatal clinics and Labour and Delivery ward of the University Hospital of the West Indies, Kingston, Jamaica. Population  Women in spontaneous labour at term. Methods  Either drug or placebo was given intravenously once the women entered active labour. Main outcome measures  The duration of the first stage of labour. Secondary outcomes included comparisons of the duration of the second and third stages of labour, blood loss at delivery, rate of caesarean section, and APGAR scores in the neonates between the two groups. Results  A total of 129 women yielded data for analysis. Of these, 69 women received the placebo and 60 received hyoscine butylbromide. The mean time for the first stage in the control group was 228 minutes, compared with 156 minutes in the drug group, representing a decrease of 31.7% (P = 0.001). There was no significant change in the duration of the second and third stages of labour, and no difference in blood loss or in APGAR scores. There was a slight (but statistically insignificant) increase in the caesarean section rate. Conclusion  Hyoscine butylbromide is effective in significantly reducing the duration of the first stage of labour, and it is not associated with any obvious adverse outcomes in mother or neonate.</description><subject>Apgar Score</subject><subject>Biological and medical sciences</subject><subject>Buscopan</subject><subject>Butylscopolammonium Bromide - therapeutic use</subject><subject>Cesarean Section - statistics &amp; numerical data</subject><subject>Childbirth &amp; labor</subject><subject>Clinical outcomes</subject><subject>Clinical trials</subject><subject>Double-Blind Method</subject><subject>Drug therapy</subject><subject>Female</subject><subject>first stage</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Hyoscine</subject><subject>Labor Stage, First - drug effects</subject><subject>Labor, Induced - methods</subject><subject>labour</subject><subject>Medical sciences</subject><subject>Obstetrics</subject><subject>Parasympatholytics - therapeutic use</subject><subject>Postpartum Hemorrhage - chemically induced</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>shortens</subject><subject>Time Factors</subject><issn>1470-0328</issn><issn>1471-0528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1P3DAQhq0KVL76FyoLqb0ljD8SO4ceWlSgFRKX5Ww5zhiyysdiJyr773HYFUg94YtHM8-MXj2EUAY5S-9inTOpWAYF1zkHUDkwWan8-RM5fhscvNaQgeD6iJzEuAZgJQfxmRwxVaW2gGOyWj0iRe_RTXT09HE7RtcOSOt52nZ1GPu2QToOdEqYb0OcaJzsAy5sZ-txDrRNQww93QR8GOzgWoxn5NDbLuKX_X9K7q9-ry5vstu76z-XP28zJ7lUGbO60YUrlG5KALDKgmpsXTkmRMm9digbBOkbtFY5zVXpCnRFrUGw2nolTsn33d1NGJ9mjJPp2-iw6-yA4xxNqaWudLWA5_-B6xR9SNkM50UJBVRlgvQOcmGMMaA3m9D2NmwNA7NoN2uz2DWLXbNoN6_azXNa_bq_P9c9Nu-Le88J-LYHbHS282ERFd-5SgotJUvcjx33r-1w--EA5tffu6USL6mYnWs</recordid><startdate>200712</startdate><enddate>200712</enddate><creator>Samuels, LA</creator><creator>Christie, L</creator><creator>Roberts‐Gittens, B</creator><creator>Fletcher, H</creator><creator>Frederick, J</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>ASE</scope><scope>FPQ</scope><scope>K6X</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>200712</creationdate><title>The effect of hyoscine butylbromide on the first stage of labour in term pregnancies</title><author>Samuels, LA ; Christie, L ; Roberts‐Gittens, B ; Fletcher, H ; Frederick, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4247-1a8d85c578d6000a7a07dab9c13362f8ce4de04fdeaa7c8276c5ec5b8031baf73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Apgar Score</topic><topic>Biological and medical sciences</topic><topic>Buscopan</topic><topic>Butylscopolammonium Bromide - therapeutic use</topic><topic>Cesarean Section - statistics &amp; numerical data</topic><topic>Childbirth &amp; labor</topic><topic>Clinical outcomes</topic><topic>Clinical trials</topic><topic>Double-Blind Method</topic><topic>Drug therapy</topic><topic>Female</topic><topic>first stage</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Hyoscine</topic><topic>Labor Stage, First - drug effects</topic><topic>Labor, Induced - methods</topic><topic>labour</topic><topic>Medical sciences</topic><topic>Obstetrics</topic><topic>Parasympatholytics - therapeutic use</topic><topic>Postpartum Hemorrhage - chemically induced</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>shortens</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Samuels, LA</creatorcontrib><creatorcontrib>Christie, L</creatorcontrib><creatorcontrib>Roberts‐Gittens, B</creatorcontrib><creatorcontrib>Fletcher, H</creatorcontrib><creatorcontrib>Frederick, J</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>British Nursing Index</collection><collection>British Nursing Index (BNI) (1985 to Present)</collection><collection>British Nursing Index</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Samuels, LA</au><au>Christie, L</au><au>Roberts‐Gittens, B</au><au>Fletcher, H</au><au>Frederick, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The effect of hyoscine butylbromide on the first stage of labour in term pregnancies</atitle><jtitle>BJOG : an international journal of obstetrics and gynaecology</jtitle><addtitle>BJOG</addtitle><date>2007-12</date><risdate>2007</risdate><volume>114</volume><issue>12</issue><spage>1542</spage><epage>1546</epage><pages>1542-1546</pages><issn>1470-0328</issn><eissn>1471-0528</eissn><coden>BIOGFQ</coden><abstract>Objective  To determine whether hyoscine butylbromide shortens the first stage of labour, without an increase in maternal or neonatal complications. Design  Randomised, double‐blinded, controlled trial. Setting  The Antenatal clinics and Labour and Delivery ward of the University Hospital of the West Indies, Kingston, Jamaica. Population  Women in spontaneous labour at term. Methods  Either drug or placebo was given intravenously once the women entered active labour. Main outcome measures  The duration of the first stage of labour. Secondary outcomes included comparisons of the duration of the second and third stages of labour, blood loss at delivery, rate of caesarean section, and APGAR scores in the neonates between the two groups. Results  A total of 129 women yielded data for analysis. Of these, 69 women received the placebo and 60 received hyoscine butylbromide. The mean time for the first stage in the control group was 228 minutes, compared with 156 minutes in the drug group, representing a decrease of 31.7% (P = 0.001). There was no significant change in the duration of the second and third stages of labour, and no difference in blood loss or in APGAR scores. There was a slight (but statistically insignificant) increase in the caesarean section rate. Conclusion  Hyoscine butylbromide is effective in significantly reducing the duration of the first stage of labour, and it is not associated with any obvious adverse outcomes in mother or neonate.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>17903230</pmid><doi>10.1111/j.1471-0528.2007.01497.x</doi><tpages>5</tpages></addata></record>
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subjects Apgar Score
Biological and medical sciences
Buscopan
Butylscopolammonium Bromide - therapeutic use
Cesarean Section - statistics & numerical data
Childbirth & labor
Clinical outcomes
Clinical trials
Double-Blind Method
Drug therapy
Female
first stage
Gynecology. Andrology. Obstetrics
Humans
Hyoscine
Labor Stage, First - drug effects
Labor, Induced - methods
labour
Medical sciences
Obstetrics
Parasympatholytics - therapeutic use
Postpartum Hemorrhage - chemically induced
Pregnancy
Pregnancy Outcome
shortens
Time Factors
title The effect of hyoscine butylbromide on the first stage of labour in term pregnancies
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