Loading…
Timing of birth for women with a twin pregnancy at term: a randomised controlled trial
There is a well recognized risk of complications for both women and infants of a twin pregnancy, increasing beyond 37 weeks gestation. Preterm birth prior to 37 weeks gestation is a recognized complication of a twin pregnancy, however, up to 50% of twins will be born after this time. The aims of thi...
Saved in:
Published in: | BMC pregnancy and childbirth 2010-10, Vol.10 (1), p.68-68, Article 68 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3 |
---|---|
cites | cdi_FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3 |
container_end_page | 68 |
container_issue | 1 |
container_start_page | 68 |
container_title | BMC pregnancy and childbirth |
container_volume | 10 |
creator | Dodd, Jodie M Crowther, Caroline A Haslam, Ross R Robinson, Jeffrey S |
description | There is a well recognized risk of complications for both women and infants of a twin pregnancy, increasing beyond 37 weeks gestation. Preterm birth prior to 37 weeks gestation is a recognized complication of a twin pregnancy, however, up to 50% of twins will be born after this time. The aims of this randomised trial are to assess whether elective birth at 37 weeks gestation compared with standard care in women with a twin pregnancy affects the risk of perinatal death, and serious infant complications.
Multicentred randomised trial.
women with a twin pregnancy at 366 weeks or more without contraindication to continuation of pregnancy. Trial Entry & Randomisation: Following written informed consent, eligible women will be randomised from 36+6 weeks gestation. The randomisation schedule uses balanced variable blocks, with stratification for centre of birth and planned mode of birth. Women will be randomised to either elective birth or standard care. Treatment Schedules: Women allocated to the elective birth group will be planned for elective birth from 37 weeks gestation. Where the plan is for vaginal birth, this will involve induction of labour. Where the plan is for caesarean birth, this will involve elective caesarean section. For women allocated to standard care, birth will be planned for 38 weeks gestation or later. Where the plan is for vaginal birth, this will involve either awaiting the spontaneous onset of labour, or induction of labour if required. Where the plan is for caesarean birth, this will involve elective caesarean section (after 38 and as close to 39 weeks as possible). Primary Study Outcome: A composite of perinatal mortality or serious neonatal morbidity.
460 women with a twin pregnancy to show a reduction in the composite outcome from 16.3% to 6.7% with adjustment for the clustering of twin infants within mothers (p = 0.05, 80% power).
This is a protocol for a randomised trial, the findings of which will contribute information about the optimal time of birth for women with an uncomplicated multiple pregnancy at and beyond 37 weeks gestation. |
doi_str_mv | 10.1186/1471-2393-10-68 |
format | article |
fullrecord | <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_783a644a5ad84886bd577c9ff05036aa</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_783a644a5ad84886bd577c9ff05036aa</doaj_id><sourcerecordid>954598984</sourcerecordid><originalsourceid>FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3</originalsourceid><addsrcrecordid>eNqFkktvEzEUhS0EoqWwZocsNl0N9fvBAolWPCpVYlPYWndm7NTRjB08E6L-exxSogZRdeXre48-Hd9jhF5T8o5So86o0LRh3PKGkkaZJ-h433l6rz5CL6ZpSQjVRpLn6IgRq7k19hj9uI5jTAucA25jmW9wyAVv8ugT3sR6BTxvYsKr4hcJUneLYcazL-P7OimQ-jzGyfe4y2kueRhqOZcIw0v0LMAw-Vd35wn6_vnT9cXX5urbl8uLj1dNqwSfG9taDr3mUgbvwVsNwDhVqlXUeCuk4oqHnnnQFiylIgCrIi0J8aETLPATdLnj9hmWblXiCOXWZYjuTyOXhYMyx27wThsOSgiQ0BthjGp7qXVnQyCScAVQWR92rNW6HX3f-fokGA6gh5MUb9wi_3LMakMZr4DzHaCN-QHA4aTLo9tm5LYZOUqcMhVyeuei5J9rP82ubrjzwwDJ5_XkrBSyJmfEo0qthORKMFKVb_9RLvO6pBqMs4RRzZiiVXS2E3UlT1PxYW-8Gtt-tv9YfXN_YXv939_FfwN7es9w</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>902172261</pqid></control><display><type>article</type><title>Timing of birth for women with a twin pregnancy at term: a randomised controlled trial</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Dodd, Jodie M ; Crowther, Caroline A ; Haslam, Ross R ; Robinson, Jeffrey S</creator><creatorcontrib>Dodd, Jodie M ; Crowther, Caroline A ; Haslam, Ross R ; Robinson, Jeffrey S</creatorcontrib><description>There is a well recognized risk of complications for both women and infants of a twin pregnancy, increasing beyond 37 weeks gestation. Preterm birth prior to 37 weeks gestation is a recognized complication of a twin pregnancy, however, up to 50% of twins will be born after this time. The aims of this randomised trial are to assess whether elective birth at 37 weeks gestation compared with standard care in women with a twin pregnancy affects the risk of perinatal death, and serious infant complications.
Multicentred randomised trial.
women with a twin pregnancy at 366 weeks or more without contraindication to continuation of pregnancy. Trial Entry & Randomisation: Following written informed consent, eligible women will be randomised from 36+6 weeks gestation. The randomisation schedule uses balanced variable blocks, with stratification for centre of birth and planned mode of birth. Women will be randomised to either elective birth or standard care. Treatment Schedules: Women allocated to the elective birth group will be planned for elective birth from 37 weeks gestation. Where the plan is for vaginal birth, this will involve induction of labour. Where the plan is for caesarean birth, this will involve elective caesarean section. For women allocated to standard care, birth will be planned for 38 weeks gestation or later. Where the plan is for vaginal birth, this will involve either awaiting the spontaneous onset of labour, or induction of labour if required. Where the plan is for caesarean birth, this will involve elective caesarean section (after 38 and as close to 39 weeks as possible). Primary Study Outcome: A composite of perinatal mortality or serious neonatal morbidity.
460 women with a twin pregnancy to show a reduction in the composite outcome from 16.3% to 6.7% with adjustment for the clustering of twin infants within mothers (p = 0.05, 80% power).
This is a protocol for a randomised trial, the findings of which will contribute information about the optimal time of birth for women with an uncomplicated multiple pregnancy at and beyond 37 weeks gestation.</description><identifier>ISSN: 1471-2393</identifier><identifier>EISSN: 1471-2393</identifier><identifier>DOI: 10.1186/1471-2393-10-68</identifier><identifier>PMID: 20973989</identifier><language>eng</language><publisher>England: BioMed Central</publisher><subject>Cesarean Section ; Elective Surgical Procedures ; Female ; Gestational Age ; Humans ; Labor, Induced ; Labor, Obstetric ; Patient Selection ; Pregnancy ; Pregnancy Outcome ; Pregnancy, Multiple ; Studies ; Study Protocol ; Term Birth ; Twins ; Womens health</subject><ispartof>BMC pregnancy and childbirth, 2010-10, Vol.10 (1), p.68-68, Article 68</ispartof><rights>2010 Dodd et al; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright ©2010 Dodd et al; licensee BioMed Central Ltd. 2010 Dodd et al; licensee BioMed Central Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3</citedby><cites>FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978123/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/902172261?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20973989$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dodd, Jodie M</creatorcontrib><creatorcontrib>Crowther, Caroline A</creatorcontrib><creatorcontrib>Haslam, Ross R</creatorcontrib><creatorcontrib>Robinson, Jeffrey S</creatorcontrib><title>Timing of birth for women with a twin pregnancy at term: a randomised controlled trial</title><title>BMC pregnancy and childbirth</title><addtitle>BMC Pregnancy Childbirth</addtitle><description>There is a well recognized risk of complications for both women and infants of a twin pregnancy, increasing beyond 37 weeks gestation. Preterm birth prior to 37 weeks gestation is a recognized complication of a twin pregnancy, however, up to 50% of twins will be born after this time. The aims of this randomised trial are to assess whether elective birth at 37 weeks gestation compared with standard care in women with a twin pregnancy affects the risk of perinatal death, and serious infant complications.
Multicentred randomised trial.
women with a twin pregnancy at 366 weeks or more without contraindication to continuation of pregnancy. Trial Entry & Randomisation: Following written informed consent, eligible women will be randomised from 36+6 weeks gestation. The randomisation schedule uses balanced variable blocks, with stratification for centre of birth and planned mode of birth. Women will be randomised to either elective birth or standard care. Treatment Schedules: Women allocated to the elective birth group will be planned for elective birth from 37 weeks gestation. Where the plan is for vaginal birth, this will involve induction of labour. Where the plan is for caesarean birth, this will involve elective caesarean section. For women allocated to standard care, birth will be planned for 38 weeks gestation or later. Where the plan is for vaginal birth, this will involve either awaiting the spontaneous onset of labour, or induction of labour if required. Where the plan is for caesarean birth, this will involve elective caesarean section (after 38 and as close to 39 weeks as possible). Primary Study Outcome: A composite of perinatal mortality or serious neonatal morbidity.
460 women with a twin pregnancy to show a reduction in the composite outcome from 16.3% to 6.7% with adjustment for the clustering of twin infants within mothers (p = 0.05, 80% power).
This is a protocol for a randomised trial, the findings of which will contribute information about the optimal time of birth for women with an uncomplicated multiple pregnancy at and beyond 37 weeks gestation.</description><subject>Cesarean Section</subject><subject>Elective Surgical Procedures</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Labor, Induced</subject><subject>Labor, Obstetric</subject><subject>Patient Selection</subject><subject>Pregnancy</subject><subject>Pregnancy Outcome</subject><subject>Pregnancy, Multiple</subject><subject>Studies</subject><subject>Study Protocol</subject><subject>Term Birth</subject><subject>Twins</subject><subject>Womens health</subject><issn>1471-2393</issn><issn>1471-2393</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqFkktvEzEUhS0EoqWwZocsNl0N9fvBAolWPCpVYlPYWndm7NTRjB08E6L-exxSogZRdeXre48-Hd9jhF5T8o5So86o0LRh3PKGkkaZJ-h433l6rz5CL6ZpSQjVRpLn6IgRq7k19hj9uI5jTAucA25jmW9wyAVv8ugT3sR6BTxvYsKr4hcJUneLYcazL-P7OimQ-jzGyfe4y2kueRhqOZcIw0v0LMAw-Vd35wn6_vnT9cXX5urbl8uLj1dNqwSfG9taDr3mUgbvwVsNwDhVqlXUeCuk4oqHnnnQFiylIgCrIi0J8aETLPATdLnj9hmWblXiCOXWZYjuTyOXhYMyx27wThsOSgiQ0BthjGp7qXVnQyCScAVQWR92rNW6HX3f-fokGA6gh5MUb9wi_3LMakMZr4DzHaCN-QHA4aTLo9tm5LYZOUqcMhVyeuei5J9rP82ubrjzwwDJ5_XkrBSyJmfEo0qthORKMFKVb_9RLvO6pBqMs4RRzZiiVXS2E3UlT1PxYW-8Gtt-tv9YfXN_YXv939_FfwN7es9w</recordid><startdate>20101025</startdate><enddate>20101025</enddate><creator>Dodd, Jodie M</creator><creator>Crowther, Caroline A</creator><creator>Haslam, Ross R</creator><creator>Robinson, Jeffrey S</creator><general>BioMed Central</general><general>BioMed Central Ltd</general><general>BMC</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>7U1</scope><scope>7U2</scope><scope>C1K</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20101025</creationdate><title>Timing of birth for women with a twin pregnancy at term: a randomised controlled trial</title><author>Dodd, Jodie M ; Crowther, Caroline A ; Haslam, Ross R ; Robinson, Jeffrey S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Cesarean Section</topic><topic>Elective Surgical Procedures</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Labor, Induced</topic><topic>Labor, Obstetric</topic><topic>Patient Selection</topic><topic>Pregnancy</topic><topic>Pregnancy Outcome</topic><topic>Pregnancy, Multiple</topic><topic>Studies</topic><topic>Study Protocol</topic><topic>Term Birth</topic><topic>Twins</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dodd, Jodie M</creatorcontrib><creatorcontrib>Crowther, Caroline A</creatorcontrib><creatorcontrib>Haslam, Ross R</creatorcontrib><creatorcontrib>Robinson, Jeffrey S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>Risk Abstracts</collection><collection>Safety Science and Risk</collection><collection>Environmental Sciences and Pollution Management</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals</collection><jtitle>BMC pregnancy and childbirth</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dodd, Jodie M</au><au>Crowther, Caroline A</au><au>Haslam, Ross R</au><au>Robinson, Jeffrey S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Timing of birth for women with a twin pregnancy at term: a randomised controlled trial</atitle><jtitle>BMC pregnancy and childbirth</jtitle><addtitle>BMC Pregnancy Childbirth</addtitle><date>2010-10-25</date><risdate>2010</risdate><volume>10</volume><issue>1</issue><spage>68</spage><epage>68</epage><pages>68-68</pages><artnum>68</artnum><issn>1471-2393</issn><eissn>1471-2393</eissn><abstract>There is a well recognized risk of complications for both women and infants of a twin pregnancy, increasing beyond 37 weeks gestation. Preterm birth prior to 37 weeks gestation is a recognized complication of a twin pregnancy, however, up to 50% of twins will be born after this time. The aims of this randomised trial are to assess whether elective birth at 37 weeks gestation compared with standard care in women with a twin pregnancy affects the risk of perinatal death, and serious infant complications.
Multicentred randomised trial.
women with a twin pregnancy at 366 weeks or more without contraindication to continuation of pregnancy. Trial Entry & Randomisation: Following written informed consent, eligible women will be randomised from 36+6 weeks gestation. The randomisation schedule uses balanced variable blocks, with stratification for centre of birth and planned mode of birth. Women will be randomised to either elective birth or standard care. Treatment Schedules: Women allocated to the elective birth group will be planned for elective birth from 37 weeks gestation. Where the plan is for vaginal birth, this will involve induction of labour. Where the plan is for caesarean birth, this will involve elective caesarean section. For women allocated to standard care, birth will be planned for 38 weeks gestation or later. Where the plan is for vaginal birth, this will involve either awaiting the spontaneous onset of labour, or induction of labour if required. Where the plan is for caesarean birth, this will involve elective caesarean section (after 38 and as close to 39 weeks as possible). Primary Study Outcome: A composite of perinatal mortality or serious neonatal morbidity.
460 women with a twin pregnancy to show a reduction in the composite outcome from 16.3% to 6.7% with adjustment for the clustering of twin infants within mothers (p = 0.05, 80% power).
This is a protocol for a randomised trial, the findings of which will contribute information about the optimal time of birth for women with an uncomplicated multiple pregnancy at and beyond 37 weeks gestation.</abstract><cop>England</cop><pub>BioMed Central</pub><pmid>20973989</pmid><doi>10.1186/1471-2393-10-68</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1471-2393 |
ispartof | BMC pregnancy and childbirth, 2010-10, Vol.10 (1), p.68-68, Article 68 |
issn | 1471-2393 1471-2393 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_783a644a5ad84886bd577c9ff05036aa |
source | Publicly Available Content Database; PubMed Central |
subjects | Cesarean Section Elective Surgical Procedures Female Gestational Age Humans Labor, Induced Labor, Obstetric Patient Selection Pregnancy Pregnancy Outcome Pregnancy, Multiple Studies Study Protocol Term Birth Twins Womens health |
title | Timing of birth for women with a twin pregnancy at term: a randomised controlled trial |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-12T13%3A44%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Timing%20of%20birth%20for%20women%20with%20a%20twin%20pregnancy%20at%20term:%20a%20randomised%20controlled%20trial&rft.jtitle=BMC%20pregnancy%20and%20childbirth&rft.au=Dodd,%20Jodie%20M&rft.date=2010-10-25&rft.volume=10&rft.issue=1&rft.spage=68&rft.epage=68&rft.pages=68-68&rft.artnum=68&rft.issn=1471-2393&rft.eissn=1471-2393&rft_id=info:doi/10.1186/1471-2393-10-68&rft_dat=%3Cproquest_doaj_%3E954598984%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-b643t-9b93ad7355feeae97aa23166b618e9456363fd2ea79a9114fa2e977500efc42f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=902172261&rft_id=info:pmid/20973989&rfr_iscdi=true |