Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/88493
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dc.contributor.authorvan der Tuuk, K.-
dc.contributor.authorKoopmans, C.-
dc.contributor.authorGroen, H.-
dc.contributor.authorMol, B.-
dc.contributor.authorvan Pampus, M.-
dc.date.issued2011-
dc.identifier.citationBJOG: an International Journal of Obstetrics and Gynaecology, 2011; 118(13):1658-1660-
dc.identifier.issn1470-0328-
dc.identifier.issn1471-0528-
dc.identifier.urihttp://hdl.handle.net/2440/88493-
dc.description.abstractWe questioned if participation in the HYPITAT trial (induction of labour versus expectant monitoring in women with gestational hypertension or pre-eclampsia at term) impacted implementation of its results and subsequently maternal health. We identified women with hypertensive disease from the Perinatal Registry, and distinguished the period before, during and after the trial. We included 43 641 women. Induction of labour increased from 58.3 to 67.1% (P < 0.001) and prevalence of eclampsia decreased from 0.85 to 0.19% (P < 0.001) before and after the trial. Concurrently, participation in the HYPITAT trial among others had immediate consequences for obstetric management and maternal health.-
dc.description.statementofresponsibilityK van der Tuuk, CM Koopmans, H Groen, BW Mol, MG van Pampus for the HYPITAT study group-
dc.language.isoen-
dc.publisherWiley-
dc.rights© 2011 The Authors-
dc.source.urihttp://dx.doi.org/10.1111/j.1471-0528.2011.03138.x-
dc.subjectEclampsia; hypertension; induction of labour; preeclampsia; pregnancy-
dc.titleImpact of the HYPITAT trial on doctors' behaviour and prevalence of eclampsia in the Netherlands-
dc.typeJournal article-
dc.identifier.doi10.1111/j.1471-0528.2011.03138.x-
pubs.publication-statusPublished-
dc.identifier.orcidMol, B. [0000-0001-8337-550X]-
Appears in Collections:Aurora harvest 7
Paediatrics publications

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