Liever inleiden dan afwachten bij aterme zwangerschapshypertensie en milde preëclampsie: HYPITAT-studie*

C. M. Koopmans, D. Bijlenga, H. Groen, S. M. C. Vijgen, J. G. Aarnoudse, D. J. Bekedam, P. P. van den Berg, K. de Boer, J. M. Burggraaff, K. W. M. Bloemenkamp, A. P. Drogtrop, A. Franx, C. J. M. de Groot, A. J. M. Huisjes, A. Kwee, A. J. van Loon, A. Lub, D. N. M. Papatsonis, J. A. M. van der Post, F. J. M. E. RoumenH. C. J. Scheepers, C. Willekes, B. W. J. Mol, M. G. van Pampus, D.G. Bekedam

Research output: Contribution to journalArticleProfessional


OBJECTIVE: To investigate what would benefit women with mild full-term pregnancy-related hypertension most: induction of labour or expectant monitoring, from the perspective of clinical effectiveness, maternal quality of life, and costs. DESIGN: Randomised clinical trial. Trial registration number ISRCTN08132825. METHODS: We undertook a multicentre randomised controlled trial in 38 hospitals in the Netherlands between October 2005 and March 2008. We enrolled patients with a singleton pregnancy in cephalic presentation at 36-41 weeks' gestation, who had gestational hypertension or mild preeclampsia. Participants were randomly allocated to receive either induction of labour or expectant monitoring. The primary outcome was a composite measure of poor maternal outcome, defined as maternal mortality, maternal morbidity (eclampsia, 'haemolysis, elevated liver enzymes, low platelets' (HELLP) syndrome, pulmonary oedema, thrombo-embolic disease and abruptio placentae), progression to severe hypertension or proteinuria, and major postpartum haemorrhage. Secondary outcomes were mode of delivery, neonatal outcome, maternal quality of life and costs. Analysis was by intention to treat. RESULTS: A total of 756 patients were allocated to receive induction of labour (n = 377 patients) or expectant monitoring (n = 379). No cases of maternal or neonatal death or eclampsia were recorded. Development of poor maternal outcome was significantly lower in the induction of labour group (117 women) than the expectant monitoring group (166 women) (31% versus 44%; relative risk 0.71 (95% CI: 0.59-0.86); p < 0.001). The caesarean section rate was lower among women in the induction of labour group (n = 54) compared to women in the expectant monitoring group (n = 72) (14% versus 19%; relative risk 0.75 (95% CI: 0.55-1.04) <p = 0.085). Neonatal outcomes and quality of life were comparable between both groups. Induction of labour is a cost saving strategy (difference euro 831). CONCLUSION: For women with full-term gestational hypertension and pre-eclampsia, induction of labour is associated with improved maternal outcome and lower costs, without the additional risk of a caserian section being necessary
Original languageDutch
Article numberA1660
Pages (from-to)A1660
JournalNederlands Tijdschrift voor Geneeskunde
Issue number22
Publication statusPublished - 2010

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