Immediate delivery versus expectant monitoring for hypertensive disorders of pregnancy between 34 and 37 weeks of gestation (HYPITAT-II): an open-label, randomised controlled trial

被引:120
作者
Broekhuijsen, Kim [20 ]
van Baaren, Gert-Jan [1 ]
van Pampus, Maria G. [3 ]
Ganzevoort, Wessel [1 ]
Sikkema, J. Marko [4 ]
Woiski, Mallory D. [5 ]
Oudijk, Martijn A. [6 ]
Bloemenkamp, Kitty W. M. [7 ]
Scheepers, Hubertina C. J. [8 ]
Bremer, Henk A. [9 ]
Rijnders, Robbert J. P. [10 ]
van Loon, Aren J. [11 ]
Perquin, Denise A. M. [12 ]
Sporken, Jan M. J. [13 ]
Papatsonis, Dimitri N. M. [14 ]
van Huizen, Marloes E. [15 ]
Vredevoogd, Corla B. [16 ]
Brons, Jozien T. J. [17 ]
Kaplan, Mesrure [18 ]
van Kaam, Anton H. [2 ]
Groen, Henk [19 ]
Porath, Martina M. [21 ]
van den Berg, Paul P. [20 ]
Mol, Ben W. J. [22 ]
Franssen, Maureen T. M. [20 ]
Langenveld, Josje [23 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Obstet & Gynaecol, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Emma Childrens Hosp, Dept Neonatol, NL-1105 AZ Amsterdam, Netherlands
[3] Onze Lieve Vrouw Hosp, Dept Obstet & Gynaecol, Amsterdam, Netherlands
[4] ZGT Almelo, Dept Obstet & Gynaecol, Almelo, Netherlands
[5] Radboud Univ Nijmegen, Dept Obstet & Gynaecol, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[6] Univ Med Ctr Utrecht, Dept Obstet, Utrecht, Netherlands
[7] Leiden Univ, Dept Obstet, Med Ctr, Leiden, Netherlands
[8] Maastricht Univ, Dept Obstet & Gynaecol, Grow, Sch Oncol & Dev Biol,Med Ctr, NL-6200 MD Maastricht, Netherlands
[9] Reinier de Graaf Gasthuis, Dept Obstet & Gynaecol, Delft, Netherlands
[10] Jeroen Bosch Hosp, Dept Obstet & Gynaecol, Shertogenbosch, Netherlands
[11] Martini Hosp, Dept Obstet & Gynaecol, Groningen, Netherlands
[12] Med Ctr Leeuwarden, Dept Obstet & Gynaecol, Leeuwarden, Netherlands
[13] Canisius Wilhelmina Hosp, Dept Obstet & Gynaecol, Nijmegen, Netherlands
[14] Amphia Hosp Breda, Dept Obstet & Gynaecol, Breda, Netherlands
[15] HagaZiekenhuis, Dept Obstet & Gynaecol, The Hague, Netherlands
[16] Med Ctr Haaglanden, Dept Obstet & Gynaecol, The Hague, Netherlands
[17] Medisch Spectrum Twente, Dept Obstet & Gynaecol, Enschede, Netherlands
[18] Ropcke Zweers Hosp, Dept Obstet & Gynaecol, Hardenberg, Netherlands
[19] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, HPC FA40, Groningen, Netherlands
[20] Univ Groningen, Univ Med Ctr Groningen, Dept Obstet & Gynaecol, Groningen, Netherlands
[21] Maxima Med Ctr, Dept Obstet & Gynaecol, Veldhoven, Netherlands
[22] Univ Adelaide, Sch Paediat & Reprod Hlth, Adelaide, SA, Australia
[23] Atrium Med Ctr Parkstad, Dept Obstet & Gynaecol, Heerlen, Netherlands
关键词
SEVERE PREECLAMPSIA; MANAGEMENT; INDUCTION; LABOR;
D O I
10.1016/S0140-6736(14)61998-X
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background There is little evidence to guide the management of women with hypertensive disorders in late preterm pregnancy. We investigated the effect of immediate delivery versus expectant monitoring on maternal and neonatal outcomes in such women. Methods We did an open-label, randomised controlled trial, in seven academic hospitals and 44 non-academic hospitals in the Netherlands. Women with non-severe hypertensive disorders of pregnancy between 34 and 37 weeks of gestation were randomly allocated to either induction of labour or caesarean section within 24 h (immediate delivery) or a strategy aimed at prolonging pregnancy until 37 weeks of gestation (expectant monitoring). The primary outcomes were a composite of adverse maternal outcomes (thromboembolic disease, pulmonary oedema, eclampsia, HELLP syndrome, placental abruption, or maternal death), and neonatal respiratory distress syndrome, both analysed by intention-to-treat. This study is registered with the Netherlands Trial Register (NTR1792). Findings Between March 1, 2009, and Feb 21, 2013, 897 women were invited to participate, of whom 703 were enrolled and randomly assigned to immediate delivery (n=352) or expectant monitoring (n=351). The composite adverse maternal outcome occurred in four (1.1%) of 352 women allocated to immediate delivery versus 11 (3.1%) of 351 women allocated to expectant monitoring (relative risk [ RR] 0.36, 95% CI 012-111; p=0069). Respiratory distress syndrome was diagnosed in 20 (5.7%) of 352 neonates in the immediate delivery group versus six (1.7%) of 351 neonates in the expectant monitoring group (RR 3.3, 95% CI 1.4-8.2; p=0.005). No maternal or perinatal deaths occurred. Interpretation For women with non-severe hypertensive disorders at 34-37 weeks of gestation, immediate delivery might reduce the already small risk of adverse maternal outcomes. However, it significantly increases the risk of neonatal respiratory distress syndrome, therefore, routine immediate delivery does not seem justified and a strategy of expectant monitoring until the clinical situation deteriorates can be considered.
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收藏
页码:2492 / 2501
页数:10
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