Induction of labour versus expectant management in women with preterm prelabour rupture of membranes between 34 and 37 weeks (the PPROMEXIL-trial)

<p>Abstract</p> <p>Background</p> <p>Preterm prelabour rupture of the membranes (PPROM) is an important clinical problem and a dilemma for the gynaecologist. On the one hand, awaiting spontaneous labour increases the probability of infectious disease for both mother and...

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Main Authors: Kars Michael M (Author), Derks Jan B (Author), Molkenboer Jan FM (Author), Porath Martina M (Author), Pernet Paula JM (Author), Wouters Maurice GAJ (Author), van Wijngaarden Wim J (Author), Bloemenkamp Kitty WM (Author), Arabin Birgit (Author), Groenewout Mariette (Author), Bijlenga Denise (Author), Opmeer Brent C (Author), van Beek Johannes J (Author), Mol Ben (Author), Nijhuis Jan G (Author), van der Ham David P (Author), Scheepers Hubertina CJ (Author), Weinans Martin JN (Author), Woiski Mallory D (Author), Wildschut Hajo IJ (Author), Willekes Christine (Author)
Format: Book
Published: BMC, 2007-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Kars Michael M  |e author 
700 1 0 |a Derks Jan B  |e author 
700 1 0 |a Molkenboer Jan FM  |e author 
700 1 0 |a Porath Martina M  |e author 
700 1 0 |a Pernet Paula JM  |e author 
700 1 0 |a Wouters Maurice GAJ  |e author 
700 1 0 |a van Wijngaarden Wim J  |e author 
700 1 0 |a Bloemenkamp Kitty WM  |e author 
700 1 0 |a Arabin Birgit  |e author 
700 1 0 |a Groenewout Mariette  |e author 
700 1 0 |a Bijlenga Denise  |e author 
700 1 0 |a Opmeer Brent C  |e author 
700 1 0 |a van Beek Johannes J  |e author 
700 1 0 |a Mol Ben  |e author 
700 1 0 |a Nijhuis Jan G  |e author 
700 1 0 |a van der Ham David P  |e author 
700 1 0 |a Scheepers Hubertina CJ  |e author 
700 1 0 |a Weinans Martin JN  |e author 
700 1 0 |a Woiski Mallory D  |e author 
700 1 0 |a Wildschut Hajo IJ  |e author 
700 1 0 |a Willekes Christine  |e author 
245 0 0 |a Induction of labour versus expectant management in women with preterm prelabour rupture of membranes between 34 and 37 weeks (the PPROMEXIL-trial) 
260 |b BMC,   |c 2007-07-01T00:00:00Z. 
500 |a 10.1186/1471-2393-7-11 
500 |a 1471-2393 
520 |a <p>Abstract</p> <p>Background</p> <p>Preterm prelabour rupture of the membranes (PPROM) is an important clinical problem and a dilemma for the gynaecologist. On the one hand, awaiting spontaneous labour increases the probability of infectious disease for both mother and child, whereas on the other hand induction of labour leads to preterm birth with an increase in neonatal morbidity (e.g., respiratory distress syndrome (RDS)) and a possible rise in the number of instrumental deliveries.</p> <p>Methods/Design</p> <p>We aim to determine the effectiveness and cost-effectiveness of immediate delivery after PPROM in near term gestation compared to expectant management. Pregnant women with preterm prelabour rupture of the membranes at a gestational age from 34<sup>+0 </sup>weeks until 37<sup>+0 </sup>weeks will be included in a multicentre prospective randomised controlled trial. We will compare early delivery with expectant monitoring.</p> <p>The primary outcome of this study is neonatal sepsis. Secondary outcome measures are maternal morbidity (chorioamnionitis, puerperal sepsis) and neonatal disease, instrumental delivery rate, maternal quality of life, maternal preferences and costs. We anticipate that a reduction of neonatal infection from 7.5% to 2.5% after induction will outweigh an increase in RDS and additional costs due to admission of the child due to prematurity. Under these assumptions, we aim to randomly allocate 520 women to two groups of 260 women each. Analysis will be by intention to treat. Additionally a cost-effectiveness analysis will be performed to evaluate if the cost related to early delivery will outweigh those of expectant management. Long term outcomes will be evaluated using modelling.</p> <p>Discussion</p> <p>This trial will provide evidence as to whether induction of labour after preterm prelabour rupture of membranes is an effective and cost-effective strategy to reduce the risk of neonatal sepsis.</p> <p>Controlled clinical trial register</p> <p>ISRCTN29313500</p> 
546 |a EN 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
655 7 |a article  |2 local 
786 0 |n BMC Pregnancy and Childbirth, Vol 7, Iss 1, p 11 (2007) 
787 0 |n http://www.biomedcentral.com/1471-2393/7/11 
787 0 |n https://doaj.org/toc/1471-2393 
856 4 1 |u https://doaj.org/article/5718588e059e4377bd08e94e5bc6139e  |z Connect to this object online.