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Low dose aspirin in the prevention of recurrent spontaneous preterm labour the APRIL study: a multicenter randomized placebo controlled trial

  • Laura Visser
  • , Marjon A. de Boer
  • , Christianne J. M. de Groot
  • , Tobias A. J. Nijman
  • , Marieke A. C. Hemels
  • , Kitty W. M. Bloemenkamp
  • , Judith E. Bosmans
  • , Marjolein Kok
  • , Judith O. van Laar
  • , Marieke Sueters
  • , Hubertina Scheepers
  • , Joris van Drongelen
  • , Maureen T. M. Franssen
  • , J. Marko Sikkema
  • , Hans J. J. Duvekot
  • , Mireille N. Bekker
  • , Joris A. M. van der Post
  • , Christiana Naaktgeboren
  • , Ben W. J. Mol
  • , Martijn A. Oudijk*
  • *Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Background: Preterm birth (birth before 37 weeks of gestation) is a major problem in obstetrics and affects an estimated 15 million pregnancies worldwide annually. A history of previous preterm birth is the strongest risk factor for preterm birth, and recurrent spontaneous preterm birth affects more than 2.5 million pregnancies each year. A recent meta-analysis showed possible benefits of the use of low dose aspirin in the prevention of recurrent spontaneous preterm birth. We will assess the (cost-) effectiveness of low dose aspirin in comparison with placebo in the prevention of recurrent spontaneous preterm birth in a randomized clinical trial.

Methods/design: Women with a singleton pregnancy and a history of spontaneous preterm birth in a singleton pregnancy (22-37 weeks of gestation) will be asked to participate in a multicenter, randomized, double blinded, placebo controlled trial. Women will be randomized to low dose aspirin (80 mg once daily) or placebo, initiated from 8 to 16 weeks up to maximal 36 weeks of gestation. The primary outcome measure will be preterm birth, defined as birth at a gestational age (GA) <37 weeks. Secondary outcomes will be a composite of adverse neonatal outcome and maternal outcomes, including subgroups of prematurity, as well as intrauterine growth restriction (IUGR) and costs from a healthcare perspective. Preterm birth will be analyzed as a group, as well as separately for spontaneous or indicated onset. Analysis will be performed by intention to treat. In total, 406 pregnant women have to be randomized to show a reduction of 35% in preterm birth from 36 to 23%. If aspirin is effective in preventing preterm birth, we expect that there will be cost savings, because of the low costs of aspirin. To evaluate this, a cost- effectiveness analysis will be performed comparing preventive treatment with aspirin with placebo.

Discussion: This trial will provide evidence as to whether or not low dose aspirin is (cost-) effective in reducing recurrence of spontaneous preterm birth.

Original languageEnglish
Article number223
Number of pages7
JournalBMC Pregnancy and Childbirth
Volume17
Issue number1
DOIs
Publication statusPublished - 14 Jul 2017

Keywords

  • Pregnancy
  • 'Spontaneous recurrent preterm birth'
  • SPTB
  • Preterm birth
  • Preterm labour
  • PTB
  • Prevention
  • Reduction
  • Aspirin
  • Acetylsalicylic acid
  • ASA
  • LOW-BIRTH-WEIGHT
  • TASK-FORCE
  • PHYSIOLOGICAL TRANSFORMATION
  • PREGNANCY COMPLICATIONS
  • SPIRAL ARTERIES
  • META-ANALYSIS
  • DELIVERY
  • MEMBRANES
  • PREECLAMPSIA
  • METAANALYSIS

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