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

Authors :
Visser, L de
Boer, M.A. de
Groot, C.J. de
Nijman, T.A.
Hemels, M.A.C.
Bloemenkamp, K.W.
Bosmans, J.E.
Kok, M. de
Laar, J.O.E.H. van
Sueters, M.
Scheepers, H.
Drongelen, J. van
Franssen, M.T.
Sikkema, J.M.
Duvekot, H.J.
Bekker, M.N.
Post, J.A. van der
Naaktgeboren, C.
Mol, B.W.
Oudijk, M.A.
Visser, L de
Boer, M.A. de
Groot, C.J. de
Nijman, T.A.
Hemels, M.A.C.
Bloemenkamp, K.W.
Bosmans, J.E.
Kok, M. de
Laar, J.O.E.H. van
Sueters, M.
Scheepers, H.
Drongelen, J. van
Franssen, M.T.
Sikkema, J.M.
Duvekot, H.J.
Bekker, M.N.
Post, J.A. van der
Naaktgeboren, C.
Mol, B.W.
Oudijk, M.A.
Source :
BMC Pregnancy and Childbirth; 223; 1471-2393; 1; 17; ~BMC Pregnancy and Childbirth~223~~~~1471-2393~1~17~~
Publication Year :
2017

Abstract

Contains fulltext : 177805.pdf (publisher's version ) (Open Access)<br />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 r

Details

Database :
OAIster
Journal :
BMC Pregnancy and Childbirth; 223; 1471-2393; 1; 17; ~BMC Pregnancy and Childbirth~223~~~~1471-2393~1~17~~
Publication Type :
Electronic Resource
Accession number :
edsoai.on1284170871
Document Type :
Electronic Resource