TY - JOUR
T1 - Maintenance tocolysis with nifedipine in threatened preterm labour: 2-year follow up of the offspring in the APOSTEL II trial
AU - Van Vliet, Eog
AU - Seinen, L
AU - Roos, C
AU - Schuit, E
AU - Scheepers, Hcj
AU - Bloemenkamp, Kwm
AU - Duvekot, Jj
AU - Van Eyck, J
AU - Kok, Jh
AU - Lotgering, Fk
AU - Van Baar, A
AU - Van Wassenaer-leemhuis, Ag
AU - Franssen, Mt
AU - Porath, Mm
AU - Van Der Post, Jam
AU - Franx, A
AU - Mol, Bwj
AU - Oudijk, Ma
PY - 2016/6
Y1 - 2016/6
N2 - Objective
To evaluate long-term effects of maintenance tocolysis with nifedipine on neurodevelopmental outcome of the infant.
Design, Setting and Population
Follow up of infants of women who participated in a multicentre randomised controlled trial on maintenance tocolysis with nifedipine versus placebo.
Methods
Two years after the APOSTEL II trial on maintenance tocolysis with nifedipine versus placebo, we asked participants to complete the Ages and Stages Questionnaire.
Main outcome measures
Infant development was measured in five domains. Developmental delay was defined as a score of ≤1 SD in one or more developmental domains. We performed exploratory subgroup analysis in women with preterm prolonged rupture of the membranes, and in women with a cervical length <10 mm at study entry.
Results
Of the 276 women eligible for follow up, 135 (52.5%) returned the questionnaire, encompassing data of 170 infants. At 2 years of age, infants of women with nifedipine maintenance tocolysis compared with placebo had a higher overall incidence of fine motor problems (22.2 versus 7.6%, OR 3.43, 95% CI 1.29–9.14, P = 0.01), and a lower incidence of poor problem-solving (21.1 versus 29.1%, OR 0.27, 95% CI 0.08-0.95, P = 0.04).
Conclusions
This follow-up study revealed no clear benefit of nifedipine maintenance tocolysis at 2 years of age. As short-term adverse perinatal outcome was not reduced in the original APOSTEL II trial, we conclude that maintenance tocolysis does not appear to be beneficial at this time.
Tweetable abstract
No clear benefit of nifedipine maintenance tocolysis in preterm labour on 2-year infant outcome.
AB - Objective
To evaluate long-term effects of maintenance tocolysis with nifedipine on neurodevelopmental outcome of the infant.
Design, Setting and Population
Follow up of infants of women who participated in a multicentre randomised controlled trial on maintenance tocolysis with nifedipine versus placebo.
Methods
Two years after the APOSTEL II trial on maintenance tocolysis with nifedipine versus placebo, we asked participants to complete the Ages and Stages Questionnaire.
Main outcome measures
Infant development was measured in five domains. Developmental delay was defined as a score of ≤1 SD in one or more developmental domains. We performed exploratory subgroup analysis in women with preterm prolonged rupture of the membranes, and in women with a cervical length <10 mm at study entry.
Results
Of the 276 women eligible for follow up, 135 (52.5%) returned the questionnaire, encompassing data of 170 infants. At 2 years of age, infants of women with nifedipine maintenance tocolysis compared with placebo had a higher overall incidence of fine motor problems (22.2 versus 7.6%, OR 3.43, 95% CI 1.29–9.14, P = 0.01), and a lower incidence of poor problem-solving (21.1 versus 29.1%, OR 0.27, 95% CI 0.08-0.95, P = 0.04).
Conclusions
This follow-up study revealed no clear benefit of nifedipine maintenance tocolysis at 2 years of age. As short-term adverse perinatal outcome was not reduced in the original APOSTEL II trial, we conclude that maintenance tocolysis does not appear to be beneficial at this time.
Tweetable abstract
No clear benefit of nifedipine maintenance tocolysis in preterm labour on 2-year infant outcome.
KW - Maintenance tocolysis
KW - nifedipine
KW - outcome
KW - preterm birth
U2 - 10.1111/1471-0528.13586
DO - 10.1111/1471-0528.13586
M3 - Article
SN - 1470-0328
VL - 123
SP - 1107
EP - 1114
JO - BJOG - An International Journal of Obstetrics and Gynaecology
JF - BJOG - An International Journal of Obstetrics and Gynaecology
IS - 7
ER -