Consortium for the Study of Pregnancy Treatments (Co-OPT): An international birth cohort to study the effects of antenatal corticosteroids

Background Antenatal corticosteroids (ACS) are widely prescribed to improve outcomes following preterm birth. Significant knowledge gaps surround their safety, long-term effects, optimal timing and dosage. Almost half of women given ACS give birth outside the “therapeutic window” and have not delivered over 7 days later. Overtreatment with ACS is a concern, as evidence accumulates of risks of unnecessary ACS exposure. Methods The Consortium for the Study of Pregnancy Treatments (Co-OPT) was established to address research questions surrounding safety of medications in pregnancy. We created an international birth cohort containing information on ACS exposure and pregnancy and neonatal outcomes by combining data from four national/provincial birth registers and one hospital database, and follow-up through linked population-level data from death registers and electronic health records. Results and discussion The Co-OPT ACS cohort contains 2.28 million pregnancies and babies, born in Finland, Iceland, Israel, Canada and Scotland, between 1990 and 2019. Births from 22 to 45 weeks’ gestation were included; 92.9% were at term (≥ 37 completed weeks). 3.6% of babies were exposed to ACS (67.0% and 77.9% of singleton and multiple births before 34 weeks, respectively). Rates of ACS exposure increased across the study period. Of all ACS-exposed babies, 26.8% were born at term. Longitudinal childhood data were available for 1.64 million live births. Follow-up includes diagnoses of a range of physical and mental disorders from the Finnish Hospital Register, diagnoses of mental, behavioural, and neurodevelopmental disorders from the Icelandic Patient Registers, and preschool reviews from the Scottish Child Health Surveillance Programme. The Co-OPT ACS cohort is the largest international birth cohort to date with data on ACS exposure and maternal, perinatal and childhood outcomes. Its large scale will enable assessment of important rare outcomes such as perinatal mortality, and comprehensive evaluation of the short- and long-term safety and efficacy of ACS.

[1]  M. Gissler,et al.  Associations Between Maternal Antenatal Corticosteroid Treatment and Mental and Behavioral Disorders in Children. , 2020, JAMA.

[2]  N. Marlow,et al.  Perinatal management of extreme preterm birth before 27 weeks of gestation: a framework for practice , 2020, Archives of Disease in Childhood.

[3]  A. Jobe Antenatal Corticosteroids-A Concern for Lifelong Outcomes. , 2020, The Journal of pediatrics.

[4]  R. Nisenbaum,et al.  Antenatal corticosteroid administration is associated with decreased growth of the fetal thymus: a prospective cohort study , 2019, Journal of Perinatology.

[5]  D. Redelmeier,et al.  Neurodevelopmental disorders among term infants exposed to antenatal corticosteroids during pregnancy: a population-based study , 2019, BMJ Open.

[6]  M. Kemp,et al.  Antenatal corticosteroids for low and middle income countries. , 2019, Seminars in perinatology.

[7]  M. Gissler,et al.  Antenatal corticosteroid therapy (ACT) and size at birth: A population-based analysis using the Finnish Medical Birth Register , 2019, PLoS medicine.

[8]  Jun Zhang,et al.  Global, regional, and national estimates of levels of preterm birth in 2014: a systematic review and modelling analysis , 2018, The Lancet. Global health.

[9]  E. Hadar,et al.  Neonatal outcomes in term pregnancies treated with antenatal corticosteroids for suspected pre-term labor , 2018, Archives of Gynecology and Obstetrics.

[10]  M. Kemp,et al.  Efficacy and safety of antenatal steroids. , 2018, American journal of physiology. Regulatory, integrative and comparative physiology.

[11]  B. Manley,et al.  The evolution of modern respiratory care for preterm infants , 2017, The Lancet.

[12]  Julie Brown,et al.  Antenatal Corticosteroids for Accelerating Fetal Lung Maturation for Women at Risk of Preterm Birth , 2007, The Cochrane database of systematic reviews.

[13]  H. Yamashita,et al.  Influence of the interval between antenatal corticosteroid therapy and delivery on respiratory distress syndrome , 2017, The journal of obstetrics and gynaecology research.

[14]  Aziz Sheikh,et al.  Establishing data-intensive healthcare: the case of Hospital Electronic Prescribing and Medicines Administration systems in Scotland. , 2016, Journal of innovation in health informatics.

[15]  D. Campbell,et al.  Data Resource Profile: The Aberdeen Maternity and Neonatal Databank (AMND). , 2016, International journal of epidemiology.

[16]  U. Valdimarsdóttir,et al.  Body Mass Index, Smoking and Hypertensive Disorders during Pregnancy: A Population Based Case-Control Study , 2016, PloS one.

[17]  G. Saade,et al.  Antenatal Betamethasone for Women at Risk for Late Preterm Delivery. , 2016, The New England journal of medicine.

[18]  A. Vintzileos,et al.  Practice patterns in the timing of antenatal corticosteroids for fetal lung maturity , 2015, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

[19]  K. Joseph,et al.  Trends in Optimal, Suboptimal, and Questionably Appropriate Receipt of Antenatal Corticosteroid Prophylaxis , 2015, Obstetrics and gynecology.

[20]  Jun Zhang,et al.  Use of antenatal corticosteroids and tocolytic drugs in preterm births in 29 countries: an analysis of the WHO Multicountry Survey on Maternal and Newborn Health , 2014, The Lancet.

[21]  M. Gissler,et al.  The Nordic medical birth registers – a potential goldmine for clinical research , 2014, Acta obstetricia et gynecologica Scandinavica.

[22]  S. Kotecha,et al.  Behavioural, educational and respiratory outcomes of antenatal betamethasone for term caesarean section (ASTECS trial) , 2013, Archives of Disease in Childhood: Fetal and Neonatal Edition.

[23]  R. Reynolds Glucocorticoid excess and the developmental origins of disease: Two decades of testing the hypothesis – 2012 Curt Richter Award Winner , 2013, Psychoneuroendocrinology.

[24]  Ann-Beth Moller,et al.  National, regional, and worldwide estimates of preterm birth rates in the year 2010 with time trends since 1990 for selected countries: a systematic analysis and implications , 2012, The Lancet.

[25]  M. Blair,et al.  Trends in the coverage of ‘universal’ child health reviews: observational study using routinely available data , 2012, BMJ Open.

[26]  M. Gissler,et al.  Should births be centralised in higher level hospitals? Experiences from regionalised health care in Finland , 2011, BJOG : an international journal of obstetrics and gynaecology.

[27]  B. Mol,et al.  Time to delivery after the first course of antenatal corticosteroids: a cohort study. , 2011, American journal of perinatology.

[28]  K. Hospital,et al.  Antenatal corticosteroids to reduce neonatal morbidity and mortality , 2022, BJOG : an international journal of obstetrics and gynaecology.

[29]  J. Garland,et al.  The effect of a prolonged time interval between antenatal corticosteroid administration and delivery on outcomes in preterm neonates: a cohort study. , 2007, American journal of obstetrics and gynecology.

[30]  C. Crowther,et al.  Effects of a single course of corticosteroids given more than 7 days before birth: A systematic review , 2003, The Australian & New Zealand journal of obstetrics & gynaecology.

[31]  A. Whitelaw,et al.  Antenatal steroids and the developing brain , 2000, Archives of disease in childhood. Fetal and neonatal edition.

[32]  A C Allen,et al.  An assessment of the validity of a computer system for probabilistic record linkage of birth and infant death records in Canada. The Fetal and Infant Health Study Group. , 2000, Chronic diseases in Canada.

[33]  Who: Recommended Definitions, Terminology and Format for Statistical Tables Related to The Perinatal Period And Use of A New Certificate For Cause of Perinatal Deaths , 1977, Acta obstetricia et gynecologica Scandinavica.

[34]  G. Liggins,et al.  A controlled trial of antepartum glucocorticoid treatment for prevention of the respiratory distress syndrome in premature infants. , 1972, Pediatrics.