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Perinatal outcomes after in-utero exposure to beta-blockers in women with heart disease: Data from the ESC EORP registry of pregnancy and cardiac disease (ROPAC).
Ramlakhan, Karishma P; Roos-Hesselink, Jolien W; Basso, Thomas; Greenslade, Jaimi; Flint, Robert B; Krieger, Eric V; Shotan, Avraham; Budts, Werner; De Backer, Julie; Hall, Roger; Johnson, Mark R; Parsonage, William A.
Affiliation
  • Ramlakhan KP; Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Obstetrics and Gynaecology, Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Roos-Hesselink JW; Department of Cardiology, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands. Electronic address: j.roos@erasmusmc.nl.
  • Basso T; Department of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, Australia.
  • Greenslade J; Emergency and Trauma Centre, Royal Brisbane and Women's Hospital, Brisbane, Australia; Australian Centre for Health Services Innovation, School of Public Health and Social Work, Centre for Healthcare Transformation, Faculty of Health, Queensland University of Technology, Brisbane, Australia.
  • Flint RB; Department of Hospital Pharmacy, Erasmus MC, University Medical Center Rotterdam, Rotterdam, The Netherlands; Department of Neonatology, Erasmus MC - Sophia Children's Hospital, University Medical Center Rotterdam, Rotterdam, The Netherlands.
  • Krieger EV; Division of Cardiology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA.
  • Shotan A; Heart Institute, Laniado Medical Center, Netanya, Adelson School of Medicine, Ariel University, Israel.
  • Budts W; Congenital and Structural Cardiology, University Hospitals Leuven, and Department of Cardiovascular Sciences, Catholic University of Leuven, Leuven, Belgium.
  • De Backer J; Department of Cardiology, Ghent University Hospital, Ghent, Belgium.
  • Hall R; Department of Cardiology, University of East Anglia, Norwich, United Kingdom.
  • Johnson MR; Department of Obstetric Medicine, Imperial College London, Chelsea and Westminster Hospital, London, United Kingdom.
  • Parsonage WA; Department of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, Australia; Australian Centre for Health Services Innovation, School of Public Health and Social Work, Centre for Healthcare Transformation, Faculty of Health, Queensland University of Technology, Brisbane, Australia.
Int J Cardiol ; 410: 132234, 2024 Sep 01.
Article in En | MEDLINE | ID: mdl-38844094
ABSTRACT

BACKGROUND:

Beta-blockers are commonly used drugs during pregnancy, especially in women with heart disease, and are regarded as relatively safe although evidence is sparse. Differences between beta-blockers are not well-studied.

METHODS:

In the Registry of Pregnancy And Cardiac disease (ROPAC, n = 5739), a prospective global registry of pregnancies in women with structural heart disease, perinatal outcomes (small for gestational age (SGA), birth weight, neonatal congenital heart disease (nCHD) and perinatal mortality) were compared between women with and without beta-blocker exposure, and between different beta-blockers. Multivariable regression analysis was used for the effect of beta-blockers on birth weight, SGA and nCHD (after adjustment for maternal and perinatal confounders).

RESULTS:

Beta-blockers were used in 875 (15.2%) ROPAC pregnancies, with metoprolol (n = 323, 37%) and bisoprolol (n = 261, 30%) being the most frequent. Women with beta-blocker exposure had more SGA infants (15.3% vs 9.3%, p < 0.001) and nCHD (4.7% vs 2.7%, p = 0.001). Perinatal mortality rates were not different (1.4% vs 1.9%, p = 0.272). The adjusted mean difference in birth weight was -177 g (-5.8%), the adjusted OR for SGA was 1.7 (95% CI 1.3-2.1) and for nCHD 2.3 (1.6-3.5). With metoprolol as reference, labetalol (0.2, 0.1-0.4) was the least likely to cause SGA, and atenolol (2.3, 1.1-4.9) the most.

CONCLUSIONS:

In women with heart disease an association was found between maternal beta-blocker use and perinatal outcomes. Labetalol seems to be associated with the lowest risk of developing SGA, while atenolol should be avoided.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Cardiovascular / Pregnancy Outcome / Registries / Adrenergic beta-Antagonists Limits: Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Int J Cardiol Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pregnancy Complications, Cardiovascular / Pregnancy Outcome / Registries / Adrenergic beta-Antagonists Limits: Adult / Female / Humans / Newborn / Pregnancy Language: En Journal: Int J Cardiol Year: 2024 Document type: Article Affiliation country: