Neurodevelopmental Outcomes After Late Preterm Antenatal Corticosteroids

Author:

Gyamfi-Bannerman Cynthia12,Clifton Rebecca G.3,Tita Alan T. N.4,Blackwell Sean C.5,Longo Monica6,de Voest Jessica A.3,O’Shea T. Michael7,Bousleiman Sabine Z.1,Ortiz Felecia5,Rouse Dwight J.8,Metz Torri D.9,Saade George R.1011,Rood Kara M.12,Heyborne Kent D.13,Thorp John M.7,Swamy Geeta K.14,Grobman William A.15,Gibson Kelly S.16,El-Sayed Yasser Y.17,Macones George A.18,

Affiliation:

1. Columbia University, New York, New York

2. University of California, San Diego, La Jolla

3. George Washington University Biostatistics Center, Washington, DC

4. University of Alabama at Birmingham

5. University of Texas Health Science Center at Houston–Children’s Memorial Hermann Hospital, Houston

6. Eunice Kennedy Shriver National Institute of Child Health and Human Development, Bethesda, Maryland

7. University of North Carolina at Chapel Hill, Chapel Hill

8. Brown University, Providence, Rhode Island

9. University of Utah Health Sciences Center, Salt Lake City

10. University of Texas Medical Branch, Galveston

11. Eastern Virginia Medical School, Norfolk

12. Ohio State University, Columbus

13. University of Colorado School of Medicine, Anschutz Medical Campus, Aurora

14. Duke University, Durham, North Carolina

15. Northwestern University, Chicago, Illinois

16. MetroHealth Medical Center-Case Western Reserve University, Cleveland, Ohio

17. Stanford University, Stanford, California

18. University of Texas at Austin

Abstract

ImportanceThe Antenatal Late Preterm Steroids (ALPS) trial changed clinical practice in the United States by finding that antenatal betamethasone at 34 to 36 weeks decreased short-term neonatal respiratory morbidity. However, the trial also found increased risk of neonatal hypoglycemia after betamethasone. This follow-up study focused on long-term neurodevelopmental outcomes after late preterm steroids.ObjectiveTo evaluate whether administration of late preterm (34-36 completed weeks) corticosteroids affected childhood neurodevelopmental outcomes.Design, Setting, and ParticipantsProspective follow-up study of children aged 6 years or older whose birthing parent had enrolled in the multicenter randomized clinical trial, conducted at 13 centers that participated in the Maternal-Fetal Medicine Units (MFMU) Network cycle from 2011-2016. Follow-up was from 2017-2022.ExposureTwelve milligrams of intramuscular betamethasone administered twice 24 hours apart.Main Outcome and MeasuresThe primary outcome of this follow-up study was a General Conceptual Ability score less than 85 (−1 SD) on the Differential Ability Scales, 2nd Edition (DAS-II). Secondary outcomes included the Gross Motor Function Classification System level and Social Responsiveness Scale and Child Behavior Checklist scores. Multivariable analyses adjusted for prespecified variables known to be associated with the primary outcome. Sensitivity analyses used inverse probability weighting and also modeled the outcome for those lost to follow-up.ResultsOf 2831 children, 1026 enrolled and 949 (479 betamethasone, 470 placebo) completed the DAS-II at a median age of 7 years (IQR, 6.6-7.6 years). Maternal, neonatal, and childhood characteristics were similar between groups except that neonatal hypoglycemia was more common in the betamethasone group. There were no differences in the primary outcome, a general conceptual ability score less than 85, which occurred in 82 (17.1%) of the betamethasone vs 87 (18.5%) of the placebo group (adjusted relative risk, 0.94; 95% CI, 0.73-1.22). No differences in secondary outcomes were observed. Sensitivity analyses using inverse probability weighting or assigning outcomes to children lost to follow-up also found no differences between groups.Conclusion and RelevanceIn this follow-up study of a randomized clinical trial, administration of antenatal corticosteroids to persons at risk of late preterm delivery, originally shown to improve short-term neonatal respiratory outcomes but with an increased rate of hypoglycemia, was not associated with adverse childhood neurodevelopmental outcomes at age 6 years or older.

Publisher

American Medical Association (AMA)

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