Neonatal outcomes following magnesium sulfate exposure in the late preterm period (34 + 0–36 + 6 weeks)

Abstract Purpose To evaluate whether antenatal magnesium sulfate exposure after 34 + 0 weeks’ gestation is associated with short and long-term neonatal outcomes in the late preterm period. Late-preterm birth was defined as delivery between 34 + 0 and 36 + 6 weeks of gestation. Methods This retrospective cohort study included children aged ≥ 2 years born at 34 + 0–36 + 6 weeks’ gestation to mothers with preeclampsia between 2013 and 2020. The primary exposure was antenatal magnesium sulfate administration. Short-term outcomes included respiratory distress, neonatal intensive care unit (NICU) admission, 5-min Apgar score ≤ 7, and umbilical cord pH ≤ 7.1. The effects of different exposure durations (< 6 h, 6–16 h, ≥ 17 h) and total dose (> 30 g) were also evaluated. The primary long-term outcome was parent-reported clinically diagnosed developmental delay (speech, cognitive, or motor), ascertained through a structured telephone questionnaire. Results Among 131 children born in the late preterm period, 59 (45%) were exposed to magnesium sulfate and 72 (55%) served as controls. Antenatal magnesium sulfate exposure was not associated with higher rates of respiratory distress, NICU admission, 5-min Apgar score ≤ 7, or cord pH ≤ 7.1. Findings were consistent across exposure durations and doses. Rates of developmental delay were similar between groups. Conclusion Magnesium sulfate administration after 34 + 0 weeks for maternal indications was not associated with statistically clear differences in the short-term neonatal or developmental outcomes assessed. However, the limited sample size, sparse adverse events, residual confounding, and incomplete long-term follow-up preclude conclusions regarding equivalence or safety.

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Publication Details

Journal
Archives of Gynecology and Obstetrics
Published
2026-10-05
DOI
https://doi.org/10.1007/s00404-026-08586-x
Primary Topic
Pregnancy and preeclampsia studies
Type
article
Field-Weighted Citation Impact
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article

Neonatal outcomes following magnesium sulfate exposure in the late preterm period (34 + 0–36 + 6 weeks)

Gil Shechter‐Maor, Tal Biron‐Shental, Adi Shilony, Gal Cohen et al.
Archives of Gynecology and Obstetrics
Pregnancy and preeclampsia studies
article

Neonatal outcomes following magnesium sulfate exposure in the late preterm period (34 + 0–36 + 6 weeks)

Gil Shechter‐Maor, Tal Biron‐Shental, Adi Shilony, Gal Cohen, Hila Shalev‐Ram, Moran Weiss
article en

Abstract

Abstract Purpose To evaluate whether antenatal magnesium sulfate exposure after 34 + 0 weeks’ gestation is associated with short and long-term neonatal outcomes in the late preterm period. Late-preterm birth was defined as delivery between 34 + 0 and 36 + 6 weeks of gestation. Methods This retrospective cohort study included children aged ≥ 2 years born at 34 + 0–36 + 6 weeks’ gestation to mothers with preeclampsia between 2013 and 2020. The primary exposure was antenatal magnesium sulfate administration. Short-term outcomes included respiratory distress, neonatal intensive care unit (NICU) admission, 5-min Apgar score ≤ 7, and umbilical cord pH ≤ 7.1. The effects of different exposure durations (< 6 h, 6–16 h, ≥ 17 h) and total dose (> 30 g) were also evaluated. The primary long-term outcome was parent-reported clinically diagnosed developmental delay (speech, cognitive, or motor), ascertained through a structured telephone questionnaire. Results Among 131 children born in the late preterm period, 59 (45%) were exposed to magnesium sulfate and 72 (55%) served as controls. Antenatal magnesium sulfate exposure was not associated with higher rates of respiratory distress, NICU admission, 5-min Apgar score ≤ 7, or cord pH ≤ 7.1. Findings were consistent across exposure durations and doses. Rates of developmental delay were similar between groups. Conclusion Magnesium sulfate administration after 34 + 0 weeks for maternal indications was not associated with statistically clear differences in the short-term neonatal or developmental outcomes assessed. However, the limited sample size, sparse adverse events, residual confounding, and incomplete long-term follow-up preclude conclusions regarding equivalence or safety.

Archives of Gynecology and Obstetrics
Tel Aviv University (IL), Meir Medical Center (IL)
Openalex Percentile: Top 8%
Pregnancy and preeclampsia studies
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