Effect of Antenatal Magnesium Sulfate Exposure on Patent Ductus Arteriosus in Premature Infants.

IF 1.5 4区 医学 Q3 OBSTETRICS & GYNECOLOGY American journal of perinatology Pub Date : 2024-09-01 Epub Date: 2024-02-06 DOI:10.1055/s-0044-1779620
Emel Okulu, Elvis Kraja, Yasemin Ezgi Kostekci, Erdal Seker, Mehmet Seckin Ozisik, Doğacan Sarısoy, Batuhan Aslan, Maide Selin Çakır, Ferhan Demirtaş, Mehmet Gökhan Ramoğlu, Tayfun Uçar, Omer Erdeve, Begum Atasay, Acar Koc, Saadet Arsan
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Abstract

Objective:  Magnesium sulfate (MgSO4) provides effective fetal neuroprotection. However, there is conflicting evidence regarding the association between antenatal MgSO4 exposure and patent ductus arteriosus (PDA). Thus, herein, we aimed to evaluate the association between antenatal MgSO4 exposure and PDA.

Study design:  Preterm infants born between 240/7 and 316/7 weeks of gestation were included in this retrospective study. Infants who died within the first 72 hours of life and those with significant congenital anomalies were excluded from the study. Echocardiographic and clinical assessment parameters were used to define PDA and hemodynamically significant PDA (hsPDA). Treatments were planned according to the standard protocols of the unit. The following data were collected from hospital medical records: perinatal characteristics, neonatal outcomes, detailed PDA follow-up findings, and maternal characteristics including MgSO4 exposure and doses.

Results:  Of the 300 included infants, 98 (32.6%) were exposed to antenatal MgSO4. hsPDA rates were similar in the infants exposed and not exposed to antenatal MgSO4, when adjusted for antenatal steroid administration, gestational age, and birth weight (OR: 1.6, 95% CI: 0.849-3.118, p = 0.146). The rates of PDA ligation and open PDA at discharge were similar between the groups. A cumulative MgSO4 dose of >20 g was associated with an increased risk of hsPDA (crude OR: 2.476, 95% CI: 0.893-6.864, p = 0.076; adjusted OR: 3.829, 95% CI: 1.068-13.728, p = 0.039). However, the cumulative dose had no effect on the rates of PDA ligation or open PDA at discharge. Rates of prematurity-related morbidities and mortality were similar between the groups.

Conclusion:  Although antenatal MgSO4 exposure may increase the incidence of hsPDA, it may not affect the rates of PDA ligation or open PDA at discharge. Further studies are required to better evaluate the dose-dependent outcomes and identify the MgSO4 dose that not only provides neuroprotection but also has the lowest risk of adverse effects.

Key points: · Antenatal exposure of MgSO4 may cause PDA.. · Antenatal MgSO4 exposure may not increase the rates of PDA ligation or open PDA at discharge.. · Further studies are required to better evaluate the dose-dependent outcomes and optimal MgSO4 dose..

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产前接触硫酸镁对早产儿动脉导管未闭的影响
目的:硫酸镁(MgSO4)能有效保护胎儿神经。然而,关于产前硫酸镁暴露与动脉导管未闭(PDA)之间的关系,目前存在相互矛盾的证据。因此,我们在此旨在评估产前硫酸镁暴露与 PDA 之间的关系:研究设计:这项回顾性研究纳入了妊娠 240/7 周至 316/7 周之间出生的早产儿。在出生后 72 小时内死亡的婴儿和有严重先天性畸形的婴儿不在研究范围内。超声心动图和临床评估参数用于定义 PDA 和血流动力学显著性 PDA(hsPDA)。治疗计划按照该单位的标准方案进行。从医院病历中收集了以下数据:围产期特征、新生儿结局、详细的PDA随访结果以及产妇特征(包括MgSO4暴露量和剂量):经调整产前类固醇用量、胎龄和出生体重后,暴露和未暴露于产前硫酸镁的婴儿的 hsPDA 发生率相似(OR:1.6,95% CI:0.849-3.118,P = 0.146)。两组患者出院时的PDA结扎率和开放性PDA率相似。累积 MgSO4 剂量大于 20 克与 hsPDA 风险增加有关(粗略 OR:2.476,95% CI:0.893-6.864,p = 0.076;调整 OR:3.829,95% CI:0.849-3.118,p = 0.146):3.829,95% CI:1.068-13.728,p = 0.039)。然而,累积剂量对出院时的 PDA 结扎率或开放性 PDA 率没有影响。两组的早产儿相关发病率和死亡率相似:结论:虽然产前接触硫酸镁可能会增加hsPDA的发病率,但可能不会影响出院时PDA结扎率或开放性PDA的发病率。需要进一步研究以更好地评估剂量依赖性结果,并确定不仅能提供神经保护且不良反应风险最低的 MgSO4 剂量:- 要点:产前接触硫酸镁可能会导致PDA。- 产前接触硫酸镁可能不会增加出院时PDA结扎或开放性PDA的发生率。- 需要进一步研究,以更好地评估剂量依赖性结果和最佳硫酸镁剂量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American journal of perinatology
American journal of perinatology 医学-妇产科学
CiteScore
5.90
自引率
0.00%
发文量
302
审稿时长
4-8 weeks
期刊介绍: The American Journal of Perinatology is an international, peer-reviewed, and indexed journal publishing 14 issues a year dealing with original research and topical reviews. It is the definitive forum for specialists in obstetrics, neonatology, perinatology, and maternal/fetal medicine, with emphasis on bridging the different fields. The focus is primarily on clinical and translational research, clinical and technical advances in diagnosis, monitoring, and treatment as well as evidence-based reviews. Topics of interest include epidemiology, diagnosis, prevention, and management of maternal, fetal, and neonatal diseases. Manuscripts on new technology, NICU set-ups, and nursing topics are published to provide a broad survey of important issues in this field. All articles undergo rigorous peer review, with web-based submission, expedited turn-around, and availability of electronic publication. The American Journal of Perinatology is accompanied by AJP Reports - an Open Access journal for case reports in neonatology and maternal/fetal medicine.
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