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Background <p>Pregnant women with mechanical heart valves (MHVs) require continuous anticoagulation; however, first-trimester exposure to warfarin raises concerns regarding fetal safety. Data on long-term pediatric outcomes after low-dose warfarin exposure remain limited. This study aimed to evaluate long-term growth, neurodevelopmental, cardiac, and endocrine outcomes in children antenatally exposed to low-dose warfarin combined with enoxaparin, compared with enoxaparin alone.</p> Methods <p>This single-center observational cohort study reports long-term pediatric follow-up outcomes of 32 children born to 30 women with MHVs who were enrolled at one participating center of the multicenter KYBELE study. Maternal data regarding anticoagulant therapy during pregnancy were obtained retrospectively from medical records, while pediatric data were collected through prospective clinical evaluations. Children underwent standardized assessments including physical examination, growth evaluation, Denver II developmental screening, skeletal radiography review, hearing and vision testing, electrocardiography, echocardiography, and thyroid and abdominal ultrasonography. Based on first-trimester anticoagulation regimen, children were classified as enoxaparin only (<i>n</i> = 12), enoxaparin plus warfarin 2.5&#xa0;mg/day (<i>n</i> = 8), or enoxaparin plus warfarin 4&#xa0;mg/day (<i>n</i> = 12).</p> Results <p>The median age at last follow-up was 61.5 months (range 9–168). No child had growth parameters below the 3rd percentile. The overall rate of prematurity was 19%. Although higher in children receiving enoxaparin plus warfarin (2.5&#xa0;mg or 4&#xa0;mg/day) compared with those receiving enoxaparin alone, the difference was not statistically significant (<i>p</i> = 0.6). Developmental delay on Denver II screening was identified in 2 of 32 children (<i>p</i> = 0.7), with no significant differences among groups. All children had normal hearing, vision, and thyroid function tests. Minor neonatal echocardiographic findings (e.g., patent ductus arteriosus or patent foramen ovale) were observed in 10 children (31%) and largely resolved during follow-up, with no child requiring cardiac intervention. No skeletal dysplasia or features suggestive of warfarin embryopathy were identified.</p> Conclusions <p>In this single-center follow-up cohort of live-born children, first-trimester exposure to low-dose warfarin combined with enoxaparin was not associated with signals of major long-term adverse outcomes in growth, neurodevelopment, cardiac status, or thyroid function compared with enoxaparin alone. These findings support cautious use of low-dose warfarin when maternal indications exist, while underscoring the need for larger multicenter studies.</p>

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Long-term pediatric outcomes after first-trimester exposure to low-dose warfarin plus enoxaparin versus enoxaparin alone in pregnancies with mechanical heart valves: the KYBELE children study

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2026年4月9日

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  • Sule Arici,
  • Ayse Inci Yildirim,
  • Gulperi Yagar Keskin,
  • Fatih Alparslan Genc,
  • Erkan Tas,
  • Serafettin Corbacioglu,
  • Ozlem Surekli Karakus,
  • Metin Sungur,
  • Ahmet Guner,
  • Sabahattin Gunduz,
  • Nuri Havan,
  • Mustafa Ozan Gursoy,
  • Mehmet Ozkan

摘要

Background

Pregnant women with mechanical heart valves (MHVs) require continuous anticoagulation; however, first-trimester exposure to warfarin raises concerns regarding fetal safety. Data on long-term pediatric outcomes after low-dose warfarin exposure remain limited. This study aimed to evaluate long-term growth, neurodevelopmental, cardiac, and endocrine outcomes in children antenatally exposed to low-dose warfarin combined with enoxaparin, compared with enoxaparin alone.

Methods

This single-center observational cohort study reports long-term pediatric follow-up outcomes of 32 children born to 30 women with MHVs who were enrolled at one participating center of the multicenter KYBELE study. Maternal data regarding anticoagulant therapy during pregnancy were obtained retrospectively from medical records, while pediatric data were collected through prospective clinical evaluations. Children underwent standardized assessments including physical examination, growth evaluation, Denver II developmental screening, skeletal radiography review, hearing and vision testing, electrocardiography, echocardiography, and thyroid and abdominal ultrasonography. Based on first-trimester anticoagulation regimen, children were classified as enoxaparin only (n = 12), enoxaparin plus warfarin 2.5 mg/day (n = 8), or enoxaparin plus warfarin 4 mg/day (n = 12).

Results

The median age at last follow-up was 61.5 months (range 9–168). No child had growth parameters below the 3rd percentile. The overall rate of prematurity was 19%. Although higher in children receiving enoxaparin plus warfarin (2.5 mg or 4 mg/day) compared with those receiving enoxaparin alone, the difference was not statistically significant (p = 0.6). Developmental delay on Denver II screening was identified in 2 of 32 children (p = 0.7), with no significant differences among groups. All children had normal hearing, vision, and thyroid function tests. Minor neonatal echocardiographic findings (e.g., patent ductus arteriosus or patent foramen ovale) were observed in 10 children (31%) and largely resolved during follow-up, with no child requiring cardiac intervention. No skeletal dysplasia or features suggestive of warfarin embryopathy were identified.

Conclusions

In this single-center follow-up cohort of live-born children, first-trimester exposure to low-dose warfarin combined with enoxaparin was not associated with signals of major long-term adverse outcomes in growth, neurodevelopment, cardiac status, or thyroid function compared with enoxaparin alone. These findings support cautious use of low-dose warfarin when maternal indications exist, while underscoring the need for larger multicenter studies.