Comparative systematic review and meta-analysis of pregnancy outcomes after kidney transplantation
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Author(s)
Bobotis, Stergios
Mavrommaths, Giorgos
Papalois, Vassilios
Type
Journal Article
Abstract
Introduction: Advancements in transplant medicine have increased the incidence of pregnancy among kidney transplant recipients. These pregnancies, however, carry elevated maternal and neonatal risks, warranting comprehensive outcome evaluation.
Materials and methods: To compare key maternal and neonatal outcomes in pregnancies following kidney transplantation with those in healthy pregnancies. A systematic search of MEDLINE, Embase, and PubMed was conducted up until December 2024. Comparative prospective and retrospective observational studies reporting maternal or neonatal outcomes in pregnancies among kidney transplant recipients and healthy controls. Risk of Bias in Non-Randomized Studies of Interventions (ROBINS-I) was used for quality assessment. Random-effects meta-analyses were conducted to calculate pooled odds ratios (ORs) with 95% confidence intervals (CIs) and heterogeneity (I2). Sensitivity analysis explored the impact of study design and bias.
Results: Eight studies encompassing 893 pregnancies post-kidney transplantation were included. Relative to healthy pregnancies, kidney-transplant recipients showed markedly higher odds of pre-eclampsia (OR: 10.17, 95% CI: 4.25–24.35; I2 = 86%), gestational hypertension (OR: 7.40, 95% CI: 2.20–24.86; I2 = 84%) and preterm birth (OR: 13.65, 95% CI: 4.79–38.92; I2 = 96%). Caesarean delivery (OR: 3.95, 95% CI: 1.67–9.31; I2 = 93%) and fetal mortality (OR: 4.84, 95% CI: 1.33–17.57; I2 = 79%) were also higher, whereas gestational diabetes did not differ (OR: 1.06, 95% CI: 0.67–1.67; I2 = 0%). Sensitivity analyses confirmed the elevated risks of pre-eclampsia and preterm birth, whereas the associations with caesarean section and fetal mortality did not remain statistically significant after adjustment for study quality.
Conclusions: Pregnancies following kidney transplantation are associated with significantly increased maternal and neonatal risks. These findings underscore the need for specialized antenatal care and further large-scale prospective studies to optimize outcomes and inform clinical guidelines.
Materials and methods: To compare key maternal and neonatal outcomes in pregnancies following kidney transplantation with those in healthy pregnancies. A systematic search of MEDLINE, Embase, and PubMed was conducted up until December 2024. Comparative prospective and retrospective observational studies reporting maternal or neonatal outcomes in pregnancies among kidney transplant recipients and healthy controls. Risk of Bias in Non-Randomized Studies of Interventions (ROBINS-I) was used for quality assessment. Random-effects meta-analyses were conducted to calculate pooled odds ratios (ORs) with 95% confidence intervals (CIs) and heterogeneity (I2). Sensitivity analysis explored the impact of study design and bias.
Results: Eight studies encompassing 893 pregnancies post-kidney transplantation were included. Relative to healthy pregnancies, kidney-transplant recipients showed markedly higher odds of pre-eclampsia (OR: 10.17, 95% CI: 4.25–24.35; I2 = 86%), gestational hypertension (OR: 7.40, 95% CI: 2.20–24.86; I2 = 84%) and preterm birth (OR: 13.65, 95% CI: 4.79–38.92; I2 = 96%). Caesarean delivery (OR: 3.95, 95% CI: 1.67–9.31; I2 = 93%) and fetal mortality (OR: 4.84, 95% CI: 1.33–17.57; I2 = 79%) were also higher, whereas gestational diabetes did not differ (OR: 1.06, 95% CI: 0.67–1.67; I2 = 0%). Sensitivity analyses confirmed the elevated risks of pre-eclampsia and preterm birth, whereas the associations with caesarean section and fetal mortality did not remain statistically significant after adjustment for study quality.
Conclusions: Pregnancies following kidney transplantation are associated with significantly increased maternal and neonatal risks. These findings underscore the need for specialized antenatal care and further large-scale prospective studies to optimize outcomes and inform clinical guidelines.
Date Issued
2025-10-13
Date Acceptance
2025-09-29
Citation
Frontiers in Transplantation, 2025, 4
ISSN
2813-2440
Publisher
Frontiers Media S.A.
Journal / Book Title
Frontiers in Transplantation
Volume
4
Copyright Statement
© 2025 Bobotis, Mavrommaths and Papalois. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
License URL
Identifier
https://www.ncbi.nlm.nih.gov/pubmed/41158299
Subjects
CYCLOSPORINE
gestational hypertension
HYPERTENSION
kidney transplantation
Life Sciences & Biomedicine
meta-analysis
pre-eclampsia
pregnancy outcomes
RECIPIENTS
Science & Technology
systematic review
Transplantation
Publication Status
Published
Coverage Spatial
Switzerland
Article Number
1689018
Date Publish Online
2025-10-13
