Vascular Ehlers‐Danlos syndrome and pregnancy: A systematic review

Author:

Haem Théo1,Benson Betty2,Dernoncourt Amandine34,Gondry Jean14,Schmidt Jean34,Foulon Arthur14ORCID

Affiliation:

1. Department of Gynaecology and Obstetrics Centre Hospitalier Universitaire Amiens Picardie Amiens France

2. Department of Gynaecology and Obstetrics Centre Hospitalier Beauvais France

3. Department of Internal Medicine and Réseau d’Epidémiologie Clinique International Francophone (RECIF) Centre Hospitalier Universitaire Amiens Picardie Amiens France

4. Faculty of Medicine Université Picardie Jules Verne Amiens France

Abstract

AbstractBackgroundVascular Ehlers‐Danlos syndrome (vEDS) is a hereditary connective tissue disorder associated with an elevated risk of vascular, uterine and digestive complications. Managing pregnancy in this context can be a challenge.ObjectivesTo systematically review the literature data on the complications in pregnancy associated with vEDS.Search strategyWe searched the Pubmed Medline and Embase databases for articles using the following terms “vascular Ehlers‐Danlos syndrome” or “vEDS” AND “pregnancy”.Selection criteriaWomen with vEDS.Data collection and analysisWe searched the PubMed® MEDLINE® database for publications evaluating obstetric outcomes in women with vEDS.Main resultsA total of 121 publications were screened, with six (accounting for 412 pregnancies) included in our review. Of the women included in this sample, 30% were infertile. The miscarriage rate was 13.8% (57/412) and 8.8% of the live births were premature. Obstetric anal sphincter injuries occurred in 11.3% (23/203) of the deliveries. The maternal mortality rate per pregnancy was 5.7%.ConclusionsWomen with vEDS present an elevated risk of uterine rupture, vascular events, digestive events and death during pregnancy. Women appear to be most at risk during the peripartum period; to avoid expulsive efforts, a caesarean section should be scheduled at 37 weeks of gestation.

Publisher

Wiley

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