医学
无症状的
产前诊断
胎儿
血管环
儿科
管理策略
干预(咨询)
产前筛查
产科
主动脉弓
怀孕
外科
主动脉
护理部
遗传学
生物
业务
工商管理
作者
Trisha V. Vigneswaran,Lindsey Hunter,J. S. Carvalho,Anna N. Seale
标识
DOI:10.1017/s1047951122002268
摘要
Abstract Objective: To investigate UK variability in prenatal and postnatal management strategy of right aortic arch and double aortic arch (RAA/DAA). Methods: Online surveys were sent to senior physicians (consultants) of the National Fetal Cardiology Working Group regarding prenatal diagnosis, counselling, and perinatal management of antenatally diagnosed RAA/DAA and to the British Congenital Cardiovascular Association regarding postnatal management strategies. Results: There were 28 prenatal and 90 postnatal surveys completed. Prenatally, there was consensus for potential associated chromosomal/genetic anomalies, but there was variation in the risk quoted. Confidence in defining aortic arch morphology was reported by 43% (12/28) of fetal cardiologists. There was variation in what was felt to be possible symptoms/signs of a compressive vascular ring, postnatal investigation, postnatal management, follow-up duration of asymptomatic patients, and indications for surgical intervention. Conclusion: This study has highlighted important areas for future research: improving accuracy of prenatal diagnosis, clarification of potential symptoms, optimal investigation strategies, and indications for surgery.
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