小儿马凡氏病专科门诊 25 年来的诊断成果和治疗意义。

IF 3 3区 医学 Q1 PEDIATRICS European Journal of Pediatrics Pub Date : 2024-11-18 DOI:10.1007/s00431-024-05857-0
Ryan E Accord, Chris Koster, Eelco Dulfer, Gideon J du Marchie Sarvaas, Saskia W M C Maass, Rolf M F Berger, Maarten P van den Berg
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引用次数: 0

摘要

本研究旨在评估一家专科门诊对怀疑患有遗传性胸主动脉疾病(HTAD)(包括马凡综合征(MFS))的儿童的诊断和治疗效果,并调查评估过程中出现的症状和发现的诊断价值。这项回顾性观察研究纳入了 1998 年至 2018 年间首次转诊时年龄小于 18 岁的所有患者。研究收集了截至 2023 年 12 月的临床数据、药物治疗、手术干预和监测期间的临床事件。利用逻辑回归分析对最终诊断为 HTAD 的患者和未诊断为 HTAD 的患者进行病例对照比较,以研究收集到的变量的诊断价值。共有 355 名儿童转诊到该诊所并接受了评估,结果有 89 例新诊断病例,HTAD 诊断率为 21%,其中包括 59 例 MFS。转诊时年龄较小、眼睑外翻、主动脉扩张和面部特征是预测 MFS 和其他 HTAD 的最有力因素,而胸肌和臂展-身高比对儿童年龄没有预测价值。在 MFS 患者中,65% 接受了降压治疗,8% 的 HTAD 患者接受了预防性主动脉手术,有些患者甚至在儿童时期就接受了手术。结论在我们的马凡氏专科门诊中,对儿童进行 HTAD 评估的诊断率很高,随后的治疗效果也很好。事实上,早期发现症状和体征并转诊到这样的专科门诊可能会导致早期诊断、监测和及时治疗,从而可能限制急性主动脉事件甚至死亡率。
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Diagnostic yield and therapeutic implications of 25 years of specialized pediatric Marfan clinic.

The purpose of this study is to evaluate the diagnostic and therapeutic yield of a specialized clinic for children with suspicion of a hereditary thoracic aortic disease (HTAD), including Marfan Syndrome (MFS), and to investigate the diagnostic value of presenting symptoms and findings during evaluation. This retrospective observational study included all patients younger than 18 years old at initial referral between 1998 and 2018. Clinical data, medical treatment, surgical interventions, and clinical events during surveillance were collected until December 2023. A case-control comparison between patients with and without an eventual diagnosis of HTAD was performed using logistic regression analysis to investigate the diagnostic value of collected variables. A total of 355 children were referred and evaluated at the clinic, resulting in 89 new diagnoses, with a diagnostic yield of 21% HTAD, including 59 cases of MFS. Younger age at referral, ectopia lentis, aortic dilatation, and facial features were among the strongest predictors of MFS and other HTAD, while pectus excavatum and arm span-height ratio had no predictive value at childhood age. Of patients with MFS, 65% received antihypertensive medication, and 8% of patients with HTAD underwent prophylactic aortic surgery, in some cases even during childhood. Conclusion: Evaluation of children for HTAD in our specialized Marfan clinic resulted in a high diagnostic yield and subsequent therapeutic implications. Indeed, early recognition of symptoms and signs and referral to such a specialized clinic may lead to early diagnosis, surveillance, and timely treatment, thereby possibly limiting acute aortic events and even mortality.

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来源期刊
CiteScore
5.90
自引率
2.80%
发文量
367
审稿时长
3-6 weeks
期刊介绍: The European Journal of Pediatrics (EJPE) is a leading peer-reviewed medical journal which covers the entire field of pediatrics. The editors encourage authors to submit original articles, reviews, short communications, and correspondence on all relevant themes and topics. EJPE is particularly committed to the publication of articles on important new clinical research that will have an immediate impact on clinical pediatric practice. The editorial office very much welcomes ideas for publications, whether individual articles or article series, that fit this goal and is always willing to address inquiries from authors regarding potential submissions. Invited review articles on clinical pediatrics that provide comprehensive coverage of a subject of importance are also regularly commissioned. The short publication time reflects both the commitment of the editors and publishers and their passion for new developments in the field of pediatrics. EJPE is active on social media (@EurJPediatrics) and we invite you to participate. EJPE is the official journal of the European Academy of Paediatrics (EAP) and publishes guidelines and statements in cooperation with the EAP.
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