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卓越遗传性出血性毛细血管扩张症中心的初步经验。

Initial experience of a hereditary hemorrhagic telangiectasia center of excellence.

作者信息

Thompson Christopher F, Suh Jeffrey D, McWilliams Justin, Duckwiler Gary, Wang Marilene B

机构信息

Department of Otolaryngology, Northwestern University, 675 N. St. Clair, Galter Pavilion 15th Floor, Room 200, Chicago, IL 60614.

出版信息

Ear Nose Throat J. 2017 Jun;96(6):E33-E36. doi: 10.1177/014556131709600607.

Abstract

Our objectives in reviewing the initial experience of a hereditary hemorrhagic telangiectasia center of excellence (HHT COE) were to better understand the interventions being performed in the comprehensive care of these patients and to present the early data as a reference for other tertiary centers considering starting an HHT COE. We conducted a retrospective review of consecutive patients referred to our newly developed HHT COE for evaluation and treatment between May 2010 and June 2013. Clinical presentation, otolaryngologic treatments, and other operative interventions were analyzed. One hundred forty-four of the 198 patients (73%) evaluated at the HHT COE had definite HHT based on the Curaçao diagnostic criteria, with 20 additional patients possibly having HHT and undergoing further evaluation to confirm the diagnosis. Sixteen of the 31 patients (52%) referred to otolaryngology required intervention in the operating room for epistaxis. Seventy-two of the 164 (44%) patients with definite or possible HHT required other interventions for internal organ arteriovenous malformations (AVMs), with interventional radiology embolization of pulmonary AVMs being the most common procedure. An HHT COE is important in providing comprehensive care for patients with this rare disease, which has significant clinical sequelae. Having an HHT COE allows for early screening and subspecialty referral within a system of specialists experienced in preventing the morbidity and mortality associated with severe epistaxis and internal organ AVMs.

摘要

我们回顾遗传性出血性毛细血管扩张症卓越中心(HHT COE)初期经验的目的,是为了更好地了解对这些患者进行综合治疗时所采取的干预措施,并呈现早期数据,为其他考虑设立HHT COE的三级中心提供参考。我们对2010年5月至2013年6月期间转诊至我们新设立的HHT COE进行评估和治疗的连续患者进行了回顾性研究。分析了临床表现、耳鼻喉科治疗及其他手术干预措施。在HHT COE接受评估的198例患者中,144例(73%)根据库拉索岛诊断标准确诊为HHT,另有20例可能患有HHT并正在接受进一步评估以确诊。转诊至耳鼻喉科的31例患者中,16例(52%)因鼻出血需要在手术室进行干预。164例确诊或可能患有HHT的患者中,72例(44%)因内脏动静脉畸形(AVM)需要其他干预措施,其中肺AVM的介入放射栓塞术是最常见的操作。HHT COE对于为这种具有严重临床后果的罕见病患者提供综合治疗非常重要。设立HHT COE能够在一个由预防严重鼻出血和内脏AVM相关发病率和死亡率方面经验丰富的专家组成的系统内实现早期筛查和专科转诊。

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