Currently managed US prevalence of cutaneous venous malformations (cVMs): a nationally representative, retrospective, real-world, subject-blinded, physician-observational probability study.
Jack Ray Gallagher, Susan Carroll, Jeffrey Martini, Michael Kelly, Maria Gnarra Buethe
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引用次数: 0
Abstract
Background: Cutaneous venous malformations (cVMs) are rare vascular anomalies characterized by progressive vessel ectasia, leading to disfigurement, pain, ulceration, and bleeding. These lesions often evade early detection and are notoriously difficult to treat due to the limited dermal bioavailability of systemic therapies. Unlike deep venous malformations, cVMs present unique management challenges and currently lack FDA-approved treatments. To address the paucity of epidemiologic data, we conducted a nationally representative, blinded, real-world observational probability study to estimate the annual treatment prevalence of cVM in the United States. A geographically representative sample of dermatologists, hematologist-oncologists, pediatricians, radiologists, and vascular surgeons was recruited via blinded invitations. Participants self-reported the number of cVM patients treated in the prior 12 months. Estimates were adjusted for comanagement to calculate the national prevalence of unique patients.
Results: Of 691 physicians who accessed the study website, 515 (74.5%) completed the survey; 376 (73.0%) reported managing at least one patient with cutaneous-only or mixed (cutaneous and internal) VMs. The estimated annual prevalence was 194,195 patients (95% CI 188,852-200,228), including 135,687 with cutaneous-only VMs and 58,508 with mixed lesions. This corresponds to a prevalence of 0.06% (US population).
Conclusions: While cVM is rare, it affects a substantial number of individuals across age groups in the U.S. These findings underscore the need for improved access to care and the development of targeted therapies for this understudied, debilitating condition.
背景:皮肤静脉畸形(cvm)是一种罕见的血管异常,其特征是血管进行性扩张,导致毁容、疼痛、溃疡和出血。由于全身治疗的皮肤生物利用度有限,这些病变往往无法早期发现,并且众所周知难以治疗。与深静脉畸形不同,cvm具有独特的管理挑战,目前缺乏fda批准的治疗方法。为了解决流行病学数据的缺乏,我们进行了一项具有全国代表性的、盲法的、真实世界的观察概率研究,以估计美国cVM的年治疗患病率。通过盲法邀请招募了具有地理代表性的皮肤科医生、血液肿瘤学家、儿科医生、放射科医生和血管外科医生。参与者自我报告在过去12个月内治疗的cVM患者数量。根据管理调整了估计值,以计算全国独特患者的患病率。结果:691名访问研究网站的医生中,515名(74.5%)完成了调查;376例(73.0%)报告至少治疗了一例皮肤性或混合性(皮肤和内部)vm。估计年患病率为194,195例(95% CI 188,852-200,228),其中135,687例为单纯皮肤vm, 58,508例为混合性病变。这相当于0.06%的患病率(美国人口)。结论:虽然cVM是罕见的,但它影响了美国各年龄组的大量个体。这些发现强调了改善护理和开发针对这种未充分研究的衰弱性疾病的靶向治疗的必要性。
期刊介绍:
Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.