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一项关于复杂主动脉瘤非标签治疗的全国性普查。

A national census for the off-label treatment of complex aortic aneurysms.

作者信息

Pitcher Grayson S, Biggs Joedd H, Dayama Anand, Newton Daniel H, Tran Kenneth, Stoner Michael C, Smeds Matthew R, Schermerhorn Marc L, Mix Doran

机构信息

Division of Vascular Surgery, University of Rochester Medical Center, Rochester, NY.

Division of Vascular Surgery, University of Kansas Medical Center, Kansas City, KS.

出版信息

J Vasc Surg. 2024 Sep;80(3):604-611. doi: 10.1016/j.jvs.2024.04.054. Epub 2024 Jun 21.

DOI:10.1016/j.jvs.2024.04.054
PMID:38904580
Abstract

OBJECTIVE

Despite regulatory challenges, device availability, and rapidly expanding techniques, off-label endovascular repair of complex aortic aneurysms (cAAs) has expanded in the past decade. Given the lack of United States Food and Drug Administration-approved endovascular technology to treat cAAs, we performed a national census to better understand volume and current practice patterns in the United States.

METHODS

Targeted sampling identified vascular surgeons with experience in off-label endovascular repair of cAAs. An electronic survey was distributed with institutional review board approval from the University of Rochester to 261 individuals with a response rate of 38% (n = 98).

RESULTS

A total of 93 respondents (95%) reported off-label endovascular repair of cAAs. Mean age was 45.7 ± 8.3 years, and 84% were male. Most respondents (59%) were within the first 10 years of practice, and 69% trained at institutions with a high-volume of off-label endovascular procedures for complex aortic aneurysms with or without a physician-sponsored investigational device exemption (PS-IDE). Twelve respondents from 11 institutions reported institutional PS-IDEs for physician-modified endografts (PMEGs), in-situ laser fenestration (ISLF), or parallel grafting technique (PGT), including sites with PS-IDEs for custom-manufactured devices. Eighty-nine unique institutions reported elective off-label endovascular repair with a mean of 20.2 ± 16.5 cases/year and ∼1757 total cases/year nationally. Eighty reported urgent/emergent off-label endovascular repair with a mean of 5.7 ± 5.4 cases/year and ∼499 total cases/year nationally. There was no correlation between high-volume endovascular institutions (>15 cases/year) and institutions with high volumes of open surgical repair for cAAs (>15 cases/year; odds ratio, 0.7; 95% confidence interval, 0.3-1.5; P = .34). Elective techniques included PMEG (70%), ISLF (30%), hybrid PMEG/ISLF (18%), and PGT (14%), with PMEG being the preferred technique for 63% of respondents. Techniques for emergent endovascular treatment of complex aortic disease included PMEG (52%), ISLF (40%), PGT (20%), and hybrid-PMEG/ISLF (14%), with PMEG being the preferred technique for 41% of respondents. Thirty-nine percent of respondents always or frequently offer referrals to institutions with PS-IDEs for custom-manufactured devices. The most common barrier for referral to PS-IDE centers included geographic distance (48%), longitudinal relationship with patient (45%), and costs associated with travel (33%). Only 61% of respondents participate in the Vascular Quality Initiative for complex endovascular aneurysm repair, and only 57% maintain a prospective institutional database. Eighty-six percent reported interest in a national collaborative database for off-label endovascular repair of cAA.

CONCLUSIONS

Estimates of off-label endovascular repair of cAAs are likely underrepresented in the literature based on this national census. PMEG was the most common technique for elective and emergent procedures. Under-reported off-label endovascular repair of cAA outcomes data appears to be limited by non-standardized PS-IDE reporting to the United States Food and Drug Administration, and the lack of Vascular Quality Initiative participation and prospective institutional data collection. Most participants are interested in a national collaborative database for endovascular repair of cAAs.

摘要

目的

尽管存在监管挑战、设备可用性问题以及技术迅速发展,但在过去十年中,复杂主动脉瘤(cAA)的非标签血管内修复术仍在不断扩展。鉴于缺乏美国食品药品监督管理局批准的用于治疗cAA的血管内技术,我们进行了一项全国性普查,以更好地了解美国的手术量和当前的实践模式。

方法

通过定向抽样确定了具有cAA非标签血管内修复经验的血管外科医生。在获得罗切斯特大学机构审查委员会批准后,向261名个体发放了电子调查问卷,回复率为38%(n = 98)。

结果

共有93名受访者(95%)报告了cAA的非标签血管内修复术。平均年龄为45.7±8.3岁,84%为男性。大多数受访者(59%)处于执业的前10年,69%在有大量复杂主动脉瘤非标签血管内手术的机构接受培训,无论这些机构是否有医生赞助的研究性器械豁免(PS-IDE)。来自11个机构的12名受访者报告了针对医生改良血管内移植物(PMEG)、原位激光开窗术(ISLF)或平行移植物技术(PGT)的机构PS-IDE,包括有定制器械PS-IDE的机构。89个不同的机构报告了选择性非标签血管内修复术,平均每年20.2±16.5例,全国每年总计约1757例。80个机构报告了紧急/急诊非标签血管内修复术,平均每年5.7±5.4例,全国每年总计约499例。高手术量血管内机构(每年>15例)与高手术量cAA开放手术修复机构(每年>15例)之间无相关性(优势比,0.7;95%置信区间,0.3 - 1.5;P = 0.34)。选择性技术包括PMEG(70%)、ISLF(,30%),、PMEG/ISLF混合技术(18%)和PGT(14%),63%的受访者首选PMEG技术。复杂主动脉疾病紧急血管内治疗技术包括PMEG(52%)、ISLF(40%)、PGT(20%)和PMEG/ISLF混合技术(14%),41%的受访者首选PMEG技术。39%的受访者总是或经常将患者转诊至有定制器械PS-IDE的机构。转诊至PS-IDE中心的最常见障碍包括地理距离(48%)、与患者的长期关系(45%)以及旅行相关费用(33%)。只有61%的受访者参与了复杂血管内动脉瘤修复的血管质量倡议,只有57%的机构维护前瞻性机构数据库。86%的受访者表示对cAA非标签血管内修复的全国协作数据库感兴趣。

结论

基于本次全国性普查,cAA非标签血管内修复术的估计数量在文献中可能被低估。PMEG是选择性和急诊手术中最常用的技术。cAA非标签血管内修复结果数据报告不足似乎受到向美国食品药品监督管理局报告PS-IDE不规范、缺乏血管质量倡议参与以及缺乏前瞻性机构数据收集的限制。大多数参与者对cAA血管内修复的全国协作数据库感兴趣。

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