Boutrous Mina L, Alvarez Alejandro C, Okoye Obi T, Laws Jennifer C, Jacobs Donald L, Smeds Matthew R
Division of Vascular and Endovascular Surgery, Department of Surgery, St. Louis University, Saint Louis, MO.
NHS Vascular LLC, SSM Health St. Mary's Hospital, Saint Louis, MO.
Ann Vasc Surg. 2019 Aug;59:225-230. doi: 10.1016/j.avsg.2019.01.024. Epub 2019 Apr 19.
Central venous occlusion may occur in hemodialysis patients, resulting in arm or facial swelling and failure of dialysis access. Endovascular management with balloon angioplasty or stenting has been described, but there are minimal data on the use of covered stents in this pathology. We sought to review a single institution's experience with the use of covered stents for central venous occlusive disease in hemodialysis patients.
A retrospective review of all patients undergoing placement of covered stents between April 2014 and December 2016 for central venous occlusive disease to preserve a failing dialysis access was performed. Patients' records were reviewed to identify demographics, medical comorbidities, operative variables, primary patency rates, and secondary interventions.
A total of 29 patients were included in the analysis. Viabahn (W.L. Gore and Associates, Flagstaff, AZ) stent grafts were exclusively used in all patients. Technical success rate was 100%. The patients were predominantly female (65.5%), with a mean age of 67.9 ± 12.1 and medical comorbidities of hypertension (86%), diabetes (76%), and tobacco use (7%). The majority (86%) had prior angioplasty and 17 of 29 (59%) patients had previous central venous catheters. The right brachiocephalic vein was the most commonly stented vessel (28%). The median stent length and diameter used were 50 millimeters (range 25-100 millimeters) and 13 millimeters (range: 9-13 millimeters), respectively. The majority of patients (83%) received a single stent, with only 2 patients requiring more than one. Median follow-up was 24 months (range: 6-41 months). Four of 29 (13.8%) patients developed symptomatic stent restenosis requiring secondary intervention, all of which occurred in patients with primary stenosis between 50% and 75%. When compared to the patients without restenosis, longer stents were found to be significantly associated with restenosis (62.5 centimeters, interquartile range [IQR]: 0] vs. 50 centimeter, IQR: 0, P = 0.002). Primary patency rates were 92.9%, 91.7%, and 80.0% at 6, 12, and 24 months respectively. Secondary patency rates were 96.4%, 95.8%, and 93.3% at 6 months, 12 months, and 24 months, respectively. The overall primary patency rate was estimated at 86.2% using Kaplan-Meier analysis at 30.5 months (95% confidence interval: 26.5-34.5 months).
Covered stent grafts have reasonable primary patency and excellent secondary patency when used for central venous stenosis in dialysis patients. Stent-graft length is associated with poorer long-term patency rates.
血液透析患者可能发生中心静脉闭塞,导致手臂或面部肿胀以及透析通路功能丧失。已有关于采用球囊血管成形术或支架置入术进行血管内治疗的描述,但关于在这种病理情况下使用覆膜支架的数据极少。我们试图回顾一家机构使用覆膜支架治疗血液透析患者中心静脉闭塞性疾病的经验。
对2014年4月至2016年12月期间因中心静脉闭塞性疾病接受覆膜支架置入以挽救功能不良的透析通路的所有患者进行回顾性分析。查阅患者记录以确定人口统计学资料、合并症、手术变量、原发性通畅率和二次干预情况。
共有29例患者纳入分析。所有患者均仅使用了威伐恩(W.L. Gore and Associates公司,弗拉格斯塔夫,亚利桑那州)覆膜支架。技术成功率为100%。患者以女性为主(65.5%),平均年龄为67.9±12.1岁,合并症包括高血压(86%)、糖尿病(76%)和吸烟(7%)。大多数患者(86%)曾接受血管成形术,29例患者中有17例(59%)曾有中心静脉导管置入史。右头臂静脉是最常置入支架的血管(28%)。使用的支架中位长度和直径分别为50毫米(范围25 - 100毫米)和13毫米(范围:9 - 13毫米)。大多数患者(83%)置入单个支架,仅2例患者需要置入多个支架。中位随访时间为24个月(范围:6 - 41个月)。29例患者中有4例(13.8%)出现有症状的支架再狭窄,需要二次干预,所有这些患者的原发性狭窄均在50%至75%之间。与无再狭窄的患者相比,发现较长的支架与再狭窄显著相关(62.5厘米,四分位间距[IQR]:0] vs. 50厘米,IQR:0,P = 0.002)。6个月、12个月和24个月时的原发性通畅率分别为92.9%、91.7%和80.0%。6个月、12个月和24个月时的继发性通畅率分别为96.4%、95.8%和93.3%。使用Kaplan - Meier分析在30.5个月时总体原发性通畅率估计为86.2%(95%置信区间:26.5 - 34.5个月)。
覆膜支架用于透析患者中心静脉狭窄时具有合理的原发性通畅率和出色的继发性通畅率。支架长度与较差的长期通畅率相关。