Nitinol stents placed in iliac veins are not associated with prolonged back pain

医学 支架 外科 人口统计学的 背痛 静脉 单中心 入射(几何) 光学 物理 病理 社会学 人口学 替代医学
作者
Chloe Snow,Sydney Pappas,Levan Sulakvelidze,Richard Kennedy,Sanjiv Lakhanpal,Peter J. Pappas
出处
期刊:Phlebology [SAGE Publishing]
卷期号:: 026835552211427-026835552211427
标识
DOI:10.1177/02683555221142710
摘要

Introduction Endovascular stenting is the standard of care for the management of symptomatic chronic venous obstruction. The increased radial resistive force and longer lengths of Nitinol stents have led to questions over persistent post-operative back pain. The purpose of this investigation was to assess the incidence and severity of post-operative back pain of Nitinol stents compared to Wallstents. Methods A retrospective review of data at the Center for Vascular Medicine was performed. Patient demographics, pre-operative, one week, three-, six,- and 12 month visual analog pain scores (VAS) for back pain, stent type, diameter, length, and vein locations were assessed. Results From April 2014 to November 2021, 627 (412 women/215 men) patients were assessed for the presence of post-operative back pain after an initial iliac vein stent placement. Stents utilized were Wallstents ( n = 114), Venovo ( n = 342), and Abre ( n = 171). The most common Nitinol stent diameter and lengths were 14 mm, 16 mm, and 120 mm, respectively ( p ≤ .03). The incidence of back pain at one week was 66% (411/627). VAS scores at one week and one, three, and six months post-operatively were the following: Wallstents-2.6 ± 3 ( n = 66), 1.7 ± 2.6 ( n = 43) 0.7 ± 2 ( n = 51), and 0 ± 0 ( n = 27); Abre-3.5 ± 3 ( n = 130), 3.8 ± 3 ( n = 19), 1.2 ± 2.5 ( n = 12), and 1 ± 2 ( n = 5); and Venovo- 2.5 ± 3 ( n = 216), 2.4 ± 3 ( n = 70), 0.9 ± 2 ( n = 68), and 0.6 ± 1.7 ( n = 49). There was no difference in the severity of back pain at any time point ( p ≥ .99). The development of back pain was unrelated to stent type, diameter, length, or covered vein territory. Conclusions Post-operative back pain was observed in 66% of patients at one week. The average pain score at one week for the entire cohort was three, which declined to less than one at one month. No difference in the severity of back pain between groups was observed at any time point, and the development of back pain is unrelated to stent type, diameter, length, or covered vein territory.
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