Angioplasty or stenting for deep venous thrombosis.

IF 8.8 2区 医学 Q1 MEDICINE, GENERAL & INTERNAL Cochrane Database of Systematic Reviews Pub Date : 2025-02-19 DOI:10.1002/14651858.CD011468.pub2
Ronald Lg Flumignan, Luis Cu Nakano, Carolina Dq Flumignan, Jose Cc Baptista-Silva
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The primary outcomes were PTS and venous thromboembolism (VTE); secondary outcomes were mortality, major bleeding, secondary patency, duration of hospitalisation, quality of life (QoL), and adverse events. We used the Cochrane RoB 1 tool to assess the risk of bias for RCTs and GRADE to assess the certainty of evidence. We performed meta-analysis where appropriate.</p><p><strong>Main results: </strong>We included two RCTs (134 participants) that were conducted in China and presented comparisons for acute obstruction after DVT based on length of follow-up (12 months (early), 24 months (intermediate), and 36 months (long term)). Angioplasty or stenting plus BMT and thrombolysis versus BMT and thrombolysis for acute obstruction due to DVT (intermediate time point) In the intermediate time point, angioplasty or stenting may have little to no effect on PTS (Venous Clinical Severity Score (VCSS): mean difference (MD) -3.21, 95% confidence interval (CI) -7.74 to 1.33; 2 studies, 133 participants; very low-certainty evidence) and adverse events (limb pain) (risk ratio (RR) 0.68, 95% CI 0.04 to 10.33; 1 study, 67 participants; very low-certainty evidence), but the evidence is very uncertain. Angioplasty or stenting may increase secondary patency (RR 0.26, 95% CI 0.11 to 0.59; 2 studies, 133 participants; very low-certainty evidence), but the evidence is very uncertain. The evidence is very uncertain about the effect of angioplasty or stenting on quality of life (MD 10.54, 95% CI -1.34 to 22.41; 2 studies, 133 participants; very low-certainty evidence), and is not estimable for VTE, mortality, or major bleeding. 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引用次数: 0

Abstract

Background: The best medical treatment (BMT) for treating deep venous thrombosis (DVT) includes anticoagulation and compression stockings. Angioplasty and stenting restore vessel patency and facilitate blood flow. In some people with DVT, angioplasty or stenting is used to minimise complications such as post-thrombotic syndrome (PTS), but their effects are under discussion.

Objectives: To assess the effects of adjunctive angioplasty or stenting on a background treatment of anticoagulation and thrombolysis, compared with BMT, sham procedure, thrombolysis, or any combination of these treatments, in people with DVT.

Search methods: We searched CENTRAL, MEDLINE, Embase, LILACS, IBECS, CINAHL, and AMED databases, as well as the World Health Organization International Clinical Trials Registry Platform and ClinicalTrials.gov trials registers, to 20 April 2023. We checked the bibliographies of included trials for further references to relevant trials and contacted specialists in the field, manufacturers, and authors of the included trials for any unpublished data.

Selection criteria: We included randomised controlled trials (RCTs) comparing angioplasty or stenting on a background treatment of anticoagulation and thrombolysis, compared with BMT, sham procedure, thrombolysis, or any combination of these treatments, in the management of people with acute obstruction due to DVT. We excluded participants who had a baseline PTS diagnosis or who had received any form of mechanical thrombectomy, as this was investigated in a separate Cochrane review.

Data collection and analysis: We used standard Cochrane methods. The primary outcomes were PTS and venous thromboembolism (VTE); secondary outcomes were mortality, major bleeding, secondary patency, duration of hospitalisation, quality of life (QoL), and adverse events. We used the Cochrane RoB 1 tool to assess the risk of bias for RCTs and GRADE to assess the certainty of evidence. We performed meta-analysis where appropriate.

Main results: We included two RCTs (134 participants) that were conducted in China and presented comparisons for acute obstruction after DVT based on length of follow-up (12 months (early), 24 months (intermediate), and 36 months (long term)). Angioplasty or stenting plus BMT and thrombolysis versus BMT and thrombolysis for acute obstruction due to DVT (intermediate time point) In the intermediate time point, angioplasty or stenting may have little to no effect on PTS (Venous Clinical Severity Score (VCSS): mean difference (MD) -3.21, 95% confidence interval (CI) -7.74 to 1.33; 2 studies, 133 participants; very low-certainty evidence) and adverse events (limb pain) (risk ratio (RR) 0.68, 95% CI 0.04 to 10.33; 1 study, 67 participants; very low-certainty evidence), but the evidence is very uncertain. Angioplasty or stenting may increase secondary patency (RR 0.26, 95% CI 0.11 to 0.59; 2 studies, 133 participants; very low-certainty evidence), but the evidence is very uncertain. The evidence is very uncertain about the effect of angioplasty or stenting on quality of life (MD 10.54, 95% CI -1.34 to 22.41; 2 studies, 133 participants; very low-certainty evidence), and is not estimable for VTE, mortality, or major bleeding. We downgraded the certainty of evidence for all reported outcomes in this comparison by two levels due to serious study limitations (risk of performance and other bias), and another level for imprecision (small numbers of events and participants). The imbalance between study group size and different vein access may also have contributed to the high heterogeneity seen in the analyses of these outcomes. We downgraded the certainty of evidence for PTS and quality of life by one level for inconsistency (no similarity of point estimates in any of the included studies, no overlap of CIs, and considerable heterogeneity in results). There is an additional difficulty with blinding personnel in this type of intervention, but the trialists should have reported blinding of outcome assessment.

Authors' conclusions: Although angioplasty or stenting may increase secondary patency in people with acute obstruction due to DVT, the evidence is very uncertain; the evidence is also very uncertain about the effect of angioplasty or stenting on PTS, quality of life, and adverse events in people with acute obstruction due to DVT. The effects on VTE, mortality, and major bleeding were not estimable or not assessed by the included studies. Future trials must be large enough to detect significant clinical outcomes, and provide data on original stenosis before angioplasty or stenting and differing times from the initial event, among other essential characteristics.

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血管成形术或支架植入术治疗深静脉血栓。
背景:治疗深静脉血栓形成(DVT)的最佳药物治疗(BMT)包括抗凝和加压袜。血管成形术和支架置入术可恢复血管通畅,促进血液流动。在一些深静脉血栓患者中,血管成形术或支架植入术可减少血栓后综合征(PTS)等并发症,但其效果仍在讨论中。目的:评估辅助血管成形术或支架置入术对DVT患者抗凝溶栓背景治疗的影响,与BMT、假手术、溶栓或这些治疗的任何组合进行比较。检索方法:我们检索了CENTRAL、MEDLINE、Embase、LILACS、IBECS、CINAHL和AMED数据库,以及世界卫生组织国际临床试验注册平台和ClinicalTrials.gov试验注册,截止到2023年4月20日。我们检查了纳入试验的参考文献,以进一步参考相关试验,并联系了该领域的专家、制造商和纳入试验的作者,以获取任何未发表的数据。选择标准:我们纳入了随机对照试验(RCTs),比较血管成形术或支架植入术在抗凝和溶栓背景治疗下与BMT、假手术、溶栓或这些治疗的任何组合在处理DVT急性梗阻患者方面的效果。我们排除了基线PTS诊断或接受过任何形式的机械取栓术的参与者,因为这在单独的Cochrane综述中进行了调查。资料收集与分析:采用标准Cochrane方法。主要结局为PTS和静脉血栓栓塞(VTE);次要结局是死亡率、大出血、二次通畅、住院时间、生活质量(QoL)和不良事件。我们使用Cochrane RoB 1工具评估随机对照试验的偏倚风险,使用GRADE评估证据的确定性。我们在适当的地方进行了meta分析。主要结果:我们纳入了在中国进行的两项随机对照试验(134名参与者),并根据随访时间(12个月(早期)、24个月(中期)和36个月(长期))对深静脉血栓栓塞后急性梗阻进行了比较。血管成形术或支架置入+ BMT +溶栓治疗急性DVT梗阻与BMT +溶栓治疗(中间时间点)在中间时间点,血管成形术或支架置入对PTS的影响可能很小或没有影响(静脉临床严重程度评分(VCSS):平均差值(MD) -3.21, 95%可信区间(CI) -7.74 ~ 1.33;2项研究,133名受试者;极低确定性证据)和不良事件(肢体疼痛)(风险比(RR) 0.68, 95% CI 0.04 ~ 10.33;1项研究,67名受试者;非常低确定性的证据),但证据非常不确定。血管成形术或支架植入可增加继发性通畅(RR 0.26, 95% CI 0.11 ~ 0.59;2项研究,133名受试者;非常低确定性的证据),但证据非常不确定。关于血管成形术或支架植入对生活质量的影响,证据非常不确定(MD 10.54, 95% CI -1.34 ~ 22.41;2项研究,133名受试者;非常低确定性的证据),并且对于静脉血栓栓塞、死亡率或大出血无法估计。由于严重的研究限制(表现风险和其他偏倚)和不精确(事件和参与者数量少),我们将本比较中所有报告结果的证据确定性降低了两个级别。研究组大小和不同静脉通路之间的不平衡也可能导致这些结果分析中的高度异质性。由于不一致,我们将PTS和生活质量证据的确定性降低了一级(在所有纳入的研究中没有相似的点估计,没有ci重叠,结果存在相当大的异质性)。在这种类型的干预中,盲化人员还有一个额外的困难,但试验人员应该报告结果评估的盲化。作者的结论是:尽管血管成形术或支架植入可能增加深静脉血栓急性梗阻患者的继发性通畅,但证据非常不确定;关于血管成形术或支架植入对深静脉血栓急性梗阻患者PTS、生活质量和不良事件的影响,证据也非常不确定。对静脉血栓栓塞(VTE)、死亡率和大出血的影响无法估计或未被纳入的研究评估。未来的试验必须足够大,以检测重要的临床结果,并提供血管成形术或支架植入前原始狭窄的数据,以及与初始事件不同的时间,以及其他基本特征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.60
自引率
2.40%
发文量
173
审稿时长
1-2 weeks
期刊介绍: The Cochrane Database of Systematic Reviews (CDSR) stands as the premier database for systematic reviews in healthcare. It comprises Cochrane Reviews, along with protocols for these reviews, editorials, and supplements. Owned and operated by Cochrane, a worldwide independent network of healthcare stakeholders, the CDSR (ISSN 1469-493X) encompasses a broad spectrum of health-related topics, including health services.
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