Department of Surgery, Division of Vascular and Endovascular Surgery, Universidade Federal de São Paulo, São Paulo, Brazil.
Evidence Based Medicine, Cochrane Brazil, Universidade Federal de São Paulo, São Paulo, Brazil.
Cochrane Database Syst Rev. 2024 Feb 14;2(2):CD013293. doi: 10.1002/14651858.CD013293.pub2.
Patients who present with problems with definitive dialysis access (arteriovenous fistula (AVF) or arteriovenous graft (AVG)) become catheter dependent (temporary access), a condition that often carries a higher risk of infections, central venous occlusions and recurrent hospitalisations. For AVG, primary patency rates are reported to be 30% to 90% in patients undergoing thrombectomy or thrombolysis. According to the National Kidney Foundation-Kidney Disease Outcomes Quality Initiative (NKF-KDOQI) guidelines, surgery is preferred when the cause of the thrombosis is a stenosis at the site of the anastomosis in thrombosed AVF. The European Best Practice Guidelines (EBPG) reported that thrombosed AVF may be preferably treated with endovascular techniques, but when the cause of thrombosis is in the anastomosis, surgery provides better results with re-anastomosis. Therefore, there is a need to carry out a systematic review to determine the effectiveness and safety of the intervention for thrombosed fistulae.
This review aims to establish the efficacy and safety of interventions for failed AVF and AVG in patients receiving haemodialysis (HD).
We searched the Cochrane Kidney and Transplant Register of Studies up to 28 January 2024 through contact with the Information Specialist using search terms relevant to this review. Studies in the Register are identified through searches of CENTRAL, MEDLINE, EMBASE, conference proceedings, the International Clinical Trials Registry Portal (ICTRP) Search Portal and ClinicalTrials.gov.
The review included randomised controlled trials (RCTs) and quasi-RCTs in people undergoing HD treatment using AVF or AVG presenting with clinical or haemodynamic evidence of thrombosis. Patients had to have used an AVF or AVG at least once.
Summary estimates of effect were obtained using a random-effects model, and results were expressed as risk ratios (RR) and their 95% confidence intervals (CI) for dichotomous outcomes. Confidence in the evidence was assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach.
Our search strategy identified 14 eligible studies (1176 randomised participants) for inclusion in this review. We included three types of interventions for the treatment of thrombosed AVF and AVG: (1) types of thrombectomy, (2) types of thrombolysis and (3) surgical procedures. Most of the included studies had a high risk of bias due to a poor study design, a low number of patients and industry involvement. Overall, there was insufficient evidence to suggest that a specific intervention was better than another for the outcomes of failure, primary patency at 30 days, technical success and adverse events (both major and minor). Primary patency at 30 days may improve with surgical compared to mechanical thrombectomy (3 studies, 404 participants: RR 1.36, 95% CI 1.07 to 1.67); however, the evidence is very uncertain. Death, access dysfunction, successful dialysis, and SONG (Standards Outcomes in Nephrology) outcomes were rarely reported. The current review is limited by the small number of available studies with a limited number of patients enrolled. Most of the studies included in this review have a high risk of bias and a low or very low certainty of evidence. Further research is required to define the most effective and clinically appropriate technique for access dysfunction.
AUTHORS' CONCLUSIONS: It remains unclear whether any intervention therapy affects the patency at 30 days or failure in any thrombosed HD AV access (very low certainty of evidence). Future research will very likely change the evidence base. Based on the importance of HD access to these patients, future studies of these interventions among people receiving HD should be a priority.
出现明确透析通路(动静脉瘘 (AVF) 或动静脉移植物 (AVG))问题的患者会依赖导管(临时通路),这种情况通常会增加感染、中心静脉阻塞和反复住院的风险。对于 AVG,接受血栓切除术或溶栓治疗的患者的原发性通畅率报告为 30% 至 90%。根据国家肾脏基金会-肾脏病结果质量倡议 (NKF-KDOQI) 指南,如果血栓形成的原因是吻合口部位的狭窄,则手术是首选。欧洲最佳实践指南 (EBPG) 报告称,对于血栓形成的 AVF,可能更适合采用血管内技术治疗,但如果血栓形成的原因是吻合口,则手术提供更好的结果,重新吻合。因此,需要进行系统评价,以确定干预血栓形成瘘的有效性和安全性。
本综述旨在确定在接受血液透析 (HD) 的患者中,治疗失败的 AVF 和 AVG 的干预措施的疗效和安全性。
我们通过与信息专家联系,使用与本次审查相关的搜索词,对截至 2024 年 1 月 28 日的 Cochrane 肾脏和移植登记册中的研究进行了搜索。通过搜索 CENTRAL、MEDLINE、EMBASE、会议论文集、国际临床试验注册门户 (ICTRP) 搜索门户和 ClinicalTrials.gov,在登记册中确定研究。
本综述纳入了使用 AVF 或 AVG 进行 HD 治疗且出现临床或血液动力学血栓形成证据的患者进行的随机对照试验 (RCT) 和准 RCT。患者必须至少使用过一次 AVF 或 AVG。
使用随机效应模型获得汇总效应估计值,并使用风险比 (RR) 和其 95%置信区间 (CI) 表示二分类结局的结果。使用 Grading of Recommendations Assessment, Development and Evaluation (GRADE) 方法评估证据的可信度。
我们的搜索策略确定了 14 项符合纳入本综述条件的研究(1176 名随机参与者)。我们纳入了三种治疗血栓形成的 AVF 和 AVG 的干预措施:(1) 血栓切除术类型,(2) 溶栓术类型,和 (3) 手术程序。大多数纳入的研究由于研究设计不佳、患者数量少和行业参与而存在高偏倚风险。总体而言,没有足够的证据表明特定的干预措施优于另一种干预措施在失败、30 天原发性通畅、技术成功和不良事件(主要和次要)方面的结果。与机械血栓切除术相比,手术可能会提高 30 天原发性通畅率(3 项研究,404 名参与者:RR 1.36,95%CI 1.07 至 1.67);然而,证据非常不确定。死亡、通路功能障碍、成功透析和 SONG(肾脏病标准结果)结局很少被报道。本综述受到可用研究数量有限且纳入患者数量有限的限制。本综述中纳入的大多数研究都存在高偏倚风险和低或非常低的证据确定性。需要进一步研究来确定最有效和最适合临床的通路功能障碍技术。
目前尚不清楚任何干预治疗是否会影响任何血栓形成的 HD AV 通路的 30 天通畅率或失败(证据确定性非常低)。未来的研究很可能会改变证据基础。基于 HD 通路对这些患者的重要性,未来在接受 HD 的人群中进行这些干预措施的研究应成为优先事项。