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静脉内消融治疗静脉性腿部溃疡。

Endovenous ablation for venous leg ulcers.

机构信息

Academic Vascular Surgical Unit, Hull York Medical School, Hull University Teaching Hospitals NHS Trust, Hull, UK.

出版信息

Cochrane Database Syst Rev. 2023 Jul 27;7(7):CD009494. doi: 10.1002/14651858.CD009494.pub3.

Abstract

BACKGROUND

Venous leg ulcers (VLUs) are a serious manifestation of chronic venous disease affecting up to 3% of the adult population. This typically recalcitrant and recurring condition significantly impairs quality of life, and its treatment places a heavy financial burden upon healthcare systems. The longstanding mainstay treatment for VLUs is compression therapy. Surgical removal of incompetent veins reduces the risk of ulcer recurrence. However, open surgery is an unpopular option amongst people with VLU, and many people are unsuitable for it. The efficacy of the newer, minimally-invasive endovenous techniques has been established in uncomplicated superficial venous disease, and these techniques can also be used in the management of VLU. When used with compression, endovenous ablation aims to further reduce pressure in the veins of the leg, which may impact ulcer healing.

OBJECTIVES

To determine the effects of superficial endovenous ablation on the healing and recurrence of venous leg ulcers and the quality of life of people with venous ulcer disease.

SEARCH METHODS

In April 2022 we searched the Cochrane Wounds Specialised Register; the Cochrane Central Register of Controlled Trials (CENTRAL); Ovid MEDLINE (including In-Process & Other Non-Indexed Citations); Ovid Embase and EBSCO CINAHL Plus. We also searched clinical trials registries for ongoing and unpublished studies, and scrutinised reference lists of relevant included studies as well as reviews, meta-analyses and health technology reports to identify additional studies. There were no restrictions on the language of publication, but there was a restriction on publication year from 1998 to April 2022 as superficial endovenous ablation is a comparatively new technology.

SELECTION CRITERIA

Randomised controlled trials (RCTs) comparing endovenous ablative techniques with compression versus compression therapy alone for the treatment of VLU were eligible for inclusion. Studies needed to have assessed at least one of the following primary review outcomes related to objective measures of ulcer healing such as: proportion of ulcers healed at a given time point; time to complete healing; change in ulcer size; proportion of ulcers recurring over a given time period or at a specific point; or ulcer-free days. Secondary outcomes of interest were patient-reported quality of life, economic data and adverse events.

DATA COLLECTION AND ANALYSIS

Two reviewers independently assessed studies for eligibility, extracted data, carried out risk of bias assessment using the Cochrane RoB 1 tool, and assessed GRADE certainty of evidence.

MAIN RESULTS

The previous version of this review found no RCTs meeting the inclusion criteria. In this update, we identified two eligible RCTs and included them in a meta-analysis. There was a total of 506 participants with an active VLU, with mean durations of 3.1 months ± 1.1 months in the EVRA trial and 60.5 months ± 96.4 months in the VUERT trial. Both trials randomised participants to endovenous treatment and compression or compression alone, however the compression alone group in the EVRA trial received deferred endovenous treatment (after ulcer healing or from six months). There is high-certainty evidence that combined endovenous ablation and compression compared with compression therapy alone, or compression with deferred endovenous treatment, improves time to complete ulcer healing (pooled hazard ratio (HR) 1.41, 95% CI 1.36 to 1.47; I = 0%; 2 studies, 466 participants). There is moderate-certainty evidence that the proportion of ulcers healed at 90 days is probably higher with combined endovenous ablation and compression compared with compression therapy alone or compression with deferred endovenous treatment (risk ratio (RR) 1.14, 95% CI 1.00 to 1.30; I = 0%; 2 studies, 466 participants). There is low-certainty evidence showing an unclear effect on ulcer recurrence at one year in people with healed ulcers with combined endovenous treatment and compression when compared with compression alone or compression with deferred endovenous treatment (RR 0.29, 95% CI 0.03 to 2.48; I = 78%; 2 studies, 460 participants). There is also low-certainty evidence that the median number of ulcer-free days at one year may not differ (306 (interquartile range (IQR) 240 to 328) days versus 278 (IQR 175 to 324) days) following combined endovenous treatment and compression when compared with compression and deferred endovenous treatment; (1 study, 450 participants). There is low-certainty evidence of an unclear effect in rates of thromboembolism between groups (RR 2.02, 95% CI 0.51 to 7.97; I = 78%, 2 studies, 506 participants). The addition of endovenous ablation to compression is probably cost-effective at one year (99% probability at GBP 20,000/QALY; 1 study; moderate-certainty evidence).

AUTHORS' CONCLUSIONS: Endovenous ablation of superficial venous incompetence in combination with compression improves leg ulcer healing when compared with compression alone. This conclusion is based on high-certainty evidence. There is moderate-certainty evidence to suggest that it is probably cost-effective at one year and low certainty evidence of unclear effects on recurrence and complications. Further research is needed to explore the additional benefit of endovenous ablation in ulcers of greater than six months duration and the optimal modality of endovenous ablation.

摘要

背景

静脉性腿部溃疡(VLUs)是一种严重的慢性静脉疾病表现,影响着高达 3%的成年人口。这种通常难以治愈且反复发作的疾病严重影响生活质量,其治疗给医疗保健系统带来了沉重的经济负担。VLUs 的长期主要治疗方法是压迫疗法。去除功能不全静脉的手术可降低溃疡复发的风险。然而,开放式手术在有 VLU 的人群中不受欢迎,许多人不适合这种手术。较新的微创静脉内技术在单纯性浅表静脉疾病中的疗效已经确立,这些技术也可用于静脉性腿部溃疡的治疗。当与压迫相结合时,静脉内消融旨在进一步降低腿部静脉的压力,这可能会影响溃疡的愈合。

目的

评估浅表静脉内消融对静脉性腿部溃疡愈合和复发以及静脉性溃疡疾病患者生活质量的影响。

检索方法

2022 年 4 月,我们检索了 Cochrane 伤口专业注册库;Cochrane 中央对照试验注册库(CENTRAL);Ovid MEDLINE(包括在处理和其他非索引引文);Ovid Embase 和 EBSCO CINAHL Plus。我们还检索了正在进行和未发表研究的临床试验登记处,并仔细审查了相关纳入研究的参考文献以及综述、荟萃分析和卫生技术报告,以确定其他研究。出版语言不受限制,但出版年份限于 1998 年至 2022 年 4 月,因为浅表静脉内消融是一种相对较新的技术。

选择标准

随机对照试验(RCTs)将静脉内消融技术与压迫疗法与单纯压迫疗法治疗静脉性腿部溃疡进行比较。研究需要评估至少一个以下主要评估指标:在给定时间点溃疡愈合的比例;完全愈合的时间;溃疡大小的变化;在给定时间段或特定时间点复发的溃疡比例;或无溃疡天数。感兴趣的次要结局包括患者报告的生活质量、经济数据和不良事件。

数据收集和分析

两位评审员独立评估研究的纳入性,提取数据,使用 Cochrane RoB 1 工具进行风险偏倚评估,并评估 GRADE 证据确定性。

主要结果

前一版综述未发现符合纳入标准的 RCTs。在本次更新中,我们确定了两项符合条件的 RCT 并将其纳入荟萃分析。共有 506 名活跃的 VLU 参与者,EVRA 试验的平均溃疡持续时间为 3.1 个月±1.1 个月,VUERT 试验的平均溃疡持续时间为 60.5 个月±96.4 个月。两项试验均将参与者随机分配到静脉内治疗和压迫或单纯压迫组,但 EVRA 试验中单纯压迫组接受延迟静脉内治疗(在溃疡愈合后或从 6 个月开始)。有高质量证据表明,与单纯压迫治疗或单纯压迫加延迟静脉内治疗相比,联合静脉内消融和压迫治疗可加快溃疡完全愈合的时间(合并危险比(HR)1.41,95%CI 1.36 至 1.47;I=0%;2 项研究,466 名参与者)。有中等质量证据表明,与单纯压迫治疗或单纯压迫加延迟静脉内治疗相比,联合静脉内消融和压迫治疗在 90 天时溃疡愈合的比例可能更高(风险比(RR)1.14,95%CI 1.00 至 1.30;I=0%;2 项研究,466 名参与者)。有低质量证据表明,在治愈的溃疡患者中,与单纯压迫治疗或单纯压迫加延迟静脉内治疗相比,联合静脉内治疗和压迫治疗在一年时溃疡复发的可能性较低(RR 0.29,95%CI 0.03 至 2.48;I=78%;2 项研究,460 名参与者)。也有低质量证据表明,与单纯压迫加延迟静脉内治疗相比,在一年时无溃疡天数的中位数可能没有差异(306(四分位距(IQR)240 至 328)天与 278(IQR 175 至 324)天);1 项研究,450 名参与者)。在组间血栓栓塞的发生率方面,也有低质量证据表明效果不明确(RR 2.02,95%CI 0.51 至 7.97;I=78%;2 项研究,506 名参与者)。与单纯压迫治疗相比,静脉内消融联合压迫治疗在一年时可能具有成本效益(GBP 20,000/QALY 的 99%概率;1 项研究;中等质量证据)。

作者结论

与单纯压迫治疗相比,浅表静脉内消融联合压迫治疗可加速腿部溃疡的愈合。这一结论基于高质量证据。有中等质量证据表明,在一年时它可能具有成本效益,且在复发和并发症方面的效果不明确。需要进一步研究来探索静脉内消融在病程超过 6 个月的溃疡中的额外益处,以及静脉内消融的最佳方式。

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