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一项针对静脉性腿部溃疡(VenUS 6)治疗的压缩疗法的随机对照试验:一项实用、多中心、平行组、三臂随机对照试验的研究方案。

A randomised controlled trial of compression therapies for the treatment of venous leg ulcers (VenUS 6): study protocol for a pragmatic, multicentre, parallel-group, three-arm randomised controlled trial.

机构信息

York Trials Unit, Department of Health Sciences, Faculty of Science, University of York, Lower Ground Floor ARRC Building, York, YO10 5DD, UK.

Centre for Health Economics, University of York, York, YO10 5DD, UK.

出版信息

Trials. 2023 May 26;24(1):357. doi: 10.1186/s13063-023-07349-2.

Abstract

BACKGROUND

Venous leg ulcer(s) are common, recurring, open wounds on the lower leg, resulting from diseased or damaged leg veins impairing blood flow. Wound healing is the primary treatment aim for venous leg ulceration, alongside the management of pain, wound exudate and infection. Full (high) compression therapy delivering 40 mmHg of pressure at the ankle is the recommended first-line treatment for venous leg ulcers. There are several different forms of compression therapy available including wraps, two-layer hosiery, and two-layer or four-layer bandages. There is good evidence for the clinical and cost-effectiveness of four-layer bandage and two-layer hosiery but more limited evidence for other treatments (two-layer bandage and compression wraps). Robust evidence is required to compare clinical and cost-effectiveness of these and to investigate which is the best compression treatment for reducing time to healing of venous leg ulcers whilst offering value for money. VenUS 6 will therefore investigate the clinical and cost-effectiveness of evidence-based compression, two-layer bandage and compression wraps for time to healing of venous leg ulcers.

METHODS

VenUS 6 is a pragmatic, multi-centre, three-arm, parallel-group, randomised controlled trial. Adult patients with a venous leg ulcer will be randomised to receive (1) compression wraps, (2) two-layer bandage or (3) evidence-based compression (two-layer hosiery or four-layer bandage). Participants will be followed up for between 4 and 12 months. The primary outcome will be time to healing (full epithelial cover in the absence of a scab) in days since randomisation. Secondary outcomes will include key clinical events (e.g. healing of the reference leg, ulcer recurrence, ulcer/skin deterioration, amputation, admission/discharge, surgery to close/remove incompetent superficial veins, infection or death), treatment changes, adherence and ease of use, ulcer related pain, health-related quality of life and resource use.

DISCUSSION

VenUS 6 will provide robust evidence on the clinical and cost-effectiveness of the different forms of compression therapies for venous leg ulceration. VenUS 6 opened to recruitment in January 2021 and is currently recruiting across 30 participating centres.

TRIAL REGISTRATION

ISRCTN67321719 . Prospectively registered on 14 September 2020.

摘要

背景

静脉性腿部溃疡是小腿上常见的、反复发作的开放性伤口,是由于腿部静脉病变或受损导致血流不畅引起的。治疗静脉性腿部溃疡的主要目标是促进伤口愈合,同时还需要控制疼痛、伤口渗出物和感染。在脚踝处提供 40mmHg 压力的全(高)压缩疗法是治疗静脉性腿部溃疡的一线推荐治疗方法。目前有多种不同形式的压缩疗法可供选择,包括包扎、两层连裤袜和两层或四层绷带。四层绷带和两层连裤袜在临床和成本效益方面有很好的证据,但其他治疗方法(两层绷带和压缩包扎)的证据则更为有限。需要有强有力的证据来比较这些治疗方法的临床和成本效益,并确定哪种压缩治疗方法最能减少静脉性腿部溃疡的愈合时间,同时提供物有所值的效果。因此,VenUS 6 将研究基于证据的压缩治疗、两层绷带和压缩包扎在促进静脉性腿部溃疡愈合方面的临床和成本效益。

方法

VenUS 6 是一项实用的、多中心的、三臂、平行组、随机对照试验。患有静脉性腿部溃疡的成年患者将被随机分配接受(1)压缩包扎、(2)两层绷带或(3)基于证据的压缩治疗(两层连裤袜或四层绷带)。参与者将接受 4 至 12 个月的随访。主要结局是自随机分组以来的愈合时间(无痂的完全上皮覆盖),以天数表示。次要结局将包括关键临床事件(例如参考腿的愈合、溃疡复发、溃疡/皮肤恶化、截肢、入院/出院、手术闭合/切除功能不全的浅静脉、感染或死亡)、治疗改变、依从性和易用性、溃疡相关疼痛、健康相关生活质量和资源使用。

讨论

VenUS 6 将提供关于静脉性腿部溃疡不同形式的压缩治疗的临床和成本效益的有力证据。VenUS 6 于 2021 年 1 月开始招募,并正在 30 个参与中心进行招募。

试验注册

ISRCTN67321719。于 2020 年 9 月 14 日前瞻性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1e5/10223923/43d0123ae0c6/13063_2023_7349_Fig1_HTML.jpg

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