Division of Interventional Radiology, University Health Network, Toronto, ON, Canada.
Centro per la cura del Piede Diabetico, Clinica San Carlo, Paderno Dugnano, MI, Italy.
J Endovasc Ther. 2022 Jun;29(3):468-477. doi: 10.1177/15266028211050309. Epub 2021 Oct 8.
To perform a systematic review assessing the safety and efficacy of percutaneous transluminal angioplasty (PTA) for treatment of critical hand ischemia (CHI) due to below-the-elbow (BTE) obstructive arterial disease.
MEDLINE and EMBASE systematic searches were performed from inception to December 2020 to identify studies assessing PTA for management of BTE obstructive arterial disease. Three independent reviewers performed abstract selection, data extraction, and quality assessment. The Newcastle-Ottawa Scale was used to assess individual study bias for non-randomized controlled trials.
Eight studies comprising 176 patients with obstructive BTE vessel disease were included. All studies had a score >5 on the Newcastle-Ottawa Scale, indicative of high quality. All studies used low-profile balloons (1.5-4 mm) for PTA of stenotic lesions or chronic total occlusions (CTOs). The weighted average technical success and clinical success rates were 89.3% (range = 82%-100%) and 69.9% (range = 19%-100%), respectively, at a mean follow-up of 29.7 ± 17.1 months. The short-term (<30 days) complication rate was low at 4.7% and most commonly included access site hematomas, pseudoaneurysms, and radial artery perforation or re-thrombosis. Nearly 20% of patients required an amputation, and most (96%) were minor (either distal phalanges or digits). Only 2 patients required above-wrist amputations. The primary and secondary patency rate at 5 years were 38% and 54%, respectively. The cumulative 5-year mortality rate was 33.1%.
PTA for CHI due to BTE obstructive arterial disease is feasible with a high technical success rate and a low short-term complication rate. Additional long-term comparative studies are required to unequivocally establish the clinical benefit of endovascular treatment compared with conservative management or surgical bypass.
系统评价经皮腔内血管成形术(PTA)治疗肘下(BTE)阻塞性动脉疾病引起的严重手部缺血(CHI)的安全性和疗效。
从建库至 2020 年 12 月,对评估 PTA 治疗 BTE 阻塞性动脉疾病的研究进行了 MEDLINE 和 EMBASE 系统检索。三名独立的审查员进行了摘要选择、数据提取和质量评估。纽卡斯尔-渥太华量表用于评估非随机对照试验的个体研究偏倚。
纳入了 8 项共 176 例 BTE 血管阻塞性疾病患者的研究。所有研究的纽卡斯尔-渥太华量表评分均>5,表明质量较高。所有研究均采用低剖面球囊(1.5-4mm)对狭窄病变或慢性完全闭塞(CTO)进行 PTA。加权平均技术成功率和临床成功率分别为 89.3%(范围为 82%-100%)和 69.9%(范围为 19%-100%),平均随访时间为 29.7±17.1 个月。短期(<30 天)并发症发生率较低,为 4.7%,最常见的包括入路部位血肿、假性动脉瘤和桡动脉穿孔或再血栓形成。近 20%的患者需要截肢,大多数(96%)为轻度(远端指骨或指)。仅 2 例患者需要腕部以上截肢。5 年时的一期和二期通畅率分别为 38%和 54%。5 年累积死亡率为 33.1%。
对于 BTE 阻塞性动脉疾病引起的 CHI,PTA 是可行的,技术成功率高,短期并发症发生率低。需要进一步进行长期的对照研究,以明确血管内治疗与保守治疗或手术旁路相比的临床获益。