Dias Miranda Nathalia de Carvalho, Marimpietri Felipe Santos, Marcolin Miranda Luccas, Carneiro de Lima Pedro Emanuel, Vasconcellos Danilo Costa Marques da Silva, Teixeira Eduardo Corvello, de Moraes Tayrine Mazotti
Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil.
Bahiana School of Medicine and Public Health, Salvador, Bahia, Brazil.
Ann Vasc Surg. 2025 Apr;113:214-220. doi: 10.1016/j.avsg.2024.12.071. Epub 2025 Jan 24.
The main treatment for chronic mesenteric ischemia (CMI) is revascularization, typically achieved through stent angioplasty of the superior mesenteric artery, and in certain cases, the celiac trunk. However, long-term outcomes using bare-metal stents (BMSs) have been less than satisfactory. Therefore, we aimed to compare the performance of covered stents (CSs) versus BMSs in patients treated for CMI.
Pubmed, Embase, and Cochrane Central Register of Controlled Trials databases were systematically searched for studies of patients with CMI who underwent stenting procedures using BMS or CS. The main outcomes were primary patency and freedom from reintervention. Statistical analysis was performed using R version 3.6.
One randomized clinical trial and 5 observational studies were included. In the pooled analysis, patients undergoing the covered stenting approach had a higher primary patency (hazard ratio 0.40; 95% confidence interval 0.23-0.68; P < 0.01). Additionally, CS also demonstrated significantly superior freedom from reintervention when compared to BMS patients (hazard ratio 0.30; 95% confidence interval 0.13-0.71; P < 0.01).
In patients undergoing transluminal angioplasty with stent placement both in the celiac trunk and superior mesenteric artery, the use of CS indicated superior primary patency and a higher rate of freedom from reintervention than BMS. These findings indicate superior outcomes with CS and may suggest their use as the preferred stent option in patients with CMI. However, these findings should be interpreted cautiously due to the limited number of studies, the moderate to serious risk of bias in the included data, and the significant heterogeneity observed. Further high-quality clinical trials are necessary to validate these results and strengthen the evidence base for clinical practice.
慢性肠系膜缺血(CMI)的主要治疗方法是血管重建,通常通过肠系膜上动脉支架血管成形术实现,在某些情况下,还包括腹腔干血管成形术。然而,使用裸金属支架(BMS)的长期疗效并不理想。因此,我们旨在比较覆膜支架(CS)与BMS在CMI患者治疗中的性能。
系统检索了PubMed、Embase和Cochrane对照试验中央注册数据库,以查找接受BMS或CS支架置入术的CMI患者的研究。主要结局指标为原发性通畅率和无需再次干预。使用R 3.6版本进行统计分析。
纳入1项随机临床试验和5项观察性研究。在汇总分析中,接受覆膜支架置入术的患者原发性通畅率更高(风险比0.40;95%置信区间0.23 - 0.68;P < 0.01)。此外,与BMS患者相比,CS在无需再次干预方面也表现出显著优势(风险比0.30;95%置信区间0.13 - 0.71;P < 0.01)。
在腹腔干和肠系膜上动脉均接受腔内血管成形术并置入支架的患者中,使用CS显示出比BMS更高的原发性通畅率和更低的再次干预率。这些发现表明CS具有更好的疗效,并可能提示其可作为CMI患者首选的支架选择。然而,由于研究数量有限、纳入数据存在中度至严重的偏倚风险以及观察到显著的异质性,这些发现应谨慎解读。需要进一步的高质量临床试验来验证这些结果,并加强临床实践的证据基础。