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首页> 外文期刊>Journal of endovascular therapy: an official journal of the International Society of Endovascular Specialists >Systematic Review of Off-the-Shelf or Physician-Modified Fenestrated and Branched Endografts
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Systematic Review of Off-the-Shelf or Physician-Modified Fenestrated and Branched Endografts

机译:对现成的或医师改良的有孔和分支状内移植物的系统评价

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Purpose: To determine the safety and efficacy of off-the-shelf fenestrated/branched grafts (OSFGs) and physician-modified stent-grafts (PMSGs) for the treatment of complex abdominal aortic aneurysms. Methods: A systematic search of the MEDLINE database via PubMed from January 2001 through March 2015 retrieved 23 relevant articles evaluating the clinical outcomes following the management of patients with pararenal or thoracoabdominal aortic aneurysms. The 15 articles on PMSGs and 8 on OSFGs contained data on 308 patients (mean age 72.93 +/- 2.89 years; 213 men). The safety endpoint was major adverse events; the efficacy outcome measure was clinical treatment success (aneurysm exclusion without type I/III endoleak, permanent paralysis, long-term dialysis, or unresolved major complications). Extracted outcome data were pooled and compared between groups; data are given as the pooled proportions and 95% confidence interval (CI). Clinical data are presented as the weighted mean. Results: Of the 308 patients analyzed, almost one third were operated on an emergency basis. The mean aneurysm diameters were 75.9 +/- 17.3 mm (range 56-115) for the PMSGs and 68.1 +/- 13.7 mm (range 60-100) for the OSFGs. A total of 936 renal and visceral vessels were targeted. Major adverse events (safety) occurred in 24 (12.8%) PMSG patients (95% CI 8.6% to 18.7%) and in 9 (7.4%) OSFG patients (95% CI 3.7% to 14%). Clinical treatment success (efficacy) was observed in 171/187 (91.4%) PMSG patients (95% CI 86.2% to 94.9%) and in 115/121 (95%) OSFG patients (95% CI 89.1% to 98.0%). Corresponding cumulative 30-day target vessel and branch stent perfusion rates were 97.2% (95% CI 95.1% to 98.4%) and 97.6% (95% CI 95.5% to 98.8%) for the PMSG group and 99.6% (95% CI 98.3% to 99.9%) and 98.4% (95% CI 96.5% to 99.4%) for the OSFG group. Six (3.2%) deaths occurred in the PMSG group only; 2 (1.1%) were aneurysm related. Overall branch patency was recorded in 443/458 (96.7%) and in 468/478 (97.9%) of target vessels in the PMSG and OSFG groups, respectively. Conclusion: Off-the-shelf and physician-modified technology seems effective and safe, in both the elective and acute settings, for the treatment of complex aortic aneurysms. Future research within a randomized trial should investigate the true limitations of these devices.
机译:目的:确定现成的开窗/分支移植物(OSFGs)和医生改良的支架移植物(PMSGs)治疗复杂腹主动脉瘤的安全性和有效性。方法:2001年1月至2015年3月间通过PubMed对MEDLINE数据库进行系统搜索,检索了23篇相关文章,评估了肾旁或胸腹主动脉瘤患者的治疗后的临床结局。关于PMSG的15篇文章和关于OSFG的8篇文章包含308例患者的数据(平均年龄72.93 +/- 2.89岁; 213例男性)。安全终点为主要不良事件。疗效结果的衡量标准是临床治疗是否成功(无I / III型内漏,永久性麻痹,长期透析或未解决的主要并发症的动脉瘤排除)。汇总提取的结果数据,并在各组之间进行比较;数据以合并比例和95%置信区间(CI)给出。临床数据以加权平均值表示。结果:在分析的308例患者中,几乎三分之一是在紧急情况下进行的。 PMSG的平均动脉瘤直径为75.9 +/- 17.3 mm(范围56-115),OSFG的平均动脉瘤直径为68.1 +/- 13.7 mm(范围60-100)。共有936个肾脏和内脏血管作为目标。 24例(12.8%)PMSG患者(95%CI 8.6%至18.7%)和9例(7.4%)OSFG患者(95%CI 3.7%至14%)发生了主要不良事件(安全性)。在171/187(91.4%)PMSG患者(95%CI 86.2%至94.9%)和115/121(95%)OSFG患者(95%CI 89.1%至98.0%)中观察到临床治疗成功(疗效)。 PMSG组相应的30天目标血管和分支支架的累积灌注率分别为97.2%(95%CI 95.1%至98.4%)和97.6%(95%CI 95.5%至98.8%)和99.6%(95%CI 98.3) OSFG组为9%至99.9%)和98.4%(95%CI为96.5%至99.4%)。仅PMSG组有6例(3.2%)死亡; 2例(1.1%)与动脉瘤有关。 PMSG和OSFG组的目标血管分别记录了443/458(96.7%)和468/478(97.9%)的总分支通畅性。结论:现成的和医生改良的技术在选择性和急性环境中对于治疗复杂的主动脉瘤似乎是有效和安全的。随机试验中的未来研究应调查这些设备的真正局限性。

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