Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA
Department of Neurologic Surgery, Mayo Clinic, Rochester, Minnesota, USA.
J Neurointerv Surg. 2024 Jun 17;16(7):706-714. doi: 10.1136/jnis-2023-020514.
Surface-modified flow diverters are increasingly used in clinical settings. However, their safety profiles and additional benefits over non-coated devices still need to be explored. In this meta-analysis, we aimed to investigate and compare the clinical outcomes of the uncoated Phenox and coated Phenox HPC flow diverters.
A systematic literature review was performed using PubMed, Scopus, Embase, and Web of Science databases. Collected data were pooled and corresponding 95% confidence intervals (CI) were calculated. Outcomes of interest included aneurysm occlusion (>6 months) and complication rates. Additionally, the safety outcomes of prophylactic single (SAPT) and dual antiplatelet treatment (DAPT) approaches were compared for patients treated with coated Phenox HPC flow diverters.
We included 17 studies with 1238 patients. The overall complete occlusion rates were 80% (95% CI 74.01% to 86.56%) for Phenox HPC and 71.3% (95% CI 59.71% to 85.20%) for non-coated Phenox flow diverters (p=0.24). Ischemic complication rates were 7.3% (95% CI 4.6% to 11.39%) with the Phenox HPC and 5.3% (95% CI 4.07% to 6.91%) with the Phenox (p=0.24). For patients treated with Phenox HPC, the SAPT (5.5%; 95% CI 2.83% to 10.85%) and DAPT (7.1%; 95% CI 1.23% to 41.45%) approaches resulted in comparable ischemic complication rates (p=0.79). The DAPT group (4.8%; 95% CI 1.46% to 16.24%) had higher hemorrhagic complication rates than the SAPT group (1.7%; 95% CI 0.52% to 6.09%), but the difference was not statistically significant for patients treated with Phenox HPC (p=0.25).
Our findings indicate that Phenox HPC is equally as safe and effective as non-coated Phenox devices. Additionally, our results suggest that prasugrel monotherapy might effectively prevent ischemic complications in patients treated with Phenox HPC flow diverters.
表面改性的血流导向装置在临床应用中越来越广泛。然而,它们的安全性和相对于非涂层装置的额外益处仍需要进一步探索。在这项荟萃分析中,我们旨在研究和比较未涂层的 Phenox 和涂层的 Phenox HPC 血流导向装置的临床结果。
使用 PubMed、Scopus、Embase 和 Web of Science 数据库进行系统文献综述。收集的数据进行汇总,并计算相应的 95%置信区间(CI)。感兴趣的结果包括动脉瘤闭塞(>6 个月)和并发症发生率。此外,还比较了接受涂层 Phenox HPC 血流导向装置治疗的患者采用预防性单(SAPT)和双重抗血小板治疗(DAPT)方法的安全性结果。
我们纳入了 17 项研究,共 1238 名患者。Phenox HPC 的总体完全闭塞率为 80%(95%CI 74.01%至 86.56%),非涂层 Phenox 血流导向装置的闭塞率为 71.3%(95%CI 59.71%至 85.20%)(p=0.24)。Phenox HPC 的缺血性并发症发生率为 7.3%(95%CI 4.6%至 11.39%),Phenox 的缺血性并发症发生率为 5.3%(95%CI 4.07%至 6.91%)(p=0.24)。对于接受 Phenox HPC 治疗的患者,SAPT(5.5%;95%CI 2.83%至 10.85%)和 DAPT(7.1%;95%CI 1.23%至 41.45%)方法的缺血性并发症发生率相当(p=0.79)。DAPT 组(4.8%;95%CI 1.46%至 16.24%)的出血性并发症发生率高于 SAPT 组(1.7%;95%CI 0.52%至 6.09%),但对于接受 Phenox HPC 治疗的患者,差异无统计学意义(p=0.25)。
我们的研究结果表明,Phenox HPC 与非涂层 Phenox 装置一样安全有效。此外,我们的结果表明,普拉格雷单药治疗可能有效预防接受 Phenox HPC 血流导向装置治疗的患者发生缺血性并发症。