Department of Cardiology, San Bortolo Hospital, Vicenza, Italy,
Department of Prevention, AULSS 8 Berica, Vicenza, Italy.
Cerebrovasc Dis. 2020;49(2):124-134. doi: 10.1159/000507317. Epub 2020 Apr 14.
Randomized-controlled trials (RCTs) reported a finding on the safety and efficacy of percutaneous patent foramen ovale (PFO) closure to prevent stroke recurrence. It showed that the Amplatzer (AMP) device appears to be superior to medical therapy (MT) in preventing strokes and episodes of atrial fibrillation (AF), than other devices. We performed a network meta-analysis (NMA) to evaluate the closure of PFO in preventing subsequent neurological events while investigating the results obtained by specific devices.
We searched 3 databases (MEDLINE, EMBASE, CENTRAL/CCTR) and identified 6 RCTs until March 2019. We performed an NMA and used pooled ORs. Analyses were done in NetMetaXL1.6-WinBUGS1.4.
Six RCTs with 3,560 patients (mean age 45.2-46.2 years) were included in the present NMA. Depending on the device, 4 groups of patients were compared with MT: 1,889 patients undergoing PFO closure were significantly less likely to experience a stroke than 1,671 patients treated with MT (ORs 0.41; 95% Cr.I. 0.27-0.60 with fixed-effects model and ORs 0.22; 95% Cr.I. 0.05-0.70 with random-effects model). The patients with AMP showed a similar risk than those treated with Helex/Cardioform (HLX/CF) or with a group of 11 multiple devices. This suggests the equality between the 2 most currently used devices. When assessing TIA and, for the safety analysis, major bleeding, both models confirm no significant difference between any devices and MT. PFO closure increased the risk of new-onset AF: MT induces AF significantly less than all the devices. In favor of the AMP, there is a reduced number of cases of AF versus MT; however, no device superiority has been established in comparing HLX/CF and other devices in a random effect model.
Our NMA provides evidence in favor of PFO closure with all the devices currently in use. We can conclude that these devices are better than MT, but not that 1 device is better than the rest in reducing stroke recurrences and AF episodes in the follow-up.
随机对照试验(RCT)报告了经皮卵圆孔未闭(PFO)封堵术预防卒中复发的安全性和有效性的发现。结果表明,相比其他装置,Amplatzer(AMP)装置在预防卒中和心房颤动(AF)发作方面似乎优于药物治疗(MT)。我们进行了一项网络荟萃分析(NMA),以评估 PFO 封堵术在预防后续神经事件方面的效果,同时调查特定装置的结果。
我们检索了 3 个数据库(MEDLINE、EMBASE、CENTRAL/CCTR),并于 2019 年 3 月前确定了 6 项 RCT。我们进行了 NMA,并使用了汇总的 OR。分析在 NetMetaXL1.6-WinBUGS1.4 中进行。
本 NMA 纳入了 6 项 RCT,共 3560 例患者(平均年龄 45.2-46.2 岁)。根据装置的不同,将 4 组患者与 MT 进行了比较:与 MT 相比,1889 例行 PFO 封堵术的患者发生卒中的可能性显著降低(OR 0.41;95%Cr.I. 0.27-0.60,固定效应模型;OR 0.22;95%Cr.I. 0.05-0.70,随机效应模型)。AMP 组与 Helex/Cardioform(HLX/CF)组或 11 种多装置组的患者风险相似。这表明目前使用的两种最常用的装置之间存在平等性。在评估 TIA 时,以及为了安全性分析,主要出血,两种模型均证实任何装置与 MT 之间均无显著差异。PFO 封堵术增加了新发 AF 的风险:MT 引起的 AF 明显少于所有装置。AMP 组的 AF 病例数减少,但在随机效应模型中,HLX/CF 和其他装置之间没有确立设备优势。
我们的 NMA 提供了支持使用目前所有装置进行 PFO 封堵术的证据。我们可以得出结论,这些装置优于 MT,但不能得出在减少随访中卒中复发和 AF 发作方面,1 种装置优于其他装置的结论。