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使用两种不同的房间隔封堵器经皮闭合卵圆孔未闭后的长期对比超声心动图检查及临床随访

Long-Term Contrast Echocardiography and Clinical Follow-Up after Percutaneous Closure of Patent Foramen Ovale Using Two Different Atrial Septal Occluder Devices.

作者信息

Scalise Filippo, Auguadro Carla, Sorropago Giovanni, Sorropago Antonio, Novelli Eugenio, Finizio Marica, Specchia Giuseppe

机构信息

Department of Interventional Cardiology, Policlinico di Monza, Monza, Italy.

Biostatistic Unit, Policlinico di Monza, Monza, Italy.

出版信息

J Interv Cardiol. 2016 Aug;29(4):406-13. doi: 10.1111/joic.12314. Epub 2016 Jun 24.

Abstract

INTRODUCTION

Percutaneous patent foramen ovale (PFO) closure by means of a septal occluder device (SOD) is a well-known therapeutic strategy for the secondary prevention of paradoxical embolic neurological events. The aim of this study was to provide long-term echocardiographic and clinical follow-up data on patients who had undergone percutaneous PFO closure with 2 different SOD.

METHODS

We selected 2 groups of patients treated with 2 different SOD: Group A: 52 patients with an Amplatzer(®) PFO Occluder and Group B: 49 patients with a Figulla Flex(®) device. All patients underwent follow-up Bubble Test Transthoracic Echocardiography (BTTE) and clinical examination. The results were compared with those recently reported in a group of patients with similar characteristics, but that had been treated conservatively, which acted as a control group.

RESULTS

The mean follow-up after PFO closure was 53 months. The Amplatzer(®) PFO Occluder and the Figulla Flex were used in 52 (51.5%) and 49 (48.5%) of patients, respectively. We found no significant difference in the rate of effective PFO closure between the devices: Amplatzer 91.4%, Figulla 93.9% (P = 0.71). One patient (1.0%) suffered a recurrent neurologic event. BTTE was positive (BTTE+) in 8 patients (8%), 5 with an Amplatzer, and 3 with a Figulla device (P = 0.516). Only 1 patient with BTTE+ had a recurrent TIA (12.5%). No significant relationship was found between device dimensions and BTTE+ (P = 0.062). In the control group (163 patients), the recurrence of neurologic events was 9.2% (15 events), that was significantly higher in respect to the patients who had undergone percutaneous closure of the PFO.

CONCLUSIONS

Percutaneous PFO closure was associated with a remarkably low risk of recurrent embolic neurological events, and no long-term device-related major complications. No statistically significant difference emerged between the 2 different SODs regarding BTTE positivity. Long-term follow-up showed that the recurrence of neurological events has been significantly higher in the group treated in a conservative way.

摘要

引言

经皮使用间隔封堵器(SOD)关闭卵圆孔未闭(PFO)是预防反常栓塞性神经事件二级预防的一种知名治疗策略。本研究的目的是提供接受两种不同SOD经皮PFO封堵术患者的长期超声心动图和临床随访数据。

方法

我们选择了两组接受两种不同SOD治疗的患者:A组:52例使用Amplatzer(®)PFO封堵器的患者,B组:49例使用Figulla Flex(®)装置的患者。所有患者均接受随访经胸超声心动图气泡试验(BTTE)和临床检查。将结果与最近报道的一组具有相似特征但接受保守治疗的患者(作为对照组)的结果进行比较。

结果

PFO封堵术后的平均随访时间为53个月。Amplatzer(®)PFO封堵器和Figulla Flex分别用于52例(51.5%)和49例(48.5%)患者。我们发现两种装置之间有效PFO封堵率无显著差异:Amplatzer为91.4%,Figulla为93.9%(P = 0.71)。1例患者(1.0%)发生复发性神经事件。8例患者(8%)BTTE呈阳性(BTTE+),5例使用Amplatzer封堵器,3例使用Figulla装置(P = 0.516)。只有1例BTTE+患者发生复发性短暂性脑缺血发作(12.5%)。未发现装置尺寸与BTTE+之间存在显著关系(P = 0.062)。在对照组(163例患者)中,神经事件复发率为9.2%(15例事件),明显高于接受经皮PFO封堵术的患者。

结论

经皮PFO封堵术与复发性栓塞性神经事件的风险极低相关,且无长期与装置相关的主要并发症。两种不同SOD在BTTE阳性方面未出现统计学显著差异。长期随访表明,保守治疗组的神经事件复发率明显更高。

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