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终末期肾病患者左心耳封堵术的植入成功率和安全性:来自意大利透析人群的围手术期结果。

Implant success and safety of left atrial appendage occlusion in end stage renal disease patients: Peri-procedural outcomes from an Italian dialysis population.

机构信息

Department of Medicine and Surgery, University of Milano-Bicocca, Monza, Italy; Nephrology Unit, San Gerardo Hospital, Monza, Italy.

Nephrology Unit, IRCCS Ospedale San Raffaele, Milano, Italy.

出版信息

Int J Cardiol. 2018 Jul 1;262:38-42. doi: 10.1016/j.ijcard.2018.03.083.

Abstract

AIMS

To estimate the safety and the efficacy of the off label left atrial appendage (LAA) occlusion in chronic dialysis patients with atrial fibrillation (AF). In this preliminary paper, we report the design of the study and the data on peri-procedural complications.

METHODS

This is a prospective cohort study. Primary endpoints are i) incidence of peri-procedural complications, ii) cumulative incidence of two-year thromboembolic events iii) cumulative incidence of two-year bleedings iiii) mortality at two years. Adverse events and death within 30 days of the procedure were recorded.

RESULTS

Fifty patients who underwent LAA occlusion between May 2014 and September 2017 were recruited. Both the mean age of the sample study and the dialysis duration were high [71.8 (9.6) years and 59.4 (78.2) months, respectively]. Most patients (84%) were hypertensive and 62% suffered a previous major bleeding. About half of them presented cardiovascular diseases. CHADSVASCs and HASBLED scores were 4.0 (1.5) and 4.4 (0.9), respectively. Most patients (88%) showed atrial dilatation and 44% left ventricular hypertrophy; 32% had left ventricular ejection fraction <50%. Fifty five percent of patients had permanent AF and 32% paroxysmal AF. All devices were implanted successfully. No deaths or major adverse events were reported during a 30-day follow-up. Three episodes of peri-procedural access site bleeding were reported, requiring no transfusion.

CONCLUSIONS

Our preliminary data suggest the feasibility and safety of LAA occlusion in patients undergoing dialysis. Only the follow-up of these patients over time can provide evidence that LAA occlusion is effective in preventing of thromboembolic events in this very high-risk population.

摘要

目的

评估在患有房颤(AF)的慢性透析患者中使用非适应证左心耳(LAA)封堵器的安全性和疗效。在本初步研究中,我们报告了研究设计和围手术期并发症的数据。

方法

这是一项前瞻性队列研究。主要终点是 i)围手术期并发症的发生率,ii)两年内血栓栓塞事件的累积发生率 iii)两年内出血的累积发生率 iiii)两年时的死亡率。记录了术后 30 天内的不良事件和死亡。

结果

2014 年 5 月至 2017 年 9 月期间,共招募了 50 名接受 LAA 封堵术的患者。样本研究的平均年龄和透析时间都很高[分别为 71.8(9.6)岁和 59.4(78.2)个月]。大多数患者(84%)患有高血压,62%曾有过大出血。约一半的患者患有心血管疾病。CHADSVASCs 和 HASBLED 评分分别为 4.0(1.5)和 4.4(0.9)。大多数患者(88%)存在心房扩张,44%存在左心室肥厚;32%的左心室射血分数<50%。55%的患者有永久性房颤,32%有阵发性房颤。所有器械均成功植入。在 30 天的随访中,没有死亡或重大不良事件报告。报告了 3 例围手术期穿刺部位出血,无需输血。

结论

我们的初步数据表明,在接受透析治疗的患者中,LAA 封堵术是可行且安全的。只有随着时间的推移对这些患者进行随访,才能提供证据证明 LAA 封堵术在预防该极高风险人群血栓栓塞事件方面是有效的。

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