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颈动脉窦综合征,我们是否应该起搏?一项多中心、随机对照试验(Safepace 2)。

Carotid sinus syndrome, should we pace? A multicentre, randomised control trial (Safepace 2).

机构信息

Falls & Blackout Unit, St James's Hospital, Dublin 8, Ireland.

出版信息

Heart. 2010 Mar;96(5):347-51. doi: 10.1136/hrt.2009.176206. Epub 2009 Nov 23.

Abstract

BACKGROUND

Cardioinhibitory carotid sinus hypersensitivity (CICSH) is highly prevalent among older people with falls.

OBJECTIVE

To assess the efficacy of dual-chamber pacing in older patients with CICSH and unexplained falls.

DESIGN

A multicentre, double blind, randomised controlled trial.

SETTING

Selection from emergency room, geriatric medicine and orthopaedic departments.

PATIENTS

Patients aged >50 years, with two unexplained falls and/or one syncopal event in the previous 12 months for which no other cause is evident apart from CICSH.

INTERVENTIONS

Patients randomised to either a 700/400 kappa, rate responsive pacemaker or implantable loop recorder (Medtronic Reveal thera RDR, Medtronic, Minneapolis, Minnesota, USA).

MAIN OUTCOME MEASURES

The primary outcome was the number falls after implantation. Secondary outcomes were time to fall event, presyncope, quality of life and cognitive function.

RESULTS

141 patients were recruited from 22 centres. Mean age was 78 years and mean follow-up 24 months. The overall relative risk of falling after device implantation compared with before was 0.23 (0.15 to 0.32). No significant reduction in falls was seen between paced and loop recorder groups (RR=0.79; 95% CI 0.41 to 1.50). Data were also consistent in both groups for syncope, quality of life and cognitive function. Conclusions These results question the use of pacing in CICSH. However, the study was underpowered and also patient characteristics differed from those in Safepace 1-participants were physically and cognitively frailer. Further work is necessary to assess cardiac pacing in this setting.

摘要

背景

在有跌倒问题的老年人中,心脏抑制型颈动脉窦敏感性(CICSH)的发病率很高。

目的

评估双腔起搏在患有 CICSH 和不明原因跌倒的老年人中的疗效。

设计

一项多中心、双盲、随机对照试验。

设置

从急诊室、老年医学科和骨科中进行选择。

患者

年龄>50 岁,在过去 12 个月内有两次不明原因的跌倒和/或一次晕厥事件,除 CICSH 外,没有其他明显原因。

干预措施

患者随机分为 700/400 kappa、频率响应起搏器或植入式环路记录器(美敦力 Reveal thera RDR,美敦力,明尼苏达州明尼阿波利斯,美国)。

主要观察指标

主要结局是植入后跌倒的次数。次要结局是跌倒事件时间、晕厥前、生活质量和认知功能。

结果

从 22 个中心共招募了 141 名患者。平均年龄为 78 岁,平均随访 24 个月。与植入前相比,设备植入后跌倒的总体相对风险为 0.23(0.15 至 0.32)。起搏组和环路记录器组之间未见跌倒明显减少(RR=0.79;95%CI 0.41 至 1.50)。在晕厥、生活质量和认知功能方面,两组的数据也一致。结论:这些结果质疑了 CICSH 中起搏的使用。然而,该研究的效力不足,且患者特征与 Safepace 1 研究参与者不同,后者的身体和认知功能更脆弱。需要进一步的工作来评估这种情况下的心脏起搏。

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