首页> 外文期刊>The Lancet >Wireless pulmonary artery haemodynamic monitoring in chronic heart failure: a randomised controlled trial.
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Wireless pulmonary artery haemodynamic monitoring in chronic heart failure: a randomised controlled trial.

机译:慢性心力衰竭的无线肺动脉血流动力学监测:一项随机对照试验。

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BACKGROUND: Results of previous studies support the hypothesis that implantable haemodynamic monitoring systems might reduce rates of hospitalisation in patients with heart failure. We undertook a single-blind trial to assess this approach. METHODS: Patients with New York Heart Association (NYHA) class III heart failure, irrespective of the left ventricular ejection fraction, and a previous hospital admission for heart failure were enrolled in 64 centres in the USA. They were randomly assigned by use of a centralised electronic system to management with a wireless implantable haemodynamic monitoring (W-IHM) system (treatment group) or to a control group for at least 6 months. Only patients were masked to their assignment group. In the treatment group, clinicians used daily measurement of pulmonary artery pressures in addition to standard of care versus standard of care alone in the control group. The primary efficacy endpoint was the rate of heart-failure-related hospitalisations at 6 months. The safety endpoints assessed at 6 months were freedom from device-related or system-related complications (DSRC) and freedom from pressure-sensor failures. All analyses were by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00531661. FINDINGS: In 6 months, 83 heart-failure-related hospitalisations were reported in the treatment group (n=270) compared with 120 in the control group (n=280; rate 0.31 vs 0.44, hazard ratio [HR] 0.70, 95% CI 0.60-0.84, p<0.0001). During the entire follow-up (mean 15 months [SD 7]), the treatment group had a 39% reduction in heart-failure-related hospitalisation compared with the control group (153 vs 253, HR 0.64, 95% CI 0.55-0.75; p<0.0001). Eight patients had DSRC and overall freedom from DSRC was 98.6% (97.3-99.4) compared with a prespecified performance criterion of 80% (p<0.0001); and overall freedom from pressure-sensor failures was 100% (99.3-100.0). INTERPRETATION: Our results are consistent with, and extend, previous findings by definitively showing a significant and large reduction in hospitalisation for patients with NYHA class III heart failure who were managed with a wireless implantable haemodynamic monitoring system. The addition of information about pulmonary artery pressure to clinical signs and symptoms allows for improved heart failure management. FUNDING: CardioMEMS.
机译:背景:先前的研究结果支持以下假设,即植入式血流动力学监测系统可能会降低心力衰竭患者的住院率。我们进行了单盲试验来评估这种方法。方法:美国64个中心纳入了纽约心脏协会(NYHA)III级心力衰竭患者,不论其左心室射血分数如何,以及先前因心力衰竭入院。通过使用集中式电子系统,将他们随机分配到无线植入式血流动力学监测(W-IHM)系统进行管理(治疗组)或对照组,至少持续6个月。只有患者被掩盖在其任务分配组中。在治疗组中,除了对照组的治疗标准和单独的治疗标准外,临床医生还每天测量肺动脉压。主要疗效终点是6个月时与心力衰竭相关的住院率。在6个月时评估的安全终点是无设备相关或系统相关并发症(DSRC),无压力传感器故障。所有分析均按意向治疗。该试验已在ClinicalTrials.gov上注册,编号为NCT00531661。结果:在6个月中,治疗组(n = 270)报告了83次与心衰相关的住院治疗,而对照组(n = 280)为120次;发生率0.31 vs 0.44,危险比[HR] 0.70,95% CI 0.60-0.84,p <0.0001)。在整个随访期间(平均15个月[SD 7]),与对照组相比,治疗组与心衰相关的住院治疗减少了39%(153 vs 253,HR 0.64,95%CI 0.55-0.75) ; p <0.0001)。 8例患者患有DSRC,与DSRC的总体自由度为98.6%(97.3-99.4),而预定的执行标准为80%(p <0.0001);并且不受压力传感器故障影响的总体自由度为100%(99.3-100.0)。解释:我们的结果与以前的发现一致,并且与以前的发现相吻合,并通过无线植入式血流动力学监测系统明确显示了NYHA III级心力衰竭患者的住院率显着降低。将有关肺动脉压力的信息添加到临床体征和症状可以改善心力衰竭的管理。资助:CardioMEMS。

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