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Effects of sacubitril/valsartan on functional status and exercise capacity in real-world patients

机译:Sacubitril / Valsartan对现实世界患者功能状况和运动能力的影响

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Background: Sacubitril/valsartan significantly reduced heart failure(HF) hospitalisations and mortality in the PARADIGM-HF-trial. However real-world data on symptomatic and functional improvement are lacking. Methods: Between December 2016 and January 2018, we retrospectively collected baseline and follow-up data including New York Heart Association (NYHA)-functional class and Cardio-pulmonary exercise data(CPET) in all HF-patients receiving sacubitril/valsartan. Additionally, in patients with an implantable electric cardiovascular device (IECD) enrolled in remote telemonitoring, we quantified patient level activity before and after initiation. Results: A total of 201 patients (82% males) were identified. NYHA-functional class was reassessed after an average of 221 +/- 114 days. Overall, 3.3% of patients improved 2 NYHA classes, 28.7% improved 1 NYHA class, 64% remained stable and 4% deteriorated 1 NYHA class. Patients with symptomatic improvement exhibited a larger reduction in Left Ventricular End Systolic Volume(LVESV) and a larger increase in Left Ventricular Ejection Fraction(LVEF[p-value both <.05]). In total, 110 patients (55%) were equipped with an IECD capable of quantifying outpatient activity-level. On an average of 364 days before sacubitril/valsartan, an activity expressed as %-of-the-day was 13 +/- 2%, vs. 18 +/- 3% the 364 days following sacubitril/valsartan initiation. Signifying a 38% improvement in the out-patient activity level. CPET-data was obtained in paired-fashion in 45 patients (22%). VO2max at baseline (14.7 +/- 3.8 mL/kg/min) did not significantly change at follow-up (14.1 +/- 4.7 mL/min/kg; p = .237). Conclusion: Real-world patients exhibit significant symptomatic and functional improvement following the initiation of sacubitril/valsartan. However, larger prospective studies are necessary to assess the impact of sacubitril/valsartan on indices of maximal exercise performance measured during CPET.
机译:背景:Sacubitril / Valsartan显着降低了心力衰竭(HF)住院治疗和帕拉维-HF试验中的死亡率。然而,缺乏现实世界症状和功能性的数据。方法:2016年12月至2018年1月,我们回顾性地收集了纽约心脏协会(NYHA)的基线和随访数据,包括接受Sacubitril / Valsartan的所有HF患者的所有HF患者。此外,在注册远程远程诊断的植入电动心血管装置(IECD)的患者中,我们在发起之前和之后量化患者水平活动。结果:鉴定了共计201例(雄性82%)。在平均221 +/- 114天后重新评估Nyha-Functional类。总体而言,3.3%的患者改善了2个NYHA课程,28.7%改善了1个NYHA课程,64%稳定,4%恶化1 NYHA课程。患有症状改善的患者在左心室收缩体积(叶管)的较大减少和左心室喷射部分的较大增加(LVEF [P值均<.05])。共有110名患者(55%)配备了能够量化门诊活动水平的IECD。在Sacubitril / Valsartan之前平均为364天,表达为-Of-Day%的活性为13 +/- 2%,与骶盐/缬沙坦的启动后364天为18 +/- 3%。在门诊活动水平中表示38%的改善。在45名患者中以配对方式获得CPET数据(22%)。在基线(14.7 +/- 3.8ml / kg / min)的vo2max在随访时没有显着变化(14.1 +/- 4.7 ml / min / kg; p = .237)。结论:在发起Sacubitril / Valsartan后,现实世界患者表现出显着的症状和功能性。然而,需要更大的前瞻性研究来评估Sacubitril / Valsartan对CPET期间测量的最大运动性能指数的影响。

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