Martens Pieter, Lambeets Seppe, Lau Chirik Wah, Dupont Matthias, Mullens Wilfried
a Department of Cardiology , Ziekenhuis Oost-Limburg , Genk , Belgium.
b Doctoral School for Medicine and Life Sciences , Hasselt University , Diepenbeek , Belgium.
Acta Cardiol. 2019 Apr;74(2):115-122. doi: 10.1080/00015385.2018.1473825. Epub 2018 Jun 17.
Sacubitril/valsartan reduced heart failure (HF)-admissions and cardiovascular mortality in the PARADIGM-HF-trial. However, real-world patients are often frailer and less able to tolerate high doses of sacubitril/valsartan.
We performed a retrospective analysis of consecutive patients prescribed sacubitril/valsartan in a single tertiary HF-clinic between December 2016 and January 2018. HF-admissions were assessed in a paired fashion, comparing the amount of antecedent HF-episodes with incident HF-episodes after the initiation. Baseline risk for adverse events was assessed by the EMPHASIS-HF-risk-score.
A total of 201-HF-patients were retrospectively identified (age = 68 ± 11 years, ejection fraction = 29 ± 8%). Real world patients were older, had higher serum creatinine and a higher New-York Heart-Association (NYHA)-class (p < .05 for all) than in the PARADIGM-HF trial. Over a mean duration of 221 ± 114 days after initiation of sacubitril/valsartan a total of 23-individual patients experienced at least one HF-episodes. Over the same time period preceding initiation of sacubitril/valsartan, 51 individual patients experienced a HF-episodes (p < .001). Sacubitril/valsartan significantly reduced the rate of incident vs. antecedent HF-admissions, in patients with low or high baseline NYHA-class (II vs. III and IV; p value = 0.019 respectively p = .004) or patients with an EMPHASIS-HF risk score below or above the mean (p = .002 respectively p = .016). Patients older than 75-years exhibited a trend towards HF-reduction. Higher doses of sacubitril/valsartan were associated with more reduction in incident versus antecedent HF-episodes.
Despite being frailer and older, real-world patients exhibit a significant and early reduction in incident HF-hospitalisations following initiation of sacubitril/valsartan. Higher doses might be associated with more reduction in HF-admissions, underscoring the importance of dose uptitration.
在PARADIGM-HF试验中,沙库巴曲缬沙坦降低了心力衰竭(HF)住院率和心血管死亡率。然而,现实世界中的患者往往身体更虚弱,更难以耐受高剂量的沙库巴曲缬沙坦。
我们对2016年12月至2018年1月期间在一家三级HF诊所连续接受沙库巴曲缬沙坦治疗的患者进行了回顾性分析。以配对方式评估HF住院情况,比较开始治疗前HF发作次数与开始治疗后新发HF发作次数。通过EMPHASIS-HF风险评分评估不良事件的基线风险。
共回顾性确定了201例HF患者(年龄=68±11岁,射血分数=29±8%)。与PARADIGM-HF试验相比,现实世界中的患者年龄更大,血清肌酐更高,纽约心脏协会(NYHA)分级更高(所有p<0.05)。在开始使用沙库巴曲缬沙坦后的平均221±114天内,共有23例患者至少经历了一次HF发作。在开始使用沙库巴曲缬沙坦之前的同一时间段内,有51例患者经历了HF发作(p<0.001)。沙库巴曲缬沙坦显著降低了新发HF住院率与既往HF住院率,无论是基线NYHA分级低或高的患者(II级与III级和IV级;p值分别为0.019和0.004),还是EMPHASIS-HF风险评分低于或高于平均值的患者(p值分别为0.002和0.016)。75岁以上的患者有HF减少的趋势。更高剂量的沙库巴曲缬沙坦与新发HF发作次数相对于既往发作次数的更多减少相关。
尽管现实世界中的患者身体更虚弱且年龄更大,但在开始使用沙库巴曲缬沙坦后,他们新发HF住院情况有显著且早期的减少。更高剂量可能与HF住院率的更多降低相关,突出了剂量滴定的重要性。