Real-world comparative effectiveness of sacubitril/valsartan versus RAS inhibition alone in patients with de novo heart failure

被引:0
作者
Bhatt, Ankeet S. [1 ,2 ,3 ]
Vaduganathan, Muthiah [4 ]
Jena, Barada P. [5 ]
Suminska, Sylwia [6 ]
Eid, Carlos [7 ]
Schwende, Heike [8 ]
Senni, Michele [9 ]
机构
[1] Kaiser Permanente San Francisco Med Ctr, San Francisco, CA USA
[2] Div Res, San Francisco, CA USA
[3] Stanford Univ, Sch Med, Div Cardiovasc Med, Palo Alto, CA USA
[4] Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA USA
[5] Novartis Global Serv Ctr, Hyderabad, India
[6] Novartis Global Serv Ctr, Dublin, Ireland
[7] Novartis Pharm Serv AG, Representat Off Middle East & North Africa, Basel, Switzerland
[8] Novartis Pharm AG, Basel, Switzerland
[9] Univ Milano Bicocca, Milan, Italy
关键词
angiotensin receptor blocker; angiotensin-converting enzyme inhibitor; de novo; heart failure; sacubitril/valsartan; NEPRILYSIN INHIBITION;
D O I
10.1002/ehf2.15183
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
AimsLarge-scale, real-world data on early initiation of sacubitril/valsartan in patients newly diagnosed (de novo) with HF with reduced ejection fraction (HFrEF) are limited. We examined the effectiveness of sacubitril/valsartan versus angiotensin-converting enzyme inhibitor (ACEi)/angiotensin receptor blocker (ARB) on all-cause and cause-specific hospitalizations among patients with de novo HFrEF from the Optum (R) dataset in the United States. MethodsThis retrospective cohort study included adult patients with de novo HFrEF (diagnosed <= 30 days) with left ventricular ejection fraction (LVEF) <= 40% who were first prescribed with sacubitril/valsartan or ACEi/ARB from 1 January 2016 to 31 March 2020. The primary endpoint (all-cause hospitalization) and secondary endpoints were analysed in propensity score-matched cohorts. ResultsA cohort of 3290 patients with de novo HFrEF who were prescribed with sacubitril/valsartan and a propensity-matched cohort of 6580 patients who were prescribed with ACEi/ARB were analysed. Overall, the mean (SD) age of patients was 63 (14) years, 34% were women, and baseline characteristics were balanced across treatment groups. Hypertension (67%), diabetes (33%) and chronic kidney disease (28%) were highly prevalent comorbidities. Patients in the sacubitril/valsartan cohort when compared with the ACEi/ARB cohort had lower annual rates of all-cause hospitalizations [incidence rate ratio (IRR): 0.81, 95% confidence interval (CI): 0.75-0.89, P < 0.001], cardiovascular (CV) hospitalizations (IRR: 0.80, 95% CI: 0.73-0.87, P < 0.001) and HF hospitalizations (IRR: 0.86, 95% CI: 0.78-0.95, P = 0.002). ConclusionsAmong patients with de novo HFrEF, sacubitril/valsartan (compared with that of ACEi/ARB) was associated with fewer all-cause, CV and HF hospitalizations. These findings are consistent with clinical trial evidence suggesting potential benefits of early initiation of sacubitril/valsartan in patients with HFrEF, including those soon after diagnosis.
引用
收藏
页码:1682 / 1692
页数:11
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