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DOI 10.1093/ehjcvp/pvaf064

Медицинская библиотека · European heart journal. Cardiovascular pharmacotherapy · 2025

Sacubitril/valsartan and quality of life assessed using the EuroQol Five-dimension Three-level questionnaire level sum score (EQ-5D-3L-LSS) in patients with HFrEF and HFmrEF/HFpEF.

Yang Mingming, Henderson Alasdair D, Anand Inder S, Desai Akshay S, Lam Carolyn S P, Maggioni Aldo P, Martinez Felipe A, Rouleau Jean L, Swedberg Karl, Vaduganathan Muthiah, van Veldhuisen Dirk J, Zannad Faiez, Zile Michael R, Packer Milton, Rizkala Adel, Lewis Eldrin F, Jhund Pardeep S, Solomon Scott D, McMurray John J V

Клиническое исследование III фазыСтатьяМногоцентровое исследованиеРандомизированное исследованиеПеревод в очереди

Аннотация

AIMS: To investigate the EQ-5D-3L Level Sum Score (LSS) in patients with heart failure (HF) and reduced (HFrEF) and mildly reduced or preserved ejection fraction (HFmrEF/HFpEF) and the effect of sacubitril/valsartan on this score using patient-level data from the PARADIGM-HF and PARAGON-HF trials.

METHODS AND

RESULTS

The LSS was calculated by summing the three levels (1-3) for each of the five domains (minimum sum score = 5; maximum sum score = 15). Patient characteristics and outcomes were compared across LSS tertiles (T1-T3) at baseline. Cox models were used to evaluate the primary endpoint [first HF hospitalization or cardiovascular death (CVD)] according to tertiles of LSS. Changes in LSS severity at 8 months were analysed using ordinal logistic regression models to estimate the effect of sacubitril/valsartan vs. enalapril or valsartan. Of 13 195 patients, 12 974 had a baseline LSS. Compared to lower LSS, patients with higher (worse) scores were older, more often women and White, and had more comorbidities and more severe HF. At 8 months, patients assigned to sacubitril/valsartan experienced more improvement and less worsening of LSS vs. the comparator: OR:1.16 (95%CI: 1.08-1.24). Sacubitril/valsartan also reduced the risk of the primary outcome across LSS tertiles: T1: HR: 0.87 (95%CI: 0.75-1.00); T2: 0.80 (95%CI: 0.71-0.90); T3: 0.87 (95%CI: 0.77-0.97); Pinteraction = 0.59. Higher LSS was independently associated with a greater risk of the primary endpoint, and the achieved LSS at 8 months may be more strongly associated with subsequent outcomes.

CONCLUSION

Sacubitril/valsartan significantly reduced the risk of HF events and improved health status across the LSS spectrum in HFrEF and HFmrEF/HFpEF.

CLINICAL TRIAL REGISTRATION: https://www.clinicaltrials.gov. Unique identifiers: NCT01920711 (PARAGON-HF), NCT01035255 (PARADIGM-HF).

Для цитирования: Yang Mingming, Henderson Alasdair D, Anand Inder S, Desai Akshay S, Lam Carolyn S P, Maggioni Aldo P, Martinez Felipe A, Rouleau Jean L, Swedberg Karl, Vaduganathan Muthiah, van Veldhuisen Dirk J, Zannad Faiez, Zile Michael R, Packer Milton, Rizkala Adel, Lewis Eldrin F, Jhund Pardeep S, Solomon Scott D, McMurray John J V. Sacubitril/valsartan and quality of life assessed using the EuroQol Five-dimension Three-level questionnaire level sum score (EQ-5D-3L-LSS) in patients with HFrEF and HFmrEF/HFpEF.. European heart journal. Cardiovascular pharmacotherapy. 2025. DOI: 10.1093/ehjcvp/pvaf064.

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