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Factors Associated With Sacubitril/Valsartan Continuation and the Methods of Combining Heart Failure Medications in Patients With Heart Failure.
Iwasaki, Erika; Kohyama, Noriko; Inamoto, Mayumi; Nagao, Michiru; Sunaga, Tomiko; Suzuki, Hiroshi; Ebato, Mio; Kogo, Mari.
Afiliación
  • Iwasaki E; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan.
  • Kohyama N; Division of Pharmacotherapeutics, Department of Clinical Pharmacy, Showa University School of Pharmacy, Tokyo, Japan.
  • Inamoto M; Department of Pharmacy, Showa University Fujigaoka Hospital, Kanagawa, Japan.
  • Nagao M; Department of Hospital Pharmaceutics, Showa University, Tokyo, Japan.
  • Sunaga T; Department of Pharmacy, Showa University Fujigaoka Hospital, Kanagawa, Japan.
  • Suzuki H; Department of Hospital Pharmaceutics, Showa University, Tokyo, Japan.
  • Ebato M; Department of Hospital Pharmaceutics, Showa University, Tokyo, Japan.
  • Kogo M; Department of Pharmacy, Showa University Dental Hospital, Tokyo, Japan.
Ann Pharmacother ; : 10600280241277354, 2024 Sep 04.
Article en En | MEDLINE | ID: mdl-39229914
ABSTRACT

BACKGROUND:

Sacubitril/valsartan (SV) is recommended for patients with heart failure (HF). In addition, a combination of 4 HF medications, including SV, is recommended in patients with HF with reduced ejection fraction (HFrEF). However, evidence on the characteristics of patients who could continue SV and its initiation methods is limited.

OBJECTIVE:

To investigate the factors associated with SV continuation and methods of combining HF medications.

METHODS:

This retrospective cohort study included HF patients who initiated with SV at our institution. The endpoint was SV continuation for 6 months after its initiation. Multivariate analysis was used to extract factors associated with SV continuation. The relationship between the methods of combining HF medications (renin-angiotensin system inhibitors, beta-blockers, mineralocorticoid receptor antagonists, or sodium-glucose cotransporter 2 inhibitors), including the number of HF medications, their combination patterns, and the timing of their initiation, and SV continuation was examined in patients with HFrEF.

RESULTS:

Of 186 eligible patients, 68.8% had HFrEF, and 79.0% continued SV for 6 months. Significant factors associated with SV continuation were albumin ≥ 3.5 g/dL (odds ratio, 4.81; 95% confidence interval, 2.19-10.59), body mass index (BMI) ≥ 18.5 kg/m2 (4.17; 1.10-15.85), and systolic blood pressure (SBP) ≥ 110 mmHg (2.66; 1.12-6.28). In patients with HFrEF, the proportion of HF medications not initiated simultaneously with SV was significantly higher in the continuation group than in the discontinuation group (67.3% vs 33.3%, P = 0.002). The number of HF medications and their combination patterns were not significantly associated with SV continuation. CONCLUSION AND RELEVANCE Albumin, BMI, and SBP are useful indicators for selecting patients who are likely to continue SV. In addition, initiating only SV without simultaneously initiating other HF medications in patients with HFrEF may lead to SV continuation.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Ann Pharmacother Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Ann Pharmacother Asunto de la revista: FARMACOLOGIA / TERAPIA POR MEDICAMENTOS Año: 2024 Tipo del documento: Article País de afiliación: Japón Pais de publicación: Estados Unidos