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Pharmacotherapy treatment patterns at hospital discharge and clinical outcomes among patients with heart failure with reduced ejection fraction

BACKGROUND: This study aimed to assess the prescribing patterns of evidence‐based pharmacotherapy and their association with clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF) in Thailand. METHODS: A retrospective cohort study of patients with HFrEF was conducted...

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Detalles Bibliográficos
Autores principales: Wongsalap, Yuttana, Poolpun, Duangkamon, Keawhai, Konrapee, Kitpluem, Napusson, Pansiri, Parichat, Malaimat, Siriluck, Senthong, Vichai, Kengkla, Kirati
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10249177/
https://www.ncbi.nlm.nih.gov/pubmed/37305111
http://dx.doi.org/10.1002/cdt3.59
Descripción
Sumario:BACKGROUND: This study aimed to assess the prescribing patterns of evidence‐based pharmacotherapy and their association with clinical outcomes in patients with heart failure with reduced ejection fraction (HFrEF) in Thailand. METHODS: A retrospective cohort study of patients with HFrEF was conducted. Treatment with a β‐blocker and renin–angiotensin system inhibitors (RASIs) with or without mineralocorticoid receptor antagonists (MRAs) at discharge was regarded as guideline‐directed medical therapy (GDMT). All others were considered non‐GDMT. The primary endpoint was the composite of all‐cause mortality or heart failure (HF) rehospitalization. Inverse‐probability‐treatment‐weighted adjusted Cox proportional hazard models were used to examine the treatment effects. RESULTS: In total, 653 patients with HFrEF (mean age 64.1 ± 14.3 years; 55.9% male) were included. GDMT with β‐blockers and RASIs with or without MRAs was prescribed at a rate of 35.4%. During a median of 1‐year follow‐up, 167 patients (27.5%) had a composite event, 81 patients (13.3%) had all‐cause mortality, and 109 patients (18.0%) had HF rehospitalization. Patients treated with GDMT at discharge showed significantly lower rates of the primary endpoint (adjusted hazard ratio [HR] 0.63; 95% CI 0.44–0.89; p = 0.009) compared with patients who did not receive GDMT. The use of GDMT was also associated with a significantly lower risk of all‐cause mortality (adjusted HR 0.59; 95% CI 0.36–0.98; p = 0.045) and HF rehospitalization (adjusted HR 0.65; 95% CI 0.43–0.96; p = 0.031). CONCLUSIONS: For HFrEF treatment, GDMT initiation at hospital discharge was associated with a significantly reduced risk of all‐cause mortality and HF rehospitalization. Nevertheless, prescribing GDMT remains underused, and it could be encouraged to improve HF outcomes in real‐world settings.