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Despite the demonstrated advantages of angiotensin receptor/neprilysin inhibitors in the management of heart failure, the pivotal Angiotensin-Neprilysin Inhibition versus Enalapril in Heart Failure (PARADIGM-HF) trial, which explored this class of medications, did not include individuals from Saudi Arabia. Recognizing that different nations and ethnic groups may exhibit unique characteristics, this study aimed to compare the demographics and outcomes of patients in Saudi Arabia who received sacubitril/valsartan (Sac/Val) with those enrolled in the PARADIGM-HF trial. In this retrospective, multicenter cohort study, we included all adult patients diagnosed with heart failure with reduced ejection fraction (HFrEF) within a tertiary healthcare system in Saudi Arabia between January 2018 and December 2021 and were initiated on Sac/Val.

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Article Synopsis
  • Current research on sacubitril/valsartan's effects on heart failure with preserved ejection fraction (HFpEF) is inconclusive, prompting further investigation into its efficacy.
  • An analysis of four trials with over 8,000 participants revealed that sacubitril/valsartan significantly decreases NT-proBNP levels and improves the Kansas City Cardiomyopathy Questionnaire (KCCQ) score, indicating improved quality of life.
  • While there were no significant changes in hospitalizations or mortality rates, sacubitril/valsartan was generally safe and showed a reduced risk of kidney function decline compared to standard treatments.
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Article Synopsis
  • U.S. guidelines suggest considering sacubitril/valsartan for chronic heart failure patients with a mildly reduced or preserved ejection fraction (EF), but its safety and effectiveness after a worsening heart failure event in patients with EF >40% was unclear.
  • The PARAGLIDE-HF trial compared sacubitril/valsartan to valsartan in patients with EF >40% who were enrolled within 30 days post-worsening heart failure, measuring the change in NT-proBNP levels as the primary endpoint.
  • Results showed that sacubitril/valsartan significantly reduced NT-proBNP levels and had some clinical benefits, although it increased cases of symptomatic hypotension; a greater treatment effect was observed in
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