Sacubitril-valsartan initiation in CHF may significantly decrease sleep apnea severity
Sleep Apnoea (SA) is a highly prevalent co-morbidity in chronic heart failure patients associated with even worse outcomes. At least 50% of CHF patients have moderate to severe SA [i.e. SA with an apnoea-hypopnoea index (AHI) of ≥15/h]. In a recent study, researchers have found that Sacubitril-valsartan (SV) for 3 months in Sleep Apnea patients is associated with a significant decrease in apnoea–hypopnoea index (AHI). The research has been published in the journal ESC Heart Failure on June 08, 2021.
The Apnea–Hypopnea Index or Apnoea–Hypopnoea Index is an index used to indicate the severity of sleep apnea. It is represented by the number of apnea and hypopnea events per hour of sleep. The apneas must last for at least 10 seconds and be associated with a decrease in blood oxygenation
Sleep apnoea [SA, either predominantly obstructive SA (OSA) or predominantly central SA (CSA)] is considered as a potential therapeutic target in CHF as underlined by the 2017 European Respiratory Society Task Force. Optimizing medical cardiac treatment for sleep apnoea (SA) in patients with chronic heart failure and reduced ejection fraction (HFrEF) is an expert Grade C recommendation based on six studies encompassing a total of 67 patients only. Whether sacubitril–valsartan (SV), a cornerstone of HFrEF medical treatment, impacts SA is unknown and requires evaluation. Therefore, Dr François Roubille and his team conducted a study to assess whether SV initiation could improve SA outcomes in HFrEF patients treated under real-life conditions.
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