Home » Health » Oral aroxybutynin, atomoxetine lowers OSA severity over 26 weeks

Oral aroxybutynin, atomoxetine lowers OSA severity over 26 weeks

by Dr. Michael Lee – Health Editor

Oral Aroxbutynin, Atomoxetine Combination‍ Shows Promise in Reducing OSA Severity

CHICAGO – A 26-week study presented at⁢ the ‍CHEST Annual Meeting this week indicates a combination of oral aroxbutynin and atomoxetine significantly lowered ​obstructive sleep apnea (OSA) severity in patients. Researchers reported improvements in apnea-hypopnea index (AHI) scores,suggesting a potential new therapeutic avenue for​ the millions affected by the condition.

Obstructive sleep apnea, a common disorder characterized by repeated interruptions⁤ in breathing during ‍sleep, impacts an estimated 22 million‌ Americans, often leading to daytime fatigue,⁤ cardiovascular problems, and reduced quality of life. Current ⁣treatments primarily involve continuous positive ⁣airway pressure (CPAP) therapy, which many patients ‍find‌ tough to ‌adhere to. This⁢ study offers a ⁤glimpse of a possibly more tolerable pharmacological approach. The findings​ could ​reshape OSA management, offering a ‍viable alternative or adjunct to existing therapies, and ‍prompting further investigation into the underlying⁣ mechanisms driving these improvements.

The study evaluated the efficacy of the drug⁢ combination over a 26-week period. Specific AHI reduction data and patient demographics were‌ not promptly available in the presented abstract.

researchers disclosed that Dr. Cronin has⁤ employment with Apnimed,‌ and ​Dr. strollo has‍ an advisory committee membership⁣ relationship with the same company.

The research was presented at the CHEST Annual Meeting, held October 19-22, 2025, in Chicago.

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