Sleep Apnea Devices: The Changing Of The Guard

The current specialty-dominated care paradigm for sleep apnea can't scale-up to meet the demands of an enormous and serious chronic disease. New companies help move diagnosis and treatment to the physicians that see patients first.

The 25-year-old field of sleep medicine, now covering some 80 different disorders, is still emerging, and the role of sleep itself remains shrouded in mystery. For the group of diseases categorized as sleep disordered breathing, however, the picture is becoming clearer. There is now widespread recognition that the breathing stoppages resulting from obstructive sleep apnea (OSA) do more than disrupt sleep. OSA has come to be viewed as a co-morbidity, a risk factor, a catalyst, or even a causal agent for many serious diseases.

Sleep apnea in all of its forms (OSA, central sleep apnea and mixes of the two) has strong links to cardiovascular conditions like atherosclerosis, myocardial infarction, hypertension, stroke, and heart...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Archive

More from Medtech Insight

Siemens Healthineers Widens FY25 EPS Range By €0.15 To Absorb Up To €300M In Tariff Costs

 
• By 

The imaging, Varian, and advanced therapies segments – which are more reliant on equipment sales – are more heavily affected, with tariffs applying to roughly 55% of their revenue base. In diagnostics, the company expects minimal exposure due to sufficient US value-added manufacturing.

FDA Rebukes Four Companies, Including One Overseas, For Procedural Failures

 

The US FDA’s device center sent warning letters to three domestic device manufacturers and one German firm for failing to adhere to protocol on several issues.

Cardiosense Advances Noninvasive Heart Monitoring With Final Validation Study

 
• By 

Cardiosense has launched a nationwide clinical study, SEISMIC-HF II, to validate its non-invasive, AI-powered technology for monitoring heart failure. The data will be used to file for US regulatory clearance of the Cardiosense heart failure monitoring platform.