Inspire Medical Systems Inc this month announced the results of a landmark long-term clinical study for its Inspire Upper Airway Stimulation (UAS) System, the first FDA-approved implantable neurostimulation treatment for people diagnosed with obstructive sleep apnea (OSA).
Inspire therapy is for some people diagnosed with moderate to severe OSA who are unable to tolerate or get relief from CPAP. In contrast to CPAP, Inspire therapy works inside the body and with a patient’s natural breathing process. Controlled by the patient sleep remote, the system includes a breathing sensor and a stimulation lead powered by a small battery. During sleep, the system senses breathing patterns and delivers mild stimulation to the tongue and other soft tissues of the throat to keep the airway open. Inspire therapy is currently available at more than 60 medical centers across the United States and Europe.
The Stimulation Therapy for Apnea Reduction (STAR) trial was conducted at 22 sleep medicine centers across the United States and Europe. One-year STAR trial outcome measures, published in the January 9, 2014 edition of the New England Journal of Medicine, showed that sleep apnea patients receiving Inspire therapy experienced significant reductions in sleep apnea events and significant improvements in quality of life measures.
The new long-term study outcomes showed that the improvements observed at one-year were sustained at the three-year follow up mark. The outcomes include:
- A 78% reduction in apnea-hypopnea index (AHI) from baseline
- An 80% reduction in oxygen desaturation events from baseline
- 80% of bed partners reported soft or no snoring as compared to 17% of bed partners at baseline
- Quality of life measures, including daytime sleepiness and functioning, showed clinically meaningful improvements and a return to normal levels over baseline
The results were published in the online issue of Otolaryngology – Head and Neck Surgery, the official peer-reviewed publication of the American Academy of Otolaryngology – Head and Neck Surgery Foundation.
New data from the STAR Trial demonstrate that more than 80% of the patients with Inspire therapy report nightly use after 3 years of being prescribed the therapy.
The data was recently presented at the annual American Academy of Otolaryngology – Head and Neck Surgery Foundation meeting in Dallas by B. Tucker Woodson, MD, chief of the Division of Sleep Medicine at Froedtert Hospital and the Medical College of Wisconsin. “The data confirms that Inspire Upper Airway Stimulation therapy is safe and effective and that the results are consistent over the long term,” says Woodson, lead author of the 36-month manuscript, in a release. “We also observed high therapy adherence rates throughout the three-year STAR trial follow-up period. It is exciting to have an effective treatment to help those sleep apnea patients who are not able to tolerate or achieve consistent benefit from CPAP.”
Tim Herbert, Inspire Medical Systems CEO, says, “The three-year study outcomes are significant as they demonstrate that improvements in both objective respiratory and subjective quality of life measures are maintained. We thank and congratulate both the STAR trial investigator group and the author team for completing the long-term follow up and publishing these important outcomes.”