AI Article Synopsis

  • Patients with obstructive sleep apnea (OSA) who can't tolerate CPAP may benefit from surgery, specifically from hypoglossal nerve stimulation (HNS) using the Inspire® device.
  • A study found that after 3 months, HNS significantly improved the quality of life for these patients, with quality of life scores rising notably in comparison to a control group.
  • The results showed that all aspects of life improved for those with the Inspire® device, particularly in daily activities and reducing anxiety, making their quality of life comparable to that of the general Spanish population.

Article Abstract

Patients with obstructive sleep apnea (OSA) that do not tolerate/accept continuous positive airway pressure (CPAP) are candidates for surgical alternatives. Hypoglossal nerve stimulation (HNS) through the implantation of the Inspire® device constitutes a minimally invasive operative option. The main objective of this study is to estimate, under real-world clinical practice conditions, the 3-month impact on the quality of life (IQoL) of the HNS in patients with moderate/severe OSA who do not tolerate or accept CPAP, compared to patients who did not receive HNS. As a baseline, the unadjusted EuroQol utility index was 0.764 (SD:0.190) in the intervention group (IGr) and 0.733 (SD:0.205) in the control group (CGr); three months later, the indexes were 0.935 (SD: 0.101) and 0.727 (SD:0.200), respectively. The positive impact on quality of life was estimated to be +0.177 (95% CI: 0.044−0.310; p = 0.010). All dimensions in the IGr improved compared to CGr, especially for usual activities (p < 0.001) and anxiety/depression (p > 0.001). At the end of the follow-up, there was no significant difference in the quality of life between the general Spanish population and the IGr (difference: 0.012; CI95%: −0.03 to −0.057; p = 0.0578) for the same age range; however, there was a difference concerning the CGr (difference: −0.196; CI95%: −0.257 to −0.135; p < 0.001). In conclusion, patients with moderate/severe OSA implanted with the Inspire® device showed a positive IQoL.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9694893PMC
http://dx.doi.org/10.3390/life12111737DOI Listing

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