Publications by authors named "Kathleen M Boyle"

Article Synopsis
  • Patients on chronic opioids are vulnerable to serious breathing issues during sleep, like central and obstructive apneas, hypopneas, and hypoxaemia.
  • Buprenorphine, a medication used for treating opioid dependency and chronic pain, has not been extensively studied for its effects on sleep-related breathing disorders.
  • In a study of 70 patients using buprenorphine/naloxone, 63% showed signs of at least mild sleep disordered breathing, with notable cases of moderate and severe sleep apnea present in 33% of participants.
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Background: Adaptive servoventilation (ASV) can be effective therapy for specific types of central apnea such as Cheyne-Stokes respiration (CSR). Patients treated chronically with opioids develop central apneas and ataxic breathing patterns (Biot's respiration), but therapy with CPAP is usually unsuccessful. There are no published studies of ASV in patients with sleep apnea complicated by chronic opioid therapy.

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Article Synopsis
  • Chronic opioid therapy has surged for pain management, yet its impact on sleep-related breathing has been insufficiently studied.
  • A study compared the sleep breathing patterns of 60 chronic opioid users to 60 non-users, finding higher apnea rates and lower oxygen saturation in the opioid group.
  • Results indicated a dose-dependent relationship where higher morphine doses correlated with more severe breathing issues during sleep, including central apneas and irregular breathing patterns.
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Background: Sleep-disordered breathing and hypoxemia frequently underlie many common medical conditions for which patients require hospitalization. Sleep apnea is associated with adverse cardiovascular, neurovascular, inflammatory, and metabolic consequences, many of which can be reversed with nasal continuous positive airway pressure. Although polysomnography is the gold standard for outpatient evaluation of sleep apnea, it has not been used for establishing the diagnosis or as a means to intervene with evidence-based therapy in the hospital setting.

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The O2 sensitivity of dissociated type I cells from rat carotid body increases with age until approximately 14-16 days. Hypoxia-induced depolarization appears to be mediated by an O2-sensitive K+ current, but other K+ currents may modulate depolarization. We hypothesized that membrane potential may be stabilized in newborn type I cells by human ether-a-go-go-related gene (HERG)-like K+ currents that inhibit hypoxia-induced depolarization and that a decrease in this current with age could underlie, in part, the developmental increase in type I cell depolarization response to hypoxia.

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