Medication-Induced Central Sleep Apnea: A Unifying Concept.
Shahrokh JavaheriW J RanderathM Safwan BadrSogol JavaheriPublished in: Sleep (2024)
Medication-induced central sleep apnea (CSA) is one of the 8 categories of causes of CSA but in the absence of awareness and careful history may be misclassified as primary CSA. While opioids are a well-known cause of respiratory depression and CSA, non-opioids medications including sodium oxybate, baclofen, valproic acid, gabapentin and ticagrelor are less well-recognized. Opioids-induced respiratory depression and CSA are mediated primarily by µ-opioid receptors, which are abundant in the pontomedullary centers involved in breathing. The non-opioid medications, sodium oxybate, baclofen, valproic acid and gabapentin, act upon brainstem gamma-aminobutyric acid (GABA) receptors, which co-colonize with µ-opioid receptors and mediate CSA. The pattern of ataxic breathing associated with these medications is like that induced by opioids on polysomnogram. Finally, ticagrelor also causes periodic breathing and CSA by increasing central chemosensitivity and ventilatory response to carbon dioxide. Given the potential consequences of CSA and the association between some of these medications with mortality, it is critical to recognize these adverse drug reactions, particularly because discontinuation of the offending agents has been shown to eliminate CSA.
Keyphrases
- chronic pain
- pain management
- sleep apnea
- adverse drug
- high glucose
- diabetic rats
- carbon dioxide
- obstructive sleep apnea
- acute coronary syndrome
- positive airway pressure
- drug induced
- healthcare
- depressive symptoms
- percutaneous coronary intervention
- oxidative stress
- emergency department
- st elevation myocardial infarction
- type diabetes
- cardiovascular disease
- antiplatelet therapy
- endothelial cells
- risk factors