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Sleep and circadian rhythm alterations associate with prolonged ventilation and worse outcomes in adult ICU patients

Sleep and circadian rhythm alterations associate with prolonged ventilation and worse outcomes in…
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Key Takeaway
Note that sleep and circadian rhythm alterations associate with worse ICU outcomes and require confirmation as therapeutic targets.

This narrative review focuses on sleep and circadian rhythm alterations among adult ICU patients. The scope covers respiratory recovery, delirium, inflammation, illness severity, mortality, post-intensive care syndrome, prolonged mechanical ventilation, weaning failure, noninvasive ventilation failure, acute brain dysfunction, systemic inflammation, cognitive impairment, psychological distress, fatigue, and reduced quality of life.

The authors synthesize findings indicating that prolonged mechanical ventilation, weaning failure, and noninvasive ventilation failure are associated with disrupted sleep architecture. Delirium and markers of acute brain dysfunction are linked to alterations in sleep and circadian rhythmicity. Systemic inflammation, disease severity, and adverse prognosis correlate with circadian rhythm disruption. Cognitive impairment, psychological distress, fatigue, and reduced quality of life may persist long after ICU discharge and contribute to these issues.

The review acknowledges that methodological limits remain. The authors state that whether these associations represent modifiable therapeutic targets that can improve prognosis requires confirmation through rigorous interventional trials. Increasing evidence suggests associations, but causality is not established. The practice relevance identifies sleep and circadian rhythms as clinically relevant biomarkers of critical illness severity and brain dysfunction.

Study Details

Study typeSystematic review
EvidenceLevel 1
PublishedMay 2026
View Original Abstract ↓
Sleep and circadian rhythms are essential regulators of physiological homeostasis, influencing immune, metabolic, cardiovascular, and neurocognitive functions. In critically ill patients, these systems are frequently disrupted by the intensive care unit (ICU) environment, therapeutic interventions, and underlying illness. Increasing evidence suggests that sleep and circadian dyssrhythmias are associated with clinical outcomes during and after critical illness. This narrative review summarizes current knowledge on sleep and circadian rhythm alterations in adult ICU patients and examines their associations with short and long-term outcomes. We review studies using a wide range of assessment tools, including polysomnography, electroencephalography, actigraphy, cardiopulmonary coupling, hormonal profiling (melatonin and cortisol), temperature rhythms and clock gene expression. The relationship between these alterations and outcomes such as respiratory recovery, delirium, inflammation, illness severity, mortality, and post-intensive care syndrome is discussed. Across multiple studies, disrupted sleep architecture, characterized by reduced total sleep time, loss of rapid eye movement sleep, and atypical electroencephalographic patterns, has been associated with prolonged mechanical ventilation, weaning failure, and noninvasive ventilation failure. Alterations in sleep and circadian rhythmicity are also linked to delirium and markers of acute brain dysfunction. Circadian rhythm disruption, reflected by blunted or phase-shifted hormonal rhythms and altered clock gene expression, correlates with systemic inflammation, disease severity, and adverse prognosis. Emerging data further indicate that sleep and circadian disturbances may persist long after ICU discharge and contribute to cognitive impairment, psychological distress, fatigue, and reduced quality of life. Although methodological limits remain, the available evidence supports sleep and circadian rhythms as clinically relevant biomarkers of critical illness severity and brain dysfunction. Whether these represent modifiable therapeutic targets that can improve prognosis requires confirmation through rigorous interventional trials designed to account for the substantial confounding inherent in this population.
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