Critical Care volume 29,
Article number: 424 (2025) Published: 07 October 2025
Abstract
Delirium is a prevalent neuropsychiatric syndrome during
critical illness and is associated with prolonged hospitalization, increased
mortality, and post-ICU cognitive decline. It is hypothesized to result from
systemic inflammation, disrupted neurotransmission, and failure of cerebral
energy metabolism. This narrative review highlights the key role of altered
neurometabolism and neuroinflammation, which occurs due to peripheral
inflammation, compromised blood-brain barrier integrity, and increased microglial
glycolysis. These changes limit neuronal glucose uptake, leading to a brain
energy crisis and consequently amplifying oxidative and inflammatory stress. We
focus on studies of ICU delirium in the setting of acute critical illness with
an emphasis on sepsis-associated encephalopathy, where mechanistic data derived
from murine models are most robust. Ketones bypass the glycolytic bottleneck
and enter the tricarboxylic acid cycle directly, activating signaling pathways
that enhance mitochondrial biogenesis, bolster antioxidant defenses, modulate
neurotransmission, and reduce inflammation. In models of neurodegenerative
diseases and traumatic brain injury, ketosis restores cerebral metabolism,
reduces neuroinflammation, and enhances cognitive function. Additionally,
preliminary human studies have demonstrated cognitive benefits and patient
tolerance of ketone supplementation. Although data in the critically ill are
limited, pilot studies suggest that enteral ketone supplementation can safely
achieve therapeutic serum concentrations without worsening acidosis or
hemodynamic instability. We hypothesize that exogenous ketone ester
supplementation may support brain energy production by providing an alternative
substrate for energy production, reducing microglial substrate competition, and
mitigating the neuronal stress that precipitates delirium. In conclusion,
exogenous ketone esters are a biologically plausible, rapidly acting metabolic
intervention that warrants rigorous clinical evaluation as a novel strategy to
prevent or treat delirium in those who are critically ill. However, randomized
controlled trials are essential for verifying safety, determining optimal
dosing, and assessing clinical effectiveness in the intensive care setting.
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