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Managing acute non-anoxic brain injuries, including hemorrhagic or ischemic strokes and traumatic brain injuries, poses a significant challenge in neurology. This challenge is compounded by the fact that fever, present in nearly 90% of patients in intensive care, is closely linked to severe neurological complications. Understanding the impact of fever on clinical outcomes is essential to optimizing therapeutic strategies and improving the quality of care. This study examines the connection between fever and neurological deterioration, offering insight into targeted intervention approaches.

Fever and brain injuries: what are the measured impacts?

The analysis is based on data from over 180 trials involving a total of 460,825 patients admitted for acute brain injuries. Key variables assessed include body temperature, study-specific definitions of fever, and neurological outcomes such as mortality and functional decline.

The findings reveal a strong association between fever and increased mortality, as well as adverse neurological outcomes. In particular, fever contributes to severe complications such as delayed cerebral ischemia, hemorrhagic transformation, and cerebral edema. These are often accompanied by increased infarct size and early worsening of neurological conditions.

Temperature control: a key to improving neurological outcomes in intensive care

This study demonstrates that fever acts as an amplifier of secondary injuries by exacerbating inflammation, vascular damage, and hemodynamic imbalances, thereby negatively affecting neurological outcomes. These harmful effects are linked to increased cerebral metabolism, inflammation, and neuronal apoptosis. While strict temperature control emerges as a promising strategy to mitigate these effects, further research is needed to establish optimal protocols. Multidisciplinary care, combining intensive monitoring and tailored temperature management, remains essential for improving patient outcomes.

Source(s) :
Grot, S., et al. (2024). Label-based meta-analysis of functional brain dysconnectivity across mood and psychotic disorders. Progress in neuro-psychopharmacology & biological psychiatry, 131, 110950 ;

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