Multimodal Brain Monitoring as an Early Warning and Prognostic Tool for Acute Brain Injury

Exclusion Criteria

• •1. Patients who were not admitted to the Intensive Care Unit (ICU) are excluded.
• •2. Patients with forms of acute brain injury other than those specified (TBI, intracranial hemorrhage, subarachnoid hemorrhage) are also excluded.
• •3. Patients with known severe liver or kidney dysfunction are excluded.
• •4. Patients whose vital signs are extremely unstable after admission, with a very poor prognosis and considered unable to survive, and whose family has decided to forgo further treatment.
• •5. Patients who had a Modified Rankin Scale greater than 2 before the onset of the current illness.
• •6. Patients with a history of congenital or acquired hemorrhagic diseases, coagulation factor deficiencies, or thrombocytopenic disorders.
• •7. Pregnant or lactating women, as well as those planning to become pregnant within the next 90 days.
• •8. Patients with severe psychiatric disorders or dementia who are unable to provide informed consent or complete follow-up requirements.
• •9. Patients who have participated in other interventional clinical trials within 30 days prior to randomization, or who are currently participating in other clinical research.
• •10. Any other reasons that the researcher deems unsuitable for participation in this trial.