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Optimal Cerebral Perfusion Pressure Management at Bedside: A Single-Center Pilot Study
Celeste Dias1, Maria João Silva, Eduarda Pereira
1Neurocritical Care Unit, Intensive Care Department, Hospital Sao Joao, Porto, Portugal, mceleste.dias@gmail.com.
Individualized cerebral perfusion pressure (CPP) management guided by cerebrovascular pressure reactivity (PRx) appears feasible for acute traumatic brain injury (TBI) patients. Significant deviations from the optimal CPP (CPPopt) were linked to adverse outcomes, suggesting a potential for improved TBI treatment.
Area of Science:
- Neuroscience
- Critical Care Medicine
- Biomedical Engineering
Background:
- Current guidelines for acute traumatic brain injury (TBI) recommend specific cerebral perfusion pressure (CPP) and intracranial pressure targets.
- However, individual patient variability in cerebral autoregulation necessitates personalized treatment strategies.
- Assessing cerebral autoregulation at the bedside can optimize CPP-guided therapy.
Purpose of the Study:
- To evaluate staff compliance with a novel autoregulation-guided treatment (CPPopt) method.
- To determine the impact of CPPopt on patient outcomes in severe TBI.
- To assess the feasibility of continuous cerebrovascular reactivity (PRx) monitoring for treatment guidance.
Main Methods:
- A prospective pilot study involving adult patients with severe TBI in a Neurocritical Care Unit (NCCU).
- Continuous multimodal brain monitoring was employed, with CPPopt automatically estimated every minute using a 4-hour window of PRx data.
- Patients were managed with CPPopt targets when feasible; otherwise, standard guidelines were followed. Offline CPPopt calculations were performed using cerebral oximetry (COx-CPPopt), brain tissue oxygenation (ORxs-CPPopt), and cerebral blood flow (CBFx-CPPopt).
Main Results:
- Eighteen patients contributed 5,520 hours of monitoring data.
- A CPPopt U-shaped curve, indicating optimal autoregulation, was observed in 61% of patients.
- Real CPP significantly correlated with calculated CPPopt (r=0.83, p<0.0001). Preserved autoregulation correlated with better Glasgow Coma Scale scores and outcomes (p=0.01).
- A discrepancy >10 mmHg between real CPP and CPPopt was associated with adverse outcomes (p=0.04). COx-CPPopt showed the lowest bias (-0.1 mmHg).
Conclusions:
- Bedside management of CPP guided by cerebrovascular pressure reactivity (CPPopt) is feasible.
- Significant deviations from CPPopt are associated with adverse outcomes in TBI patients.
- The non-invasive COx-CPPopt method using NIRS warrants further investigation for clinical application.
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