Abstract
Purpose
To assess the feasibility of Transcranial Doppler ultrasonography (TCD) neuromonitoring in a general intensive care environment, in the prognosis and outcome prediction of patients who are in coma due to a variety of critical conditions.
Methods
The prospective trial was performed between March 2017 and March 2019 Addenbrooke’s Hospital, Cambridge, UK. Forty adult patients who failed to awake appropriately after resuscitation from cardiac arrest or were in coma due to conditions such as meningitis, seizures, sepsis, metabolic encephalopathies, overdose, multiorgan failure or transplant were eligible for inclusion. Gathered data included admission diagnosis, duration of ventilation, length of stay in the ICU, length of stay in hospital, discharge status using Cerebral Performance Categories (CPC). All patients received intermittent extended TCD monitoring following inclusion in the study. Parameters of interest included TCD-based indices of cerebral autoregulation, non-invasive intracranial pressure, autonomic system parameters (based on heart rate variability), critical closing pressure, the cerebrovascular time constant and indices describing the shape of the TCD pulse waveform.
Results
Thirty-seven patients were included in the final analysis, with 21 patients classified as good outcome (CPC 1-2) and 16 as poor neurological outcomes (CPC 3-5). Three patients were excluded due to inadequacies identified in the TCD acquisition. The results indicated that irrespective of the primary diagnosis, non-survivors had significantly disturbed cerebral autoregulation, a shorter cerebrovascular time constant and a more distorted TCD pulse waveform (all p<0.05).
Conclusions
Preliminary results from the trial indicate that multi-parameter TCD neuromonitoring increases outcome-predictive power and TCD-based indices can be applied to general intensive care monitoring.
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Acknowledgements
This study was sponsored by the Cambridge University Hospitals NHS Foundation Trust R&D and led by MSD (IRAS Project ID: 165207).
Funding
This work was supported by Cambridge Commonwealth, European & International Trust Scholarship (University of Cambridge) in the form of Scholarship funding for DC, and NIHR Brain Injury Healthcare Technology Co-operative, Cambridge, UK in the form of equipment funding for DC, LC, and MC. The sponsors had no role in the design or conduct of this manuscript.
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LC, DC, MC, MSD designed and led the study, performed the statistical analysis, and drafted the first version of the manuscript. All the authors participated in data interpretation, collection, and editing of the first version of the manuscript. All authors approved the final version of the manuscript and authorship requirements have been met.
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MC and PS share financial interest in a portion of ICM+ software licensing fees. The remaining authors disclose no conflicts of interest.
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This manuscript complies with all instructions to authors and adhere to ethical guidelines and indicate ethical approvals (IRB) and use of informed consent. The experimental protocol and informed consent were approved by the institutional review board at Addenbrooke’s Hospital, Cambridge University Hospitals Foundation Trust (“Non-invasive multimodal brain monitoring in Clinical Neuroscience”, IRAS ID 165207, REC (IRB) reference 16/LO/1971).
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Informed consent was obtained for all individual participants included in the study. As patients were unable to provide informed consent themselves at the point of inclusion, they were included either by a process of deferred assent by next of kin or of inclusion by professional assent through treating physicians, who were not involved in the trial.
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Calviello, L.A., Cardim, D., Czosnyka, M. et al. Feasibility of non-invasive neuromonitoring in general intensive care patients using a multi-parameter transcranial Doppler approach. J Clin Monit Comput 36, 1805–1815 (2022). https://doi.org/10.1007/s10877-022-00829-x
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DOI: https://doi.org/10.1007/s10877-022-00829-x