Feasibility of non-invasive neuro-monitoring during extracorporeal membrane oxygenation in children

Author:

McDevitt William M1ORCID,Farley Margaret2,Martin-Lamb Darren1,Jones Timothy J34,Morris Kevin P25,Seri Stefano16,Scholefield Barnaby R27

Affiliation:

1. Department of Neurophysiology, Birmingham Children’s Hospital Birmingham, UK

2. Paediatric Intensive Care Unit, Birmingham Children’s Hospital, Birmingham, UK

3. Department of Cardiac Surgery, Birmingham Children’s Hospital, Birmingham, UK

4. Institute of Cardiovascular Sciences, University of Birmingham, Birmingham, UK

5. Institute of Applied Health Research, University of Birmingham, Birmingham, UK

6. Aston Brain Centre, School of Life and Health Sciences, Aston University, Birmingham, UK

7. Birmingham Acute Care Research Group, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, UK

Abstract

Introduction Detection of neurological complications during extracorporeal membrane oxygenation (ECMO) may be enhanced with non-invasive neuro-monitoring. We investigated the feasibility of non-invasive neuro-monitoring in a paediatric intensive care (PIC) setting. Methods In a single centre, prospective cohort study we assessed feasibility of recruitment, and neuro-monitoring via somatosensory evoked potentials (SSEP), electroencephalography (EEG) and near infrared spectroscopy (NIRS) during venoarterial (VA) ECMO in paediatric patients (0–15 years). Measures were obtained within 24h of cannulation, during an intermediate period, and finally at decannulation or echo stress testing. SSEP/EEG/NIRS measures were correlated with neuro-radiology findings, and clinical outcome assessed via the Pediatric cerebral performance category (PCPC) scale 30 days post ECMO cannulation. Results We recruited 14/20 (70%) eligible patients (median age: 9 months; IQR:4–54, 57% male) over an 18-month period, resulting in a total of 42 possible SSEP/EEG/NIRS measurements. Of these, 32/42 (76%) were completed. Missed recordings were due to lack of access/consent within 24 h of cannulation (5/42, 12%) or PIC death/discharge (5/42, 12%). In each patient, the majority of SSEP (8/14, 57%), EEG (8/14, 57%) and NIRS (11/14, 79%) test results were within normal limits. All patients with abnormal neuroradiology (4/10, 40%), and 6/7 (86%) with poor outcome (PCPC ≥4) developed indirect SSEP, EEG or NIRS measures of neurological complications prior to decannulation. No study-related adverse events or neuro-monitoring data interpreting issues were experienced. Conclusion Non-invasive neuro-monitoring (SSEP/EEG/NIRS) during ECMO is feasible and may provide early indication of neurological complications in this high-risk population.

Funder

National Institute for Health Research

Publisher

SAGE Publications

Subject

Advanced and Specialized Nursing,Cardiology and Cardiovascular Medicine,Safety Research,Radiology, Nuclear Medicine and imaging,General Medicine

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