Characterization and prognostic relevance of neuron specific enolase after cardiopulmonary resuscitation with extracorporeal circulation (e-CPR)

Background The use of veno-arterial extracorporeal membrane oxygenation (VA-ECMO) is recommended in the current resuscitation guidelines of the European Resuscitation Council as a rescue attempt for selected patients for whom extended resuscitation measures do not lead to the establishment of a spontaneous circulation (ROSC). We aim to characterize and investigate the value of neuron specific enolase (NSE) for assessing the neurological prognosis after cardiopulmonary resuscitation (CPR) as these have so far only been evaluated in resuscitated patients without extracorporeal circulatory support. Methods We retrospectively analyzed the records of patients, who received a VA-ECMO under ongoing CPR between 2004 and 2021 and were treated in a cardiac intensive care unit (ICU) of a university, tertiary care center. Outcome will be measured clinically by using the Glasgow Outcome Score (GOS) four weeks after ICU discharge. Neurological prognosis will be estimated by serum concentration of NSE (baseline until 96h). Serum free hemoglobin (fHb, baseline until 96h) serves as a marker for identifying a potential confounding effect of relevant parallel hemolysis. Results 190 patients were included in our study (baseline characteristics, Figure 1). 154 patients (84.5%) died within 4 weeks after ICU admission or remained unconscious (GOS 1+2), 29 survived (15.5%) with a residual slight to severe neurological deficit (GOS 3–5). Mean duration of VA-ECMO treatment was 103.4±112.1 h. In a wake-up attempt 48–96 h after CPR, patients with GOS 3–5 showed significantly more frequent adequate responses to speech (84% vs. 30.3%; p Conclusion The neuroprotein NSE makes an early, neurological, prognostic assessment of resuscitated patients possible even during VA-ECMO treatment and could be used in sedated patients as a biomarker for evaluation of treatment decision in acute heart failure such as therapy continuation, eligibility for heart transplantation or LVAD implantation. Funding Acknowledgement Type of funding sources: None.