AI Article Synopsis

  • The study investigates whether specific biomarkers (S-100b and neuron-specific enolase) can predict cognitive impairment in patients who survived out-of-hospital cardiac arrest with good neurological outcomes.
  • A total of 79 patients were monitored for cognitive function six months after resuscitation, with memory impairment identified as the most common issue.
  • The findings reveal that neuron-specific enolase measured 48 hours after reaching a targeted temperature could accurately predict cognitive impairment, showing 100% sensitivity and 56% specificity, regardless of the duration of targeted temperature management.

Article Abstract

Background: Patients surviving out-of hospital cardicac arrest, with good neurological outcome according to Cerebral Performance Category, frequently have neuropsychological impairment. We studied whether biomarker data (S-100b and neuron-specific enolase) obtained during the ICU stay predicted cognitive impairment 6 months after resuscitation.

Methods: Patients (N = 79) with a CPC-score ≤2 were recruited from two trial sites taking part in the TTH48 trial comparing targeted temperature management (TTM) for 48 h vs. 24 h at 33 ± 1 °C. We assessed patients 6 months after the OHCA. We measured biomarkers S-100b and NSE at arrival and at 24, 48 and 72 h after reaching the target temperature of 33 ± 1 °C. Four cognitive domain z-scores were calculated, and global cognitive impairment was defined as z < -1.67 on at least 3 out of 13 cognitive tests. Non-parametric correlations were used to assess the relationship between cognitive domain and biomarkers. ROC curves were used to assess prediction of cognitive impairment from the biomarkers. Logistic regression was used to investigate whether TTM duration moderated biomarker prediction of cognitive impairment.

Results: Cognitive impairment was present in 22% of the patients with memory impairment being the most common. The biomarkers correlated significantly with several cognitive domain scores and NSE at 48 h predicted cognitive impairment with 100% sensitivity and 56% specificity. The predictive properties of NSE at 48 h was unaffected by duration of TTM.

Conclusions: Early biomarker prognostication of cognitive impairment is feasible even in OHCA survivors with good neurological outcome as defined by CPC. NSE at 48 h predicted cognitive impairment.

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Source
http://dx.doi.org/10.1016/j.resuscitation.2021.02.025DOI Listing

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