Format

Send to

Choose Destination
Intensive Care Med. 2003 Feb;29(2):189-95. Epub 2002 Dec 10.

Serum neuron-specific enolase predicts outcome in post-anoxic coma: a prospective cohort study.

Author information

1
Intensive Care Unit, Reinier de Graaf Gasthuis, Reinier de Graafweg 3-11, 2625 AD, Delft, Netherlands. meynaar@rdgg.nl

Abstract

OBJECTIVE:

The aim of this study was to investigate whether serial serum neuron-specific enolase (NSE) can be used to predict neurological prognosis in patients remaining comatose after cardiopulmonary resuscitation (CPR). DESIGN. Observational cohort study. Clinicians were blinded to NSE results.

SETTING:

Eighteen-bed general ICU.

PATIENTS:

Comatose patients admitted to the ICU after CPR.

INTERVENTIONS:

Serum NSE was measured at admission and daily for 5 days.

MEASUREMENTS AND RESULTS:

Patients received full intensive treatment until recovery or until absence of cortical response to somatosensory evoked potentials more than 48 h after CPR proved irreversible coma. Of the 110 patients included (mean GCS at ICU admission 3, range 3--9), 34 regained consciousness, five of whom died in hospital. Seventy-six patients did not regain consciousness, 72 of whom died in hospital. Serum NSE at 24 h and at 48 h after CPR was significantly higher in patients who did not regain consciousness than in patients who regained consciousness (at 24 h: median NSE 29.9 microg/l, range 1.8-250 vs 9.9 microg/l, range 4.5-21.5, P<0.001; at 48 h: median 37.8 microg/l, range 4.4-411 vs 9.5 microg/l, range 6.2-22.4, P= 0.001). No patient with a serum NSE level >25.0 microg/l at any time regained consciousness. Addition of NSE to GCS and somatosensory evoked potentials increased predictability of poor neurological outcome from 64% to 76%.

CONCLUSIONS:

High serum NSE levels in comatose patients at 24 h and 48 h after CPR predict a poor neurological outcome. Addition of NSE to GCS and somatosensory evoked potentials increases predictability of neurological outcome.

PMID:
12594583
DOI:
10.1007/s00134-002-1573-2
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Springer
Loading ...
Support Center