Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation

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Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation. / Hasslacher, Julia; Lehner, Georg Franz; Harler, Ulrich; Beer, Ronny; Ulmer, Hanno; Kirchmair, Rudolf; Fischer-Colbrie, Reiner; Bellmann, Romuald; Dunzendorfer, Stefan; Joannidis, Michael.

In: INTENS CARE MED, Vol. 40, No. 10, 10.2014, p. 1518-27.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Hasslacher, J, Lehner, GF, Harler, U, Beer, R, Ulmer, H, Kirchmair, R, Fischer-Colbrie, R, Bellmann, R, Dunzendorfer, S & Joannidis, M 2014, 'Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation', INTENS CARE MED, vol. 40, no. 10, pp. 1518-27. https://doi.org/10.1007/s00134-014-3423-4

APA

Hasslacher, J., Lehner, G. F., Harler, U., Beer, R., Ulmer, H., Kirchmair, R., Fischer-Colbrie, R., Bellmann, R., Dunzendorfer, S., & Joannidis, M. (2014). Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation. INTENS CARE MED, 40(10), 1518-27. https://doi.org/10.1007/s00134-014-3423-4

Vancouver

Bibtex

@article{fc0de44721c741e78e8f5d5d92160512,
title = "Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation",
abstract = "PURPOSE: The neuropeptide secretoneurin (SN) shows widespread distribution in the brain. We evaluated whether SN is elevated after cardiopulmonary resuscitation (CPR) and could serve as a potential new biomarker for hypoxic brain injury after CPR.METHODS: This was a prospective observational clinical study. All patients admitted to a tertiary medical intensive care unit after successful CPR with expected survival of at least 24 h were consecutively enrolled from September 2008 to April 2013. Serum SN and neuron-specific enolase were determined in 24 h intervals starting with the day of CPR for 7 days. Neurological outcome was assessed with the Cerebral Performance Categories Scale (CPC) at hospital discharge.RESULTS: A total of 134 patients were included with 49 % surviving to good neurological outcome (CPC 1-2). SN serum levels peaked within the first 24 h showing on average a sixfold increase above normal. SN levels were significantly higher in patients with poor (CPC 3-5) than in patients with good neurological outcome [0-24 h: 75 (43-111) vs. 38 (23-68) fmol/ml, p < 0.001; 24-48 h: 45 (24-77) vs. 23 (16-39) fmol/ml, p < 0.001]. SN determined within the first 48 h showed a receiver operating characteristic (ROC) area under the curve (AUC) of 0.753 (0.665-0.841). NSE in the first 72 h had a ROC-AUC of 0.881 (0.815-0.946). When combining the two biomarkers an AUC of 0.925 (0.878-0.972) for outcome prediction could be reached.CONCLUSIONS: SN is a promising early biomarker for hypoxic brain injury. Further studies will be required for confirmation of these results.",
keywords = "APACHE, Aged, Area Under Curve, Biomarkers, Cardiopulmonary Resuscitation, Diagnostic Techniques, Neurological, Female, Heart Arrest, Humans, Hypoxia, Brain, Intensive Care Units, Male, Middle Aged, Multivariate Analysis, Neuropeptides, Organ Dysfunction Scores, Out-of-Hospital Cardiac Arrest, Phosphopyruvate Hydratase, Predictive Value of Tests, Prospective Studies, ROC Curve, Secretogranin II, Tertiary Care Centers, Time-to-Treatment, Journal Article",
author = "Julia Hasslacher and Lehner, {Georg Franz} and Ulrich Harler and Ronny Beer and Hanno Ulmer and Rudolf Kirchmair and Reiner Fischer-Colbrie and Romuald Bellmann and Stefan Dunzendorfer and Michael Joannidis",
year = "2014",
month = oct,
doi = "10.1007/s00134-014-3423-4",
language = "English",
volume = "40",
pages = "1518--27",
journal = "INTENS CARE MED",
issn = "0342-4642",
publisher = "Springer",
number = "10",

}

RIS

TY - JOUR

T1 - Secretoneurin as a marker for hypoxic brain injury after cardiopulmonary resuscitation

AU - Hasslacher, Julia

AU - Lehner, Georg Franz

AU - Harler, Ulrich

AU - Beer, Ronny

AU - Ulmer, Hanno

AU - Kirchmair, Rudolf

AU - Fischer-Colbrie, Reiner

AU - Bellmann, Romuald

AU - Dunzendorfer, Stefan

AU - Joannidis, Michael

PY - 2014/10

Y1 - 2014/10

N2 - PURPOSE: The neuropeptide secretoneurin (SN) shows widespread distribution in the brain. We evaluated whether SN is elevated after cardiopulmonary resuscitation (CPR) and could serve as a potential new biomarker for hypoxic brain injury after CPR.METHODS: This was a prospective observational clinical study. All patients admitted to a tertiary medical intensive care unit after successful CPR with expected survival of at least 24 h were consecutively enrolled from September 2008 to April 2013. Serum SN and neuron-specific enolase were determined in 24 h intervals starting with the day of CPR for 7 days. Neurological outcome was assessed with the Cerebral Performance Categories Scale (CPC) at hospital discharge.RESULTS: A total of 134 patients were included with 49 % surviving to good neurological outcome (CPC 1-2). SN serum levels peaked within the first 24 h showing on average a sixfold increase above normal. SN levels were significantly higher in patients with poor (CPC 3-5) than in patients with good neurological outcome [0-24 h: 75 (43-111) vs. 38 (23-68) fmol/ml, p < 0.001; 24-48 h: 45 (24-77) vs. 23 (16-39) fmol/ml, p < 0.001]. SN determined within the first 48 h showed a receiver operating characteristic (ROC) area under the curve (AUC) of 0.753 (0.665-0.841). NSE in the first 72 h had a ROC-AUC of 0.881 (0.815-0.946). When combining the two biomarkers an AUC of 0.925 (0.878-0.972) for outcome prediction could be reached.CONCLUSIONS: SN is a promising early biomarker for hypoxic brain injury. Further studies will be required for confirmation of these results.

AB - PURPOSE: The neuropeptide secretoneurin (SN) shows widespread distribution in the brain. We evaluated whether SN is elevated after cardiopulmonary resuscitation (CPR) and could serve as a potential new biomarker for hypoxic brain injury after CPR.METHODS: This was a prospective observational clinical study. All patients admitted to a tertiary medical intensive care unit after successful CPR with expected survival of at least 24 h were consecutively enrolled from September 2008 to April 2013. Serum SN and neuron-specific enolase were determined in 24 h intervals starting with the day of CPR for 7 days. Neurological outcome was assessed with the Cerebral Performance Categories Scale (CPC) at hospital discharge.RESULTS: A total of 134 patients were included with 49 % surviving to good neurological outcome (CPC 1-2). SN serum levels peaked within the first 24 h showing on average a sixfold increase above normal. SN levels were significantly higher in patients with poor (CPC 3-5) than in patients with good neurological outcome [0-24 h: 75 (43-111) vs. 38 (23-68) fmol/ml, p < 0.001; 24-48 h: 45 (24-77) vs. 23 (16-39) fmol/ml, p < 0.001]. SN determined within the first 48 h showed a receiver operating characteristic (ROC) area under the curve (AUC) of 0.753 (0.665-0.841). NSE in the first 72 h had a ROC-AUC of 0.881 (0.815-0.946). When combining the two biomarkers an AUC of 0.925 (0.878-0.972) for outcome prediction could be reached.CONCLUSIONS: SN is a promising early biomarker for hypoxic brain injury. Further studies will be required for confirmation of these results.

KW - APACHE

KW - Aged

KW - Area Under Curve

KW - Biomarkers

KW - Cardiopulmonary Resuscitation

KW - Diagnostic Techniques, Neurological

KW - Female

KW - Heart Arrest

KW - Humans

KW - Hypoxia, Brain

KW - Intensive Care Units

KW - Male

KW - Middle Aged

KW - Multivariate Analysis

KW - Neuropeptides

KW - Organ Dysfunction Scores

KW - Out-of-Hospital Cardiac Arrest

KW - Phosphopyruvate Hydratase

KW - Predictive Value of Tests

KW - Prospective Studies

KW - ROC Curve

KW - Secretogranin II

KW - Tertiary Care Centers

KW - Time-to-Treatment

KW - Journal Article

U2 - 10.1007/s00134-014-3423-4

DO - 10.1007/s00134-014-3423-4

M3 - SCORING: Journal article

C2 - 25138227

VL - 40

SP - 1518

EP - 1527

JO - INTENS CARE MED

JF - INTENS CARE MED

SN - 0342-4642

IS - 10

ER -