Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial

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Copeptin as a marker of outcome after cardiac arrest : a sub-study of the TTM trial. / Düring, Joachim; Annborn, Martin; Cronberg, Tobias; Dankiewicz, Josef; Devaux, Yvan; Hassager, Christian; Horn, Janneke; Kjaergaard, Jesper; Kuiper, Michael; Nikoukhah, Homa Rafi; Stammet, Pascal; Undén, Johan; Wanscher, Michael Jaeger; Wise, Matt; Friberg, Hans; Nielsen, Niklas.

In: Critical Care, Vol. 24, 185, 04.2020.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Düring, J, Annborn, M, Cronberg, T, Dankiewicz, J, Devaux, Y, Hassager, C, Horn, J, Kjaergaard, J, Kuiper, M, Nikoukhah, HR, Stammet, P, Undén, J, Wanscher, MJ, Wise, M, Friberg, H & Nielsen, N 2020, 'Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial', Critical Care, vol. 24, 185. https://doi.org/10.1186/s13054-020-02904-8

APA

Düring, J., Annborn, M., Cronberg, T., Dankiewicz, J., Devaux, Y., Hassager, C., Horn, J., Kjaergaard, J., Kuiper, M., Nikoukhah, H. R., Stammet, P., Undén, J., Wanscher, M. J., Wise, M., Friberg, H., & Nielsen, N. (2020). Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial. Critical Care, 24, [185]. https://doi.org/10.1186/s13054-020-02904-8

Vancouver

Düring J, Annborn M, Cronberg T, Dankiewicz J, Devaux Y, Hassager C et al. Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial. Critical Care. 2020 Apr;24. 185. https://doi.org/10.1186/s13054-020-02904-8

Author

Düring, Joachim ; Annborn, Martin ; Cronberg, Tobias ; Dankiewicz, Josef ; Devaux, Yvan ; Hassager, Christian ; Horn, Janneke ; Kjaergaard, Jesper ; Kuiper, Michael ; Nikoukhah, Homa Rafi ; Stammet, Pascal ; Undén, Johan ; Wanscher, Michael Jaeger ; Wise, Matt ; Friberg, Hans ; Nielsen, Niklas. / Copeptin as a marker of outcome after cardiac arrest : a sub-study of the TTM trial. In: Critical Care. 2020 ; Vol. 24.

Bibtex

@article{d43c41d9628944419582f605c1afbb73,
title = "Copeptin as a marker of outcome after cardiac arrest: a sub-study of the TTM trial",
abstract = "Background: Arginine vasopressin has complex actions in critically ill patients, involving vasoregulatory status, plasma volume, and cortisol levels. Copeptin, a surrogate marker for arginine vasopressin, has shown promising prognostic features in small observational studies and is used clinically for early rule out of acute coronary syndrome. The objective of this study was to explore the association between early measurements of copeptin, circulatory status, and short-term survival after out-of-hospital cardiac arrest. Methods: Serial blood samples were collected at 24, 48, and 72 h as part of the target temperature management at 33 °C versus 36 °C after cardiac arrest trial, an international multicenter randomized trial where unconscious survivors after out-of-hospital cardiac arrest were allocated to an intervention of 33 or 36 °C for 24 h. Primary outcome was 30-day survival with secondary endpoints circulatory cause of death and cardiovascular deterioration composite; in addition, we examined the correlation with extended the cardiovascular sequential organ failure assessment (eCvSOFA) score. Results: Six hundred ninety patients were included in the analyses, of whom 203 (30.3%) developed cardiovascular deterioration within 24 h, and 273 (39.6%) died within 30 days. Copeptin measured at 24 h was found to be independently associated with 30-day survival, hazard ratio 1.17 [1.06-1.28], p = 0.001; circulatory cause of death, odds ratio 1.03 [1.01-1.04], p = 0.001; and cardiovascular deterioration composite, odds ratio of 1.05 [1.02-1.08], p < 0.001. Copeptin at 24 h was correlated with eCvSOFA score with rho 0.19 [0.12-0.27], p < 0.001. Conclusion: Copeptin is an independent marker of severity of the post cardiac arrest syndrome, partially related to circulatory failure. Trial registration: Clinical Trials, NCT01020916. Registered November 26, 2009.",
keywords = "Arginine vasopressin, AVP protein human, Biomarkers, Copeptin, Critical illness, Humans, Out-of hospital cardiac arrest, Prognosis, Survivors",
author = "Joachim D{\"u}ring and Martin Annborn and Tobias Cronberg and Josef Dankiewicz and Yvan Devaux and Christian Hassager and Janneke Horn and Jesper Kjaergaard and Michael Kuiper and Nikoukhah, {Homa Rafi} and Pascal Stammet and Johan Und{\'e}n and Wanscher, {Michael Jaeger} and Matt Wise and Hans Friberg and Niklas Nielsen",
year = "2020",
month = apr,
doi = "10.1186/s13054-020-02904-8",
language = "English",
volume = "24",
journal = "Critical Care",
issn = "1364-8535",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - Copeptin as a marker of outcome after cardiac arrest

T2 - a sub-study of the TTM trial

AU - Düring, Joachim

AU - Annborn, Martin

AU - Cronberg, Tobias

AU - Dankiewicz, Josef

AU - Devaux, Yvan

AU - Hassager, Christian

AU - Horn, Janneke

AU - Kjaergaard, Jesper

AU - Kuiper, Michael

AU - Nikoukhah, Homa Rafi

AU - Stammet, Pascal

AU - Undén, Johan

AU - Wanscher, Michael Jaeger

AU - Wise, Matt

AU - Friberg, Hans

AU - Nielsen, Niklas

PY - 2020/4

Y1 - 2020/4

N2 - Background: Arginine vasopressin has complex actions in critically ill patients, involving vasoregulatory status, plasma volume, and cortisol levels. Copeptin, a surrogate marker for arginine vasopressin, has shown promising prognostic features in small observational studies and is used clinically for early rule out of acute coronary syndrome. The objective of this study was to explore the association between early measurements of copeptin, circulatory status, and short-term survival after out-of-hospital cardiac arrest. Methods: Serial blood samples were collected at 24, 48, and 72 h as part of the target temperature management at 33 °C versus 36 °C after cardiac arrest trial, an international multicenter randomized trial where unconscious survivors after out-of-hospital cardiac arrest were allocated to an intervention of 33 or 36 °C for 24 h. Primary outcome was 30-day survival with secondary endpoints circulatory cause of death and cardiovascular deterioration composite; in addition, we examined the correlation with extended the cardiovascular sequential organ failure assessment (eCvSOFA) score. Results: Six hundred ninety patients were included in the analyses, of whom 203 (30.3%) developed cardiovascular deterioration within 24 h, and 273 (39.6%) died within 30 days. Copeptin measured at 24 h was found to be independently associated with 30-day survival, hazard ratio 1.17 [1.06-1.28], p = 0.001; circulatory cause of death, odds ratio 1.03 [1.01-1.04], p = 0.001; and cardiovascular deterioration composite, odds ratio of 1.05 [1.02-1.08], p < 0.001. Copeptin at 24 h was correlated with eCvSOFA score with rho 0.19 [0.12-0.27], p < 0.001. Conclusion: Copeptin is an independent marker of severity of the post cardiac arrest syndrome, partially related to circulatory failure. Trial registration: Clinical Trials, NCT01020916. Registered November 26, 2009.

AB - Background: Arginine vasopressin has complex actions in critically ill patients, involving vasoregulatory status, plasma volume, and cortisol levels. Copeptin, a surrogate marker for arginine vasopressin, has shown promising prognostic features in small observational studies and is used clinically for early rule out of acute coronary syndrome. The objective of this study was to explore the association between early measurements of copeptin, circulatory status, and short-term survival after out-of-hospital cardiac arrest. Methods: Serial blood samples were collected at 24, 48, and 72 h as part of the target temperature management at 33 °C versus 36 °C after cardiac arrest trial, an international multicenter randomized trial where unconscious survivors after out-of-hospital cardiac arrest were allocated to an intervention of 33 or 36 °C for 24 h. Primary outcome was 30-day survival with secondary endpoints circulatory cause of death and cardiovascular deterioration composite; in addition, we examined the correlation with extended the cardiovascular sequential organ failure assessment (eCvSOFA) score. Results: Six hundred ninety patients were included in the analyses, of whom 203 (30.3%) developed cardiovascular deterioration within 24 h, and 273 (39.6%) died within 30 days. Copeptin measured at 24 h was found to be independently associated with 30-day survival, hazard ratio 1.17 [1.06-1.28], p = 0.001; circulatory cause of death, odds ratio 1.03 [1.01-1.04], p = 0.001; and cardiovascular deterioration composite, odds ratio of 1.05 [1.02-1.08], p < 0.001. Copeptin at 24 h was correlated with eCvSOFA score with rho 0.19 [0.12-0.27], p < 0.001. Conclusion: Copeptin is an independent marker of severity of the post cardiac arrest syndrome, partially related to circulatory failure. Trial registration: Clinical Trials, NCT01020916. Registered November 26, 2009.

KW - Arginine vasopressin

KW - AVP protein human

KW - Biomarkers

KW - Copeptin

KW - Critical illness

KW - Humans

KW - Out-of hospital cardiac arrest

KW - Prognosis

KW - Survivors

U2 - 10.1186/s13054-020-02904-8

DO - 10.1186/s13054-020-02904-8

M3 - Journal article

C2 - 32345356

AN - SCOPUS:85084107249

VL - 24

JO - Critical Care

JF - Critical Care

SN - 1364-8535

M1 - 185

ER -

ID: 242716470