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Increase in plasma glucagon, a factor in hyperglycemia, is related to neurological outcome in postcardiac-arrest patients.

AbstractAIM OF THE STUDY:
In postcardiac-arrest (PCA) patients, hyperglycemia is a factor reflecting an unfavorable outcome, and might be caused by the inflammation and stress of "sepsis-like" syndrome. In this study, plasma glucagon, a representative glycogenolytic and gluconeogenic hormone, was measured and assessed the correlation for neurological outcome in PCA patients.
METHODS:
This study was a retrospective, single-medical-center analysis, conducted in the intensive care unit of a university hospital. Twenty-four sequential PCA patients were included. Plasma samples were collected from the patients on days 1, 2, and 3 after the return of spontaneous circulation (ROSC). Glucagon was compared in patients with favorable and unfavorable neurological outcomes.
RESULTS:
At all time points, plasma glucagon was significantly higher in patients with an unfavorable outcome (P<0.05). Glucagon on day 1 had remarkable sensitivity (88.2%) and specificity (85.8%) as an indicator of outcome, and correlated with the collapse-ROSC interval, the start of cardiopulmonary resuscitation (CPR)-ROSC interval, and the epinephrine dose during CPR.
CONCLUSIONS:
Plasma glucagon reflects unfavorable outcomes in PCA patients, and might be related to ischemic and reperfusion stress.
AuthorsChiyomi Oshima, Tadashi Kaneko, Ryosuke Tsuruta, Yasutaka Oda, Takashi Miyauchi, Motoki Fujita, Yoshikatsu Kawamura, Shunji Kasaoka, Tsuyoshi Maekawa
JournalResuscitation (Resuscitation) Vol. 81 Issue 2 Pg. 187-92 (Feb 2010) ISSN: 1873-1570 [Electronic] Ireland
PMID20015588 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright 2009 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Glucagon
Topics
  • Adult
  • Aged
  • Aged, 80 and over
  • Female
  • Glucagon (blood)
  • Heart Arrest (blood, complications)
  • Humans
  • Hyperglycemia (blood)
  • Male
  • Middle Aged
  • Nervous System Diseases (etiology)
  • Prognosis
  • Retrospective Studies
  • Risk Factors

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