Prognostic Importance of Myocardial Injury in Critically Ill Dogs with Systemic Inflammation
Background In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (ICU) death independent of prognostic composite scoring. Hypothesis Presence of myocardial injury predicts short‐term death in cr...
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Published in | Journal of veterinary internal medicine Vol. 27; no. 4; pp. 895 - 903 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Blackwell Publishing Ltd
01.07.2013
John Wiley & Sons, Inc |
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Abstract | Background
In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (ICU) death independent of prognostic composite scoring.
Hypothesis
Presence of myocardial injury predicts short‐term death in critically ill dogs with systemic inflammation and provides additional prognostic information when combined with established canine prognostic composite scores.
Animals
Forty‐two dogs admitted to the ICU with evidence of systemic inflammation and no primary cardiac disease.
Methods
Prospective cohort study. Blood samples were obtained at ICU admission for the measurement of cTnI and cTnT, C‐reactive protein, and several cytokines. The acute patient physiologic and laboratory evaluation (APPLE) score and the survival prediction index were calculated within the first 24 hours of admission. Receiver operating characteristic (ROC) curves were used to examine the prognostic capacity of each biomarker and severity score. Multiple logistic regression analysis was performed to evaluate whether cardiac markers significantly contributed to severity scores.
Results
Twenty‐eight day case fatality rate was 26% (11/42 dogs). cTnI concentrations were (median [range]) 0.416 [0.004–141.5] ng/mL and cTnT concentrations were 13.5 [<13–3,744] ng/L. cTnI, cTnT, and the APPLE score were all significant prognosticators with areas under the ROC curves [95% CI] of 0.801 [0.649; 0.907], 0.790 [0.637; 0.900], and 0.776 [0.621; 0.889], respectively. cTnI significantly contributed to the APPLE score in providing additional prognostic specificity (P = .025).
Conclusions and Clinical Importance
Markers of myocardial injury predict short‐term death in dogs with systemic inflammation and cTnI significantly contributes to the APPLE score. |
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AbstractList | Background
In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (
ICU
) death independent of prognostic composite scoring.
Hypothesis
Presence of myocardial injury predicts short‐term death in critically ill dogs with systemic inflammation and provides additional prognostic information when combined with established canine prognostic composite scores.
Animals
Forty‐two dogs admitted to the
ICU
with evidence of systemic inflammation and no primary cardiac disease.
Methods
Prospective cohort study. Blood samples were obtained at
ICU
admission for the measurement of cTnI and cTnT, C‐reactive protein, and several cytokines. The acute patient physiologic and laboratory evaluation (
APPLE
) score and the survival prediction index were calculated within the first 24 hours of admission. Receiver operating characteristic (ROC) curves were used to examine the prognostic capacity of each biomarker and severity score. Multiple logistic regression analysis was performed to evaluate whether cardiac markers significantly contributed to severity scores.
Results
Twenty‐eight day case fatality rate was 26% (11/42 dogs). cTnI concentrations were (median [range]) 0.416 [0.004–141.5] ng/mL and cTnT concentrations were 13.5 [<13–3,744] ng/L. cTnI, cTnT, and the
APPLE
score were all significant prognosticators with areas under the
ROC
curves [95% CI] of 0.801 [0.649; 0.907], 0.790 [0.637; 0.900], and 0.776 [0.621; 0.889], respectively. cTnI significantly contributed to the
APPLE
score in providing additional prognostic specificity (
P
= .025).
Conclusions and Clinical Importance
Markers of myocardial injury predict short‐term death in dogs with systemic inflammation and cTnI significantly contributes to the
APPLE
score. BACKGROUNDIn noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (ICU) death independent of prognostic composite scoring.HYPOTHESISPresence of myocardial injury predicts short-term death in critically ill dogs with systemic inflammation and provides additional prognostic information when combined with established canine prognostic composite scores.ANIMALSForty-two dogs admitted to the ICU with evidence of systemic inflammation and no primary cardiac disease.METHODSProspective cohort study. Blood samples were obtained at ICU admission for the measurement of cTnI and cTnT, C-reactive protein, and several cytokines. The acute patient physiologic and laboratory evaluation (APPLE) score and the survival prediction index were calculated within the first 24 hours of admission. Receiver operating characteristic (ROC) curves were used to examine the prognostic capacity of each biomarker and severity score. Multiple logistic regression analysis was performed to evaluate whether cardiac markers significantly contributed to severity scores.RESULTSTwenty-eight day case fatality rate was 26% (11/42 dogs). cTnI concentrations were (median [range]) 0.416 [0.004-141.5] ng/mL and cTnT concentrations were 13.5 [<13-3,744] ng/L. cTnI, cTnT, and the APPLE score were all significant prognosticators with areas under the ROC curves [95% CI] of 0.801 [0.649; 0.907], 0.790 [0.637; 0.900], and 0.776 [0.621; 0.889], respectively. cTnI significantly contributed to the APPLE score in providing additional prognostic specificity (P = .025).CONCLUSIONS AND CLINICAL IMPORTANCEMarkers of myocardial injury predict short-term death in dogs with systemic inflammation and cTnI significantly contributes to the APPLE score. Background In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (ICU) death independent of prognostic composite scoring. Hypothesis Presence of myocardial injury predicts short‐term death in critically ill dogs with systemic inflammation and provides additional prognostic information when combined with established canine prognostic composite scores. Animals Forty‐two dogs admitted to the ICU with evidence of systemic inflammation and no primary cardiac disease. Methods Prospective cohort study. Blood samples were obtained at ICU admission for the measurement of cTnI and cTnT, C‐reactive protein, and several cytokines. The acute patient physiologic and laboratory evaluation (APPLE) score and the survival prediction index were calculated within the first 24 hours of admission. Receiver operating characteristic (ROC) curves were used to examine the prognostic capacity of each biomarker and severity score. Multiple logistic regression analysis was performed to evaluate whether cardiac markers significantly contributed to severity scores. Results Twenty‐eight day case fatality rate was 26% (11/42 dogs). cTnI concentrations were (median [range]) 0.416 [0.004–141.5] ng/mL and cTnT concentrations were 13.5 [<13–3,744] ng/L. cTnI, cTnT, and the APPLE score were all significant prognosticators with areas under the ROC curves [95% CI] of 0.801 [0.649; 0.907], 0.790 [0.637; 0.900], and 0.776 [0.621; 0.889], respectively. cTnI significantly contributed to the APPLE score in providing additional prognostic specificity (P = .025). Conclusions and Clinical Importance Markers of myocardial injury predict short‐term death in dogs with systemic inflammation and cTnI significantly contributes to the APPLE score. In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit (ICU) death independent of prognostic composite scoring. Presence of myocardial injury predicts short-term death in critically ill dogs with systemic inflammation and provides additional prognostic information when combined with established canine prognostic composite scores. Forty-two dogs admitted to the ICU with evidence of systemic inflammation and no primary cardiac disease. Prospective cohort study. Blood samples were obtained at ICU admission for the measurement of cTnI and cTnT, C-reactive protein, and several cytokines. The acute patient physiologic and laboratory evaluation (APPLE) score and the survival prediction index were calculated within the first 24 hours of admission. Receiver operating characteristic (ROC) curves were used to examine the prognostic capacity of each biomarker and severity score. Multiple logistic regression analysis was performed to evaluate whether cardiac markers significantly contributed to severity scores. Twenty-eight day case fatality rate was 26% (11/42 dogs). cTnI concentrations were (median [range]) 0.416 [0.004-141.5] ng/mL and cTnT concentrations were 13.5 [<13-3,744] ng/L. cTnI, cTnT, and the APPLE score were all significant prognosticators with areas under the ROC curves [95% CI] of 0.801 [0.649; 0.907], 0.790 [0.637; 0.900], and 0.776 [0.621; 0.889], respectively. cTnI significantly contributed to the APPLE score in providing additional prognostic specificity (P = .025). Markers of myocardial injury predict short-term death in dogs with systemic inflammation and cTnI significantly contributes to the APPLE score. |
Author | King, L.G. Thawley, V. Willesen, J.L. Langhorn, R. Trafny, D.J. Machen, M.C. Oyama, M.A. Kjelgaard-Hansen, M. Tarnow, I. |
Author_xml | – sequence: 1 givenname: R. surname: Langhorn fullname: Langhorn, R. email: rel@sund.ku.dk organization: Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, Frederksberg C, Denmark – sequence: 2 givenname: M.A. surname: Oyama fullname: Oyama, M.A. organization: Department of Clinical Studies - Philadelphia, School of Veterinary Medicine, University of Pennsylvania, PA, Philadelphia – sequence: 3 givenname: L.G. surname: King fullname: King, L.G. organization: Department of Clinical Studies - Philadelphia, School of Veterinary Medicine, University of Pennsylvania, PA, Philadelphia – sequence: 4 givenname: M.C. surname: Machen fullname: Machen, M.C. organization: Department of Clinical Studies - Philadelphia, School of Veterinary Medicine, University of Pennsylvania, PA, Philadelphia – sequence: 5 givenname: D.J. surname: Trafny fullname: Trafny, D.J. organization: Department of Clinical Studies - Philadelphia, School of Veterinary Medicine, University of Pennsylvania, PA, Philadelphia – sequence: 6 givenname: V. surname: Thawley fullname: Thawley, V. organization: Department of Clinical Studies - Philadelphia, School of Veterinary Medicine, University of Pennsylvania, PA, Philadelphia – sequence: 7 givenname: J.L. surname: Willesen fullname: Willesen, J.L. organization: Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, Frederksberg C, Denmark – sequence: 8 givenname: I. surname: Tarnow fullname: Tarnow, I. organization: Chr. Hansen A/S, Horsholm, Denmark – sequence: 9 givenname: M. surname: Kjelgaard-Hansen fullname: Kjelgaard-Hansen, M. organization: Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, Frederksberg C, Denmark |
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In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high... In noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive care unit... BackgroundIn noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive... BACKGROUNDIn noncardiac critical disease in humans, myocardial injury as detected by cardiac troponin I and T (cTnI and cTnT) has been linked to high intensive... |
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SubjectTerms | Animals Biomarker Biomarkers Cardiac troponin Cohort Studies Companion animals Critical Illness Cytokines Cytokines - blood Cytokines - genetics Cytokines - metabolism Dog Diseases - etiology Dog Diseases - pathology Dogs Emergency medical care Female Gene Expression Regulation Heart attacks Heart Diseases - etiology Heart Diseases - pathology Heart Diseases - veterinary Inflammation - veterinary Intensive care Male Medical prognosis Mortality Risk factors Sepsis Severity scores Survival analysis Troponin I - blood Tumor necrosis factor-TNF Veterinary medicine |
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Title | Prognostic Importance of Myocardial Injury in Critically Ill Dogs with Systemic Inflammation |
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