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 inJournal of veterinary internal medicine Vol. 27; no. 4; pp. 895 - 903
Main Authors Langhorn, R., Oyama, M.A., King, L.G., Machen, M.C., Trafny, D.J., Thawley, V., Willesen, J.L., Tarnow, I., Kjelgaard-Hansen, M.
Format Journal Article
LanguageEnglish
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.
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.
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Keywords Companion animals
Biomarker
Cardiac troponin
Severity scores
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2002; 16
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2004; 22
2007; 167
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2010; 38
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2008; 36
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1999; 82
1995; 273
2001; 62
2003; 32
2005; 23
2004; 32
2002; 28
2006; 42
2003; 348
2010; 25
2010; 24
2004; 18
2000; 102
1989; 169
1984; 16
2002; 221
2005; 31
1997; 16
2003; 29
2002; 90
2013
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2006; 228
2010; 5
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Snippet 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...
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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