Table 3

Logistic regression analyses for predictors of 30-day major adverse cardiovascular event rate

VariableOdds ratio95% confidence intervalP-value
A. Univariate logistic regression analysis
Post-operative hs-cTnI quartiles<0.001
 2nd quartile0.760.42–1.40.38
 3rd quartile0.970.49–1.90.93
 4th quartile17.711.9–26.4<0.001
hs-cTnI >13 000 ng/L21.215.1–29.7<0.001
Age1.031.01–1.050.001
EuroSCORE II1.111.07–1.15<0.001
Statin use0.570.41–0.810.001
CPB use3.272.29–4.67<0.001
Time on CPB1.011.009–1.02<0.001
LVEF0.980.97–0.990.004
History of AF2.01.1–3.70.02
VariableOdds ratio95% confidence intervalP-value
A. Univariate logistic regression analysis
Post-operative hs-cTnI quartiles<0.001
 2nd quartile0.760.42–1.40.38
 3rd quartile0.970.49–1.90.93
 4th quartile17.711.9–26.4<0.001
hs-cTnI >13 000 ng/L21.215.1–29.7<0.001
Age1.031.01–1.050.001
EuroSCORE II1.111.07–1.15<0.001
Statin use0.570.41–0.810.001
CPB use3.272.29–4.67<0.001
Time on CPB1.011.009–1.02<0.001
LVEF0.980.97–0.990.004
History of AF2.01.1–3.70.02
B. Multivariate logistic regression analysis for CV outcomes (females and males)
hs-cTnI >13 000 ng/L21.915.5–30.8<0.001
EuroSCORE II1.101.05–1.140.001
Statin use0.650.46–0.930.02
B. Multivariate logistic regression analysis for CV outcomes (females and males)
hs-cTnI >13 000 ng/L21.915.5–30.8<0.001
EuroSCORE II1.101.05–1.140.001
Statin use0.650.46–0.930.02
C. Multivariate analysis for 30-day MACE applying gender-specific cut-off values
 Females (>9400 ng/L)
Males (>13 300 ng/L)
20.114.3–28.2<0.001
EuroSCORE II1.11.05–1.13<0.001
Statin use0.660.46–0.930.007
C. Multivariate analysis for 30-day MACE applying gender-specific cut-off values
 Females (>9400 ng/L)
Males (>13 300 ng/L)
20.114.3–28.2<0.001
EuroSCORE II1.11.05–1.13<0.001
Statin use0.660.46–0.930.007
D. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the study cohort
ThresholdEvents/totalAdjusted odds ratioa95% confidence intervalP-value
<10×URL1/1311.0Reference
≥10–<35× URL7/5721.40.17–11.70.74
≥35–<70×URL17/10531.90.25–14.30.54
≥70–<500×URL40/25411.80.24–13.00.58
≥500×URL94/38734.54.6–250.8<0.001
D. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the study cohort
ThresholdEvents/totalAdjusted odds ratioa95% confidence intervalP-value
<10×URL1/1311.0Reference
≥10–<35× URL7/5721.40.17–11.70.74
≥35–<70×URL17/10531.90.25–14.30.54
≥70–<500×URL40/25411.80.24–13.00.58
≥500×URL94/38734.54.6–250.8<0.001
E. Univariate logistic regression analysis of derived hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
VariableOdds ratio95% confidence intervalP-value
hs-cTnI > 13 000 ng/L17.56.0–51.2<0.001
Gender-specific cut-off values5.971.21–29.40.013
E. Univariate logistic regression analysis of derived hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
VariableOdds ratio95% confidence intervalP-value
hs-cTnI > 13 000 ng/L17.56.0–51.2<0.001
Gender-specific cut-off values5.971.21–29.40.013
F. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
ThresholdEvents/totalUnivariate OR (95% CI)Univariate P-valueAdjusteda OR (95% CI)P-value
<35×URLb3/184 (1.6)1.01.0 (reference)
≥35–<70× URL3/186 (1.6)1.26 (0.30–5.35)0.751.35 (0.31–5.82)0.69
≥70–<500× URL10/240 (4.2)2.17 (0.61–7.80)0.222.43 (0.64–9.12)0.19
≥500× URL6/18 (33)26.2 (6.73–102)<0.00137.9 (8.85–163)<0.001
F. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
ThresholdEvents/totalUnivariate OR (95% CI)Univariate P-valueAdjusteda OR (95% CI)P-value
<35×URLb3/184 (1.6)1.01.0 (reference)
≥35–<70× URL3/186 (1.6)1.26 (0.30–5.35)0.751.35 (0.31–5.82)0.69
≥70–<500× URL10/240 (4.2)2.17 (0.61–7.80)0.222.43 (0.64–9.12)0.19
≥500× URL6/18 (33)26.2 (6.73–102)<0.00137.9 (8.85–163)<0.001

hs-cTnI, high-sensitivity cardiac troponin I; MACE, major adverse cardiovascular events; CPB, cardiopulmonary bypass; LVEF, left ventricular ejection fraction; AF, atrial fibrillation; URL, upper reference limit.

a

Adjusted for EuroSCORE II and statin use.

b

Zero outcomes for the group of <10×URL (0/22), so group combined with 10–<35× URL as reference.

Table 3

Logistic regression analyses for predictors of 30-day major adverse cardiovascular event rate

VariableOdds ratio95% confidence intervalP-value
A. Univariate logistic regression analysis
Post-operative hs-cTnI quartiles<0.001
 2nd quartile0.760.42–1.40.38
 3rd quartile0.970.49–1.90.93
 4th quartile17.711.9–26.4<0.001
hs-cTnI >13 000 ng/L21.215.1–29.7<0.001
Age1.031.01–1.050.001
EuroSCORE II1.111.07–1.15<0.001
Statin use0.570.41–0.810.001
CPB use3.272.29–4.67<0.001
Time on CPB1.011.009–1.02<0.001
LVEF0.980.97–0.990.004
History of AF2.01.1–3.70.02
VariableOdds ratio95% confidence intervalP-value
A. Univariate logistic regression analysis
Post-operative hs-cTnI quartiles<0.001
 2nd quartile0.760.42–1.40.38
 3rd quartile0.970.49–1.90.93
 4th quartile17.711.9–26.4<0.001
hs-cTnI >13 000 ng/L21.215.1–29.7<0.001
Age1.031.01–1.050.001
EuroSCORE II1.111.07–1.15<0.001
Statin use0.570.41–0.810.001
CPB use3.272.29–4.67<0.001
Time on CPB1.011.009–1.02<0.001
LVEF0.980.97–0.990.004
History of AF2.01.1–3.70.02
B. Multivariate logistic regression analysis for CV outcomes (females and males)
hs-cTnI >13 000 ng/L21.915.5–30.8<0.001
EuroSCORE II1.101.05–1.140.001
Statin use0.650.46–0.930.02
B. Multivariate logistic regression analysis for CV outcomes (females and males)
hs-cTnI >13 000 ng/L21.915.5–30.8<0.001
EuroSCORE II1.101.05–1.140.001
Statin use0.650.46–0.930.02
C. Multivariate analysis for 30-day MACE applying gender-specific cut-off values
 Females (>9400 ng/L)
Males (>13 300 ng/L)
20.114.3–28.2<0.001
EuroSCORE II1.11.05–1.13<0.001
Statin use0.660.46–0.930.007
C. Multivariate analysis for 30-day MACE applying gender-specific cut-off values
 Females (>9400 ng/L)
Males (>13 300 ng/L)
20.114.3–28.2<0.001
EuroSCORE II1.11.05–1.13<0.001
Statin use0.660.46–0.930.007
D. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the study cohort
ThresholdEvents/totalAdjusted odds ratioa95% confidence intervalP-value
<10×URL1/1311.0Reference
≥10–<35× URL7/5721.40.17–11.70.74
≥35–<70×URL17/10531.90.25–14.30.54
≥70–<500×URL40/25411.80.24–13.00.58
≥500×URL94/38734.54.6–250.8<0.001
D. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the study cohort
ThresholdEvents/totalAdjusted odds ratioa95% confidence intervalP-value
<10×URL1/1311.0Reference
≥10–<35× URL7/5721.40.17–11.70.74
≥35–<70×URL17/10531.90.25–14.30.54
≥70–<500×URL40/25411.80.24–13.00.58
≥500×URL94/38734.54.6–250.8<0.001
E. Univariate logistic regression analysis of derived hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
VariableOdds ratio95% confidence intervalP-value
hs-cTnI > 13 000 ng/L17.56.0–51.2<0.001
Gender-specific cut-off values5.971.21–29.40.013
E. Univariate logistic regression analysis of derived hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
VariableOdds ratio95% confidence intervalP-value
hs-cTnI > 13 000 ng/L17.56.0–51.2<0.001
Gender-specific cut-off values5.971.21–29.40.013
F. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
ThresholdEvents/totalUnivariate OR (95% CI)Univariate P-valueAdjusteda OR (95% CI)P-value
<35×URLb3/184 (1.6)1.01.0 (reference)
≥35–<70× URL3/186 (1.6)1.26 (0.30–5.35)0.751.35 (0.31–5.82)0.69
≥70–<500× URL10/240 (4.2)2.17 (0.61–7.80)0.222.43 (0.64–9.12)0.19
≥500× URL6/18 (33)26.2 (6.73–102)<0.00137.9 (8.85–163)<0.001
F. Logistic regression analysis of different hs-cTnI thresholds to predict 30-day MACE in the external validation cohort from The Alfred Hospital
ThresholdEvents/totalUnivariate OR (95% CI)Univariate P-valueAdjusteda OR (95% CI)P-value
<35×URLb3/184 (1.6)1.01.0 (reference)
≥35–<70× URL3/186 (1.6)1.26 (0.30–5.35)0.751.35 (0.31–5.82)0.69
≥70–<500× URL10/240 (4.2)2.17 (0.61–7.80)0.222.43 (0.64–9.12)0.19
≥500× URL6/18 (33)26.2 (6.73–102)<0.00137.9 (8.85–163)<0.001

hs-cTnI, high-sensitivity cardiac troponin I; MACE, major adverse cardiovascular events; CPB, cardiopulmonary bypass; LVEF, left ventricular ejection fraction; AF, atrial fibrillation; URL, upper reference limit.

a

Adjusted for EuroSCORE II and statin use.

b

Zero outcomes for the group of <10×URL (0/22), so group combined with 10–<35× URL as reference.

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