Brief Article
Copyright ©2013 Baishideng Publishing Group Co.
World J Cardiol. Jun 26, 2013; 5(6): 196-206
Published online Jun 26, 2013. doi: 10.4330/wjc.v5.i6.196
Table 1 Prediction of mid-term bleeding events in univariate analysis
Bleeding eventNo bleeding eventP value
Age (yr) 74.6 67.2< 0.001
Female gender41.40%34.50%0.292
NSTEMI67.20%57.50%0.095
Diabetes mellitus50.00%33.50%0.011
Previous arterial hypertension84.50%73.80%0.072
Smoking habits29.30%17.20%0.049
History of stroke/TIA17.50%8.10%0.015
Atrial fibrillation at admission16.70%13.50%0.516
Bleeding during hospitalization19.30%7.10%0.001
Maximum killip class 1.62 1.390.004
Hemoglobin at admission (g/dL)12.0 13.5< 0.001
GFR at admission (mL/min)55.0 71.6< 0.001
Blood urea nitrogen at admission (mg/dL)  13.5 8.7< 0.001
Submitted to revascularization procedures58.60%63.90%0.422
Table 2 Calculation of the BLEED-myocardial infarction score
VariablePoints assigned
Age (yr)
< 650
65-741
≥ 752
GFR at admission (MDRD formula, mL/min)
≥ 600
30-59.91
< 302
History of stroke or transient ischemic attack1
No0
Yes1
Heart failure during hospitalization2
No0
Yes1
History of hypertension
No0
Yes1
Antithrombotic therapy3
1 agent1
2 agents2
3 agents3
Hemoglobin at admission (g/dL)
≥ 120
10-11.91
< 102
Blood urea nitrogen at admission (mg/dL)
< 100
10-251
> 252
History of major hemorrhage or bleeding event during hospitalization4
No0
Yes1
Smoking habits (until hospitalization)
No0
Yes1
History of diabetes mellitus
No0
Yes1
Table 3 Description of derivation and validation samples
CharacteristicDerivation sample (n = 1050)Validation sample (n = 852)
Age (yr)67.9 ± 13.567.9 ± 13.6
Male gender686 (64.7)578 (68.0)
Type of myocardial infarction
STEMI42.1%38.8%
NSTEMI57.9%61.2%
Diabetes mellitus380 (35.9)266 (31.2)
Previous hypertension796 (75.2)631 (74.2)
Hyperlipidemia59629 (56.3)475 (59.6)
Smoking habits287 (27.1)281 (33.1)
Previously known coronary disease283 (26.7)243 (28.6)
History of stroke/TIA94 (9.0)77 (9.1)
Atrial fibrillation at admission144 (13.7)99 (12.4)
Admission killip class  1.40 ± 0.61.36 ± 0.7
Maximum killip class 1.56 ± 0.81.46 ± 0.8
Average number of vessels with significant lesions1.60 ± 0.97 1.54 ± 0.99
GFR at admission68.6 ± 38.472.6 ± 32.0
BUN at admission (mmol/L)9.58 ± 6.818.85 ± 6.20
Hemoglobin at admission (mg/dL)  13.3 ± 2.113.8 ± 6.14
NT-proBNP at admission (ng/L)  4202 ± 134006393 ± 15950
Submitted to revascularization procedures645 (61.4)663 (77.8)
Clinically significant bleeding during hospitalization87 (8.3)55 (6.5)
Average GRACE score for intrahospital mortality153.9 (P25 124; P50 151; P75 179)145.6 (P25 114; P50 143; P75 173)
Average GRACE score for 6-mo mortality128.0 (P25 102; P50 125; P75 149)121.0 (P25 94; P50 118; P75 145)
Moderate-severe left ventricular systolic dysfunction19.50%23.00%
Discharged on dual anti-platelet therapy818 (89.2)723 (90.6)
Discharged on anticoagulant treatment36 (3.9)37 (4.6)
Intrahospital mortality8.60%6.10%
Post-discharge mortality (mo)165 (16.5) (Follow-up: 19.9 ± 6.7)88 (11.0) (Follow-up: 13.4 ± 8.1)
Bleeding events during follow-up (mo)62 (6.8) (Follow-up: 19.9 ± 6.7)60 (7.5) (Follow-up: 13.4 ± 8.1)
Table 4 Hemorrhagic and combined event rates according to the BLEED-myocardial infarction score risk-group stratification
CategoryLow riskIntermediate riskHigh riskGamma for trendP value
Clinically significant bleeding events
Derivation cohort (follow-up: 19.9 ± 6.7 mo)Incidence0.80%3.40%14.40%0.70 ± 0.08< 0.001
Validation cohort (follow-up: 13.4 ± 8.1 mo)Incidence1.30%5.00%14.10%0.61 ± 0.08< 0.001
Composite endpoint (bleeding + all-cause mortality)
Derivation cohort (follow-up: 19.9 ± 6.7 mo)Incidence3.10%11.40%45.70%0.76 ± 0.04< 0.001
Validation cohort (follow-up: 13.4 ± 8.1 mo)Incidence1.30%9.30%31.30%0.73 ± 0.05< 0.001
Table 5 Primary and secondary endpoint event rates according to the BLEED-myocardial infarction score
SampleBLEED-MI scoreBleeding event rateComposite endpoint event rate
Derivation sample0-10.80%3.10%
2-32.70%10.00%
4-57.90%19.10%
6-713.60%50.40%
8-920.00%65.90%
10-1125.00%71.40%
Gamma for trend0.60 ± 0.070.70 ± 0.04
P value < 0.001 < 0.001
Validation sample0-10.00%0.00%
2-31.20%1.80%
4-55.40%8.80%
6-76.50%16.10%
8-913.90%25.70%
10-1117.80%39.70%
12-1323.10%48.00%
14-15-60.00%
Gamma for trend0.52 ± 0.070.63 ± 0.05
P value < 0.001 < 0.001
Table 6 Number of patients reaching the primary endpoint in the validation sample at different time points
Time (mo)Low riskIntermediate riskHigh risk
0-31421
4-6053
7-9146
10-12034
13-15003
16-18000
19-21001
22-24001