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
Published online Jun 26, 2013. doi: 10.4330/wjc.v5.i6.196
Table 1 Prediction of mid-term bleeding events in univariate analysis
Bleeding event | No bleeding event | P value | |
Age (yr) | 74.6 | 67.2 | < 0.001 |
Female gender | 41.40% | 34.50% | 0.292 |
NSTEMI | 67.20% | 57.50% | 0.095 |
Diabetes mellitus | 50.00% | 33.50% | 0.011 |
Previous arterial hypertension | 84.50% | 73.80% | 0.072 |
Smoking habits | 29.30% | 17.20% | 0.049 |
History of stroke/TIA | 17.50% | 8.10% | 0.015 |
Atrial fibrillation at admission | 16.70% | 13.50% | 0.516 |
Bleeding during hospitalization | 19.30% | 7.10% | 0.001 |
Maximum killip class | 1.62 | 1.39 | 0.004 |
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 procedures | 58.60% | 63.90% | 0.422 |
Table 2 Calculation of the BLEED-myocardial infarction score
Variable | Points assigned |
Age (yr) | |
< 65 | 0 |
65-74 | 1 |
≥ 75 | 2 |
GFR at admission (MDRD formula, mL/min) | |
≥ 60 | 0 |
30-59.9 | 1 |
< 30 | 2 |
History of stroke or transient ischemic attack1 | |
No | 0 |
Yes | 1 |
Heart failure during hospitalization2 | |
No | 0 |
Yes | 1 |
History of hypertension | |
No | 0 |
Yes | 1 |
Antithrombotic therapy3 | |
1 agent | 1 |
2 agents | 2 |
3 agents | 3 |
Hemoglobin at admission (g/dL) | |
≥ 12 | 0 |
10-11.9 | 1 |
< 10 | 2 |
Blood urea nitrogen at admission (mg/dL) | |
< 10 | 0 |
10-25 | 1 |
> 25 | 2 |
History of major hemorrhage or bleeding event during hospitalization4 | |
No | 0 |
Yes | 1 |
Smoking habits (until hospitalization) | |
No | 0 |
Yes | 1 |
History of diabetes mellitus | |
No | 0 |
Yes | 1 |
Table 3 Description of derivation and validation samples
Characteristic | Derivation sample (n = 1050) | Validation sample (n = 852) |
Age (yr) | 67.9 ± 13.5 | 67.9 ± 13.6 |
Male gender | 686 (64.7) | 578 (68.0) |
Type of myocardial infarction | ||
STEMI | 42.1% | 38.8% |
NSTEMI | 57.9% | 61.2% |
Diabetes mellitus | 380 (35.9) | 266 (31.2) |
Previous hypertension | 796 (75.2) | 631 (74.2) |
Hyperlipidemia | 59629 (56.3) | 475 (59.6) |
Smoking habits | 287 (27.1) | 281 (33.1) |
Previously known coronary disease | 283 (26.7) | 243 (28.6) |
History of stroke/TIA | 94 (9.0) | 77 (9.1) |
Atrial fibrillation at admission | 144 (13.7) | 99 (12.4) |
Admission killip class | 1.40 ± 0.6 | 1.36 ± 0.7 |
Maximum killip class | 1.56 ± 0.8 | 1.46 ± 0.8 |
Average number of vessels with significant lesions | 1.60 ± 0.97 | 1.54 ± 0.99 |
GFR at admission | 68.6 ± 38.4 | 72.6 ± 32.0 |
BUN at admission (mmol/L) | 9.58 ± 6.81 | 8.85 ± 6.20 |
Hemoglobin at admission (mg/dL) | 13.3 ± 2.1 | 13.8 ± 6.14 |
NT-proBNP at admission (ng/L) | 4202 ± 13400 | 6393 ± 15950 |
Submitted to revascularization procedures | 645 (61.4) | 663 (77.8) |
Clinically significant bleeding during hospitalization | 87 (8.3) | 55 (6.5) |
Average GRACE score for intrahospital mortality | 153.9 (P25 124; P50 151; P75 179) | 145.6 (P25 114; P50 143; P75 173) |
Average GRACE score for 6-mo mortality | 128.0 (P25 102; P50 125; P75 149) | 121.0 (P25 94; P50 118; P75 145) |
Moderate-severe left ventricular systolic dysfunction | 19.50% | 23.00% |
Discharged on dual anti-platelet therapy | 818 (89.2) | 723 (90.6) |
Discharged on anticoagulant treatment | 36 (3.9) | 37 (4.6) |
Intrahospital mortality | 8.60% | 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
Category | Low risk | Intermediate risk | High risk | Gamma for trend | P value | |
Clinically significant bleeding events | ||||||
Derivation cohort (follow-up: 19.9 ± 6.7 mo) | Incidence | 0.80% | 3.40% | 14.40% | 0.70 ± 0.08 | < 0.001 |
Validation cohort (follow-up: 13.4 ± 8.1 mo) | Incidence | 1.30% | 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) | Incidence | 3.10% | 11.40% | 45.70% | 0.76 ± 0.04 | < 0.001 |
Validation cohort (follow-up: 13.4 ± 8.1 mo) | Incidence | 1.30% | 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
Sample | BLEED-MI score | Bleeding event rate | Composite endpoint event rate |
Derivation sample | 0-1 | 0.80% | 3.10% |
2-3 | 2.70% | 10.00% | |
4-5 | 7.90% | 19.10% | |
6-7 | 13.60% | 50.40% | |
8-9 | 20.00% | 65.90% | |
10-11 | 25.00% | 71.40% | |
Gamma for trend | 0.60 ± 0.07 | 0.70 ± 0.04 | |
P value | < 0.001 | < 0.001 | |
Validation sample | 0-1 | 0.00% | 0.00% |
2-3 | 1.20% | 1.80% | |
4-5 | 5.40% | 8.80% | |
6-7 | 6.50% | 16.10% | |
8-9 | 13.90% | 25.70% | |
10-11 | 17.80% | 39.70% | |
12-13 | 23.10% | 48.00% | |
14-15 | - | 60.00% | |
Gamma for trend | 0.52 ± 0.07 | 0.63 ± 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 risk | Intermediate risk | High risk |
0-3 | 1 | 4 | 21 |
4-6 | 0 | 5 | 3 |
7-9 | 1 | 4 | 6 |
10-12 | 0 | 3 | 4 |
13-15 | 0 | 0 | 3 |
16-18 | 0 | 0 | 0 |
19-21 | 0 | 0 | 1 |
22-24 | 0 | 0 | 1 |
- Citation: Barra S, Providência R, Caetano F, Almeida I, Paiva L, Dinis P, Leitão Marques A. BLEED-Myocardial Infarction Score: Predicting mid-term post-discharge bleeding events. World J Cardiol 2013; 5(6): 196-206
- URL: https://www.wjgnet.com/1949-8462/full/v5/i6/196.htm
- DOI: https://dx.doi.org/10.4330/wjc.v5.i6.196