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. 2016 Nov;107(5):403–410. doi: 10.5935/abc.20160149

Table 1.

Baseline characteristics

  Tirofiban (%) Placebo (%) Ω p
Patients 24 (41.4%) 34 (58.6%)  
Age 59.5 (±10.5) 58.3 (±11.9) (=0.70) Ţ
Male 19 (79.2%) 30 (88.2%) (=0.46) ƒ
Caucasian 22 (91.6%) 27 (79.4%) (=0.28) ƒ
BMI   ≥ 30 5 (20.8 %) 7 (20.6%) (=1.00) ƒ
Hypertension 16 (66.6%) 23 (67.6%) (=0.84) χ
Smokers 13 (54.2%) 16 (47.1%) (=0.79) χ
Dyslipidemia 10 (41.6%) 11 (32.4%) (=0.58) χ
CAD Family History 5 (20.8%) 12 (35.3%) (=0.26) ƒ
Diabetes 3 (12.5%) 7 (20.6%) (=0.49) ƒ
ACEI/ARB 10 (41.6%) 15 (44.1%) (=1.00) ƒ
Oral antidiabetic 3 (12.5%) 8 (23.5%) (=0.33) ƒ
Statin 6 (25%) 3 (8.8%) (=0.14) ƒ
ASA 2 (8.3%) 4 (11.7%) (=1.00) ƒ
Diuretics 1 (4.2%) 5 (14.7%) (=0.38) ƒ

BMI: body mass index; CAD: coronary artery disease; ACEI: angiotensin converting enzyme inhibitor; ARB: angiotensin receptor blocker; ASA: acetylsalicylic acid; p: p-value;

ƒ

p-value calculated by Fisher Exact Test;

Ţ

p-value calculated by “t” Student Test (95% IC 4.86-7.26);

Χ

p-value calculated by Chi-square Test;

tirofiban percentage group;

Ω

placebo percentage group