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Table 3 Multivariate analysis based on the therapeutic window

From: An optimal window of platelet reactivity by LTA assay for patients undergoing percutaneous coronary intervention

One-year outcome

IW*

OW

HR

95%CI

P

506

1203

n(%)

n(%)

Net adverse clinical events

85 (16.8)

278 (23.1)

1.44

1.12–1.85

0.004

Ischemic events

11 (2.2)

34 (2.8)

1.34

0.68–2.64

0.403

 Death

5 (1.0)

15 (1.2)

1.27

0.46–3.51

0.640

 MI

5 (1.0)

15 (1.2)

1.30

0.47–3.59

0.608

 ST

5 (1.0)

16 (1.3)

1.41

0.52–3.87

0.500

 TVR

1 (0.2)

10 (0.8)

4.49

0.57–35.17

0.150

Bleeding events

80 (15.8)

248 (20.6)

1.33

1.03–1.72

0.028

 Major + Minor

10 (2.0)

221 (1.8)

0.86

0.40–1.84

0.700

 Minimal

70 (13.8)

226 (18.8)

1.38

1.05–1.81

0.022

  1. Risk factors included in the analysis of net clinical outcome: Sex, age, BMI, Smoking, Hypertension, Diabetes, CABG history, PCI history, Hemoglobin, Platelet count, eGFR, APTT, INR; Risk factors included in the analysis of MACE: Sex, Age, BMI, Smoking, Hypertension, Diabetes, CABG history, PCI history; Risk factors included in the analysis of bleeding: Sex, Age, Hypertension, Diabetes, Hemoglobin, Platelet count, eGFR, INR, APTT
  2. * IW: 25.5% ≤ PLADP < 37.5%; OW: PLADP < 25.5% or ≥ 37.5%