Table 1 Ischemic cardiovascular and bleeding event risk by CYP2C19 status and P2Y12 inhibitor maintenance therapy in patients initiated on clopidogrel during the index PCI (n = 601)

From: Frequency and clinical outcomes of CYP2C19 genotype-guided escalation and de-escalation of antiplatelet therapy in a real-world clinical setting

Clinical outcome by

Event

Event rate

Log-rank P valued

Log-rank P valued

Adjusted HR

P value

CYP2C19 phenotype–selected P2Y12 inhibitor

No. (%)a

(Per 100 patient-years)c

(Unadjusted)

(Adjusted)

(95% CI)

MACCE or clinically significant bleeding events

  Continue clopidogrel (IM/PM)

24 (27.6%)

51.8

  

2.89 (1.44–6.13)

0.003

  Continue clopidogrel (UM/RM/NM)

74 (17.5%)

26.6

  

1.37 (0.76–2.70)

0.304

  Escalation to prasugrel/ticagrelor (IM/PM)

12 (13.3%)

19.4

P = 0.007

P = 0.003

Reference

 

MACCE

  Continue clopidogrel (IM/PM)b

23 (26.4%)

49.5

  

5.72 (2.41–15.8)

<0.001

  Continue clopidogrel (UM/RM/NM)

59 (13.9%)

20.9

  

2.27 (1.04–5.96)

0.038

  Escalation to prasugrel/ticagrelor (IM/PM)

6 (6.7%)

9.5

P < 0.001

P < 0.001

Reference

 

Clinically significant bleeding events

  Continue clopidogrel (IM/PM)b

2 (2.3%)

4.3

  

0.46 (0.07–2.07)

0.329

  Continue clopidogrel (UM/RM/NM)

20 (4.7%)

7.2

  

0.64 (0.26–1.81)

0.378

  Escalation to prasugrel/ticagrelor (IM/PM)

6 (6.7%)

9.7

P = 0.587

P = 0.559

Reference

 
  1. CI confidence interval, HR hazard ratio, IM intermediate metabolizer, MACCE major adverse cardiovascular or cerebrovascular event, NM normal metabolizer, PCI percutaneous coronary intervention, PM poor metabolizer, RM rapid metabolizer, UM ultrarapid metabolizer.
  2. aData are presented as the number (%) of patients in each group who experienced the event over 12 months of follow-up after the index PCI.
  3. bDue to the rare use of clopidogrel in CYP2C19 PMs, 22 of the 23 MACCE events and both bleeding events in this group occurred in IMs.
  4. cThe event rate was calculated as the number of events per 100 patient-years of follow-up.
  5. dUnadjusted and covariate-adjusted log-rank P values across the three CYP2C19 phenotype-antiplatelet strata. The small subset of 11 patients with an UM/RM/NM phenotype who were escalated to alternative (prasugrel or ticagrelor) therapy were not included in the analysis.