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Table 5 Effect of various factors like diabetes, ACS, EF, reason for stopping ticagrelor, time of stopping ticagrelor, and nature of new drug added instead of ticagrelor on our primary outcome

From: Effect of discontinuation of ticagrelor and switching-over to other P2Y12 agents in patients with acute coronary syndrome: a single-center real-world experience from India

 

Primary outcome happened, N-17

Primary outcome did not happen, N-292

p value

n

n%

n

n%

Diabetes

7

41.2

130

44.5

0.79

Acute coronary syndrome group

USA

7

41.2

118

40.4

0.99

NSTEMI

2

11.8

35

12.0

STEMI

8

47.1

139

47.6

Ejection fraction

 

EF ≤ 30%

0

0.0

8

2.7

0.8

EF ≥ 55%

11

64.75

170

58.2

EF-30–45%

3

17.6

55

18.8

EF-45–55%

3

17.6

59

20.2

Culprit vessel

  

Left anterior descending artery (LAD)

7

41.2

160

54.8

0.32

Circumflex (LCX)

2

11.85

49

16.8

Right coronary artery (RCA)

8

47.1

78

26.7

Left main or triple vessel disease

0

0.0

5

1.7

Reason for stopping

 

0.70

Ticagrelor - not stooped

6

35.6

67

22.9

Ticagrelor stopped - physician-based decision

1

5.9

1

14.7

Ticagrelor stopped - cost

10

58.8

178

61.0

Ticagrelor stopped - non-availability of drug

0

0.0

3

1.0

Ticagrelor stopped - side effects

0

0.0

1

0.3

Nature of drug that was used during switch-over from ticagrelor

     

Ticagrelor continued

6

35.3

67

22.9

0.45

Clopidogrel

11

64.7

219

75.0

Prasugrel

0

0.0

6

2.1

Timing of ticagrelor stopped and event

     

Not stopped

6

35.3

66

22.6

 

Stopped < 1 month

2

11.8

13

4.5

0.44

Stopped 1–3 months

1

5.9

31

10.6

 

Stopped 3–6 months

2

11.8

29

9.9

 

Stopped 6–12 months

3

17.6

49

16.8

 

Stopped > 12 months

3

17.6

104

35.6