Description

Patients receiving thrombolytic therapy following myocardial infarction may experience bleeding as a complication. The risk for moderate to severe bleeding can be estimated from the thrombolytic regimen and clinical features of the patient.


Patients studied: The 41,021 patients in the GUSTO-I trial.

 

Therapeutic regimens:

(1) streptokinase (SK) plus subcutaneous heparin

(2) streptokinase plus IV heparin

(3) tissue plasminogen activator (tPA)

(4) combination therapy of tPA plus streptokinase plus IV heparin

 

The most common sources of bleeding were procedure related, with lower rates if the patient did not undergo catheterization or other invasive procedure.

 

Risk factors associated with hemorrhage:

(1) therapeutic regimens: streptokinase + IV heparin; combination regimen

(2) older age

(3) lighter body weight

(4) female sex

(5) African ancestry

 

Prediction of Moderate or Severe Bleeding Event with Invasive Procedure

 

Parameter

Finding

Points

age in years

30

18

 

40

27

 

50

36

 

60

45

 

70

54

 

80

63

 

90

72

body weight in kilograms

40

87

 

60

74

 

80

61

 

100

52

 

120

43

 

140

35

diastolic blood pressure

60

30

 

80

25

 

100

21

 

120

17

 

140

13

 

160

8

 

180

4

 

200

0

pulse in beats per minute

0

0

 

40

4

 

80

8

 

120

12

 

160

16

 

200

19

 

240

23

miscellaneous risk factors

female sex

12

 

African ancestry

10

 

current smoker

8

 

hypertension

7

 

previous angina

3

 

previous myocardial infarction

2

Killip class and treatment interaction

Killip I and streptokinase + subcutaneous heparin

38

 

Killip I and TPA

32

 

Killip I and streptokinase + IV heparin

43

 

Killip I and combination therapy (SK+TPA)

39

 

Killip II and streptokinase + subcutaneous heparin

46

 

Killip II and TPA

39

 

Killip II and streptokinase + IV heparin

50

 

Killip II and combination therapy (SK+TPA)

42

 

Killip III and streptokinase + subcutaneous heparin

53

 

Killip III and TPA

48

 

Killip III and streptokinase + IV heparin

57

 

Killip III and combination therapy (SK+TPA)

54

 

Killip IV and streptokinase + subcutaneous heparin

60

 

Killip IV and TPA

55

 

Killip IV and streptokinase + IV heparin

65

 

Killip IV and combination therapy (SK+TPA)

60

 

 

total points =

= SUM(all predictive factors present)

 

Total Points

Risk of Moderate to Severe Bleeding

182

10%

210

20%

228

30%

243

40%

257

50%

271

60%

286

70%

 

if this data is plugged into JMP,

 

risk of bleeding in percent =

= (0.0022386 * ((points) ^2)) - (0.454114 * (points)) + 17.819422

 

Risk of Bleeding in Noncatheterized Patients

 

Parameter

Finding

Points

age in years

40

0

 

50

6

 

60

18

 

70

29

 

80

41

 

90

53

 

100

64

 

110

76

body weight in kilograms

40

37

 

60

20

 

80

4

 

100

0

 

120

0

pulse in beats per minute

40

91

 

60

91

 

80

96

 

100

100

 

120

98

 

140

91

 

160

77

 

180

57

 

200

32

miscellaneous risk factors

female sex

12

 

streptokinase + IV heparin treatment

13

ancestry + TPA use

non-African and no TPA

0

 

non-African and TPA

0

 

African and no TPA

15

 

African and TPA

43

Killip class and combination therapy

Killip I and no combo therapy

3

 

Killip I and combo therapy

15

 

Killip II and no combo therapy

0

 

Killip II and combo therapy

25

 

Killip III or IV and no combo therapy

7

 

Killip III or IV  and combo therapy

11

 

total points =

= SUM(all predictive factors present)

 

Total Points

Risk of Moderate to Severe Bleeding

142

5%

162

10%

175

15%

185

20%

192

25%

199

30%

206

35%

211

40%

217

45%

223

50%

 

if this data is plugged into JMP,

 

risk of bleeding in percent =

= (0.005285 * ((points) ^2)) - (1.367107 * (points)) + 92.553427


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