Description

Fanola et al reported the TIMI-AF score for determining the risk of adverse events in a patient with atrial fbrillation. This can help decide what therapy may be best for the patient. The authors are from Brigham and Women's Hospital and Daiichi Sankyo Pharma.


Patient selection: atrial fibrillation with CHADS2 or CHA2DS2-VASc >= 2

 

Exclusions: creatinine clearance < 30 mL per minute, reversible cause of AF, dual antiplatelet therapy, acute coronary syndrome within past 30 days, acute stroke within 30 days, mitral stenosis, or mechanical valves

 

Outcome: disabling stroke, life-threatening bleeding, all-cause mortality

 

Parameters:

(1) age in years

(2) left ventricular function with ejection fraction in percent

(3) hemoglobin in g/dL

(4) race

(5) baseline atrial fibrillation or atrial flutter (associated with sustained or permanent arrhythmia or longer history)

(6) prior ischemic stroke

(7) prior myocardial infarction

(8) serum creatinine in µmol/L

(9) gender

(10) diabetes mellitus

(11) history of carotid artery disease

 

Parameter

Finding

Points

age in years

< 66 years

0

 

66 to 74 years

2

 

>= 75 years

3

LVEF in percent

unknown

1

 

>= 50%

0

 

30 to 49%

2

 

< 30%

3

hemoglobin

>= 13 g/dL

0

 

< 13 g/dL

2

race

white

0

 

other

2

baseline atrial fibrillation or flutter

no

0

 

yes

1

prior ischemic stroke

no

0

 

yes

1

prior MI

no

0

 

yes

1

serum creatinine

< 110 µmol/L

0

 

>= 110 µmol/L

1

gender

female

0

 

male

1

diabetes mellitus

no

0

 

yes

1

history of carotid artery disease

no

0

 

yes

1

 

total score =

= SUM(points for all 11 parameters)

 

Interpretation:

• minimum score: 0

• maximum score: 17

• The higher the score the greater the risk for an adverse event.

• A non-vitamin K antagonist oral anticoagulant (such as edoxaban) is preferred for a vitamin K antagonist naive patient (<= 60 days of therapy prior to enrollment) with intermediate or high risk.

• A vitamin K antagonist should be used in a patient who is vitamin K experienced or a patient who is vitamin K antagonist naive and low risk.

 

Total Score

Risk

Event Rate per Year

0 to 6

low

3.5%

7 to 9

intermediate

10%

10 to 17

high

21%

 


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