The Cardiovascular
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Canadian Syncope Risk Score

Predicts 30-day serious adverse events after emergency department syncope.

Canadian Syncope Risk Score
Predisposition to vasovagal symptoms (reassuring)
History of clinically significant heart disease
Any systolic BP reading <90 or >180 mmHg in the ED
Elevated troponin (above normal for local assay)
Abnormal QRS axis (<-30 or >100 degrees)
QRS duration >130 ms
Corrected QT interval >480 ms
ED diagnosis of vasovagal syncope
ED diagnosis of cardiac syncope
Result0 points

Approximate 30-day risk of a serious adverse event is very low (<=0.9%).

30-day serious adverse event risk
very low (<=0.9%)

When to use

  • Risk-stratifying adult emergency department patients with syncope for 30-day serious adverse events, including arrhythmia and death.

Formula

Sum of: predisposition to vasovagal symptoms (-1), heart disease history (+1), SBP <90 or >180 mmHg (+2), elevated troponin (+2), abnormal QRS axis (+1), QRS duration >130ms (+1), QTc >480ms (+2), ED diagnosis of vasovagal syncope (-2), ED diagnosis of cardiac syncope (+2). Range -3 to +11.

References

  1. Thiruganasambandamoorthy V, Kwong K, Wells GA, et al. Development of the Canadian Syncope Risk Score to predict serious adverse events after emergency department assessment of syncope. CMAJ. 2016;188(12):E289-98.