Table 3.
Variable | Anticoagulation initiation in ED or within 30 days | |||
---|---|---|---|---|
| ||||
Univariate models | Multivariable model | |||
|
|
|||
Odds ratio* | 95% CI | Adjusted odds ratio* | 95% CI | |
Age, per year | 0.93 | 0.89, 0.96 | 0.89 | 0.82, 0.96 |
Gender | ||||
Female | Reference | -- | Reference | -- |
Male | 0.65 | 0.41, 1.04 | 1.58 | 0.91, 2.74 |
Race | ||||
White | Reference | -- | Reference | -- |
Non-white | 1.27 | 0.69, 2.34 | 0.85 | 0.42, 1.74 |
Clinical characteristics at index ED visit | ||||
Rhythm diagnosis | ||||
AF, any | Reference | -- | Reference | -- |
AFL, isolated | 3.18 | 1.38, 7.33 | 2.20 | 0.84, 5.77 |
AF/FL history | ||||
Prior AF/FL diagnosis | Reference | -- | Reference | -- |
New AF/FL diagnosis | 2.93 | 1.81, 4.73 | 3.10 | 1.72, 5.58 |
Onset of symptoms | ||||
Recent-onset (<48 hrs) | Reference | -- | Reference | -- |
Not recent (≥48 hrs) | 2.06 | 1.15, 3.69 | 2.31 | 1.03, 5.21 |
Unclear | 1.54 | 0.91, 2.62 | 1.10 | 0.54, 2.23 |
AF/AFL categorization | ||||
Chronic/unremitting | Reference | -- | Reference | -- |
Intermittent/recurrent | 2.61 | 1.19, 5.74 | 4.56 | 1.65, 12.60 |
Unclear | 3.44 | 1.42, 8.38 | 3.43 | 1.14, 10.34 |
ED cardiologist consultation | ||||
No | Reference | -- | Reference | -- |
Yes | 2.47 | 1.54, 3.96 | 1.89 | 1.10,3.23 |
ED discharge rhythm | ||||
Sinus rhythm | Reference | -- | Reference | -- |
AF/FL | 1.67 | 1.05, 2.64 | 2.65 | 1.35, 5.21 |
ATRIA stroke risk | ||||
Score, per point increase above 6 | 0.90 | 0.84, 0.96 | 1.10 | 0.96, 1.26 |
HAS-BLED hemorrhage risk score | ||||
Score, per point increase | 0.86 | 0.73, 1.02 | ||
Categorical | ||||
Low risk (<3) | Reference | -- | ||
High risk (≥3) | 0.59 | 0.34, 1.01 |
ED, emergency department; AF, atrial fibrillation; AFL, atrial flutter; AF/FL, atrial fibrillation or flutter; ATRIA, Anticoagulation and Risk Factors in Atrial Fibrillation; HAS-BLED, Hypertension, Abnormal renal/liver function, Stroke, Bleeding history or predisposition, Labile international normalized ratio, Elderly (>65 years), Drugs or alcohol; CI, confidence interval.
Reference group includes individuals with no anticoagulation initiation by 30 days after the index ED visit.