Abstract
BACKGROUND:
Patients with atrial fibrillation frequently seek emergency care. Rates of guideline-concordant oral anticoagulant therapy for stroke prevention are suboptimal in the community. We assessed the association between prescribing of oral anticoagulants in the emergency department (relative to referral to a longitudinal care provider for treatment initiation) and long-term use of oral anticoagulants.
METHODS:
This retrospective cohort study performed at 15 hospitals in Ontario, Canada, involved patients aged 65 years or older who visited the emergency department between 2009 and 2014, who had a primary diagnosis of atrial fibrillation, were discharged home, and were eligible for and willing to take stroke-prevention therapy. We used inverse probability-of-treatment weighting based on the propensity score to compare patients who were and were not given a prescription for an oral anticoagulant. The primary outcome was a prescription fill for an oral anticoagulant 6 months later. Secondary outcomes included a prescription fill at 1 year, all-cause mortality, and strokes or bleeding events leading to hospital admission.
RESULTS:
Of 2132 eligible patients, 402 (18.9%) were given a prescription for an oral anticoagulant in the emergency department. After weighting, 67.8% of these patients had filled a prescription for an oral anticoagulant at 6 months versus 37.2% of those who did not receive a prescription in the emergency department (absolute risk increase [ARI] 30.6%, number needed to treat [NNT] 3). At 1 year, the ARI was 23.2% and the NNT was 4. Rates of death, stroke and bleeding events did not differ significantly.
INTERPRETATION:
In patients with atrial fibrillation who were eligible for stroke prevention, prescribing an oral anticoagulant in the emergency department was associated with substantially higher long-term use of oral anticoagulants compared with deferring to the longitudinal care provider to initiate this therapy. Physicians working in the emergency department should consider initiating oral anticoagulation in eligible patients who are being discharged to home.
More than 33 million people have atrial fibrillation worldwide, 1 and the prevalence is expected to double in the coming decades.2,3 Atrial fibrillation is associated with a fivefold increase in the risk of stroke,4,5 for which the 1-year mortality rate is 50%.6 Stroke prevention with oral anticoagulation therapy decreases the risk by about 60%,7,8 and numerous guidelines endorse this type of therapy for high-risk patients with atrial fibrillation.9–11 Nonetheless, many studies have documented suboptimal use of oral anticoagulants.12–14
Patients with atrial fibrillation often present to the emergency department because of symptoms such as palpitations, shortness of breath and chest pain.15,16 In Ontario, there are about 20 000 emergency department visits per year for atrial fibrillation, and most of these patients (63%) are sent home after emergency care (v. 31% in the United States).17 Therefore, the emergency department may be an important setting for improvement of suboptimal prescribing rates for oral anticoagulants.18–20 The advent of direct oral anticoagulants, 21–24 which do not require bridging or monitoring of the international normalized ratio, may improve the willingness of emergency physicians to initiate a long-term medication that may cause bleeding. However, current usual care is referral to the longitudinal care provider (e.g., primary care provider or cardiologist) to initiate such medications, as that provider will have the patient’s complete medical history, can follow the patient for potential adverse effects and dose adjustments, and has more time for shared decision-making, possibly over more than 1 visit.25,26 In addition, there are limited data on whether initiation of oral anticoagulants in the emergency department results in greater long-term use.27
We assessed the long-term use of oral anticoagulants after provision of a prescription in the emergency department, compared with deferral to the longitudinal health care provider for initiation of therapy.
Methods
Study design
This retrospective cohort study was performed at 15 emergency departments (listed in Appendix 1, Table A1, available at www.cmaj.ca/lookup/suppl/doi:10.1503/cmaj.190747/-/DC1) in Ontario, Canada, with linkage to province-wide health data sets.
Data sources and data collection
We identified potential study patients from the National Ambulatory Care Reporting System of the Canadian Institute for Health Information, which collects data on all emergency department visits in Ontario.28 Because the data set does not include information about provision of prescriptions, a trained physician abstracted the identified charts at each hospital. This allowed confirmation that, for all patients, atrial fibrillation (code I480) had been diagnosed in the emergency department.18 The abstractor collected chart data using standardized definitions. Chart data were linked at ICES (via unique, encoded identifiers) to numerous databases containing the following Ontario-wide data: hospital admissions, mortality (including out-of-hospital deaths), instances of filling a prescription for an anticoagulant, billings by any physician and physician specialty (Appendix 1, Table A2).29–32
Study participants
Patients eligible for inclusion were those aged 65 years or older who were seen between Apr. 1, 2009, and Mar. 31, 2014, and were discharged home from the emergency department with a primary diagnosis of atrial fibrillation/flutter (i.e., the first diagnosis written on the chart by the managing physician). Thus, we included both incident and prevalent cases of atrial fibrillation. Because age 65 years or older was a qualifying criterion for use of oral anticoagulants in the 2014 Canadian guidelines for atrial fibrillation (based on the CHADS-65 algorithm),33 all of these patients qualified for this therapy. We excluded patients who were already taking these drugs (i.e., prescription fill within the previous 90 d) and those whose international normalized ratio was greater than 1.2. A physician’s reluctance to prescribe for patients perceived to be at higher risk for bleeding or a patient’s resistance to taking an anticoagulant might affect both emergency department prescribing and the primary outcome measure (subsequent prescribing). Therefore, we excluded patients with relative contraindications to oral anticoagulants or the potential for clinician perception of a high risk of bleeding, specifically those from a nursing home and those with a history of major cancer, hemorrhagic stroke, major gastrointestinal bleeding or HAS-BLED score of 4 or higher,34 as well as cases in which the managing physician documented patient refusal.
The exposure group consisted of patients who received a prescription for an oral anticoagulant in the emergency department (“emergency department prescription group”), and the nonexposed group consisted of those who did not receive a prescription (“no emergency department prescription group”).
Outcome measures
The primary outcome measure was a prescription fill for an oral anticoagulant at 6 months after the emergency visit. Prescriptions in Ontario can have a maximum duration of 100 days to be eligible for payment by the Ontario Drug Benefit Program, so we defined our outcome measure as a prescription fill between 130 and 230 days after discharge. Medications included in the analysis were warfarin, apixaban, dabigatran and rivaroxaban; at the time of the study, edoxaban had not yet been approved in Canada. Secondary outcomes included a prescription fill for an oral anticoagulant at 1 year (315–415 d after discharge), all-cause mortality, and stroke (hemorrhagic or ischemic) or bleeding event leading to hospital admission. Strokes and bleeding events (gastrointestinal, genitourinary or respiratory bleeding; intracranial hemorrhage) were determined using the Discharge Abstract Database (codes listed in Appendix 1, Table A3).35 Adherence to anticoagulant therapy was defined as 80% or higher, and discontinuation was defined as a gap in medication fill of 30 days or more.
Statistical analysis
Univariable comparisons between exposure groups were performed using χ2 and t tests, as appropriate. The proportion of days covered by oral anticoagulant therapy was calculated for each group at 30, 90, 180 and 365 days. All patients were eligible for stroke prevention with an oral anticoagulant; however, we adjusted for differences between groups using inverse probability-of-treatment weighting based on the propensity score. This increases the likelihood that we were comparing 2 groups with a similar distribution of baseline covariables that might influence prescribing of oral anticoagulants both in the emergency department and in follow-up (i.e., covariables related to perceived bleeding risk). Using patients who were alive at the time of outcome assessment (to avoid immortal time bias36), we estimated a propensity score by regressing prescription provision on 29 variables selected a priori.15,27,37 This method weights participants by the inverse of the probability of actual treatment received.38 Balance between groups was assessed using weighted standardized differences. 39 We calculated absolute risk differences between groups, as well as numbers needed to treat (NNTs).
We performed the following sensitivity analyses. We used logistic regression in the unweighted sample for prescription fill outcomes. We repeated the inverse-weighting analysis in a cohort without exclusions based on HAS-BLED score,34 because that score was not meant to prevent physicians from initiating oral anticoagulants, but rather to address risk factors for bleeding (which an emergency physician is in no position to do on a continuing basis).10,11 We performed the analysis for only those patients with electrocardiographic (ECG) or rhythmstrip proof of atrial fibrillation in the chart.
All analyses were performed with SAS software (version 9.3).
Ethics approval
Ethics approval was obtained from the pertinent research ethics boards of all sites, as listed in Appendix 1, Table A1.
Results
Of 2132 eligible patients, 402 (18.9%) had chart documentation that an oral anticoagulant prescription had been provided in the emergency department (Table 1). Of these prescriptions, 296 (73.6%) were written by the managing emergency physician, not a consulting physician (Appendix 1, Table A4). The prescribing rate varied widely across hospitals (7.3%–38.2%). For more than 90% of all patients, an instruction to follow up with a relevant provider was documented in the chart.
Table 1:
Characteristics of patients who did and did not receive an oral anticoagulant (OAC) prescription in the emergency department
| Characteristic | Group; no. (%) of patients* | ||
|---|---|---|---|
| All n = 2132 |
Received OAC prescription n = 402 |
Did not receive OAC prescription n = 1730 |
|
| Patient | |||
| Age, yr | |||
| Mean ± SD | 75.9 ± 7.3 | 77.2 ± 6.8 | 75.7 ± 7.3 |
| Median (IQR) | 75.0 (70.0–81.0) | 77.0 (72.0–82.0) | 75.0 (70.0–81.0) |
| Sex, female | 1256 (58.9) | 216 (53.7) | 1040 (60.1) |
| Rural residence | 45 (2.1) | 13 (3.2) | 32 (1.8) |
| Income quintile | |||
| 1 (lowest) | 302 (14.2) | 59 (14.7) | 243 (14.0) |
| 2 | 380 (17.8) | 69 (17.2) | 311 (18.0) |
| 3 | 418 (19.6) | 76 (18.9) | 342 (19.8) |
| 4 | 533 (25.0) | 96 (23.9) | 437 (25.3) |
| 5 (highest) | 499 (23.4) | 102 (25.4) | 397 (22.9) |
| Came from doctor’s office (v. home) | 569 (26.7) | 159 (39.6) | 410 (23.7) |
| Medical history | |||
| Atrial fibrillation | 568 (26.6) | 66 (16.4) | 502 (29.0) |
| Heart failure | 224 (10.5) | 47 (11.7) | 177 (10.2) |
| Hypertension | 1615 (75.8) | 332 (82.6) | 1283 (74.2) |
| Diabetes mellitus | 385 (18.1) | 87 (21.6) | 298 (17.2) |
| Stroke or TIA | 23 (1.1) | † | † |
| Coronary artery disease | 421 (19.7) | 84 (20.9) | 337 (19.5) |
| Valvular disease | 36 (1.7) | 10 (2.5) | 26 (1.5) |
| Chronic obstructive pulmonary disease | 131 (6.1) | 27 (6.7) | 104 (6.0) |
| Chronic renal failure | 30 (1.4) | 7 (1.7) | 23 (1.3) |
| Dementia | 40 (1.9) | 8 (2.0) | 32 (1.8) |
| History of falls | 41 (1.9) | 9 (2.2) | 32 (1.8) |
| ADG score, median (IQR) | 13 (10–15) | 12 (10–15) | 13 (10–15) |
| CHADS2 score | |||
| 0 | 216 (10.1) | 19 (4.7) | 197 (11.4) |
| 1 | 780 (36.6) | 112 (27.9) | 668 (38.6) |
| 2 | 812 (38.1) | 196 (48.8) | 616 (35.6) |
| ≥ 3 | 324 (15.2) | 75 (18.7) | 249 (14.4) |
| CHA2DS2-VASc score | |||
| 1 | 97 (4.5) | 7 (1.7) | 90 (5.2) |
| 2 | 384 (18.0) | 57 (14.2) | 327 (18.9) |
| 3 | 681 (31.9) | 118 (29.4) | 563 (32.5) |
| 4 | 611 (28.7) | 149 (37.1) | 462 (26.7) |
| 5 | 260 (12.2) | 57 (14.2) | 203 (11.7) |
| ≥ 6 | 99 (4.6) | 14 (3.5) | 85 (4.9) |
| HAS-BLED score 1 or 2 (v. 3) | 942 (44.2) | 179 (44.5) | 763 (44.1) |
| Warfarin therapy failed in the past | 9 (0.4) | 0 (0.0) | 9 (0.5) |
| History of GI bleed | 19 (0.9) | † | † |
| History of other bleed | 10 (0.5) | 0 (0.0) | 10 (0.6) |
| Smoking history | |||
| Current | 83 (3.9) | 10 (2.5) | 73 (4.2) |
| Previous | 138 (6.5) | 35 (8.7) | 103 (6.0) |
| ASA | 775 (36.4) | 147 (36.6) | 628 (36.3) |
| Clopidogrel | 44 (2.1) | 8 (2.0) | 36 (2.1) |
| ASA + clopidogrel40 | 50 (2.3) | 6 (1.5) | 44 (2.5) |
| ED arrival and care | |||
| Arrival by ambulance | 581 (27.3) | 78 (19.4) | 503 (29.1) |
| Triage score‡ | |||
| 1 or 2 | 426 (20.0) | 96 (23.9) | 330 (19.1) |
| 3, 4 or 5 | 1706 (80.0) | 306 (76.1) | 1400 (80.9) |
| Presenting heart rate, median (IQR) | 113 (88–136) | 110 (85–132) | 114 (89–138) |
| Proof of atrial fibrillation by ECG or rhythm strip | 1949 (91.4) | 389 (96.8) | 1560 (90.2) |
| Creatinine, μmol/L, median (IQR) | 82 (68–98) | 87 (72–103) | 81 (68–97) |
| Discharge | |||
| Discharge rhythm | |||
| Normal sinus rhythm | 1142 (53.6) | 93 (23.1) | 1049 (60.6) |
| Atrial fibrillation | 875 (41.0) | 274 (68.2) | 601 (34.7) |
| Other | 95 (4.5) | 30 (7.5) | 65 (3.8) |
| Unknown | 20 (0.9) | † | † |
| New prescription of ASA and/or clopidogrel | 380 (17.8) | † | † |
| ED physician prescribed OAC | 296 (13.9) | 296 (73.6) | – |
| ED physician documented that prescribing OAC was considered | 308 (14.4) | † | † |
| Consultation provided by cardiologist or internist in ED | 341 (16.0) | 106 (26.4) | 235 (13.6) |
| Documented follow-up advice | |||
| Follow up with relevant provider (PCP, cardiologist, internist) | 1952 (91.6) | 386 (96.0) | 1566 (90.5) |
| Follow up with other provider | 39 (1.8) | 12 (3.0) | 27 (1.6) |
Note: ADG = Adjusted Diagnostic Group,41 ASA = acetylsalicylic acid, ECG = electrocardiogram, ED = emergency department, GI = gastrointestinal, IQR = interquartile range, PCP = primary care provider, SD = standard deviation, TIA = transient ischemic attack.
Except where indicated otherwise.
Owing to a privacy agreement between the Canadian Institute for Health Information and ICES, these data values are not reported either because n ≤ 5, or to prevent the calculation of values ≤ 5.
According to Canadian Triage and Acuity Score.42
In univariable analyses, 280 (71.8%) of the 390 patients who received an emergency department prescription for an oral anticoagulant and were alive at 6 months filled a prescription at 6 months (Table 2). Among the 1672 patients who were discharged without a prescription and were still alive at 6 months, 615 (36.8%) filled a prescription for an oral anticoagulant at 6 months. In the emergency department prescription group, 75.1% (302/402) had an outpatient physician visit within 7 days, and 96.3% (387/402) had such a visit by 30 days (Table 3), compared with 57.5% (994/1730) and 88.3% (1528/1730), respectively, among the no emergency department prescription group. Patients who were given a prescription for an oral anticoagulant in the emergency department filled it a median of 1 day after discharge (mean 12 d; Table 2). Among those in the no-prescription group who actually filled a prescription at some point during the 1-year follow-up (46.0%), median time to fill the prescription was 28 days (mean 76 d).
Table 2:
Univariable outcomes in relation to receipt of an oral anticoagulant (OAC) prescription in the emergency department
| Outcome | Group; no. (%) of patients* | ||
|---|---|---|---|
| All n = 2132 |
Received OAC prescription n = 402 |
Did not receive OAC prescription n = 1730 |
|
| Prescriptions for OAC | |||
| At 6 mo (130–230 d after discharge) | |||
| Filled prescription for OAC | 895 (42.0) | 280 (69.7) | 615 (35.5) |
| Died | 70 (3.3) | 12 (3.0) | 58 (3.4) |
| At 1 yr (315–415 d after discharge) | |||
| Filled prescription for OAC | 934 (43.8) | 261 (64.9) | 673 (38.9) |
| Died | 110 (5.2) | 23 (5.7) | 87 (5.0) |
| Filled ≥ 1 prescription for OAC up to 1 yr (415 d) after ED visit | |||
| No. (%) of patients | 1150 (53.9) | 355 (88.3) | 795 (46.0) |
| Time to first fill, median (IQR) | 10 (1–61) | 1 (0–1) | 28 (7–100) |
| Time to first fill, mean ± SD | 56 ± 94 | 12 ± 46 | 76 ± 103 |
| Discontinuation of OAC therapy | |||
| Filled ≥ 1 prescription within 180 d, but discontinued before d 230 | |||
| Discontinued† | 427/1035 (41.3) | 168/355 (47.3) | 259/680 (38.1) |
| No discontinuation | 608/1035 (58.7) | 187/355 (52.6) | 421/680 (61.9) |
| Filled ≥ 1 prescription within 365 d, but discontinued before d 415 | |||
| Discontinued† | 564/1129 (50.0) | 207/354 (58.5) | 357/775 (46.1) |
| No discontinuation | 565/1129 (50.0) | 147/354 (41.5) | 418/775 (53.9) |
| Secondary outcomes | |||
| Death | |||
| 30 d | 9 (0.4) | ‡ | ‡ |
| 90 d | 33 (1.5) | 8 (2.0) | 25 (1.4) |
| 180 d | 58 (2.7) | 10 (2.5) | 48 (2.8) |
| 1 yr | 99 (4.6) | 19 (4.7) | 80 (4.6) |
| 2 yr | 176 (8.3) | 35 (8.7) | 141 (8.2) |
| Stroke, any type | |||
| 180 d | 17 (0.8) | ‡ | ‡ |
| 1 yr | 24 (1.1) | 6 (1.5) | 18 (1.0) |
| 2 yr | 44 (2.1) | 7 (1.7) | 37 (2.1) |
| Bleeding event | |||
| 180 d | 16 (0.8) | 6 (1.5) | 10 (0.6) |
| 1 yr | 27 (1.3) | 9 (2.2) | 18 (1.0) |
| 2 yr | 44 (2.1) | 13 (3.2) | 31 (1.8) |
Note: IQR = interquartile range, SD = standard deviation.
Except where noted otherwise.
Denominator shown excludes patients who died and those who did not fill a prescription for OAC within the specified time frame.
Owing to a privacy agreement between the Canadian Institute for Health Information and ICES, these data values are not reported either because n ≤ 5, or to prevent the calculation of values ≤ 5.
Table 3:
Univariable results for type of follow-up care in relation to receipt of an oral anticoagulant (OAC) prescription in the emergency department
| Outcome | Group; no. (%) of patients | ||
|---|---|---|---|
| All n = 2132 |
Received OAC prescription n = 402 |
Did not receive OAC prescription n = 1730 |
|
| Follow-up care within 7 d | |||
| No. (%) of patients | 1296 (60.8) | 302 (75.1) | 994 (57.5) |
| Specialty of first follow-up | |||
| Cardiology | 213 (10.0) | 40 (10.0) | 173 (10.0) |
| Internal medicine | 228 (10.7) | 41 (10.2) | 187 (10.8) |
| Family medicine | 855 (40.1) | 221 (55.0) | 634 (36.6) |
| No follow-up | 836 (39.2) | 100 (24.9) | 736 (42.5) |
| Filled prescription for OAC within 30 d of follow-up* | |||
| Cardiology | 83/213 (39.0) | 25/40 (62.5) | 58/173 (33.5) |
| Internal medicine | 92/228 (40.4) | 28/41 (68.3) | 64/187 (34.2) |
| Family medicine | 276/855 (32.3) | 135/221 (61.1) | 141/634 (22.2) |
| Follow-up care within 30 d | |||
| No. (%) of patients | 1915 (89.8) | 387 (96.3) | 1528 (88.3) |
| Specialty of first follow-up | |||
| Cardiology | 392 (18.4) | 57 (14.2) | 335 (19.4) |
| Internal medicine | 292 (13.7) | 54 (13.4) | 238 (13.8) |
| Family medicine | 1231 (57.7) | 276 (68.7) | 955 (55.2) |
| No follow-up | 217 (10.2) | 15 (3.7) | 202 (11.7) |
| Filled prescription for OAC within 30 d of follow-up* | |||
| Cardiology | 135/392 (34.4) | 32/57 (56.1) | 103/335 (30.7) |
| Internal medicine | 109/292 (37.3) | 32/54 (59.3) | 77/238 (32.4) |
| Family medicine | 357/1231 (29.0) | 162/276 (58.7) | 195/955 (20.4) |
For patients seen by each type of specialist.
After inverse probability-of-treatment weighting, the groups were well balanced,38 other than slightly more patients in the highest-income quintile in the emergency department prescription group (Appendix 1, Table A5). After weighting, the proportions who filled a prescription for an oral anticoagulant at 6 months were 67.8% in the emergency department prescription group and 37.2% in the no-prescription group (absolute risk increase [ARI] 30.6%, NNT 3) (Table 4). At 1 year, the corresponding proportions were 63.7% and 40.5%, respectively (ARI 23.2, NNT 4).
Table 4:
Subsequent prescription fills in relation to receipt of an oral anticoagulant (OAC) prescription in the emergency department
| Timing and group | Univariable analysis | After propensity-score weighting | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|
|
|
|
|||||||||
| Filled prescription, % | p value | ARI | NNT | Died, % | Filled prescription, % | p value | ARI | NNT | Died, % | |
| At 6 mo | ||||||||||
|
| ||||||||||
| Received OAC prescription in ED | 69.7 | < 0.001 | 34.2 | 3 | 3.0 | 67.8 | < 0.001 | 30.6 | 3 | 3.3 |
|
| ||||||||||
| Did not receive OAC prescription in ED | 35.5 | 3.4 | 37.2 | 3.6 | ||||||
|
| ||||||||||
| At 1 yr | ||||||||||
|
| ||||||||||
| Received OAC prescription in ED | 64.9 | < 0.001 | 26.0 | 4 | 5.7 | 63.7 | < 0.001 | 23.2 | 4 | 6.1 |
|
| ||||||||||
| Did not receive OAC prescription in ED | 38.9 | 5.0 | 40.5 | 5.4 | ||||||
Note: ARI = absolute risk increase, ED = emergency department, NNT = number needed to treat.
In the sensitivity analyses using logistic regression, the adjusted odds for a prescription fill at 6 months for the emergency department prescription group relative to the no-prescription group were 3.26 (95% CI 2.66–4.01), and the adjusted odds at 1 year were 2.37 (95% CI 1.86–3.02). Results were similar for the cohort without HAS-BLED score exclusions and for patients with ECG or rhythmstrip proof of atrial fibrillation documented in the chart.
In the 30 days after discharge, adherence (based on proportion of days covered) was 74.6% in the emergency department prescription group and 14.0% in the no-prescription group (Figure 1). By 6 months, adherence was 60.2% and 21.7%, respectively, and at 1 year, it had fallen to 56.0% in the emergency department prescription group and 24.3% in the no-prescription group. At all time points, those in the emergency department prescription group had a higher proportion of days covered than those in the no-prescription group. Discontinuations are shown in Table 2 and Appendix 1, Figure A1.
Figure 1:
Among all patients, the proportion of days covered ( PDC) by filled prescriptions for anticoagulant therapy for patients who received a prescription for an oral anticoagulant in the emergency department (ED Rx) and those who did not receive such a prescription (No ED Rx).
Among the 1296 patients who obtained 7-day outpatient followup care, 39.0% (83/213) of those who saw a cardiologist filled a prescription for an oral anticoagulant within 30 days of that appointment: 62.5% (25/40) in the emergency department prescription group and 33.5% (58/173) in the no-prescription group (Table 3) (ARI 29.0%). Among patients who saw an internist, the ARI was 34.1%. Most patients who obtained 7-day follow-up saw a primary care provider (66.0% [855/1296]), and 61.1% (135/221) of the emergency department prescription group filled an oral anticoagulant prescription within 30 days of the appointment compared with 22.2% (141/634) of the no-prescription group (ARI 38.9%).
Strokes leading to hospital admission were uncommon in both groups (Table 2), and most were ischemic. After inverse weighting, the absolute event rates for death and for strokes were not statistically different between groups (Appendix 1, Table A6). Bleeding events were not statistically different at any follow-up time, including after weighting.
Interpretation
In this multicentre study in Ontario, Canada, providing an oral anticoagulant prescription in the emergency department to patients with atrial fibrillation who were older than 65 years was associated with a marked increase in long-term use of this therapy. The NNT for 1 additional patient to fill a prescription for an oral anticoagulant at 6 months after the emergency visit was 3. The NNT had increased to 4 by 1 year, which was expected because persistence with this therapy is known to decline over time.43,44 To prevent 1 stroke at 1 year, the NNT with oral anticoagulants is 1.7;7 therefore, the NNT for oral anticoagulant prescriptions in the emergency department to prevent a stroke is about 7. By comparison, the NNT for statins to prevent nonfatal myocardial infarction in patients with a history of heart disease is 39.45
There may be several explanations for our findings. Patients who receive a prescription during an emergency care episode may be more likely to fill such a prescription than patients who wait a week or a month to see their regular provider and experience no untoward event (e.g., stroke) during that delay. The finding that 75% of patients who received an emergency department prescription filled it within 2 days of discharge supports the hypothesis that the emergency department encounter is influential with patients.
A primary care provider may be more likely to continue a prescription initiated by another physician or may be reassured that another physician has initiated oral anticoagulant therapy. Among patients who received a prescription in the emergency department, there was an almost 40% absolute increase in prescription fills after follow-up with the primary care provider, relative to patients referred to longitudinal care providers to consider initiation of therapy. This effect was attenuated but still present (> 25% absolute improvement) when internists and cardiologists provided the first follow-up appointment. Although an emergency department prescription does not guarantee subsequent refills (probably in some cases for good reason, such as a contraindication of which the emergency physician was not aware), it did substantially increase the proportion of patients with such refills. In addition, prescription fill rates after a follow-up appointment were similar among provider types for patients who received a prescription in the emergency department (56%–59% at 30 days), whereas the range among provider types was wider for the noprescription group (20%–32%). This result suggests that emergency department prescribing was associated with an increase in prescribing rates by primary care providers, to levels similar to those of cardiologists.
In a small study of 137 patients with atrial fibrillation discharged from the emergency department in Ontario, ARI was 43% for 6-month prescription fills among patients who received a prescription in the emergency department relative to those who did not.27 Our adjusted results in a larger population were similar but attenuated (ARI 31%).
Increasing the proportion of eligible patients receiving oral anticoagulants at the population level has been associated with a lower incidence of atrial fibrillation–related stroke;13 however, we found no reduction in deaths or strokes. Our study may have been underpowered because of low event rates.18 Subsequent discontinuation among those in the emergency department prescription group combined with initiation of oral anticoagulants in the no-prescription group would also be expected to reduce between-group differences in outcomes. Notably, prescribing of oral anticoagulants in the emergency department was not associated with an increase in major bleeding events.
Rates of oral anticoagulant initiation were much lower for patients who left the emergency department in sinus rhythm than for patients who left in atrial fibrillation, similar to results from the PINNACLE registry and other studies.46,47 This finding suggests the need to educate emergency physicians about use of oral anticoagulants regardless of atrial fibrillation type (paroxysmal v. persistent or permanent). Discontinuations and nonadherence were modestly more frequent in the emergency department prescription group; however, at all time points the proportion of patients without stroke protection was much higher in the no-prescription group. The discontinuation rates may highlight other steps required to improve long-term use of oral anticoagulants, such as patient education.48
Prescribing tools can simplify decision-making for busy emergency physicians;49 however, preventive care in the emergency department may be hindered by factors such as the potential for a longer stay in the emergency department.50,51 Importantly, with initiation of a new long-term medication, it is recommended that these patients be followed over time, to ensure the dosage is correct and adverse effects are managed.52 Because emergency physicians are not in a position to follow patients, they rarely initiate long-term medications. This may explain the low rate of oral anticoagulant initiation in our study (18.9%; similar to other North American studies47,53,54). For many patients, treatment with acetylsalicylic acid may have been considered adequate: until 2012, guidelines endorsed this agent for patients with CHADS2 score of 0 or (possibly) 1.55,56
An approach of “default short-term anticoagulation therapy” has been suggested, whereby the emergency physician prescribes an oral anticoagulant for several weeks, followed by an appointment with the longitudinal care provider,25 who decides whether to renew the prescription (based on a more thorough knowledge of the patient’s medical history), provides shared decision-making and addresses HAS-BLED risk factors.10,25 If the patient does not obtain follow-up care, the prescription ends, as does the risk of bleeding. Given our results, we believe that emergency physicians should consider adapting this approach. Future work is needed to establish a reliable follow-up system that directly connects patients to longitudinal care.
Limitations
We used propensity-score methods to adjust for group differences but were unable to account for unmeasured covariables. However, in this circumstance a randomized trial is likely neither ethical nor feasible. Our study ended in 2014, and most prescriptions were for warfarin; however, warfarin use is decreasing as direct oral anticoagulant use is increasing.57,58 This shift may make it more likely that emergency and family physicians will initiate oral anticoagulation, but the impact of starting oral anticoagulation in the emergency department is unlikely to change substantially. We included all patients who qualified for stroke prevention on the basis of CHADS-65, but in the earlier years of this study, CHADS2 combined with CHA2DS2-VASc was recommended; 55 therefore, some of the early patients would not have qualified for oral anticoagulants. There was only 1 chart abstractor, but she performed data abstraction for our previous study, which used many of the same variables and had high inter-rater agreement.15 We assessed only strokes leading to admission, because transient ischemic attacks and minor strokes are not well coded in administrative data.35 This may have resulted in an underestimation of the frequency of minor strokes and reduced our power to detect differences in stroke outcomes.
Conclusion
In this multicentre study of patients older than 65 years with atrial fibrillation and without high-risk factors for bleeding who were discharged from the emergency department, provision of an oral anticoagulant prescription in the emergency department was associated with a 31% absolute increase in the risk of filling a prescription at 6 months, compared with referral to the longitudinal care provider to initiate this therapy. Physicians working in the emergency department should consider initiating oral anticoagulants in similar patients who are being discharged home, because this action is associated with improved use of stroke prevention long after the patient leaves the emergency department.
Footnotes
CMAJ Podcasts: author interview at https://soundcloud.com/cmajpodcasts/190747-res
Competing interests: For activities outside the submitted work, Paul Dorian has received personal fees from Bayer and Servier as well as grants and personal fees from BMS and Pfizer, and Ratika Parkash has received grants from Pfizer, Boehringer-Ingelheim, Medtronic and Abbott as well as honoraria from Servier. No other competing interests were declared.
This article has been peer reviewed.
Contributors: All of the authors contributed to the concept and design of the study, and participated in the analysis and interpretation of data. Clare Atzema and Alice Chong acquired the data. Clare Atzema, Cynthia Jackevicius, Alice Chong and Peter Austin performed the statistical analysis. Clare Atzema drafted the manuscript, and all of the authors critically revised the manuscript for important intellectual content. Clare Atzema obtained the funding. All of the authors approved the final version to be published and agreed to be held accountable for the work. Clare Atzema had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.
Funding: This project was supported by a grant from C-SPIN (Canadian Stroke Prevention Intervention Network), which was funded by a Canadian Institutes for Health Research (CIHR) Emerging Network Grant under the Institute of Circulatory and Respiratory Health. Clare Atzema was supported by a Mid-Career Investigator Award from the Heart and Stroke Foundation of Ontario (HSFO), the Practice Plan of the Department of Emergency Services at Sunnybrook Health Sciences Centre and the Sunnybrook Research Institute. Paul Dorian and Ratika Parkash were supported by the Cardiac Arrhythmia Network of Canada (CaNET) National Centre of Excellence. Noah Ivers was supported by a New Investigator Award from the CIHR. Peter Austin was supported by a Mid-Career Investigator Award from the HSFO.
Data sharing: The data set from this study is held securely in coded form at ICES. While data-sharing agreements prohibit ICES from making the data set publicly available, access may be granted to those who meet prespecified criteria for confidential access, available at www.ices.on.ca/DAS. The full data set creation plan and underlying analytic code are available from the authors upon request, on the understanding that the programs may rely upon coding templates or macros that are unique to ICES.
Disclaimers: The Heart and Stroke Foundation of Ontario had no involvement in the design or conduct of the study, data management or analysis, or manuscript preparation, review, or authorization for submission. This study was supported by ICES, which is funded by an annual grant from the Ontario Ministry of Health and Long-Term Care (MOHLTC). The opinions, results and conclusions reported in this paper are those of the authors and are independent from the funding sources. No endorsement by ICES or the Ontario MOHLTC is intended or should be inferred.
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