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| Name | Class |
|---|---|
| Heart and Stroke Foundation of Canada | OTHER |
| Canadian Cardiovascular Society | OTHER |
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Multicentre, prospective cohort study in patients with a history of HF with preserved or reduced ejection fraction admitted to hospital with acutely decompensated HF. Eligible and consenting patients will be enrolled at 3 Hamilton, Ontario area hospitals and receive 28-day ECG monitoring implemented at the time of hospital discharge. Patients will be followed for a total of 1 year from hospital discharge.
In patients discharged from hospital after an admission for acute heart failure (HF) decompensation, subclinical atrial fibrillation (AF) of 30 minutes or greater in duration is common (at least 15% of patients without prior AF) and is associated with increased risk of re-hospitalization within 30-days.
Study Objectives:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Enrolled Patients |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| ECG Patch, pocket ECG monitor | Device | Two consecutive 14-day ECG monitor patches or one single 28-day pocket ECG monitor (28-days total monitoring) implemented at the time of hospital discharge . |
| Measure | Description | Time Frame |
|---|---|---|
| Subclinical atrial fibrillation ≥30 minutes in duration | 30 days post-discharge |
| Measure | Description | Time Frame |
|---|---|---|
| Heart failure re-hospitalization | 30 days post-discharge |
| Measure | Description | Time Frame |
|---|---|---|
| Subclinical atrial fibrillation >6 minutes in duration | 30 days post-discharge | |
| Clinical atrial fibrillation | 30 days post-discharge | |
| Heart Failure re-hospitalization |
Inclusion Criteria:
Exclusion Criteria:
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Patients with a history of HF who are admitted to hospital with acutely decompensated HF and have no prior history of AF.
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| Name | Affiliation | Role |
|---|---|---|
| Jorge A Wong, MD, MPH | Population Health Research Institute | Principal Investigator |
| Stuart Connolly, MD | Population Health Research Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hamilton General Hospital | Hamilton | Ontario | Canada | |||
| Juravinski Hospital |
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| 1 year post-discharge |
| All-cause re-hospitalization | 30 days and 1 year post-discharge |
| All-cause and cardiovascular mortality | 30 days and 1 year post-discharge |
| Incident stroke/TIA or systemic thromboembolism | 30 days and 1 year post-discharge |
| Myocardial infarction | 30 days and 1 year post-discharge |
| Patient acceptance of device monitoring | Measured by simple questionnaire that has not been validated. Patients will be asked to respond to satisfaction questions on a scale of a) strongly agree b) agree c) somewhat agree d) disagree or e) strongly disagree. The questions will ask about their experience with the device, such as: were instructions on using the device clear, the device was easy to use, the device did not limit my usual daily activities, the size of the device was not cumbersome, etc. | 30 days post-discharge |
| Hamilton |
| Ontario |
| Canada |
| St. Joseph's Healthcare Hamilton | Hamilton | Ontario | Canada |
| St. Mary's Hospital | Kitchener | Ontario | N2M1B2 | Canada |
| St. Catherines General Hospital | St. Catharines | Ontario | L2S0A9 | Canada |
| ID | Term |
|---|---|
| D006333 | Heart Failure |
| D001281 | Atrial Fibrillation |
| ID | Term |
|---|---|
| D006331 | Heart Diseases |
| D002318 | Cardiovascular Diseases |
| D001145 | Arrhythmias, Cardiac |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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