A.Fib Emergency Department Study Atrial Fibrillation

NCT ID: NCT03127085

Last Updated: 2019-02-15

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 297 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2017-04-21
• Study Completion Date: 2018-09-27

Brief Summary

Patients with a history of atrial fibrillation (AF) who frequently attend the emergency department (ED) with symptoms may not require emergency treatment, and may be more appropriately managed in an alternative outpatient setting. This may be the result of inappropriate or inadequate advice or a lack of patient understanding. The main research objective pertains to the reason for seeking medical attention for AF in the ED, ED management of the patient, outcomes of ED care and alternative strategies.

Detailed Description

This study is a multi-centre, multi-provincial, patient survey using mixed methods. 778 patients will be enrolled from 9 centres in 3 provinces from academic, urban, and rural centres to achieve geographical and health system heterogeneity. The planned duration of the entire study (enrollment through follow-up) is approximately 12 months. Patients presenting to the ED with a primary diagnosis of AF and with a prior diagnosis of established AF will be approached to participate. Each centre will be responsible for obtaining local consent. Data will be stored confidentially and securely at the coordinating centre (Queens University, Kingston, Ontario).

Patients who meet the inclusion criteria will be invited to take part at the time of presentation to the ED or after their ED visit. For all enrolled patients, one follow up telephone call will be made within one to four weeks of the ED visit by a social scientist with specialised training in questionnaires based in Queens University, Kingston, Ontario.

Conditions

Atrial Fibrillation

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• Male or female ≥ 18 years of age
• Atrial fibrillation is the primary reason for ED visit (documented by 12-lead ECG or Holter rhythm strip by a member of the healthcare team providing care to the patient).
• Patients with an established history of AF (prior diagnosis with ECG / rhythm strip evidence of AF)
• Patient must be literate in English
• Patient must provide informed consent

Exclusion Criteria

• Male or female < 18 years of age
• Non-English speaking
• unable and/or unwilling to consent
• Acute coronary syndrome (ischemic chest pain, ST changes, + troponin [mild troponin elevation alone does not exclude the patient])
• Cardiogenic shock or class IV congestive heart failure at the time of visit
• Enrolled in a cardiovascular drug or device research study
• New onset atrial fibrillation

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cardiac Arrhythmia Network of Canada

OTHER

Sponsor Role: collaborator

Queen's University

OTHER

Sponsor Role: lead

Responsible Party

Dr. Benedict Glover

Chief of Cardiac Arrhythmia Service, Queen's University, Kingston, Ontario

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Benedict Glover, MD

Role: PRINCIPAL_INVESTIGATOR

Queen's University

Locations

Kingston Health Sciences Centre - Kingston General Hospital Site

Kingston, Ontario, Canada

Countries

Canada

References

Hong KL, Babiolakis C, Zile B, Bullen M, Haseeb S, Halperin F, Hohl CM, Magee K, Sandhu RK, Tian SY, Kennedy A, Lobban T, Mariano Z, Dorian P, Angaran P, Evans M, Leong-Sit P, Glover BM. Canada-wide mixed methods analysis evaluating the reasons for inappropriate emergency department presentation in patients with a history of atrial fibrillation: the multicentre AF-ED trial. BMJ Open. 2020 Apr 16;10(4):e033482. doi: 10.1136/bmjopen-2019-033482.

Reference Type: DERIVED

PMID: 32303514 (View on PubMed)

Other Identifiers

AF ED

Identifier Type: -

Identifier Source: org_study_id