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Trial Review
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Trial registered on ANZCTR
Registration number
ACTRN12618001890224
Ethics application status
Approved
Date submitted
15/11/2018
Date registered
21/11/2018
Date last updated
21/11/2018
Date data sharing statement initially provided
21/11/2018
Type of registration
Retrospectively registered
Titles & IDs
Public title
A review of hospital based management of atrial fibrillation
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Scientific title
A review of the inpatient and emergency department management of atrial fibrillation
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Secondary ID [1]
296622
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None
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Universal Trial Number (UTN)
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Trial acronym
REVIEW-AF
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Linked study record
This study is linked to the Home Based Education and Learning Package for atrial fibrillation study (HELP AF). ACTRN12611000607976. Participants for the current trial were individuals who underwent preliminary screening for eligibility in the HELP AF study.
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Health condition
Health condition(s) or problem(s) studied:
Atrial Fibrillation
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Condition category
Condition code
Cardiovascular
309150
309150
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0
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Other cardiovascular diseases
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
The aim of this study is to characterise hospital based health care resource utilisation in a cohort of individuals with atrial fibrillation. The cohort of individuals comprises of participants who presented to the emergency departments of three hospitals over a one year period (2013-2014) primarily due to atrial fibrillation. Emergency department presentations and hospital admissions over an approximate four year follow up period (ranging from 2013-2018) will be recorded with a view towards characterising reasons for re-presentations to the emergency department and hospital admissions. This information will be obtained retrospectively by electronic medical review. The management of atrial fibrillation will be explored including the use of rate and rhythm control therapies and appropriate use of oral anticoagulation to reduce stroke risk. Factors predictive of re-presentation and hospitalisation will be examined.
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Intervention code [1]
312925
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Not applicable
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Comparator / control treatment
No control group.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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The primary outcome measure will be to characterise reasons for emergency department re-presentations and/or hospital admissions in a cohort of individuals with AF. These will be characterised as related to: 1: atrial fibrillation 2: other cardiovascular causes 3: all other causes. This is a composite endpoint. Data will be collected by retrospective electronic medial review.
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Assessment method [1]
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Timepoint [1]
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Over an approximate four year follow up time period. This time period ranges from 2013-2018.
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Primary outcome [2]
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To determine factors predictive of re-hospitalisation for atrial fibrillation
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Assessment method [2]
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Timepoint [2]
308172
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Over an approximate four year follow up period (ranging from 2013-2018).
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Secondary outcome [1]
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To determine hospital based management of atrial fibrillation, including the use of rate and rhythm control strategies, and the appropriate use of oral anticoagulation to reduce stroke risk.
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Assessment method [1]
354148
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Timepoint [1]
354148
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Over an approximate four year follow up period (ranging from 2013-2018).
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Eligibility
Key inclusion criteria
Individuals presenting to the emergency department of three public hospitals in South Australia with a principal diagnosis, by ICD-9 or ICD-10 coding, of atrial fibrillation and/or atrial flutter.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Individuals residing in states other than South Australia, overseas visitors, individuals presenting to hospital for elective AF related procedures, individuals presenting to hospitals which do not publish their emergency department or hospital admission correspondence on electronic health databases.
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Study design
Purpose
Natural history
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Duration
Longitudinal
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Selection
Defined population
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Timing
Retrospective
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Statistical methods / analysis
The study sample consists of all individuals presenting to the emergency department of participating hospitals (for the HELP AF study) over a one year period. All individuals with a principal diagnosis of atrial fibrillation were eligible for inclusion. Descriptive analyses will be used to examine reasons for emergency department re-presentations and admissions over the follow up period. A logistic regression model will be used to examine factors predictive of re-presentation or admission to hospital. Descriptive analyses will be employed to examine the use of rate and rhythm control therapies and appropriate use of oral anticoagulation.
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
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Actual
5/07/2016
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Date of last participant enrolment
Anticipated
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Actual
19/07/2018
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Date of last data collection
Anticipated
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Actual
19/07/2018
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Sample size
Target
400
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Accrual to date
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Final
438
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Recruitment in Australia
Recruitment state(s)
SA
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Recruitment hospital [1]
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The Royal Adelaide Hospital - Adelaide
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Recruitment hospital [2]
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The Queen Elizabeth Hospital - Woodville
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Recruitment hospital [3]
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Lyell McEwin Hospital - Elizabeth Vale
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Recruitment postcode(s) [1]
24702
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5000 - Adelaide
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Recruitment postcode(s) [2]
24703
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5011 - Woodville
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Recruitment postcode(s) [3]
24704
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5112 - Elizabeth Vale
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Centre for Heart Rhythm Disorders, University of Adelaide
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Address [1]
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Centre for Heart Rhythm Disorders
c/-Royal Adelaide Hospital
Department of Cardiology
Port Road
Adelaide SA 5000
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Country [1]
301199
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Australia
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Primary sponsor type
University
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Name
Centre for Heart Rhythm Disorders, University of Adelaide
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Address
Centre for Heart Rhythm Disorders
c/-Royal Adelaide Hospital
Department of Cardiology
Port Road
Adelaide SA 5000
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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None
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Address [1]
300826
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N/A
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Country [1]
300826
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Royal Adelaide Hospital Human Research Ethics Committee
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Ethics committee address [1]
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Port Road Adelaide SA 5000
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Ethics committee country [1]
301940
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Australia
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Date submitted for ethics approval [1]
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06/10/2015
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Approval date [1]
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06/11/2015
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Ethics approval number [1]
301940
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HREC/15/RAH/447
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Summary
Brief summary
The aim of this study is to examine reasons for re-presentation to emergency departments or admissions to hospital in a cohort of individuals with atrial fibrillation (AF). The use of treatment for AF, including rate and rhythm controlling strategies, and blood thinning medications (anticoagulation) to reduce the risk of stroke will also be explored. Factors associated with emergency department re-presentations and/or hospital admissions will also be examined.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Prof Prashanthan Sanders
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Address
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Centre for Heart Rhythm Disorders
c/- Department of Cardiology
Royal Adelaide Hospital
Port Road
Adelaide SA 5000
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Country
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Australia
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Phone
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+61 8 83139000
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Fax
88634
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Email
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[email protected]
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Contact person for public queries
Name
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Celine Gallagher
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Address
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Centre for Heart Rhythm Disorders
c/- Department of Cardiology
Royal Adelaide Hospital
Port Road
Adelaide SA 5000
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Country
88635
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Australia
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Phone
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+61 8 8313 9000
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Fax
88635
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Email
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[email protected]
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Contact person for scientific queries
Name
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Prashanthan Sanders
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Address
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Centre for Heart Rhythm Disorders
c/- Department of Cardiology
Royal Adelaide Hospital
Port Road
Adelaide SA 5000
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Country
88636
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Australia
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Phone
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+61 8 83139000
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Fax
88636
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Email
88636
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
Not applicable
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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