Atrial Fibrillation Clinical Trial
Official title:
Treatment of Atrial Fibrillation in Finland - the FinFib 2 Study
FINFIB 2 is an observational investigator-driven study that seeks to examine current treatment practice for atrial fibrillation in Finland. The investigators hypothesis is that the treatment of atrial fibrillation has improved since the introduction of new antiarrhythmic drugs and anticoagulants.
FINFIB 2 is an observational investigator-driven study that seeks to examine current
treatment practice for atrial fibrillation (AF) in Finland. It will produce important
information such as whether the introduction of the new agents has taken place in accordance
with the treatment guidelines in different parts of Finland.
Working hypothesis is that the treatment of AF has improved since the introduction of new
antiarrhythmic drugs and anticoagulants. However, the investigators also expect to find out
that there are geographical differences in the use of these agents. The expect outcome is
that the investigators will identify these differences and be able to better homogenize the
treatment of AF in different parts of the country and different levels of the health care
system.
The study data will be obtained in the form of a cross-section sampling over two weeks. All
patients with ECG-diagnosed AF who attend emergency clinics for examination or treatment of
arrhythmia or other cardiac diseases during the study period will be included. The
investigators estimate the number of patients will be about 1000. Aside from background
information, risk data (e.g. CHA2DS2VASc), symptoms (EHRA classification), medication,
examinations and the choice of treatment, the only data recorded about each patient with AF
will be date of birth and gender. The patients will be divided into four groups according to
type of AF: 1. New onset AF, 2. Paroxysmal AF, 3. Persistent AF, 4. Permanent AF. The data
will be obtained by the local study doctor using online, protected data collection program.
The data will be stored on a secured server, which can be accessed for data entry by the
investigators at the study centers. The database is not a personal data register, as
identity codes will not be stored at any point and individual patients cannot be identified
later through the database. Only the investigator group will have the rights to use the
database.
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Observational Model: Cohort, Time Perspective: Prospective
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