Aortic Valve Stenosis Clinical Trial
Official title:
Study to Improve Outcomes in Aortic Stenosis. International, Multi-center, Prospective, Observation and Interventional Cohort Registry
The purpose of this study is to narrow the gap between patients being diagnosed with severe aortic stenosis and those being appropriately monitored and treated. For this purpose a prospective survey of current practice (3 months) will be conducted followed by a six month period of intervention during which a variety of quality improvements measures will be implemented. There will then be a 3 month follow-up period during which the legacy of this initiative will be monitored during which no intervention will be carried out.
All patients meeting pre-specified criteria (severe aortic stenosis whether with or without
symptoms) will be collected. There will be three phases at each site observation A,
intervention, observation B. Observation A: In this phase, the nurse identifies cases with
severe AS and collects their data. Baseline data for each patient will be collected and a
follow-up will be done after three months for each patient to determine his/her outcome and
the treatment that was decided on. There will also be an optional telephone follow-up to find
out the patient's outcome.
Intervention: In this phase, the physician referring a patient for echocardiography will be
notified of a finding of severe aortic stenosis: the nurse brings cases with severe AS to the
attention of the referring physician within a week (via phone, e-mail or letter) to make them
aware of the diagnosis.
Baseline and follow-up data will be collected for each patient as before. Moreover, more
detailed data with regard to the patient's health status will be documented.
Observation B: Same as Observation Phase A
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