This single-center observational registry follows contemporary efficacy and short-term complications of elective electric cardioversion.
Study Type
OBSERVATIONAL
Enrollment
5,000
Electric cardioversion in short sedation according to established clinical practice and indications
Institute for Clinical and Experimental Medicine (IKEM)
Prague, Czechia
RECRUITINGAcute major complications
Major thromboembolic events or events related to cardioversion requiring unplanned hospitalisation (bleeding, severe bradycardia, anesthesia-related complications, heart failure etc)
Time frame: Within 24 hours from the procedure
Subacute major complications
Major thromboembolic events or events related to cardioversion requiring unplanned hospitalisation (bleeding, severe bradycardia, anesthesia-related complications, acute heart failure etc), evaluated by structured phone call.
Time frame: 24 hours to 30 days after the procedure
Acute minor complications
Minor procedure-related complications not requiring acute hospitalisation (asymptomatic bradycardia, post-anesthesia spasms)
Time frame: Within 24 hours from the procedure
Acute efficacy
Presence of sinus rhythm on continous ECG (5-lead) monitoring
Time frame: Within 2 hours from the procedure
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