Cardiology
Conditions
Interventions
AHRE group
Non AHRE group
Sponsors
Assiut University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: • Patients = 18 years with dual-chamber pacemakers, CRT or ICDs with atrial leads. • Device capable of AHRE detection. • Sinus rhythm at baseline.
Exclusion criteria
Exclusion criteria: • Permanent or diagnosed paroxysmal AF (by documented 12 lead surface ECG) or atrial flutter. • History of prior catheter ablation. • Severe valvular heart disease or Cardiac valve prosthesis. • Poor echocardiographic window
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint: •To study the association between AHRE detected on CIED patients and LA strain parameters | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary effectiveness endpoints: 1. To detect association between atrial mechanical dysfunction with AHRE burden. 2. To assess the additive value of advanced imaging (STE) over conventional echocardiographic parameters. 3. To assess association between AHRE and thromboembolic events including cerebrovascular stroke, limb ischemia and other embolic manifestations. 4. To assess association between LA dysfunction and thromboembolic events including cerebrovascular stroke, limb ischemia and other embolic manifestations. | — |
Countries
Egypt
Contacts
Public ContactMohamed Aboelhassan Abdelrady
Physician
Outcome results
None listed