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Get With the Guidelines Atrial Fibrillation Registry

Recruiting
Conditions
Atrial Flutter
Atrial Fibrillation
Registration Number
NCT06245187
Lead Sponsor
American Heart Association
Brief Summary

Get With The Guidelines-Atrial Fibrillation is designed to assist hospital care teams in consistently providing the latest evidence-based treatment for their AFib patients. At the same time, it offers a means of monitoring the quality of AFib care in U.S. hospitals and building a database for continued research and further quality improvement.

Detailed Description

Get With The Guidelines-Atrial Fibrillation was initiated in 2013 with over 88 U.S. hospitals participating is designed to assist hospital care teams in consistently providing the latest evidence-based treatment for their AFib patients. At the same time, it offers a means of monitoring the quality of AFib care in U.S. hospitals and building a database for continued research and further quality improvement.

Achievement measures tracked through Get With The Guidelines-Atrial Fibrillation:

1. ACEI/ARB at discharge for LVSD

2. Assessment of thromboembolic risk factors

3. Beta Blocker at discharge

4. Discharged on FDA-approved anticoagulation therapy

5. PT/INR planned follow-up

6. Statin at discharge in AF patients with CAD, CVA/TIA or PVD.

Quality measures tracked through Get With The Guidelines-Atrial Fibrillation:

1. Aldosterone antagonist at discharge

2. Atrial fibrillation patient education

3. Anticoagulation therapy education

4. CHA2DS2-VASC reported

5. Discharge heart rate \<110bpm

6. Smoking cessation

7. Warfarin at discharge for valvular atrial fibrillation

Additional measures collected by Get With The Guidelines-Atrial Fibrillation can be viewed at: http://www.heart.org/idc/groups/heart-public/@private/@wcm/@hcm/@gwtg/documents/downloadable/ucm_451183.pdf

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
17198
Inclusion Criteria
  • Patients hospitalized with nonvalvular Atrial Fibrillation or Atrial Flutter
Exclusion Criteria
  • Patients who do not have nonvalvular Atrial Fibrillation or Atrial Flutter
  • Patients under 18 years of age
  • Patients not admitted as inpatients.
  • Patients on comfort care only
  • Patients discharged to hospice.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cardiac Tamponade and/or Pericardiocentesis Following Ablation30 days

Percent of patients with cardiac tamponade and/or pericardiocentesis occurring within 30 days following ablation procedure.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Amy Bennett

🇺🇸

Dallas, Texas, United States

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