Inclusion criteria for all AF subjects: Must be between 18 and 100 years old with a diagnosis of atrial fibrillation. Additionally, subject must have a family member with known AF.
Item
Inclusion criteria for all AF subjects: Must be between 18 and 100 years old with a diagnosis of atrial fibrillation. Additionally, subject must have a family member with known AF.
boolean
C1512693 (UMLS CUI [1,1])
C1706256 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C0001779 (UMLS CUI [1,4])
C0086282 (UMLS CUI [1,5])
C0004238 (UMLS CUI [1,6])
Exclusion criteria for all AF subjects: New onset AF occurring within 3 months of CABG or valve surgery; AF occurring post heart transplant; Post allogeneic bone marrow transplant.
Item
Exclusion criteria for all AF subjects: New onset AF occurring within 3 months of CABG or valve surgery; AF occurring post heart transplant; Post allogeneic bone marrow transplant.
boolean
C0680251 (UMLS CUI [1,1])
C1706256 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C1442461 (UMLS CUI [1,4])
C0010055 (UMLS CUI [1,5])
C2066019 (UMLS CUI [1,6])
C0680251 (UMLS CUI [2,1])
C1706256 (UMLS CUI [2,2])
C0231290 (UMLS CUI [2,3])
C0018823 (UMLS CUI [2,4])
C0680251 (UMLS CUI [3,1])
C1706256 (UMLS CUI [3,2])
C0231290 (UMLS CUI [3,3])
C0194037 (UMLS CUI [3,4])
Controls were defined as those subjects who satisfied the following criteria (AFFIRM) after treatment with 2 or fewer AV nodal-blocking agents: average heart rate (HR) ≤ 80 bpm at rest, in addition to either an average 24-hour HR ≤ 100 bpm and no maximal 24-hr HR > 110% of the predicted age-adjusted maximum exercise HR, or a HR ≤ 110 bpm during a 6-minute walk test.
Item
Controls were defined as those subjects who satisfied the following criteria (AFFIRM) after treatment with 2 or fewer AV nodal-blocking agents: average heart rate (HR) ≤ 80 bpm at rest, in addition to either an average 24-hour HR ≤ 100 bpm and no maximal 24-hr HR > 110% of the predicted age-adjusted maximum exercise HR, or a HR ≤ 110 bpm during a 6-minute walk test.
boolean
C1512693 (UMLS CUI [1,1])
C0009932 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,4])
C4523943 (UMLS CUI [1,5])
C0018810 (UMLS CUI [1,6])
Cases were defined as those subjects who failed to satisfy the AFFIRM criteria after combined therapy with 3 AV nodal-blocking agents and required AV node ablation and pacemaker implantation.
Item
Cases were defined as those subjects who failed to satisfy the AFFIRM criteria after combined therapy with 3 AV nodal-blocking agents and required AV node ablation and pacemaker implantation.
boolean
C1706256 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C4523943 (UMLS CUI [1,4])
C1514873 (UMLS CUI [1,5])
C3275044 (UMLS CUI [1,6])
C0189863 (UMLS CUI [1,7])
Criteria for post-op patients with no AF: All adult patients scheduled for elective cardiothoracic surgery who are capable of providing informed consent will be eligible for the study. Emergency patients or hemodynamically unstable patients for whom discussion of consent would delay surgery or who are incapable of providing consent will be excluded.
Item
Criteria for post-op patients with no AF: All adult patients scheduled for elective cardiothoracic surgery who are capable of providing informed consent will be eligible for the study. Emergency patients or hemodynamically unstable patients for whom discussion of consent would delay surgery or who are incapable of providing consent will be excluded.
boolean
C1512693 (UMLS CUI [1,1])
C1549444 (UMLS CUI [1,2])
C0004238 (UMLS CUI [1,3])
C2242990 (UMLS CUI [1,4])
C0085732 (UMLS CUI [1,5])
C0021430 (UMLS CUI [1,6])
C0680251 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
C1640361 (UMLS CUI [2,3])
C0543467 (UMLS CUI [2,4])