Table 3.
Variable | Amiodarone (N=210) | Propafenone (N=42) | Antazoline (N=109) | Antazoline+Amiodarone (N=53) | Antazoline+Propafenone (N=13) | Amiodarone+Propafenone (N=18) | Antazoline+Amiodarone+Propafenone (N=5) | Antazoline vs Amiodarone P Value | Antazoline vs Propafenone P Value | Multiple Comparisons Test P Value |
---|---|---|---|---|---|---|---|---|---|---|
Age, y | 67.7±11.2 | 64.2±12.4 | 62.8±12.0 | 67.4±10.7 | 59.4±11.8 | 58.4±15.6 | 69.0±4.1 | <0.001a | 0.292a | 0.001b |
Male sex | 95 (45.2%) | 9 (21.4%) | 60 (55.0%) | 29 (54.7%) | 7 (53.8%) | 10 (55.6%) | 2 (40.0%) | 0.096c | <0.001c | 0.012d |
EHRA class | 3 (2–3) | 2 (2–3) | 3 (2–3) | 3 (2–3) | 2 (2–3) | 3 (2–3) | 3 (2.5–3) | 0.995e | 0.756e | 0.846f |
CHA2DS2‐VASc [pts] | 2.9±1.6 | 2.6±1.7 | 2.6±1.5 | 3.0±1.5 | 2.2±1.7 | 2.1±1.5 | 2.2±0.8 | 0.082a | 0.986a | 0.072b |
Heart rate, /min | 119.8±25.8 | 122.2±19.8 | 122.1±23.8 | 121.6±25.9 | 111.3±25.4 | 125.3±23.8 | 114.0±41.0 | 0.478a | 0.830a | 0.758b |
AF episode duration, h | 12 (5–24) | 12 (6–15) | 7 (4–18) | 10 (4–24) | 7 (4–13) | 12 (6–15) | 9.5 (8–17) | 0.051e | 0.210e | 0.449f |
Persistent AF | 13 (6.2%) | 2 (4.8%) | 0 (0.0%) | 1 (1.9%) | 0 (0.0%) | 2 (11.1%) | 0 (0.0%) | 0.007c | 0.016c | 0.086d |
Urgent hospital admission | 95 (45.2%) | 12 (28.6%) | 18 (16.5%) | 20 (37.7%) | 4 (30.8%) | 8 (44.4%) | 4 (80.0%) | <0.001c | 0.102c | <0.001d |
Arterial hypertension | 156 (74.3%) | 25 (59.5%) | 77 (70.6%) | 45 (84.9%) | 10 (76.9%) | 11 (61.1%) | 4 (80.0%) | 0.435c | 0.165c | 0.087d |
Diabetes mellitus | 40 (19.1%) | 4 (9.5%) | 17 (15.6%) | 14 (26.4%) | 2 (15.4%) | 2 (11.1%) | 0 (0.0%) | 0.422c | 0.324c | 0.299d |
CAD/PAD | 65 (30.9%) | 9 (21.4%) | 44 (40.4%) | 17 (32.1%) | 5 (38.5%) | 4 (22.2%) | 0 (0.0%) | 0.111c | 0.029c | 0.169d |
Former TIA/stroke | 11 (5.2%) | 3 (7.1%) | 5 (4.6%) | 1 (1.9%) | 0 (0.0%) | 0 (0.0%) | 0 (0.0%) | 0.786c | 0.530c | 0.756d |
TnT, pg/mL | 12 (8–21) | 9 (4–13) | 8 (7–12) | 9 (7–16) | 7 (5–10) | 8 (5–14) | 27 (7–45) | <0.001e | 0.908e | 0.001f |
eGFR, mL/min | 70.5±18.0 | 71.9±18.8 | 72.1±16.6 | 70.6±18.0 | 71.9±15.5 | 77.1±18.6 | 70.6±12.6 | 0.576a | 0.819a | 0.694b |
K+ level, mEq/L | 4.3±0.5 | 4.2±0.3 | 4.2±0.4 | 4.3±0.4 | 4.1±0.4 | 4.4±0.4 | 3.9±0.5 | 0.468a | 0.669a | 0.570b |
WBC, ×1000/μL | 7.95±2.39 | 7.27±1.63 | 7.42±2.25 | 8.38±5.55 | 7.15±1.20 | 7.36±1.58 | 7.45±4.66 | 0.038a | 0.866a | 0.237b |
Hemoglobin, g/dL | 14.1±1.6 | 14.5±1.2 | 14.5±1.5 | 14.6±1.3 | 14.6±1.4 | 14.4±1.8 | 13.5±2.3 | 0.040a | 0.583a | 0.349b |
LVEF, % | 51.6±10.6 | 54.7±8.2 | 55.0±5.9 | 51.4±8.9 | 55.4±3.6 | 52.2±9.1 | 52.0±4.5 | 0.064a | 0.662a | 0.229b |
LVEF <50% | 38 (18.1%) | 3 (7.1%) | 8 (7.3%) | 13 (24.5%) | 0 (0.0%) | 3 (16.7%) | 1 (20.0%) | 0.027c | 0.933c | 0.062d |
LAd, mm | 42.6±5.1 | 39.5±5.8 | 42.3±4.5 | 42.8±4.8 | 42.5±4.7 | 41.5±6.6 | 40.4±6.7 | 0.937a | 0.009a | 0.092b |
Electrical cardioversion | 17 (8.1%) | 4 (9.5%) | 7 (6.4%) | 5 (9.4%) | 3 (23.1%) | 3 (17.7%) | 0 (0.0%) | 0.568c | 0.485c | 0.380d |
IV potassium use | 132 (62.9%) | 29 (69.0%) | 63 (57.8%) | 32 (60.4%) | 10 (76.9%) | 12 (66.7%) | 3 (60.0%) | 0.346c | 0.226c | 0.799d |
β‐blocker use | 58 (27.6%) | 23 (54.8%) | 39 (35.8%) | 20 (37.7%) | 4 (30.8%) | 10 (55.5%) | 2 (40.0%) | 0.163c | 0.034c | 0.018d |
Successful pharmacological cardioversion | 140 (66.7%) | 33 (78.6%) | 93 (85.3%) | 29 (54.7%) | 6 (46.2%) | 11 (61.1%) | 2 (40.0%) | <0.001c | 0.317c | <0.001d |
AF indicates atrial fibrillation; bpm, beats per minute; CAD, coronary artery disease; eGFR, estimated glomerular filtration rate; EHRA, European Heart Rhythm Association; IV, intravenous; LAd, left atrial diameter; LVEF, left ventricular ejection fraction; PAD, peripheral artery disease; SCr, serum creatinine concentration; SD, standard deviation; TIA, transient ischemic attack; TnT, troponin T concentration; WBC, white blood cell count.
Student t test.
ANOVA test.
Chi‐squared test.
Multiple comparisons chi‐squared test.
Mann‐Whitney U test.
Kruskal‐Wallis test.