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. 2021 Sep 2;24(4):552–564. doi: 10.1093/europace/euab200

Table 1.

Cardiovascular therapies given to patients in the EAST-AFNET 4 trial at discharge from the baseline visit, at 12 months follow-up, and at 24 months follow-up

Randomized group
Early rhythm control (N = 1395) Usual care (N = 1394) Total (N = 2789) P-value
Patients receiving oral anticoagulation
 Anticoagulation (discharge from baseline) 1267/1389 (91.2%) 1250/1393 (89.7%) 2517/2782 (90.5%) 0.149
 NOACs (discharge from BL) 800/1389 (57.6%) 763/1393 (54.8%) 1563/2782 (56.2%) 0.103
 Vitamin K antagonists (discharge from BL) 467/1389 (33.6%) 490/1393 (35.2%) 957/2782 (34.4%) 0.397
 Anticoagulation (12 months FU) 1087/1230 (88.4%) 1121/1241 (90.3%) 2208/2471 (89.4%) 0.111
 NOACs (12 months FU) 713/1230 (58.0%) 704/1241 (56.7%) 1417/2471 (57.3%) 0.657
 Vitamin K antagonists (12 months FU) 376/1230 (30.6%) 421/1241 (33.9%) 797/2471 (32.3%) 0.100
 Anticoagulation (24 months FU) 1020/1159 (88.0%) 1065/1171 (90.9%) 2085/2330 (89.5%) 0.021
 NOACs (24 months FU) 690/1159 (59.5%) 699/1171 (59.7%) 1389/2330 (59.6%) 0.774
 Vitamin K antagonists (24 months FU) 330/1159 (28.5%) 366/1171 (31.3%) 696/2330 (29.9%) 0.202
Patients receiving rate control therapy (beta adrenoreceptor blocker, verapamil, diltiazem, or digitalis glycosides)
 Rate control (discharge from BL) 1088/1389 (78.3%) 1235/1393 (88.7%) 2323/2782 (83.5%) <0.001
 Rate control (12 months FU) 883/1230 (71.8%) 1055/1241 (85.0%) 1938/2471 (78.4%) <0.001
 Rate control (24 months FU) 799/1159 (68.9%) 986/1171 (84.2%) 1785/2330 (76.6%) <0.001
Patients receiving any rate controlling medication (beta adrenoreceptor blocker, verapamil, diltiazem, digitalis glycosides, or antiarrhythmic drugs with rate controlling propertiesa)
 Patients receiving any rate controlling medication (discharge from BL) 1259/1389 (90.6%) 1250/1393 (89.7%) 2509/2782 (90.2%) 0.382
 Patients receiving any rate controlling medication (12 months FU) 1065/1230 (86.6%) 1084/1241 (87.3%) 2149/2471 (87.0%) 0.588
 Patients receiving any rate controlling medication (24 months FU) 968/1159 (83.5%) 1013/1171 (86.5%) 1981/2330 (85.0%) 0.042
Patients receiving diuretics
 Diuretics (discharge from BL) 559/1389 (40.2%) 561/1393 (40.3%) 1120/2782 (40.3%) 0.987
 Diuretics (12 months FU) 508/1230 (41.3%) 521/1241 (42.0%) 1029/2471 (41.6%) 0.788
 Diuretics (24 months FU) 478/1159 (41.2%) 507/1171 (43.3%) 985/2330 (42.3%) 0.299
Patients receiving heart failure and antihypertensive therapy (ACE inhibitor, angiotensin receptor blocker, mineralocorticoid antagonists, and neprilysin/valsartan)
 Heart failure and antihypertensive therapies (discharge from BL) 964/1389 (69.4%) 988/1393 (70.9%) 1952/2782 (70.2%) 0.397
 Heart failure and antihypertensive therapies (12 months FU) 854/1230 (69.4%) 878/1241 (70.7%) 1732/2471 (70.1%) 0.482
 Heart failure and antihypertensive therapies (24 months FU) 798/1159 (68.9%) 837/1171 (71.5%) 1635/2330 (70.2%) 0.163
Patients receiving diabetes therapy (oral antidiabetic medication and insulin)
 Antidiabetic therapy (discharge from BL) 256/1389 (18.4%) 254/1393 (18.2%) 510/2782 (18.3%) 0.873
 Antidiabetic therapy (12 months FU) 238/1230 (19.3%) 237/1241 (19.1%) 475/2471 (19.2%) 0.870
 Antidiabetic therapy (24 months FU) 228/1159 (19.7%) 227/1171 (19.4%) 455/2330 (19.5%) 0.924
Patients receiving statins
 Statins (discharge from BL) 628/1389 (45.2%) 568/1393 (40.8%) 1196/2782 (43.0%) 0.016
 Statins (12 months FU) 587/1230 (47.7%) 526/1241 (42.4%) 1113/2471 (45.0%) 0.006
 Statins (24 months FU) 576/1159 (49.7%) 529/1171 (45.2%) 1105/2330 (47.4%) 0.020

All patient numbers are given split by randomized group and in total. Proportions indicate proportions of patients receiving each therapy at each time point as a fraction of the totality of patients still in follow-up and with available medication information at that time point. Anticoagulation, therapy with heart failure and antihypertensive drugs, antidiabetic therapy, and rate control therapy were used in most patients.

ACE inhibitor, angiotensin-converting enzyme inhibitor; BL, baseline visit; FU, follow-up; NOAC, novel oral anticoagulant.

a

Antiarrhythmic drugs with rate controlling properties are amiodarone, dronedarone, propafenone, and sotalol. P-values resulting from mixed logistic regression with centre as random effect.