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. 2023 Jun 21;109(10):2914–2925. doi: 10.1097/JS9.0000000000000566

Table 2.

Baseline and operative characteristics of patients at Stage II and III.

Characteristic Pilot study (N=20) Clinical trial (N=120) Ablation (N=97) P *
Sex, no (male/female) 20 (7/13) 120 (46/74) 97 (38/59) 0.899
Age, years 49.6±9.6 52.3±8.0 56.7±8.7 <0.001
NYHA Class III or Class IV, no. (%) 20 (100) 112 (93.3) 84 (86.6) 0.095
Atrial fibrillation duration, months 19.4±6.5 23.6±9.7 21.5±8.1 <0.001
Left ventricular ejection fraction, n (%) 57.1±8.1 60.5±8.7 61.0±9.3 0.708
Left atrial anteroposterior diameter, mm 55.0±3.3 54.8±9.3 51.5±8.3 0.007
Mitral lesion, no. (%) 20 (100) 120 (100) 89 (91.8) 0.004
Aortic lesion, no. (%) 0 58 (48.3) 52 (53.6) 0.44
Tricuspid lesion, no. (%) 0 85 (70.8) 79 (81.4) 0.071
Coronary Heart Disease, no. (%) 0 3 (2.5) 1 (1.0) 0.77
Hypertension, no. (%) 1 (5.0) 13 (10.8) 7 (7.2) 0.36
Prior cerebrovascular accident, no. (%) 0 12 (10) 9 (9.3) 0.858
Diabetes, no. (%) 1 (5.0) 5 (4.2) 6 (6.2) 0.717
Smoking history, no. (%) 2 (10.0) 25 (20.8) 11 (11.3) 0.062
Use of amiodarone, no. (%) 1 (5.0) 3 (2.5) 5 (5.2) 0.484
Use of digoxin, no. (%) 11 (55.0) 69 (57.5) 47 (48.5) 0.241
Use of beta-blocker, no. (%) 5 (25.0) 23 (19.2) 49 (50.5) <0.001
Preoperative NT-proBNP level, pg/ml 1553.2±1233.2 1482.3±1321.8 1486.7±1470.9 0.982
Preoperative creatine level, μmol/l 77.5±16.3 79.4±44.9 78.1±18.4 0.219
EuroScore I 1.8±1.6 1.8±1.4 1.8±1.5 0.842
Mitral valve procedure, no. (%)
 Mitral valve replacement 20 (100) 109 (90.8) 88 (90.7) 0.977
 Mitral valve repair 0 11 (9.2) 9 (9.3) 0.807
Aortic valve replacement, no. (%) 0 35 (29.2) 20 (20.6) 0.15
Tricuspid valve repair, no. (%) 0 38 (31.7) 33 (34.0) 0.713
CABG, no. (%) 0 3 (2.5) 0 0.325
Blood loss, ml 216.5±127.0 260.8±158.7 317.7±176.5 0.013
Extubation time, h 14.3±8.28 13.6±10.8 20.6±20.9 0.003
Total surgery time, min 221.6±33.9 230.7±48.4 284.4±47.4 <0.001
Total cardiopulmonary bypass time, min 95.5±19.0 106.8±33.4 169.3±39.1 <0.001
Aortic cross-clamp time, min 44.4±17.8 52.5±23.5 108.2±24.6 <0.001
*

P value was obtained by the comparison between clinical trial group and ablation group.