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. 2022 Mar 29;11(7):e023776. doi: 10.1161/JAHA.121.023776

Table 4.

Clinical Outcomes at 2 Years According to Various Usage Pattern of Vasodilator

Overall

(n=1895)

No vasodilator

(n=359)

Vasodilator P value*

Nonnitrate

vasodilator

(n=1187)

Conventional

nitrate

(n=209)

Combination

(n=140)

Primary end point 89 (4.7) 18 (5.0) 44 (3.7) 15 (7.2) 12 (8.6) 0.017
Cardiac death 4 (0.2) 2 (0.6) 2 (0.2) 0 0 0.410
Acute coronary syndrome 58 (3.1) 8 (2.2) 25 (2.1) 13 (6.2) 12 (8.6) <0.001
Non–ST‐segment–elevation myocardial infarction 4 (0.2) 0 1 (0.1) 1 (0.5) 2 (1.4) 0.007
Unstable angina 54 (2.8) 8 (2.2) 24 (2.0) 12 (5.7) 10 (7.1) <0.001
Arrhythmia 31 (1.6) 9 (2.5) 20 (1.7) 2 (1.0) 0 0.200
Atrial fibrillation 10 (0.5) 3 (0.8) 7 (0.6) 0 0 0.460
Atrioventricular block 7 (0.4) 4 (1.1) 2 (0.2) 1 (0.5) 0 0.063
ventricular tachycardia or ventricular fibrillation 7 (0.4) 0 6 (0.5) 1 (0.5) 0 0.473
Cardiac arrest 3 (0.2) 1 (0.3) 2 (0.2) 0 0 0.828
All‐cause death 13 (0.7) 6 (1.7) 5 (0.4) 0 2 (1.4) 0.030
Rehospitalization 295 (15.6) 53 (14.8) 187 (15.8) 29 (13.9) 26 (18.6) 0.654
Medication change § 1172 (62.7) 203 (60.8) 747 (62.9) 132 (63.2) 90 (64.7) 0.844

Values are expressed as n (%).

*

The P values are derived from the chi‐square test for group comparison.

The primary end point was a composite of cardiac death, acute coronary syndrome, and new‐onset arrhythmia.

There was no ST‐segment–elevation myocardial infarction in all groups.

§

Data for medication change were available in 334 (93.0%) with no vasodilator group, 1187 (100%) with nonnitrate vasodilator group, 209 (100%) with conventional nitrate group, and 139 (99.3%) with combination group.