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. 2008 Dec 5;10(12):930–935. doi: 10.1111/j.1751-7176.2008.00050.x

Table II.

 Patients’ Distribution According to Number and Class of Additional Antihypertensive Drugs Being Taken at Each Time Point of BP Determination (1 or 2 and 12 Weeks of Treatment)

Early BP Determination Group Standard BP Determination Group
1 Week (n=331) 12 Weeks (n=186) 2 Weeks (n=1890) 12 Weeks (n=1372)
No.
 0 330 (99.7) 161 (86.6) 1856 (98.2) 1187 (86.5)
 1 1 (0.3) 20 (10.8) 33 (1.7) 163 (11.9)
 2 0 (0.0) 5 (2.7) 1 (0.1) 21 (1.5)
 3 0 (0.0) 0 (0.0) 0 (0.0) 1 (0.1)
 ≥4 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
Class
 Diuretic 0 (0.0) 5 (2.7) 9 (0.5) 35 (2.6)
 α‐Blocker 0 (0.0) 2 (1.1) 1 (0.1) 10 (0.7)
 β‐Blocker 0 (0.0) 1 (0.5) 1 (0.1) 14 (1.0)
 CCB 1 (0.3) 20 (10.8) 23 (1.2) 144 (10.5)
 ACE inhibitor 0 (0.0) 0 (0.0) 1 (0.1) 4 (0.3)
 ARB 0 (0.0) 0 (0.0) 0 (0.0) 0 (0.0)
 Other 0 (0.0) 2 (1.1) 0 (0.0) 0 (0.0)

Abbreviations: ACE, angiotensin‐converting enzyme; ARB, angiotensin II type 1 receptor blocker; BP, blood pressure; CCB, calcium channel blocker. Values are No. (%). The patients’ distribution represents that in 1 day prior to BP determination at 1, 2, and 12 weeks.