Effects of celecoxib and rofecoxib on blood pressure and edema in patients ≥65 years of age with systemic hypertension and osteoarthritis

被引:224
作者
Whelton, A
White, WB
Bello, AE
Puma, JA
Fort, JG
机构
[1] Universal Clin Res Ctr Inc, Baltimore, MD USA
[2] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[3] Univ Connecticut, Sch Med, Farmington, CT USA
[4] Illinois Bone & Joint Inst, Chicago, IL USA
[5] Heart & Vasc Ctr, Mt Airy, NC USA
[6] Duke Univ, Med Ctr, Durham, NC USA
[7] Pharmacia Corp, Peapack, NJ USA
关键词
D O I
10.1016/S0002-9149(02)02661-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Concomitant use of nonsteroidal anti-inflammatory drugs (NSAIDs), including the cyclooxygenase-2 (COX-2) specific inhibitors, with antihypertensive medication is common practice for many patients with arthritis. This study evaluated the effects of celecoxib 200 mg/day and rofecoxib 25 mg/day on blood pressure (BP) and edema in a 6-week, randomized, parallel-group, double-blind study in patients greater than or equal to65 years of age with osteoarthritis who. were treated with fixed antihypertensive regimens. One thousand ninety-two patients received study medication (celecoxib, n = 549; rofecoxib, n = 543). Significantly more patients in the rofecoxib group compared with the celecoxib group developed increased systolic BP (change >20 mm Hg plus absolute value greater than or equal to140 mm Hg) at any time point (14.9% vs 6.9%, p <0.01). Rofecoxib caused the greatest increase in systolic BP in patients receiving angiotensin-converting enzyme inhibitors or β blockers, whereas those on calcium channel antagonists or diuretic monotherapy receiving either celecoxib or rofecoxib showed no significant increases in BP. Clinically significant new-onset or worsening edema associated with weight gain developed in a greater percentage of patients in the rofecoxib group (7.7%) compared with the celecoxib group (4.7%) (p <0.05). Thus, in patients with controlled hypertension on a fixed antihypertensive regimen, careful monitoring of BP is warranted after the initiation of celecoxib or rofecoxib therapy. (C) 2002 by Excerpta Medica, Inc.
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页码:959 / 963
页数:5
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