Results of a Meta-Analysis Comparing the Tolerability of Lercanidipine and Other Dihydropyridine Calcium Channel Blockers

被引:31
|
作者
Makarounas-Kirchmann, Kelly [1 ,2 ]
Glover-Koudounas, Sophie [3 ]
Ferrari, Paolo [4 ,5 ]
机构
[1] KMC Hlth Care, Frankston, Vic, Australia
[2] Monash Univ, Dept Epidemiol & Prevent Med, Melbourne, Vic 3004, Australia
[3] Solvay Pharmaceut Australia, Pymble, NSW, Australia
[4] Fremantle Hosp, Dept Nephrol, Perth, WA, Australia
[5] Univ Western Australia, Sch Med & Pharmacol, Perth, WA 6009, Australia
关键词
calcium channel blocker; dihydropyridines; lercanidipine; edema; adverse events; tolerability; GASTROINTESTINAL THERAPEUTIC SYSTEM; ANTIHYPERTENSIVE DRUGS; HYPERTENSIVE PATIENTS; PERSISTENCE; LACIDIPINE; NIFEDIPINE; AMLODIPINE; PRESSURE; AGENTS;
D O I
10.1016/j.clinthera.2009.08.010
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Results from clinical studies suggest that the dihydropyridine calcium channel blocker (CCB) lercanidipine may be associated with a lower incidence of peripheral edema than are older dihydropyridine CCBs. Objective: The objective of the present study was to conduct a meta-analysis of published data from randomized controlled trials (RCTs) to assess the relative risk (RR) of dihydropyridine CCB-specific adverse events with lercanidipine versus the older dihydropyridine CCBs (first generation: amlodipine, felodipine, and nifedipine), and versus the other lipophilic dihydropyridine CCBs (second generation: lacidipine and manidipine). Methods: A systematic literature search (all years through August 11, 2008) of MEDLINE, EMBASE, and the Cochrane Library was conducted for English-language reports of single- or double-blind RCTs of >= 4 weeks' duration that compared the tolerability of lercanidipine with other dihydropyridine CCBs in participants with mild (140-159/90-99 mm Hg) to moderate (160-179/100-109 mm Hg) hypertension. Results: Eight RCTs (6 used first-generation drugs, and 4 used second-generation drugs) met the criteria for inclusion. Efficacy outcomes for lowering blood pressure did not differ statistically between lercanidipine and either generation of medications. Compared with the first generation, lercanidipine was associated with a reduced risk of peripheral edema (52/742 with lercanidipine vs 88/627 with first generation; RR = 0.44 [95% CI, 0.31-0.62]), but not flushing or headache. The frequency of peripheral edema, flushing, and headache did not differ statistically between lercanidipine and the second-generation drugs. Study participants were less likely to withdraw from the RCTs because of peripheral edema (RR = 0.24 [95% CI, 0.12-0.47]) or any adverse event (RR = 0.51 [95% CI, 0.33-0.77]) when treated with lercanidipine rather than a drug from the first generation, but not when treated with lercanidipine rather than second-generation drugs. Conclusion: In this meta-analysis, lercanidipine was associated with a lower risk of peripheral edema and a lower risk of treatment withdrawal because of peripheral edema than were the first-generation, but not the second-generation, dihydropyridine CCBs. (Clin Ther. 2009;31:1652-1663) (C) 2009 Excerpta Medica Inc.
引用
收藏
页码:1652 / 1663
页数:12
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