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尼莫地平。老年人中药物相互作用的可能性。

Nimodipine. Potential for drug-drug interactions in the elderly.

作者信息

Mück W, Ahr G, Kuhlmann J

机构信息

Institute of Clinical Pharmacology International, Bayer AG, Wuppertal, Germany.

出版信息

Drugs Aging. 1995 Mar;6(3):229-42. doi: 10.2165/00002512-199506030-00006.

Abstract

Nimodipine is indicated for a variety of conditions in elderly patients. Elderly patients often have multiple morbidity and receive treatment with a variety of drugs. Therefore, it is important to investigate the possible pharmacokinetic and pharmacodynamic interactions of nimodipine with various drugs commonly prescribed for elderly patients. There were no clinically relevant interactions of nimodipine with any of the following specific agents studied: the antiarrhythmics mexiletine, propafenone, disopyramide or quinidine, digoxin, the beta-adrenoceptor antagonists propranolol or atenolol, nifedipine, warfarin, diazepam, indomethacin, ranitidine or glibenclamide (glyburide). However, there were some notable interactions. In epileptic patients taking the anticonvulsants carbamazepine, phenobarbital (phenobarbitone) and/or phenytoin, there was a 7-fold decrease in the area under the plasma concentration versus time curve (AUC) and an 8- to 10-fold decrease in the maximum plasma concentration of nimodipine. These effects were to be expected, considering the hepatic enzyme-inducing properties of these anticonvulsant drugs. Therefore concomitant use of these agents with oral nimodipine is not recommended. In contrast, epileptic patients treated with nimodipine and valproic acid (sodium valproate) showed an increase in both the AUC (approximately 50%) and maximum plasma concentrations (approximately 30%) of nimodipine, which may be explained by valproic acid inhibiting the presystemic oxidative metabolism of nimodipine. Concomitant administration of cimetidine produced an approximate doubling of the bioavailability of nimodipine. This again was to be expected, considering the known inhibitory effect of cimetidine on cytochrome P450. However, no changes in haemodynamics, clinical or laboratory status or tolerability were observed, and dose adjustment did not appear to be clinically necessary.

摘要

尼莫地平适用于老年患者的多种病症。老年患者常患有多种疾病,并接受多种药物治疗。因此,研究尼莫地平与老年患者常用的各种药物之间可能存在的药代动力学和药效学相互作用具有重要意义。尼莫地平与以下任何一种特定药物之间均未发现具有临床相关性的相互作用:抗心律失常药美西律、普罗帕酮、丙吡胺或奎尼丁、地高辛、β肾上腺素受体拮抗剂普萘洛尔或阿替洛尔、硝苯地平、华法林、地西泮、吲哚美辛、雷尼替丁或格列本脲(优降糖)。然而,也存在一些值得注意的相互作用。在服用抗惊厥药卡马西平、苯巴比妥和/或苯妥英的癫痫患者中,尼莫地平的血浆浓度-时间曲线下面积(AUC)降低了7倍,最大血浆浓度降低了8至10倍。考虑到这些抗惊厥药物的肝酶诱导特性,这些作用是可以预期的。因此,不建议这些药物与口服尼莫地平同时使用。相比之下,接受尼莫地平和丙戊酸(丙戊酸钠)治疗的癫痫患者,尼莫地平的AUC(约50%)和最大血浆浓度(约30%)均有所增加,这可能是因为丙戊酸抑制了尼莫地平的首过氧化代谢。西咪替丁的同时给药使尼莫地平的生物利用度增加了约一倍。考虑到西咪替丁对细胞色素P450的已知抑制作用,这同样是可以预期的。然而,未观察到血流动力学、临床或实验室状态或耐受性的变化,且似乎没有临床必要进行剂量调整。

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