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氯吡格雷对健康志愿者中萘普生所致胃肠道失血的影响。

Effect of clopidogrel on naproxen-induced gastrointestinal blood loss in healthy volunteers.

作者信息

van Hecken A, Depré M, Wynants K, Vanbilloen H, Verbruggen A, Arnout J, Vanhove P, Cariou R, De Schepper P J

机构信息

Centre for Clinical Pharmacology, UZ Gasthuisberg, K.U.Leuven, Belgium.

出版信息

Drug Metabol Drug Interact. 1998;14(3):193-205. doi: 10.1515/dmdi.1998.14.3.193.

Abstract

The effect of clopidogrel, a potent inhibitor of platelet aggregation, on naproxen-induced faecal blood loss was investigated in 30 healthy volunteers in a randomized, double-blind, placebo-controlled, two parallel treatment groups study. All subjects first received naproxen 250 mg b.i.d. during 7 days, after which they were randomly allocated to additionally receive either clopidogrel 75 mg once daily (n = 15) or matching placebo (n = 15) for 11 days. Faecal blood loss was measured by the 51Cr-labelled erythrocyte method during the last four days of each of the four study periods, i.e. baseline, treatment with naproxen alone, combined treatment and wash-out. Mean daily faecal blood loss was below 0.5 ml/day during the baseline period in both treatment groups and increased during treatment with naproxen alone to (mean +/- SD) 1.14 +/- 0.58 ml/day in the naproxen + placebo group and to 1.93 +/- 1.51 ml/day in the naproxen + clopidogrel group. Addition of clopidogrel to naproxen treatment was associated with an increase of the mean daily blood loss to 6.83 +/- 9.32 ml/day, which was statistically significantly higher than 1.75 +/- 1.40 ml/day observed during treatment with naproxen + placebo. During the wash-out period, mean daily blood loss decreased to 0.98 +/- 0.51 ml/day in the naproxen + placebo group and to 1.07 +/- 0.46 ml/day in the naproxen + clopidogrel group. Based on these results, it can be concluded that clopidogrel increases naproxen-induced gastrointestinal blood loss in healthy volunteers. Caution should therefore be called for when these drugs are coadministered.

摘要

在一项随机、双盲、安慰剂对照、两个平行治疗组的研究中,对30名健康志愿者研究了血小板聚集强效抑制剂氯吡格雷对萘普生所致粪便失血的影响。所有受试者首先在7天内每日两次服用250 mg萘普生,之后他们被随机分配额外接受每日一次75 mg氯吡格雷(n = 15)或匹配的安慰剂(n = 15),持续11天。在四个研究阶段的每个阶段的最后四天,即基线期、单独使用萘普生治疗期、联合治疗期和洗脱期,采用51Cr标记红细胞法测量粪便失血量。在两个治疗组的基线期,平均每日粪便失血量均低于0.5 ml/天,在单独使用萘普生治疗期间增加,在萘普生+安慰剂组增加至(均值±标准差)1.14±0.58 ml/天,在萘普生+氯吡格雷组增加至1.93±1.51 ml/天。在萘普生治疗中加用氯吡格雷使平均每日失血量增加至6.83±9.32 ml/天,这在统计学上显著高于萘普生+安慰剂治疗期间观察到的1.75±1.40 ml/天。在洗脱期,萘普生+安慰剂组的平均每日失血量降至0.98±0.51 ml/天,萘普生+氯吡格雷组降至1.07±0.46 ml/天。基于这些结果,可以得出结论,氯吡格雷会增加健康志愿者中萘普生所致的胃肠道失血。因此,当联合使用这些药物时应谨慎。

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