Danqi Piantan Jiaonang does not modify hemostasis, hematology, and biochemistry in normal subjects and stroke patients

被引:37
作者
Gan, Robert [1 ]
Lambert, Caroline [2 ]
Jiao Lianting [6 ]
Chan, Edwin S. Y. [3 ]
Venketasubramanian, N. [1 ]
Chen, Christopher [4 ]
Chan, Bernard P. L. [5 ]
Samama, Michel Meyer [7 ]
Bousser, Marie Germaine [8 ]
机构
[1] Natl Inst Neurosci, Dept Neurol, Singapore 308433, Singapore
[2] Moleac Pte Ltd, Singapore, Singapore
[3] Evidence Based Med Clin Trials & Epidemiol Res Un, Singapore, Singapore
[4] Natl Univ Singapore, Dept Pharmacol, Singapore 117548, Singapore
[5] Natl Univ Singapore Hosp, Div Neurol, Singapore 117548, Singapore
[6] Tianjin Univ Tradit Chinese Med, Teaching Hosp 1, Biol Lab, Tianjin, Peoples R China
[7] Hotel Dieu Univ Hosp, APHP, Dept Hematol, Paris, France
[8] Paris Diderot Univ, Fac Med, Lariboisiere Hosp, Dept Neurol, Paris, France
关键词
Danqi Piantan Jiaonang; stroke; traditional Chinese medicine; safety studies;
D O I
10.1159/000126919
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Objective: Previous studies on Danqi Piantan Jiaonang (DPJ, NeuroAid (R)), a traditional Chinese medicine, in stroke patients showed promising results. Our aim was to determine the safety of DPJ in normal subjects and stroke patients through a series of studies assessing its immediate and long-term effects, alone and in combination with aspirin, on hematological, hemostatic, and biochemical parameters. Methods: We conducted 3 studies from December 2004 to May 2006. Study 1 was a case series which recruited 32 healthy volunteers who were given 2 oral doses of 4 DPJ capsules (0.4 g/capsule) 6 h apart. Study 2 was a randomized controlled trial of 22 healthy volunteers who received either 1 oral dose of aspirin 300 mg alone or a combination of 1 dose of aspirin 300 mg and 2 doses of 4 DPJ capsules taken 6 h apart. For both studies 1 and 2, hemostatic parameters (prothrombin time, activated partial thromboplastin time, fibrinogen, platelet aggregation, D-dimer) were tested at baseline, and after 2 and 8 h. Study 3 was a case series which recruited 10 patients with recent ischemic stroke (within 7 days) who were given 4 DPJ capsules taken orally 3 times a day for 1 month. Blood tests for hemostatic, hematological (complete blood count), and biochemical parameters (glucose, creatinine, alanine aminotransferase, aspartate transaminase, C-reactive protein) were performed at baseline, and after 1 and 4 weeks. Results: Apart from the expected changes in platelet aggregation in subjects taking aspirin, no significant differences were detected in hemostatic parameters at baseline, and 2 and 8 h after oral intake of DPJ alone or in combination with aspirin. Likewise, no significant differences were observed in hematological, hemostatic, and biochemical parameters at baseline, and after 1 and 4 weeks of oral intake of DPJ. Conclusion: DPJ does not significantly modify hematological, hemostatic, and biochemical parameters in normal subjects and stroke patients. Copyright (C) 2008 S. Karger AG, Basel.
引用
收藏
页码:450 / 456
页数:7
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