Efficacy of 24-week treatment with compound aspirin on platelet aggregation in patients with cardiovascular disease
Yishi Li
Abstract
Yishi Li
Abstract
Objective: To evaluate the inhibition of platelet aggregation after 24-week therapy of compound aspirin(dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin) in cardiovascular patients.Methods: A total of 103 cardiovascular patients with high platelet aggregation rate were enrolled,who needed the treatment of aspirin.They were treated with oral doses of dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin(contain 162 mg aspirin) daily for 24 weeks.Platelet aggregation was measured before and 6,12,24 weeks after administration.Results: The platelet aggregation was significantly inhibited 6,12 and 24 weeks after administration.There were significant differences in the platelet aggregation between baseline and post-treatment.The inhibition rate of platelet aggregation at 6,12,24 weeks after administration were-(20.49±22.35)%,-(28.10±22.88)%,and-(23.23±22.68)%,respectively.The platelet aggregation was inhibited at 12 weeks more than at 6 weeks follow-up,but less at 24 weeks than at 12 weeks follow-up(P0.05).Conclusion: The inhibitive effect of dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin tablet on platelet aggregation is conclusive;however,this effect is lower at 24 weeks than at 12 weeks.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To evaluate the inhibition of platelet aggregation after 24-week therapy of compound aspirin(dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin) in cardiovascular patients.Methods: A total of 103 cardiovascular patients with high platelet aggregation rate were enrolled,who needed the treatment of aspirin.They were treated with oral doses of dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin(contain 162 mg aspirin) daily for 24 weeks.Platelet aggregation was measured before and 6,12,24 weeks after administration.Results: The platelet aggregation was significantly inhibited 6,12 and 24 weeks after administration.There were significant differences in the platelet aggregation between baseline and post-treatment.The inhibition rate of platelet aggregation at 6,12,24 weeks after administration were-(20.49±22.35)%,-(28.10±22.88)%,and-(23.23±22.68)%,respectively.The platelet aggregation was inhibited at 12 weeks more than at 6 weeks follow-up,but less at 24 weeks than at 12 weeks follow-up(P0.05).Conclusion: The inhibitive effect of dihydroxyaluminum aminoacetate-heavy magnesium carbonate-aspirin tablet on platelet aggregation is conclusive;however,this effect is lower at 24 weeks than at 12 weeks.
Key concepts: Aspirin, Platelet aggregation, Platelet, Medicine, Magnesium, Oral administration, Platelet aggregation inhibitor, Internal medicine