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Comparative effect of clopidogrel and aspirin versus aspirin alone on laboratory parameters: a retrospective,
Insights
Combination therapy with clopidogrel and aspirin may lead to greater hematological adverse effects, specifically a reduction in white blood cell count, compared to aspirin monotherapy. This study evaluated laboratory parameters in patients receiving these antiplatelet agents.
Area of Science:
- Cardiovascular Medicine
- Pharmacology
- Clinical Laboratory Science
Background:
- Clopidogrel and aspirin are crucial antiplatelet agents for preventing recurrent cardiovascular events.
- Combination therapy increases hemorrhage risk, but its impact on laboratory parameters requires further study in clinical practice.
Purpose of the Study:
- To compare the effects of clopidogrel plus aspirin versus aspirin monotherapy on laboratory parameters.
- To assess changes in serum levels and hematological parameters in patients undergoing antiplatelet therapy.
Main Methods:
- Retrospective analysis of 159 clopidogrel/aspirin users and 834 aspirin monotherapy users from November 2004 to April 2011.
- Multivariable regression and propensity score adjustment were used to compare mean changes in laboratory values.
- Evaluated serum creatinine, liver enzymes, hemoglobin, hematocrit, and various blood cell counts up to two months post-initiation.
Main Results:
- Combination therapy showed a significantly greater reduction in white blood cell (WBC) count compared to aspirin alone.
- No other statistically significant differences were observed in other tested laboratory parameters between the groups.
- Clopidogrel plus aspirin increased the risk of gastrointestinal bleeding (RR 2.06-2.61).
Conclusions:
- Hematological adverse effects, particularly decreased WBC count, may be more pronounced with clopidogrel and aspirin combination therapy.
- Findings suggest careful monitoring of laboratory parameters in patients on dual antiplatelet therapy.
Background:
Clopidogrel and aspirin are antiplatelet agents that are recommended to reduce the risk of recurrent stroke and other cardiovascular events. Combination therapy of clopidogrel and aspirin has been shown to increase the risk of hemorrhage, but the effects of the drugs on laboratory parameters have not been well studied in patients in routine clinical practice. Therefore, we evaluated and compared the effects of combination therapy with clopidogrel plus aspirin and aspirin monotherapy on laboratory parameters using a clinical database.
Methods:
We used data from the Clinical Data Warehouse of Nihon University School of Medicine obtained between November 2004 and April 2011, to identify cohorts of new users (n = 159) of clopidogrel (75 mg/day) plus aspirin (100 mg/day) and new users (n = 834) of aspirin alone (100 mg/day). We used a multivariable regression model and regression adjustment with the propensity score to adjust for differences in baseline covariates between settings, and compare the mean changes in serum levels of creatinine, aspartate aminotransferase, alanine aminotransferase and hematological parameters, including hemoglobin level, hematocrit, and white blood cell (WBC), red blood cell and platelet counts up to two months after the start of study drug administration.
Results:
After adjustment, the reduction of WBC count in clopidogrel plus aspirin users was significantly greater than that in aspirin alone users. All other tests showed no statistically significant difference in the mean change from baseline to during the exposure period between clopidogrel plus aspirin users and aspirin alone users. The combination of clopidogrel and aspirin increased the risk of gastrointestinal bleeding compared with aspirin alone, with a relative risk ranging from 2.06 (95% CI, 1.02 to 4.13; p = 0.043) for the multivariate model and 2.61 (95% CI, 1.18 to 5.80; p = 0.0184) for propensity adjustment.
Conclusion:
Our findings suggested that hematological adverse effects may be greater with combination therapy of clopidogrel plus aspirin than with aspirin monotherapy.
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