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A multicomponent intervention incorporating CYP2C19 genotype-guided therapy and integrated pharmaceutical care
Dan Zhang1, Zhongru Meng1, Yufei Li1
1Department of Pharmacy, The First People's Hospital of Yancheng, Yancheng First Hospital Affiliated Hospital of Nanjing University Medical School, Yancheng, Jiangsu, China.
Insights
Integrating CYP2C19 genotype-guided antiplatelet therapy with pharmacist care improved medication adherence and reduced hospitalizations in ischemic stroke patients, especially high-risk individuals. This approach enhances patient outcomes without increasing adverse reactions.
Area of Science:
- Pharmacogenomics
- Clinical Pharmacy
- Stroke Medicine
Background:
- Ischemic stroke patients face challenges with antiplatelet therapy due to CYP2C19 genetic variations and poor medication adherence.
- The effectiveness of combining genetic testing with comprehensive pharmaceutical care for stroke prevention is not well-established across different risk groups.
Purpose of the Study:
- To evaluate a pharmacist-led intervention integrating CYP2C19 genotype-guided antiplatelet therapy versus routine care in ischemic stroke patients.
- To assess the impact on medication adherence, hospitalization frequency, and adverse drug reactions.
Main Methods:
- A single-center, prospective, randomized controlled trial involving 300 ischemic stroke patients.
- Intervention group received CYP2C19 genotype-guided antiplatelet therapy and pharmacist care; control group received routine care.
- Outcomes assessed included medication adherence, hospitalization rates, and adverse reactions over one year.
Main Results:
- The individualized treatment group showed significantly higher medication adherence (adjusted mean difference=0.533, p<0.001) and lower hospitalization frequency (IRR=0.700, p=0.049) compared to the control group.
- Benefits were more pronounced in high-risk patients (ESRS ≥ 3), with significantly reduced hospitalizations (IRR=0.640, p=0.033).
- No significant difference in adverse reactions was observed between groups (OR=0.543, p=0.072).
Conclusions:
- A multicomponent intervention combining CYP2C19 genotype-guided therapy and pharmacist care improves adherence and reduces hospitalizations in ischemic stroke patients.
- High-risk patients experienced the most significant benefits in reducing hospitalizations.
- The intervention enhanced outcomes without increasing adverse drug reactions, though the specific contribution of genotyping alone requires further study.
Background:
In ischemic stroke patients, antiplatelet therapy faces challenges from CYP2C19 genetic variability and poor post-discharge medication adherence, yet the value of integrating genotyping with comprehensive pharmaceutical care remains unclear across different recurrence risk populations.
Methods:
This single-center, prospective, parallel-group, open-label, assessor-blinded randomized controlled trial enrolled 300 ischemic stroke patients to evaluate a complex pharmacist-led intervention incorporating CYP2C19 genotype-guided antiplatelet therapy (individualized group, n = 150) versus routine care (control group, n = 150).
Results:
In the individualized treatment group, the proportion of patients with intermediate or poor CYP2C19 metabolizer phenotypes who received antiplatelet therapy adjustments was significantly higher (48.72 and 77.27% vs. 10.00%, p < 0.001), and genotype was positively correlated with medication adjustment (ρ = 0.476, p < 0.001). After 1 year, negative binomial regression showed that the individualized group had significantly lower hospitalization frequency than the control group (IRR = 0.700, 95% CI: 0.491-0.999, p = 0.049), and ANCOVA revealed significantly higher medication adherence (adjusted mean difference = 0.533, 95% CI: 0.250-0.815, p < 0.001). Subgroup analysis stratified by ESRS score showed that the beneficial effect of individualized treatment on reducing hospitalization was more pronounced in high-risk patients (ESRS ≥ 3: IRR = 0.640, 95% CI: 0.425-0.965, p = 0.033), whereas the effect in the low-risk group (ESRS < 3) did not reach statistical significance. After multivariable adjustment, the between-group difference in adverse reactions was not statistically significant (OR = 0.543, 95% CI: 0.279-1.057, p = 0.072).
Conclusion:
A multicomponent intervention comprising CYP2C19 genotype-guided therapy and intensive pharmacist-led integrated pharmaceutical care significantly improved medication adherence and reduced hospitalization frequency, with more pronounced benefits observed in patients at high risk of stroke recurrence, without increasing the risk of adverse drug reactions. However, the specific contribution of genotyping alone cannot be isolated from the overall care package.
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