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Evaluation of clinical application of the acceptance drug Levetiracetam Tablets volume-based procurement |
YANG Li1,2 DONG Xianzhe1 CUI Xiaohui1 LU Song2 LIU Wenna1 LI Lin1 YUE Xiaolin1 ZHANG Lan1 |
1.Department of Pharmacy, Xuanwu Hospital, Capital Medical University, Beijing 100053, China;
2.College of Pharmacy, Zunyi Medical University, Guizhou Province, Zunyi 563000, China |
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Abstract Objective To preliminarily evaluate the clinical application consistency of the volume-based procurement of Jiyike of Levetiracetam (LEV) Tablets and Keppra from original LEV tablets based on prescription data. Methods Retrospective analysis was made on the prescription data of patients who used Jiyike and Keppra in outpatient department of Xuanwu Hospital, Capital Medical University before the implementation of the volume-based policy (March 2018 to January 2019) and after the implementation of the volume-based policy (March 2019 to January 2020). According to the 1∶1 nearest-neighbor propensity score matching method, the medication possession ratio, the continuous single drug use rate, the rate of continuous treatment for 3, 6 and 9 months, the abnormal upregulation rate of continuous treatment dose, and the continuous use rate after the first diagnosis were counted, and the drug replacement situation of the two was compared. The drug costs of Keppra and Jiyike after the implementation of the volume-based policy and the drug costs of LEV before and after the implementation of the volume-based policy were compared. Results There were no significant differences in the proportion of patients with ≥80%medication possession ratio between Jiyike group and Keppra group (P > 0.05). The proportion of patients in Keppra group was higher than that in Jiyike group after 3, 6 and 9 months of continuous treatment (P < 0.05). The abnormal upregulation rate of continuous treatment dose and continuous single drug use rate in Keppra group was significantly higher than that in Jiyike group (P < 0.05). There was no significant difference in the continuous use rate between the two groups after the first diagnosis (P > 0.05). There was no statistical significance in drug replacement between Jiyike group and Keppra group (P > 0.05). The per capita annual drug cost in Jiyike group was lower than that in Keppra group, the difference was statistically significant (P < 0.05). The per capita annual cost of LEV after the implementation of the volume-based policy was significantly lower than that before the implementation of the volume-based policy, with statistical significance (P < 0.05). Conclusion The clinical application of Jiyike and Keppra is basically the same, and it can reduce the economic burden of patients to a large extent.
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