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Rapid health technology assessment of baloxavir marboxil in the treatment of influenza / 中国药房
China Pharmacy ; (12): 2402-2408, 2023.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-996399
Responsible library: WPRO
ABSTRACT
OBJECTIVE To evaluate the effectivenesssafety and economy of baloxavir marboxil in the treatment of influenza, and to provide evidence-based reference for the introduction of new drugs in hospitals and clinical medication decisions. METHODS Retrieved from PubMed, Embase, Web of Science, Cochrane Library, Epistemonikos, CBM, CNKI, VIP, Wanfang database, official websites and relevant databases of health technology assessment (HTA) institutions, the results of the included studies were descriptively analyzed after literature screening, data extraction and quality evaluation. RESULTS A total of 11 studies were included, involving 6 systematic reviews/meta-analyses and 5 pharmacoeconomic studies. Compared with placebo, baloxavir marboxil significantly shortened the time to alleviation of symptoms (TTAS) and time to resolution of fever (TTRF), reduced the virus titer change from baseline at 24 h and 48 h after treatment and the incidence of bronchitis, with statistical significance (P< 0.05). Compared with neuraminidase inhibitors (NAIs), there were no significant differences in shortening TTRF and reducing the incidence of complicationspneumonia and bronchitis (P>0.05). The majority of studies suggested that there were no significant differences in shortening TTAS (P>0.05). Only very low-quality literature suggested that baloxavir marboxil could significantly reduce the virus titer change from baseline at 24 h and 48 h after treatment. In terms of safety, the incidences of adverse events (AEs) and drug-related adverse events (DRAEs) induced by baloxavir marboxil showed no significant differences, compared with peramivir and zanamivir (P>0.05). Some studies considered that the incidences of AEs and DRAEs with baloxavir marboxil were lower than placebo, oseltamivir and laninamivir. Compared with oseltamivir in China and laninamivir in Japan, baloxavir marboxil showed cost-effectiveness advantages. CONCLUSIONS Compared with placebo, baloxavir marboxil has good efficacysafety and economy. Compared with NAIs (oseltamivir), baloxavir marboxil has good economic advantages in China, but further high-quality studies are still needed regarding its safety and efficacy.

Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.8 Achieve universal access to health Database: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 2023 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being Health problem: Target 3.8 Achieve universal access to health Database: WPRIM (Western Pacific) Language: Chinese Journal: China Pharmacy Year: 2023 Document type: Article
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