Comparison of Hospitalization Incidence in Influenza Outpatients Treated With Baloxavir Marboxil or Neuraminidase Inhibitors: A Health Insurance Claims Database Study

Author:

Komeda Takuji1,Takazono Takahiro23ORCID,Hosogaya Naoki24,Miyazaki Taiga23,Ogura Eriko5,Iwata Shinpei1,Miyauchi Hideyuki1,Honda Keiichi1,Fujiwara Masakazu6,Ajisawa Yoshikazu7,Watanabe Hideaki7,Kitanishi Yoshitake6,Hara Kanae8,Mukae Hiroshi29

Affiliation:

1. PMS & Pharmacoepidemiology Department, Shionogi Pharmacovigilance Center Co, Ltd, Osaka, Japan

2. Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan

3. Department of Infectious Diseases, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

4. Nagasaki University Hospital, Clinical Research Center, Nagasaki, Japan

5. Global Development Division, Shionogi & Co, Ltd, Osaka, Japan

6. Data Science Office, Shionogi & Co, Ltd, Osaka, Japan

7. Biostatistics Center, Shionogi & Co, Ltd, Osaka, Japan

8. Pharmacovigilance Department, Shionogi & Co, Ltd, Osaka, Japan

9. Department of Respiratory Medicine, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

Abstract

Abstract Background Baloxavir marboxil (baloxavir) is a single-dose, oral antiinfluenza drug with a novel mechanism of action. We compared the incidence of hospitalization in patients treated with baloxavir vs neuraminidase inhibitors. Methods In this retrospective, observational, cohort study, we used real-world patient data extracted from a Japanese health insurance claims database. The enrollment period was 1 October 2018 to 17 April 2019. On day 1, eligible patients (N = 339 007) received baloxavir, oseltamivir, zanamivir, or laninamivir. Baseline characteristics were standardized using the inverse probability of treatment weighting method. The primary end point was the incidence of hospitalization (days 2–14). Secondary end points included antibacterial use, secondary pneumonia, and additional antiinfluenza drug use. Results Compared with the baloxavir group, the incidence of hospitalization was greater in the oseltamivir group (risk ratio [RR] and 95% confidence interval [CI], 1.41 [1.00–2.00]; risk difference [RD] and 95% CI, 0.06 [.01–.12]) and zanamivir group (RR, 1.85 [1.23–2.78]; RD, 0.11 [.02–.20]). Oseltamivir-treated patients were less likely to require antibacterials than baloxavir-treated patients (RR, 0.87 [.82–.91]). However, oseltamivir-treated patients were more likely to be hospitalized with antibacterials (RR, 1.70 [1.21–2.38]) or antibacterial injection (RR, 1.67 [1.17–2.38]) than baloxavir-treated patients (post hoc analysis). Compared with baloxavir-treated patients, additional antiinfluenza drug use was greater in oseltamivir-, zanamivir-, and laninamivir-treated patients (RR, 1.51 [1.05–2.18], 2.84 [2.04–3.96], and 1.68 [1.35–2.10], respectively). Conclusions Baloxavir is an efficacious antiinfluenza treatment that may reduce hospitalization compared with oseltamivir and zanamivir. Clinical Trials Registration University hospital Medical Information Network Clinical Trials Registry (UMIN000038159).

Funder

Shionogi

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Microbiology (medical)

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