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Real-World Effectiveness of Ensitrelvir in Reducing Severe Outcomes in Outpatients at High Risk for COVID-19.
Takazono, Takahiro; Fujita, Satoki; Komeda, Takuji; Miyazawa, Shogo; Yoshida, Yuki; Kitanishi, Yoshitake; Kinoshita, Masahiro; Kojima, Satoshi; Shen, Huilian; Uehara, Takeki; Hosogaya, Naoki; Iwanaga, Naoki; Mukae, Hiroshi.
Affiliation
  • Takazono T; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Fujita S; Data Science Department, Shionogi & Co., Ltd., 4F, Midosuji MTR Bldg., 3-6-3, Awajimachi, Chuo-ku, Osaka, 541-0047, Japan. satoki.fujita@shionogi.co.jp.
  • Komeda T; Data Science Department, Shionogi & Co., Ltd., 4F, Midosuji MTR Bldg., 3-6-3, Awajimachi, Chuo-ku, Osaka, 541-0047, Japan.
  • Miyazawa S; Data Science Department, Shionogi & Co., Ltd., 4F, Midosuji MTR Bldg., 3-6-3, Awajimachi, Chuo-ku, Osaka, 541-0047, Japan.
  • Yoshida Y; Data Science Department, Shionogi & Co., Ltd., 4F, Midosuji MTR Bldg., 3-6-3, Awajimachi, Chuo-ku, Osaka, 541-0047, Japan.
  • Kitanishi Y; Data Science Department, Shionogi & Co., Ltd., 4F, Midosuji MTR Bldg., 3-6-3, Awajimachi, Chuo-ku, Osaka, 541-0047, Japan.
  • Kinoshita M; Medical Affairs Department, Shionogi & Co., Ltd., Osaka, Japan.
  • Kojima S; Medical Affairs Department, Shionogi & Co., Ltd., Osaka, Japan.
  • Shen H; Medical Affairs Department, Shionogi & Co., Ltd., Osaka, Japan.
  • Uehara T; Drug Development and Regulatory Science Division, Shionogi & Co., Ltd., Osaka, Japan.
  • Hosogaya N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Iwanaga N; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
  • Mukae H; Department of Respiratory Medicine, Nagasaki University Hospital, Nagasaki, Japan.
Infect Dis Ther ; 13(8): 1821-1833, 2024 Aug.
Article in En | MEDLINE | ID: mdl-38941067
ABSTRACT

INTRODUCTION:

This study aimed to evaluate the effectiveness of ensitrelvir, an oral antiviral, in reducing hospitalization risk in outpatients at high-risk for severe COVID-19 during the Omicron era.

METHODS:

This was a retrospective study using a large Japanese health insurance claims database. It included high-risk outpatients for severe symptoms who received their first COVID-19 diagnosis between November 2022 and July 2023. The study included outpatients aged ≥ 18 years. The primary endpoint was all-cause hospitalization during the 4-week period from the date of outpatient diagnosis and medication, comparing the ensitrelvir group (n = 5177) and the no antiviral treatment group (n = 162,133). The risk ratio and risk difference were evaluated after adjusting patient background distribution by the inverse probability of treatment weight (IPTW) method. Secondary endpoints were incidence of respiratory and heart rate monitoring, oxygen therapy, ventilator use, intensive care admission, and all-cause death.

RESULTS:

The risk ratio for all-cause hospitalization between the ensitrelvir group (n = 167,385) and the no antiviral treatment group (n = 167,310) after IPTW adjustment was 0.629 [95% confidence interval (CI) 0.420, 0.943]. The risk difference was - 0.291 [95% CI - 0.494, - 0.088]. The incidence of both respiratory and heart rate monitoring and oxygen therapy was lower in the ensitrelvir group. Ventilator use, intensive care admission, and all-cause death were difficult to assess because of the limited events.

CONCLUSIONS:

The incidence of all-cause hospitalization was significantly lower in the ensitrelvir group than in the no antiviral treatment group, suggesting ensitrelvir is an effective treatment in patients at risk of severe COVID-19.
COVID-19 still poses a risk for patients with serious health conditions and weakened immune systems, who are more likely to develop severe illness. Several studies have indicated that some oral antiviral medications might be effective in preventing severe disease. This study aimed to evaluate if ensitrelvir, an oral antiviral medication, can help prevent hospitalization in outpatients who are at risk of developing severe symptoms from the Omicron variant of the SARS-CoV-2 virus. The hospitalization rates of patients who received ensitrelvir was compared with those who did not receive any antiviral treatment, using medical records from a large health insurance database in Japan focused on outpatients who were at risk of severe symptoms and were diagnosed with COVID-19 between November 2022 and July 2023. Respiratory and heart rate monitoring, oxygen therapy, ventilator use, intensive care admission, and all-cause death were also evaluated. The study found that patients who received ensitrelvir had a lower risk of being hospitalized compared to those who did not receive any antiviral treatment. The ensitrelvir group also had lower rates of respiratory and heart rate monitoring and oxygen therapy. However, it was challenging to assess the effects on ventilator use, intensive care admission, and all-cause death due to the small number of events in the population under evaluation. Based on these findings, ensitrelvir appears to be an effective treatment for reducing the risk of hospitalization in patients at risk of severe COVID-19.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Infect Dis Ther Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Infect Dis Ther Year: 2024 Document type: Article