英文摘要 |
infection and rheumatic diseases receiving rituximab. Methods: We recruited patients with chronic HBV infection and rheumatic diseases admitted and placed on rituximab from July 1, 2019, to December 31, 2019. The patients were divided into antiviral-receiving and nonantiviral-receiving groups according to their baseline medications. The primary endpoint was set as acute hepatitis flare. After a 210-day follow-up period, we assessed the differences in baseline characteristics and primary outcome between these two groups. Results: There was no significant difference in baseline characteristics between the antiviral-receiving and nonantiviral-receiving groups, except that hepatitis B core antibody (anti-HBc) levels were higher in nonantiviral-receiving group. Two flare events developed during the 210-day follow-up period. The flare rates were 40.0% and 0.0% in the nonantiviral-receiving and antiviral-receiving groups, respectively, but the difference in flare rates was not significant due to the small sample size. The receiver operating characteristic (ROC) curve for anti-HBc levels provided the predictability of the flare. Conclusion: Patients with chronic HBV infection have a higher risk for hepatitis B flare and reactivation. Antiviral agents are effective in preventing flares. |