医学
内科学
拉米夫定
人口
乙型肝炎表面抗原
乙型肝炎病毒
乙型肝炎
美罗华
回顾性队列研究
共病
血清学
免疫学
丙型肝炎病毒
入射(几何)
流行病学
病毒学
丙型肝炎
作者
M. C. Ditto,Simone Parisi,V. Varisco,R. Talotta,Alberto Batticciotto,M. Antivalle,Maria Chiara Gerardi,M. Agosti,Richard Borrelli,Enrico Fusaro,Piercarlo Sarzi-Puttini
出处
期刊:Clinical and Experimental Rheumatology
日期:2020-09-16
卷期号:39 (3): 546-554
被引量:1
标识
DOI:10.55563/clinexprheumatol/c25fja
摘要
Hepatitis B (HBV) is a common comorbidity among rheumatic patients. The prevalence of HBV infection and the rate of reactivation remain unclear. The literature data suggested a higher risk in chronic than in past infection. Currently, the literature data are mostly focused on anti-TNF and rituximab. This retrospective observational study aimed to analyse the prevalence of HBV infection and the risk of viral reactivation in a population of rheumatic patients undergoing anti-TNF and non-anti-TNF agents.We analysed 1216 rheumatic patients, treated with both csDMARDs and bDMARDs between 2006 and 2017. Serologic markers for HBV (HBsAg, anti-HBs, anti-HBc) were performed prior and during biologic treatment. Patients with chronic or resolved infection were monitored every 3 months.The prevalence of HBV in our cohort was 15.7% (chronic infection: 0.4%, resolved infection: 12.6%, anti-HBc positivity alone: 2.6%). 12 (6.2%) out of 191 HBV infected patients experienced a reactivation. All of them showed markers of past infection. One patient experienced HBV reactivation despite lamivudine. Only one patient experienced acute hepatitis, probably due to the interruption of immunosuppressors in anticipation of surgery, not preceded by any HBV prophylactic treatment.HBV reactivation is a rare event in patients treated with a bDMARD and it can also occur while taking lamivudine, not only in chronic carriers (as per the literature data) but also in inactive ones. Regular screening followed by prompt treatment can prevent symptoms or complications. Due to the risk of hepatitis following the immune reconstitution, an antiviral therapy should be considered in the case of sudden discontinuation of csDMARDs or bDMARD.
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