对接受免疫抑制治疗患者的 HBV 再激活和抗病毒预防进行评估

Ahmet ŞAHİN, Selda ASLAN
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 Material and Method: The study included 375 patients over 18 years of age who received tumor necrosis factor-α (TNF-α) inhibitor, tyrosine kinase inhibitor, steroids, methotrexate or anti-CD20 antibodies due to rheumatic diseases in a training and research hospital between May 2022 and May 2023. Hepatitis B surface antigen (HbsAg), hepatitis B surface antibody (anti-Hbs), hepatitis B core protein antibody (anti-Hbc IgG) serologies, immunosuppressive therapies and oral antivirals were retrospectively analyzed.
 Results: The average age of the 375 patients included in the study was 43.77±13.07 years. 193 (51.5%) of the patients were male. 11 patients were HbsAg positive, 150 patients were anti-Hbs positive, 19 patients were isolated anti-Hbc IgG positive, and 79 patients were both anti-Hbs and anti-Hbc IgG positive. According to serological findings, 109 (29%) patients had HBV exposure. All three test results of 194 (51.7%) patients were negative. A total of 85 (22.7%) patients received oral antiviral prophylaxis due to the use of immunosuppressive agents. In terms of HBVr, 16.5% were evaluated as high risk, 75.3% as moderate risk, and 8.2% as low risk. Out of 85 patients 79 received entecavir, 5 reveived tenofovir disoproxil fumarate (TDF) and 1 received tenofovir alafenamide fumarate (TAF). The mean duration for the immunosuppressive therapy was 6.41±4.20 years. The mean duration of oral antiviral prophylaxis among patients was 1.02±1.72 years. HBVr was not observed in any of our patients.
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 Material and Method: The study included 375 patients over 18 years of age who received tumor necrosis factor-α (TNF-α) inhibitor, tyrosine kinase inhibitor, steroids, methotrexate or anti-CD20 antibodies due to rheumatic diseases in a training and research hospital between May 2022 and May 2023. Hepatitis B surface antigen (HbsAg), hepatitis B surface antibody (anti-Hbs), hepatitis B core protein antibody (anti-Hbc IgG) serologies, immunosuppressive therapies and oral antivirals were retrospectively analyzed.
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引用次数: 0

摘要

目的:慢性乙型肝炎患者和有乙型肝炎(HBV)感染史的人在接受免疫抑制治疗时存在HBV再激活(HBVr)的风险。在这项研究中,我们旨在评估因风湿病而接受各种免疫抑制治疗的患者的乙肝血清学、危险人群和抗病毒预防。 材料和方法:该研究纳入了375例18岁以上的患者,这些患者于2022年5月至2023年5月在一家培训和研究医院因风湿病接受肿瘤坏死因子-α (TNF-α)抑制剂、酪氨酸激酶抑制剂、类固醇、甲氨蝶呤或抗cd20抗体。回顾性分析乙型肝炎表面抗原(HbsAg)、乙型肝炎表面抗体(anti-Hbs)、乙型肝炎核心蛋白抗体(anti-Hbc IgG)血清学、免疫抑制治疗及口服抗病毒药物。 结果:纳入研究的375例患者平均年龄为43.77±13.07岁。男性193例(51.5%)。HbsAg阳性11例,抗hbs阳性150例,分离抗hbc IgG阳性19例,抗hbs和抗hbc IgG均阳性79例。根据血清学结果,109例(29%)患者有HBV暴露。194例(51.7%)患者三项检测结果均为阴性。85例(22.7%)患者因使用免疫抑制剂而接受了口服抗病毒预防治疗。在HBVr方面,16.5%的人被评估为高风险,75.3%为中度风险,8.2%为低风险。85例患者中,79例接受恩替卡韦治疗,5例接受富马酸替诺福韦二氧吡酯(TDF)治疗,1例接受富马酸替诺福韦阿拉胺(TAF)治疗。免疫抑制治疗的平均持续时间为6.41±4.20年。患者口服抗病毒药物预防的平均持续时间为1.02±1.72年。在我们的所有患者中未观察到HBVr。 结论:患者在接受免疫抑制治疗前,应首先评估乙型肝炎血清学和预防指征。此外,作为一项预防医学活动,应尽快完成未接种疫苗患者的乙肝疫苗接种。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
İmmunsupresif Tedavi Alan Hastalarda HBV Reaktivasyonu ve Antiviral Profilaksinin Değerlendirilmesi
Aim: Patients with chronic hepatitis B and people with a history of hepatitis B (HBV) infection are at risk of HBV reactivation (HBVr) when they receive immunosuppressive therapy. In this study, we aimed to evaluate the hepatitis B serology, risk groups and antiviral prophylaxis of patients receiving various immunosuppressive therapies due to rheumatological diseases. Material and Method: The study included 375 patients over 18 years of age who received tumor necrosis factor-α (TNF-α) inhibitor, tyrosine kinase inhibitor, steroids, methotrexate or anti-CD20 antibodies due to rheumatic diseases in a training and research hospital between May 2022 and May 2023. Hepatitis B surface antigen (HbsAg), hepatitis B surface antibody (anti-Hbs), hepatitis B core protein antibody (anti-Hbc IgG) serologies, immunosuppressive therapies and oral antivirals were retrospectively analyzed. Results: The average age of the 375 patients included in the study was 43.77±13.07 years. 193 (51.5%) of the patients were male. 11 patients were HbsAg positive, 150 patients were anti-Hbs positive, 19 patients were isolated anti-Hbc IgG positive, and 79 patients were both anti-Hbs and anti-Hbc IgG positive. According to serological findings, 109 (29%) patients had HBV exposure. All three test results of 194 (51.7%) patients were negative. A total of 85 (22.7%) patients received oral antiviral prophylaxis due to the use of immunosuppressive agents. In terms of HBVr, 16.5% were evaluated as high risk, 75.3% as moderate risk, and 8.2% as low risk. Out of 85 patients 79 received entecavir, 5 reveived tenofovir disoproxil fumarate (TDF) and 1 received tenofovir alafenamide fumarate (TAF). The mean duration for the immunosuppressive therapy was 6.41±4.20 years. The mean duration of oral antiviral prophylaxis among patients was 1.02±1.72 years. HBVr was not observed in any of our patients. Conclusion: Before patients receive immunosuppressive therapy, hepatitis B serologies and prophylaxis indication should be evaluated firstly. In addition, as a preventive medicine activity, hepatitis B vaccinations of unvaccinated patients should be completed as quickly as possible.
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