Publication:
Current antiviral practice and course of Hepatitis B virus infection in inflammatory arthritis: a multicentric observational study (A + HBV study)

dc.contributor.authorsUmut KALYONCU;Hakan EMMUNGİL;Ahmet Mesut ONAT;SEDAT YILMAZ;TİMUÇİN KAŞİFOĞLU;Servet AKAR;GÜZİDE NEVSUN İNANÇ;FATİH YILDIZ;ORHAN KÜÇÜKŞAHİN;ÖMER KARADAĞ;RIDVAN MERCAN;Cemal BES;VELİ YAZISIZ;BARIŞ YILMAZER;MUSTAFA ÖZMEN;Şükran ERTEN;Soner ŞENEL;AYTEN YAZICI;Etem Koray TAŞCILAR;Melike KALFA;Sedat KİRAZ;Bünyamin KISACIK;Yavuz PEHLİVAN;LEVENT KILIÇ;İSMAİL ŞİMŞEK;AYŞE ÇEFLE;NURULLAH AKKOÇ;RAFİ HANER DİRESKENELİ;Eren ERKEN;TAHSİN MURAT TURGAY;Mehmet Akif ÖZTÜRK;Mehmet SOY;KENAN AKSU;Ayhan DİNÇ;İhsan ERTENLİ
dc.date.accessioned2022-04-04T12:54:17Z
dc.date.accessioned2026-01-11T18:37:13Z
dc.date.available2022-04-04T12:54:17Z
dc.date.issued2015
dc.description.abstract0
dc.description.abstractObjective: The reactivation of hepatitis B virus (HBV) infection is a well-known event in hepatitis B surface antigen (HbsAg)-positive patients receiving immunosuppressive therapy. The objective of this study was to assess the antiviral practice and course of HBV infection in inflammatory arthritis. Material and Methods: Nineteen rheumatology centers participated in this retrospective study. HbsAg-positive patients who were taking disease-modifying antirheumatic drugs and who were being tested for HBV viral load at a minimum of two different time points were included. The case report form (CRF) consisted of demographic data, rheumatic diseases, treatment profiles, transaminase levels, viral hepatitis serological markers, and HBV viral load. The reactivation of HBV was defined as the abrupt rise in HBV replication by an increase in serum HBV DNA levels in a patient with a previously inactive HBV infection. Results: In total, the data of 101 (female 50.5%) patients were included (76 patients with inactive HBV carriers and 25 patients with chronic HBV infection). The mean age of patients was 44±12 years, and the mean follow-up duration was 31±22 months. Of the 101 patients, 70 (69.3%) received antiviral treatment. HBV reactivation was detected in 13 of 76 (17.1%) patients with inactive HBV carriers. HBV reactivation was observed less frequently, not although significantly, in those patients receiving antiviral prophylaxis compared with those not receiving prophylaxis [5/41 (12.2%) vs. 8/33 (24.2%), p=0.17]. Forty-two patients (31 patients had inactive HBV carriers) were using anti-tumor necrosis factor agents. HBV reactivation was detected in 6 of the 31 (19.3%) patients. Twenty-five patients had chronic hepatitis, and five (20%) of them had not received antiviral prophylaxis. HBV viral loads were persistently elevated in 7 (28%) of 25 patients (three patients under and four patients not under antiviral treatment). Conclusion: HBV reactivation was observed in approximately 17% of patients under immunosuppressive treatments. HBV reactivation was more frequently observed in those who did not receive antiviral prophylaxis.
dc.identifier.issn2147-9720;2148-4279
dc.identifier.urihttps://hdl.handle.net/11424/258288
dc.language.isoeng
dc.relation.ispartofEuropean Journal of Rheumatology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectRomatoloji
dc.titleCurrent antiviral practice and course of Hepatitis B virus infection in inflammatory arthritis: a multicentric observational study (A + HBV study)
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage154
oaire.citation.issue4
oaire.citation.startPage149
oaire.citation.titleEuropean Journal of Rheumatology
oaire.citation.volume2

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