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Risk of hepatitis B virus reactivation in patients with asthma or chronic obstructive pulmonary disease treated with corticosteroids

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dc.contributor.authorKim, Tae-Wan-
dc.contributor.authorKim, Mi-Na-
dc.contributor.authorKwon, Jae-Woo-
dc.contributor.authorKim, Kyung-Mook-
dc.contributor.authorKim, Won-
dc.contributor.authorChang, Yoon-Seok-
dc.contributor.authorMin, Kyung-Up-
dc.contributor.authorKim, You-Young-
dc.contributor.authorCho, Sang-Heon-
dc.contributor.authorPark, Heung-Woo-
dc.contributor.authorKim, Sae-Hoon-
dc.date.accessioned2012-06-27T05:51:02Z-
dc.date.available2012-06-27T05:51:02Z-
dc.date.issued2010-10-
dc.identifier.citationRESPIROLOGY; Vol.15 7; 1092-1097ko_KR
dc.identifier.issn1323-7799-
dc.identifier.urihttps://hdl.handle.net/10371/77587-
dc.description.abstractBackground and objective: Reactivation of hepatitis B virus (HBV) is thought to be associated with immunosuppressive treatments, but insufficient information is available on the effect of corticosteroids. The aim of this study was to evaluate the risk of HBV reactivation in hepatitis B surface antigen-seropositive patients with asthma or COPD, who were treated with systemic corticosteroids (SCS) in addition to inhaled corticosteroids (ICS). Methods: Patients with asthma or COPD (n = 198), who were hepatitis B surface antigen-seropositive and had been treated with ICS, were identified retrospectively. To evaluate the additional effects of SCS, the SCS group was divided into those who received intermittent or continuous SCS (>= 3 months of continuous SCS treatment), and into those who received low-dose (<= 20 mg/day of prednisolone) or medium-to-high-dose SCS. The study outcome was HBV reactivation. Results: HBV reactivation occurred in 11.1% of patients in the SCS group, which was significantly higher than the reactivation rate in the ICS group. HBV reactivation was more frequent in the SCS group compared with the ICS group (OR 3.813, 95% CI: 1.106-13.145, P = 0.032), and in the continuous and medium-to-high-dose SCS subgroups compared with the ICS group (OR 5.719, 95% CI: 1.172-27.905, P = 0.048 and OR 4.884, 95% CI: 1.362-17.511, P = 0.014, respectively). Conclusions: These results suggest that addition of SCS to ICS increases the risk of HBV reactivation, especially when SCS are administered chronically or at high doses.ko_KR
dc.description.sponsorshipThis work was supported by a Korean Health 21
R&D Project Grant from the Ministry of Health &
Welfare, Republic of Korea (A040153 & A030001).
ko_KR
dc.language.isoenko_KR
dc.publisherWILEY-BLACKWELLko_KR
dc.subjectasthmako_KR
dc.subjectchronic obstructive pulmonary diseaseko_KR
dc.subjectsystemic corticosteroidko_KR
dc.subjectinhaled corticosteroidko_KR
dc.subjecthepatitis B virus reactivationko_KR
dc.titleRisk of hepatitis B virus reactivation in patients with asthma or chronic obstructive pulmonary disease treated with corticosteroidsko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김태완-
dc.contributor.AlternativeAuthor김미나-
dc.contributor.AlternativeAuthor권재우-
dc.contributor.AlternativeAuthor김경묵-
dc.contributor.AlternativeAuthor김새훈-
dc.contributor.AlternativeAuthor김원-
dc.contributor.AlternativeAuthor박흥우-
dc.contributor.AlternativeAuthor장윤석-
dc.contributor.AlternativeAuthor조상헌-
dc.contributor.AlternativeAuthor민경업-
dc.contributor.AlternativeAuthor김유영-
dc.identifier.doi10.1111/j.1440-1843.2010.01798.x-
dc.citation.journaltitleRESPIROLOGY-
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