2019
DOI: 10.1007/s40257-019-00457-3
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Managing Psoriasis in Patients with HBV or HCV Infection: Practical Considerations

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Cited by 35 publications
(71 citation statements)
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References 142 publications
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“…In contrast, some reports considering treatment options for patients with HBV and HCV infection indicated that the use of cyclosporine was associated with a moderate (1-10%) risk of HBV reactivation during psoriasis treatment, including the need for concomitant anti-HBV prophylactic therapy and the checking of HBV DNA levels every three months [14].…”
Section: Hepatitis B Virusmentioning
confidence: 98%
See 1 more Smart Citation
“…In contrast, some reports considering treatment options for patients with HBV and HCV infection indicated that the use of cyclosporine was associated with a moderate (1-10%) risk of HBV reactivation during psoriasis treatment, including the need for concomitant anti-HBV prophylactic therapy and the checking of HBV DNA levels every three months [14].…”
Section: Hepatitis B Virusmentioning
confidence: 98%
“…Hepatitis C [15][16][17] Influenza virus infection [28] Rotavirus infection [29,30] Human Immunodeficiency Virus infection [26,33,34] Coronavirus infection [39][40][41][42][43] Hepatitis B [10][11][12][13][14] Hepatitis D [12,20] Herpes simplex infection [26,27] Herpes Zoster Virus infection [35,36] Hepatitis E [21] Cytomegalovirus infection [19,20,22] Human Papilloma Virus infection [29,30] Human Herpesvirus-8 (Kaposi Sarcoma virus) infection [42,43] The possible beneficial effect of cyclosporine on the course of COVID-19 seems very probable. Thus, it is not justified to suggest that patients with autoimmune diseases should discontinue cyclosporine therapy solely because of the COVID-19 pandemic.…”
Section: Possible Negative Effect Of Cyclosporine On Disease Coursementioning
confidence: 99%
“…11,13,27 Monitoring of liver enzymes and HBV DNA every 3 months is mandatory during treatment and for 6 to 12 months after drug discontinuation since HBV reactivation typically occurred during and after immune reconstitution. 11,13,27 Data relating to the use of biologic agents in HBV patients with psoriasis are increasingly available, and most of the available data are specific to anti-TNFs (in more than 200 patients with psoriasis). 5 Similar to other conventional therapies for psoriasis, HBsAg+ patients are at higher risk than HBsAg−/HBcAb+ patients for HBV reactivation.…”
Section: Discussionmentioning
confidence: 99%
“…44,45 There is also limited data supporting the use of the IL12/23 inhibitor ustekinumab, and the IL17 inhibitors secukinumab and ixekizumab. 46,47 Results from the first active comparator (ACCEPT) study of psoriasis biologic agents comparing ustekinumab and the TNF antagonist etanercept demonstrated that it is more appropriate to use etanercept rather than ustekinumab in psoriasis patients with hepatitis C infection. 48 We note a lack of data with the other IL23/p19 inhibitors: guselkumab, risankizumab and tildrakizumab; and the IL17 receptor blocker: brodalumab, and with the synthetic drug apremilast, in these patients.…”
Section: Chronic Infectionsmentioning
confidence: 99%
“…Data from two large clinical trials also show that the risk of hepatitis B infection is similar with or without apremilast treatment. 46,53 The only reports from reactivation of hepatitis B with cyclosporin are from severe immunosuppressed patients. 54 Reactivation of hepatitis B occurred in 39% of HBsAg+ patients treated with TFN-a-blockers for autoimmune diseases but not in HBsAg-/anti-HBc+ patients.…”
Section: Chronic Infectionsmentioning
confidence: 99%