Literature DB >> 21689211

The burden of HCV treatment in patients with inherited bleeding disorders.

D E Fransen van de Putte1, K Fischer, D Posthouwer, E P Mauser-Bunschoten.   

Abstract

Many patients with inherited bleeding disorders are infected with hepatitis C virus (HCV). Antiviral treatment, consisting of pegylated interferon and ribavirin, has many side-effects. The aim of the study was to prospectively assess the occurrence and course of side-effects and changes in health-related quality of life (HRQoL) during antiviral treatment in patients with inherited bleeding disorders and chronic HCV. Forty-seven patients were followed during antiviral treatment. Side-effects of treatment were recorded, and the Beck Depression Inventory and the RAND-36 HRQoL questionnaire were administered at regular intervals. Frequently reported side-effects were fatigue (100%), headache (94%), pruritus and skin rash (94%), concentration problems (89%), decreased appetite (89%), fever, irritability and hair loss (all 85%). Many side-effects disappeared soon after end of treatment, but 4 weeks after cessation fatigue, concentration problems and sleeping problems were still present in more than 30% of patients. Dose reduction was necessary in 21 patients (45%), mostly because of decreasing weight or haemoglobin levels. Two patients stopped treatment prematurely because of side-effects. Depression was present in 28 patients (60%). HRQoL decreased significantly during treatment in all RAND-36 domains, and increased again within 4 weeks after treatment. Major side-effects were similar in patients with successful (n = 31, 66%) and unsuccessful antiviral treatment. In patients with inherited bleeding disorders and chronic HCV, antiviral treatment has many, but mostly transient side-effects and a significant impact on quality of life. Careful follow-up and management of side-effects will ensure optimal compliance and treatment results.
© 2011 Blackwell Publishing Ltd.

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Year:  2011        PMID: 21689211     DOI: 10.1111/j.1365-2516.2011.02602.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  3 in total

1.  Assessment of factors associated with the quality of life of patients living with HIV/HCV co-infection.

Authors:  Marco Pereira; Renata Fialho
Journal:  J Behav Med       Date:  2016-08-09

2.  Hepatitis C virus in hemophilia: Health-related quality of life after successful treatment in the sixth Hemophilia in the Netherlands study.

Authors:  Cas J Isfordink; Samantha C Gouw; Erna C van Balen; Shermarke Hassan; Erik A M Beckers; Johanna G van der Bom; Michiel Coppens; Jeroen Eikenboom; Kathelijn Fischer; Louise Hooimeijer; Frank W G Leebeek; Frits R Rosendaal; Saskia E M Schols; Cees Smit; Lize F D van Vulpen; Eveline P Mauser-Bunschoten
Journal:  Res Pract Thromb Haemost       Date:  2021-11-17

Review 3.  Hepatitis C infection in patients with hereditary bleeding disorders: epidemiology, natural history, and management.

Authors:  Nikolaos Papadopoulos; Vasiliki Argiana; Melanie Deutsch
Journal:  Ann Gastroenterol       Date:  2017-10-26
  3 in total

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