Literature DB >> 9011469

Managing patients on interferon therapy.

R Esteban1.   

Abstract

Interferon (IFN) has become the standard therapy for chronic hepatitis C. The use of IFN should be accompanied by adequate diagnosis and management using standard practices as well as new and sophisticated techniques now available. A liver biopsy performed prior to IFN therapy initiation remains the standard for adequate histological diagnosis of HCV disease as well as determination of disease severity and the presence of liver cirrhosis. ALT normalization is not adequate to determine complete short-term response to IFN treatment. Adverse effects resulting from IFN therapy include a flulike syndrome, hematologic effects, neuropsychiatric effects, and thyroid abnormalities. The majority of these can be adequately managed without discontinuation of IFN treatment. However, preexisting psychiatric conditions are a contraindication to IFN therapy. IFN treatment also is contraindicated in patients with autoimmune hepatitis (AIH). Therefore, it is important to distinguish AIH from chronic HCV infection using HCV-RNA analysis and determination of autoimmune titers (including anti-LKM antibodies, anti-SMA, and ANA). Recently reported adverse effects of IFN include respiratory and ocular effects. Serological diagnosis of HCV infection has evolved to the use of second- and third-generation ELISA tests. Although sophisticated, these tests cannot distinguish between active and quiescent infection, and therefore are of limited value in monitoring treatment response. Several other techniques have been suggested: the ratio between IgG and IgM class anti-HCV core antibodies, detection of antibodies against a glycosylated recombinant product of the E2 envelope glycoprotein, and several different polymerase chain reaction (PCR) techniques. The latter appears to be the most promising. Use of these techniques should be incorporated into the monitoring of IFN therapy to assist in the evaluation of adequate treatment response, the need for treatment alteration, and estimation of relapse risk upon treatment cessation.

Entities:  

Mesh:

Substances:

Year:  1996        PMID: 9011469     DOI: 10.1007/bf02087887

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  17 in total

Review 1.  Side effects of alpha interferon.

Authors:  P F Renault; J H Hoofnagle
Journal:  Semin Liver Dis       Date:  1989-11       Impact factor: 6.115

2.  Sustained hypothyroidism induced by recombinant alpha interferon in patients with chronic hepatitis C.

Authors:  P Marcellin; M Pouteau; P Renard; J M Grynblat; N Colas Linhart; P Bardet; B Bok; J P Benhamou
Journal:  Gut       Date:  1992-06       Impact factor: 23.059

3.  Antibody to hepatitis C virus second envelope (HCV-E2) glycoprotein: a new marker of HCV infection closely associated with viremia.

Authors:  R Lesniewski; G Okasinski; R Carrick; C Van Sant; S Desai; R Johnson; J Scheffel; B Moore; I Mushahwar
Journal:  J Med Virol       Date:  1995-04       Impact factor: 2.327

4.  Liver/kidney microsome antibody type 1 and hepatitis C virus infection.

Authors:  F Lunel; N Abuaf; L Frangeul; P Grippon; M Perrin; Y Le Coz; D Valla; E Borotto; A M Yamamoto; J M Huraux
Journal:  Hepatology       Date:  1992-09       Impact factor: 17.425

5.  Psychiatric complications of long-term interferon alfa therapy.

Authors:  P F Renault; J H Hoofnagle; Y Park; K D Mullen; M Peters; D B Jones; V Rustgi; E A Jones
Journal:  Arch Intern Med       Date:  1987-09

6.  Reversibility of thyroid dysfunction induced by recombinant alpha interferon in chronic hepatitis C.

Authors:  E Baudin; P Marcellin; M Pouteau; N Colas-Linhart; J P Le Floch; C Lemmonier; J P Benhamou; B Bok
Journal:  Clin Endocrinol (Oxf)       Date:  1993-12       Impact factor: 3.478

7.  Interferon-associated retinopathy.

Authors:  D R Guyer; J Tiedeman; L A Yannuzzi; J S Slakter; D Parke; J Kelley; R A Tang; M Marmor; G Abrams; J W Miller
Journal:  Arch Ophthalmol       Date:  1993-03

8.  A comparison of three interferon alfa-2b regimens for the long-term treatment of chronic non-A, non-B hepatitis. Multicenter Study Group.

Authors:  T Poynard; P Bedossa; M Chevallier; P Mathurin; C Lemonnier; C Trepo; P Couzigou; J L Payen; M Sajus; J M Costa
Journal:  N Engl J Med       Date:  1995-06-01       Impact factor: 91.245

9.  High prevalence of serological markers of autoimmunity in patients with chronic hepatitis C.

Authors:  B D Clifford; D Donahue; L Smith; E Cable; B Luttig; M Manns; H L Bonkovsky
Journal:  Hepatology       Date:  1995-03       Impact factor: 17.425

10.  Loss of serum HCV RNA at week 4 of interferon-alpha therapy is associated with more favorable long-term response in patients with chronic hepatitis C.

Authors:  E Orito; M Mizokami; K Suzuki; K Ohba; T Ohno; M Mori; K Hayashi; K Kato; S Iino; J Y Lau
Journal:  J Med Virol       Date:  1995-06       Impact factor: 2.327

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.