Management of chronic viral hepatitis in patients with thalassemia: recommendations from an international panel

Author:

Di Marco Vito123,Capra Marcello14,Angelucci Emanuele15,Borgna-Pignatti Caterina16,Telfer Paul7,Harmatz Paul8,Kattamis Antonis9,Prossamariti Luciano110,Filosa Aldo111,Rund Deborah12,Gamberini Maria Rita113,Cianciulli Paolo114,De Montalembert Marianne15,Gagliardotto Francesco14,Foster Graham16,Grangè Jean Didier17,Cassarà Filippo118,Iacono Angela19,Cappellini Maria Domenica2021,Brittenham Gary M.22,Prati Daniele223,Pietrangelo Antonello224,Craxì Antonio23,Maggio Aurelio118,

Affiliation:

1. Italian Society for the Study of Thalassemia and Haemoglobinopathies, Rome, Italy;

2. Italian Association for the Study of the Liver, Rome, Italy;

3. Sezione di Gastroenetrologia ed Epatologia, Dipartimento Biomedico di Medicina Interna e Specialistica, University of Palermo, Palermo, Italy;

4. UOC Ematologia-Emoglobinopatie, ARNAS Civico, Di Cristina, Benfratelli, Palermo, Italy;

5. Unità Operativa di Ematologia e Centro Trapianti, Ospedale Oncologico di Riferimento Regionale Armando Businco, Cagliari, Italy;

6. Department of Clinical and Experimental Medicine-Pediatrics, University of Ferrara, Ferrara, Italy;

7. Centre for Haematology, Barts and The London School of Medicine and Dentistry, Department of Haematology, Royal London Hospital, London, United Kingdom;

8. Division of Gastroenterology, Children's Hospital & Research Center, Oakland, CA;

9. First Department of Pediatrics, University of Athens, Medical School, Aghia Sophia Children's Hospital, Thivon and Levadias, Athens, Greece;

10. UOC Ematologia-Talassemia, AORN A. Cardarelli, Napoli, Italy;

11. UOS Talassemia Pediatrica, AORN A. Cardarelli, Napoli, Italy;

12. Hebrew University Hadassah Medical Organization, Jerusalem, Israel;

13. Department of Reproduction and Growth, Pediatric and Adolescent Unit, S. Anna Hospital, Ferrara, Italy;

14. Day Hospital Talassemia, Ospedale S. Eugenio, Roma, Italy;

15. Service de Pediatrie Generale, Hopital Necker, Paris, France;

16. Queen Mary's University of London, Barts and The London School of Medicine, The Liver Unit, London, United Kingdom;

17. Service d'Hépatogastroenterologie, Hopital Tenon, Paris, France;

18. UOC Ematologia con Talassemia, AO Riuniti Villa Sofia-V. Cervello, Palermo, Italy;

19. Foundation Leonardo Giambrone, Naples, Italy;

20. Policlinico, Mangiagalli, Regina Elena Foundation IRCCS, University of Milan, Milan, Italy;

21. Fondazione IRCCS Ca Granda Policlinico, Università di Milano, Milan, Italy;

22. Children's Hospital of New York, NY;

23. Department of Transfusion Medicine and Hematology, Ospedale Alessandro Manzoni, Lecco, Italy and Center of Transfusion Medicine, Cellular Therapy and Cryobiology, IRCCS Foundation Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy; and

24. Division of Internal Medicine and Center for Hemochromatosis, University Hospital of Modena, Modena, Italy

Abstract

AbstractChelation therapy with new drugs prevents cardiac damage and improves the survival of thalassemia patients. Liver diseases have emerged as a critical clinical issue. Chronic liver diseases play an important role in the prognosis of thalassemia patients because of the high frequency of viral infections and important role of the liver in regulating iron metabolism. Accurate assessment of liver iron overload is required to tailor iron chelation therapy. The diagnosis of hepatitis B virus– or hepatitis C virus–related chronic hepatitis is required to detect patients who have a high risk of developing liver complications and who may benefit by antiviral therapy. Moreover, clinical management of chronic liver disease in thalassemia patients is a team management issue requiring a multidisciplinary approach. The purposes of this paper are to summarize the knowledge on the epidemiology and the risks of transmission of viral infections, to analyze invasive and noninvasive methods for the diagnosis of chronic liver disease, to report the knowledge on clinical course of chronic viral hepatitis, and to suggest the management of antiviral therapy in thalassemia patients with chronic hepatitis B or C virus or cirrhosis.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference99 articles.

1. Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major.;Brittenham;N Engl J Med,1994

2. Survival in medically treated patients with homozygous β-thalassemia.;Olivieri;N Engl J Med,1994

3. Improving survival with deferiprone treatment in patients with thalassemia major: a prospective multicenter randomised clinical trial.;Maggio;Blood Cells Mol Dis,2009

4. Iron overload following red blood cell transfusion and its impact on disease severity.;Ozment;Biochim Biophys Acta,2009

5. Survival and complications in patients with thalassemia major treated with transfusion and deferoxamine.;Borgna-Pignatti;Haematologica,2004

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3