Access to care in rare liver diseases: New challenges and new opportunities

被引:21
作者
Jones, David E. J. [1 ,2 ]
Sturm, Ekkehard [1 ,3 ]
Lohse, Ansgar W. [1 ,4 ]
机构
[1] RARE LIVER European Reference Network, Newcastle Upon Tyne, Tyne & Wear, England
[2] Newcastle Univ, Inst Cellular Med, Newcastle Upon Tyne, Tyne & Wear, England
[3] Univ Childrens Hosp, Tubingen, Germany
[4] Univ Med Ctr Hamburg Eppendorf, Dept Med, Hamburg, Germany
基金
英国医学研究理事会;
关键词
Rare disease; Transitional care; Care delivery; Genetic disease; PRIMARY SCLEROSING CHOLANGITIS; PRIMARY BILIARY-CIRRHOSIS; QUALITY-OF-LIFE; AUTOIMMUNE HEPATITIS; CHILDHOOD DISEASES; BRUCELLA INFECTION; WILSON DISEASE; ACID; PREVALENCE; TRANSPLANTATION;
D O I
10.1016/j.jhep.2017.11.004
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Patients with rare diseases are often disadvantaged, particularly those with rare liver diseases. Reasons for disadvantage include delayed or overlooked diagnosis, lack of local expertise and high-quality care, poor scientific understanding of the disease process and limited therapeutic options. In adult liver disease this can be compounded by prejudices towards patients with liver disease in general, because of a perception (incorrect for all rare liver diseases) that liver disease is lifestyle related and thus "selfinflicted". In paediatric rare liver diseases, such as biliary atresia, optimising outcomes requires a particularly timely diagnosis. Irrespective of patient age, the scientific and medical community must rise to the challenge of advancing our understanding of rare liver disease, searching for more effective and specific therapies, and providing the infrastructure to provide the best care for all patients, infants, children, young and older adults. The European Reference Network for Rare Liver Diseases is an important step in this direction. (C) 2017 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:577 / 585
页数:9
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