A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
Author(s) -
Nesrin Beşbaş,
Diana Karpman,
Daniel Landau,
Chantal Loirat,
Willem Proesmans,
Giuseppe Remuzzi,
Gianfranco Rizzoni,
Carol M. Taylor,
N. Van de Kar,
L. B. Zimmerhackl
Publication year - 2006
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/sj.ki.5001581
Subject(s) - thrombotic thrombocytopenic purpura , etiology , medicine , causation , disease , intensive care medicine , pediatrics , immunology , platelet , political science , law
The diagnostic terms hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are based on historical and overlapping clinical descriptions. Advances in understanding some of the causes of the syndrome now permit many patients to be classified according to etiology. The increased precision of a diagnosis based on causation is important for considering logical approaches to treatment and prognosis. It is also essential for research. We propose a classification that accommodates both a current understanding of causation (level 1) and clinical association in cases for whom cause of disease is unclear (level 2). We tested the classification in a pediatric disease registry of HUS. The revised classification is a stimulus to comprehensive investigation of all cases of HUS and TTP and is expected to increase the proportion of cases in whom a level 1 etiological diagnosis is confirmed.
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