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The incidence of thrombotic thrombocytopenic purpura‐hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS‐13 deficiency
Author(s) -
TERRELL D. R.,
WILLIAMS L. A.,
VESELY S. K.,
LÄMMLE B.,
HOVINGA J. A. K.,
GEORGE J. N.
Publication year - 2005
Publication title -
journal of thrombosis and haemostasis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.947
H-Index - 178
eISSN - 1538-7836
pISSN - 1538-7933
DOI - 10.1111/j.1538-7836.2005.01436.x
Subject(s) - thrombotic thrombocytopenic purpura , medicine , incidence (geometry) , adamts , schistocyte , hemolytic anemia , atypical hemolytic uremic syndrome , thrombotic microangiopathy , immunology , platelet , antibody , complement system , disease , metalloproteinase , physics , thrombospondin , matrix metalloproteinase , optics
Summary.  Background:  Accurate estimates of the incidence of thrombotic thrombocytopenic purpura (TTP) are important to assess the resources required for current treatments as well as to anticipate the need to develop new treatments. Previous estimates have been indirect and have not reported data on patients with ADAMTS‐13 deficiency. Objective:  To determine the incidence of patients with TTP‐hemolytic uremic syndrome (HUS) in three categories: all patients with clinically suspected TTP‐HUS, patients with idiopathic TTP‐HUS, and patients with severe ADAMTS‐13 deficiency. Methods:  Incidence rates were estimated from the Oklahoma TTP‐HUS Registry, analyzing all 206 consecutive patients from January 1, 1996 to June 30, 2004 who were treated with plasma exchange for their initial episode of clinically suspected TTP‐HUS. ADAMTS‐13 activity was measured in 186 (90%) of the 206 patients. Results:  The age–sex–race standardized annual incidence rates were 11.29 × 10 6 (95% CI: 9.70–12.88) for all patients with clinically suspected TTP‐HUS; 4.46 × 10 6 (95% CI: 3.43–5.50) for patients with idiopathic TTP‐HUS; and 1.74 × 10 6 (95% CI: 1.06–2.41) for patients with severe ADAMTS‐13 deficiency (<5% activity). In all three categories, the incidence rates were greater for women and for blacks. For patients with severe ADAMTS‐13 deficiency, the age–sex standardized incidence rate ratio of blacks to non‐blacks was 9.29 (95% CI: 4.33–19.93). Conclusions:  Accurate incidence rate estimates for all patients with clinically suspected TTP‐HUS, idiopathic TTP‐HUS, and TTP associated with severe ADAMTS‐13 deficiency have been determined. The greater incidence among women and blacks is comparable with their increased risk for other autoimmune disorders.

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