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Systemic Lupus ErythematosusA Statistical Evaluation of Mortality Based on a Consecutive Series of 299 Patients
ROBERT E. KELLUM, MD;
JOHN R. HASERICK, MD
Arch Intern Med. 1964;113(2):200-207.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text PDF and any section headings. |
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In a review of the literature we have found no recent statistical evaluation of the long-term prognosis in patients with systemic lupus erythematosus (hereinafter designated as SLE). Though a dire prognosis was attributed to SLE prior to the early 1950's, the disease actually covers a wide range of severity, from the acute fulminating variety with an unpredictable response to corticosteroids, to the chronic, "smoldering" forms that are compatible with a long life expectancy.1-3 This report summarizes a statistical survey based on 11 years' experience in observing and treating 299 patients with SLE and includes an analysis of factors such as sex, race, and the use of steroid therapy.
Material
The material for this study comprises a consecutive series of patients in an 11-year period, or all of the 299 patients with systemic lupus erythematosus who were examined and treated at the Cleveland Clinic between January, 1949, and December, 1959.
. . . [Full Text PDF of this Article]
Author Affiliations
CLEVELAND
From The Department of Dermatology, The Cleveland Clinic Foundation.
Footnotes
Received for publication July 9, 1963; accepted Sept 16.
Formerly Fellow in The Department of Dermatology, Cleveland Clinic; present address: University of Oregon Medical School, Portland 1 (Dr. Kellum).
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