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Autoimmune hemolytic anemia in patients with systemic lupus erythematosus

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dc.contributor.author Kokori, SIG en
dc.contributor.author Ioannidis, JPA en
dc.contributor.author Voulgarelis, M en
dc.contributor.author Tzioufas, AG en
dc.contributor.author Moutsopoulos, HM en
dc.date.accessioned 2014-03-01T01:49:46Z
dc.date.available 2014-03-01T01:49:46Z
dc.date.issued 2000 en
dc.identifier.issn 0002-9343 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/25914
dc.subject.classification Medicine, General & Internal en
dc.subject.other CONSENSUS-STUDY-GROUP en
dc.subject.other ANTIPHOSPHOLIPID ANTIBODIES en
dc.subject.other RHEUMATOLOGY RESEARCH en
dc.subject.other CLINICAL-SIGNIFICANCE en
dc.subject.other EUROPEAN WORKSHOP en
dc.subject.other DISEASE-ACTIVITY en
dc.subject.other MANIFESTATIONS en
dc.subject.other AUTOANTIBODIES en
dc.subject.other SPECIFICITY en
dc.subject.other THROMBOSIS en
dc.title Autoimmune hemolytic anemia in patients with systemic lupus erythematosus en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2000 en
heal.abstract PURPOSE: We sought to evaluate the clinical and serologic associations with, and outcomes of, autoimmune hemolytic anemia, as compared with other types of anemia, in patients with systemic lupus erythematosus (SLE). SUBJECTS AND METHODS: We studied 41 consecutive patients with SLE with clinically manifest autoimmune hemolytic anemia, including 27 (66%) in whom hemolysis was the initial disease manifestation. We matched each patient for age and disease duration with a patient with SLE with anemia resulting from a different cause. RESULTS: The 41 patients had a total of 50 episodes of autoimmune hemolytic anemia. The recurrence rate was 4 per 100 person-years. Cases and controls had similar mean (+/- SD) lupus activity indexes (2.1 +/- 1.5 vs 2.4 +/- 1.3, P = 0.5). Patients with autoimmune hemolytic anemia at any time could be distinguished from patients with other causes of anemia, because they were more likely to have elevated titers of IgG anticardiolipin antibodies [odds ratio (OR) = 5.8; 95% confidence interval (CI), 1.4 to 24] and thrombosis (OR = 4.6; 95% CI, 1.0 to 21). Autoimmune hemolytic anemia at the onset of SLE was independently associated with renal involvement (OR = 5.4; 95% CI, 1.0 to 28), thrombocytopenia (OR = 7.3; 95% CI, 1.1 to 4&), and possibly thrombotic episodes during follow-up (OR = 11; 95% CI, 0.8 to 160) when compared with controls with other types of anemia at the onset of SLE. CONCLUSIONS: Autoimmune hemolytic anemia usually occurs at the onset of SLE, and its recurrence rate is low among treated patients. The association with IgG anticardiolipin antibodies and thrombosis suggests that the occurrence of autoimmune hemolytic anemia may define a subgroup of patients with SLE who have characteristic serologic and clinical manifestations. (C) 2000 by Excerpta Medica, Inc. en
heal.publisher EXCERPTA MEDICA INC en
heal.journalName AMERICAN JOURNAL OF MEDICINE en
dc.identifier.isi ISI:000085334500003 en
dc.identifier.volume 108 en
dc.identifier.issue 3 en
dc.identifier.spage 198 en
dc.identifier.epage 204 en


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