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Title:
Adult-onset Stillās disease: an Italian multicentre retrospective observational study of manifestations and treatments in 245 patients | Clinical Rheumatology
Description:
Adult-onset Stillās disease (AOSD) is a systemic inflammatory condition of unknown aetiology characterized by typical episodes of spiking fever, evanescent rash, arthralgia, leukocytosis and hyperferritinemia. Given the lack of data in Italian series, we promote a multicentric data collection to characterize the clinical phenotype of Italian patients with AOSD. Data from 245 subjects diagnosed with AOSD were collected by 15 centres between March and May 2013. The diagnosis was made following Yamaguchiās criteria. Data regarding clinical manifestations, laboratory features, disease course and treatments were reported and compared with those presented in other published series of different ethnicity. The most frequent features were the following: arthritis (93 %), pyrexia (92.6 %), leukocytosis (89 %), negative ANA (90.4 %) and neutrophilia (82 %). As compared to other North American, North European, Middle Eastern and Far Eastern cohorts, Italian data show differences in clinical and laboratory findings. Regarding the treatments, in 21.9 % of cases, corticosteroids and traditional DMARDs have not been able to control the disease while biologics have been shown to be effective in 48 to 58 patients. This retrospective work summarizes the largest Italian multicentre series of AOSD patients and presents clinical and laboratory features that appear to be influenced by the ethnicity of the affected subjects.
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Keywords {š}
disease, stills, article, pubmed, google, scholar, adultonset, clinical, cas, rheumatol, rheumatology, university, italy, department, patients, clin, adult, medicine, unit, data, italian, study, rheum, retrospective, stefano, privacy, cookies, content, research, systemic, laboratory, arthritis, onset, publish, search, treatments, sfriso, priori, valesini, aosd, subjects, features, access, central, ann, dis, fautrel, exp, division, information,
Topics {āļø}
month download article/chapter carlo maurizio montecucco systemic inflammatory condition systemic autoimmune diseases systemic autoinflammatory diseases full article pdf privacy choices/manage cookies laboratory findings retrospective work summarizes silvia rossi gianfranco ferraccioli michele colaci clodoveo ferri daniela iacono gabriele valentini unknown aetiology characterized nationwide epidemiological survey schumacher hr jr liossis s-nc francesco caso conditions privacy policy article sfriso clinical presentation current clinical evidence european economic area corticosteroid sparing effect santāanna hospital multicentric data collection giovanni lapadula applied clinical science accepting optional cookies linda carli stefano alivernini raffaele scarpa valentina bagnari ilaria piazza silvano adami biologic agents de stefano retrospective study related subjects refractory adult-onset early adult-onset chronic joint disease article log main content log stefano bombardieri disease article 30 journal finder publish italy anna
Questions {ā}
- A retrospective study of patients with adult-onset Stillās disease: is pericarditis a possible predictor for biological disease-modifying anti-rheumatic drugs need?
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headline:Adult-onset Stillās disease: an Italian multicentre retrospective observational study of manifestations and treatments in 245 patients
description:Adult-onset Stillās disease (AOSD) is a systemic inflammatory condition of unknown aetiology characterized by typical episodes of spiking fever, evanescent rash, arthralgia, leukocytosis and hyperferritinemia. Given the lack of data in Italian series, we promote a multicentric data collection to characterize the clinical phenotype of Italian patients with AOSD. Data from 245 subjects diagnosed with AOSD were collected by 15 centres between March and May 2013. The diagnosis was made following Yamaguchiās criteria. Data regarding clinical manifestations, laboratory features, disease course and treatments were reported and compared with those presented in other published series of different ethnicity. The most frequent features were the following: arthritis (93Ā %), pyrexia (92.6Ā %), leukocytosis (89Ā %), negative ANA (90.4Ā %) and neutrophilia (82Ā %). As compared to other North American, North European, Middle Eastern and Far Eastern cohorts, Italian data show differences in clinical and laboratory findings. Regarding the treatments, in 21.9Ā % of cases, corticosteroids and traditional DMARDs have not been able to control the disease while biologics have been shown to be effective in 48 to 58 patients. This retrospective work summarizes the largest Italian multicentre series of AOSD patients and presents clinical and laboratory features that appear to be influenced by the ethnicity of the affected subjects.
datePublished:2016-05-20T00:00:00Z
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Adult-onset Stillās disease
Biologic drugs
Clinical presentation
Laboratory findings
Retrospective study
Rheumatology
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headline:Adult-onset Stillās disease: an Italian multicentre retrospective observational study of manifestations and treatments in 245 patients
description:Adult-onset Stillās disease (AOSD) is a systemic inflammatory condition of unknown aetiology characterized by typical episodes of spiking fever, evanescent rash, arthralgia, leukocytosis and hyperferritinemia. Given the lack of data in Italian series, we promote a multicentric data collection to characterize the clinical phenotype of Italian patients with AOSD. Data from 245 subjects diagnosed with AOSD were collected by 15 centres between March and May 2013. The diagnosis was made following Yamaguchiās criteria. Data regarding clinical manifestations, laboratory features, disease course and treatments were reported and compared with those presented in other published series of different ethnicity. The most frequent features were the following: arthritis (93Ā %), pyrexia (92.6Ā %), leukocytosis (89Ā %), negative ANA (90.4Ā %) and neutrophilia (82Ā %). As compared to other North American, North European, Middle Eastern and Far Eastern cohorts, Italian data show differences in clinical and laboratory findings. Regarding the treatments, in 21.9Ā % of cases, corticosteroids and traditional DMARDs have not been able to control the disease while biologics have been shown to be effective in 48 to 58 patients. This retrospective work summarizes the largest Italian multicentre series of AOSD patients and presents clinical and laboratory features that appear to be influenced by the ethnicity of the affected subjects.
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Biologic drugs
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