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Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review
BACKGROUND: Adult-onset Still disease (AOSD) is a rare systemic inflammatory disorder. A few patients develop organ complications that can be life-threatening. Our objectives were to describe the disease course and phenotype of life-threatening AOSD, including response to therapy and long-term outco...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896069/ https://www.ncbi.nlm.nih.gov/pubmed/29642928 http://dx.doi.org/10.1186/s13054-018-2012-2 |
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author | Néel, Antoine Wahbi, Anaïs Tessoulin, Benoit Boileau, Julien Carpentier, Dorothée Decaux, Olivier Fardet, Laurence Geri, Guillaume Godmer, Pascal Goujard, Cécile Maisonneuve, Hervé Mari, Arnaud Pouchot, Jacques Ziza, Jean-Marc Bretonnière, Cédric Hamidou, Mohamed |
author_facet | Néel, Antoine Wahbi, Anaïs Tessoulin, Benoit Boileau, Julien Carpentier, Dorothée Decaux, Olivier Fardet, Laurence Geri, Guillaume Godmer, Pascal Goujard, Cécile Maisonneuve, Hervé Mari, Arnaud Pouchot, Jacques Ziza, Jean-Marc Bretonnière, Cédric Hamidou, Mohamed |
author_sort | Néel, Antoine |
collection | PubMed |
description | BACKGROUND: Adult-onset Still disease (AOSD) is a rare systemic inflammatory disorder. A few patients develop organ complications that can be life-threatening. Our objectives were to describe the disease course and phenotype of life-threatening AOSD, including response to therapy and long-term outcome. METHODS: A multicenter case series of intensive care medicine (ICU) patients with life-threatening AOSD and a systematic literature review. RESULTS: Twenty patients were included. ICU admission mostly occurred at disease onset (90%). Disease manifestations included fever (100%), sore throat (65%), skin rash (65%), and arthromyalgia (55%). Serum ferritin was markedly high (median: 29,110 ng/mL). Acute respiratory failure, shock and multiple organ failure occurred in 15 (75%), 10 (50%), and 7 (35%) cases, respectively. Hemophagocytosis was demonstrated in eight cases. Two patients died. Treatment delay was significant. All patients received corticosteroids. Response rate was 50%. As second-line, intravenous immunoglobulins were ineffective. Anakinra was highly effective. After ICU discharge, most patients required additional treatment. Literature analysis included 79 cases of AOSD with organ manifestations, which mainly included reactive hemophagocytic syndrome (42%), acute respiratory failure (34%), and cardiac complications (23%). Response rate to corticosteroids was 68%. Response rates to IVIgs, cyclosporin, and anakinra were 50%, 80%, and 100%, respectively. CONCLUSIONS: AOSD should be recognized as a rare cause of sepsis mimic in patients with fever of unknown origin admitted to the ICU. The diagnosis relies on a few simple clinical clues. Early intensive treatment may be discussed. IVIgs should be abandoned. Long-term prognosis is favorable. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2012-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5896069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-58960692018-04-20 Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review Néel, Antoine Wahbi, Anaïs Tessoulin, Benoit Boileau, Julien Carpentier, Dorothée Decaux, Olivier Fardet, Laurence Geri, Guillaume Godmer, Pascal Goujard, Cécile Maisonneuve, Hervé Mari, Arnaud Pouchot, Jacques Ziza, Jean-Marc Bretonnière, Cédric Hamidou, Mohamed Crit Care Research BACKGROUND: Adult-onset Still disease (AOSD) is a rare systemic inflammatory disorder. A few patients develop organ complications that can be life-threatening. Our objectives were to describe the disease course and phenotype of life-threatening AOSD, including response to therapy and long-term outcome. METHODS: A multicenter case series of intensive care medicine (ICU) patients with life-threatening AOSD and a systematic literature review. RESULTS: Twenty patients were included. ICU admission mostly occurred at disease onset (90%). Disease manifestations included fever (100%), sore throat (65%), skin rash (65%), and arthromyalgia (55%). Serum ferritin was markedly high (median: 29,110 ng/mL). Acute respiratory failure, shock and multiple organ failure occurred in 15 (75%), 10 (50%), and 7 (35%) cases, respectively. Hemophagocytosis was demonstrated in eight cases. Two patients died. Treatment delay was significant. All patients received corticosteroids. Response rate was 50%. As second-line, intravenous immunoglobulins were ineffective. Anakinra was highly effective. After ICU discharge, most patients required additional treatment. Literature analysis included 79 cases of AOSD with organ manifestations, which mainly included reactive hemophagocytic syndrome (42%), acute respiratory failure (34%), and cardiac complications (23%). Response rate to corticosteroids was 68%. Response rates to IVIgs, cyclosporin, and anakinra were 50%, 80%, and 100%, respectively. CONCLUSIONS: AOSD should be recognized as a rare cause of sepsis mimic in patients with fever of unknown origin admitted to the ICU. The diagnosis relies on a few simple clinical clues. Early intensive treatment may be discussed. IVIgs should be abandoned. Long-term prognosis is favorable. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-018-2012-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-11 /pmc/articles/PMC5896069/ /pubmed/29642928 http://dx.doi.org/10.1186/s13054-018-2012-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Néel, Antoine Wahbi, Anaïs Tessoulin, Benoit Boileau, Julien Carpentier, Dorothée Decaux, Olivier Fardet, Laurence Geri, Guillaume Godmer, Pascal Goujard, Cécile Maisonneuve, Hervé Mari, Arnaud Pouchot, Jacques Ziza, Jean-Marc Bretonnière, Cédric Hamidou, Mohamed Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title | Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title_full | Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title_fullStr | Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title_full_unstemmed | Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title_short | Diagnostic and management of life-threatening Adult-Onset Still Disease: a French nationwide multicenter study and systematic literature review |
title_sort | diagnostic and management of life-threatening adult-onset still disease: a french nationwide multicenter study and systematic literature review |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896069/ https://www.ncbi.nlm.nih.gov/pubmed/29642928 http://dx.doi.org/10.1186/s13054-018-2012-2 |
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