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Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers
BACKGROUND: Adult-onset Still’s disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes, lymphadenopathy, hepatosplenomegaly, and serositis. The m...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131497/ https://www.ncbi.nlm.nih.gov/pubmed/27903264 http://dx.doi.org/10.1186/s12916-016-0738-8 |
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author | Ruscitti, Piero Cipriani, Paola Masedu, Francesco Iacono, Daniela Ciccia, Francesco Liakouli, Vasiliki Guggino, Giuliana Carubbi, Francesco Berardicurti, Onorina Di Benedetto, Paola Valenti, Marco Triolo, Giovanni Valentini, Gabriele Giacomelli, Roberto |
author_facet | Ruscitti, Piero Cipriani, Paola Masedu, Francesco Iacono, Daniela Ciccia, Francesco Liakouli, Vasiliki Guggino, Giuliana Carubbi, Francesco Berardicurti, Onorina Di Benedetto, Paola Valenti, Marco Triolo, Giovanni Valentini, Gabriele Giacomelli, Roberto |
author_sort | Ruscitti, Piero |
collection | PubMed |
description | BACKGROUND: Adult-onset Still’s disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes, lymphadenopathy, hepatosplenomegaly, and serositis. The multi-visceral involvement of the disease and the different complications, such as macrophage activation syndrome, may strongly decrease the life expectancy of AOSD patients. METHODS: This study aimed to identify the positive and negative features correlated with the outcome of patients. A retrospective analysis of AOSD patients prospectively admitted to three rheumatologic centers was performed to identify the clinical features present at the time of diagnosis and to predict the possible outcome. Furthermore, we investigated the as yet to be validated prognostic value of the systemic score previously proposed. RESULTS: One hundred consecutive AOSD patients were enrolled. The mean systemic score showed that the majority of patients had a multi-organ involvement. Sixteen patients showed different complications, mainly the macrophage activation syndrome. A strong increase of inflammatory markers was observed. All patients received steroids at different dosages, 55 patients in association with immunosuppressive drugs and 32 in association with biologic agents. Sixteen patients died during the follow-up. Regression analysis showed that the higher values of the systemic score and the presence of AOSD-related complications, assessed at the time of diagnosis, were significantly correlated with patient mortality. A prognostic impact of the systemic score of ≥ 7.0 was reported. CONCLUSIONS: Our study showed that a higher systemic score and the presence of AOSD-related complications at the time of diagnosis were significantly associated with mortality. Of note, a cut-off at 7.0 of the systemic score showed a strong prognostic impact in identifying patients at risk of AOSD-related death. |
format | Online Article Text |
id | pubmed-5131497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51314972016-12-12 Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers Ruscitti, Piero Cipriani, Paola Masedu, Francesco Iacono, Daniela Ciccia, Francesco Liakouli, Vasiliki Guggino, Giuliana Carubbi, Francesco Berardicurti, Onorina Di Benedetto, Paola Valenti, Marco Triolo, Giovanni Valentini, Gabriele Giacomelli, Roberto BMC Med Research Article BACKGROUND: Adult-onset Still’s disease (AOSD) is rare inflammatory disease of unknown etiology that usually affects young adults. The more common clinical manifestations are spiking fevers, arthritis, evanescent rash, elevated liver enzymes, lymphadenopathy, hepatosplenomegaly, and serositis. The multi-visceral involvement of the disease and the different complications, such as macrophage activation syndrome, may strongly decrease the life expectancy of AOSD patients. METHODS: This study aimed to identify the positive and negative features correlated with the outcome of patients. A retrospective analysis of AOSD patients prospectively admitted to three rheumatologic centers was performed to identify the clinical features present at the time of diagnosis and to predict the possible outcome. Furthermore, we investigated the as yet to be validated prognostic value of the systemic score previously proposed. RESULTS: One hundred consecutive AOSD patients were enrolled. The mean systemic score showed that the majority of patients had a multi-organ involvement. Sixteen patients showed different complications, mainly the macrophage activation syndrome. A strong increase of inflammatory markers was observed. All patients received steroids at different dosages, 55 patients in association with immunosuppressive drugs and 32 in association with biologic agents. Sixteen patients died during the follow-up. Regression analysis showed that the higher values of the systemic score and the presence of AOSD-related complications, assessed at the time of diagnosis, were significantly correlated with patient mortality. A prognostic impact of the systemic score of ≥ 7.0 was reported. CONCLUSIONS: Our study showed that a higher systemic score and the presence of AOSD-related complications at the time of diagnosis were significantly associated with mortality. Of note, a cut-off at 7.0 of the systemic score showed a strong prognostic impact in identifying patients at risk of AOSD-related death. BioMed Central 2016-12-01 /pmc/articles/PMC5131497/ /pubmed/27903264 http://dx.doi.org/10.1186/s12916-016-0738-8 Text en © The Author(s). 2016 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 Article Ruscitti, Piero Cipriani, Paola Masedu, Francesco Iacono, Daniela Ciccia, Francesco Liakouli, Vasiliki Guggino, Giuliana Carubbi, Francesco Berardicurti, Onorina Di Benedetto, Paola Valenti, Marco Triolo, Giovanni Valentini, Gabriele Giacomelli, Roberto Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title | Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title_full | Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title_fullStr | Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title_full_unstemmed | Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title_short | Adult-onset Still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
title_sort | adult-onset still’s disease: evaluation of prognostic tools and validation of the systemic score by analysis of 100 cases from three centers |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5131497/ https://www.ncbi.nlm.nih.gov/pubmed/27903264 http://dx.doi.org/10.1186/s12916-016-0738-8 |
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