Literature DB >> 26865703

2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative.

Angelo Ravelli1, Francesca Minoia2, Sergio Davì2, AnnaCarin Horne3, Francesca Bovis2, Angela Pistorio2, Maurizio Aricò4, Tadej Avcin5, Edward M Behrens6, Fabrizio De Benedetti7, Lisa Filipovic8, Alexei A Grom8, Jan-Inge Henter3, Norman T Ilowite9, Michael B Jordan8, Raju Khubchandani10, Toshiyuki Kitoh11, Kai Lehmberg12, Daniel J Lovell8, Paivi Miettunen13, Kim E Nichols14, Seza Ozen15, Jana Pachlopnik Schmid16, Athimalaipet V Ramanan17, Ricardo Russo18, Rayfel Schneider19, Gary Sterba20, Yosef Uziel21, Carol Wallace22, Carine Wouters23, Nico Wulffraat24, Erkan Demirkaya25, Hermine I Brunner8, Alberto Martini1, Nicolino Ruperto2, Randy Q Cron26.   

Abstract

To develop criteria for the classification of macrophage activation syndrome (MAS) in patients with systemic juvenile idiopathic arthritis (JIA). A multistep process, based on a combination of expert consensus and analysis of real patient data, was conducted. A panel of 28 experts was first asked to classify 428 patient profiles as having or not having MAS, based on clinical and laboratory features at the time of disease onset. The 428 profiles comprised 161 patients with systemic JIA-associated MAS and 267 patients with a condition that could potentially be confused with MAS (active systemic JIA without evidence of MAS, or systemic infection). Next, the ability of candidate criteria to classify individual patients as having MAS or not having MAS was assessed by evaluating the agreement between the classification yielded using the criteria and the consensus classification of the experts. The final criteria were selected in a consensus conference. Experts achieved consensus on the classification of 391 of the 428 patient profiles (91.4%). A total of 982 candidate criteria were tested statistically. The 37 best-performing criteria and 8 criteria obtained from the literature were evaluated at the consensus conference. During the conference, 82% consensus among experts was reached on the final MAS classification criteria. In validation analyses, these criteria had a sensitivity of 0.73 and a specificity of 0.99. Agreement between the classification (MAS or not MAS) obtained using the criteria and the original diagnosis made by the treating physician was high (κ=0.76). We have developed a set of classification criteria for MAS complicating systemic JIA and provided preliminary evidence of its validity. Use of these criteria will potentially improve understanding of MAS in systemic JIA and enhance efforts to discover effective therapies, by ensuring appropriate patient enrollment in studies. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

Entities:  

Keywords:  Adult Onset Still's Disease; Amyloidosis; Analgesics; Ankylosing Spondylitis; Ant-CCP

Mesh:

Year:  2016        PMID: 26865703     DOI: 10.1136/annrheumdis-2015-208982

Source DB:  PubMed          Journal:  Ann Rheum Dis        ISSN: 0003-4967            Impact factor:   19.103


  110 in total

Review 1.  The rheumatology/hematology interface: CAPS and MAS diagnosis and management.

Authors:  John M Gansner; Nancy Berliner
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

2.  Impact of biologics on disease course in systemic onset juvenile idiopathic arthritis.

Authors:  Hatice Ezgi Baris; Edwin Anderson; Betul Sozeri; Fatma Dedeoglu
Journal:  Clin Rheumatol       Date:  2018-09-20       Impact factor: 2.980

3.  Macrophage activation syndrome in Still's disease: analysis of clinical characteristics and survival in paediatric and adult patients.

Authors:  Piero Ruscitti; Carmela Rago; Luciana Breda; Paola Cipriani; Vasiliki Liakouli; Onorina Berardicurti; Francesco Carubbi; Caterina Di Battista; Alberto Verrotti; Roberto Giacomelli
Journal:  Clin Rheumatol       Date:  2017-09-15       Impact factor: 2.980

Review 4.  Pediatric hemophagocytic lymphohistiocytosis.

Authors:  Scott W Canna; Rebecca A Marsh
Journal:  Blood       Date:  2020-04-16       Impact factor: 22.113

5.  [Clinical characteristics and treatment outcomes of macrophage activation syndrome in adults: A case series of 67 patients].

Authors:  H H Yao; Y N Wang; X Zhang; J X Zhao; Y Jia; Z Wang; Z G Li
Journal:  Beijing Da Xue Xue Bao Yi Xue Ban       Date:  2019-12-18

6.  Combining multiple biomarkers differentiates between active SJIA, SJIA-MAS and EBV-HLH.

Authors:  L K Weaver
Journal:  Clin Exp Immunol       Date:  2017-10-26       Impact factor: 4.330

7.  Systemic lupus erythematosus presenting to haematology with pancytopenia and features of macrophage activation syndrome.

Authors:  Jayna Mistry; Graham Knee; Vishal Jayakar
Journal:  BMJ Case Rep       Date:  2018-02-21

Review 8.  Adult-onset Still's disease with macrophage activation syndrome diagnosed and treated based on cytokine profiling: a case-based review.

Authors:  Ken Goda; Tsuneaki Kenzaka; Masahiko Hoshijima; Akihiro Yachie; Hozuka Akita
Journal:  Rheumatol Int       Date:  2019-09-20       Impact factor: 2.631

9.  Keeping up with the progress in the diagnosis and management of pediatric rheumatic diseases.

Authors:  Hong-Mei Song
Journal:  World J Pediatr       Date:  2020-02       Impact factor: 2.764

10.  Characteristic elevation of soluble TNF receptor II : I ratio in macrophage activation syndrome with systemic juvenile idiopathic arthritis.

Authors:  M Shimizu; N Inoue; M Mizuta; Y Nakagishi; A Yachie
Journal:  Clin Exp Immunol       Date:  2017-09-15       Impact factor: 4.330

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