Assessment of the HScore for reactive haemophagocytic syndrome in patients with rheumatic diseases

被引:54
作者
Batu, E. D. [1 ]
Erden, A. [2 ]
Seyhoglu, E. [3 ]
Kilic, L. [2 ]
Buyukasik, Y. [4 ]
Karadag, O. [2 ]
Bilginer, Y. [1 ]
Bilgen, S. A. [2 ]
Akdogan, A. [2 ]
Kiraz, S. [2 ]
Ertenli, A. I. [2 ]
Ozen, S. [1 ]
Kalyoncu, U. [2 ]
机构
[1] Hacettepe Univ, Div Rheumatol, Dept Paediat, Fac Med, Ankara, Turkey
[2] Hacettepe Univ, Div Rheumatol, Dept Internal Med, Fac Med, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Dept Internal Med, Fac Med, Ankara, Turkey
[4] Hacettepe Univ, Div Haematol, Dept Internal Med, Fac Med, Ankara, Turkey
关键词
MACROPHAGE ACTIVATION SYNDROME; JUVENILE IDIOPATHIC ARTHRITIS; HISTIOCYTIC HYPERPLASIA; CLINICAL-FEATURES; DIAGNOSIS; ADULTS;
D O I
10.3109/03009742.2016.1167951
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Objectives: Reactive haemophagocytic syndrome (RHS) is a hyperinflammatory disorder often occurring in the background of several disorders such as infections, malignancies, and rheumatic diseases. Recently, a score known as the HScore was developed for the diagnosis of RHS. In the original study, most of the patients had underlying haematological malignancy or infection and the best cut-off value for the HScore was 169 (sensitivity 93%; specificity 86%). In this study we aimed to analyse the performance of the HScore in rheumatic disease-related RHS.Method: The patients with rheumatic disorders evaluated in the Departments of Rheumatology and Paediatric Rheumatology at Hacettepe University, Ankara, Turkey between 2002 and 2014 were reviewed retrospectively. The first group (n=30) consisted of patients with RHS; the control group (n=64) included patients with active rheumatic diseases without RHS.Results: In the RHS group, 14 (46.7%) had adult-onset Still's disease (AOSD), 10 (33.3%) systemic juvenile idiopathic arthritis (SJIA), and six (20%) systemic lupus erythematosus (SLE). The control group (n=64) consisted of 32 (50%) AOSD, 13 (20.3%) SJIA, and 19 (29.7%) SLE patients. Applying the HScore to the RHS patients, the best cut-off value was 190.5 with a sensitivity of 96.7% and specificity of 98.4%. When we excluded the patients from the control group who had not had bone marrow aspiration (n=23), the same cut-off (190.5) performed best (sensitivity 96.7%; specificity 97.6%). Applying the 2004 haemophagocytic lymphohistiocytosis (HLH-2004) criteria gave a sensitivity of 56.6% and a specificity of 100% in the whole study group.Conclusions: In our study, a cut-off value for the HScore different from the original study performed better. Further studies are warranted to determine optimum cut-off values in different studies.
引用
收藏
页码:44 / 48
页数:5
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