Skip to main content
. 2016 Jan 19;2(1):e000161. doi: 10.1136/rmdopen-2015-000161

Table 1.

Comparison of demographic, clinical and histopathological features, triggers, treatments and outcome between patients classified as MAS or non-MAS, by the expert panel*

N Patients classified as MAS (n=70) N Patients classified as non-MAS (n=33) p Value
Demographic characteristics
Sex 70 33 0.81
 Female 42 (60.0) 19 (57.6)
 Male 28 (40.0) 14 (42.4)
Age at onset of MAS, median (IQR), years 69 10.5 (4.4–14.6) 32 7.6 (4.1–11.6) 0.01
Duration of systemic JIA at MAS onset, median (IQR), years 69 0.9 (0.1–2.4) 31 1.5 (0.1–4.1) 0.31
Clinical manifestations at onset of MAS
Fever 69 68 (98.5) 33 28 (84.9) 0.01†
Hepatomegaly 67 50 (74.6) 33 16 (48.5) 0.01
Splenomegaly 65 37 (56.9) 33 16 (48.5) 0.43
Lymphadenopathy 65 36 (55.4) 32 8 (25.0) 0.005
Active arthritis 69 42 (60.9) 33 17 (51.5) 0.37
Central nervous system involvement 65 31 (47.7) 33 8 (24.2) 0.02
Haemorrhagic manifestations 67 26 (38.8) 33 4 (12.1) 0.006
Heart, lung or kidney failure 69 13 (18.8) 33 1 (3.0) 0.03
Triggers 0.49‡
Active disease 58 28 (48.3) 27 14 (51.8)
Infection 58 23 (39.6) 27 7 (25.9)
Treatment toxicity 58 1 (1.7) 27 3 (11.1)
Other 58 3 (5.2) 27 2 (7.4)
Unknown 58 3 (5.2) 27 2 (7.4)
Histopathological features
Bone marrow aspiration and/or biopsy of l ymphnode and/or liver 69 54 (78.3) 33 16 (48.5) 0.002
Haemophagocytosis on bone marrow aspiration and/or biopsy of lymphnode and/or liver 54 31 (57.4) 16 11 (68.7) 0.42
Therapeutic interventions
Any corticosteroids 69 68 (98.5) 33 33 (100.0) 1.0
Cyclosporine 69 47 (68.1) 33 24 (72.7) 0.64
Intravenous immunoglobulin 68 27 (39.7) 33 10 (30.3) 0.36
Biological medications† 68 17 (25.0) 33 9 (27.3) 0.81
Etoposide 67 10 (14.9) 33 4 (12.1) 1.0
Other immunosuppressants 66 5 (7.6) 32 3 (9.1) 0.71
Plasma exchange 67 6 (9.0) 33 2 (6.1) 1.0
Outcome
ICU admission 58 26 (44.8) 29 5 (17.2) 0.01
Death 69 7 (10.1) 33 0 (0.0) 0.01

*Except where indicated otherwise, data are the number (%).

†Administered biological medications included anakinra, tocilizumab, canakinumab, etanercept, abatacept, rituximab, alentuzumab.

‡The statistical comparison was made on the ensemble of triggering factors.

ICU, intensive care unit; JIA, juvenile idiopathic arthritis; MAS, macrophage activation syndrome.