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. 2017 Jul 17;17:168. doi: 10.1186/s12887-017-0926-5

Table 2.

Clinical characteristics of the study sample (children)

Group1 Group2
TN → SC* SC → TN*
(n = 30) (n = 25)
Diagnosis
 Behçet syndrom 0 1 (4%)
 JIA (enthesitis-related) 9 (30%) 7 (26%)
 JIA (undifferenciated) 1 (3%) 2 (8%)
 JIA (oligoarticular) 5 (17%) 10 (37%)
 JIA (polyarticular) 0 4 (15%)
 JIA (systemic) 1 (3%) 0
 Chronic osteomyelitis 1 (3%) 1 (4%)
 Auto-inflammatory disease 0 (0%) 1 (4%)
 Juvenile dermatomyositis (JDM) 1 (3%) 0 (0%)
 Uveitis 2 (7%) 1 (4%)
 Chronic infantile neurological cutaneous articular (CINCA) syndrom 1 (3%) 0
 Lupus 1 (3%) 0
 Crohn’s disease 1 (3%) 0
 Undetermined 4 (13%) 0
Severity a
 Mild/moderate 27 (90%) 23 (92%)
 Severe 3 (10%) 2 (8%)

Allocation order of TN telenursing; SC standard care, for 12 months each. JIA juvenile idiopathic arthritis

aSeverity of the disease was assessed prior randomization, by the treating physician using the

JADAS