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. 2021 Apr 28;9:665815. doi: 10.3389/fped.2021.665815

Table 1.

Baseline features at diagnosis, medication and complication*.

KD KD/sJIA P-value
(n = 1765) (n = 8)
Demographics
Sex (male) 1,091 (62%) 6 (75%) 0.72
Age at diagnosis, years (median, IQR) 3.1 (1.7–5.3) 4.7 (2.1–5.3) 0.81
Less than 1 year old 218 (12%) 0 (0%) 0.61
Greater than 9 years old 130 (7%) 0 (0%) 1.00
Classic Kawasaki disease clinical signs
Number of days of fever pre–diagnosis 6 (5–8) 5 (5–6) 0.20
Incomplete Kawasaki disease 483 (29%) 4 (50%) 0.24
Bilateral conjunctival injection 1,433 (88%) 4 (50%) 0.01
Oral changes 1,424 (87%) 7 (88%) 1.00
Extremity changes 1,250 (77%) 6 (75.0%) 1.00
Polymorphous skin rash 1,436 (88%) 8 (100%) 0.61
Cervical lymphadenopathy 962 (59%) 3 (38%) 1.00
Laboratory investigations
Albumin (g/L) 35 ± 6 29 ± 5 0.01
Alanine transaminase (U/L) 28 (16–67) 21 (11–29) <0.001
Aspartate transaminase (U/L) 37 (27–55) 30 (28–52) 0.04
C-reactive protein (mg/L) 35 (28–47) 35 (31–202) 0.32
Erythrocytes sedimentation rate (mm/h) 68 (41–95) 104 (62–120) 0.08
Hematocrit 0.334 (0.311–0.358) 0.322 (0.266–0.329) 0.11
Hemoglobin (g/L) 113 ± 13 102 ± 17 0.13
Lymphocytes (109 cells per L) 2.6 (1.6–4.2) 1.9 (1.0–3.6) 0.09
Platelets (109 cells per L) 355 (267–462) 408 (315–546) 0.54
Red blood cells (1012 cells per L) 4.2 ± 0.5 3.9 ± 0.4 0.14
White blood cells (109 cells per L) 13.0 (9.3–16.9) 17.0 (15.1–20.6) 0.03
Treatment
Multiple intravenous immunoglobulin 221 (14%) 6 (75%) <0.001
Intravenous steroids 115 (7%) 7 (88%) <0.001
Oral steroids 56 (3%) 5 (63%) <0.001
Complications
No coronary artery aneurysms (z-score <2.5) 1,271 (86%) 6 (75%) 0.32
Small coronary artery aneurysms (z-score 2.5–5.0) 125 (9%) 2 (25%) 0.14
Large coronary artery aneurysms (z-score 5.0–10.0) 40 (3%) 0 (0%) <0.001
Giant coronary artery aneurysms (z-score >10) 43 (3%) 0 (0%) <0.001
Macrophage activation syndrome 16 (1%) 1 (13%) 0.07
*

Data are reported as frequencies with percentages, means with standard deviation or median with interquartile range.

Obtained from comparison between patients from the KD cohort and KD patients with a co-diagnosis of sJIA.

KD, Kawasaki disease; sJIA, systemic idiopathic arthritis; KD/sJIA, Kawasaki disease patients with a co-diagnosis of systemic juvenile idiopathic arthritis.