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. Author manuscript; available in PMC: 2023 Dec 1.
Published in final edited form as: Pediatr Crit Care Med. 2022 Sep 30;23(12):968–979. doi: 10.1097/PCC.0000000000003074

Table 1.

Clinical characteristics by CRP-ferritin multi- trajectory group1

CRP-ferritin Multi- Trajectory Group

Group 1 (N = 8) Group 2 (N = 80) Group 3 (N = 16) Group 4 (N = 121) Group 5 (N = 30) P-value
Age at onset of organ failure (in years) 1 [0, 2] 3 [1, 8] 4 [0, 11] 8 [3, 14] 10 [6, 13] <.0012

Male 3 (38%) 42 (53%) 9 (56%) 75 (62%) 14 (47%) 0.3533

PRISM 6 [0, 12] 7 [3, 12] 15 [8, 22] 9 [5, 15] 9 [5, 13] 0.0192

OFI on Day 0 1 [1, 2] 2 [1, 2] 3 [1, 3] 2 [1, 2] 2 [1, 3] 0.0992

Cancer 0 (0%) 2 (3%) 3 (19%) 6 (5%) 15 (50%) <.0013

Transplant 0 (0%) 2 (3%) 2 (13%) 5 (4%) 11 (37%) <.0013

Chronic illness 4 (50%) 41 (51%) 11 (69%) 64 (53%) 23 (77%) 0.1043

INFECTIONS AT ELIGIBILITY4

 Bacterial 3 (38%) 22 (28%) 4 (25%) 55 (45%) 13 (43%) 0.2753

 Viral 4 (50%) 35 (44%) 4 (25%) 25 (21%) 8 (27%) 0.0883

 Fungal 0 (0%) 0 (0%) 0 (0%) 2 (2%) 1 (3%) 0.6273
1

Only subjects with the first two samples were included in biomarker trajectory analyses.

2

Kruskal-Wallis test.

3

Fisher’s exact test (Monte Carlo approximation).

4

Documented infections at the time of study eligibility are reported. The statistical tests compare documented vs. suspected infections.