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. 2022 Sep 5;7:51. doi: 10.1038/s41525-022-00326-9

Table 3.

Comparison between diagnostic and non-diagnostic rapid ES in the NICU in Phase II.

[number (%) unless otherwise noted] Diagnostic n = 22 Non-diagnostic n = 58 p valuea
Male sex 9 (41) 32 (55) 0.319
GA (weeks; median (IQR)) 37 (36, 39.8) 36 (32, 37) 0.028
Prematurity <37 weeks 8 (36) 32 (55) 0.210
BW (grams; median (IQR)) 2945 (2270, 3515) 2600 (1550, 3050) 0.011
Low BW <2500 grams 8 (36) 27 (47) 0.459
Age at genetics consult (days; median (range)) 6 (3.3, 13) 15 (4, 61) 0.123
Phenotypic criteria
Neurologic (e.g., hypotonia, seizures) 11 (50) 20 (34) 0.304
Congenital anomaly/anomalies 12 (55) 22 (38) 0.211
Suspected metabolic disease 4 (18) 17 (29) 0.401
Dysmorphic features 10 (45) 18 (31) 0.295
Failure to thrive 2 (9) 2 (3) 0.303
End of life 0 (0) 3 (5) 0.557
Family history of the genetic disorder 1 (5) 0 (0) 0.275
Likely Mendelian disorder 0 (0) 2 (3) 0.523
Critical illness
Respiratory support (CPAP, NIPPV, or intubation) 17 (77) 48 (83) 0.749
Inotropic support 5 (23) 23 (40) 0.195
Dialysis 2 (9) 2 (3) 0.303
Mortality (by 12 months) 8 (36) 13 (22) 0.257

aCalculated using two-tailed Fisher’s exact test or Mann-Whitney test.