Table 1.
Primary diagnosis of neonatal cholestasis.
| Primary diagnosis for neonatal cholestasis | Dataset |
|
|---|---|---|
| Complete-case n = 2661 (%) | Whole-case n = 4028 (%) | |
| Prematurity and birth-related issues | 654 (24.6%) | 1426 (35.4%) |
| Congenital heart anomaly and other problems | 663 (24.9%) | 751 (18.6%) |
| Liver origin diseases including biliary atresia and hepatitis | 416 (15.6%) | 461 (11.4%) |
| Gastrointestinal anomaly and other problems | 345 (13%) | 369 (9.2%) |
| Neonatal jaundice in healthy newborns | 58 (2.2%) | 299 (7.4%) |
| Respiratory anomaly and related issues | 178 (6.7%) | 222 (5.5%) |
| Genetic/chromosomal disorders | 141 (5.3%) | 174 (4.3%) |
| Renal anomalies and urinary tract issues | 55 (2.1%) | 81 (2.0%) |
| Malignancy and tumour | 57 (2.1%) | 59 (1.5%) |
| Brain anomalies and other neurologic issues | 32 (1.2%) | 48 (1.2%) |
| Infection | 15 (0.6%) | 43 (1.1%) |
| Haematologic disorders | 16 (0.6%) | 38 (0.9%) |
| Hypopituitarism/hypothyroidism | 9 (0.3%) | 27 (0.7%) |
| Others | 22 (0.8%) | 30 (0.7%) |