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. Author manuscript; available in PMC: 2019 Aug 1.
Published in final edited form as: Pediatr Nephrol. 2018 Sep 7;34(2):261–267. doi: 10.1007/s00467-018-4072-6

Table 3.

Patients with ≥ 1 infection vs. no infection

Infection (N = 148) No infection (N = 222) p value

Age (years) at first hospitalization (median, IQR) 5.9 years (3.1, 10.5) 6.6 years (3.5, 11.3) 0.008
Sex (n, %) 0.486
  Male 94 (63.5) 133 (59.9)
Race/ethnicity (n, %) 0.185
  White 59 (47.2) 86 (46.2)
  Hispanic 29 (23.2) 33 (17.7)
  Black 21 (16.8) 49 (26.3)
  Other 16(12.8) 18(9.7)
Clinical pattern of NS (n, %) 0.002
  Steroid sensitive-infrequently relapsing 29 (19.6) 75 (33.8)
  Steroid sensitive-frequently relapsing 26 (17.6) 32 (14.4)
  Steroid sensitive-steroid dependent 31 (21.0) 57 (25.7)
  Steroid-resistant 53 (35.8) 46 (20.7)
  Congenital or infantile 4 (2.7) 1 (0.5)
Biopsy diagnosis (n, %) 0.441
  Minimal change disease (± mild mesangial hypercellularity) 48 (32.4) 63 (28.4)
  FSGS or FGGS 38 (25.7) 47 (21.2)
  Membranous, MPGN, others 9 (6.1) 15 (6.8)
  No biopsy 53 (35.8) 97 (43.7)
Baseline eGFR ml/min/1.73m2 (median, IQR) 129.5 (99.0, 173.1) 128.9 (95.0, 166.4) 0.633
Number of hospitalizations (median, IQR) 2 (1,3.5) 1 (1,2) <0.001
Overall hospital days (median, IQR) 10(6,22) 5 (3,8) <0.001
ICU days (median, IQR) 0 (0, 0) 0 (0, 0) <0.001

NS nephrotic syndrome, eGFR estimated glomerular filtration rate, ICU Intensive Care Unit, FGGS focal global glomerulosclerosis, FSGS focal segmental glomerulosclerosis, MPGN membranoproliferative glomerulonephritis