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. 2017 Feb 23;33(2):356–364. doi: 10.1093/ndt/gfw444

Table 3.

Cox regression model on the effect of age group at RRT start on mortality, adjusting age group by other variables

Variable Hazard ratio 95% CI P-value
Age group (years)
 11–<16 1.00
 16–<21 1.87 0.95–3.67 0.07
 21–<26 2.12 1.11–4.05 0.02
 26–30 2.04 1.07–3.87 0.03
Sex
 Male 1.00
 Female 1.13 0.88–1.46 0.3
Ethnicity
 White 1.00
 Asian 0.59 0.36–0.98 0.04
 Black 0.71 0.43–1.15 0.2
 Other 0.64 0.30–1.38 0.3
Year of start
 1999-2002 1.35 1.00–1.83 0.05
 2003-2005 0.97 0.71–1.33 0.9
 2006-2008 1.00
Modality
 Transplant 1.00
 Dialysis, transplant listed 4.20 2.61–6.75 <0.0001
 Dialysis, not transplant listed 16.6 10.8–25.4 <0.0001
Primary renal diagnosis
 Glomerular Diseasea 1.00
 Familial/hereditary nephropathies
  Other familial/hereditary nephropathies 0.59 0.21–1.66 0.3
  Polycystic kidney disease 1.07 0.33–3.44 0.9
 Miscellaneous renal disorders 1.88 1.28–2.76 0.001
 Systemic diseases affecting the kidney
  Diabetesb 4.03 2.71–6.01 <0.0001
  Other systemic diseasesc 1.93 1.08–3.48 0.03
 Tubulointerstitial disease
  Obstructive 1.37 0.78–2.40 0.3
  Renal dysplasia ± reflux 0.43 0.20–0.97 0.04
  Other tubulointerstitial diseased 6.49 4.07–10.4 <0.0001

Data based on 3243 patients and 248 events and excludes those with a missing ethnicity or PRD.

a

Glomerular disease was chosen as a comparator, as it was the most frequent diagnosis.

b

There was a significant non-proportionality over time between those with and without diabetes, with the effect seen only after 230 days and no effect on other HRs when using a piecewise Cox regression analysis; this model presents the overall HR for the entire follow-up period.

c

PRD codes in the ‘other systemic diseases’ group include amyloid, haemolytic uraemic syndrome, renovascular diseases and hypertension. Of those with amyloid (n = 15), 33.3% died, while the proportion of death from other conditions was 6.6, 8.6 and 6.5%, respectively.

d

PRD codes in the ‘other tubulointerstitial disease’ group include drug-induced tubulopathies and interstitial nephritis; of those with drug-induced tubulopathies (n = 65), 32.3% died and of those with interstitial nephritis (n = 45), 15.6% died.