Patient subgroup | No of GLR patients with SLE with ESRD attributed to SLE in USRDS | No of GLR patients with SLE progressing to ESRD | Attribution of ESRD to SLE (95% CI) |
---|---|---|---|
Overall | 198 | 251 | 78.9% (73.3% to 83.8%) |
Demographics | |||
Age at SLE diagnosis, years | |||
<18 | 77 | 82 | 93.9% (86.3% to 98.0%) |
18–30 | 80 | 91 | 87.9% (79.4% to 93.8%) |
>30 | 41 | 78 | 52.6% (40.9% to 64.0%) |
p Value* | <0.001 | ||
Sex | |||
Male | 31 | 38 | 81.6% (65.7% to 92.3%) |
Female | 167 | 213 | 78.4% (72.3% to 83.7%) |
p Value* | 0.66 | ||
Race† | |||
Black | 184 | 232 | 79.3% (73.5% to 84.3%) |
White | 13 | 18 | 72.2% (46.5% to 90.3%) |
p Value* | 0.48 | ||
% black residents in residential census tract | |||
Above median | 93 | 116 | 80.2% (71.7% to 87.0%) |
Below median | 88 | 114 | 77.2% (68.4% to 84.5%) |
p Value* | 0.58 | ||
% living below poverty in residential census tract | |||
Above median | 87 | 115 | 75.7% (66.8% to 83.2%) |
Below median | 94 | 115 | 81.7% (73.5% to 88.3%) |
p Value* | 0.26 | ||
% high-school dropouts in residential census tract | |||
Above median | 89 | 115 | 77.4% (68.7% to 84.7%) |
Below median | 92 | 115 | 80.0% (71.5% to 86.9%) |
p Value* | 0.63 | ||
Access to care | |||
Insurance at start of ESRD | |||
Private | 66 | 91 | 72.5% (62.2% to 81.4%) |
Medicaid | 56 | 65 | 86.2% (75.3% to 93.5%) |
Other | 30 | 42 | 71.4% (55.4% to 84.3%) |
None | 29 | 31 | 93.5% (78.6% to 99.2%) |
p Value* | 0.02 | ||
Pre-ESRD nephrology care‡ | |||
Yes | 56 | 77 | 72.7% (61.4% to 82.3%) |
No | 21 | 23 | 91.3% (72.0% to 98.9%) |
p Value* | 0.06 | ||
Physician stating final SLE diagnosis | |||
No rheumatologist, dermatologist or nephrologists | 20 | 33 | 60.6% (42.1% to 77.1%) |
Rheumatologist | 61 | 83 | 73.5% (62.7% to 82.6%) |
Dermatologist | 3 | 4 | 75.0% (19.4% to 99.4%) |
Nephrologist | 32 | 39 | 82.1% (66.5% to 92.5%) |
Combination of rheumatologist, dermatologist or nephrologist | 81 | 91 | 89.0% (80.7% to 94.6%) |
p Value* | 0.008 | ||
At least one renal biopsy | |||
Yes | 141 | 173 | 81.5% (74.9% to 87.0%) |
No | 57 | 78 | 73.1% (61.8% to 82.5%) |
p Value* | 0.13 | ||
Multiple renal biopsies | |||
Yes | 129 | 169 | 76.3% (69.2% to 82.5%) |
No | 69 | 82 | 84.2% (74.4% to 91.3%) |
p Value* | 0.16 | ||
Clinical | |||
Duration of SLE prior to ESRD start, years | |||
<5 | 64 | 80 | 80.0% (69.6% to 88.1%) |
5–10 | 52 | 64 | 81.3% (69.5% to 89.9%) |
>10 | 82 | 107 | 76.6% (67.5% to 84.3%) |
p Value* | 0.74 | ||
Physician-stated SLE-related diagnosis | |||
SLE | 184 | 219 | 84.0% (78.5% to 88.6%) |
SLE and connective tissue disease | 10 | 22 | 45.5% (24.4% to 67.8%) |
Drug-induced lupus | 0 | 1 | 0% |
Specified connective tissue disease | 2 | 5 | 40.0% (5.3% to 85.3%) |
Unspecified diffuse connective tissue disease | 1 | 1 | 100% |
p Value* | <0.001 | ||
ACR criteria, % | |||
≥4 criteria | 157 | 193 | 81.4% (75.1% to 86.6%) |
<3 criteria | 41 | 58 | 70.7% (57.3% to 81.9%) |
p Value* | 0.08 | ||
ACR criterion present | |||
Malar rash | 63 | 72 | 87.5% (77.6% to 94.1%) |
Discoid rash | 29 | 35 | 82.9% (66.4% to 93.4%) |
Photosensitivity | 42 | 47 | 89.4% (76.9% to 96.5%) |
Mucocutaneous ulcers | 37 | 43 | 86.1% (72.1% to 94.7%) |
Arthritis | 136 | 161 | 84.5% (77.9% to 89.7%) |
Serositis | 99 | 119 | 83.2% (75.2% to 89.4%) |
Renal | 190 | 241 | 78.8% (73.1% to 83.8%) |
Neurological | 51 | 59 | 86.4% (75.0% to 94.0%) |
Haematological | 188 | 231 | 81.4% (75.8% to 86.2%) |
Immunological | 158 | 184 | 85.9% (80.0% to 90.6%) |
ANA | 162 | 206 | 78.6% (72.4% to 84.0%) |
Year of ESRD start | |||
Before 1995 | 22 | 27 | 81.5% (61.9% to 93.7%) |
1995–2004 | 96 | 120 | 80.0% (71.7% to 86.7%) |
2005 or later | 80 | 104 | 76.9% (67.6% to 84.6%) |
p Value* | 0.80 |
*By χ2 or Fisher's exact test.
†Restricted to white and black patients only.
‡Pre-ESRD nephrology care collected 2005+ only.
ACR, American College of Rheumatology; ESRD, end-stage renal disease; ESRD Medical Eligibility Form 2728; SLE, systemic lupus erythematosus; USRDS, United States Renal Data System.