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. Author manuscript; available in PMC: 2017 Mar 1.
Published in final edited form as: Arthritis Care Res (Hoboken). 2016 Mar;68(3):357–365. doi: 10.1002/acr.22685

Table 2.

Incidence of all-cause end-stage renal disease among SLE patients in the Georgia Lupus Registry, through 4/30/11a

Cohort No. of
patients
at risk
No. of
ESRD
events
Total
patient-
years at
risk
Median (IQR)
years to
ESRDb
Incidence rate,
per 1000
patient-years
(95% CI)
5-year
cumulative
incidence,c
%
Incident SLE by
combined case
definitiond
344 29 2603.8 4.1 (2.0-5.9) 11.1 (7.7-16.0) 5.2
Incident SLE by≥4
ACR criteria only
266 25 2007.8 4.1 (1.3-5.8) 12.5 (8.4-18.4) 6.0
Point prevalent
SLEe by combined
case definitiond
1488 95 --- 2.6 (1.6-4.6) --- 5.2

ACR, American College of Rheumatology; ESRD, end-stage renal disease; IQR, interquartile range; SLE, systemic lupus erythematosus.

a

Last date of death follow-up in the Georgia Lupus Registry. A total of 30 patients initiated ESRD treatment between date of SLE diagnosis and 9/30/12, the last date of ESRD follow-up.

b

Among those who progress to ESRD by 4/30/11.

c

Representing 18, 16, and 78 ESRD events within 5 years for the three cohorts listed.

d

Combined case definition, ≥4 ACR criteria, 3 ACR criteria plus treating rheumatologist’s diagnosis, or renal involvement as indicated by biopsy consistent with class II-VI lupus nephritis or ESRD requiring dialysis or renal transplantation.

e

Point prevalent cohort of patients in the GLR alive with an existing diagnosis of SLE (primary combined case definition) and free of ESRD on 12/31/04. Because patients who died with SLE prior to 12/31/04 were at risk for ESRD, patient-years and incidence rates were not calculated for this cohort.