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602 Childhood-onset Systemic Lupus Erythematosus: Long-term outcomes in a large multi-ethnic Ontario cohort
  1. Steve Jeoung1,
  2. Roberta A Berard2,
  3. Janet E Pope3,
  4. Johannes Roth4,
  5. J Carter Thorne5,
  6. Earl D Silverman6 and
  7. Deborah M Levy6
  1. 1University of Toronto, Kuan Liu, University of Toronto
  2. 2Children’s Hospital of Western Ontario, Wesley Fidler, St. Joseph’s Hospital
  3. 3St. Joseph’s Health Care, University of Western Ontario
  4. 4University of Ottawa
  5. 5Southlake Regional Health Centre
  6. 6The Hospital for Sick Children, University of Toronto
  7. 7The Hospital for Sick Children and University of Toronto


Background/Purpose The long-term morbidity and mortality of childhood-onset SLE (cSLE) after transition to adult care is not well documented. The present study aims to fill this knowledge gap by analyzing outcomes in a large province-wide cSLE clinical cohort linked to multiple administrative healthcare databases. Our objectives were to: 1) determine all-cause and cause-specific mortality rates, adverse renal event rates, cardiovascular event rates, and cancer rates in cSLE; and 2) determine baseline characteristics associated with higher rates of transition between 3 different states: event-free (entry), adverse renal event, and death.

Methods Clinical data were abstracted for cSLE patients (<18 years at diagnosis) diagnosed between January 1990 and March 2011 and followed for ≥1 year after contacting all pediatric and adult rheumatologists and nephrologists practicing in Ontario. Data and Ontario Health Insurance Plan (OHIP) numbers were securely transferred to the Institute for Clinical and Evaluative Sciences (ICES). OHIP numbers were transformed into an encrypted ICES key number (IKN) used to link the cohort to multiple administrative datasets to determine the outcomes of interest. We examined descriptive summaries of major outcomes including death, adverse renal events (end-stage kidney disease [ESKD] requiring chronic dialysis and renal transplant), cardiovascular events (including angina, transient ischemic attack, endocarditis, myocardial infarction, pericarditis, stroke), and cancer. In addition, we modeled the disease progression with a multi-state Cox model (figure 1) to determine baseline demographic and clinical characteristics that were significantly associated with higher rates of transition from being event-free to experiencing an adverse renal event, from being event-free to experiencing death, and from experiencing an adverse renal event to experiencing death.

Results There were 38 deaths in a cohort of 615 patients with the mean follow-up time of 14.4 person years. The all-cause mortality rate was 3.36 per 1000 person-years. The rates for end- stage kidney disease (ESKD) requiring chronic dialysis and renal transplant were 3.87 and 2.43 per 1000 person-years, respectively. The rate for any type of cardiovascular event and cancer were 6.49 and 3.47 per 1000 person-years, respectively. The multi-state Cox model indicated that the Black ethnic group (HR, 3.58; 95% CI, 1.6-8.0) and the presence of renal involvement at baseline (HR, 2.19; 95% CI, 1.2-4.1) were significantly associated with higher rates of transition from event-free to adverse renal event. Additionally, the Black ethnic group (HR, 5.45; 95% CI, 1.6-18.8) was significantly associated with higher rates of transition from event-free to death.

None of the variables were significantly associated with higher rates of transition from adverse renal event to death.

Conclusion In this large Canadian multi-ethnic long-term cSLE cohort, ethnicity was associated with adverse outcomes including adverse renal events and death. Further analyses will help inform risk for adverse outcomes to improve clinical care for the highest risk patients.

Abstract 602 Table 1

Baseline table stratified by death status

Abstract 602 Table 2

Descriptive summary of major outcomes of cSLE

Abstract 602 Figure 1

Multi-state model diagram

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