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The bm12 Inducible Model of Systemic Lupus Erythematosus SLE in C57BL/6 Mice
Published on: November 1, 2015
Outcomes in hospitalized pediatric patients with systemic lupus erythematosus
Mary Beth F Son1, Victor M Johnson, Aimee O Hersh
1Division of Immunology, Boston Children's Hospital, 300 Longwood Ave, Boston, MA 02115. marybeth.son@childrens.harvard.edu.
Insights
Racial and ethnic disparities impact outcomes for children with childhood-onset systemic lupus erythematosus (SLE). Hispanic patients experienced longer hospital stays and higher mortality, while African American race was linked to ICU admissions and death.
Area of Science:
- Pediatric Rheumatology
- Health Disparities Research
- Systemic Lupus Erythematosus (SLE) Studies
Background:
- Documented outcome disparities exist in adults with systemic lupus erythematosus (SLE).
- Limited data are available on sociodemographic factors influencing outcomes in childhood-onset SLE.
- Understanding these disparities is crucial for improving care in pediatric SLE patients.
Purpose of the Study:
- To investigate associations between sociodemographic factors and hospital admission volume.
- To examine the relationship between these factors and hospitalization characteristics.
- To identify risk factors for poor outcomes in patients with childhood-onset SLE.
Main Methods:
- Analysis of 10,724 admissions for 2775 patients (aged 3–17 years) with SLE from January 2006 to September 2011 using the Pediatric Health Information System.
- Descriptive statistics and univariable analyses for demographic characteristics, readmissions, and length of stay.
- Multivariable logistic regression controlling for covariates to assess risk factors for adverse outcomes.
Main Results:
- Hispanic patients had longer hospital stays, more readmissions, and higher in-hospital mortality.
- African American race was significantly associated with intensive care unit (ICU) admission.
- African American race and Hispanic ethnicity were linked to end-stage renal disease and death.
Conclusions:
- Race and ethnicity are significantly associated with adverse outcomes in hospitalized children with SLE.
- Hospital volume and location did not show significant associations with patient outcomes.
- Further research is necessary to fully understand the complex relationship between sociodemographic factors and poor outcomes in childhood-onset SLE.
Objective:
Disparities in outcomes among adults with systemic lupus erythematosus (SLE) have been documented. We investigated associations between sociodemographic factors and volume of annual inpatient hospital admissions with hospitalization characteristics and poor outcomes among patients with childhood-onset SLE.
Methods:
By using the Pediatric Health Information System, we analyzed admissions for patients aged 3 to <18 years at index admission with ≥ 1 International Classification of Diseases, Ninth Revision code for SLE from January 2006 to September 2011. Summary statistics and univariable analyses were used to examine demographic characteristics of hospital admissions, readmissions, and lengths of stay. We used multivariable logistic regression analyses, controlling for patient gender, age, race, ethnicity, insurance type, hospital volume, US census region, and severity of illness, to examine risk factors for poor outcomes.
Results:
A total of 10,724 admissions occurred among 2775 patients over the study period. Hispanic patients had longer lengths of stay, more readmissions, and higher in-hospital mortality. In multivariable analysis, African American race was significantly associated with ICU admission. African American race and Hispanic ethnicity were associated with end-stage renal disease and death. Volume of patients with SLE per hospital and hospital location were not significantly associated with outcomes.
Conclusions:
In this cohort of hospitalized children with SLE, race and ethnicity were associated with outcomes. Further studies are needed to elucidate the relationship between sociodemographic factors and poor outcomes in patients with childhood-onset SLE.
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