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Published on: November 1, 2015
Risk factors for mortality in 1528 Brazilian childhood-onset systemic lupus erythematosus patients
Ana P Sakamoto1, Clovis A Silva2, Ana C Pita2
1Pediatric Rheumatology Unit, Universidade Federal de Sao Paulo, Sao Paulo, SP, Brazil.
Insights
Mortality in childhood-onset systemic lupus erythematosus (cSLE) is low but concerning. Neuropsychiatric lupus (NP-SLE) and chronic kidney disease (CKD) are significant risk factors for death in cSLE patients.
Area of Science:
- Pediatric Rheumatology
- Systemic Lupus Erythematosus Research
- Clinical Epidemiology
Background:
- Childhood-onset systemic lupus erythematosus (cSLE) is a chronic autoimmune disease with potential for significant morbidity and mortality.
- Understanding mortality patterns and risk factors in cSLE is crucial for improving patient outcomes and guiding clinical management.
Purpose of the Study:
- To identify associations between mortality and patient characteristics in cSLE.
- To evaluate risk factors for mortality in cSLE patients.
- To determine the primary causes of death in this population.
Main Methods:
- A multicenter retrospective cohort study involving 1,528 cSLE patients from 27 Brazilian pediatric rheumatology centers.
- Review of medical records for demographic, clinical, disease activity, damage scores, and treatment data.
- Univariate and multivariate Cox regression analyses to identify mortality risk factors; Kaplan-Meier plots for survival rates.
Main Results:
- A total of 63/1,528 (4.1%) patients died. Sepsis (42.8%) and opportunistic infections (11.1%) were leading causes of death.
- Neuropsychiatric lupus (NP-SLE) (HR=2.56) and chronic kidney disease (CKD) (HR=4.33) were significant risk factors for mortality.
- Overall 5, 10, and 15-year survival rates were 97%, 95.4%, and 93.8%, respectively.
Conclusions:
- The mortality rate in cSLE in Brazil is low but warrants attention.
- NP-SLE and CKD represent major risk factors, highlighting the severity of these manifestations in cSLE-related mortality.
Objectives:
To identify associations between mortality in cSLE patients and their characteristics: clinical and laboratory features, disease activity and damage scores, and treatment; to evaluate risk factors associated with mortality in cSLE; and to determine the most frequent causes of death in this group of patients.
Methods:
We performed a multicenter retrospective cohort using data from 1,528 cSLE patients followed in 27 pediatric rheumatology tertiary centers in Brazil. Patients' medical records were reviewed according to a standardized protocol, in which information regarding demographic and clinical features, disease activity and damage scores, and treatment were collected and compared between deceased cSLE patients and survivors. Univariate and multivariate analyses by Cox regression model were used to calculate risk factors for mortality, whereas survival rates were analyzed by Kaplan-Meier plots.
Results:
A total of 63/1,528 (4.1%) patients deceased, 53/63 were female (84.1%), median age at death was 11.9 (9.4-13.1) years and median time interval between cSLE diagnosis and death was 3.2 (0.5-5.3) years. Sepsis was the main cause of death in 27/63 (42.8%) patients, followed by opportunistic infections in 7/63 (11.1%), and alveolar hemorrhage in 6/63 (9.5%) patients. The regression models resulted in neuropsychiatric lupus (NP-SLE) (HR = 2.56, 95% CI = 1.48-4.42) and chronic kidney disease (CKD) (HR = 4.33, 95% CI = 2.33-4.72), as risk factors significantly associated with mortality. Overall patient survival after cSLE diagnosis at 5, 10, and 15 years were 97%, 95.4%, and 93.8%, respectively.
Conclusions:
This study confirmed that the recent mortality rate in cSLE in Brazil is low, but still of concern. NP-SLE and CKD were the main risk factors for mortality, indicating that the magnitude of these manifestations was significantly high.
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