Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus

Abstract Background Morbidity and mortality in childhood onset systemic lupus erythematosus (SLE) is more severe than adult onset SLE. Long-term follow up is needed to determine the prognosis. The objectives of this study are to describe the mortality of childhood SLE in a single tertiary care centr...

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Main Authors: Pondtip Jongvilaikasem, Edward B. McNeil, Pornsak Dissaneewate, Prayong Vachvanichsanong
Format: Article
Language:English
Published: BMC 2018-09-01
Series:Pediatric Rheumatology Online Journal
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12969-018-0274-5
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author Pondtip Jongvilaikasem
Edward B. McNeil
Pornsak Dissaneewate
Prayong Vachvanichsanong
author_facet Pondtip Jongvilaikasem
Edward B. McNeil
Pornsak Dissaneewate
Prayong Vachvanichsanong
author_sort Pondtip Jongvilaikasem
collection DOAJ
description Abstract Background Morbidity and mortality in childhood onset systemic lupus erythematosus (SLE) is more severe than adult onset SLE. Long-term follow up is needed to determine the prognosis. The objectives of this study are to describe the mortality of childhood SLE in a single tertiary care centre over three decades, compare trends in survival over time, and determine predictors for survival. Methods We retrospectively reviewed the medical records of children aged < 18 years who were diagnosed with SLE at the Department of Pediatrics, Songklanagarind Hospital, Thailand, from 1985 to 2016. Results There were 331 children (272 girls, 59 boys) with a mean age at presentation of 11.5 ± 2.6 years. The mean follow-up duration was 7.0 ± 5.0 (range 1–28) years, 77 children (23.3%) died, 28.6% within the first year after diagnosis. The overall mortality rate was 3.3 per 100 person-years. Survival rates at 1, 5 and 10 years were 93.4%, 83.1% and 72.6%, respectively. Ten-year survival rates for the children diagnosed in the decades 1985–1996, 1997–2006 and 2007–2016 were 67.4%, 63.4% and 82.8%, respectively (p < 0.001). Boys had worse survival than girls (hazard ratio = 2.3, 95% CI: 1.4–3.7) even after adjusting for decade of diagnosis. Lupus nephritis (LN) class IV had similar survival compared to LN classes II/III/V combined (hazard ratio = 1.0, 95% CI: 0.6–1.7). Conclusion In our setting, the survival rate of childhood onset SLE has improved during the past 10 years, but mortality is still high compared to developed countries, particularly in boys.
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spelling doaj.art-7ff2f2bf37c44d4c8fe46e5a3b5232c22022-12-21T19:15:44ZengBMCPediatric Rheumatology Online Journal1546-00962018-09-011611710.1186/s12969-018-0274-5Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosusPondtip Jongvilaikasem0Edward B. McNeil1Pornsak Dissaneewate2Prayong Vachvanichsanong3Department of Pediatrics, Faculty of Medicine, Prince of Songkla UniversityEpidemiology Unit, Faculty of Medicine, Prince of Songkla UniversityDepartment of Pediatrics, Faculty of Medicine, Prince of Songkla UniversityDepartment of Pediatrics, Faculty of Medicine, Prince of Songkla UniversityAbstract Background Morbidity and mortality in childhood onset systemic lupus erythematosus (SLE) is more severe than adult onset SLE. Long-term follow up is needed to determine the prognosis. The objectives of this study are to describe the mortality of childhood SLE in a single tertiary care centre over three decades, compare trends in survival over time, and determine predictors for survival. Methods We retrospectively reviewed the medical records of children aged < 18 years who were diagnosed with SLE at the Department of Pediatrics, Songklanagarind Hospital, Thailand, from 1985 to 2016. Results There were 331 children (272 girls, 59 boys) with a mean age at presentation of 11.5 ± 2.6 years. The mean follow-up duration was 7.0 ± 5.0 (range 1–28) years, 77 children (23.3%) died, 28.6% within the first year after diagnosis. The overall mortality rate was 3.3 per 100 person-years. Survival rates at 1, 5 and 10 years were 93.4%, 83.1% and 72.6%, respectively. Ten-year survival rates for the children diagnosed in the decades 1985–1996, 1997–2006 and 2007–2016 were 67.4%, 63.4% and 82.8%, respectively (p < 0.001). Boys had worse survival than girls (hazard ratio = 2.3, 95% CI: 1.4–3.7) even after adjusting for decade of diagnosis. Lupus nephritis (LN) class IV had similar survival compared to LN classes II/III/V combined (hazard ratio = 1.0, 95% CI: 0.6–1.7). Conclusion In our setting, the survival rate of childhood onset SLE has improved during the past 10 years, but mortality is still high compared to developed countries, particularly in boys.http://link.springer.com/article/10.1186/s12969-018-0274-5Childhood-onsetSurvival ratesSystemic lupus erythematosusThai
spellingShingle Pondtip Jongvilaikasem
Edward B. McNeil
Pornsak Dissaneewate
Prayong Vachvanichsanong
Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
Pediatric Rheumatology Online Journal
Childhood-onset
Survival rates
Systemic lupus erythematosus
Thai
title Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
title_full Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
title_fullStr Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
title_full_unstemmed Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
title_short Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus
title_sort improvement of survival rates in the last decade in thai childhood onset systemic lupus erythematosus
topic Childhood-onset
Survival rates
Systemic lupus erythematosus
Thai
url http://link.springer.com/article/10.1186/s12969-018-0274-5
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AT pornsakdissaneewate improvementofsurvivalratesinthelastdecadeinthaichildhoodonsetsystemiclupuserythematosus
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