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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2018-09-01T00:00:00Z.
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LEADER | 00000 am a22000003u 4500 | ||
---|---|---|---|
001 | doaj_7ff2f2bf37c44d4c8fe46e5a3b5232c2 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Pondtip Jongvilaikasem |e author |
700 | 1 | 0 | |a Edward B. McNeil |e author |
700 | 1 | 0 | |a Pornsak Dissaneewate |e author |
700 | 1 | 0 | |a Prayong Vachvanichsanong |e author |
245 | 0 | 0 | |a Improvement of survival rates in the last decade in Thai childhood-onset systemic lupus erythematosus |
260 | |b BMC, |c 2018-09-01T00:00:00Z. | ||
500 | |a 10.1186/s12969-018-0274-5 | ||
500 | |a 1546-0096 | ||
520 | |a 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. | ||
546 | |a EN | ||
690 | |a Childhood-onset | ||
690 | |a Survival rates | ||
690 | |a Systemic lupus erythematosus | ||
690 | |a Thai | ||
690 | |a Pediatrics | ||
690 | |a RJ1-570 | ||
690 | |a Diseases of the musculoskeletal system | ||
690 | |a RC925-935 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Pediatric Rheumatology Online Journal, Vol 16, Iss 1, Pp 1-7 (2018) | |
787 | 0 | |n http://link.springer.com/article/10.1186/s12969-018-0274-5 | |
787 | 0 | |n https://doaj.org/toc/1546-0096 | |
856 | 4 | 1 | |u https://doaj.org/article/7ff2f2bf37c44d4c8fe46e5a3b5232c2 |z Connect to this object online. |