唐氏综合征和脓毒症患儿的死亡风险

来源 :世界核心医学期刊文摘(儿科学分册) | 被引量 : 0次 | 上传用户:wangjuekenan
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Objective: To determine differences in case fatality rates between children with and without Down syndrome. Study design: We used the Pediatric Health Information System (PHIS) database, which includes demographic and diagnostic data from freestanding children’s hospitals. Using Poisson regression, we determined the risk of mortality from sepsis for children with Down syndrome, after controlling for potential confounding factors. Results: A total of 35,645 patients met our inclusion criteria, of which 3936 (11%) died during hospitalization. Altogether, 620 of the included patients also had a diagnosis of Down syndrome; 106 (17%) of these died during hospitalization. Children with Down syndrome had significantly elevated risk of mortality (mortality rate ratio = 1.30; 95%confidence interval = 1.06 to 1.59) after adjusting for potential confounding factors including demographics, pathogens, and concomitant conditions. Conclusions: Children with Down syndrome and sepsis have elevated risk of mortality. These findings have implications for treatment decisions, communications about prognosis, and future research. Study design: We used the Pediatric Health Information System (PHIS) database, which includes demographic and diagnostic data from freestanding children’s hospitals. Using Poisson regression, we determined the risk of mortality from sepsis for children with Down syndrome, after controlling for potential confounding factors. Results: A total of 35,645 patients with our inclusion criteria, of which 3936 (11%) died during hospitalization. Altogether, 620 of the included patients also had children with Down syndrome had significantly elevated risk of mortality (mortality rate ratio = 1.30; 95% confidence interval = 1.06 to 1.59) after adjusting for potential confounding factors including demographics, pathogens, and concomitant conditions. Conclusions: Children with Down syndrome and sepsis have elevated risk of mortality. These findings have implications for treatment decisions, communications about prognosis, and future research.
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