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The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

机译：新生儿假阳性筛查结果对健康系统的影响：一项中链酰基辅酶A脱氢酶缺乏症

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摘要

BackgroundThere is no consensus in the literature regarding the impact of false positive newborn screening results on early health care utilization patterns. We evaluated the impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency (MCADD) in a cohort of Ontario infants.

机译：背景文献中关于假阳性新生儿筛查结果对早期医疗利用模式的影响尚无共识。我们评估了安大略省婴儿队列中假阳性新生儿筛查结果对中链酰基辅酶A脱氢酶缺乏症（MCADD）的影响。

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期刊名称 Orphanet Journal of Rare Diseases
作者
Maria D. Karaceper; Pranesh Chakraborty; Doug Coyle; Kumanan Wilson; Jonathan B. Kronick; Steven Hawken; Christine Davies; Marni Brownell; Linda Dodds; Annette Feigenbaum; Deshayne B. Fell; Scott D. Grosse; Astrid Guttmann; Anne-Marie Laberge; Aizeddin Mhanni; Fiona A. Miller; John J. Mitchell; Meranda Nakhla; Chitra Prasad; Cheryl Rockman-Greenberg; Rebecca Sparkes; Brenda J. Wilson; Beth K. Potter;
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年(卷),期 2016(11),-1
年度 2016
页码 12
总页数 9
原文格式 PDF
正文语种
中图分类医学史 ;
关键词
Neonatal screening Metabolic diseases Health services utilization;

机译：新生儿筛查;代谢性疾病;卫生服务利用;

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专利

1. HEALTH SYSTEM IMPACT OF FALSE-POSITIVE NEWBORN SCREENING RESULTS FOR MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY AND PHENYLKETONURIA IN ONTARIO, CANADA [J] . Feigenbaum Annette, Khangura S. D., Karaceper M. D., Molecular genetics and metabolism . 2016 ,第3期

机译：加拿大安大略省中链酰基辅酶A脱氢酶缺乏症和苯丙酮尿症的假阳性新生儿筛查结果对健康系统的影响
2. The epidemiology and health service impact of medium-chain acyl-CoA dehydrogenase deficiency among affected children and those with false positive newborn screening results in Ontario [J] . Karaceper Maria D., Brownell Marni, Casey Robin, Clinical Biochemistry . 2014 ,第15期

机译：安大略省中链酰基辅酶A脱氢酶缺乏症对患病儿童和新生儿筛查结果为假阳性的儿童的流行病学和卫生服务影响
3. Correcting false positive medium-chain acyl-CoA dehydrogenase deficiency results from newborn screening; synthesis, purification, and standardization of branched-chain C8 acylcarnitines for use in their selective and accurate absolute quantitation by UHPLC-MS/MS [J] . Minkler Paul E., Stoll Maria S. K., Ingalls Stephen T., Molecular genetics and metabolism . 2017 ,第4期

机译：校正新生儿筛选的假阳性中链酰基-CoA脱氢酶缺乏症结果; 支链C8酰基氨基碱的合成，纯化和标准化，用于通过UHPLC-MS / MS的选择性和准确的绝对定量使用
4. Screening of glucose-6-phosphate dehydrogenase (G6PD) deficiency in two high endemic malaria populations, West Papua province and North Moluccas [C] . Hanna S. I. Kawulur, Hana Krismawati, Clara Imaniar International Conference on Biological Science . 2020

机译：筛选葡萄糖-6-磷酸盐脱氢酶（G6PD）缺乏两种高处理疟疾群体，西巴布亚省和北莫尔卡斯
5. Discussion of the potential benefits, implications and applications of research and data on parental experiences of children identified as a carrier for medium-chain acyl-CoA dehydrogenase deficiency. [D] . Davar, Ushtavaity V. 2005

机译：讨论被确定为中链酰基辅酶A脱氢酶缺乏症携带者的儿童的父母经验的研究和数据的潜在益处，影响和应用。
6. Health services use among children diagnosed with medium-chain acyl-CoA dehydrogenase deficiency through newborn screening: a cohort study in Ontario Canada [O] . Maria D. Karaceper, Sara D. Khangura, Kumanan Wilson, 2019

机译：通过新生儿筛查被诊断出患有中链酰基辅酶A脱氢酶缺乏症的儿童中的卫生服务使用：加拿大安大略省的一项队列研究
7. The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study [O] . 2016

机译：新生儿假阳性筛查结果对健康系统的影响：一项中链酰基辅酶A脱氢酶缺乏症

The health system impact of false positive newborn screening results for medium-chain acyl-CoA dehydrogenase deficiency: a cohort study

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