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在一家大都市医院进行代谢疾病筛查。

Screening for metabolic disease in a metropolitan hospital.

作者信息

Krieger I, Nigro M, Taqi Q

出版信息

Am J Dis Child. 1982 Feb;136(2):125-8. doi: 10.1001/archpedi.1982.03970380037009.

Abstract

Screening for metabolic diseases at Children's Hospital of Michigan, Detroit during 1978 and 1979 led to the discovery of 7.5 cases per year, representing a marked increase over previous years. Five cases of organic aciduria were identified during this two-year period by use of urinary gas chromatography. Four of these were found to have methylmalonic aciduria. The increase in detection rate was due to the addition of an organic acid screening technique and greater use of two standard screening tests. The yield of screening by these two tests also improved, which we attribute to the better use of specific criteria. Inclusion of a simple urine screening test for methylmalonic acid is recommended in the workup of infants with episodic vomiting, lethargy, acidosis, or catastrophic illness.

摘要

1978年至1979年期间,在底特律的密歇根儿童医院对代谢性疾病进行筛查,结果发现每年有7.5例,相较于前几年有显著增加。在这两年期间,通过尿液气相色谱法鉴定出5例有机酸尿症。其中4例被发现患有甲基丙二酸尿症。检测率的提高归因于增加了一种有机酸筛查技术以及更广泛地使用了两项标准筛查测试。这两项测试的筛查产出也有所提高,我们将其归因于对特定标准的更好应用。对于患有发作性呕吐、嗜睡、酸中毒或重症疾病的婴儿,建议在检查过程中加入一项针对甲基丙二酸的简单尿液筛查测试。

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