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外分泌胰腺功能的筛查(作者译)

[Screening of exocrine pancreatic function (author's transl)].

作者信息

Stock K P, Schenk J, Schmack B, Domschke W

出版信息

Dtsch Med Wochenschr. 1981 Jul 31;106(31-32):983-7. doi: 10.1055/s-2008-1070438.

Abstract

The validity of oral pancreatic function tests (fluoresceine dilaurate-[FDL-], N-benzoyl-L-tyrosyl-para-amino-benzoic-acid-[PABA-]test) was assessed intra-individually in 67 patients in comparison with the secretin-pancreozymin test corrected for volume loss. Faecal chymotrypsin (CH-F) estimation was included in the comparison. According to the result of the secretin-pancreozymin test, patients were divided into those with normal pancreatic function (n = 28), those with borderline restricted function (n = 18), and those with manifest exocrine insufficiency (n = 21). Results show that in borderline decreased pancreatic function the diagnostic value of all screening tests is limited. The sensitivity (true pathological results) was 38% in the FDL-test, 40% in the PABA-test, and 31% in CH-F. In manifest exocrine pancreatic insufficiency FDL- and PABA-test as well as CH-F showed similar sensitivity of 67, 63, and 62%, respectively. Results show that oral pancreatic function tests, particularly the simple FDL-test, represent a diagnostic alternative to the relatively complicated CH-F assessment. However, none of the tests are able to replace the secretin-pancreozymin test as the most valid diagnostic investigation.

摘要

对67例患者进行了口服胰腺功能试验(荧光素二月桂酸酯-[FDL-]、N-苯甲酰-L-酪氨酰-对氨基苯甲酸-[PABA-]试验)的个体内有效性评估,并与校正了容量损失的促胰液素-胰酶泌素试验进行比较。比较中包括了粪便糜蛋白酶(CH-F)测定。根据促胰液素-胰酶泌素试验结果,患者被分为胰腺功能正常者(n = 28)、临界性功能受限者(n = 18)和明显外分泌功能不全者(n = 21)。结果显示,在临界性胰腺功能降低时,所有筛查试验的诊断价值均有限。FDL试验的敏感性(真正的病理结果)为38%,PABA试验为40%,CH-F为31%。在明显的胰腺外分泌功能不全时,FDL试验、PABA试验以及CH-F的敏感性相似,分别为67%、63%和62%。结果表明,口服胰腺功能试验,尤其是简单的FDL试验,是相对复杂的CH-F评估的一种诊断替代方法。然而,没有一种试验能够取代促胰液素-胰酶泌素试验成为最有效的诊断检查方法。

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