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健康受试者中促胰液素刺激的内镜和德赖林管胰腺功能测试方法的随机交叉研究。

A randomized crossover study of secretin-stimulated endoscopic and dreiling tube pancreatic function test methods in healthy subjects.

作者信息

Stevens Tyler, Conwell Darwin L, Zuccaro Gregory, Van Lente Frederick, Purich Edward, Khandwala Farah, Fein Seymour

机构信息

Department of Gastroenterology and Hepatology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.

出版信息

Am J Gastroenterol. 2006 Feb;101(2):351-5. doi: 10.1111/j.1572-0241.2006.00407.x.

Abstract

OBJECTIVES

We have developed an endoscopic method of secretin endoscopic pancreatic function testing (ePFT) to simplify duodenal fluid collection. Validation of the ePFT requires a direct comparison to the traditional PFT using a Dreiling tube (DT). Our aim was to compare bicarbonate concentrations [HCO3-] obtained by the ePFT and DT methods in healthy subjects (HS).

METHODS

HS were randomized to either DT or ePFT, then crossed over to the other test after a minimum 1-wk washout. An age/weight-based sedation bolus was used for each test. DT protocol: Endoscopic placement of a DT was confirmed by fluoroscopy. After a baseline 15-min collection and administration of IV synthetic secretin, fluid was continuously collected in 15-min aliquots for an hour. ePFT protocol: Endoscopy was performed using a 6-mm endoscope. After gastric aspiration and discard and IV secretin, duodenal aspirates were obtained every 15-min for an hour. Fluid specimens were auto-analyzed for [HCO3-].

RESULTS

Twelve HS were enrolled (6F, mean age 37 yr). The difference in [HCO3-] between the two methods was not significant at the 0-, 30-, 45-, or 60-min collections. An excellent correlation in peak [HCO3-] was observed (R2 = 0.84, p < 0.001). Using a peak [HCO3-] cutpoint 80 mEq/L, there was 100% agreement between the methods; using cutpoint 90 mEq/L, there was 83% agreement.

CONCLUSIONS

The accuracy of the ePFT is similar to DT: There were minimal differences in [HCO3-] at each of the timed collections and at peak. There is an excellent correlation in peak [HCO3-] and high level of diagnostic agreement between the tests.

摘要

目的

我们开发了一种内镜下促胰液素内镜胰腺功能测试(ePFT)方法,以简化十二指肠液的采集。ePFT的验证需要与使用德赖林管(DT)的传统胰腺功能测试进行直接比较。我们的目的是比较健康受试者(HS)中通过ePFT和DT方法获得的碳酸氢盐浓度[HCO3-]。

方法

将HS随机分为DT组或ePFT组,然后在至少1周的洗脱期后交叉进行另一项测试。每次测试均使用基于年龄/体重的镇静推注剂量。DT方案:通过荧光透视确认DT的内镜放置。在进行15分钟的基线采集并静脉注射合成促胰液素后,以15分钟的等份连续采集液体1小时。ePFT方案:使用6毫米的内镜进行内镜检查。在抽吸并弃去胃液并静脉注射促胰液素后,每隔15分钟采集十二指肠抽吸物1小时。对液体标本自动分析[HCO3-]。

结果

纳入了12名HS(6名女性,平均年龄37岁)。在0、30、45或60分钟采集时,两种方法之间的[HCO3-]差异不显著。观察到峰值[HCO3-]具有良好的相关性(R2 = 0.84,p < 0.001)。使用峰值[HCO3-]切点80 mEq/L时,两种方法之间的一致性为100%;使用切点90 mEq/L时,一致性为83%。

结论

ePFT的准确性与DT相似:在每个定时采集点和峰值时,[HCO3-]的差异极小。峰值[HCO3-]之间具有良好的相关性,且两种测试之间的诊断一致性水平较高。

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