Stevens Tyler, Conwell Darwin L, Zuccaro Gregory, Van Lente Frederick, Purich Edward, Khandwala Farah, Fein Seymour
Department of Gastroenterology and Hepatology, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Am J Gastroenterol. 2006 Feb;101(2):351-5. doi: 10.1111/j.1572-0241.2006.00407.x.
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).
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-].
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.
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.
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-]。
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-]。
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%。
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。