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13C-尿素呼气试验检测幽门螺杆菌感染的最低分析要求

Minimum analysis requirements for the detection of Helicobacter pylori infection by the 13C-urea breath test.

作者信息

Klein P D, Graham D Y

机构信息

Department of Pediatrics, Baylor College of Medicine, Houston, Texas.

出版信息

Am J Gastroenterol. 1993 Nov;88(11):1865-9.

PMID:8237934
Abstract

BACKGROUND

In an attempt to identify the minimum criteria for scoring the 13C-urea breath test, we examined test results from 96 healthy subjects, 270 duodenal ulcer patients undergoing treatment to eradicate Helicobacter pylori, and 1000 consecutive breath tests analyzed in our laboratory.

METHODS

The 13CO2/12CO2 isotope ratio in a baseline sample was compared with that of samples collected at 20, 30, 40, and 50 min post-dosing. A positive test was defined as an average increase in the ratio of 6/1000 over baseline. Values for a two-sample analysis (baseline and one other) and for a single-sample analysis were extracted from the data and compared with the original analysis outcome.

RESULTS

Test results were negative for 186 patients and positive for 84. The two-sample method had high specificity (94-99/1000), sensitivity (95-99/1000), and positive predictive value (88-97/1000). False-positive results occurred most often with samples collected at 20 min and least often with the sample at 40 min (11 and 1, respectively). Analyses based on a single sample collected beyond 20 min, in which samples with an isotope ratio > or = -15/1000 versus the standard were defined as positive, gave comparable specificity (98-99/1000), slightly reduced sensitivity (92-94%), and positive predictive value (96-99%). The analyses of 1000 consecutive breath tests yielded approximately 1% false-positive and false-negative results by the two-sample method; the single-sample method yielded a 2% false-positive and false-negative result.

CONCLUSION

The 13C-urea breath test can determine H. pylori infective status from a single breath sample collected at least 30 min post-dose in which the absolute 13C abundance is > or = -15/1000 versus the standard.

摘要

背景

为了确定13C-尿素呼气试验的最低评分标准,我们检查了96名健康受试者、270名接受根除幽门螺杆菌治疗的十二指肠溃疡患者的检测结果,以及在我们实验室分析的1000次连续呼气试验。

方法

将基线样本中的13CO2/12CO2同位素比值与给药后20、30、40和50分钟采集的样本的该比值进行比较。阳性试验定义为该比值较基线平均升高6/1000。从数据中提取用于双样本分析(基线和另一个样本)和单样本分析的值,并与原始分析结果进行比较。

结果

186例患者检测结果为阴性,84例为阳性。双样本法具有较高的特异性(94 - 99/1000)、敏感性(95 - 99/1000)和阳性预测值(88 - 97/1000)。假阳性结果最常出现在20分钟采集的样本中,最少出现在40分钟采集的样本中(分别为11例和1例)。基于给药20分钟后采集的单个样本进行分析,其中同位素比值相对于标准>或 = -15/1000的样本被定义为阳性,其特异性相当(98 - 99/1000),敏感性略有降低(92 - 94%),阳性预测值(96 - 99%)。通过双样本法对1000次连续呼气试验进行分析,产生了约1%的假阳性和假阴性结果;单样本法产生了2%的假阳性和假阴性结果。

结论

13C-尿素呼气试验可根据给药后至少30分钟采集的单个呼气样本确定幽门螺杆菌感染状态,其中相对于标准的绝对13C丰度>或 = -15/1000。

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