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标准剂量和高剂量雷尼替丁对[13C]尿素呼气试验结果的影响。

Effect of standard and high dose ranitidine on [13C]urea breath test results.

作者信息

Cutler A F, Elnaggar M, Brooks E, O'Mara K

机构信息

Department of Internal Medicine, Sinai Hospital, Detroit, Michigan 48235, USA.

出版信息

Am J Gastroenterol. 1998 Aug;93(8):1297-9. doi: 10.1111/j.1572-0241.1998.00412.x.

DOI:10.1111/j.1572-0241.1998.00412.x
PMID:9707054
Abstract

OBJECTIVE

It has been suggested that standard dose H2 blockers will affect the [14-C]urea breath test. The aim of this study was to evaluate the effect of standard and high dose ranitidine on the [13C]urea breath test in a prospective cross-over study.

METHODS

Volunteers found to be positive for H. pylori by IgG serology and [13C]urea breath test were given either ranitidine 150 mg b.i.d. or 300 mg b.i.d. for 14 days. Repeat breath tests were completed on the last day of antisecretory dosing and study patients were immediately crossed over to the other ranitidine dose. The third breath test was performed at 14 days after initiation of the new dose.

RESULTS

A total of 20 volunteers were enrolled. Using the established cut-off of 2.4% for the commercial breath test, only one patient developed negative results on H2 blockers. This patient had negative breath tests on both ranitidine doses and remained test-negative off all medications 6 wk after study completion, suggesting either a false positive baseline test or an unexpected bacterial eradication. No specific trend in breath test results was observed for the group (p=NS). On ranitidine 300 mg, six of 19 patients elevated their breath results from 23% to 112% (mean 76%) above baseline.

CONCLUSION

Ranitidine at standard or high doses did not generate a reproducible decline in breath test results. Histamine 2 blockers do not need to be discontinued before urea breath testing.

摘要

目的

有人提出标准剂量的H2受体阻滞剂会影响[14-C]尿素呼气试验。本研究的目的是在一项前瞻性交叉研究中评估标准剂量和高剂量雷尼替丁对[13C]尿素呼气试验的影响。

方法

通过IgG血清学和[13C]尿素呼气试验发现幽门螺杆菌呈阳性的志愿者,给予雷尼替丁150毫克,每日两次或300毫克,每日两次,持续14天。在抗分泌给药的最后一天完成重复呼气试验,研究患者立即交叉使用另一种雷尼替丁剂量。在开始新剂量14天后进行第三次呼气试验。

结果

共招募了20名志愿者。使用商业呼气试验既定的2.4%的临界值,只有一名患者在使用H2受体阻滞剂后出现阴性结果。该患者在两种雷尼替丁剂量下呼气试验均为阴性,并且在研究完成6周后停用所有药物后仍为试验阴性,这表明要么基线试验为假阳性,要么出现了意外的细菌根除。该组在呼气试验结果中未观察到特定趋势(p=无显著性差异)。在使用雷尼替丁300毫克时,19名患者中有6名的呼气结果从基线以上的23%升高到112%(平均76%)。

结论

标准剂量或高剂量的雷尼替丁不会使呼气试验结果出现可重复的下降。在进行尿素呼气试验之前无需停用组胺2受体阻滞剂。

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