Department of General Medicine and Community Health Science, Sasayama Medical Center, Hyogo College of Medicine, Nishinomiya, Hyogo, Japan.
J Gastroenterol Hepatol. 2012 Apr;27 Suppl 3:100-2. doi: 10.1111/j.1440-1746.2012.07080.x.
Ecabet sodium is reported to have a bactericidal effect on Helicobacter pylori and inhibit urease activity in vitro.
Seven male volunteers (mean age, 51.3 years; range, 45-55 years) with H. pylori infection were medicated with 1 g ecabet sodium t.i.d. for 4 weeks. The urea breath test (UBT) was performed 10 times per person: before medication, seven times in 2 weeks, and once in the third and fourth weeks. Stool antigen tests (HpSA PLUS and Testmate pylori antigen) were performed five times per person: before medication and weekly during medication.
The premedication UBT value ranged from 4.9 ‰ to 77.4 ‰ and from 2.9 ‰ to 44 ‰ at the end of the treatment period. Not one of the subjects had a negative UBT result during medication. The optical densities of the HpSA and Testmate pylori antigen tests ranged from 0.4 to > 3.0 premedication and from 0.0 to > 3.0 at the end of treatment. HpSA and Testmate pylori antigen were negative in two cases.
In this study, ecabet sodium did not effect the results of UBT in volunteers with H. pylori infection. Ecabet sodium may influence stool antigens because in two of seven cases the H. pylori stool antigen tests returned negative results.
依卡倍特钠据报道具有杀菌作用,可抑制幽门螺杆菌(Helicobacter pylori)的体外脲酶活性。
7 名男性志愿者(平均年龄 51.3 岁;范围 45-55 岁)感染幽门螺杆菌,接受依卡倍特钠 1 g,每日 3 次,共 4 周治疗。每位志愿者进行 10 次尿素呼气试验(UBT):用药前、2 周内 7 次、第 3 周和第 4 周各 1 次。每位志愿者进行 5 次粪便抗原检测(HpSA PLUS 和 Testmate 幽门螺杆菌抗原):用药前和用药期间每周 1 次。
用药前 UBT 值范围为 4.9‰至 77.4‰,治疗结束时为 2.9‰至 44‰。在用药期间,没有一个志愿者的 UBT 结果为阴性。HpSA 和 Testmate 幽门螺杆菌抗原检测的光密度值范围为用药前 0.4 至>3.0,治疗结束时 0.0 至>3.0。两种情况下 HpSA 和 Testmate 幽门螺杆菌抗原检测结果均为阴性。
在这项研究中,依卡倍特钠对幽门螺杆菌感染志愿者的 UBT 结果没有影响。依卡倍特钠可能会影响粪便抗原,因为在 7 例中,有 2 例 H. pylori 粪便抗原检测结果为阴性。