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每日一次服用10毫克奥美拉唑与每日两次服用20毫克法莫替丁相比,哪种药物的抑酸效果更佳?对日本细胞色素P450 2C19基因野生型幽门螺杆菌阴性患者单次或重复给药的效果。

Which has superior acid-suppressive effect, 10 mg omeprazole once daily or 20 mg famotidine twice daily? Effects of single or repeated administration in Japanese Helicobacter pylori-negative CYP2C19 extensive metabolizers.

作者信息

Shimatani Tomohiko, Inoue Masaki, Kuroiwa Tomoko, Moriwaki Mutsuko, Xu Jing, Ikawa Kazuro, Morikawa Norifumi, Tazuma Susumu

机构信息

Department of General Medicine, Hiroshima University Hospital, 1-2-3 Kasumi, Hiroshima, Japan.

出版信息

Dig Dis Sci. 2007 Feb;52(2):390-5. doi: 10.1007/s10620-006-9490-9. Epub 2007 Jan 9.

Abstract

Low-dose omeprazole is superior to full-dose famotidine in maintenance therapy for gastroesophageal reflux disease, whereas "on-demand" famotidine is more effective for relief of episodes of heartburn. To explain this apparent discrepancy, intragastric pH was measured for 24-hr seven times in eight Japanese Helicobacter pylori-negative cytochrome P450 2C19 extensive metabolizers; on Days 1, 8, and 15 of repeated administration of 10 mg of omeprazole once daily and of 20 mg of famotidine twice daily and before medication. During repeated administration of omeprazole, mean intragastric pH and % time that intragastric pH > 4.0 were significantly higher and became greater. With famotidine, although these parameters were significantly higher, the degrees became smaller. Consequently, acid-suppressive effect was in the order; omeprazole < famotidine on Day 1, omeprazole approximately famotidine on Day 8, and omeprazole >famotidine on Day 15. This discrepancy possibly results from the "potentiation" of acid-suppressive effect of omeprazole and the "tolerance" phenomenon in respect to famotidine.

摘要

低剂量奥美拉唑在胃食管反流病维持治疗中优于全剂量法莫替丁,而“按需服用”法莫替丁对缓解烧心发作更有效。为解释这一明显差异,对8名日本细胞色素P450 2C19广泛代谢型幽门螺杆菌阴性患者进行了7次24小时胃内pH值测量;在每日一次重复给予10mg奥美拉唑和每日两次重复给予20mg法莫替丁的第1、8和15天以及用药前进行测量。在重复给予奥美拉唑期间,平均胃内pH值和胃内pH值>4.0的时间百分比显著更高且增加。对于法莫替丁,虽然这些参数也显著更高,但增幅较小。因此,抑酸效果顺序为:第1天奥美拉唑<法莫替丁,第8天奥美拉唑≈法莫替丁,第15天奥美拉唑>法莫替丁。这种差异可能是由于奥美拉唑抑酸作用的“增强”以及法莫替丁的“耐受”现象所致。

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