Volume 22, Issue 9 pp. 1429-1434

Low-dose intravenous pantoprazole for optimal inhibition of gastric acid in Korean patients

Jung-Hwan Oh

Jung-Hwan Oh

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Myung-Gyu Choi

Corresponding Author

Myung-Gyu Choi

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Dr Myung-Gyu Choi, Division of Gastroenterology, Department of Internal Medicine, Kangnam St Mary's Hospital, 505 Banpo-dong, Seocho-gu, Seoul 137-040, Korea. Email: [email protected]Search for more papers by this author
Mi-Sook Dong

Mi-Sook Dong

School of Life Science and Biotechnology, Korea University, Seoul, Korea

Search for more papers by this author
Jae-Myung Park

Jae-Myung Park

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Chang-Nyol Paik

Chang-Nyol Paik

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Yu-Kyung Cho

Yu-Kyung Cho

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Jeong-Jo Jeong

Jeong-Jo Jeong

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
In-Seok Lee

In-Seok Lee

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Sang-Woo Kim

Sang-Woo Kim

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Sok-Won Han

Sok-Won Han

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
Kyu-Yong Choi

Kyu-Yong Choi

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
In-Sik Chung

In-Sik Chung

Division of Gastroenterology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, and

Search for more papers by this author
First published: 15 August 2007
Citations: 18

Abstract

Background and Aim: Proton-pump inhibitor (PPI) therapy for bleeding ulcers is more efficacious in Asian patients than in non-Asian patients. The aim of this study was to evaluate the efficacy of various doses of pantoprazole on intragastric acidity in Korean patients.

Methods: A prospective randomized study was conducted in 52 patients either with bleeding peptic ulcers after successful endotherapy or who received endoscopic mucosal resection for gastric neoplasms. Patients were randomized into two doses of intravenous pantoprazole: 40 mg q.d. and 40 mg b.i.d. We compared these results with our preliminary study utilizing high-dose pantoprazole (80 mg + 8 mg/h). The potential contribution of CYP2C19 genetic polymorphisms and the presence of Helicobacter pylori were also assessed.

Results: Pantoprazole 40 mg b.i.d. and high-dose pantoprazole demonstrated better inhibition of intragastric acid than pantoprazole q.d. (P < 0.05). The pantoprazole 40 mg q.d. group exhibited significant variations in acid inhibition correlating with CYP2C19 genotype. Median 24 h pH values did not differ significantly between the pantoprazole b.i.d. and high-dose pantoprazole groups, regardless of H. pylori infection status. A median intragastric pH < 6.0 was observed in only three of 28 patients in the 40 mg b.i.d. group; these three patients were extensive metabolizers.

Conclusion: A 40 mg b.i.d. dose of pantoprazole is sufficient to maintain pH > 6.0 in Korean patients, except for patients with extensive metabolizing CYP2C19 genotypes.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.