Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Clinical Trial
. 2000 Apr;118(4):696-704.
doi: 10.1016/s0016-5085(00)70139-9.

Intravenous pantoprazole rapidly controls gastric acid hypersecretion in patients with Zollinger-Ellison syndrome

Affiliations
Clinical Trial

Intravenous pantoprazole rapidly controls gastric acid hypersecretion in patients with Zollinger-Ellison syndrome

E A Lew et al. Gastroenterology. 2000 Apr.

Abstract

Background & aims: Parenteral control of gastric acid hypersecretion in conditions such as Zollinger-Ellison syndrome (ZES) or idiopathic gastric acid hypersecretion is necessary perioperatively or when oral medications cannot be taken for other reasons (e.g., during chemotherapy, acute upper gastrointestinal bleeding, or in intensive care unit settings).

Methods: We evaluated the efficacy and safety of 15-minute infusions of the proton pump inhibitor pantoprazole (80-120 mg every 8-12 hours) in controlling acid output for up to 7 days. Effective control was defined as acid output >10 milliequivalents per hour (mEq/h) (<5 mEq/h in patients with prior acid-reducing surgery) for 24 hours.

Results: The 21 patients enrolled had a mean age of 51.9 years (range, 29-75) and a mean disease duration of 8.1 years (range, <0.5-21); 13 were male, 7 had multiple endocrine neoplasia syndrome type I, 4 had undergone acid-reducing surgery, 2 had received chemotherapy, and 13 had undergone gastrinoma resections without cure. Basal acid output (mean +/- SD) was 40.2 +/- 27.9 mEq/h (range, 11.2-117.9). In all patients, acid output was controlled within the first hour (mean onset of effective control, 41 minutes) after an initial 80-mg intravenous pantoprazole dose. Pantoprazole, 80 mg every 12 hours, was effective in 17 of 21 patients (81%) for up to 7 days. Four patients required upward dose titration, 2 required 120 mg pantoprazole every 12 hours, and 2 required 80 mg every 8 hours. At study end, acid output remained controlled for 6 hours beyond the next expected dose in 71% of patients (n = 15); mean acid output increased to 4.0 mEq/h (range, 0-9.7). No serious or unexpected adverse events were observed.

Conclusions: Intravenous pantoprazole, 160-240 mg/day administered in divided doses by 15-minute infusion, rapidly and effectively controlled acid output within 1 hour and maintained control for up to 7 days in all ZES patients.

PubMed Disclaimer

Figures

Figure 1.
Figure 1.
Inhibition of mean gastric acid output over the first 2 hours after the initial IV administration of 80 mg pantoprazole. Collection periods were 15 minutes long. Baseline value for these data is based on a 15-minute collection period, whereas data in Table 3 for initial acid output are based on a 1-hour collection period.
Figure 2.
Figure 2.
Gastric acid output curves after IV pantoprazole in 4 representative ZES patients. For 17 of 21 patients (81% of the study cohort), acid secretion was controlled with 80 mg IV pantoprazole every 12 hours (a representative example of this pattern of control is shown in A). Two patients (9.5%) required 120 mg IV pantoprazole every 12 hours (a representative example of this pattern of control is shown in B). (Cand D) Two patients (9.5%) required 80 mg IV pantoprazole every 8 hours. (C)The patient’s condition was uncontrolled with twice daily therapy, but after the study protocol was amended to permit dosing every 8 hours, control was achieved rapidly. (D) The dose interval was shortened to 8 hours in a patient after the first control measurement showing loss of control with immediate results.

References

    1. Metz DC, Jensen RT. Endocrine tumors of the pancreas. In: Haubrich WB, Schaffner F, Berk JE, eds. Bockus gastroenterology 5th ed. Volume 4 Philadelphia: Saunders, 1994:3002–3034.
    1. Metz DC. Peptic ulcer disease; diagnosis and treatment. In: DiMarino AJ, Benjamin SB, eds. Gastrointestinal disease: an endoscopic approach Volume 1 Cambridge: Blackwell Science, 1997:285–304.
    1. Zollinger RM, Ellison EC. Primary peptic ulcerations of the jejunum associated with islet cell tumors of the pancreas. Ann Surg 1955;142:709–728. - PMC - PubMed
    1. Zollinger RM, Ellison EC, OíDorisio TM, Sparks J. Thirty years experience with gastrinoma. World J Surg 1984;8:427–435. - PubMed
    1. Metz DC, Pisegna JR, Fishbeyn VA, Benya RV, Jensen RV. The control of gastric acid hypersecretion in the management of patients with Zollinger–Ellison syndrome. In: Progress symposium on the treatment of islet cell tumors. World J Surg 1993;17:468–480. - PMC - PubMed

Publication types

MeSH terms

LinkOut - more resources