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维持性口服泮托拉唑治疗对卓-艾综合征和特发性胃酸分泌过多患者有效。

Maintenance oral pantoprazole therapy is effective for patients with Zollinger-Ellison syndrome and idiopathic hypersecretion.

作者信息

Metz David C, Soffer Elaine, Forsmark Chris E, Cryer Byron, Chey William, Bochenek Wieslaw, Pisegna Joseph R

机构信息

University of Pennsylvania Medical Center, Division of Gastroenterology, Philadelphia 19104, USA.

出版信息

Am J Gastroenterol. 2003 Feb;98(2):301-7. doi: 10.1111/j.1572-0241.2003.07262.x.

Abstract

OBJECTIVE

Maintenance proton pump inhibitor (PPI) therapy is effective for gastric acid hypersecretory states, although data with pantoprazole are limited. The aim of this study was to evaluate the safety and efficacy of long term p.o. pantoprazole in individuals with hypersecretion.

METHODS

All subjects had Zollinger-Ellison syndrome or idiopathic hypersecretion. Baseline acid output was measured in the presence of prior maintenance antisecretory therapy before pantoprazole exposure. The starting dose was 40 mg b.i.d. in most cases, and the dose was adjusted to document control within the first 2 wk of therapy. The maximal allowable dose was 240 mg daily. Acid output was measured on day 28 and then quarterly from month 3. The primary efficacy endpoint was documented control of acid secretion at 6 months, i.e., acid output in the last 1 h before the next dose of therapy of <10 mEq/h (<5 mEq/h in subjects with prior acid-reducing surgery).

RESULTS

A total of 26 subjects had Zollinger-Ellison syndrome (six with multiple endocrine neoplasia syndrome type 1) and nine had idiopathic hypersecretion. Pre-enrollment therapy included omeprazole in 27 subjects and lansoprazole in eight, and 82.4% of subjects were controlled on their prior regimens. With upward dose titration, acid output was controlled in all subjects by day 10 and in all but two (6%) at the 6-month time point. Median acid secretion on therapy at 6 months was <2 mEq/h (mean 2.2 mEq/h; range 0-10.5 mEq/h) at a dose of 40 mg b.i.d. for 24 subjects, 80 mg b.i.d. for seven subjects, and 120 mg b.i.d. for two subjects. During the course of the study, five subjects required doses of 240 mg daily. Pantoprazole was generally well tolerated. No cases of anterior optic ischemic neuropathy occurred. Five subjects died during follow-up, all because of events unrelated to the study drug.

CONCLUSIONS

Maintenance p.o. pantoprazole therapy at a dose of 80-240 mg/day in divided doses was both effective and generally well tolerated for patients with Zollinger-Ellison syndrome and idiopathic hypersecretion.

摘要

目的

维持质子泵抑制剂(PPI)治疗对胃酸分泌过多状态有效,尽管泮托拉唑的相关数据有限。本研究旨在评估长期口服泮托拉唑治疗胃酸分泌过多患者的安全性和有效性。

方法

所有受试者均患有卓艾综合征或特发性胃酸分泌过多。在暴露于泮托拉唑之前,在先前维持性抗分泌治疗的情况下测量基础酸排量。大多数情况下起始剂量为40mg,每日两次,在治疗的前2周内调整剂量以记录控制情况。最大允许剂量为每日240mg。在第28天测量酸排量,然后从第3个月开始每季度测量一次。主要疗效终点是记录6个月时酸分泌的控制情况,即在下一次给药前最后1小时的酸排量<10mEq/h(先前接受过抑酸手术的受试者中<5mEq/h)。

结果

共有26名受试者患有卓艾综合征(6名患有1型多发性内分泌肿瘤综合征),9名患有特发性胃酸分泌过多。入组前治疗包括27名受试者使用奥美拉唑,8名受试者使用兰索拉唑,82.4%的受试者在先前治疗方案下得到控制。随着剂量向上滴定,所有受试者在第10天时酸排量得到控制,在6个月时间点时,除两名(6%)外所有受试者均得到控制。6个月治疗时,24名受试者剂量为40mg,每日两次,7名受试者剂量为80mg,每日两次,2名受试者剂量为120mg,每日两次,酸分泌中位数<2mEq/h(平均2.2mEq/h;范围0 - 10.5mEq/h)。在研究过程中,5名受试者需要每日240mg的剂量。泮托拉唑总体耐受性良好。未发生前部缺血性视神经病变病例。5名受试者在随访期间死亡,均因与研究药物无关的事件。

结论

对于卓艾综合征和特发性胃酸分泌过多患者,每日80 - 240mg分剂量口服泮托拉唑维持治疗有效且总体耐受性良好。

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