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兰索拉唑治疗儿童胃食管反流病的安全性

Safety of lansoprazole in the treatment of gastroesophageal reflux disease in children.

作者信息

Tolia Vasundhara, Fitzgerald Joseph, Hassall Eric, Huang Bidan, Pilmer Betsy, Kane Robert

机构信息

Children's Hospital of Michigan, Detroit, Michigan 48201, USA.

出版信息

J Pediatr Gastroenterol Nutr. 2002;35 Suppl 4:S300-7. doi: 10.1097/00005176-200211004-00002.

Abstract

OBJECTIVES

To evaluate the safety of lansoprazole in children between 1 and 11 years of age.

METHODS

In a phase I/II, open-label, multicenter (11 sites) study, children with symptomatic gastroesophageal reflux disease (GERD), erosive esophagitis (> or = grade 2), and/or esophageal pH < 4 for > 4.2% of the 24-hour period were assigned, on the basis of body weight, to lansoprazole 15 mg (< or = 30 kg) or 30 mg (> 30 kg) once daily for 8 to 12 weeks. At the discretion of the investigator, the dosage of lansoprazole was increased up to 60 mg daily in children who continued to be symptomatic after 2 weeks of treatment. Safety for all study participants was monitored by adverse event reports and laboratory evaluations.

RESULTS

Sixty-six children were enrolled in the study and were included in the safety analysis. Throughout the treatment period, no child discontinued therapy because of an adverse event and no clinically significant changes in laboratory values were observed. Three of the 32 children (9%) who received lansoprazole 15 mg once daily (mean exposure 50.3 days) and 6 of the 34 children (18%) who received the 30 mg once-daily dose (mean exposure 49.4 days) experienced one or more treatment-related adverse events before any dose increase. The three children in the lansoprazole 15 mg treatment group were treated with doses of 0.6 mg to 1.2 mg/kg/day; those in the lansoprazole 30 mg treatment group were treated with doses of 0.7 mg to 0.9 mg/kg/day. Only one child experienced a new treatment-related adverse event after an increase in lansoprazole dose to 1.3 mg/kg/day. Treatment-related events experienced by two or more children were: constipation (lansoprazole 15 mg QD, two children; lansoprazole 30 mg QD, one child), and headache (lansoprazole 30 mg QD, two children). Mean fasting serum gastrin levels were significantly increased from 58.0 pg/mL at baseline to 112.4 pg/mL at week 2 and 121.9 pg/mL at the final visit (P < or = 0.001 for each comparison). However, the median fasting serum gastrin levels at the week 2 and the final visit were within the normal range (25-111 pg/mL).

CONCLUSION

Lansoprazole, when administered on the basis of body weight in children between 1 and 11 years of age, is safe and well-tolerated.

摘要

目的

评估兰索拉唑在1至11岁儿童中的安全性。

方法

在一项I/II期、开放标签、多中心(11个地点)研究中,将有症状性胃食管反流病(GERD)、糜烂性食管炎(≥2级)和/或24小时食管pH值<4的时间超过4.2%的儿童,根据体重分配至每日一次服用15毫克(≤30千克)或30毫克(>30千克)兰索拉唑,疗程为8至12周。根据研究者的判断,对于治疗2周后仍有症状的儿童,兰索拉唑剂量可增至每日60毫克。通过不良事件报告和实验室评估监测所有研究参与者的安全性。

结果

66名儿童入组该研究并纳入安全性分析。在整个治疗期间,没有儿童因不良事件而停药,也未观察到实验室值有临床显著变化。每日一次服用15毫克兰索拉唑的32名儿童中有3名(9%)(平均暴露50.3天),每日一次服用30毫克兰索拉唑的34名儿童中有6名(18%)(平均暴露49.4天)在任何剂量增加之前出现了一种或多种与治疗相关的不良事件。兰索拉唑15毫克治疗组的3名儿童接受的剂量为0.6毫克至1.2毫克/千克/天;兰索拉唑30毫克治疗组的儿童接受的剂量为0.7毫克至0.9毫克/千克/天。只有一名儿童在兰索拉唑剂量增加至1.3毫克/千克/天后出现了新的与治疗相关的不良事件。两名或更多儿童经历的与治疗相关的事件有:便秘(兰索拉唑15毫克每日一次,两名儿童;兰索拉唑30毫克每日一次,一名儿童)和头痛(兰索拉唑30毫克每日一次,两名儿童)。空腹血清胃泌素平均水平从基线时的58.0皮克/毫升显著增至第2周时的112.4皮克/毫升以及末次访视时的121.9皮克/毫升(每次比较P≤0.001)。然而,第2周和末次访视时空腹血清胃泌素水平中位数在正常范围内(25 - 111皮克/毫升)。

结论

在1至11岁儿童中,根据体重服用兰索拉唑是安全且耐受性良好的。

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