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新生儿和婴儿质子泵抑制剂的处方模式

Proton pump inhibitor prescribing patterns in newborns and infants.

作者信息

Illueca Marta, Alemayehu Berhanu, Shoetan Nze, Yang Huiying

机构信息

AstraZeneca LP, Wilmington, Delaware.

出版信息

J Pediatr Pharmacol Ther. 2014 Oct-Dec;19(4):283-7. doi: 10.5863/1551-6776-19.4.283.

Abstract

OBJECTIVES

In 2011, the Food and Drug Administration (FDA) approved intravenous esomeprazole 0.5 mg/day for children aged >1 month and oral esomeprazole for infants aged 1 month to <1 year at doses of 2.5, 5, and 10 mg based on weight. Prior to 2011, proton pump inhibitors (PPIs) were not approved for use in infants aged <1 year. This study determined PPI usage rates prior to the FDA approval among newborns and infants in both the inpatient and outpatient settings and compared PPI and histamine-2 receptor antagonist (H2RA) usage in the inpatient setting.

METHODS

We conducted a retrospective analysis of PPI prescribing patterns for newborns and infants from 2003 to 2008 using data from the Premier Perspective Inpatient Hospital Database and the PharMetrics Patient-Centric Database for inpatient and outpatient data, respectively. PPI use and diagnoses were determined from clinical and charge records from more than 500 hospitals. Descriptive statistics were used to summarize the findings.

RESULTS

Our analysis showed that PPIs were prescribed for approximately 5000 newborns (0.13%) and 15,000 infants (2.65%) each year in the hospital setting and 1.6% of newborns and infants, as a group, in the outpatient setting. Newborns and infants receiving PPIs most often had diagnoses of gastroesophageal reflux disease (GERD) and were generally prescribed an adult PPI dose, although the actual dose administered could not be substantiated.

CONCLUSIONS

Although no PPI was approved by the FDA for patients aged <1 year at the time of this study, results of this analysis indicate that PPIs were commonly prescribed for newborns and infants, mostly in hospital, but also in outpatient settings. Most PPIs were prescribed for infants with a diagnosis of GERD.

摘要

目的

2011年,美国食品药品监督管理局(FDA)批准静脉注射艾司奥美拉唑,剂量为0.5毫克/天,用于1个月以上儿童;批准口服艾司奥美拉唑,用于1个月至不满1岁婴儿,根据体重分别给予2.5毫克、5毫克和10毫克的剂量。2011年之前,质子泵抑制剂(PPI)未被批准用于1岁以下婴儿。本研究确定了FDA批准之前住院和门诊环境中新生儿和婴儿使用PPI的比例,并比较了住院环境中PPI和组胺-2受体拮抗剂(H2RA)的使用情况。

方法

我们分别使用Premier Perspective住院医院数据库和PharMetrics以患者为中心的数据库中的数据,对2003年至2008年新生儿和婴儿的PPI处方模式进行了回顾性分析。PPI的使用和诊断是根据500多家医院的临床和收费记录确定的。使用描述性统计来总结研究结果。

结果

我们的分析表明,在医院环境中,每年约有5000名新生儿(0.13%)和15000名婴儿(2.65%)使用PPI;在门诊环境中,作为一个群体,有1.6%的新生儿和婴儿使用PPI。接受PPI治疗的新生儿和婴儿最常见的诊断是胃食管反流病(GERD),并且通常使用成人PPI剂量,尽管实际给药剂量无法得到证实。

结论

尽管在本研究时FDA未批准任何PPI用于1岁以下患者,但该分析结果表明,PPI在新生儿和婴儿中普遍使用,大多是在医院,但在门诊环境中也有使用。大多数PPI是开给诊断为GERD的婴儿。

相似文献

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Proton pump inhibitor prescribing patterns in newborns and infants.新生儿和婴儿质子泵抑制剂的处方模式
J Pediatr Pharmacol Ther. 2014 Oct-Dec;19(4):283-7. doi: 10.5863/1551-6776-19.4.283.

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