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对正在接受多潘立酮治疗的囊性纤维化儿科患者的血清催乳素进行监测。

Monitoring of serum prolactin in pediatric patients with cystic fibrosis who are receiving domperidone.

作者信息

Cho Eva, Ho Sharon, Gerber Patricia, Davidson A George F

机构信息

, BScPharm, ACPR, is with the Pharmacy, Children's and Women's Health Centre of British Columbia, Vancouver, British Columbia.

出版信息

Can J Hosp Pharm. 2009 Mar;62(2):119-26. doi: 10.4212/cjhp.v62i2.440.

Abstract

BACKGROUND

Since 2003, it has been routine practice at Children's and Women's Health Centre of British Columbia to monitor serum levels of prolactin in pediatric patients with cystic fibrosis who are receiving domperidone. Although a pharmacologic relationship between domperidone and prolactin has been documented in the literature, there is no information about routine monitoring of prolactin, and guidance on interpretation of prolactin values is lacking.

OBJECTIVES

To characterize how prolactin levels were being used in monitoring patients with cystic fibrosis who were receiving domperidone therapy at this institution, to evaluate the need for this practice, and to formulate recommendations accordingly.

METHODS

A chart review was conducted for pediatric patients with cystic fibrosis who had been receiving domperidone therapy and whose serum prolactin levels had been monitored between June 1, 2001, and October 1, 2005.

RESULTS

A total of 219 samples had been drawn, from 49 patients, for determination of prolactin level. Of these, 100 (45.7%) were above the normal range. Of the values above the normal range, 86 (86%) led to no dosage adjustment of domperidone and 14 (14%) led to either a decrease in dose or discontinuation of therapy. None of the elevated prolactin levels were associated with supratherapeutic doses of domperidone.

CONCLUSION

The role of routine monitoring of prolactin in this patient population requires further study. In particular, more information is needed about prolactin levels in pediatric patients and the relationship of prolactin level to domperidone dose.

摘要

背景

自2003年以来,不列颠哥伦比亚省儿童与妇女健康中心一直对接受多潘立酮治疗的囊性纤维化儿科患者进行血清催乳素水平监测。尽管文献中已记录了多潘立酮与催乳素之间的药理关系,但尚无关于催乳素常规监测的信息,且缺乏催乳素值解读的指导。

目的

描述在该机构中催乳素水平如何用于监测接受多潘立酮治疗的囊性纤维化患者,评估这种做法的必要性,并据此制定建议。

方法

对2001年6月1日至2005年10月1日期间接受多潘立酮治疗且血清催乳素水平已被监测的囊性纤维化儿科患者进行病历审查。

结果

共采集了49例患者的219份样本用于测定催乳素水平。其中,100份(45.7%)高于正常范围。在高于正常范围的值中,86份(86%)未导致多潘立酮剂量调整,14份(14%)导致剂量减少或停药。催乳素水平升高均与多潘立酮超治疗剂量无关。

结论

在该患者群体中常规监测催乳素的作用需要进一步研究。特别是,需要更多关于儿科患者催乳素水平以及催乳素水平与多潘立酮剂量关系的信息。

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Electrogastrography reveals post-prandial gastric dysmotility in children with cystic fibrosis.
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