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医生如何看待和利用来自致畸物信息服务机构(母婴风险计划)的信息。

How physicians perceive and utilize information from a teratogen information service: the Motherisk Program.

作者信息

Einarson Adrienne, Park Andrew, Koren Gideon

机构信息

The Motherisk Program, The Hospital for Sick Children Toronto, Canada.

出版信息

BMC Med Educ. 2004 Apr 5;4:6. doi: 10.1186/1472-6920-4-6.

Abstract

BACKGROUND

Teratogen information services have been developed around the world to disseminate information regarding the safety of maternal exposures during pregnancy. The Motherisk Program in Toronto, Canada, fields thousands of these inquiries per year. Our primary objective was to evaluate the perception and utilization of information received from us by physicians. Our secondary objective was to examine their information seeking behavior, in particular regarding teratogen information.

METHODS

A one page survey was sent to physicians who had called Motherisk for information concerning pregnancy exposures in the previous 30 days for three months. Among the questions that were asked were demographics, which included gender, years in practice, specialty, information resources, and how they utilized the information received from Motherisk.

RESULTS

We received 118/200 completed questionnaires (59% response rate). The mean age of the respondents was: 42 +/- 9 years, mean years of practice was: 14 +/- 8 years, males: 46(38%) and females 72(62%) and 95(80%) were family physicians. 56(48%) researched their question prior to calling Motherisk, 106(91%) and passed on the information received to their patient verbatim. The top four resources for information were: 1) The CPS (PDR), 2) textbooks, 3) journals and 4) colleagues. Only 8% used the Medline for gathering information.

CONCLUSIONS

Physicians feel that a teratogen information service is an important component in the management of women exposed to drugs, chemicals, radiation and infections diseases etc. during pregnancy. Despite the advent of the electronic age, a minority of the physicians in our survey elected to use electronic means to seek information.

摘要

背景

世界各地都设立了致畸物信息服务机构,以传播孕期母体接触相关物质安全性的信息。加拿大多伦多的母婴风险计划每年要处理数千起此类咨询。我们的主要目标是评估医生对从我们这里获取信息的认知和利用情况。次要目标是研究他们的信息寻求行为,特别是关于致畸物信息的行为。

方法

向在过去三个月内致电母婴风险计划咨询孕期接触情况的医生发送了一份单页调查问卷。所提问题包括人口统计学信息,如性别、从业年限、专业、信息来源以及他们如何利用从母婴风险计划获得的信息。

结果

我们共收到118份/200份完整问卷(回复率59%)。受访者的平均年龄为:42±9岁,平均从业年限为:14±8年,男性46人(38%),女性72人(62%),95人(80%)为家庭医生。56人(48%)在致电母婴风险计划之前就已对问题进行了研究,106人(91%)将所获信息逐字传达给了患者。信息的前四大来源是:1)《加拿大医学会杂志》(《医师案头参考》),2)教科书,3)期刊,4)同事。只有8%的人利用医学在线数据库获取信息。

结论

医生们认为致畸物信息服务是孕期接触药物、化学物质、辐射和传染病等的女性管理中的一个重要组成部分。尽管已进入电子时代,但在我们的调查中,仍有少数医生选择使用电子手段来寻求信息。

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