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英格兰东北部无糖药品宣传活动评估:药品使用情况的定量分析。

Evaluation of a sugar-free medicines campaign in north east England: quantitative analysis of medicines use.

作者信息

Maguire A, Evans D J, Rugg-Gunn A J, Butler T J

机构信息

Dental School, University of Newcastle upon Tyne, UK.

出版信息

Community Dent Health. 1999 Sep;16(3):138-44.

Abstract

OBJECTIVE

The aim of the study was to evaluate the effectiveness of a sugar-free medicines campaign using suitable prescribing and purchasing indicators.

BASIC RESEARCH DESIGN

Quantitative analysis of sugar-free medicine use, before (1995) and after (1996) the campaign.

CLINICAL SETTING

Two test and two control districts in north east England.

PARTICIPANTS

General medical practitioners (GPs) and community pharmacists.

INTERVENTION

A 12-month campaign involving development and distribution of information packs designed to increase the proportion of prescriptions dispensed sugar-free for paediatric use.

MAIN OUTCOME MEASURES

Changes in the proportion of the following which were sugar-free: (a) for target prescribed medicines (i) number of prescriptions dispensed. (ii) number of prescribed daily amounts (PDA); (b) for target over the counter (OTC) medicines, (i) number of bottles sold, (ii) number of standard daily amounts (SDA) sold.

RESULTS

Quantitative analysis of prescriptions and OTC sales showed statistically highly significant changes towards sugar-free prescribing and dispensing of prescribed medicines but only small increases in the proportion of some sugar-free OTC sales.

CONCLUSIONS

The impact of the campaign was shown to be greatest in changing prescribing habits of GPs with less effect on OTC medicine use. The outcome measures used were suitable for quantitative evaluation of the campaign. POST-CAMPAIGN DEVELOPMENT: Sustainable changes in GPs' prescribing behaviour can be facilitated by software suppliers' modifications to computing software used for prescription writing.

摘要

目的

本研究旨在通过合适的处方和购买指标评估无糖药品推广活动的效果。

基础研究设计

对无糖药品使用情况进行定量分析,对比推广活动前(1995年)和推广活动后(1996年)的情况。

临床环境

英格兰东北部的两个试验区和两个对照区。

参与者

全科医生(GPs)和社区药剂师。

干预措施

开展为期12个月的活动,内容包括编制和分发信息包,以提高儿科使用的无糖配方药品的配药比例。

主要观察指标

以下各项中无糖产品的比例变化:(a)针对目标处方药,(i)配药处方数量。(ii)规定日剂量(PDA)数量;(b)针对目标非处方药,(i)售出瓶数,(ii)售出标准日剂量(SDA)数量。

结果

对处方和非处方药销售情况的定量分析显示,在无糖处方和处方药配药方面有统计学上高度显著的变化,但在一些无糖非处方药销售比例方面仅有小幅增加。

结论

该推广活动在改变全科医生的处方习惯方面影响最大,对非处方药使用的影响较小。所采用的观察指标适用于对该推广活动进行定量评估。活动后发展:软件供应商对用于书写处方的计算软件进行修改,有助于全科医生的处方行为实现可持续变化。

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