Evaluating the effect of making the indication field compulsory in electronic prescriptions: A pre-post study in a hospital prescribing system.

IF 3.1 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Lorna Pairman, Paul Chin, Matthew Doogue
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Abstract

Aims: Recording the indication for a medicine in the prescription supports communication. In May 2023, our district hospitals made the free-text indication field in prescriptions compulsory for all medicines in the inpatient prescribing system. This study aimed to evaluate the effect of introducing a compulsory indication field in an inpatient prescribing system.

Methods: Text in the indication field was manually classified as an indication, 'other text', 'rubbish text', 'to be determined' and 'blank'. Prescribing data were extracted from the district data warehouse. The change in proportion of prescriptions with an indication was compared for 8 weeks after introduction of a compulsory indication field to an equivalent 8 weeks in 2022. Secondary outcomes included medication cessation and indication recording before discharge.

Results: We analysed 81 634 prescriptions before and 82 726 after indications were made compulsory. The proportion of prescriptions with an indication increased from 29.2% to 75.6%. 'Rubbish text' increased from 0% to 2.3%, 'other text' from 2.5% to 14.7%, and 'to be determined' from 0.0% to 6.6%. Of 5557 prescriptions with 'to be determined' initially, 18.1% were ceased and 2.7% had an indication before discharge.

Conclusions: After making the prescription indication field compulsory, the proportion of medicines with an indication increased from 29% to 76%, with only a small increase in 'rubbish text'. Following the system change, the quality of information recording improved but there was no change in medicine use. Compulsory fields should be combined with improvements in other components of care to improve medicine use.

评价电子处方强制填写指征字段的效果:医院处方系统的前后研究。
目的:在处方中记录药物的适应症,便于沟通。2023年5月,我区医院将处方中自由文本指征字段强制纳入住院处方系统中所有药品。本研究旨在评估在住院病人处方系统中引入强制指征字段的效果。方法:手工将指示字段中的文本分为指示、“其他文本”、“垃圾文本”、“待确定”和“空白”。处方数据从地区数据仓库中提取。在引入强制性适应证领域后的8周内,比较了具有适应证的处方比例的变化与2022年等效的8周。次要结局包括停药和出院前适应证记录。结果:分析了强制适应证实施前处方81 634张,强制适应证实施后处方82 726张。有适应证的处方比例由29.2%提高到75.6%。“垃圾短信”从0%增加到2.3%,“其他短信”从2.5%增加到14.7%,“待定”从0.0%增加到6.6%。在5557张最初带有“待定”字样的处方中,18.1%的处方被停用,2.7%的处方在出院前有指征。结论:处方指征字段强制执行后,有指征的药品比例由29%增加到76%,仅有“垃圾文字”略有增加。系统变更后,信息记录的质量有所提高,但用药情况没有变化。强制性领域应与其他保健组成部分的改进相结合,以改善药物使用。
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来源期刊
CiteScore
6.30
自引率
8.80%
发文量
419
审稿时长
1 months
期刊介绍: Published on behalf of the British Pharmacological Society, the British Journal of Clinical Pharmacology features papers and reports on all aspects of drug action in humans: review articles, mini review articles, original papers, commentaries, editorials and letters. The Journal enjoys a wide readership, bridging the gap between the medical profession, clinical research and the pharmaceutical industry. It also publishes research on new methods, new drugs and new approaches to treatment. The Journal is recognised as one of the leading publications in its field. It is online only, publishes open access research through its OnlineOpen programme and is published monthly.
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