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大型儿童医院实施肠外营养电子化处方和配制后用药差错的频次和严重程度

 SIBCS 2020-11-25

  2016年4月,美国肠外肠内营养学会(ASPEN)官方期刊《营养临床实践》(NCP)正式发表了犹他州盐湖城第一儿童医院发表的临床观察,发现根据肠外营养指南和推荐意见实施电子化处方和配制后,近7年来84503例肠外营养处方出现用药差错230例(0.27%),与全国近1.5年4730例处方用药差错74例(1.6%)相比较低。在肠外营养的处方、抄写、配制、输注过程中,无抄写差错,绝大多数(95%)差错发生于输注过程中。

Nutr Clin Pract. 2016 Apr;31(2):195-206.

Frequency and Severity of Parenteral Nutrition Medication Errors at a Large Children's Hospital After Implementation of Electronic Ordering and Compounding.

MacKay M, Anderson C, Boehme S, Cash J, Zobell J.

  • Primary Children's Hospital, Salt Lake City, Utah.

  • Intermountain Healthcare, Salt Lake City, Utah.

INTRODUCTION: The Institute for Safe Medication Practices has stated that parenteral nutrition (PN) is considered a high-risk medication and has the potential of causing harm. Three organizations-American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.), American Society of Health-System Pharmacists, and National Advisory Group-have published guidelines for ordering, transcribing, compounding and administering PN. These national organizations have published data on compliance to the guidelines and the risk of errors. The purpose of this article is to compare total compliance with ordering, transcription, compounding, administration, and error rate with a large pediatric institution.

METHOD: A computerized prescriber order entry (CPOE) program was developed that incorporates dosing with soft and hard stop recommendations and simultaneously eliminating the need for paper transcription. A CPOE team prioritized and identified issues, then developed solutions and integrated innovative CPOE and automated compounding device (ACD) technologies and practice changes to minimize opportunities for medication errors in PN prescription, transcription, preparation, and administration. Thirty developmental processes were identified and integrated in the CPOE program, resulting in practices that were compliant with A.S.P.E.N. safety consensus recommendations. Data from 7 years of development and implementation were analyzed and compared with published literature comparing error, harm rates, and cost reductions to determine if our process showed lower error rates compared with national outcomes.

RESULTS: The CPOE program developed was in total compliance with the A.S.P.E.N. guidelines for PN. The frequency of PN medication errors at our hospital over the 7 years was 230 errors/84,503 PN prescriptions, or 0.27% compared with national data that determined that 74 of 4730 (1.6%) of prescriptions over 1.5 years were associated with a medication error. Errors were categorized by steps in the PN process: prescribing, transcription, preparation, and administration. There were no transcription errors, and most (95%) errors occurred during administration.

CONCLUSION: We conclude that PN practices that conferred a meaningful cost reduction and a lower error rate (2.7/1000 PN) than reported in the literature (15.6/1000 PN) were ascribed to the development and implementation of practices that conform to national PN guidelines and recommendations. Electronic ordering and compounding programs eliminated all transcription and related opportunities for errors.

PMID: 26214511

DOI: 10.1177/0884533615591606

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