ICD-10-AM 代码在澳大利亚维多利亚州血液学-肿瘤学病例组合中用于医院获得性肺炎质量改进监测的性能。

Jake C Valentine, Elizabeth Gillespie, Karin M Verspoor, Lisa Hall, Leon J Worth
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引用次数: 0

摘要

背景:澳大利亚医院获得性并发症(HAC)政策的出台是为了促进澳大利亚医院使用 ICD-10-AM 代码进行负经费调整:本研究旨在确定 HAC 框架中的 ICD-10-AM 代码在检测癌症患者医院获得性肺炎方面的阳性预测值 (PPV),并描述本中心实施电子病历 (EMR) 前后 PPV 的变化情况:对澳大利亚墨尔本 Peter MacCallum 癌症中心在两个时间段(2015 年 7 月 1 日至 2017 年 6 月 30 日[EMR 前]和 2020 年 9 月 1 日至 2021 年 2 月 28 日[EMR 前])发生的所有编码肺炎病例进行回顾性病例审查,以确定符合标准化监测定义的事件比例:在研究期间的 41,260 例离职人员中,3.66%(n = 151)发生了 HAC 编码肺炎。在 151 例编码为肺炎的离职人员中,有 27 例符合共识监控标准,总 PPV 为 0.18(95% CI:0.12, 0.25)。EMR实施后,PPV提高了约三倍(0.34 [95% CI: 0.19, 0.53] 对 0.13 [95% CI: 0.08, 0.21]; p = .013):结论:目前的HAC定义对癌症患者医院获得性肺炎的分类能力较差到中等,因此可能无法准确反映医院层面的质量改进情况。EMR的实施确实提高了病例的发现率,未来为支持强有力的监测框架而对行政编码数据进行的改进应侧重于EMR系统:尽管澳大利亚医疗机构可随时获得 ICD-10-AM 数据,但这些数据不足以监测和报告血液肿瘤科患者的医院获得性肺炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Performance of ICD-10-AM codes for quality improvement monitoring of hospital-acquired pneumonia in a haematology-oncology casemix in Victoria, Australia.

Background: The Australian hospital-acquired complication (HAC) policy was introduced to facilitate negative funding adjustments in Australian hospitals using ICD-10-AM codes.

Objective: The aim of this study was to determine the positive predictive value (PPV) of the ICD-10-AM codes in the HAC framework to detect hospital-acquired pneumonia in patients with cancer and to describe any change in PPV before and after implementation of an electronic medical record (EMR) at our centre.

Method: A retrospective case review of all coded pneumonia episodes at the Peter MacCallum Cancer Centre in Melbourne, Australia spanning two time periods (01 July 2015 to 30 June 2017 [pre-EMR period] and 01 September 2020 to 28 February 2021 [EMR period]) was performed to determine the proportion of events satisfying standardised surveillance definitions.

Results: HAC-coded pneumonia occurred in 3.66% (n = 151) of 41,260 separations during the study period. Of the 151 coded pneumonia separations, 27 satisfied consensus surveillance criteria, corresponding to an overall PPV of 0.18 (95% CI: 0.12, 0.25). The PPV was approximately three times higher following EMR implementation (0.34 [95% CI: 0.19, 0.53] versus 0.13 [95% CI: 0.08, 0.21]; p = .013).

Conclusion: The current HAC definition is a poor-to-moderate classifier for hospital-acquired pneumonia in patients with cancer and, therefore, may not accurately reflect hospital-level quality improvement. Implementation of an EMR did enhance case detection, and future refinements to administratively coded data in support of robust monitoring frameworks should focus on EMR systems.

Implications: Although ICD-10-AM data are readily available in Australian healthcare settings, these data are not sufficient for monitoring and reporting of hospital-acquired pneumonia in haematology-oncology patients.

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