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How Well Do Codes Predict True Congenital Heart Defects? A Centers for Disease Control and Prevention-Based Multisite Validation Project.这些代码能多准确地预测真正的先天性心脏缺陷?一项基于疾病控制与预防中心的多地点验证项目。
J Am Heart Assoc. 2022 Aug 2;11(15):e024911. doi: 10.1161/JAHA.121.024911. Epub 2022 Jul 19.
2
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Int J Cardiol. 2022 Jul 1;358:34-38. doi: 10.1016/j.ijcard.2022.04.019. Epub 2022 Apr 11.
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Lifespan Perspective on Congenital Heart Disease Research: JACC State-of-the-Art Review.先天性心脏病研究的寿命期视角:JACC 最新综述。
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阳性预测值 、 和 编码在先天性心脏病识别中的应用。

Positive Predictive Value of , and , Codes for Identification of Congenital Heart Defects.

机构信息

Division of Cardiology Emory University School of Medicine Division of Cardiology Atlanta GA USA.

Children's Healthcare of Atlanta Cardiology Atlanta GA USA.

出版信息

J Am Heart Assoc. 2023 Aug 15;12(16):e030821. doi: 10.1161/JAHA.123.030821. Epub 2023 Aug 7.

DOI:10.1161/JAHA.123.030821
PMID:37548168
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10492959/
Abstract

Background Administrative data permit analysis of large cohorts but rely on (), and () codes that may not reflect true congenital heart defects (CHDs). Methods and Results CHDs in 1497 cases with at least 1 encounter between January 1, 2010 and December 31, 2019 in 2 health care systems, identified by at least 1 of 87 / CHD codes were validated through medical record review for the presence of CHD and CHD native anatomy. Interobserver and intraobserver reliability averaged >95%. Positive predictive value (PPV) of / codes for CHD was 68.1% (1020/1497) overall, 94.6% (123/130) for cases identified in both health care systems, 95.8% (249/260) for severe codes, 52.6% (370/703) for shunt codes, 75.9% (243/320) for valve codes, 73.5% (119/162) for shunt and valve codes, and 75.0% (39/52) for "other CHD" (7 / codes). PPV for cases with >1 unique CHD code was 85.4% (503/589) versus 56.3% (498/884) for 1 CHD code. Of cases with secundum atrial septal defect / codes 745.5/Q21.1 in isolation, PPV was 30.9% (123/398). Patent foramen ovale was present in 66.2% (316/477) of false positives. True positives had younger mean age at first encounter with a CHD code than false positives (22.4 versus 26.3 years; =0.0017). Conclusions CHD / codes have modest PPV and may not represent true CHD cases. PPV was improved by selecting certain features, but most true cases did not have these characteristics. The development of algorithms to improve accuracy may improve accuracy of electronic health records for CHD surveillance.

摘要

背景

行政数据允许对大量队列进行分析,但依赖于()和()代码,这些代码可能无法反映真实的先天性心脏病(CHD)。

方法和结果

在 2 个医疗保健系统中,在 2010 年 1 月 1 日至 2019 年 12 月 31 日期间至少有 1 次就诊记录的 1497 例患者中,至少使用 87 个 /CHD 代码中的 1 个识别出 CHD,并通过病历回顾确认 CHD 及 CHD 原生解剖的存在。观察者间和观察者内可靠性平均 >95%。/代码诊断 CHD 的阳性预测值(PPV)总体为 68.1%(1020/1497),2 个医疗保健系统均识别的病例为 94.6%(123/130),严重程度代码为 95.8%(249/260),分流代码为 52.6%(370/703),瓣膜代码为 75.9%(243/320),分流和瓣膜代码为 73.5%(119/162),“其他 CHD”(7 个 / 代码)为 75.0%(39/52)。>1 个独特的 CHD 代码的病例的 PPV 为 85.4%(503/589),而 1 个 CHD 代码的病例为 56.3%(498/884)。单纯孤立性房间隔缺损 / 代码 745.5/Q21.1 的病例,PPV 为 30.9%(123/398)。卵圆孔未闭在 66.2%(316/477)的假阳性中存在。真正的阳性病例首次出现 CHD 代码的平均年龄低于假阳性病例(22.4 岁对 26.3 岁;=0.0017)。

结论

CHD / 代码的阳性预测值适中,可能无法代表真实的 CHD 病例。通过选择某些特征可以提高 PPV,但大多数真实病例没有这些特征。开发用于提高准确性的算法可能会提高电子健康记录用于 CHD 监测的准确性。