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Pulmonary Arterial Hypertension: Too Complex for Physicians, Too Complex for ICD Diagnosis Codes

机译:肺动脉高压:对于医师而言过于复杂,对于ICD诊断代码而言过于复杂

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We read with interest the recent article “Accuracy of Algorithms to Identify Pulmonary Arterial Hypertension in Administrative Data: A Systematic Review” by Gillmeyer et?alsup1/sup in this issue of CHEST. The authors characterize the ample limitations and poor diagnostic accuracy posed by analyzing electronic health records of patients with purported pulmonary hypertension. Intriguing arguments made on the results of their meta-analysis are “a need for revision of ICD diagnosis codes to allow discrimination between different WHO PH groups” and the incorporation of “PAH-specific medications in the case definition.” While we applaud the authors for bringing forth this tremendous problem in the field of pulmonary hypertension, we would recommend caution in assuming these changes would improve the accuracy of pulmonary arterial hypertension (PAH) diagnosis.
机译:我们感兴趣地阅读了Gillmeyer等人在本期CHEST上发表的最新文章“识别行政数据中肺动脉高压的算法准确性:系统综述”。作者通过分析据称患有肺动脉高压的患者的电子健康记录来描述其局限性和诊断准确性差。关于荟萃分析结果的有趣观点是“需要修订ICD诊断规范,以区分不同的WHO PH组”,以及将“ PAH专用药物纳入病例定义”。尽管我们赞扬作者在肺动脉高压领域提出了这个巨大的问题,但我们建议谨慎考虑这些变化将改善肺动脉高压(PAH)诊断的准确性。

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