Center for Innovations in Quality, Effectiveness and Safety, Michael E. DeBakey VA Medical Center, (MEDVAMC 152), 2002 Holcombe Blvd., Houston, TX 77030, USA.
Baylor College of Medicine, One Baylor Plaza, Houston, TX 77030, USA.
Int J Qual Health Care. 2020 Jul 20;32(6):405-411. doi: 10.1093/intqhc/mzaa066.
Diagnostic errors in psychiatry are understudied partly because they are difficult to measure. The current study aimed to adapt and test the Safer Dx Instrument, a structured tool to review electronic health records (EHR) for errors in medical diagnoses, to evaluate errors in anxiety diagnoses to improve measurement of psychiatric diagnostic errors.
The iterative adaptation process included a review of the revised Safer Dx-Mental Health Instrument by mental health providers to ensure content and face validity and review by a psychometrician to ensure methodologic validity and pilot testing of the revised instrument.
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Pilot testing was conducted on 128 records of patients diagnosed with anxiety in integrated primary care mental health clinics. Cases with anxiety diagnoses documented in progress notes but not included as a diagnosis for the encounter (n = 25) were excluded.
INTERVENTION(S): None.
MAIN OUTCOME MEASURE(S): None.
Of 103 records meeting the inclusion criteria, 62 likely involved a diagnostic error (42 from use of unspecified anxiety diagnosis when a specific anxiety diagnosis was warranted; 20 from use of unspecified anxiety diagnosis when anxiety symptoms were either undocumented or documented but not severe enough to warrant diagnosis). Reviewer agreement on presence/absence of errors was 88% (κ = 0.71).
The revised Safer Dx-Mental Health Instrument has a high reliability for detecting anxiety-related diagnostic errors and deserves testing in additional psychiatric populations and clinical settings.
精神科诊断错误的研究较少,部分原因是其难以衡量。本研究旨在改编和测试 Safer Dx 仪器,这是一种用于审查电子健康记录(EHR)中医疗诊断错误的结构化工具,用于评估焦虑症诊断中的错误,以改善精神科诊断错误的测量。
迭代改编过程包括精神卫生提供者对修订后的 Safer Dx-心理健康仪器进行审查,以确保内容和表面效度,并由心理计量学家进行审查,以确保方法学有效性,并对修订后的仪器进行试点测试。
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在综合初级保健心理健康诊所中对 128 份被诊断为焦虑症的患者记录进行了试点测试。排除了在进度记录中记录有焦虑症诊断但不作为就诊诊断的病例(n=25)。
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在符合纳入标准的 103 份记录中,有 62 份可能存在诊断错误(42 份是因为使用了未指明的焦虑症诊断,而应明确特定的焦虑症诊断;20 份是因为使用了未指明的焦虑症诊断,而焦虑症状既没有记录也没有记录到足以诊断的严重程度)。评估者对错误存在/不存在的一致性为 88%(κ=0.71)。
修订后的 Safer Dx-心理健康仪器具有很高的可靠性,可用于检测与焦虑相关的诊断错误,值得在其他精神科人群和临床环境中进行测试。