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Response to Spitzer et al. letter

机译:对Spitzer等人的回应。信件

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摘要

Homage must be paid to the DSM-III field trials (1) that strongly influenced the design of the DSM-5 field trials. It could hardly be otherwise, since methods for evaluating categorical diagnoses were developed for DSM-III by Dr. Spitzer and his colleagues, Drs. Fleiss and Cohen. However, in the 30 years after 1979, the methodology and the understanding of kappa have advanced (2), and DSM-5 reflects that as well.Like DSM-III, DSM-5 field trials sampled typical clinic patients. However, in the DSM-III field trials, participating clinicians were allowed to select the patients to evaluate and were trusted to report all results. In the DSM-5 field trials, symptomatic patients at each site were referred to a research associate for consent, assigned to an appropriate stratum, and randomly assigned to two participating clinicians for evaluation, with electronic data entry. In DSM-III field trials, the necessary independence of the two clinicians evaluating each patient was taken on trust. Stronger blinding protections were implemented in the DSM-5 field trials. Selection bias and lack of blindness tend to inflate kappas.
机译:必须向严重影响DSM-5野外试验设计的DSM-III野外试验(1)致敬。 Spitzer博士和他的同事Drs。Spitzer为DSM-III开发了用于评估分类诊断的方法,这几乎不可能。弗莱斯和科恩。然而,在1979年之后的30年中,对Kappa的方法和理解有了进一步的发展(2),而DSM-5也反映出这一点。与DSM-III类似,DSM-5现场试验对典型的临床患者进行了采样。但是,在DSM-III现场试验中,允许参与的临床医生选择要评估的患者,并被信任报告所有结果。在DSM-5现场试验中,将每个部位有症状的患者转介给研究助理以征得他们的同意,分配给适当的阶层,并随机分配给两名参与的临床医生进行评估,并输入电子数据。在DSM-III现场试验中,信任评估了两名评估每个患者的临床医生的必要独立性。在DSM-5现场试验中实施了更强的致盲保护。选择偏见和盲目性往往会使卡帕斯膨胀。

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