Rettew David C, Lynch Alicia Doyle, Achenbach Thomas M, Dumenci Levent, Ivanova Masha Y
Department of Psychiatry, University of Vermont College of Medicine, Burlington, VT 05401, USA.
Int J Methods Psychiatr Res. 2009 Sep;18(3):169-84. doi: 10.1002/mpr.289.
Standardized diagnostic interviews (SDIs) have become de facto gold standards for clinical research. However, because clinical practitioners seldom use SDIs, it is essential to determine how well SDIs agree with clinical diagnoses. In meta-analyses of 38 articles published from 1995 to 2006 (N = 15,967 probands), mean kappas (z-transformed) between diagnoses from clinical evaluations versus SDIs were 0.27 for a broad category of all disorders, 0.29 for externalizing disorders, and 0.28 for internalizing disorders. Kappas for specific disorders ranged from 0.19 for generalized anxiety disorder to 0.86 for anorexia nervosa (median = 0.48). For diagnostic clusters (e.g. psychotic disorders), kappas ranged from 0.14 for affective disorders (including bipolar) to 0.70 for eating disorders (median = 0.43). Kappas were significantly higher for outpatients than inpatients and for children than adults. However, these effects were not significant in meta-regressions.
Diagnostic agreement between SDIs and clinical evaluations varied widely by disorder and was low to moderate for most disorders. Thus, findings from SDIs may not fully apply to diagnoses based on clinical evaluations of the sort used in the published studies. Rather than implying that SDIs or clinical evaluations are inferior, characteristics of both may limit agreement and generalizability from SDI findings to clinical practice.
标准化诊断访谈(SDIs)已成为临床研究事实上的金标准。然而,由于临床医生很少使用SDIs,因此确定SDIs与临床诊断的一致性程度至关重要。在对1995年至2006年发表的38篇文章(N = 15967名先证者)进行的荟萃分析中,临床评估诊断与SDIs诊断之间的平均卡帕值(z转换后),对于所有疾病的广泛类别为0.27,外化性疾病为0.29,内化性疾病为0.28。特定疾病的卡帕值范围从广泛性焦虑症的0.19到神经性厌食症的0.86(中位数 = 0.48)。对于诊断集群(如精神障碍),卡帕值范围从情感障碍(包括双相情感障碍)的0.14到饮食障碍的0.70(中位数 = 0.43)。门诊患者的卡帕值显著高于住院患者,儿童的卡帕值显著高于成人。然而,在荟萃回归中这些效应并不显著。
SDIs与临床评估之间的诊断一致性因疾病而异,差异很大,大多数疾病的一致性为低到中等。因此,SDIs的研究结果可能无法完全适用于基于已发表研究中所使用的那种临床评估的诊断。这并不意味着SDIs或临床评估较差,两者的特点都可能限制一致性以及从SDIs研究结果到临床实践的可推广性。