Comparative Diagnostic Accuracy of Nursing Delirium Screening Scale Versus Confusion Assessment Method for Postoperative Delirium: A Systematic Review and Meta‐Analysis

谵妄 医学 荟萃分析 心理信息 混乱 梅德林 重症监护室 急诊医学 内科学 重症监护医学 心理学 精神分析 政治学 法学
作者
Chia‐Jou Lin,Donna M. Fick,Victoria Traynor,Yi‐Chen Chen,Hui‐Fen Hsiang,Hsiao‐Yean Chiu
出处
期刊:Journal of Clinical Nursing [Wiley]
卷期号:34 (1): 287-298 被引量:2
标识
DOI:10.1111/jocn.17467
摘要

ABSTRACT Aims To synthesise the evidence on and to compare the diagnostic accuracy of the Nu‐DESC and CAM in detecting postoperative delirium among hospitalised patients. Design Systematic review and diagnostic meta‐analysis. Data Sources The PubMed, Embase, Cumulative Index to Nursing and Allied Health Literature, ProQuest Dissertations and Theses A&I, and PsycINFO databases were systematically searched from their inception to February 10, 2023. Results In total, 10 ( n = 1950) and seven ( n = 830) reports were included for the Nu‐DESC and CAM, respectively. For Nu‐DESC and CAM, the pooled sensitivities were 0.69 and 0.65, respectively, while the summary specificities were 0.99 for Nu‐DESC and 0.92 for CAM. The pooled specificity differed significantly between the two tools ( p < 0.001), despite comparable pooled sensitivities. The duration of stay in the intensive care unit significantly moderated the summary specificity of Nu‐DESC ( B = −0.0003, p = 0.009). Regarding CAM, the percentage of female participants showed a positive correlation with its pooled sensitivity ( B = 0.005, p = 0.02). Furthermore, studies where clinical specialists served as assessors demonstrated a higher summary sensitivity than those assessed by nurses (0.87 vs. 0.25, p = 0.01). Conclusion The sensitivities of the Nu‐DESC and CAM for detecting postoperative delirium did not achieve optimal levels. Therefore, developing more accurate tools to detect postoperative delirium by integrating features from related risk factors or incorporating technology‐based algorithms to enhance the screening capability is warranted. Reporting Method The study has adhered to PRISMA‐DTA guideline. Patient or Public Contribution No patient or public contribution. Trial Registration The study protocol has been registered on PROSPERO (CRD42023398961)
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