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检验医学中的系统评价:原则、流程及实际考量

Systematic reviews in laboratory medicine: principles, processes and practical considerations.

作者信息

Horvath Andrea Rita, Pewsner Daniel

机构信息

Committee on Evidence-Based Laboratory Medicine, International Federation of Clinical Chemistry and Laboratory Medicine and Department of Clinical Chemistry, University of Szeged, Faculty of Medicine, Szeged, Hungary.

出版信息

Clin Chim Acta. 2004 Apr;342(1-2):23-39. doi: 10.1016/j.cccn.2003.12.015.

Abstract

BACKGROUND

Systematic reviews and meta-analyses are generally accepted to represent the highest level of evidence, and are a cornerstone in practising evidence-based medicine. So far, these efforts have been largely confined to the evaluation of the efficacy and effectiveness of therapeutic and preventive interventions. Systematic reviews in laboratory medicine are scarce and many of them do not meet essential quality criteria [Clin. Chem. Lab. Med. 38 (2000) 577]. Most of these problems are related to the poor design and heterogeneity of primary research, and that there are no agreed methods or quality standards for making systematic reviews in laboratory medicine.

AIMS AND OBJECTIVES

For better evidence in laboratory medicine, not only higher quality primary studies but also standardized methodologies for designing, conducting and reporting systematic reviews in diagnostics are needed. The aim of this review is to present the general principles and provide a step-by-step process of systematic reviewing in laboratory medicine.

METHODS

This narrative review is based on the overview of the medical literature on the methodology of systematic reviewing and that of the "state of the art" of evidence-based diagnosis.

RESULTS

Systematic reviews of diagnostic interventions differ from that of therapeutic interventions in the methods of question formulation, the choice of study design, the assessment of study quality and the statistical methods used to combine results. Therefore, the general principles of systematic reviewing are adapted to the specialist field of laboratory medicine. The process of systematic reviewing consists of six key steps: (1) preparation for the review, (2) systematic search of the primary literature, (3) selection of papers for review, (4) critical appraisal of the selected literature, (5) analysis and synthesis of data, and (6) interpretation of data. The most important technical and methodological aspects of each step and the essential elements of a good systematic review in laboratory medicine are presented.

CONCLUSIONS

Systematic reviews of diagnostic interventions support clinical and policy decisions, the development of practice guidelines, clinical audit, technology assessment, economic evaluations, education and training, and identify gaps in our knowledge for future research. Systematic reviewing of laboratory data is expected to result in better, bigger and more reliable primary studies, which hopefully will support the diffusion of new diagnostic technologies with scientifically proven efficacy and effectiveness in the future.

摘要

背景

系统评价和荟萃分析通常被认为代表了最高级别的证据,是实施循证医学的基石。到目前为止,这些工作主要局限于对治疗和预防干预措施的疗效和有效性评估。检验医学领域的系统评价较少,且其中许多不符合基本质量标准[《临床化学与检验医学》38 (2000) 577]。这些问题大多与原始研究设计不佳和异质性有关,并且在检验医学领域进行系统评价尚无公认的方法或质量标准。

目的

为了在检验医学中获得更好的证据,不仅需要更高质量的原始研究,还需要用于设计、开展和报告诊断方面系统评价的标准化方法。本综述的目的是阐述一般原则,并提供检验医学系统评价的逐步流程。

方法

本叙述性综述基于对医学文献中系统评价方法以及循证诊断“最新技术水平”的概述。

结果

诊断性干预措施的系统评价在问题提出方法、研究设计选择、研究质量评估以及用于合并结果的统计方法等方面与治疗性干预措施的系统评价不同。因此,系统评价的一般原则适用于检验医学专业领域。系统评价过程包括六个关键步骤:(1) 综述准备;(2) 对原始文献进行系统检索;(3) 选择纳入综述的论文;(4) 对所选文献进行严格评价;(5) 数据的分析与综合;(6) 数据解读。阐述了每个步骤最重要的技术和方法学方面以及检验医学中良好系统评价的基本要素。

结论

诊断性干预措施的系统评价有助于临床和政策决策、实践指南的制定、临床审计、技术评估、经济评价、教育与培训,并识别我们知识中的空白以供未来研究。对检验数据进行系统评价有望产生更好、规模更大且更可靠的原始研究,有望在未来支持具有科学验证疗效和有效性的新诊断技术的推广。

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