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免疫组织化学检测分析验证的原则:美国病理学家学会病理学和实验室质量中心指南。

Principles of analytic validation of immunohistochemical assays: Guideline from the College of American Pathologists Pathology and Laboratory Quality Center.

机构信息

From the Department of Pathology, St. Jude Medical Center, Fullerton, California (Dr Fitzgibbons); the Department of Pathology and Laboratory Medicine, Women & Infants Hospital/Brown University, Providence, Rhode Island (Dr Bradley); the College of American Pathologists, Northfield, Illinois (Ms Fatheree and Mr Smith); the Department of Pathology, Kaiser Permanente - Los Angeles Medical Center, Los Angeles, California (Dr Alsabeh); PhenoPath Laboratories, Seattle, Washington (Dr Fulton); the Department of Pathology, Beth Israel Deaconess Medical Center, Boston, Massachusetts (Dr Goldsmith); the Department of Pathology, Mercy Hospital, Janesville, Wisconsin (Dr Haas); the Department of Pathology, Montefiore Medical Center, New York, New York (Dr Karabakhtsian); Regional Medical Laboratory, St John's Medical Center, Tulsa, Oklahoma (Ms Loykasek); the Department of Pathology, University of Minnesota Medical Center, Fairview, Minneapolis (Dr Marolt); the Department of Pathology, The Methodist Hospital, Houston, Texas (Dr Shen); and the Department of Pathology, University of Washington Medical Center, Seattle (Dr Swanson).

出版信息

Arch Pathol Lab Med. 2014 Nov;138(11):1432-43. doi: 10.5858/arpa.2013-0610-CP. Epub 2014 Mar 19.

Abstract

CONTEXT

Laboratories must validate all assays before they can be used to test patient specimens, but currently there are no evidence-based guidelines regarding validation of immunohistochemical assays.

OBJECTIVE

To develop recommendations for initial analytic validation and revalidation of immunohistochemical assays.

DESIGN

The College of American Pathologists Pathology and Laboratory Quality Center convened a panel of pathologists and histotechnologists with expertise in immunohistochemistry to develop validation recommendations. A systematic evidence review was conducted to address key questions. Electronic searches identified 1463 publications, of which 126 met inclusion criteria and were extracted. Individual publications were graded for quality, and the key question findings for strength of evidence. Recommendations were derived from strength of evidence, open comment feedback, and expert panel consensus.

RESULTS

Fourteen guideline statements were established to help pathology laboratories comply with validation and revalidation requirements for immunohistochemical assays.

CONCLUSIONS

Laboratories must document successful analytic validation of all immunohistochemical tests before applying to patient specimens. The parameters for cases included in validation sets, including number, expression levels, fixative and processing methods, should take into account intended use and should be sufficient to ensure that the test accurately measures the analyte of interest in specimens tested in that laboratory. Recommendations are also provided for confirming assay performance when there are changes in test methods, reagents, or equipment.

摘要

背景

实验室在将检测患者样本的检测方法投入使用前,必须对其进行验证,但目前尚缺乏免疫组织化学检测方法验证的循证指南。

目的

制定免疫组织化学检测方法初始分析验证和再验证的推荐意见。

设计

美国病理学家协会病理和实验室质量中心召集了一组在免疫组织化学方面具有专业知识的病理学家和组织技术人员,制定验证建议。进行了系统的证据审查,以解决关键问题。电子搜索确定了 1463 篇出版物,其中 126 篇符合纳入标准并被提取。对单个出版物进行了质量分级,并对证据强度的关键问题发现进行了分级。建议来自证据强度、公开意见反馈和专家小组共识。

结果

建立了 14 条指南性声明,以帮助病理实验室遵守免疫组织化学检测方法的验证和再验证要求。

结论

实验室在将免疫组织化学检测方法应用于患者样本之前,必须记录所有免疫组织化学检测方法的成功分析验证情况。验证集中包含的病例参数,包括数量、表达水平、固定剂和处理方法,应考虑预期用途,并且应足以确保该检测在该实验室检测的样本中准确测量感兴趣的分析物。当检测方法、试剂或设备发生变化时,还提供了确认检测性能的建议。

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