Recommendations for European laboratories based on the KDIGO 2024 Clinical Practice Guideline for the Evaluation and Management of Chronic Kidney Disease.

IF 3.8 2区 医学 Q1 MEDICAL LABORATORY TECHNOLOGY Clinical chemistry and laboratory medicine Pub Date : 2024-11-26 DOI:10.1515/cclm-2024-1082
Etienne Cavalier, Tomáš Zima, Pradip Datta, Konstantinos Makris, Elke Schaeffner, Michel Langlois, Mario Plebani, Pierre Delanaye
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Abstract

The 2024 Kidney Disease: Improving Global Outcomes (KDIGO) guidelines for chronic kidney disease (CKD) evaluation and management bring important updates, particularly for European laboratories. These guidelines emphasize the need for harmonization in CKD testing, promoting the use of regional equations. In Europe, the European Kidney Function Consortium (EKFC) equation is particularly suited for European populations, particularly compared to the CKD-EPI 2021 race-free equation. A significant focus is placed on the combined use of creatinine and cystatin C to estimate glomerular filtration rate (eGFRcr-cys), improving diagnostic accuracy. In situations where eGFR may be inaccurate or clinically insufficient, the guidelines encourage the use of measured GFR (mGFR) through exogenous markers like iohexol. These guidelines emphasize the need to standardize creatinine and cystatin C measurements, ensure traceability to international reference materials, and adopt harmonized reporting practices. The recommendations also highlight the importance of incorporating risk prediction models, such as the Kidney Failure Risk Equation (KFRE), into routine clinical practice to better tailor patient care. This article provides a European perspective on how these KDIGO updates should be implemented in clinical laboratories to enhance CKD diagnosis and management, ensuring consistency across the continent.

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根据《KDIGO 2024 慢性肾脏病评估与管理临床实践指南》为欧洲实验室提出的建议。
2024 年肾脏病:改善全球结果》(KDIGO)慢性肾脏病(CKD)评估和管理指南带来了重要的更新,尤其是对欧洲实验室而言。这些指南强调了统一 CKD 检测的必要性,提倡使用地区性方程。在欧洲,欧洲肾功能联盟(EKFC)方程特别适合欧洲人群,尤其是与 CKD-EPI 2021 无种族差异方程相比。重点是结合使用肌酐和胱抑素 C 来估算肾小球滤过率(eGFRcr-cys),从而提高诊断的准确性。在 eGFR 可能不准确或临床效果不佳的情况下,指南鼓励通过碘海醇等外源性标记物来测量 GFR(mGFR)。这些指南强调有必要实现肌酐和胱抑素 C 测量的标准化,确保与国际参考材料的可追溯性,并采用统一的报告方法。这些建议还强调了将肾衰竭风险方程(KFRE)等风险预测模型纳入常规临床实践的重要性,以便更好地为患者提供量身定制的治疗。本文从欧洲的角度阐述了临床实验室应如何实施这些 KDIGO 更新以加强 CKD 诊断和管理,同时确保整个欧洲大陆的一致性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical chemistry and laboratory medicine
Clinical chemistry and laboratory medicine 医学-医学实验技术
CiteScore
11.30
自引率
16.20%
发文量
306
审稿时长
3 months
期刊介绍: Clinical Chemistry and Laboratory Medicine (CCLM) publishes articles on novel teaching and training methods applicable to laboratory medicine. CCLM welcomes contributions on the progress in fundamental and applied research and cutting-edge clinical laboratory medicine. It is one of the leading journals in the field, with an impact factor over 3. CCLM is issued monthly, and it is published in print and electronically. CCLM is the official journal of the European Federation of Clinical Chemistry and Laboratory Medicine (EFLM) and publishes regularly EFLM recommendations and news. CCLM is the official journal of the National Societies from Austria (ÖGLMKC); Belgium (RBSLM); Germany (DGKL); Hungary (MLDT); Ireland (ACBI); Italy (SIBioC); Portugal (SPML); and Slovenia (SZKK); and it is affiliated to AACB (Australia) and SFBC (France). Topics: - clinical biochemistry - clinical genomics and molecular biology - clinical haematology and coagulation - clinical immunology and autoimmunity - clinical microbiology - drug monitoring and analysis - evaluation of diagnostic biomarkers - disease-oriented topics (cardiovascular disease, cancer diagnostics, diabetes) - new reagents, instrumentation and technologies - new methodologies - reference materials and methods - reference values and decision limits - quality and safety in laboratory medicine - translational laboratory medicine - clinical metrology Follow @cclm_degruyter on Twitter!
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