Toward harmonization of clinical molecular diagnostic reports: findings of an international survey

Author:

Payne Deborah A.1,Baluchova Katarina2,Russomando Graciela3,Ahmad-Nejad Parviz45,Mamotte Cyril6,Rousseau Francois7,van Schaik Ron H.N.8,Marriott Kristin9,Maekawa Masato10,Chan K.C. Allen11

Affiliation:

1. American Pathology Partners-Unipath LLC – Clinical Trials and Development , Denver, CO , USA

2. Comenius University in Bratislava , Jessenius Faculty of Medicine in Martin, Biomedical Center, Division of Oncology , Martin , Slovakia

3. Universidad Nacional de Asunción , Molecular Biology and Biotechnology Department , Instituto de Investigaciones en Ciencias de la Salud , San Lorenzo , Paraguay

4. Institute for Medical Laboratory Diagnostics, Centre for Clinical and Translational Research (CCTR) , Wuppertal , Germany

5. Universitat Witten/Herdecke , Witten , Germany

6. Curtin University, School of Biomedical Sciences and CHIRI Biosciences , Perth , Australia

7. CHU de Québec, Université Laval , Department of Laboratory Medicine and Department of Molecular Biology , Medical Biochemistry and Pathology, Faculty of Medicine, Centre de recherché , Québec City, Quebec , Canada

8. Erasmus Medical Center, IFCC Expert Center Pharmacogenetics, Department of Clinical Chemistry , Rotterdam , The Netherlands

9. KSchmidt Consulting, LLC. , Littleton, CO , USA

10. Hamamatsu University School of Medicine, Department of Laboratory Medicine , Hamamatsu , Japan

11. The Chinese University of Hong Kong, Department of Chemical Pathology , Hong Kong SAR , P.R. China

Abstract

Abstract Background: The International Organization for Standardization (ISO) 15189 standard provides recommendations for the postexamination reporting phase to enhance quality in clinical laboratories. The purpose of this study was to encourage a broad discussion on current reporting practices for molecular diagnostic tests by conducting a global survey of such practices. Methods: The International Federation of Clinical Chemistry and Laboratory Medicine’s Committee for Molecular Diagnostics (IFCC C-MD) surveyed laboratories on selected ISO 15189 recommendations and topics. The survey addressed the following aspects: (1) laboratory demographics, (2) report format, (3) result reporting/layout, (4) comments in report and (5) interpretation and clinical decision-making information. Additionally, participants indicated categories needing standardization. Results: Sixteen responses from laboratories located in Asia, Europe, the Middle East, North America and South America were received. Several categories yielded 100% agreement between laboratories, whereas other categories had less than or equal to 50% concordance. Participants scored “nomenclature” and “description of methodologies” as the two most frequently cited aspects needing standardization. Conclusions: The postexamination phase requires extensive and consistent communication between the laboratory, the healthcare provider and the end user. Surveyed laboratories were most likely to follow explicit ISO 15189 recommendations vs. recommendations when the term(s) “where appropriate or where applicable” was used. Interpretation and reporting of critical values varied among participants. Although the outcome of this study may not fully represent the practices of all molecular testing laboratories in countries around the world, the survey identified and specified several recommendations that are requirements for harmonized reporting in molecular diagnostics.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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