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180702 r ||| eng |
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|a 9789241502054
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|a Weyer, Karin
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|a Commercial serodiagnostic tests for diagnosis of tuberculosis
|h Elektronische Ressource
|b policy statement
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|a Geneva, Switzerland
|b World Health Organization
|c 2011, 2011
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|a 1 PDF file (19 pages)
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|a Includes bibliographical references
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|a Diagnostic Tests, Routine
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|a Tuberculosis, Pulmonary / diagnosis
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|a Serologic Tests / standards
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|a Mirzayev, Fuad
|e [author]
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|a Gemert, Wayne van
|e [author]
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|a Gilpin, Christopher
|e [author]
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|a World Health Organization
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|a eng
|2 ISO 639-2
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|b NCBI
|a National Center for Biotechnology Information
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|a Title from PDF title page. - "WHO/HTM/TB/2011.5"--Title page verso. - "This document was prepared by Karin Weyer, Fuad Mirzayev, Wayne van Gemert, and Christopher Gilpin (WHO Stop TB Department) on the basis of consensus at an international Expert Group Meeting convened by WHO in Geneva on 22 July 2010."--Acknowledgements page
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|u https://www.ncbi.nlm.nih.gov/books/NBK304212
|3 Volltext
|n NLM Bookshelf Books
|3 Volltext
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|a 610
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|a An antibody detection-based diagnostic test in a user-friendly format could potentially replace microscopy and extend tuberculosis diagnosis to lower levels of health services. Dozens of commercial serological tests for tuberculosis are being marketed in many parts of the world, despite previous systematic reviews having reported variable sensitivity and specificity of these tests. Since the publication of these reviews, the evidence base has grown, methods for meta-analyses of diagnostic tests have evolved, and the WHO Stop TB Department (STB) has implemented a systematic approach to evidence synthesis for TB diagnostic policy development involving systematic reviews and meta-analyses, assessment of the evidence base by Expert Group review, and implementation of the GRADE process for evidence synthesis
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