Interpretative commenting
- PMID: 18852867
- PMCID: PMC2556593
Interpretative commenting
Abstract
* Clinical laboratories should be able to offer interpretation of the results they produce. * At a minimum, contact details for interpretative advice should be available on laboratory reports.Interpretative comments may be verbal or written and printed. * Printed comments on reports should be offered judiciously, only where they would add value; no comment preferred to inappropriate or dangerous comment. * Interpretation should be based on locally agreed or nationally recognised clinical guidelines where available. * Standard tied comments ("canned" comments) can have some limited use.Individualised narrative comments may be particularly useful in the case of tests that are new, complex or unfamiliar to the requesting clinicians and where clinical details are available. * Interpretative commenting should only be provided by appropriately trained and credentialed personnel. * Audit of comments and continued professional development of personnel providing them are important for quality assurance.
References
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- ISO 15189:2003. Medical laboratories – Particular requirements for quality and competence. Geneva, Switzerland: ISO; 2003.
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- National Pathology Accreditation Advisory Council. Requirements for pathology laboratories (2007 Edition) [(Accessed 26 February 2008)]. http://www.health.gov.au/internet/main/publishing.nsf/Content/4B4BC09A2A....
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- Code of practice for clinical biochemists (chemical pathologists) and clinical biochemistry services. [(Accessed 26 February 2008)]. http://www.rcpath.org/resources/pdf/G027-ClinBioCodeOfPractice-May05.pdf.
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- Clinical Pathology Accreditation (UK) Ltd. Standards for the Medical Laboratory. [(Accessed 26 February 2008)]. http://www.cpa-uk.co.uk/files/pdlabst.pdf?bcsi_scan_276FAA45874D151E=0&b....
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- The Royal College of Pathologists. Guidelines for the provision of interpretative comments on biochemical reports. Bull R Coll Pathol. 1998;104:25.
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