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dc.contributor.authorCoskun, Abdurrahman
dc.contributor.authorSandberg, Sverre
dc.contributor.authorUnsal, Ibrahim
dc.contributor.authorYavuz, Fulya G.
dc.contributor.authorCavusoglu, Coskun
dc.contributor.authorSerteser, Mustafa
dc.contributor.authorKilercik, Meltem
dc.contributor.authorAarsand, Aasne Karine
dc.date.accessioned2022-04-08T11:06:36Z
dc.date.available2022-04-08T11:06:36Z
dc.date.created2022-01-26T13:18:31Z
dc.date.issued2022
dc.identifier.issn1434-6621
dc.identifier.urihttps://hdl.handle.net/11250/2990751
dc.description.abstractFor many measurands, physicians depend on population-based reference intervals (popRI), when assessing laboratory test results. The availability of personalized reference intervals (prRI) may provide a means to improve the interpretation of laboratory test results for an individual. prRI can be calculated using estimates of biological and analytical variation and previous test results obtained in a steady-state situation. In this study, we aim to outline statistical approaches and considerations required when establishing and implementing prRI in clinical practice. Data quality assessment, including analysis for outliers and trends, is required prior to using previous test results to estimate the homeostatic set point. To calculate the prRI limits, two different statistical models based on ‘prediction intervals’ can be applied. The first model utilizes estimates of ‘within-person biological variation’ which are based on an individual’s own data. This model requires a minimum of five previous test results to generate the prRI. The second model is based on estimates of ‘within-subject biological variation’, which represents an average estimate for a population and can be found, for most measurands, in the EFLM Biological Variation Database. This model can be applied also when there are lower numbers of previous test results available. The prRI offers physicians the opportunity to improve interpretation of individuals’ test results, though studies are required to demonstrate if using prRI leads to better clinical outcomes. We recommend that both popRIs and prRIs are included in laboratory reports to aid in evaluating laboratory test results in the follow-up of patients.en_US
dc.language.isoengen_US
dc.publisherDe Gruyteren_US
dc.titlePersonalized reference intervals - Statistical approaches and considerationsen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 De Gruyteren_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1515/cclm-2021-1066
dc.identifier.cristin1990462
dc.source.journalClinical Chemistry and Laboratory Medicineen_US
dc.source.pagenumber629-635en_US
dc.identifier.citationClinical Chemistry and Laboratory Medicine. 2022, 60(4), 629-635.en_US
dc.source.volume60en_US
dc.source.issue4en_US


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