Protocol and standard operating procedures for common use in a worldwide multicenter study on reference values
dc.contributor.author | Ichihara, Kiyoshi | |
dc.contributor.author | Barth, Julian H. | |
dc.contributor.author | Klee, George | |
dc.contributor.buuauthor | Özarda, Yeşim | |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/Biyokimya Anabilim Dalı. | tr_TR |
dc.contributor.researcherid | AAL-8873-2021 | tr_TR |
dc.contributor.scopusid | 35741320500 | tr_TR |
dc.date.accessioned | 2022-03-21T12:50:25Z | |
dc.date.available | 2022-03-21T12:50:25Z | |
dc.date.issued | 2013-05 | |
dc.description.abstract | The reference intervals (RIs) given in laboratory reports have an important role in aiding clinicians in interpreting test results in reference to values of healthy populations. In this report, we present a proposed protocol and standard operating procedures (SOPs) for common use in conducting multicenter RI studies on a national or international scale. The protocols and consensus on their contents were refined through discussions in recent C-RIDL meetings. The protocol describes in detail (1) the scheme and organization of the study, (2) the target population, inclusion/exclusion criteria, ethnicity, and sample size, (3) health status questionnaire, (4) target analytes, (5) blood collection, (6) sample processing and storage, (7) assays, (8) cross-check testing, (9) ethics, (10) data analyses, and (11) reporting of results. In addition, the protocol proposes the common measurement of a panel of sera when no standard materials exist for harmonization of test results. It also describes the requirements of the central laboratory, including the method of cross-check testing between the central laboratory of each country and local laboratories. This protocol and the SOPs remain largely exploratory and may require a reevaluation from the practical point of view after their implementation in the ongoing worldwide study. The paper is mainly intended to be a basis for discussion in the scientific community. | en_US |
dc.description.sponsorship | Japan Society for the Promotion of Science (24256003) | en_US |
dc.identifier.citation | Özarda, Y. vd. (2013). "Protocol and standard operating procedures for common use in a worldwide multicenter study on reference values". Clinical Chemistry and Laboratory Medicine, 51(5), 1027-1040. | en_US |
dc.identifier.endpage | 1040 | tr_TR |
dc.identifier.issn | 1434-6621 | |
dc.identifier.issn | 1437-4331 | |
dc.identifier.issue | 5 | tr_TR |
dc.identifier.pubmed | 23633469 | tr_TR |
dc.identifier.scopus | 2-s2.0-84882276801 | tr_TR |
dc.identifier.startpage | 1027 | tr_TR |
dc.identifier.uri | https://doi.org/10.1515/cclm-2013-0249 | |
dc.identifier.uri | https://www.degruyter.com/document/doi/10.1515/cclm-2013-0249/html | |
dc.identifier.uri | http://hdl.handle.net/11452/25237 | |
dc.identifier.volume | 51 | tr_TR |
dc.identifier.wos | 000318495900024 | tr_TR |
dc.indexed.pubmed | Pubmed | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.wos | SCIE | en_US |
dc.language.iso | en | en_US |
dc.publisher | Walter De Gruyter Gmbh | de |
dc.relation.collaboration | Yurt dışı | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.relation.journal | Clinical Chemistry and Laboratory Medicine | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.subject | Medical laboratory technology | en_US |
dc.subject | Cross-check study | en_US |
dc.subject | Harmonization | en_US |
dc.subject | Multicenter study | en_US |
dc.subject | Panel of sera | en_US |
dc.subject | Reference interval | en_US |
dc.subject | Standardization | en_US |
dc.subject | Approved recommendation 1987 | en_US |
dc.subject | Collected reference values | en_US |
dc.subject | Reference intervals | en_US |
dc.subject | Statistical treatment | en_US |
dc.subject | Serum | en_US |
dc.subject | Tubes | en_US |
dc.subject | Individuals | en_US |
dc.subject | Specimens | en_US |
dc.subject | Proposal | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Blood sampling | en_US |
dc.subject.emtree | Blood storage | en_US |
dc.subject.emtree | Ethnicity | en_US |
dc.subject.emtree | Health status | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Multicenter study (topic) | en_US |
dc.subject.emtree | Normal human | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Quality control | en_US |
dc.subject.emtree | Questionnaire | en_US |
dc.subject.emtree | Reference value | en_US |
dc.subject.emtree | Sample size | en_US |
dc.subject.mesh | Blood specimen collection | en_US |
dc.subject.mesh | Calibration | en_US |
dc.subject.mesh | Clinical chemistry tests | en_US |
dc.subject.mesh | Healthy volunteers | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Laboratories | en_US |
dc.subject.mesh | Quality control | en_US |
dc.subject.mesh | Reference values | en_US |
dc.subject.scopus | Clinical Chemistry; Thyrotropin; Chemical Species | en_US |
dc.subject.wos | Medical laboratory technology | en_US |
dc.title | Protocol and standard operating procedures for common use in a worldwide multicenter study on reference values | en_US |
dc.type | Article | |
dc.wos.quartile | Q1 | en_US |