Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/65277
Full metadata record
DC FieldValueLanguage
dc.contributor.authorThanin Lokeskraweeen_US
dc.contributor.authorSombat Muengtaweepongsaen_US
dc.contributor.authorPattarapol Inbunlengen_US
dc.contributor.authorPhichayut Phinyoen_US
dc.contributor.authorJayanton Patumanonden_US
dc.date.accessioned2019-08-05T04:31:12Z-
dc.date.available2019-08-05T04:31:12Z-
dc.date.issued2019-04-01en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-85064155404en_US
dc.identifier.other10.1371/journal.pone.0214874en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85064155404&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/65277-
dc.description.abstract© 2019 Lokeskrawee et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Background The standard treatment of acute ischemic stroke patients is thrombolytic therapy within 60 minutes of a patient’s arrival in stroke center hospitals. Based on the policy of the Lampang Referral System Committee, blood samples of suspected stroke patients need to be collected before transfer to the stroke center (Lampang Hospital). It was still questionable as to whether these blood samples are valid for clinical use and the present study aimed to confirm or deny their validity. Methods A diagnostic study was conducted from June 2015 to May 2016. After exclusion, 340 patients were deemed eligible for analysis. Blood samples were collected just before normal saline infusion at referring hospitals and stored in blood collecting tube boxes set during transportation. At the stroke center, informed consents was requested, blood samples were re-collected to serve as a ‘gold standard’. Prothrombin time (PT), international normalized ratio (INR), activated partial thromboplastin time (aPTT), platelet count, hemoglobin (Hb), hematocrit (Hct), blood urea nitrogen (BUN), and creatinine (Cr) were compared using paired t-tests. Binary regression was used to analyze for accuracy (%) to adjust for extraneous influences and was presented by modified Bland-Altman plots. Results The laboratory results of referring hospitals vs. the stroke center were: PT, 12.4±3.2 vs. 12.5±3.0 sec; INR: 1.0±0.3 vs. 1.0±0.3; and platelet count: 239.8±77.1 vs. 239.8±74.8 (x103/μL). The adjusted accuracy of the PT, INR, and platelet counts were 96.8%, 96.8%, and 95.3% respectively. Conclusion Laboratory tests from referring hospital were determined to be valid. Blood samples should thus be collected at referring hospitals in order to avoid unnecessary blood collection at the stroke center.en_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMultidisciplinaryen_US
dc.titleAccuracy of laboratory tests collected at referring hospitals versus tertiary care hospitals for acute stroke patientsen_US
dc.typeJournalen_US
article.title.sourcetitlePLoS ONEen_US
article.volume14en_US
article.stream.affiliationsLampang Hospitalen_US
article.stream.affiliationsThammasat Universityen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsMae Sai District Hospitalen_US
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.