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Comparison of an immature platelet fraction and reticulated platelet in liver cirrhosis

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dc.contributor.authorKim, Hye Ryoun-
dc.contributor.authorPark, Bo Rae G.-
dc.contributor.authorLee, Mi Kyung-
dc.contributor.authorPark, Ae Ja-
dc.contributor.authorAhn, Jeong Yeal-
dc.date.available2019-05-30T06:35:41Z-
dc.date.issued2007-02-
dc.identifier.issn1598-6535-
dc.identifier.issn2234-3814-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24154-
dc.description.abstractBackground : The main causes of thrombocytopenia in cirrhosis are thought to be platelet destruction and the reduction of thrombopoietin (TPO) expression in the liver. Immature platelet fraction (IPF) has been measured by a fully automated analyzer (Sysmex XE-2100, Japan) as reticulated platelet (RP), which is reflected with thrombopoiesis in bone marrow. In this study, we tried to compare the percentage of IPF (IPF) with that of RP (RP) in patients with liver cirrhosis (LC) and controls. Methods : We compared IPF to RP in 72 liver cirrhosis patients and 30 healthy normal controls. RP was stained with acridine orange, followed by FC500 (Beckman Coulter, USA) analysis and the IPF was identified by flow cytometry with the use of a nucleic acid specific dye in the reticulocyte channel on the Sysmex XE-2100 (TOA Medical Electronics Co., Ltd,, Japan). Results : IPF value in the healthy control was 2.2% (1.7-5.2). RP and IPF were significantly higher in the patients with liver cirrhosis (P < 0,05). IPF appeared to be correlated with RP (y=0.19x+3.35, r=0,34, P < 0.05). In ROC for diagnosis of LC, IPF was significantly more useful than RP. Conclusions : This results show that a rapid, inexpensive automated method for measuring the IPF is feasible and should become a standard parameter in evaluating reticulated platelets.-
dc.format.extent6-
dc.language한국어-
dc.language.isoKOR-
dc.publisherKOREAN SOC LABORATORY MEDICINE-
dc.titleComparison of an immature platelet fraction and reticulated platelet in liver cirrhosis-
dc.typeArticle-
dc.identifier.doi10.3343/kjlm.2007.27.1.7-
dc.identifier.bibliographicCitationKOREAN JOURNAL OF LABORATORY MEDICINE, v.27, no.1, pp 7 - 12-
dc.identifier.kciidART001039054-
dc.description.isOpenAccessN-
dc.identifier.wosid000254719600002-
dc.identifier.scopusid2-s2.0-51049085161-
dc.citation.endPage12-
dc.citation.number1-
dc.citation.startPage7-
dc.citation.titleKOREAN JOURNAL OF LABORATORY MEDICINE-
dc.citation.volume27-
dc.type.docTypeArticle-
dc.publisher.location대한민국-
dc.subject.keywordAuthorreticulated platelet-
dc.subject.keywordAuthorimmature platelet fraction-
dc.subject.keywordAuthorsysmex XE-2100-
dc.subject.keywordAuthorliver cirrhosis-
dc.subject.keywordPlusTHIAZOLE ORANGE-
dc.subject.keywordPlusTHROMBOCYTOPENIA-
dc.subject.keywordPlusCHEMOTHERAPY-
dc.subject.keywordPlusIPF-
dc.relation.journalResearchAreaMedical Laboratory Technology-
dc.relation.journalWebOfScienceCategoryMedical Laboratory Technology-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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