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dc.contributor.author이영열-
dc.date.accessioned2018-02-15T06:33:13Z-
dc.date.available2018-02-15T06:33:13Z-
dc.date.issued2011-06-
dc.identifier.citationINTERNATIONAL JOURNAL OF HEMATOLOGY, Vol.93 No.2 [2011], 163-169en_US
dc.identifier.issn0925-5710-
dc.identifier.urihttp://link.springer.com/article/10.1007%2Fs12185-011-0771-5-
dc.description.abstractThe clinical significance of ADAMTS13 activity for response to treatment, mortality rate, recurrence, and prognosis is unclear. Therefore, we investigated the characteristics of severe ADAMTS13 deficiency and evaluated its prognostic features in Thrombotic thrombocytopenic purpura (TTP). The Korean TTP Registry includes 66 patients from 13 teaching hospitals in Korea who received the diagnosis of TTP from January 2005 to December 2008. Blood samples obtained upon admission were sent for ADAMTS13 analysis (multimer analysis by sodium dodecyl sulfate electrophoresis) to a central laboratory along with patient clinical information. Patients with severe ADAM-TS13 deficiency had lower serum creatinine levels (P = 0.001) than patients with non-severe ADAMTS13 deficiency. Although severe ADAMTS13 deficiency was associated with better response rate (75 vs. 53%, P = 0.145), remission rate (81 vs. 61%, P = 0.209), and mortality rate (19 vs. 31%, P = 0.508) than non-severe ADAMTS13 deficiency, treatment outcomes did not differ significantly between groups. After adjusting for clinical and laboratory features, multivariate analysis did not reveal any independent risk factors for TTP-associated mortality. Patients with severe ADAMTS13 deficiency had lower serum creatinine levels at presentation, but severe ADAMTS13 activity deficiency at TTP diagnosis does not appear to have prognostic significance.en_US
dc.language.isoenen_US
dc.publisherSPRINGER TOKYO, 1-11-11 KUDAN-KITA, CHIYODA-KU, TOKYO, 102-0073, JAPANen_US
dc.subjectADAMTS-13en_US
dc.subjectThrombotic thrombocytopenic purpura (TTP)en_US
dc.subjectVon Willebrand factor (VWF) cleaving proteaseen_US
dc.subjectPlasma exchange (PE)en_US
dc.subjectMicroangiopathic hemolytic anemiaen_US
dc.titleClinical features of severe acquired ADAMTS13 deficiency in thrombotic thrombocytopenic purpura: the Korean TTP registry experienceen_US
dc.typeArticleen_US
dc.relation.no2-
dc.relation.volume93-
dc.identifier.doi10.1007/s12185-011-0771-5-
dc.relation.page163-169-
dc.relation.journalINTERNATIONAL JOURNAL OF HEMATOLOGY-
dc.contributor.googleauthorJang, Moon Ju-
dc.contributor.googleauthorChong, So Young-
dc.contributor.googleauthorKim, In-Ho-
dc.contributor.googleauthorKim, Jee-Hyun-
dc.contributor.googleauthorJung, Chul-Won-
dc.contributor.googleauthorKim, Ja Young-
dc.contributor.googleauthorPark, Ji-Chan-
dc.contributor.googleauthorLee, Sun Min-
dc.contributor.googleauthorKim, Yeo-Kyeoung-
dc.contributor.googleauthorLee, Young-Yiul-
dc.relation.code2011204217-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidleeyy-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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