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dc.contributor.author김규남-
dc.date.accessioned2019-10-28T06:00:34Z-
dc.date.available2019-10-28T06:00:34Z-
dc.date.issued2019-05-
dc.identifier.citationACTA HAEMATOLOGICA, Page. 1-5en_US
dc.identifier.issn0001-5792-
dc.identifier.issn1421-9662-
dc.identifier.urihttps://www.karger.com/Article/FullText/499362-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/111607-
dc.description.abstractGlanzmann thrombasthenia is an uncommon hereditary disease that involves an abnormal platelet function leading to complicated hemostatic problems. In situations of anticipated hemorrhage, irradiated apheresed platelets are the first line of treatment. In addition, a combination of recombinant factor VIIa and an antifibrinolytic agent such as tranexamic acid can be utilized to minimize bleeding. Here we are present stable management of a pediatric patient with Glanzmann thrombasthenia admitted for traumatic epidural hematoma removal. Due to the condition of the operation site, some blood loss was unavoidable. However, hemostasis was successfully controlled, and the patient was discharged without additional complications.en_US
dc.language.isoenen_US
dc.publisherKARGERen_US
dc.subjectGlanzmann thrombastheniaen_US
dc.subjectAntifibrinolytic agentsen_US
dc.subjectRecombinant factor VIIaen_US
dc.titlePerioperative hemostatic management of a pediatric patient with Glanzmann thrombasthenia undergoing osteoplastic craniotomy and hematoma removal: A case reporten_US
dc.typeArticleen_US
dc.identifier.doi10.1159/000499362-
dc.relation.page1-5-
dc.relation.journalACTA HAEMATOLOGICA-
dc.contributor.googleauthorLee, Sung Min-
dc.contributor.googleauthorKim, Kyu Nam-
dc.contributor.googleauthorKim, Soo Yeon-
dc.relation.code2019001189-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF MEDICINE[S]-
dc.sector.departmentDEPARTMENT OF MEDICINE-
dc.identifier.pidknkim9-
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COLLEGE OF MEDICINE[S](의과대학) > MEDICINE(의학과) > Articles
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