Publication:
Hemostatic Side Effects of High-Dose Methotrexate in Childhood Acute Lymphoblastic Leukemia

dc.authorscopusid6602890385
dc.authorscopusid6601991412
dc.authorscopusid7102824836
dc.authorscopusid6602784315
dc.authorscopusid6507222394
dc.authorscopusid56695326700
dc.authorscopusid56695326700
dc.contributor.authorFišgin, T.
dc.contributor.authorYarali, N.
dc.contributor.authorKara, A.
dc.contributor.authorBozkurt, C.
dc.contributor.authorBirgen, D.
dc.contributor.authorErten, U.
dc.contributor.authorDuru, F.
dc.date.accessioned2020-06-21T15:43:32Z
dc.date.available2020-06-21T15:43:32Z
dc.date.issued2004
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Fišgin] Tunç, Department of Pediatric Hematology, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Yarali] Hüsniye Neşe, Department of Pediatric Hematology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Kara] Abdurrahman, Department of Pediatric Hematology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Bozkurt] Ceyhun, Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Birgen] Dilek, Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Erten] Ulya, Department of Pediatric Oncology, Dr. Sami Ulus Children's Hospital, Ankara, Turkey; [Duru] Feride, Department of Pediatric Hematology, Dr. Sami Ulus Children's Hospital, Ankara, Turkeyen_US
dc.description.abstractThe purpose of this study is to investigate the hemostatic side effects of HDMTX. Between 2001 and 2002, 20 children with acute lymphoblastic leukemia at the Dr. Sami Ulus Children's Hospital, Department of Pediatric Hematology and Oncology, treated according to the St. Jude ALL XIII protocol were eligible to this study. Methotrexate at a dose of 2 g/m2 was infused over 24 hours. Coagulation screening studies included prothrombin time (PT), APTT, fibrinogen, fibrin degradation product (D-Dimer), factor II, factor V, factor VII, factor VIII, factor IX, factor X, PC, PS, AT-III determinations before HDMTX therapy (PreT), 1 day after (Post1D), and 1 week after (PostT1W) the end of the HDMTX infusion. We found that PT and APTT were prolonged, PC, PS, and AT-III levels were decreased with a slight increase in D-Dimer 1 day after the administration of HDMTX and all of them returned to the normal levels by 7 days. In addition we found that FVII, FIX, FX were significantly decreased 1 day after therapy and normalised by 7 days.en_US
dc.identifier.doi10.1080/08880010490264064
dc.identifier.endpage83en_US
dc.identifier.issn0888-0018
dc.identifier.issn1521-0669
dc.identifier.issue1en_US
dc.identifier.pmid14660309
dc.identifier.scopus2-s2.0-0345872389
dc.identifier.scopusqualityQ3
dc.identifier.startpage77en_US
dc.identifier.urihttps://doi.org/10.1080/08880010490264064
dc.identifier.urihttps://hdl.handle.net/20.500.12712/21652
dc.identifier.volume21en_US
dc.identifier.wosWOS:000186930500010
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofPediatric Hematology and Oncologyen_US
dc.relation.journalPediatric Hematology and Oncologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleHemostatic Side Effects of High-Dose Methotrexate in Childhood Acute Lymphoblastic Leukemiaen_US
dc.typeArticleen_US
dspace.entity.typePublication

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