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The Clinical Effect of Deferoxamine Mesylate on Edema after Intracerebral Hemorrhage

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  • Yao Yu
  • Wei Zhao
  • Chunpeng Zhu
  • Zhiping Kong
  • Yan Xu
  • Guangzhi Liu
  • Xuguang Gao

Abstract

Background and Purpose: It has been shown that 3 days of 62 mg/kg/day deferoxamine infusion (maximum dose not to exceed 6000 mg/day) is safe and tolerated by intracerebral hemorrhage (ICH) patients. The aim of this study was to investigate the efficacy of deferoxamine mesylate for edema resolution and hematoma absorption after ICH. Methods: From February 2013 to May 2014, spontaneous ICH patients diagnosed by computed tomography (CT) within 18 hours of onset were evaluated. Patients were randomly divided into two groups: an experimental group and a control group. The treatment of the two groups was similar except that the experimental group received deferoxamine mesylate. Patients were evaluated by CT and neurology scale at the time of admission, and on the fourth, eighth, and fifteenth day (or at discharge) after admission. Patients were followed up for the first 30 days and clinical data of the two groups were compared. Results: Forty-two patients completed 30 days of follow-up by May 2014; 21 cases in the experimental group and 21 cases in the control group. The control group’s relative edema volume on the fifteenth day (or discharge) was 10.26 ± 17.54, which was higher than the experimental group (1.91 ± 1.94; P

Suggested Citation

  • Yao Yu & Wei Zhao & Chunpeng Zhu & Zhiping Kong & Yan Xu & Guangzhi Liu & Xuguang Gao, 2015. "The Clinical Effect of Deferoxamine Mesylate on Edema after Intracerebral Hemorrhage," PLOS ONE, Public Library of Science, vol. 10(4), pages 1-13, April.
  • Handle: RePEc:plo:pone00:0122371
    DOI: 10.1371/journal.pone.0122371
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