Pharmacotherapy of Traumatic Brain Injury: State of the Science and the Road Forward: Report of the Department of Defense Neurotrauma Pharmacology Workgroup

被引:182
作者
Diaz-Arrastia, Ramon [1 ]
Kochanek, Patrick M. [2 ]
Bergold, Peter [3 ]
Kenney, Kimbra [4 ]
Marx, Christine E. [5 ,6 ]
Grimes, Jamie B. [7 ]
Loh, Yince [8 ]
Adam, Gina E. [9 ]
Oskvig, Devon
Curley, Kenneth C. [9 ]
Salzer, Wanda [9 ]
机构
[1] Uniformed Serv Univ Hlth Sci, Dept Neurol, Bethesda, MD 20814 USA
[2] Univ Pittsburgh, Sch Med, Dept Crit Care Med, Pittsburgh, PA USA
[3] Suny Downstate Med Ctr, Dept Physiol & Pharmacol, Brooklyn, NY 11203 USA
[4] Uniformed Serv Univ Hlth Sci, Dept Neurol, Rockville, MD USA
[5] Duke Univ, Med Ctr, Dept Psychiat & Behav Sci, Durham, NC USA
[6] Durham VA Med Ctr, Durham, NC USA
[7] Def & Vet Brain Injury Ctr, Silver Spring, MD USA
[8] Madigan Army Med Ctr, Dept Neurol, Tacoma, WA 98431 USA
[9] US Army Med Res & Mat Command, Ft Detrick, MD USA
基金
美国国家卫生研究院;
关键词
animal studies; head trauma; human studies; pharmacology; traumatic brain injury; RECOMBINANT-HUMAN-ERYTHROPOIETIN; SEX STEROID-HORMONES; POTENTIAL NEUROPROTECTIVE MECHANISM; ANEURYSMAL SUBARACHNOID HEMORRHAGE; CHRONIC METHYLPHENIDATE TREATMENT; CONTROLLED CORTICAL IMPACT; WATER MAZE PERFORMANCE; DIFFUSE AXONAL INJURY; CLOSED-HEAD INJURY; CYCLOSPORINE-A;
D O I
10.1089/neu.2013.3019
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Despite substantial investments by government, philanthropic, and commercial sources over the past several decades, traumatic brain injury (TBI) remains an unmet medical need and a major source of disability and mortality in both developed and developing societies. The U.S. Department of Defense neurotrauma research portfolio contains more than 500 research projects funded at more than $700 million and is aimed at developing interventions that mitigate the effects of trauma to the nervous system and lead to improved quality of life outcomes. A key area of this portfolio focuses on the need for effective pharmacological approaches for treating patients with TBI and its associated symptoms. The Neurotrauma Pharmacology Workgroup was established by the U.S. Army Medical Research and Materiel Command (USAMRMC) with the overarching goal of providing a strategic research plan for developing pharmacological treatments that improve clinical outcomes after TBI. To inform this plan, the Workgroup (a) assessed the current state of the science and ongoing research and (b) identified research gaps to inform future development of research priorities for the neurotrauma research portfolio. The Workgroup identified the six most critical research priority areas in the field of pharmacological treatment for persons with TBI. The priority areas represent parallel efforts needed to advance clinical care; each requires independent effort and sufficient investment. These priority areas will help the USAMRMC and other funding agencies strategically guide their research portfolios to ensure the development of effective pharmacological approaches for treating patients with TBI.
引用
收藏
页码:135 / 158
页数:24
相关论文
共 265 条
  • [41] Neuroprotection with erythropoietin administration following controlled cortical impact injury in rats
    Cherian, Leela
    Clay Goodman, J.
    Robertson, Claudia
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2007, 322 (02) : 789 - 794
  • [42] Improved Cerebrovascular Function and Reduced Histological Damage with Darbepoietin Alfa Administration after Cortical Impact Injury in Rats
    Cherian, Leela
    Goodman, J. Clay
    Robertson, Claudia
    [J]. JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2011, 337 (02) : 451 - 456
  • [43] Pharmacology of riluzole in acute spinal cord injury
    Chow, Diana S. L.
    Teng, Yang
    Toups, Elizabeth G.
    Aarabi, Bizhan
    Harrop, James S.
    Shaffrey, Christopher I.
    Johnson, Michele M.
    Boakye, Maxwell
    Frankowski, Ralph F.
    Fehlings, Michael G.
    Grossman, Robert G.
    [J]. JOURNAL OF NEUROSURGERY-SPINE, 2012, 17 : 129 - 140
  • [44] The effects of cyclosporin-A on axonal conduction deficits following traumatic brain injury in adult rats
    Colley, Beverly S.
    Phillips, Linda L.
    Reeves, Thomas M.
    [J]. EXPERIMENTAL NEUROLOGY, 2010, 224 (01) : 241 - 251
  • [45] Creyghton Wouter M, 2004, Semin Vasc Med, V4, P167, DOI 10.1055/s-2004-835375
  • [46] Progesterone improves acute recovery after traumatic brain injury in the aged rat
    Cutler, Sarah M.
    Cekic, Milos
    Miller, Darren M.
    Wali, Bushra
    VanLandingham, Jacob W.
    Stein, Donald G.
    [J]. JOURNAL OF NEUROTRAUMA, 2007, 24 (09) : 1475 - 1486
  • [47] Slow-release and injected progesterone treatments enhance acute recovery after traumatic brain injury
    Cutler, Sarah M.
    VanLandingham, Jacob W.
    Murphy, Anne Z.
    Stein, Donald G.
    [J]. PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2006, 84 (03) : 420 - 428
  • [48] Involvement of the Glycogen Synthase Kinase-3 Signaling Pathway in TBI Pathology and Neurocognitive Outcome
    Dash, Pramod K.
    Johnson, Daniel
    Clark, Jordan
    Orsi, Sara A.
    Zhang, Min
    Zhao, Jing
    Grill, Raymond J.
    Moore, Anthony N.
    Pati, Shibani
    [J]. PLOS ONE, 2011, 6 (09):
  • [49] Defense Medical Surveillance System and Theater Medical Data Store, 2012, DOD NUMB TRAUM BRAIN
  • [50] Growth hormone therapy in critically ill patients
    Demling, R
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (11) : 837 - 839