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CNS Drugs

, Volume 30, Issue 9, pp 791–806 | Cite as

Pharmacologic Neuroprotection for Functional Outcomes After Traumatic Brain Injury: A Systematic Review of the Clinical Literature

  • Shaun E. Gruenbaum
  • Alexander Zlotnik
  • Benjamin F. Gruenbaum
  • Denise Hersey
  • Federico BilottaEmail author
Systematic Review

Abstract

Introduction

Traumatic brain injury (TBI) is a major cause of death and disability worldwide. The deleterious effects of secondary brain injury may be attenuated by early pharmacological therapy in the emergency room and intensive care unit (ICU). Current medical management of acute TBI is primarily supportive, aimed at reducing intracranial pressure (ICP) and optimizing cerebral perfusion. There are no pharmacological therapies to date that have been unequivocally demonstrated to improve neurological outcomes after TBI.

Objectives

The purpose of this systematic review was to evaluate the recent clinical studies from January 2013 through November 2015 that investigated neuroprotective functional outcomes of pharmacological agents after TBI.

Methods

The following databases were searched for relevant studies: MEDLINE (OvidSP January Week 1, 2013–November Week 2 2015), Embase (OvidSP 2013 January 1–2015 November 24), and the unindexed material in PubMed (National Library of Medicine/National Institutes of Health [NLM/NIH]). This systematic review included only full-length clinical studies and case series that included at least five patients and were published in the English language. Only studies that examined functional clinical outcomes were included.

Results

Twenty-five of 527 studies met our inclusion criteria, which investigated 15 independent pharmacological therapies. Eight of these therapies demonstrated possible neuroprotective properties and improved functional outcomes, of which five were investigated with randomized clinical trials: statins, N-acetyl cysteine (NAC), Enzogenol, Cerebrolysin, and nitric oxide synthase inhibitor (VAS203). Three pharmacological agents did not demonstrate neuroprotective effects, and four agents had mixed results.

Conclusions

While there is currently no single pharmacological therapy that will unequivocally improve clinical outcomes after TBI, several agents have demonstrated promising clinical benefits for specific TBI patients and should be investigated further.

Keywords

Growth Hormone Traumatic Brain Injury Glibenclamide Rosuvastatin Growth Hormone Deficiency 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Notes

Compliance with Ethical Standards

Funding

Shaun Gruenbaum is an Investigative Medicine MD to PhD Program graduate student. This publication was made possible by Clinical and Translational Science Awards (CTSA) Grant number UL1 TR000142 from the National Center for Advancing Translational Science (NCATS), a component of the NIH. Its contents are solely the responsibility of the authors and do not necessarily represent the official view of the NIH.

Conflicts of interest

Shaun Gruenbaum, Alexander Zlotnik, Benjamin Gruenbaum, Denise Hersey, and Federico Bilotta declare no conflicts of interest.

Supplementary material

40263_2016_355_MOESM1_ESM.pdf (77 kb)
Supplementary material 1 (PDF 77 kb)

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Copyright information

© Springer International Publishing Switzerland 2016

Authors and Affiliations

  • Shaun E. Gruenbaum
    • 1
  • Alexander Zlotnik
    • 2
  • Benjamin F. Gruenbaum
    • 1
  • Denise Hersey
    • 3
  • Federico Bilotta
    • 4
    Email author
  1. 1.Department of AnesthesiologyYale University School of MedicineNew HavenUSA
  2. 2.Department of Anesthesiology and Critical CareBen-Gurion University of the NegevBeer-ShevaIsrael
  3. 3.Cushing/Whitney Medical LibraryYale UniversityNew HavenUSA
  4. 4.Department of Anesthesiology, Critical Care and Pain Medicine‘La Sapienza’ University of RomeRomeItaly

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