Evidence-based pharmacotherapy for cerebral vasospasm

Neurol Res. 2009 Jul;31(6):615-20. doi: 10.1179/174313209X382377. Epub 2008 Dec 23.

Abstract

Introduction: The vast amount of literature on the pharmaceutical treatment of cerebral vasospasm after aneurysmal subarachnoid hemorrhage remains daunting. Optimal treatment regimens for patients can be obscured by studies not statistically powered to draw evidenced-based conclusions.

Methods: In this chapter, we reviewed the English literature using the National Library of Medicine for studies regarding pharmacotherapies for the treatment of cerebral vasospasm. These studies were then categorized according to the US Preventative Services Task Force ranking system for evidence based medicine and reviewed each pharmacotherapy for its efficacy in the treatment of cerebral vasospasm.

Results: Nimodipine (Nimotop), HMG Co-A reductase inhibitor (statins) and enoxaparin (Lovenox) were the only drugs with level-1 evidence available for the treatment of vasospasm from aneurysmal subarachnoid hemorrhage as defined by the US Preventative Services Task Force.

Conclusion: As the understanding of the pathophysiological mechanisms of vasospasm after aneurysmal subarachnoid hemorrhage evolves in the basic science laboratory, novel medications are being trialed in humans. However, significantly more work must be carried out in this area before we have an effective medical treatment that can prevent or reverse the devastating events of cerebral vasospasm.

Publication types

  • Review

MeSH terms

  • Animals
  • Cardiovascular Agents / therapeutic use*
  • Enoxaparin / therapeutic use
  • Evidence-Based Medicine*
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use
  • Nimodipine / therapeutic use
  • Subarachnoid Hemorrhage / complications
  • Subarachnoid Hemorrhage / drug therapy*
  • Vasospasm, Intracranial / complications
  • Vasospasm, Intracranial / drug therapy*
  • Vasospasm, Intracranial / prevention & control*

Substances

  • Cardiovascular Agents
  • Enoxaparin
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Nimodipine