Fast awakening from minimally conscious state with apomorphine

Brain Inj. 2009 Feb;23(2):172-7. doi: 10.1080/02699050802649662.

Abstract

Background: Traumatic brain injury (TBI) can induce long-term severe disorders of consciousness. Evidence suggests an underlying dopaminergic deficit. Dopamine agonists may therefore play an important role in recovery of consciousness.

Objective: To explore the response to continuous subcutaneous administration of apomorphine in a patient who had remained in minimally conscious state for 104 days and to evaluate the anatomical substrate of the effect.

Design: A prospective, open-label, daily treatment, dose-escalation single case clinical study, with retrospective diffusion tensor image (DTI) evaluation.

Results: On the fist day of treatment, the patient was able to move his limbs on command and answer yes/no questions which had not been the case prior to apomorphine administration. Subsequently there was a full recovery of consciousness and substantial functional recovery that was sustained even after apomorphine discontinuation. At the highest dose, mild dyskinesias were observed. These resolved with a lowering of the dose. DTI demonstrated a decrease of thalamocortical and corticothalamic projections in this MCS patient compared to normal volunteers.

Conclusion: Although this is an open-label single-patient case report, the data are consistent with the theory that a dopaminergic deficit underlies MCS and that it may be overcome with apomorphine administration.

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Activities of Daily Living
  • Adult
  • Apomorphine / therapeutic use*
  • Brain Injuries / drug therapy*
  • Brain Injuries / physiopathology
  • Dopamine Agonists / therapeutic use*
  • Humans
  • Male
  • Persistent Vegetative State / drug therapy*
  • Persistent Vegetative State / physiopathology
  • Recovery of Function / drug effects*
  • Recovery of Function / physiology
  • Treatment Outcome

Substances

  • Dopamine Agonists
  • Apomorphine