CC BY-NC-ND 4.0 · J Neuroanaesth Crit Care 2016; 03(03): 233-238
DOI: 10.4103/2348-0548.190069
Original Article
Thieme Medical and Scientific Publishers Private Ltd.

Deep Brain Stimulation Utilizing Dexmedetomidine: A Clinical Report from the University of Miami Miller School of Medicine

Derek B. Covington
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Meredith M. Degnan
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Yiliam F. Rodriguez-Blanco
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Ankeet A. Choxi
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Rupa S. Prasad
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Jonathan R. Jagid
Department of Anesthesiology, University of Miami Miller School of Medicine, Miami, FL 33136
,
Thomas M. Fuhrman
1   Bay Pines Veterans Administration Medical Center, Bay Pines, FL 33744, USA
› Author Affiliations
Further Information

Publication History

Publication Date:
05 May 2018 (online)

Abstract

Background: Deep brain stimulation (DBS) is an increasingly utilized technique to treat symptoms of neurological movement disorders, most commonly, Parkinson’s Disease. Patients and surgeons alike appreciate the minimally invasive nature of this procedure, as well as its reversibility. As these surgeries are being performed more often, it is becoming increasingly important to optimize our anesthetic management during these cases. Methods: We conducted a retrospective review of the DBS procedures that have been performed at our institution utilizing monitored anaesthesia care (MAC) via dexmedetomidine infusion to report on the frequency and type of perioperative complications as well as to assess the effectiveness of this technique. Results: A total of 150 patients and 174 lead placements were included in this study. Dexmedetomidine was the sole anaesthetic used in 85.6% of cases. The remaining cases used a combination of dexmedetomidine and adjuvant agents. A total of one perioperative complication was found in our series, resulting in a total complication rate percentage per patient of 0.6%.Conclusions: We found very few perioperative complications associated with the use of dexmedetomidine during these challenging cases. With its anxiolytic, sedative, and analgesic properties coupled with preservation of respiration and a short half-life, dexmedetomidine has ideal properties for DBS procedures.

 
  • REFERENCES

  • 1 Chakrabarti R, Ghazanwy M, Tewari A. Anesthetic challenges for deep brain stimulation: A systematic approach. N Am J Med Sci 2014; 6: 359-69
  • 2 Mayberg HS, Lozano AM, Voon V, McNeely HE, Seminowicz D, Hamani C. et al. Deep brain stimulation for treatment-resistant depression. Neuron 2005; 45: 651-60
  • 3 Greenberg BD, Malone DA, Friehs GM, Rezai AR, Kubu CS, Malloy PF. et al. Three-year outcomes in deep brain stimulation for highly resistant obsessive-compulsive disorder. Neuropsychopharmacology 2006; 31: 2384-93
  • 4 Young RF, Brechner T. Electrical stimulation of the brain for relief of intractable pain due to cancer. Cancer 1986; 57: 1266-72
  • 5 Wu C, Sharan AD. Neurostimulation for the treatment of epilepsy: A review of current surgical interventions. Neuromodulation 2013; 16: 10-24
  • 6 Venkatraghavan L, Luciano M, Manninen P. Review article: Anesthetic management of patients undergoing deep brain stimulator insertion. Anesth Analg 2010; 110: 1138-45
  • 7 Deiner S, Hagen J. Parkinson's disease and deep brain stimulator placement. Anesthesiol Clin 2009; 27: 391-415
  • 8 Khatib R, Ebrahim Z, Rezai A, Cata JP, Boulis NM, John Doyle D. et al. Perioperative events during deep brain stimulation: The experience at cleveland clinic. J Neurosurg Anesthesiol 2008; 20: 36-40
  • 9 Precedex: Redefining Sedation, a Clinical Monograph. Chicago: Abbott Laboratories; 2001
  • 10 Rozet I, Muangman S, Vavilala MS, Lee LA, Souter MJ, Domino KJ. et al. Clinical experience with dexmedetomidine for implantation of deep brain stimulators in Parkinson's disease. Anesth Analg 2006; 103: 1224-8
  • 11 Sassi M, Zekaj E, Grotta A, Pollini A, Pellanda A, Borroni M. et al. Safety in the use of dexmedetomidine (precedex) for deep brain stimulation surgery: Our experience in 23 randomized patients. Neuromodulation 2013; 16: 401-6
  • 12 Bala R, Chaturvedi A, Pandia MP, Birthal PK. Anaesthetic management and perioperative complications during deep brain stimulation surgery: Our institutional experience. J Neuroanaesth Crit Care 2016; 3: 119-25
  • 13 Binder DK, Rau GM, Starr PA. Risk factors for hemorrhage during microelectrode-guided deep brain stimulator implantation for movement disorders. Neurosurgery 2005; 56: 722-32
  • 14 Gorgulho A, De Salles AA, Frighetto L, Behnke E. Incidence of hemorrhage associated with electrophysiological studies performed using macroelectrodes and microelectrodes in functional neurosurgery. J Neurosurg 2005; 102: 888-96
  • 15 Velly LJ, Rey MF, Bruder NJ, Gouvitsos FA, Witjas T, Regis JM. et al. Differential dynamic of action on cortical and subcortical structures of anesthetic agents during induction of anesthesia. Anesthesiology 2007; 107: 202-12
  • 16 Mack PF, Perrine K, Kobylarz E, Schwartz TH, Lien CA. Dexmedetomidine and neurocognitive testing in awake craniotomy. J Neurosurg Anesthesiol 2004; 16: 20-5
  • 17 Ard J, Doyle W, Bekker A. Awake craniotomy with dexmedetomidine in pediatric patients. J Neurosurg Anesthesiol 2003; 15: 263-6
  • 18 Bustillo MA, Lazar RM, Finck AD, Fitzsimmons B, Berman MF, Pile-Spellman J. et al. Dexmedetomidine may impair cognitive testing during endovascular embolization of cerebral arteriovenous malformations: A retrospective case report series. J Neurosurg Anesthesiol 2002; 14: 209-12