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Correspondence|Articles in Press

Dual-Target Deep Brain Stimulation for Obsessive-Compulsive Disorder and Tourette Syndrome

      Deep brain stimulation (DBS) has been used effectively for both treatment-resistant obsessive-compulsive disorder (OCD) and Tourette syndrome (TS) (
      • Gadot R.
      • Najera R.
      • Hirani S.
      • Anand A.
      • Storch E.
      • Goodman W.K.
      • et al.
      Efficacy of deep brain stimulation for treatment-resistant obsessive-compulsive disorder: Systematic review and meta-analysis [published online ahead of print Sep 20].
      ,
      • Martinez-Ramirez D.
      • Jimenez-Shahed J.
      • Leckman J.F.
      • Porta M.
      • Servello D.
      • Meng F.G.
      • et al.
      Efficacy and safety of deep brain stimulation in Tourette syndrome: The International Tourette Syndrome Deep Brain Stimulation Public Database and Registry.
      ). While DBS of the anterior limb of the internal capsule is Food and Drug Administration approved for use in OCD under a Humanitarian Device Exemption, DBS for TS is still considered investigational (
      • Billnitzer A.
      • Jankovic J.
      Current management of tics and Tourette syndrome: Behavioral, pharmacologic, and surgical treatments.
      ,
      • Arya S.
      • Filkowski M.M.
      • Nanda P.
      • Sheth S.A.
      Deep brain stimulation for obsessive-compulsive disorder.
      ). Several DBS targets for TS have been studied, most prominently the globus pallidus internus (GPi) and centromedian/parafascicular thalamus, though no single best target has emerged (
      • Martinez-Ramirez D.
      • Jimenez-Shahed J.
      • Leckman J.F.
      • Porta M.
      • Servello D.
      • Meng F.G.
      • et al.
      Efficacy and safety of deep brain stimulation in Tourette syndrome: The International Tourette Syndrome Deep Brain Stimulation Public Database and Registry.
      ,
      • Baldermann J.C.
      • Hennen C.
      • Schüller T.
      • Andrade P.
      • Visser-Vandewalle V.
      • Horn A.
      • et al.
      Normative functional connectivity of thalamic stimulation for reducing tic severity in Tourette syndrome.
      ). Up to two-thirds of patients with TS present with comorbid OCD (
      • Hirschtritt M.E.
      • Lee P.C.
      • Pauls D.L.
      • Dion Y.
      • Grados M.A.
      • Illmann C.
      • et al.
      Lifetime prevalence, age of risk, and genetic relationships of comorbid psychiatric disorders in Tourette syndrome.
      ). In many cases, treatment-resistant dual-diagnosis patients have been treated with one pair of leads in the hope of improving both. In an attempt to optimize outcomes for both disorders, and given the increasing utilization of multilead implantation strategies (
      • Oliveria S.F.
      • Rodriguez R.L.
      • Bowers D.
      • Kantor D.
      • Hilliard J.D.
      • Monari E.H.
      • et al.
      Safety and efficacy of dual-lead thalamic deep brain stimulation for patients with treatment-refractory multiple sclerosis tremor: A single-centre, randomised, single-blind, pilot trial.
      ,
      • Mitchell K.T.
      • Schmidt S.L.
      • Cooney J.W.
      • Grill W.M.
      • Peters J.
      • Rahimpour S.
      • et al.
      Initial clinical outcome with bilateral, dual-target deep brain stimulation trial in Parkinson disease using Summit RC + S.
      ,
      • Gadot R.
      • Shofty B.
      • Najera R.A.
      • Anand A.
      • Banks G.
      • Khan A.B.
      • et al.
      Case report: Dual target deep brain stimulation with externalized programming for post-traumatic complex movement disorder.
      ,
      • Kobayashi K.
      • Katayama Y.
      • Oshima H.
      • Watanabe M.
      • Sumi K.
      • Obuchi T.
      • et al.
      Multitarget, dual-electrode deep brain stimulation of the thalamus and subthalamic area for treatment of Holmes' tremor.
      ), we opted for a dual-target strategy in 2 patients with severe TS and OCD. We also utilized recently available sensing-capable implantable pulse generators (IPGs), which present a unique opportunity to study the disease-modifying effects of DBS on OCD- and TS-associated neurophysiology.
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