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Focal cooling of brain parenchyma in a transient large vessel occlusion model: proof-of-concept.
Caroff, Jildaz; King, Robert M; Mitchell, Jennifer E; Marosfoi, Miklos; Licwinko, Joseph R; Gray-Edwards, Heather L; Puri, Ajit S; Merrill, Thomas L; Gounis, Matthew J.
Afiliação
  • Caroff J; Interventional Neuroradiology, NEURI Center, Bicêtre Hospital, Le Kremlin- Bicêtre, France.
  • King RM; New England Center for Stroke Research, Department of Radiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Mitchell JE; Department of Biomedical Engineering, Worcester Polytechnic Institute, Worcester, MA, USA.
  • Marosfoi M; FocalCool, Mullica Hill, New Jersey, USA.
  • Licwinko JR; New England Center for Stroke Research, Department of Radiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Gray-Edwards HL; FocalCool, Mullica Hill, New Jersey, USA.
  • Puri AS; New England Center for Stroke Research, Department of Radiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Merrill TL; New England Center for Stroke Research, Department of Radiology, University of Massachusetts Medical School, Worcester, Massachusetts, USA.
  • Gounis MJ; FocalCool, Mullica Hill, New Jersey, USA.
J Neurointerv Surg ; 12(2): 209-213, 2020 Feb.
Article em En | MEDLINE | ID: mdl-31363042
ABSTRACT

INTRODUCTION:

The neuroprotective benefit of therapeutic hypothermia (TH) has been demonstrated, but systemic side effects and time required to achieve effective TH in acute ischemic stroke (AIS) care limits clinical use. We investigate rapid and localized cooling using a novel insulated catheter in an ischemia-reperfusion model.

METHODS:

In phase I (n=4), cold saline was delivered to the canine internal carotid artery via an insulated catheter. Temperature was measured using intracerebral thermocouples. The coolant flow rate was varied to meet a target temperature of 31-32°C in the hemisphere infused. In phase II (n=8), a temporary middle cerebral artery occlusion was created. Five dogs underwent localized TH at the optimal flow rate from phase I, and the remaining animals were untreated controls. Cooling was initiated 5 min before recanalization and continued for an additional 20 min following 45 min of occlusion duration. The outcome was infarct volume and neurological function.

RESULTS:

Ipsilateral tissue cooling rates were 2.2±2.5°C/min at a flow rate of 20-40 mL/min with an observed minimum of 23.8°C. Tissue cooling was localized to the ipsilateral side of the infusion with little impact on temperatures of the core or contralateral hemisphere of the brain. In phase II, animals tolerated TH with minimal systemic impact. Infarct volume in treated animals was 0.2±0.2 cm3, which was smaller than in sham animals (3.8±1.0 cm3) as well as six untreated historical control animals (4.0±2.8 cm3) (p=0.013).

CONCLUSIONS:

Proof-of-concept data show that localised brain TH can be quickly and safely achieved through a novel insulated catheter. The small infarct volumes suggest potential benefit for this approach.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isquemia Encefálica / Crioterapia / Acidente Vascular Cerebral / Infarto da Artéria Cerebral Média / Estudo de Prova de Conceito Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Isquemia Encefálica / Crioterapia / Acidente Vascular Cerebral / Infarto da Artéria Cerebral Média / Estudo de Prova de Conceito Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2020 Tipo de documento: Article