电穿孔消融支气管平滑肌细胞:一种新的非热哮喘治疗方法。

Pulmonary and critical care medicine Pub Date : 2016-12-01 Epub Date: 2016-11-06 DOI:10.15761/PCCM.1000120
Jason A Tri, Christopher V DeSimone, Craig Daniels, Roshini S Asirvatham, Susan B Mikell, Dorothy J Ladewig, Kelly Krajnick, Samuel J Asirvatham
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引用次数: 2

摘要

目的:哮喘是一种常见病,给美国医疗保健系统带来了巨大的负担,并可能与显著的患者发病率和死亡率相关。目前的医学疗法既昂贵又无疗效。射频消融术是一种永久性哮喘治疗的新方法。然而,这种射频方法是基于热的,可能导致对气道的有害影响,如狭窄或溃疡。我们描述了一种新的,改进的平滑肌消融治疗方法,使用非热直流电穿孔消融。方法:我们开发并测试了原型电穿孔消融装置,该装置可通过内窥镜和支气管镜进入气道。我们测试了这种方法的可行性,并在2只杂种狗身上进行了概念验证。为了评估平滑肌功能,我们进行了消融术前和消融术后的功能研究,以评估气道可逆性。我们也通过支气管镜直视评估支气管病变。结果:我们开发了一种新的电穿孔导管,通过内窥镜途径将能量输送到支气管平滑肌。我们在2个急性犬类研究中测试了这些导管,并成功地证明了通过新颖的原型和盐水冲洗来破坏平滑肌组织的能力,用于广泛的非热电穿孔消融。我们的功能研究证明了这种方法的有效性。结论:我们报告了一种使用新型原型和生理盐水电穿孔的非热支气管平滑肌消融新方法。这些早期发现需要在更大的慢性犬类研究中进一步评估,以评估其作为潜在治疗方法的使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Electroporation ablation of bronchial smooth muscle cells: A novel non-thermal asthma therapy.

Electroporation ablation of bronchial smooth muscle cells: A novel non-thermal asthma therapy.

Electroporation ablation of bronchial smooth muscle cells: A novel non-thermal asthma therapy.

Electroporation ablation of bronchial smooth muscle cells: A novel non-thermal asthma therapy.

Objective: Asthma is a common disease which places significant burden on the US healthcare system and which can be associated with significant patient morbidity and mortality. Current medical therapies are costly and not curative. A new approach for a more permanent asthma treatment is the use of radiofrequency ablation. However, this radiofrequency approach is thermal-based and can result in deleterious effects to the airways, such as stenosis or ulceration. We describe a novel, improved therapeutic approach for smooth muscle ablation using non-thermal DC electroporation ablation.

Methods: We developed and tested prototype electroporation ablation devices that access the airways both endoscopically and via a bronchoscope. We tested the feasibility of this approach and demonstrated proof-of-concept in 2 mongrel dogs. In order to assess for smooth muscle function, we performed functional studies pre and post ablation with methacholine challenge to assess for airway reversibility. We also evaluated bronchial lesions via direct vision with bronchoscopy.

Results: We developed novel electroporation catheters to delivery energy to the bronchial smooth muscle through an endoscopic approach. We tested these catheters in 2 acute canine studies and successfully demonstrated the ability to destroy smooth muscle tissue via novel prototypes and saline irrigation for widespread non-thermal electroporation ablation. Our functional studies demonstrate the efficacy of this approach.

Conclusion: We report a novel method for non-thermal bronchial smooth muscle ablation using novel prototypes and electroporation with normal saline. These early findings require further evaluation in larger, chronic canine studies to assess for use as a potential curative therapy.

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