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一种用于阻塞性睡眠呼吸暂停微创外科治疗的新型植入式装置:设计与临床前安全性评估。

A novel implantable device for a minimally invasive surgical treatment of obstructive sleep apnea: design and preclinical safety assessment.

作者信息

Gillis Edward, Rampersaud Charles, Pease Emmanuelle, Buscemi Paul

机构信息

ReVENT Medical, Inc., Newark, CA, USA.

出版信息

Nat Sci Sleep. 2016 Jul 20;8:249-58. doi: 10.2147/NSS.S99353. eCollection 2016.

Abstract

BACKGROUND

In obstructive sleep apnea (OSA), occlusion of the upper airway by soft tissue causes intermittent hypoxemia and can have serious sequelae. A novel implantable medical device for OSA is composed of a linear silicone elastic element held in an extended state by a bioabsorbable external sheath. The implant is delivered to the tongue base or soft palate via a minimally invasive approach. Normal tissue healing anchors the device at the attachment points before the bioabsorbable material dissolves and the elastic element contracts to stabilize the surrounding tissue.

METHODS

Device prototypes were evaluated in multiple investigations: 1) a finite elements analysis model simulated the movement of the tongue base during sleep with and without the implant; 2) dynamic mechanical testing simulated 10 years' normal use; 3) cadaveric implantations were conducted; 4) an ovine study in which implants of varying design were evaluated via gross pathology and histological assessment; and 5) a canine study in which implants of varying design in the tongue base and soft palate were evaluated via gross pathology and histological assessment.

RESULTS

  1. The implant was capable of reducing ~95% of tongue base movement during simulated sleep; 2) implants remained intact throughout the testing with no evidence of creep fatigue or change in dynamic modulus; 3) the device could be reliably deployed in the desired placement locations and was appropriate for various anatomies; and 4) all implants were well tolerated through 1 year, with minimal inflammatory responses.

CONCLUSION

This new minimally invasive device for OSA has been demonstrated, through various bench and animal testing, to be safe, well tolerated, suitable for long-term use, and to function as intended. No adverse health consequences were observed in the animals, and histological evaluation indicated good healing. This study establishes proof of concept and supports human trials.

摘要

背景

在阻塞性睡眠呼吸暂停(OSA)中,软组织对上气道的阻塞会导致间歇性低氧血症,并可能产生严重的后遗症。一种用于OSA的新型可植入医疗器械由一个线性硅胶弹性元件组成,该元件由生物可吸收外部护套保持在伸展状态。该植入物通过微创方法输送到舌根或软腭。在生物可吸收材料溶解且弹性元件收缩以稳定周围组织之前,正常的组织愈合将装置固定在附着点处。

方法

在多项研究中对设备原型进行了评估:1)有限元分析模型模拟了有植入物和无植入物时睡眠期间舌根的运动;2)动态力学测试模拟了10年的正常使用情况;3)进行了尸体植入;4)一项绵羊研究,通过大体病理学和组织学评估对不同设计的植入物进行了评估;5)一项犬类研究,通过大体病理学和组织学评估对舌根和软腭中不同设计的植入物进行了评估。

结果

1)该植入物在模拟睡眠期间能够减少约95%的舌根运动;2)在整个测试过程中,植入物保持完好,没有蠕变疲劳或动态模量变化的迹象;3)该装置能够可靠地部署在所需的放置位置,并且适用于各种解剖结构;4)所有植入物在1年内耐受性良好,炎症反应极小。

结论

通过各种台架试验和动物试验证明,这种用于OSA的新型微创装置是安全的,耐受性良好,适合长期使用,并且能按预期发挥作用。在动物身上未观察到不良健康后果,组织学评估表明愈合良好。本研究建立了概念验证并支持人体试验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a618/4959767/6dfa6cf17b15/nss-8-249Fig1.jpg

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