新型DYNAtraq装置稳定气管切开术导管概念的临床证明。

IF 1.3 Q4 ENGINEERING, BIOMEDICAL
Medical Devices-Evidence and Research Pub Date : 2022-07-13 eCollection Date: 2022-01-01 DOI:10.2147/MDER.S366829
Mauricio Orozco-Levi, Carlos Reyes, Neikel Quintero, Diana Tiga-Loza, Mabel Reyes, Sandra Sanabria, Camilo Pizarro, Juan De Hoyos, Norma Serrano, Victor Castillo, Alba Ramírez-Sarmiento
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引用次数: 0

摘要

简介:气管切开术是重症监护病房(ICU)最常见的手术策略之一,可为多种适应症提供相关的临床益处。然而,根据不同的系列,与使用相关的并发症从5%到40%不等。如果固定策略和气管造口管相对于气管轴的对齐得到改善,这些并发症的风险可以降低。目的:建立一种用于气管造口插管固定和对准的呼吸医学技术创新功能装置(简称DYNAtraq),并在机械通气患者中进行初步研究,评估其可行性和安全性。方法:研究分四个阶段进行:(1)设备的设计工程和功能原型;(2)细胞毒性和对牵引力和推力的耐受性研究;(3)气管造口和机械通气患者使用的可行性和安全性的初步研究;(4)卫生工作者满意度研究。结果:创新的DYNAtraq装置的设计,一方面包括一个连接器,在套管和通气管之间插入很少的额外死区,另一方面,一个带有两个支撑物的轴,用于粘附在胸部皮肤上,具有非常高的耐受性(几公斤)拉和推。在患者中,该装置矫正了气管造口管在侧侧角(p < 0.001)和头尾角(p < 0.001)的错位。其效果在整个随访期间保持不变(p < 0.001)。使用DYNAtraq未引起严重不良事件,对患者并发症的保护作用为70% (RR = 0.3, p < 0.001)。结论:DYNAtraq是一种新型的呼吸内科设备,可用于机械通气患者气管造口管的稳定、对准和固定。它的使用为传统形式的支撑提供了额外的好处,因为它纠正了错位,增加了对习惯性或强迫运动的容忍度。DYNAtraq是一种安全的元素,可以减少气管造口管的并发症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Clinical Proof of Concept for Stabilization of Tracheostomy Tubes Using Novel DYNAtraq Device.

Clinical Proof of Concept for Stabilization of Tracheostomy Tubes Using Novel DYNAtraq Device.

Clinical Proof of Concept for Stabilization of Tracheostomy Tubes Using Novel DYNAtraq Device.

Clinical Proof of Concept for Stabilization of Tracheostomy Tubes Using Novel DYNAtraq Device.

Introduction: Tracheostomy is one of the most common surgical strategies in intensive care units (ICU) and provides relevant clinical benefit for multiple indications. However, the complications associated with its use range from 5 to 40% according to different series. The risk of these complications could be reduced if fixation strategies and alignment of the tracheostomy tube with respect to the tracheal axis are improved.

Aim: To build a functional device of technological innovation in respiratory medicine for the fixation and alignment of tracheostomy cannula (acronym DYNAtraq) and to evaluate its feasibility and safety in a pilot study in mechanically ventilated patients.

Methods: Study carried out in four phases: (1) design engineering and functional prototyping of the device; (2) study of cytotoxicity and tolerance to the force of traction and push; (3) pilot study of feasibility and safety of its use in tracheostomized and mechanically ventilated patients; and (4) health workers satisfaction study.

Results: The design of the innovative DYNAtraq device included, on the one hand, a connector with very little additional dead space to be inserted between the cannula and the ventilation tubes, and, on the other hand, a shaft with two supports for adhesion to the skin of the thorax with very high tolerance (several kilograms) to pull and push. In patients, the device corrected the malpositioned tracheostomy tubes for the latero-lateral (p < 0.001) and cephalo-caudal angles (p < 0.001). Its effect was maintained throughout the follow-up time (p < 0.001). The use of DYNAtraq did not induce serious adverse events and showed a 70% protective effect for complications (RR = 0.3, p < 0.001) in patients.

Conclusion: DYNAtraq is a new device for respiratory medicine that allows the stabilization, alignment and fixation of tracheostomy tubes in mechanically ventilated patients. Its use provides additional benefits to traditional forms of support as it corrects misalignment and increases tolerance to habitual or forced movements. DYNAtraq is a safe element and can reduce the complications of tracheostomy tubes.

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来源期刊
Medical Devices-Evidence and Research
Medical Devices-Evidence and Research ENGINEERING, BIOMEDICAL-
CiteScore
2.80
自引率
0.00%
发文量
41
审稿时长
16 weeks
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