Majid Adnan, Alape Daniel, Kheir Fayez, Folch Erik, Ochoa Sebastian, Folch Alejandro, Gangadharan Sidhu P
Division of Thoracic Surgery and Interventional Pulmonology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Respiration. 2016;92(6):389-396. doi: 10.1159/000450961. Epub 2016 Oct 29.
Patients with severe symptomatic expiratory central airway collapse (ECAC) undergo a stent trial to determine whether they are candidate for tracheobronchoplasty. Most stent trials were done using silicone stents. However, there was a higher number of silicone stent-related complications.
The aim of this study was to evaluate the safety and efficacy of short-term uncovered self-expanding metallic airway stents (USEMAS) in patients with ECAC.
This was a retrospective review. Baseline measurements were compared to those obtained after 7-14 days. Measurements included: Modified Medical Research Council (mMRC), Cough Quality of Life Questionnaire (CQLQ), spirometry testing, and 6-Minute Walk Test (6MWT). Stent- and procedure-related complications were reported.
33 patients (median age, 52 years) underwent the USEMAS trial. Presenting symptoms were dyspnea in 100%, intractable cough in 90.3%, recurrent infection in 42.2%, and inability to clear secretions in 21.4%. Dyspnea, cough, and secretion clearance improved in 88, 70, and 57%, respectively. Overall, there was a significant improvement in mMRC (p < 0.001), CQLQ (p = 0.015), and 6MWT (p = 0.015). There was 1 airway infection, 1 stent migration, and 1 pneumothorax. The median duration of USEMAS was 7 days. All stents were removed without any complications. At the time of stent removal, no granulation tissue was observed in 30.9%, and mild granulation tissue was observed in 69.1%.
The short-term USEMAS trial improves respiratory symptoms, quality of life, and exercise capacity with few complications in patients with severe symptomatic ECAC when performed by a multidisciplinary airway team in highly specialized centers with experience in the evaluation and treatment of this patient population.
患有严重症状性呼气性中央气道塌陷(ECAC)的患者会接受支架试验,以确定他们是否适合进行气管支气管成形术。大多数支架试验使用的是硅酮支架。然而,与硅酮支架相关的并发症数量较多。
本研究的目的是评估短期裸金属自膨式气道支架(USEMAS)在ECAC患者中的安全性和有效性。
这是一项回顾性研究。将基线测量结果与7 - 14天后获得的测量结果进行比较。测量指标包括:改良医学研究委员会(mMRC)、咳嗽生活质量问卷(CQLQ)、肺功能测试和6分钟步行试验(6MWT)。报告了与支架和手术相关的并发症。
33例患者(中位年龄52岁)接受了USEMAS试验。主要症状为呼吸困难(100%)、顽固性咳嗽(90.3%)、反复感染(42.2%)和无法清除分泌物(21.4%)。呼吸困难、咳嗽和分泌物清除情况分别有88%、70%和57%得到改善。总体而言,mMRC(p < 0.001)、CQLQ(p = 0.015)和6MWT(p = 0.015)均有显著改善。发生1例气道感染、1例支架移位和1例气胸。USEMAS的中位使用时间为7天。所有支架均顺利取出,无任何并发症。在取出支架时,30.9%未观察到肉芽组织,69.1%观察到轻度肉芽组织。
由多学科气道团队在对该患者群体进行评估和治疗方面经验丰富的高度专业化中心进行短期USEMAS试验,可改善严重症状性ECAC患者的呼吸症状、生活质量和运动能力,且并发症较少。