Tracheomalacia

气管软化
  • 文章类型: Case Reports
    背景:Ohtahara综合征是一种进行性发育性和癫痫性脑病,表现在婴儿早期。这种罕见疾病的特征是顽固性癫痫发作,精神运动性迟钝,预后不良。迄今为止,关于Ohtahara综合征儿童的麻醉管理的病例报道很少。然而,存在困难气道的Ohtahara综合征患者的报告有限。本报告描述了我们对患有Ohtahara综合征的儿科患者的气道发现和全身麻醉管理,该患者正在接受诊断支气管镜检查以治疗严重的吸气性喘鸣。
    方法:14个月大,9公斤,Ohtahara综合征的男性患者有一年的严重吸气喘鸣病史,并计划进行支气管镜检查并进行灌洗。在考试中,病人呼吸嘈杂,是非语言发育迟缓的,头部控制不佳,有明显的中枢张力减退。患者用氯胺酮诱导,全身麻醉用丙泊酚维持。支气管镜检查顺利完成,并诊断为喉气管软化症。患者的呼吸在整个过程中保持自发,没有发现癫痫发作。在麻醉后护理室,患者的呼吸和心血管功能稳定。
    结论:本报告记录了一名14个月大的儿童被诊断为Ohtahara综合征的严重吸气喘鸣的异常发现,以及我们在其诊断支气管镜检查期间的麻醉管理。目前,Ohtahara综合征患者存在的复杂气道病理学的文献有限,应进一步评估。这将有助于儿科麻醉师,因为这些患者可能需要仔细的术前评估,周到的气道管理,和手术替代品待命。
    BACKGROUND: Ohtahara syndrome is a progressive developmental and epileptic encephalopathy that manifests in the early infantile period. This rare condition is characterized by intractable seizures, psychomotor retardation, and poor prognosis. To date, there are a handful of case reports regarding the anesthetic management of children with Ohtahara syndrome. However, limited reports exist of patients with Ohtahara syndrome who present with difficult airways. This report describes our airway findings and general anesthetic management of a pediatric patient with Ohtahara syndrome undergoing diagnostic bronchoscopy for severe inspiratory stridor.
    METHODS: A 14-month-old, 9 kg, male patient with Ohtahara syndrome presented with a year-long history of severe inspiratory stridor and was scheduled for bronchoscopy with lavage. On exam, the patient had noisy breathing, was non-verbal with developmental delay, and had poor head control with significant central hypotonia. The patient was induced with ketamine and general anesthesia was maintained with propofol. Bronchoscopic evaluation was completed uneventfully and revealed a diagnosis of laryngotracheomalacia. The patient\'s breathing was maintained spontaneously throughout the procedure and no seizures were noted. In the post anesthesia care unit, the patient\'s respiratory and cardiovascular function were stable.
    CONCLUSIONS: This report documents the unusual finding of severe inspiratory stridor in a 14-month-old child diagnosed with Ohtahara syndrome and our anesthetic management during their diagnostic bronchoscopy. Currently, documentation of complex airway pathology present in patients with Ohtahara syndrome is limited and should be further evaluated. This will assist pediatric anesthesiologists as these patients may require careful preoperative assessment, thoughtful airway management, and surgical alternatives on standby.
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  • 文章类型: Journal Article
    背景:由聚二恶烷酮制成的可生物降解(BD)支架仅用于人体气道。这些支架结合了经典气管支架的优点,由于它们的生物相容性和在气道中的时间限制,预计副作用较少。然而,出现了新的临床后果。这里,作者分享了他们使用BD支架治疗气管适应症的经验,关注其安全性和有效性。
    方法:这是对2013年9月至2022年12月在布拉格第一医学院呼吸内科和Thomayer大学医院接受生物可降解气管支架植入的成年患者数据库的回顾性回顾。适应症包括功能显着的非恶性气管狭窄和气管软化。自膨胀,可生物降解,ELLA-CSLtd.制造的聚二恶烷酮气管支架(HradecKralove,捷克共和国)在全身麻醉下进行刚性支气管镜检查。所有患者均在该部门进行了随访,并获得了必要的护理。使用描述性统计和Fisher精确分析了主要疗效和安全性参数及其关系,威尔科克森和克鲁斯卡尔·瓦利斯测试。
    结果:47例成人患者共植入65个支架。在植入后的头两个月,当预期有足够的功能时,在完成这一时期的39例患者中,有26例(66.7%)发现支架有效.临床有效率达89.7%,由于早期再狭窄大多是轻度的,只有4例患者需要治疗。显著粘液停滞的频率,迁移和肉芽组织生长为2.6%,7.5%和23.1%,分别,在此期间。34名参与者在第一次或第二次支架插入后完成了半年的随访期,有些人在这段时间之后得到了跟进。症状控制不佳,再狭窄的发展和需要干预是这一时期的特征,因为支架退化.经历了气管腔重塑或稳定的22例患者达到了无支架状态。7名患者接受了随后的手术治疗。
    结论:BD支架是安全的,并在开始降解之前提供足够的气管支持。BD支架的使用需要密切监测患者并对可能的再狭窄进行准确治疗。
    背景:基于项目NT14146-大型气道管理中的可生物降解支架(2013-2015,MZ0/NT),于2013年5月1日在捷克共和国的研发与创新信息系统和ClinicalTrials.gov(reg。不。NCT02620319,2015年12月2日)。
    BACKGROUND: Biodegradable (BD) stents made from polydioxanone have been used only in human airways. These stents combine the advantages of classical tracheal stents, and fewer side effects are expected due to their biocompatibility and their time-limited presence in airways. However, new clinical consequences have arisen. Here, the authors share their experiences with BD stents for tracheal indications, focusing on their safety and efficacy.
    METHODS: This was a retrospective review of a collected database of adult patients who underwent implantation of biodegradable tracheal stents between September 2013 and December 2022 at the Department of Respiratory Medicine of the 1st Faculty of Medicine in Prague and Thomayer University Hospital. The indications included functionally significant nonmalignant tracheal stenosis and tracheomalacia. Self-expandable, biodegradable, polydioxanone tracheal stents manufactured by ELLA-CS Ltd. (Hradec Kralove, Czech Republic) were implanted during rigid bronchoscopy under general anaesthesia. All patients were followed up in the department and were provided with the necessary care. The main efficacy and safety parameters and relationships were analysed using descriptive statistics and Fisher´s exact, Wilcoxon and Kruskal‒Wallis tests.
    RESULTS: A total of 65 stents were implanted in 47 adult patients. During the first two months after implantation, when adequate function was expected, the stent was found to be effective in 26 out of 39 patients who completed this period (66.7%). The clinical effectiveness reached 89.7%, as early restenoses were mostly mild and necessitated treatment in only 4 patients. The frequencies of significant mucostasis, migration and granulation tissue growth were 2.6%, 7.5% and 23.1%, respectively, during this period. Thirty-four participants completed the half-year follow-up period after the first or second stent insertion, and some were followed up beyond this period. Poor control of symptoms, the development of restenosis and the need for interventions were characteristic of this period as the stents degraded. Twenty-two patients who experienced remodelling or stabilization of the tracheal lumen achieved a stent-free state. Seven patients underwent subsequent surgical treatment.
    CONCLUSIONS: BD stents are safe and provide adequate tracheal support until they begin to degrade. The use of BD stents necessitates close monitoring of patients and accurate treatment of possible restenosis.
    BACKGROUND: Based on project NT14146 - Biodegradable stents in the management of the large airways (2013-2015, MZ0/NT), registered on May 1, 2013, in the Research and Development and Innovation Information System of the Czech Republic and at ClinicalTrials.gov (reg. no. NCT02620319, December 2, 2015).
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  • 文章类型: Case Reports
    气管支气管软化(TBM)是由于气管软骨部分的弱化而发生的,导致气道功能受损并导致呼吸困难等症状,咳嗽,无法清除分泌物。闭塞性细支气管炎综合征(BOS)是接受异基因造血干细胞移植(HSCT)的患者中最常见的晚期非感染性肺部并发症。因此,同种异体HSCT后出现进行性呼吸困难和慢性咳嗽的患者,新的阻塞性肺功能测试模式,通常被诊断为移植后BOS。然而,值得注意的是,TBM在肺功能测试中也可表现为阻塞性缺陷模式.据报道,气管软化是同种异体干细胞移植的罕见并发症。我们介绍了两名在同种异体HSCT后发展为TBM的患者,最初接受了移植后BOS治疗,但症状没有改善。然而,持续气道正压通气治疗后,他们的症状消退了。
    Tracheobronchomalacia (TBM) occurs due to the weakening of cartilaginous part of the trachea, resulting in compromised airway function and leading to symptoms such as dyspnea, cough, and inability to clear secretions. Bronchiolitis obliterans syndrome (BOS) is the most prevalent late noninfectious pulmonary complication in patients who underwent allogeneic haematopoietic stem cell transplantation (HSCT). Therefore, patients experiencing progressive dyspnea and chronic cough after allogenic HSCT, with new obstructive pattern on pulmonary function test, are typically diagnosed with post-transplant BOS. However, it is important to note that TBM can also manifest as an obstructive defect pattern on pulmonary function test. Tracheomalacia has been reported as a rare complication of allogenic stem cell transplantation. We present two patients who developed TBM following allogeneic HSCT and were initially treated for post-transplant BOS but did not experience symptom improvement. However, after treatment with continuous positive airway pressure, their symptom subsided.
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  • 文章类型: Journal Article
    背景:一些研究提到了SARS-CoV-2肺炎后的实质发现,但是很少有研究提到气道的改变。这项研究的目的是估计气管软化的患病率并分析SARS-CoV-2患者队列的临床特征。
    方法:研究人群由所有SARS-CoV-2患者组成,该患者入院服务于50万居民。患者在出院后2至6个月之间就诊。在这次访问中,所有患者都接受了详尽的临床问卷并接受了临床检查,肺功能检查和胸部CT。
    结果:从2020年2月至2021年8月,将1920例患者纳入队列,在呼气HRCT成像中观察到15例(0.8%)气管软化。所有气管软化症患者在CT扫描中也出现磨玻璃影,12例患者有气道后遗症。
    结论:气管软化是SARS-CoV-2幸存者的特殊后遗症。
    BACKGROUND: Several studies mentioned parenchymal findings after SARS-CoV-2 pneumonia, but few studies have mentioned alterations in the airways. The aim of this study was to estimate the prevalence of tracheomalacia and to analyse the clinical characteristics in a cohort of patients with SARS-CoV-2.
    METHODS: The study population consisted of all patients with SARS-CoV-2 admitted a hospital serving a population of 500 000 inhabitants. Patients were visited between 2 and 6 months after hospital discharge. In this visit, all patients were subjected to an exhaustive clinical questionnaire and underwent clinical examination, pulmonary function tests and chest CT.
    RESULTS: From February 2020 to August 2021, 1920 patients were included in the cohort and tracheomalacia was observed in 15 (0.8%) on expiratory HRCT imaging. All patients with tracheomalacia also presented ground glass opacities in the CT scan and 12 patients had airway sequelae.
    CONCLUSIONS: Tracheomalacia is an exceptional sequela of SARS-CoV-2 survivors.
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  • 文章类型: Editorial
    气管内袖带压力监测是重症监护病房患者护理的重要组成部分,确保机械通气的安全性和有效性。尽管它很重要,仍然缺乏关于最佳压力目标和文档实践的标准化协议。这篇社论探讨了气管内压力监测在提高患者预后方面的重要性,强调临床实践中的挑战和潜在解决方案。
    Endotracheal cuff-pressure monitoring is a critical component of patient care in the intensive care unit, ensuring the safety and efficacy of mechanical ventilation. Despite its importance, there remains a lack of standardized protocols regarding optimal pressure targets and documentation practices. This editorial examines the significance of endotracheal intracuff-pressure monitoring in enhancing patient outcomes, highlighting the challenges and potential solutions in clinical practice.
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  • 文章类型: Journal Article
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  • 文章类型: Journal Article
    背景:观察不同时间点不同直径的自膨式金属(SEM)气道支架植入后相关并发症的发生,为临床上现有气道支架的优化设计提供理论依据。
    方法:健康新西兰大白兔胸部CT检查后建立良性气管狭窄模型。将气道狭窄超过50%的四五个模型兔分为两组。A组21只兔植入小直径SEM支架(支架直径与气道直径之比近1.0),B组24只兔植入大直径气管支架(支架直径与气道直径之比大于1.2)。第2次支架植入术后观察支架相关并发症,第四,8th,第12周通过支气管镜大体解剖,病理和IL-1RA的表达,IL-8和MMP9受累气管。
    结果:B组支架后气管软化的发生率(24/24100%)明显高于A组(1/21,4.8%)(P<0.05)。支架两端瘢痕挛缩发生率B组(11/24,45.8%)明显高于A组(2/21,9.5%)(P<0.05)。病理结果A、B均显示支气管粘膜柱状上皮开始损伤和脱落,炎症细胞浸润后第2周和第4周的支架,上皮被修复了,固有层腺体几乎消失了,胶原纤维增生明显,在第8周和第12周后形成疤痕。ELISA结果显示IL-1RA的表达,支架组比良性气管狭窄模型兔IL-8和MMP9升高。B组IL-1RA和MMP9在不同时期升高,但A组IL-1RA和MMP9的表达在早期呈先升高后降低的趋势。
    结论:金属支架可引起兔良性气管狭窄不同程度的支架相关并发症。B组支架诱导气管软化和瘢痕挛缩的发生率高于A组。IL-8和MMP9可能参与了支架植入术后并发症的发生和B组峰值向后移动。ING.
    BACKGROUND: To observe the occurrence of related complications after self-expandable metallic (SEM) airway stents implantation with different diameters at different time points, and to provide theoretical basis for the optimal chioce of existing airway stents in clinical practice.
    METHODS: Healthy New Zealand white rabbits were used to establish benign tracheal stenosis models after chest CT examination. Forty-fivemodel rabbits with more than 50% of airway stenosis were divided into two groups. Small-diameter SEM stents (The ratio of stent diameter to airway diameter is nearly 1.0) were implanted in Group A in 21 rabbits, and large-diameter tracheal stents (The ratio of stent diameter to airway diameter is more than 1.2) were implanted in Group B in 24 rabbits. Stent-related complications were observed after stent implantation in 2nd,4th,8th, and 12th week by bronchoscopygross anatomy, pathological and the expressions of IL-1RA, IL-8 and MMP9 in involved tracheal.
    RESULTS: The incidence rate of tracheomalacia of stent was significantly higher in group B (24/24 100%) than that in group A (1 /21,4.8%) (P < 0.05). The incidence rate of scar contracture at both ends of stent was significantly higher than in group B (11 / 24,45.8%) that in group A (2 /21, 9.5%) (P < 0.05). The pathological results of both A and B showed that the columnar epithelium of bronchial mucosa began to damage and detach, inflammatory cells infiltrated after 2nd and 4th week of stenting, The epithelium was repaired, the lamina propria glands almost disappeared, collagen fiber proliferation was obvious, and scars were formed after 8th and 12th week of stenting. ELISA results revealed that the expressions of IL-1RA, IL-8, and MMP9 were increased in the stent group than in model rabbit with benign tracheal stenosis. IL-1RA and MMP9 increased at different periods in group B, but the expression of IL-1RA and MMP9 showed a tread of increasing in the early stage and then decreasing in group A.
    CONCLUSIONS: Metal stents can cause different degrees of stent-related complications in rabbits with benign tracheal stenosis. The incidence of stent-induced tracheomalacia and scar contracture were higher in Group B than that in Group A. IL-1RA, IL-8 and MMP9 may be involved in the development of complications after stentimplantation and peak value of group B movered backward. ing.
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  • 文章类型: Journal Article
    唐氏综合症(DS)是与生命相容的最常见的染色体异常。反复呼吸道感染(RRIs)会严重影响DS患者的生活,导致住院率上升,对重症监护和死亡率的需求更高。通过文献综述,我们在这里总结了该类患者中RRI的主要病因,特别关注气道畸形,如气管软化,气管支气管和支气管软化,与该综合征相关的合并症,比如先天性心脏病,吞咽困难,胃食管反流,肌肉骨骼受累和肥胖,和免疫损伤,涉及先天免疫和适应性免疫。对于这些患者来说,多学科的方法是必要的,以及一些预防策略,特别是根据其国家免疫计划接种疫苗。
    Down Syndrome (DS) is the most common chromosomal abnormality compatible with life. The life of patients suffering from DS can be strongly impacted by Recurrent Respiratory tract Infections (RRIs), leading to an increased rate of hospitalisation, a higher need for intensive care and fatality. With a literature review, we summarise here the main etiological factors for RRI in this category of patients, particularly focusing on airway malformations such as tracheomalacia, tracheal bronchus and bronchomalacia, comorbidities associated with the syndrome, like congenital heart diseases, dysphagia, gastroesophageal reflux, musculoskeletal involvement and obesity, and immunologic impairments, involving both innate and adaptive immunity. For these patients, a multidisciplinary approach is imperative as well as some preventive strategies, in particular vaccinations in accordance with their national schedule for immunization.
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  • 文章类型: Case Reports
    背景:无毒结节性甲状腺肿是全球最常见的甲状腺疾病之一。甲状腺切除术治疗大型甲状腺肿术后气道阻塞的风险相对较高,气管软化是潜在的并发症之一。
    方法:一名61岁女性主诉颈部肿块45年。节点逐渐扩大,但她没有呼吸困难,声音嘶哑,或吞咽时疼痛。然后进行全甲状腺切除术。组织病理学检查显示胶体甲状腺肿。在手术过程中,气管评估显示气管软化,然后对病人进行了气管切开术。经过三个月的随访,病人不再有气管软化症,气管造口术成功关闭.
    结论:手术被认为是治疗非毒性甲状腺肿的一种可接受的方法。最常见的适应症是压迫症状,胸骨下延伸,无法通过药物控制甲状腺功能亢进,还有恶性肿瘤的嫌疑.然而,甲状腺切除术治疗大型甲状腺肿,术后呼吸道阻塞的风险相对较高。诊断气管软化可能具有挑战性,通常依靠支气管镜检查来评估气道并观察软骨和膜的塌陷。可以通过内部或外部支架或气管造口术来管理获得的气管软化。
    结论:甲状腺全切除术已被推荐为无毒和毒性多结节性甲状腺肿的合适手术。甲状腺切除术后甲状腺肿大患者可能会发生气管软化。气管造口术通过在软化区的病灶段创建通道,有效地管理气管软化,恢复气道的通畅。
    BACKGROUND: Nontoxic nodular goiter is one of the most prevalent thyroid conditions worldwide. Thyroidectomy for large goiters has a relatively high risk of postoperative airway obstruction, with tracheomalacia being one of the potential complications.
    METHODS: A 61-year-old woman complained of a lump in her neck for 45 years. The node is progressively enlarged, but she did not experience any breathing difficulty, hoarseness, or pain while swallowing. A total thyroidectomy was then performed. The histopathologic examination revealed colloid goiter. During the procedure, evaluation of the trachea revealed a tracheomalacia, so a tracheotomy was then performed on the patient. After a follow-up period of three months, the patient was no longer experiencing tracheomalacia, and the tracheostomy was successfully closed.
    CONCLUSIONS: Surgery has been considered an acceptable approach for managing non-toxic goiter. The most common indications are compressive symptoms, substernal extension, inability to control hyperthyroidism through medication, and a suspicion of malignancy. However, thyroidectomy for large goiter carries a relatively high risk of postoperative respiratory obstruction. Diagnosing tracheomalacia can be challenging and often relies on bronchoscopy to assess the airway and observe the collapse of cartilage and membranes. Acquired tracheomalacia can be managed through internal or external stenting or tracheostomy.
    CONCLUSIONS: Total thyroidectomy has been recommended as a suitable procedure for non-toxic and toxic multinodular goiter. Tracheomalacia may occur following thyroidectomy in patients with thyroid enlargement. Tracheostomy effectively manages tracheomalacia by creating a channel across the malacia\'s focal segment, restoring the airway\'s patency.
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  • 文章类型: Journal Article
    目标:在患有气管支气管软化症的儿童中,应针对最严重的病例进行手术治疗,并针对气管支气管软化的类型和位置。这项研究的目的是描述患有严重气管支气管软化症的儿童接受手术的表现和结果。
    方法:回顾性病例系列,包括2003年至2023年在三级医院接受严重气管支气管软化手术的20名儿童。数据收集了诊断时的症状年龄,相关的合并症,以前的手术,手术年龄,手术入路,随访时间,和结果。手术成功被定义为症状改善。
    结果:严重的气管支气管软化症最常见的症状是喘鸣(50%),紫癜(50%),和反复呼吸道感染(45%)。所有患者都有一种或多种潜在疾病,最常见的食管闭锁(40%)和早产(35%)。所有患者均行支气管镜检查。根据病因,患者接受了以下手术:前主动脉固定术(n=15/75%),后气管固定术(n=4/20%),和/或后降主动脉(n=4/20%)。三名患者接受了前主动脉固定术和后气管固定术。经过12个月的中位随访,16例(80%)患者呼吸道症状改善。在8例先前气管切开术的患者中,有3例(37.5%)实现了拔管。诊断时死亡咒语的存在与手术失败有关。
    结论:在80%的严重气管支气管软化症患儿中,单独或联合外科手术可改善呼吸道症状。手术的选择应个体化,并以病因为指导:前主动脉固定术用于前压迫,后气管固定术用于膜质侵入,左支气管阻塞后降主动脉固定术。
    OBJECTIVE: In children with tracheobronchomalacia, surgical management should be reserved for the most severe cases and be specific to the type and location of tracheobronchomalacia. The goal of this study is to describe the presentation and outcomes of children with severe tracheobronchomalacia undergoing surgery.
    METHODS: Retrospective case series of 20 children operated for severe tracheobronchomalacia at a tertiary hospital from 2003 to 2023. Data were collected on symptoms age at diagnosis, associated comorbidities, previous surgery, age at surgery, operative approach, time of follow-up, and outcome. Surgical success was defined as symptom improvement.
    RESULTS: The most frequent symptoms of severe tracheobronchomalacia were stridor (50 %), cyanosis (50 %), and recurrent respiratory infections (45 %). All patients had one or more underlying conditions, most commonly esophageal atresia (40 %) and prematurity (35 %). Bronchoscopy were performed in all patients. Based on etiology, patients underwent the following procedures: anterior aortopexy (n = 15/75 %), posterior tracheopexy (n = 4/20 %), and/or posterior descending aortopexy (n = 4/20 %). Three patients underwent anterior aortopexy and posterior tracheopexy procedures. After a median follow-up of 12 months, 16 patients (80 %) had improvement in respiratory symptoms. Decannulation was achieved in three (37.5 %) out of eight patients with previous tracheotomy. The presence of dying spells at diagnosis was associated with surgical failure.
    CONCLUSIONS: Isolated or combined surgical procedures improved respiratory symptoms in 80 % of children with severe tracheobronchomalacia. The choice of procedure should be individualized and guided by etiology: anterior aortopexy for anterior compression, posterior tracheopexy for membranous intrusion, and posterior descending aortopexy for left bronchus obstruction.
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