Tracheomalacia

气管软化
  • 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: Case Reports
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  • 文章类型: Case Reports
    先天性脊柱侧凸患者的气管狭窄和气管软化是先天性发育不良引起的严重和罕见的疾病,插管后损伤,创伤,和气管肿瘤.患有气管狭窄的儿童的麻醉对于麻醉师来说是具有挑战性的。我们描述了一名8岁的女性患者在种植先天性脊柱侧弯的棒植入后出现了严重的气管狭窄和气管软化。术前综合评估肺功能和气道形态,这在临床上可以忽略,应在先天性脊柱侧凸患者中进行。
    Tracheal stenosis and tracheomalacia in patients with congenital scoliosis are serious and rare conditions caused by congenital dysplasia, postintubation injury, trauma, and tracheal tumor. Anesthesia of a child with tracheal stenosis is challenging for anesthesiologists. We describe an 8-year-old female patient developed severe tracheal stenosis and tracheomalacia after growing rod implantation for congenital scoliosis. Comprehensive assessment of preoperative pulmonary function and airway morphology, which can be neglected clinically, should be performed in congenital scoliosis patients.
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  • 文章类型: Journal Article
    有呼吸道症状的严重气管软化(TM)患者需要手术干预,包括主动脉固定术,内支架或外夹板。虽然一些患者在气管缓解后仍有呼吸道症状,没有证据支持任何一种手术疗法。在这里,我们介绍了三维(3D)打印的生物可吸收气道外夹板治疗患有严重TM的先天性心脏病(CHD)患者的临床安全性和有效性。从2019年5月至2020年9月,招募了9名重度TM患者。中位年龄为5个月(范围,3-25个月),中位体重为7.5公斤(范围,3-15公斤)。所有病人都有喘息,两名患者术前接受机器通气(MV)辅助。TM的中值长度为1.5cm(范围,1.0-3.0厘米)。所有患者均接受“C”形腔气道外夹板悬吊,在SOLIDWORKS中设计并由聚己内酯(PCL)制成。气道外夹板可以提供至少6个月的有效支持,并在2-3年内完全降解为二氧化碳和水。术后机器辅助通气的中位时间为23.7h(范围,3.3-223.4小时),ICU住院时间中位数为9天(范围,4-25天)。中位随访时间为18个月(范围,12-24个月)。呼吸道症状全部缓解,没有发生外夹板相关并发症。3D计算机断层扫描重建显示无气道狭窄。个性化3D打印生物可吸收气道外夹板不仅可以限制外部压缩,防止气道塌陷,还可以确保气道的生长潜力,这是一个保险箱,TM治疗冠心病可靠有效。
    Severe tracheomalacia (TM) patients with respiratory symptoms need surgical intervention, including aortopexy, internal stents or external splint. While some patients continue to have respiratory symptoms after tracheal relief, and there is no evidence to support any one surgery therapy over another. Here we introduce a clinical safety and efficacy of the three-dimensional (3D)-printed bioresorbable airway external splints in treating congenital heart disease (CHD) patients with severe TM. From May 2019 to September 2020, nine patients with severe TM were enrolled. The median age was 5 months (range, 3-25 months), and the median weight was 7.5 kg (range, 3-15 kg). All patients had wheezing, and two patients were assisted by machine ventilation (MV) preoperatively. The median length of TM was 1.5 cm (range, 1.0-3.0 cm). All patients underwent suspension of a \"C\"-shaped lumen airway external splint, which were designed in SOLIDWORKS and made of polycaprolactone (PCL). The airway external splint could provided effective support for at least 6 months and was completely degraded into carbon dioxide and water within 2-3 years. The median time of postoperative machine assisted ventilation was 23.7 h (range, 3.3-223.4 h), and the median time of ICU stay was 9 days (range, 4-25 days). The median follow-up time was 18 months (range, 12-24 months). Respiratory symptoms were all relieved, and no external splint-associated complications occurred. The 3D computed tomography reconstruction showed no airway stenosis. Personalized 3D-printed bioresorbable airway external splint can not only limit external compression and prevent airway collapse but also ensure the growth potential of the airway, which is a safe, reliable and effective treatment for CHD with TM.
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  • 文章类型: Journal Article
    气管上皮是肺部疾病的主要目标,因为它为环境和肺叶之间的气流提供了管道。气道上皮细胞增殖和分化的细胞和分子机制仍然知之甚少。Hedgehog(HH)信号协调肺上皮细胞和间充质细胞之间的通讯,它调节基质细胞增殖,分化和信号传导回上皮。这里,我们揭示了气道上皮细胞中HH信号的自分泌功能。配体Sonichedgehog(SHH)或其效应物平滑(SMO)的上皮细胞消耗会导致上皮细胞增殖和分化的缺陷。在培养的原代人气道上皮细胞中,HH信号传导抑制也阻碍细胞增殖和分化。上皮HH功能是介导的,至少在某种程度上,通过转录激活,HH信号传导抑制导致小鼠气管和人气道上皮细胞中细胞类型特异性转录因子基因的下调。这些结果为HH信号在气道发育过程中上皮细胞增殖和分化中的作用提供了新的见解。
    The tracheal epithelium is a primary target for pulmonary diseases as it provides a conduit for air flow between the environment and the lung lobes. The cellular and molecular mechanisms underlying airway epithelial cell proliferation and differentiation remain poorly understood. Hedgehog (HH) signaling orchestrates communication between epithelial and mesenchymal cells in the lung, where it modulates stromal cell proliferation, differentiation and signaling back to the epithelium. Here, we reveal a previously unreported autocrine function of HH signaling in airway epithelial cells. Epithelial cell depletion of the ligand sonic hedgehog (SHH) or its effector smoothened (SMO) causes defects in both epithelial cell proliferation and differentiation. In cultured primary human airway epithelial cells, HH signaling inhibition also hampers cell proliferation and differentiation. Epithelial HH function is mediated, at least in part, through transcriptional activation, as HH signaling inhibition leads to downregulation of cell type-specific transcription factor genes in both the mouse trachea and human airway epithelial cells. These results provide new insights into the role of HH signaling in epithelial cell proliferation and differentiation during airway development.
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  • 文章类型: Journal Article
    OBJECTIVE: Vascular rings are rare anomalies of congenital heart disease that cause respiratory and gastrointestinal symptoms. This study assessed the long-term outcomes of patients with vascular ring division.
    METHODS: A multi-institution retrospective review of 371 patients with vascular rings undergoing surgical division at 3 paediatric cardiac institutions between November 2007 and October 2019 was performed.
    RESULTS: The complete vascular rings consisted of a double aortic arch (24.5%), right aortic arch with left ligamentum arteriosum (36.7%) and left aortic arch, with right ligamentum arteriosum (0.5%). The incomplete vascular rings consisted of a pulmonary artery sling (22.9%), left aortic arch with aberrant right subclavian artery (15.1%) and innominate artery compression syndrome (0.3%). Respiratory symptoms included stridor (71.4%), wheezing (49.1%), coughing (31.5%), gastrointestinal symptoms included choking (12.4%), dysphagia (3.2%) and emesis (1.9%). Only one patient died after discharge, yielding a late mortality rate of 0.3% (1/360). The 10-year overall survival rate was 96.8%. Postoperative complications were reported in 51 patients, 15 of whom required reoperation. The 10-year freedom from reoperation rate was 95.9%. Follow-up was completed in 95.4% (354/371) of patients, with a mean follow-up time of 4.3 ± 2.9 years (range from 1 to 13 years). Twenty patients (5.6%) experienced residual symptoms during long-term follow-up.
    CONCLUSIONS: The outcomes of vascular ring division are excellent. A Kommerell diverticulum >1.5 times the aberrant left subclavian artery origin is an operative indication for primary resection. Tracheomalacia is a risk factor for reoperation and residual symptoms, and preoperative fibrobronchoscopy is important for evaluation.
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  • 文章类型: Journal Article
    Flexible bronchoscopy (FB), developed in the 1960s, is widely used in the clinical practice of pediatrics and has demonstrated fundamental value in clinical diagnoses and treatment. However, as an invasive procedure, the use of FB is limited due to concerns regarding the tolerance of the procedure and the possible complications in neonatal units. Thus, the present study aimed to investigate the clinical safety and efficacy of flexible bronchoscopy (FB) in a neonatal intensive care unit (NICU). Neonates (n=54) who received FB in the NICU of Shanghai Children\'s Hospital between January 2012 and December 2016 were enrolled as the experimental group and another 54 neonates who required nebulization and tracheal secretion suction treatments were the control group. Indicators including blood gas, complete blood count, C-reactive protein (CRP), X-ray, patient breathing rate, temperature and blood pressure were monitored prior to and following the procedure. No significant differences in sex, gestational age, birth weight or postnatal age were observed between the experimental group and the control group (P>0.05). Among the 54 FB patients, several cases with side effect were identified, including 18 (33.3%) with respiratory tract stenosis, nine (16.7%) with malacia and stenosis and six (11.1%) with esophagotracheal fistula. Among the 54 members of the control group, 44 neonates (81.4%) were discharged with improved condition, five (9.3%) succumbed and five patients (9.3%) abandoned the treatment and left the hospital. Bronchoalveolar lavage demonstrated consistent results with respiratory secretion culture or tracheal tube culture. In comparison between the experimental and the control groups, no significant difference in pH, partial pressure of carbon dioxide (PCO2), partial pressure of oxygen (PO2) and HCO3 - was observed, while there were no statistical differences in the values of pH, PCO2 and HCO3 - (P>0.05). However, PO2 was significantly increased, and CRP was significantly reduced, following FB procedure compared with prior to FB (P<0.05). No pneumothorax, shock, other severe complications, fever or diffused pneumonia were observed during or after FB. The data from the present study demonstrated that FB is a safe and effective strategy for the diagnosis and differentiation of neonatal respiratory diseases in NICU.
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  • 文章类型: Journal Article
    BACKGROUND: Tracheomalacia may be caused by long-standing compression of retrosternal goitre because of destruction of support of tracheal cartilages. Life-threatening airway collapses may occur after surgical removal of goitre. However, available literature on management methods of tracheomalacia is sparse. Our study highlights prolonged endotracheal intubation as a feasible treatment method.
    METHODS: This retrospective study analysed 106 thyroidectomies for retrosternal goitre performed between 1994 and 2019. We recorded each patient\'s clinical profile. Severe tracheomalacia was confirmed through the following: soft and floppy trachea on intra-operative palpation and the collapse of cross-sectional tracheal area measured in computed tomography (CT) images by >80%. We assessed the extent of airway stenosis of these cases. All severe cases were treated by prolonged endotracheal intubation.
    RESULTS: Surgical treatment was successfully performed in all 106 retrosternal goitre patients with no mortality. Seventeen severe tracheomalacia cases were confirmed. The extent of airway stenosis was assessed: the minimal tracheal diameter of compressed trachea was 0.2-0.4 [mean 0.31, standard deviation (SD) 0.06] cm, and the narrow tracheal length was 4-6.7 (mean 5.1, SD 0.6) cm. These patients underwent endotracheal intubation for 17-47 h after surgery. All patients were transferred to the general ward after extubation and successfully discharged. There were no cases of tracheal stenosis on follow-up.
    CONCLUSIONS: Tracheomalacia is a rare but serious complication of retrosternal goitre surgery. Based on our experience, prolonged endotracheal intubation is a feasible treatment for tracheomalacia after retrosternal goitre surgery.
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  • 文章类型: Journal Article
    This study is to investigate the status and clinical significance of respiratory viruses in bronchoalveolar lavage fluid (BALF) of children with PBB.
    Sixty-eight children with PBB aged from 3 months to 5 years were enrolled and retrospectively reviewed from January 2014 to December 2017. Thirty-five children with persistent pneumonia or chronic pneumonia were matched as controls. Bronchoalveolar lavage fluid samples were collected for respiratory virus detection and bacterial culture.
    The detection rate of bacteria in BALF of children with PBB was 61.8%, which was significantly higher than that of control group (20%) (P < 0.001). The detection rate of virus in BALF of children with PBB was 23.5%, including 6 (8.8%) of rhinovirus, 4 (5.9%) of parainfluenza virus type 3, 2(2.9%) of bocavirus, 2 (2.9%) of respiratory syncytial virus 1 (1.5%) of human metapneumonia virus and 1 (1.5%) of influenza virus A. 10 cases (28.6%) of virus were detected in the control group, including 3 (8.6%) respiratory syncytial virus, 3 (8.6%) rhinovirus and 2 (5.7%) bocavirus. There was no significant difference of viral detection rate between the two groups (P = 0.577).
    Respiratory viruses can be detected in BALF of children with PBB, However, there is no evidence that PBB is virus-induced.
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  • 文章类型: Case Reports
    BACKGROUND: Tracheomalacia (TM), caused by anterior mediastinal tumorectomy, most likely to deteriorate condition of patient life.
    METHODS: A 63-year-old patient felt serious dyspnea diagnosis as TM caused by the recurrent cervical schwannoma. The narrowest diameter of the TM was only 0.446 cm and the length of malacic segment was 7.47 cm. Here we designed a novel tracheal suspension technique by using autogenous rib cartilage graft to treat severe TM. The obvious effect was observed that the inner diameter increased from 0.446 cm to 1.390 cm,and the airway symptom was alleviated.
    CONCLUSIONS: The autogenous rib cartilage graft used for suspending the malacic trachea was safe and effective.
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