Site Logo

Register your email below and receive our newsletter with news.

Continuous and bimonthly publication
ISSN (on-line): 1806-3756

Licença Creative Commons
11118
Views
Back to summary
Open Access Peer-Reviewed
Cartas ao Editor

Tracheobronchomalacia in a patient on invasive mechanical ventilation: the role of electrical impedance tomography in its detection and positive end-expiratory pressure titration

Traqueobroncomalácia em paciente sob ventilação mecânica invasiva: o papel da tomografia de impedância elétrica na sua detecção e na titulação da pressão expiratória final positiva

Olívia Meira Dias1, Eduardo Leite Vieira Costa2, Daniel Antunes Silva Pereira3, Caroline Nappi Chaves3, Samia Zahi Rached3, Carmen Silvia Valente Barbas2

To the Editor:

Tracheobronchomalacia (TBM) is a disorder caused by weakness of the tracheal and bronchial walls, together with softening of the supporting cartilage, resulting in excessive expiratory collapse. (1) Although some individuals with TBM are asymptomatic, others present with symptoms such as dyspnea, hemoptysis, wheezing, and chronic cough.(1-3) Because the symptoms are nonspecific, TBM can be easily overlooked or misdiagnosed as other obstructive airway diseases, including asthma and COPD.(4)

In TBM patients with acute respiratory failure, noninvasive ventilation is a therapeutic option, because positive end-expiratory pressure (PEEP) can prevent airway collapse.(5-7) Kandaswamy et al.(8) reported that, among patients with respiratory distress who failed weaning from mechanical ventilation or required reintubation in the ICU, the prevalence of TBM, identified on CT scans of the chest acquired only days before intubation, was 1.6%. However, to our knowledge, there have been no reports of TBM being diagnosed during invasive mechanical ventilation.

Electrical impedance tomography (EIT) is a noninvasive, radiation-free monitoring tool that provides real-time imaging of ventilation at the bedside. Here, we report a case in which the combination of CT and EIT scans of the chest allowed us to make the diagnosis of TBM and to determine the best PEEP titration for preventing airway collapse in an intubated patient.

A 66-year-old female was admitted to the emergency room complaining of breathlessness. She had a history of recurrent episodes of wheezing and dry cough, both of which partially improved after treatment with aminophylline and inhaled short-acting bronchodilators. Her past medical history included orotracheal intubation, for severe bronchospasm, five years prior. She reported no fever, sputum production, or other symptoms. She stated that she had not been exposed to any inhaled allergens, had no known allergies, and had no family history of asthma. She reported that she was not a tobacco user but had long been exposed to biomass smoke from cooking.

On physical examination, she was in respiratory distress, presenting with accessory muscle use, her RR was 28 breaths/min, and her SpO2 was 96% while breathing room air. Examination of the lungs revealed prolonged expiration and diffuse wheezing.

The results of the radiographic assessment and laboratory exams were unremarkable. Partial symptomatic relief was achieved after inhalation therapy with ipratropium bromide and fenoterol, together with intravenous hydrocortisone. She was discharged home but returned to the emergency room with bronchospasm minutes later. Although she was then treated with additional doses of inhaled bronchodilators, as well as intravenous magnesium sulfate, her dyspnea worsened. A few hours later, she became comatose, requiring orotracheal intubation and admission to the ICU.

At ICU admission, the patient was deeply sedated with fentanyl and midazolam, was started on inhaled albuterol (400 g/h), received intravenous hydrocortisone (200 mg every 6 h), and was started on continuous cisatracurium infusion. Respiratory mechanics were measured during volume-controlled ventilation; the PEEP was set at 5 cmH2O; the FiO2 was set at 40%; the RR was 12 breaths/min; the flow rate was set at 60 L/min; the inspiratory pause duration on plateau pressure was 2 s; and the tidal volume (10 mL/kg) revealed low lung compliance (26 mL/cmH2O), high airway resistance (24 cmH2O/L/s), and an intrinsic PEEP of 8 cmH2O. The expiratory flow curve was indicative of airway obstruction (Figure 1). Chest X-rays performed 24 and 48 h after ICU admission showed atelectasis of the left lower lobe and of the right lower lobe, respectively, without any differences between the two time points, in terms of the ventilatory parameters.



At 48 h after ICU admission, an HRCT scan of the chest showed bilateral small pleural effusions with partial lower lobe atelectasis, and a reduction in the cross-sectional diameters of the trachea and main bronchi, mainly in the subsegmental divisions of the lower lobes, bilaterally, all of which is consistent with a diagnosis of TBM (Figure 1). On the basis of that working hypothesis, the patient was maintained on pressure-controlled ventilation and the PEEP level was changed from 5 cmH2O to 15 cmH2O, all other parameters remaining unchanged. The wheezing on auscultation suddenly disappeared, tidal volume increased from 227 mL to 398 mL, and the shape of the expiratory flow curve dramatically improved, no longer indicating flow limitation (Figure 1).

In order to choose the PEEP level that would represent the best compromise-maintaining airway patency while avoiding lung overdistension-we titrated PEEP with EIT (Table 1). After a lung recruitment maneuver, we kept a constant driving pressure of 15 cmH2O and decreased the PEEP level by 2 cmH2O every 2 min until we reached a PEEP of zero. The PEEP level that allowed minimal lung overdistension and prevented airway collapse was 12 cmH2O (Figures 1D and 1E).



The patient showed considerable improvement in her ventilation parameters. However, because of difficult weaning, she was tracheostomized at discharge.

The conventional approach to detecting TBM is by fluoroscopy or through direct observation on bronchoscopy, in which a narrowing of > 50% in the sagittal diameter of the trachea is considered diagnostic of the disorder.(4) Expiratory CT scans have been validated as a method to evaluate collapse of the airways, a 50% expiratory reduction in the cross-sectional area of the airway lumen being considered diagnostic of TBM in symptomatic individuals.(4,9-11) Although we cannot guarantee that, in the case presented here, the CT scan was obtained at full expiration, the clinical history and CT findings were highly suggestive of TBM. Our patient had also undergone bronchoscopy during a percutaneous tracheotomy performed in the ICU, with sedation and muscle paralysis. However, a detailed evaluation of the respiratory dynamics was not possible, because the patient was not breathing spontaneously.

Previous reports have addressed the importance of noninvasive ventilation to maintaining airway patency, decreasing pulmonary resistance, improving expiratory airflow obstruction, and reducing the inspiratory transpulmonary pressures required to initiate airflow, thus decreasing the work of breathing.(5-7) To our knowledge, this is the first study to address the use of EIT in the ventilatory management of TBM in patients on invasive mechanical ventilation. The respiratory flow curves seen after we increased the PEEP helped show the importance of PEEP as a pneumatic stent to open the previously collapsed airways. In addition, the use of EIT allowed the bedside diagnosis of TBM and the titration of the PEEP. It is noteworthy that EIT was extremely helpful in that it informed decisions regarding changes in the ventilatory strategy, because high PEEP levels are not desirable in patients with obstructive lung disease, who are at a high risk for the development of dynamic hyperinflation. Coincidentally, the PEEP level that was set empirically was similar to that determined to be ideal based on the EIT analysis.

The lability of airway opening and closing in TBM predisposes patients to severe bronchospasm crises that are refractory to conventional therapy. Even for pulmonologists and critical care physicians, the diagnosis of TBM is a challenge. Therefore, it should be included in the differential diagnosis of refractory bronchospasm in ICU patients presenting with predisposing factors for TBM.

References


1. Feist JH, Johnson TH, Wilson RJ. Acquired tracheomalacia: etiology and differential diagnosis. Chest. 1975;68(3):340-5. http://dx.doi.org/10.1378/chest.68.3.340

2. Nuutinen J. Acquired tracheobronchomalacia. Eur J Respir Dis. 1982;63(5):380-7.

3. Jokinen K, Palva T, Sutinen S, Nuutinen J. Acquired tracheobronchomalacia. Ann Clin Res. 1977;9(2):52-7.

4. Aquino SL, Shepard JA, Ginns LC, Moore RH, Halpern E, Grillo HC, et al. Acquired tracheomalacia: detection by expiratory CT scan. J Comp Assist Tomogr. 2001;25(3):394-9. http://dx.doi.org/10.1097/00004728-200105000-00011

5. Ferguson GT, Benoist J. Nasal continuous positive airway pressure in the treatment of tracheobronchomalacia. Am Rev Respir Dis. 1993;147(2):457-61. http://dx.doi.org/10.1164/ajrccm/147.2.457

6. Adliff M, Ngato D, Keshavjee S, Brenaman S, Granton JT. Treatment of diffuse tracheomalacia secondary to relapsing polychondritis with continuous positive airway pressure. Chest. 1997;112(6):1701-4. http://dx.doi.org/10.1378/chest.112.6.1701

7. Lin JY, Kuo PH. A 92-year old woman with expiratory wheezing refractory to inhaled bronchodilators. Chest. 2009;135(6):1680-3. http://dx.doi.org/10.1378/chest.08-2559

8. Kandaswamy C, Bird G, Gill N, Math E, Vempilly JJ. Severe tracheomalacia in the ICU: identification of diagnostic criteria and risk factor analysis from a case
9. control study. Respir Care. 2013;58(2):340-7. http://dx.doi.org/10.4187/respcare.01866

10. Carden KA, Boiselle PM, Waltz DA, Ernst A. Tracheomalacia and tracheobronchomalacia in children and adults: an in-depth review. Chest. 2005;127(3):984-1005. http://dx.doi.org/10.1378/chest.127.3.984

11. Marchiori E, Pozes AS, Junior AS, Escuissato DL, Irion KL, Araujo Neto Cd, et al. Diffuse abnormalities of the trachea: computed tomography findings. J Bras

12. Pneumol. 2008;34(1):47-54. http://dx.doi.org/10.1590/S1806-37132008000100009

13. Lee EY, Litmanovich D, Boiselle PM. Multidetector CT evaluation of tracheobronchomalacia. Radiol Clin N Am. 2009;47(2):261-9. http://dx.doi.org/10.1016/j.rcl.2008.11.007





Indexes

Development by:

© All rights reserved 2024 - Jornal Brasileiro de Pneumologia