Skip to main content
Advertisement
Browse Subject Areas
?

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Tracheostomy in COVID-19 acute respiratory distress syndrome patients and follow-up: A parisian bicentric retrospective cohort

  • Diane Evrard ,

    Roles Conceptualization, Investigation, Methodology, Writing – original draft, Writing – review & editing

    evrard.diane@gmail.com

    Affiliation Department of Otorhinolaryngology, Bichat Hospital, Paris, France

  • Igor Jurcisin,

    Roles Data curation, Investigation

    Affiliation Department of Anesthesiology and Critical Care, Beaujon hospital, DMU Parabol, AP-HP.Nord, Paris, France

  • Maksud Assadi,

    Roles Data curation, Investigation

    Affiliation Department of Anesthesia and Surgical Intensive Care Unit, Bichat Hospital, Université de Paris, UFR Denis Diderot, INSERM UMR 1152, ANR10-LABX-17, Paris, France

  • Juliette Patrier,

    Roles Data curation, Investigation

    Affiliation Medical Intensive Care Unit, Bichat Hospital, Paris, France

  • Victor Tafani,

    Roles Conceptualization, Data curation, Investigation, Methodology

    Affiliation Department of Otorhinolaryngology, Bichat Hospital, Paris, France

  • Nicolas Ullmann,

    Roles Data curation, Investigation

    Affiliation Department of Oral and Maxillofacial surgery, Beaujon Hospital, Paris, France

  • Jean-François Timsit,

    Roles Validation

    Affiliation Medical Intensive Care Unit, Bichat Hospital, Paris, France

  • Philippe Montravers,

    Roles Supervision, Validation

    Affiliation Department of Anesthesia and Surgical Intensive Care Unit, Bichat Hospital, Université de Paris, UFR Denis Diderot, INSERM UMR 1152, ANR10-LABX-17, Paris, France

  • Béatrix Barry,

    Roles Supervision, Validation

    Affiliation Department of Otorhinolaryngology, Bichat Hospital, Paris, France

  • Emmanuel Weiss,

    Roles Supervision, Validation

    Affiliations Department of Anesthesiology and Critical Care, Beaujon hospital, DMU Parabol, AP-HP.Nord, Paris, France, Inserm UMR-S1149, Inserm et Université de Paris, Paris, France

  • Sacha Rozencwajg

    Roles Data curation, Investigation, Methodology, Writing – original draft

    Affiliation Department of Anesthesia and Surgical Intensive Care Unit, Bichat Hospital, Université de Paris, UFR Denis Diderot, INSERM UMR 1152, ANR10-LABX-17, Paris, France

Abstract

Background

Tracheostomy has been proposed as an option to help organize the healthcare system to face the unprecedented number of patients hospitalized for a COVID-19-related acute respiratory distress syndrome (ARDS) in intensive care units (ICU). It is, however, considered a particularly high-risk procedure for contamination. This paper aims to provide our experience in performing tracheostomies on COVID-19 critically ill patients during the pandemic and its long-term local complications.

Methods

We performed a retrospective analysis of prospectively collected data of patients tracheostomized for a COVID-19-related ARDS in two university hospitals in the Paris region between January 27th (date of first COVID-19 admission) and May 18th, 2020 (date of last tracheostomy performed). We focused on tracheostomy technique (percutaneous versus surgical), timing (early versus late) and late complications.

Results

Forty-eight tracheostomies were performed with an equal division between surgical and percutaneous techniques. There was no difference in patients’ characteristics between surgical and percutaneous groups. Tracheostomy was performed after a median of 17 [1222] days of mechanical ventilation (MV), with 10 patients in the “early” group (≤ day 10) and 38 patients in the “late” group (> day 10). Survivors required MV for a median of 32 [22–41] days and were ultimately decannulated with a median of 21 [1534] days spent on cannula. Patients in the early group had shorter ICU and hospital stays (respectively 15 [1219] versus 35 [25–47] days; p = 0.002, and 21 [1628] versus 54 [35–72] days; p = 0.002) and spent less time on MV (respectively 17 [1420] and 35 [27–43] days; p<0.001). Interestingly, patients in the percutaneous group had shorter hospital and rehabilitation center stays (respectively 44 [34–81] versus 92 [61–118] days; p = 0.012, and 24 [1138] versus 45 [22–71] days; p = 0.045). Of the 30 (67%) patients examined by a head and neck surgeon, 17 (57%) had complications with unilateral laryngeal palsy (n = 5) being the most prevalent.

Conclusions

Tracheostomy seems to be a safe procedure that could help ICU organization by delegating work to a separate team and favoring patient turnover by allowing faster transfer to step-down units. Following guidelines alone was found sufficient to prevent the risk of aerosolization and contamination of healthcare professionals.

Introduction

The SARS-CoV-2 pandemic created new challenges for healthcare professionals all over the globe. In particular, intensive care units (ICU) have been overwhelmed with patients suffering from acute respiratory distress syndrome (ARDS), the most severe form of respiratory failure. The understanding of coronavirus infectious disease 19 (COVID-19) related ARDS pathophysiology has led to personalized care for these patients [1].

Among these critically ill patients, some will experience prolonged mechanical ventilation (MV) or difficult weaning. Tracheostomy is often proposed as a weaning strategy for these patients due to its proven benefits: less need for deep sedation, shorter weaning time, and shorter ICU and hospital stay [2]. In the context of the COVID-19 pandemic, tracheostomy (especially early tracheostomy) has also been seen as a good option to optimize the organization of the healthcare system [3] in a context of limited availability of ICU beds and sedative drugs [4]. Nevertheless, tracheostomy is considered a particularly high-risk procedure for the healthcare professionals involved due to droplets and spillage of blood and bronchial secretions. Indeed, the World Health Organization reported an increased risk of contamination for healthcare workers performing tracheostomies [57]. Thus, benefits and harms of tracheostomy during the COVID-19 pandemic need to be evaluated.

This paper provides our experience in performing tracheostomies for COVID-19-related ARDS patients during the pandemic. We analyzed tracheostomy techniques, early outcomes and airway complications as well as the serology of staff involved.

Methods

Study design

The study was approved by Paris-North Ethically Committee and the French Anesthesiology and Critical Care Medicine Society Ethical Committee, and informed consent was waived as part of a public health outbreak investigation. We performed a retrospective analysis of prospectively collected data from all consecutive patients who underwent a tracheostomy for a COVID-19 respiratory failure at Bichat and Beaujon University Hospitals in the Paris region (France) during the “first wave” between January 27th (date of first COVID-19 admission) and May 18th, 2020 (last tracheostomy performed). The study was approved by the local ethical committee and informed consent was waived as part of a public health outbreak investigation.

Population

Patient management in ICU.

Patient management was discussed daily within the ICU team. It followed current best practice and local guidelines that included regular assessment of sedation, MV parameters and ventilator-associated pneumonia criteria according to guidelines in place [810]. COVID-19 specific treatments were only given as part of ongoing concomitant clinical trials.

Tracheostomy decision and procedure.

The decision to perform a tracheostomy was taken by a multidisciplinary team and general indications were prolonged MV and difficult weaning [11]. Also, as the pandemic progressed, an increased turnover of patients in ICU was needed to ensure that new patients could be admitted. This objective could only be met by transferring patients recovering from ARDS to “step-down units” (i.e., units which can support tracheostomized patients without any other organ dysfunction). Thus, some tracheostomies were performed based on this particular indication.

As recommended [1215], surgical tracheostomies (ST) were performed by two senior head and neck surgeons, one intensivist and/or anesthesiologist, two operating theater nurses and one ICU nurse. Percutaneous tracheostomies (PT) were performed by two intensivists and/or anesthesiologists.

To reduce the risk of exposure to the virus, the following rules were applied [1215]: clamping endotracheal tube (ETT) when the trachea is open and fast insertion of cannula and balloon inflation.

For both, protective apparel included a waterproof cap, goggles with an anti-spitting splash screen, a filtering facepiece particles 2 (FFP2) mask, a disposable waterproof surgical apron, two pairs of surgical gloves, and plastic shoe covers. For all procedures, a portion of the tracheal ring in the shape of a square was excised.

As defined by most studies [16, 17], we considered tracheostomies “early” if they were performed before day 10 from the intubation and “late” otherwise.

Outcomes

Patients and procedure.

Patient data included demographics, date of first COVID-19 symptoms and polymerase chain reaction (PCR) results, level of respiratory support (oxygen therapy, MV support), ICU and hospital outcomes (length of MV, length of stay at hospital, vital status). Patients were also evaluated six months after hospital discharge to evaluate MV and tracheostomy complications as part of a routine post-ICU consultation.

Procedure data included timing of tracheostomy, length of procedure, and complications.

Healthcare professionals’ SARS-CoV-2 status

Healthcare professionals had a PCR nasal swab performed if considered contact cases on clinical suspicion of contamination. Also, as part of an ongoing study looking at healthcare professionals’ seroconversion status (SEROCOV NCT04304690), a SARS-CoV-2 serology was performed between two and four weeks after their last tracheostomy.

Statistical analysis

Data are expressed in median [interquartile range] or percentages as appropriate. Comparison analyses were performed using a Chi-squared test. A p-value below .05 was considered statistically significant. Statistics were performed using Prism 8.0 (GraphPad, La Jolla, USA).

Results

During the study period, among 1733 patients hospitalized for COVID-19 at Bichat and Beaujon University Hospitals, 300 were hospitalized in ICU, all requiring invasive MV. Forty-eight tracheostomies were performed representing 16% of mechanically ventilated patients with an equal division between surgical and percutaneous techniques. Patients’ characteristics are summarized in Table 1. Ten tracheostomies were considered early and 38 were considered late (Fig 1).

thumbnail
Fig 1. Flow chart.

Abbreviations: COVID-19 = coronavirus infectious disease 19; ICU = intensive care unit.

https://doi.org/10.1371/journal.pone.0261024.g001

thumbnail
Table 1. Patients characteristics during intensive care unit hospitalization with early and late tracheostomy.

https://doi.org/10.1371/journal.pone.0261024.t001

Regarding surgical tracheostomies, 18 (75%) were performed in negative-pressure ICU rooms and 6 (25%) in the operating theater.

Tracheostomy procedure and complications

Tracheostomy was performed after a median of 17 [1222] days of MV. The mean duration for the ST procedure was 21 [1035] minutes. No data was available concerning the duration for the percutaneous tracheostomy (PT) procedure.

Three complications were reported during PT due to technical difficulties, all leading to severe hypoxemia with 2 conversions to a surgical technique. One patient presented a cardiac arrest (no flow null, low flow of 2 minutes) due to hypoxemia, with no neurological consequences. These two patients were included in the ST group.

Patient outcomes

Patient outcomes are summarized in Table 2 and Fig 2. At 6 months, overall survival was 85%. Five patients died in ICU (1 septic shock due to abdominal abscess, 4 withdrawal of care) and 2 later during hospitalization (1 patient died of a septic shock due to a ventilator-associated pneumonia, the other one after withdrawal of care). The median length of stay in ICU and in hospital for survivors was 31 [18–46] days and 48 [24–61] days respectively. Survivors required MV for 32 [25–41] days and were spontaneously breathing on cannulation for 7 [214] days. All survivors were ultimately decannulated with a median of 21 [1534] days spent on cannula.

thumbnail
Fig 2. Timeline of surviving patients tracheostomized after COVID-19 ARDS.

Abbreviations: ARDS = acute respiratory distress syndrome; COVID-19 = coronavirus infectious disease 19; ICU = intensive care unit; MV = mechanical ventilation.

https://doi.org/10.1371/journal.pone.0261024.g002

thumbnail
Table 2. Patients outcomes after intensive care unit hospitalization with early and late tracheostomy.

https://doi.org/10.1371/journal.pone.0261024.t002

Healthcare professionals’ SARS-CoV-2 status

The eight implicated surgeons remained healthy after performing all ST. Their serology blood tests for SARS-CoV-2 tested 3 weeks after the last tracheostomy were all negative. No intensivist and/or anesthesiologist had serology blood conversion due to professional exposure.

Comparison between early and late tracheostomies

Patients in the two subgroups were similar except for the time from hospitalization to ICU admission (respectively 3 [25] versus 1 [0–3] days for the early and late group; p = 0.035), and the need for prone positioning before tracheostomy (respectively 30% versus 78%; p<0.001). Patients in the early group had shorter ICU and hospital stay (respectively 15 [1219] and 35 [25–47] days; p = 0.002 and 21 [1628] versus 54 [35–72] days; p = 0.002) and spent less time on MV (respectively 17 [1420] and 35 [27–43] days; p<0.001) but statistically similar time on cannula (respectively 14 [1118] and 23 [1535] days; p = 0.056) (Table 2).

Comparison between surgical and percutaneous techniques

Patients in the two subgroups were similar except for BMI>30 kg/m2 (respectively 15 (63%) for surgical and 6 (25%) for percutaneous tracheostomies; p = 0.02). Patients in the percutaneous group had shorter hospital and rehabilitation center stay (respectively 44 [34–81] versus 92 [61–118] days; p = 0.012 and 24 [1138] versus 45 [22–71] days; p = 0.045) (S1 Table).

Long-term head and neck complications

Thirty patients (63%) were examined by a head and neck senior consultant with a median of 121 [79–147] days after being discharged from ICU. Of the 30 patients examined, 17 (57%) had complications due to prolonged intubation. Unilateral laryngeal palsy was found in 5 (17%) patients. The other complications were dysphonia (30%), laryngeal edema (13%), dysphagia (20%), tracheal stenosis (6.7%) and laryngeal sensitivity dysfunction (10%). No significant difference for long-term head and neck complications was found either between early and late tracheostomies or between surgical and percutaneous ones. A vocal fold fat injection was performed 4 months after decannulation for one patient with symptomatic unilateral laryngeal palsy. The mean follow-up of these 30 patients was 277 [42–532] days and no further complication was noted.

Discussion

How to perform and manage tracheostomy in coronavirus disease (COVID)-19 patients is interesting in terms of procedure, ICU organization and caregivers’ protection [13]. In our study, tracheostomy was performed in 16% of our patients. This rate is almost twice higher than in French COVID-ICU study which reported a rate of 9% [18], which might be explained by the high severity of our population. We report 3 (6.3%) complications directly linked to the procedure. The rate of per-procedure complications varied tremendously in published studies ranging from 10.1% [19] to 100% [20]. In a recent meta-analysis [21], Benito et al. analyzed 18 studies reporting tracheostomy in COVID-19 patients. Their report showed a large disparity in patient outcomes: weaning from ventilator ranged between 23.3% [22] and 89.3% [23], and successful decannulation between 3.1% [24] and 96.6% [3].

Our study is the first to report long-term complications with a standardized exam by a head and neck senior consultant. We reported a 57% complication rate due to prolonged intubation and/or tracheostomy with no difference depending on timing nor technique used. This study highlights the importance of a head and neck monitoring for these patients. Piazza et al. underlined the increase of long-term airways complications due to intubations and tracheostomies for COVID-19 patients [25] and asks for a real “call to action”. These complications require specific expertise, must be precociously detected and therefore clinicians must be well aware of those. Our cohort analyzed for the first time these complications with more a year of hindsight.

With the appropriate protection [26], tracheostomy was a safe procedure for the healthcare professionals involved. Similar to previously published studies [3], no contamination was observed after tracheostomy was performed.

Although PT was recommended in ICU by the French National ICU Societies (Société de Réanimation de Langue Française—SRLF and Société Française d’Anesthésie Réanimation—SFAR) experts [11], ST were realized for 50% of patients in our cohort. Particular anatomy of these patients, often with obesity and availability of surgeons could explain this choice.

Timing of tracheostomy in COVID-19 patients remains subject to vivid debate as studies report heterogeneous results [15, 2730]. In our study with two comparable groups, no difference was observed between the early and late tracheostomies. The debate will most likely be difficult to settle due to the retrospective design of studies performed during the pandemic.

Classic benefits of tracheostomy include reduction of sedation doses, easier mobilization and suction, reduced airway dead space as well as feeding; harms are represented mostly by early and late complications. In the COVID-19 pandemic, potential benefits also included early transfer to step-down units for patients less severe and harms included aerosolization and contamination of healthcare professionals. Due to its retrospective design, our study could shed light on all questions. Nevertheless, several interesting results are worth mentioning.

First, tracheostomy could be performed in these severe critically ill patients without an increased risk of complications. Indeed, the literature reports a global risk of 4.3% for all tracheostomies performed [31].

Second, despite the fact that expert opinions differ on the recommended technique [32], we found no difference between a percutaneous and a surgical approach. For patients with a difficult anatomy or high BMI, we preferred performing a surgical procedure by two senior surgeons in the operating room.

Third, we found that the procedure was safe for healthcare professionals as long as guidelines were respected. Some teams have proposed the use of supplementary protection gear (such as surgical field isolation drape, negative flow hood, snorkeling masks with specific adaptors) [3335] that may prevent some teams from using the technique. In our study, it seems that standard protective apparel and appropriate rules described by scientific societies are sufficient [14, 15, 36]. Indeed, no surgeons presented any symptoms or a change in SARS-CoV-2 serology 2 weeks after the last procedure, as found in other studies [14, 28, 37].

Fourth, patients who had an early tracheostomy in order to be transferred to step-down units–to help turnover in the context of shortage of ICU beds–showed similar outcomes compared to patients receiving a tracheostomy at a later stage. We even report here that patients had a significantly shorter time in ICU, in hospital and on mechanical ventilation. This is most likely due to the selection of our population who would benefit from an early tracheostomy. Indeed, “late tracheostomies” were performed after a risk-benefits balance had been clearly weighed and patient’s risk was considered minimal. On the other side, “early tracheostomies” were performed on patient that were less severe with only 30% proned, none on ECMO, and only one patient had renal replacement therapy. Nevertheless, this is an interesting finding as some authors caution against performing tracheostomy before day 10 of MV [17, 38]. We suggest that timing of tracheostomy should be assessed on a case-by-case basis rather than follow a strict rule. This would allow for more severe patients–who might require additional therapies such as renal replacement therapy or extracorporeal membrane oxygenation (ECMO)–to be admitted to ICU.

Fifth, as ICU staff may be overwhelmed by the amount of work, tracheostomies could be delegated to a separate team. In our case, head and neck surgeons not used to regularly perform percutaneous tracheostomies were trained over a week.

Strengths and limitations of our study

Our study is the first to report prolonged long-term complications after tracheostomy performed in COVID-19 patients. In a follow-up consultation, local examination highlighted that more than half of the patients presented at least one pharyngo-laryngeal complication. The prevalence of complications is comparable with those reported for non-COVID-19 patients requiring prolonged MV or tracheostomy [39].

Our study suffers some limitations. First, due to its retrospective design and the relatively low number of patients, no causality can be demonstrated. Thus, our conclusions are only associative and need to be taken with precautions. In particular, while duration of MV or length of stay in ICU or hospital was significantly shorter in the early group, this is most likely due to the lower severity of these patients as shown by the lower need for prone positioning. Second, our study took place in two tertiary hospitals, Bichat being an expert center for epidemiological and biological risk, thus generalizability to other settings and hospitals may be limited. Nevertheless, similar results, especially regarding contamination of healthcare professionals, were found in other studies.

Tracheostomy seems to be a safe procedure that could help ICU organization by delegating work to a separate team and favoring patient turnover by allowing faster transfer to step-down units. Following guidelines alone was sufficient to prevent the risk of aerosolization and contamination of healthcare professionals.

Supporting information

S1 Table. Patients characteristics during intensive care unit hospitalization and outcomes after intensive care unit hospitalization with surgical and percutaneous tracheostomy.

Abbreviations: BMI = body mass index; COVID-19 = coronavirus infectious disease-19; ECMO = extracorporeal membrane oxygenation; ICU = intensive care unit; IQR = interquartile range; MV = mechanical ventilation; PCR = polymerase chain reaction; PEEP = positive end-expiratory pressure SAPS 2 = severity acute physiologic score 2.

https://doi.org/10.1371/journal.pone.0261024.s001

(DOCX)

Acknowledgments

We would like to thank Marie Lyager for her English proofreading.

References

  1. 1. Gattinoni L, Chiumello D, Caironi P, Busana M, Romitti F, Brazzi L, et al. COVID-19 pneumonia: different respiratory treatments for different phenotypes? Intensive Care Med. 2020 Apr 14;1–4. pmid:32291463
  2. 2. Durbin CG. Tracheostomy: Why, When, and How? Respir Care. 2010 Aug 1;55(8):1056–68. pmid:20667153
  3. 3. Williamson A, Roberts MT, Phillips J, Saha R. Early percutaneous tracheostomy for patients with COVID‐19. Anaesthesia. 2020 Jul 11. pmid:32652565
  4. 4. Constantin J-M, Maury E, Aubrun F. Rapport SFAR: Preconisations-pour-lutilisation-parcimonieuse-des-molecules-en-tension-durant-la-pandemie-covid-19. 2020 Apr. Available from: https://sfar.org/download/preconisations-pour-lutilisation-parcimonieuse-des-molecules-en-tension-durant-la-pandemie-covid-19/?wpdmdl = 26081&refresh = 5ea1be84aec4f1587658372
  5. 5. Tran K, Cimon K, Severn M, Pessoa-Silva CL, Conly J. Aerosol generating procedures and risk of transmission of acute respiratory infections to healthcare workers: a systematic review. PloS One. 2012;7(4):e35797. pmid:22563403
  6. 6. Brown J, Gregson FKA, Shrimpton A, Cook TM, Bzdek BR, Reid JP, et al. A quantitative evaluation of aerosol generation during tracheal intubation and extubation. Anaesthesia. 2021 Feb;76(2):174–81. pmid:33022093
  7. 7. Klompas M, Baker M, Rhee C. What Is an Aerosol-Generating Procedure? JAMA Surg. 2020 Dec 15;
  8. 8. Sauder P, Andreoletti M, Cambonie. Sédation-analgésie en réanimation (nouveau-né exclu). In: Réanimation. Masson, Elsevier. 2008. Available from: https://www.em-consulte.com/article/179487/sedation-analgesie-en-reanimation-nouveau-ne-exclu https://doi.org/10.1016/j.reaurg.2008.01.006 pmid:32288723
  9. 9. Papazian L, Aubron C, Brochard L, Chiche J-D. Prise en charge du Syndrome de Détresse Respiratoire Aigüe (SDRA) de l’adulte à la phase initiale- Recommandations Formalisées d’Experts. SRLF; 2018.
  10. 10. Recommandations d’experts portant sur la prise en charge en réanimation des patients en période d’épidémie à SARS-CoV2—La SFAR. Société Française d’Anesthésie et de Réanimation. 2020. Available from: https://sfar.org/recommandations-dexperts-portant-sur-la-prise-en-charge-en-reanimation-des-patients-en-periode-depidemie-a-sars-cov2/
  11. 11. Trouillet JL, Collange O, Belafia F, Blot F, Capellier G, Cesareo E, et al. Tracheotomy in the intensive care unit: guidelines from a French expert panel. Ann Intensive Care. 2018 Mar 15;8. pmid:29344743
  12. 12. Wei WI, Tuen HH, Ng RWM, Lam LK. Safe tracheostomy for patients with severe acute respiratory syndrome. The Laryngoscope. 2003;113(10):1777–9. pmid:14520105
  13. 13. Bassi M, Ruberto F, Poggi C, Diso D, Anile M, De Giacomo T, et al. Is Surgical Tracheostomy Better Than Percutaneous Tracheostomy in COVID-19–Positive Patients? Anesth Analg. 2020 Oct;131(4):1000–1005. pmid:32925315
  14. 14. Broderick D, Kyzas P, Sanders K, Sawyerr A, Katre C, Vassiliou L. Surgical tracheostomies in Covid-19 patients: important considerations and the “5Ts” of safety. Br J Oral Maxillofac Surg. 2020 Jun;58(5):585–9. pmid:32321662
  15. 15. McGrath BA, Brenner MJ, Warrillow SJ, Pandian V, Arora A, Cameron TS, et al. Tracheostomy in the COVID-19 era: global and multidisciplinary guidance. Lancet Respir Med. 2020 Jul;8(7):717–25. pmid:32422180
  16. 16. Andriolo BN, Andriolo RB, Saconato H, Atallah ÁN, Valente O. Early versus late tracheostomy for critically ill patients. Cochrane Database Syst Rev. 2015 Jan 12;2015(1). pmid:25581416
  17. 17. Young D, Harrison DA, Cuthbertson BH, Rowan K, TracMan Collaborators for the. Effect of Early vs Late Tracheostomy Placement on Survival in Patients Receiving Mechanical Ventilation: The TracMan Randomized Trial. JAMA. 2013 May 22;309(20):2121. pmid:23695482
  18. 18. Clinical characteristics and day-90 outcomes of 4244 critically ill adults with COVID-19: a prospective cohort study. Intensive Care Med. 2020 Oct 29;1–14. pmid:33211135
  19. 19. Tornari C, Surda P, Takhar A, Amin N, Dinham A, Harding R, et al. Tracheostomy, ventilatory wean, and decannulation in COVID-19 patients. Eur Arch Otorhinolaryngol. 2020 Aug.
  20. 20. Sancho J, Ferrer S, Lahosa C, Posadas T, Bures E, Bañuls P, et al. Tracheostomy in patients with COVID-19: predictors and clinical features. Eur Arch Otorhinolaryngol. 2021 Jan 1 pmid:33386436
  21. 21. Benito DA, Bestourous DE, Tong JY, Pasick LJ, Sataloff RT. Tracheotomy in COVID-19 Patients: A Systematic Review and Meta-analysis of Weaning, Decannulation, and Survival. Otolaryngol Neck Surg. 2021 Jan 5;194599820984780.
  22. 22. Zuazua-Gonzalez A, Collazo-Lorduy T, Coello-Casariego G, Collazo-Lorduy A, Leon-Soriano E, Torralba-Moron A, et al. Surgical Tracheostomies in COVID-19 Patients: Indications, Technique, and Results in a Second-Level Spanish Hospital. OTO Open. 2020 Jul 1;4(3):2473974X20957636. pmid:32974425
  23. 23. Glibbery N, Karamali K, Walker C, Fitzgerald O’Connor I, Fish B, Irune E. Tracheostomy in the coronavirus disease 2019 patient: evaluating feasibility, challenges and early outcomes of the 14-day guidance. J Laryngol Otol.:1–8. pmid:32758308
  24. 24. Turri-Zanoni M, Battaglia P, Czaczkes C, Pelosi P, Castelnuovo P, Cabrini L. Elective Tracheostomy During Mechanical Ventilation in Patients Affected by COVID-19: Preliminary Case Series From Lombardy, Italy. Otolaryngol Neck Surg. 2020 Jul 1;163(1):135–7. pmid:32396455
  25. 25. Piazza C, Filauro M, Dikkers FG, Nouraei SAR, Sandu K, Sittel C, et al. Long-term intubation and high rate of tracheostomy in COVID-19 patients might determine an unprecedented increase of airway stenoses: a call to action from the European Laryngological Society. Eur Arch Otorhinolaryngol. 2020 Jun 6;1–7.
  26. 26. Rovira A, Dawson D, Walker A, Tornari C, Dinham A, Foden N, et al. Tracheostomy care and decannulation during the COVID-19 pandemic. A multidisciplinary clinical practice guideline. Eur Arch Otorhinolaryngol. 2020 Jun 17 pmid:32556788
  27. 27. Tang Y, Wu Y, Zhu F, Yang X, Huang C, Hou G, et al. Tracheostomy in 80 COVID-19 Patients: A Multicenter, Retrospective, Observational Study. Front Med. 2020;7 pmid:33425960
  28. 28. Volo T, Stritoni P, Battel I, Zennaro B, Lazzari F, Bellin M, et al. Elective tracheostomy during COVID-19 outbreak: to whom, when, how? Early experience from Venice, Italy. Eur Arch Otorhinolaryngol. 2020 Jul 12;1–9. pmid:32656673
  29. 29. Martin-Villares C, Perez Molina-Ramirez C, Bartolome-Benito M, Bernal-Sprekelsen M. Outcome of 1890 tracheostomies for critical COVID-19 patients: a national cohort study in Spain. Eur Arch Otorhinolaryngol. 2020 Aug 4;1–8. pmid:32749607
  30. 30. Rosano A, Martinelli E, Fusina F, Albani F, Caserta R, Morandi A, et al. Early Percutaneous Tracheostomy in Coronavirus Disease 2019: Association With Hospital Mortality and Factors Associated With Removal of Tracheostomy Tube at ICU Discharge. A Cohort Study on 121 Patients*. Crit Care Med. 2021 Feb;49(2):261–270. pmid:33201005
  31. 31. Goldenberg D, Ari EG, Golz A, Danino J, Netzer A, Joachims HZ. Tracheotomy Complications: A Retrospective Study of 1130 Cases. Otolaryngol Neck Surg. 2000 Oct 1;123(4):495–500. pmid:11020193
  32. 32. Chiesa Estomba CM, Araujo da Costa AS, Schmitz TR, Lago PV. Base of Tongue Tuberculosis: A Case Report. Iran J Otorhinolaryngol. 2015 May;27(80):239–42. pmid:26082907
  33. 33. Tanaka L, Alexandru M, Jbyeh S, Desbrosses C, Bouzit Z, Cheisson G, et al. A hybrid approach to tracheostomy in COVID‐19 patients ensuring staff safety. Br J Surg. 2020 May 17 pmid:32418207
  34. 34. Prabhakaran K, Malcom R, Choi J, Chudner A, Moscatello A, Panzica P, et al. Open tracheostomy for covid19 positive patients: a method to minimize aerosolization and reduce risk of exposure. J Trauma Acute Care Surg. 2020 May 11 pmid:32404630
  35. 35. Thierry B, Célérier C, Simon F, Lacroix C, Khonsari R-H. How and why use the EasyBreath® surface snorkeling mask as a personal protective equipment during the COVID-19 pandemic? Eur Ann Otorhinolaryngol Head Neck Dis. 2020 Sep;137(4):329–31. pmid:32493648
  36. 36. Schultz P, Morvan J-B, Fakhry N, Morinière S, Vergez S, Lacroix C, et al. French consensus regarding precautions during tracheostomy and post-tracheostomy care in the context of COVID-19 pandemic. Eur Ann Otorhinolaryngol Head Neck Dis. 2020 May;137(3):167–9. pmid:32307265
  37. 37. Angel L, Kon ZN, Chang SH, Rafeq S, Palasamudram Shekar S, Mitzman B, et al. Novel Percutaneous Tracheostomy for Critically Ill Patients With COVID-19. Ann Thorac Surg. 2020 Sep;110(3):1006–11. pmid:32339508
  38. 38. Cheung NH, Napolitano LM. Tracheostomy: Epidemiology, Indications, Timing, Technique, and OutcomesDiscussion. Respir Care. 2014 Jun 1;59(6):895–919. pmid:24891198
  39. 39. Brodsky MB, Levy MJ, Jedlanek E, Pandian V, Blackford B, Price C, et al. Laryngeal Injury and Upper Airway Symptoms after Oral Endotracheal Intubation with Mechanical Ventilation During Critical Care: A Systematic Review. Crit Care Med. 2018 Dec;46(12):2010–7. pmid:30096101