Literature DB >> 32653759

Safe percutaneous dilational tracheostomy in 5 patients with ARDS by Covid-19.

Manuel Taboada1, Sara Vazquez2, Julia Regueira2, Agustín Cariñena2, Francisco Aneiros2, Valentin Caruezo2, Alberto Naveira2, Pablo Otero2.   

Abstract

Entities:  

Keywords:  Acute respiratory distress syndrome (ARDS); COVID-19; Percutaneous tracheostomy

Mesh:

Year:  2020        PMID: 32653759      PMCID: PMC7340012          DOI: 10.1016/j.jclinane.2020.109977

Source DB:  PubMed          Journal:  J Clin Anesth        ISSN: 0952-8180            Impact factor:   9.452


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To the Editor: Coronavirus disease 2019 (Covid-19), caused by the novel severe acute respiratory syndrome coronavirus (SARS-CoV-2), is a disease with a clinical spectrum that ranges from asymptomatic to critical disease requiring Intensive Care Unit (ICU) admission, intubation, and prolonged mechanical ventilation due to a severe acute respiratory distress syndrome (ARDS) [1]. Despite the large and growing number of cases of Covid-19 disease around the world, there are few publications related to the performance of tracheostomies in Covid-19 patients who require prolonged mechanical ventilation. We describe our experience in 5 patients with laboratory-confirmed COVID-19 admitted in the ICU of Clinical Hospital of Santiago de Compostela who underwent elective bedside percutaneous dilational tracheostomies (PDT) during April 2020. This prospective case series was approved by the Research Ethics Committee of the Galicia, Spain, number 2020-188. Informed consent for the procedure was provided by all patients or a close relative of the patient. All patients were admitted with severe ARDS. Patient demographics, comorbidities, clinical ICU course and treatments are described in Table 1 . Tracheostomy was performed after a mean of 16 (13-27) days of invasive mechanical ventilation and the patients presented a PaO2/FiO2 ratio of 167 (92-206). PTD took place in ICU, in a closed room. Team that performed PTD consisted of 3 anesthesiologists and a circulation nurse. One anesthesiologist managed airway and bronchoscopy, and the other two performed the PTD. Each person wore standard personal protective equipment PPE (FFP3 mask, surgical cap, goggles, surgical gown, and double gloves). During procedure, all patients were deep sedated and paralyzed. During tracheal puncture mechanical ventilation was stopped and we used a Single-Step dilatation technique (Ciaglia Blue Rhino G2 Advanced Percutaneous Tracheostomy Kit (Cook Medical)) with the help of a bronchoscope to control the puncture site, the direction of guidewire, and the location of tracheostomy. PTD was performed at the bedside in all five patients without difficulty, and no complications were found. Neither the nurse nor the anesthetists who participated in the PTD developed symptoms or tested positive for Covid-19 fourteen days after procedure.
Table 1

Clinical Characteristics patients with severe ARDS by COVID-19 where tracheostomy was performed.

Patient 1Patient 2Patient 3Patient 4Patient 5
Characteristics
 Age, yr6870706368
 Sex,FMMMM
 Weight, kg6592759097
 Height, cm165165162176166
 APACHE II score2117211620
 PaO2/FiO2 in ICU admission (mmHg)18020692133173
 PaO2 in ICU admission (mmHg)8012492106104
 Chronic medical illness
 HypertensionNoYesYesNoYes
 DiabetesNoNoNoNoYes
 Chronic obstructive pulmonary diseaseYesNoNoNoNo
 Heart diseaseNoYesSiNoYes
 Laboratory parameters
 Leukocytes count per mL179808400480034507400
 Lymphocytes count per mL2305101802801080
 C-reactive protein, mg/L25155717
 D-dimer, ng/mL487070719003571295
 Lactate dehydrogenase, U/L989600248519913
 Creatine kinase, ng/mL2911403311054
 Serum Ferritin, μg/L53126506892898653
 Interleukin-6, pg/mL15885181967077
 Procalcitonin, ng/mL13,30,32640,460,22
 Triglycerides, mg/dL127195118256117
 Treatment
 HydroxychloroquineYesYesYesYesYes
 Lopinavir/ritonavirYesYesYesYesYes
 AzithromycinYesYesYesYesYes
 TocilizumabNoNoYesNoYes
 GlucocorticoidsYesYesYesYesYes
Clinical ICU course
 Duration since intubation to tracheostomy (days)1327171616
 Length of ICU stay (days)3931384039a
 Survival at 21 after PTDYesYesNoNoYes

Remained ICU, PTD: percutaneous dilational tracheostomies.

Clinical Characteristics patients with severe ARDS by COVID-19 where tracheostomy was performed. Remained ICU, PTD: percutaneous dilational tracheostomies. PTD is a common, minimally invasive procedure to facilitate tracheostomy placement, and it represents an alternative to traditional open tracheostomy. We prefer to perform PTD because it is fast, safe, and with low complications. It is performed in our ICU at bedside, avoiding transport of Covid-19 patients to the operating room with repeated connection and disconnection of ventilatory circuits during transfer. Although open tracheostomies were favored over PTD during the SARS outbreak [2], techniques for PTD have advanced since then. We used a single stage “Rhino” dilator technique avoiding multiple entries. Procedure was performed under deep sedation and full neuromuscular blockade to prevent coughing, and we stopped mechanical ventilation just before performing the PTD, to minimize aerosol generation. Although the use of the bronchoscope could generate an increase in aerosols, we believe that it is worth using it due to the increased safety for the patient when performing the procedure. During the procedure we paid meticulous attention to the details of infection control, to minimize cross-contamination and our risk of contracting the illness [3,4]. The optimal timing of tracheostomy in ventilated Covid-19 patients remains controversial. We perform our PTD 14 days after endotracheal intubation (IOT) as recommends the American of Otolaryngology-Head and Neck surgery [5]. In conclusion, there is no evidence whether PTD or surgical open tracheotomy is less aerosol generating. We considered that PTD may be a safe and effective technique for COVID-19 patients with ARDS. Future studies will determine the role of percutaneous tracheostomy in Covid-19 patients with difficult disconnection from mechanical ventilation. Clinical trial number: Code No. 2020-188.

Prior presentations

No.

Funding statement

No funding provided.

Support

Support was provided solely from institutional and departmental sources.

Authors contributions

Conception of the study: Manuel Taboada, Valentin Caruezo Study design: Manuel Taboada, Data collection: Manuel Taboada, Agustín Cariñena, Francisco Aneiros, Albero Naveira, Pablo Otero. Data analysis: Manuel Taboada Drafting the manuscript: All authors helped to revise the draft of the manuscript Editing and approval of the manuscript: All authors

Declaration of competing interest

The authors declare the absence of conflict of interests.
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