key: cord-0692124-tbfx0wfs
authors: Nadeem, Rashid; Zahra, Ahmed Najah; Hassan, Mustafa; Parvez, Yusuf; Gundawar, Nilesh; Hussein, Mohammed A.M.; Younis, Manal; Mathews, Manoj P.; Khan, Wasim; Saleh, Majid Ahmed; Mumtaz, Imran; Aljaghoub, Hebah Rami; Elfatih, Ahd; Waleed, Alaa; Ghoneem, Alaa
title: Prevalence and Timing of Tracheostomy and Its Impact on Clinical Outcomes in COVID-19 Pneumonia Patients in Dubai Hospital
date: 2021-04-14
journal: Dubai Medical Journal
DOI: 10.1159/000515209
sha: 25be237f02e99e88bcf35953f5a63b5a74073878
doc_id: 692124
cord_uid: tbfx0wfs

INTRODUCTION: Coronavirus has caused more than a million deaths as of October 2020. Hospitals consider tracheostomy after the patient is virus negative, usually after 3 weeks. Prevalence and timing of tracheostomy and its impact on survival among COVID patients are unknown. METHODS: A retrospective, single-center study of all patients with COVID-19 ARDS who underwent tracheostomy was conducted. Patients with age <18 and patients treated with ECMO were excluded. Duration of ventilation before tracheostomy was recorded. Clinical variables, outcome variables, and confounding variables were recorded and compared between patients with tracheostomy and without tracheostomy. The aim was to determine prevalence and timing of tracheostomy and its impact on clinical outcomes. RESULTS: We found that tracheostomies were performed only in 21 out of 196 patients (10.8%). Tracheostomies were performed after 3 weeks on average (22.1 ± 7.5 days). Survival was significantly higher in patients who underwent tracheostomy (85.7 vs. 42.5%, p = 0.001). LOSICU was longer for tracheostomy patients than patients without tracheostomy (median [IQR]: 35 [23–47] vs. 15 [9–21], p = 0.001). Patients who underwent tracheostomy had a higher proportion of treatment with continuous renal replacement therapy (CRRT) (52 vs. 30%, p = 0.04), more COVID-19 swab testing (6.5 [4.5–8.5] vs. 5 [3–7], p = 0.002), more days on mechanical ventilation (34.5 [24–45] vs. 11 [5.5–16.5], p = 0.001), and more length of stay in the hospital (54 [38–70] vs. 20 [10.5–29.5], p = 0.001). All other factors were not statistically different between the 2 groups. Approximately 29% of patients had possible false-negative testing as their swab became positive after being negative. CONCLUSION: Tracheostomy was performed only in 10% of our patients with COVID-19 ARDS. Time to tracheostomy was after 3 weeks on average. Survival was better in patients with tracheostomy, but tracheostomized patients stayed longer in the ICU and hospital and utilized more days of mechanical ventilation and CRRT.

ly higher in patients who underwent tracheostomy (85.7 vs. 42.5%, p = 0.001). LOSICU was longer for tracheostomy patients than patients without tracheostomy (median [IQR]: 35 vs. 15 [9] [10] [11] [12] [13] [14] [15] [16] [17] [18] [19] [20] [21] , p = 0.001). Patients who underwent tracheostomy had a higher proportion of treatment with continuous renal replacement therapy (CRRT) (52 vs. 30%, p = 0.04), more COVID-19 swab testing (6.5 [4.5-8.5 ] vs. 5 [3] [4] [5] [6] [7] , p = 0.002), more days on mechanical ventilation (34.5 vs. 11 [5.5-16.5] , p = 0.001), and more length of stay in the hospital (54 vs. 20 [10.5-29.5] , p = 0.001). All other factors were not statistically different between the 2 groups. Approximately 29% of patients had possible falsenegative testing as their swab became positive after being negative. Conclusion: Tracheostomy was performed only in 10% of our patients with COVID-19 ARDS. Time to tracheostomy was after 3 weeks on average. Survival was better in patients with tracheostomy, but tracheostomized patients stayed longer in the ICU and hospital and utilized more days of mechanical ventilation and CRRT.

Coronavirus has caused more than a million deaths as of October 2020 [1] . Severe infection with coronavirus causes pneumonia leading to acute respiratory distress syndrome and respiratory failure requiring invasive mechanical ventilation. Prolonged invasive mechanical ventilation often leads to ventilator-associated pneumonia and other complications as it is associated with longer use of sedatives, narcotics, muscle paralysis leading to longer need for invasive central catheters, and stationary position of the patient causing line infection and pressure injuries to the skin, respectively. Therefore, tracheostomy is considered for mechanically ventilated patients after 7-10 days if patients are expected to be ventilator dependent for a longer time [2] . Most hospitals consider tracheostomy only after the patient is virus negative since the tracheostomy procedure generates a high aerosol risk of virus transmission [3] . A case series of 14 patients showed that most patients were seronegative after 2 weeks, which suggests it is safer to consider tracheostomy after 2 weeks and seroconversion [4] . Many centers report performing tracheostomy for COVID-19 patients within 14 days [5] . We aim to measure the prevalence of tracheostomy and its timing for COVID-19 patients in our patient population. We compare the outcomes of patients who underwent tracheostomies (28-day survival and length of stay [LOS] in the ICU and hospital).

We conductive a retrospective, single-center study of electronic medical records of all consecutive patients with proven COVID-19 infection admitted to Dubai hospital, UAE. We included all patients admitted between January 1, 2020, and June 30, 2020. We only excluded patients <18 years of age and those treated with extracorporeal membrane oxygenation. All patients who underwent tracheostomy comprise the cases. The control group comprised all other CO-VID-19 patients with respiratory failure who did not have a tracheostomy. The Otorhinolaryngology team performed all tracheostomies in operation theaters. We recorded the duration of invasive mechanical ventilation (days) before tracheostomy. We recorded demographics (age, gender, and BMI) and confounding factors to compare the 2 groups. Confounding factors include clinical symptoms and signs on admission. We also recorded laboratory data including white blood cell counts, lymphocyte counts, platelets count, blood chemistries, renal indices, coagulation profile, liver function tests, and inflammatory and disease markers including C-reactive protein, ferritin, procalcitonin, lactate, creatinine kinase, and D-dimers.

Our hospital policy required virus-negative status of the patient to perform tracheostomy. Repeated swab test results recorded seroconversion as per protocol until 2 consecutive swabs were reported as negative. We recorded the number of days to seroconver-sion and the number of swabs performed. Treatment profiles were recorded for use of chloroquine, antivirals, antibacterial, and steroids. All laboratory tests, including PCR confirmation of CO-VID-19, were performed at the Dubai Hospital Laboratory.

Sample characteristics were compared between the tracheostomy group and those who did not have tracheostomy. Numerical data were presented as median and interquartile range (IQR), and categorical data were presented as count (%). Fisher exact tests were performed for categorical variables and the Mann-Whitney U test for continuous variables (as data were not normally distributed). Data are presented as median and IQR. We used IBM SPSS Statistics for Windows, version 26 (IBM Corp., Armonk, NY, USA).

We found that tracheostomies were performed only in 21 out of 194 patients (10.8%). All tracheostomies were performed after 3 weeks (22.1 ± 7.5 days) on average. Survival was significantly higher in patients who underwent tracheostomy (85. (Tables 1-2) . Possible false-negative swab test results were 28.8% (N = 56) as swab became positive after being negative (nasal swab = 37, tracheal swab = 10, sputum swab = 4, and nasopharyngeal swab = 5). There was no difference between tracheostomy and no tracheostomy groups. We could not perform long-term temporal follow-up on our patients as the majority of patients transferred to other hospitals, long-term ventilator facilities, or rehabilitation centers owing to relatively limited inpatient beds during CO-VID-19 pandemic peak time.

Prolonged mechanical ventilation beyond 10 days with a clinical condition requiring more time usually necessitates tracheostomy, which is known to provide comfort, Values are presented as n (%). Bold type denotes significance. CRRT, continuous renal replacement therapy. * Fisher's exact test was done to assess the difference between groups. reduces amounts of sedatives and paralytic medications, and improves dead space in the respiratory system [5] . Delay in tracheostomy is associated with more sequelae of prolonged sedation and paralysis, neuropathy, and myopathy of critical illness, which may further delay the weaning process [6] . Moreover, prolonged endotracheal intubation requires prolonged invasive indwelling central lines leading to line infection and bacteremia. Prolonged endotracheal intubation frequently requires muscle paralysis leading to increase in the occurrence of pressure injuries and ulcers. We have studied both of these complications in our sample, and data are presently under review (not presented here). Therefore, it is worthwhile to consider tracheostomy in these patients. Aerosol generation during tracheostomy makes it a high-risk procedure; therefore, guidelines suggest that the procedure be delayed until COVID-19 patients have a lower viral burden or become seronegative [7, 8] . Most institutions require 2 reliable negative swabs before tracheostomy is performed since false-negative test results are significantly high [9] . In our sample, 28.8% of patients had possible false-negative testing as swab again became positive after being negative.

Tracheostomies were performed after 3 weeks in our COVID-19 patients (22.1 ± 7.5 days). Chao et al. [10] reported the average time of intubation to tracheostomy as 19.7 ± 6.9 days, with a range of 8-42 days. In Spanish hospitals, the median timing of tracheostomy was 12 days (4-42 days) since orotracheal intubation [11] . Current protocols recommended delaying tracheostomy for at least 14 days or longer or until a negative PCR [7, 8] .

Survival was higher in our sample (85%) for tracheostomy patients. Martin-Villares et al. [11] reported that for 52.1% of tracheostomized patients, weaning was achieved, while 24.2% were still under mechanical ventilation, and only 23.7% patients had died from COVID-19, so their survival was 76.3%. Others reported similarly 67-70% survival as well [12, 13] . Weaning details for our sample were unknown as most patients were transferred out of the ICU to another hospital, chronic ventilator-dependent patients' facilities, or rehabilitation centers.

LOSICU was surprisingly prolonged in our tracheostomized patients. Although tracheostomy helps optimally utilize ICU resources, bed crises and cultural and administrative reasons preclude discharging tracheostomized patients to the medical ward.

Days on mechanical ventilation were more in the tracheostomy group. Since more patients survived, they stayed longer on ventilators, ICU, and CRRT. Our region has minimal chronic ventilator-dependent patients' facilities.

We identified the following limitations of our study. The study is a single-center retrospective chart review with a small sample size and low power. Otorhinolaryngologists performed all tracheostomies in the operation theater (no bedside percutaneous tracheostomies are performed). Therefore, results may not apply to other hospitals in the United Arab Emirates or other populations.

Tracheostomy was performed only in 10% of our patients with COVID-19 ARDS. Time to tracheostomy was after 3 weeks on average. Survival was better in patients with tracheostomy, but tracheostomized patients stayed longer in the ICU, in the hospital, on mechanical ventilation, and on CRRT.

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Tracheostomy guidelines developed at a large academic medical center during the CO-VID-19 pandemic

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The authors would like to acknowledge all members of the CO-VID-19 tracheostomy team who were instrumental in performing tracheostomies (Otorhinolaryngology Department): A.G., I.H., J.K., T.M., K.K., and H.T.

No conflicts to declare.

The authors did not receive any funding. 

Ethical approval was provided by DSREC DSREC-07/2020_10/ approved on 23 July 2020. Data source bank was the electronic medical records system (Salama/Epic). Patients' data privacy and confidentiality of information was considered. Only deidentified data were collected. All authors have proper training to exercise strict confidentiality and privacy in data collection. Therefore, strict data security measures were taken to ensure privacy and confidentiality.