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Acta Clinica Croatica logoLink to Acta Clinica Croatica
. 2022 Dec;61(4):707–710. doi: 10.20471/acc.2022.61.04.18

HIGH-FLOW NASAL CANNULA COMBINED WITH PRONE POSITIONING AS AN INTUBATION ALTERNATIVE IN COVID-19: A CASE REPORT AND REVIEW OF THE LITERATURE

Nataša Sojčić 1, Jasminka Peršec 1,2, Andrej Šribar 1,2,
PMCID: PMC10588387  PMID: 37868176

SUMMARY

The use of high-flow nasal cannula (HFNC) in COVID-19 patients is a controversial topic due to the benefits and risks which may occur in patients and healthcare workers. The goal of this treatment modality is potential avoidance of invasive mechanical ventilation, but generation of aerosol and increased healthcare professional infection risk must be considered. We present a case of a SARS-CoV-2-positive 71-year-old male with acute hypoxemic respiratory failure, who was successfully treated with HFNC combined with prone positioning. Furthermore, we discuss recent literature concerning potential issues of HFNC treatment in COVID-19 patients.

Key words: Noninvasive ventilation, COVID-19, SARS-CoV-2, Oxygen inhalation therapy, Respiratory failure

Introduction

The use of high-flow nasal cannula (HFNC) to provide oxygen supplementation and improve the ventilation-perfusion ratio is a well-established treatment modality in patients with hypoxemic respiratory failure (HRF) (1). However, its use in COVID-19 patients is discouraged due to the potential aerosol spread and increased infection risk (2). We present a patient with borderline moderate to severe HRF in whom invasive mechanical ventilation was avoided by combined use of HFNC and prone positioning.

Case Report

In April 2020, a 71-year-old male patient with arterial hypertension and mild obesity (body mass index 27.5 kg/m2) was admitted to the Intensive Care Unit (ICU) in primary respiratory intensive care center specialized for COVID-19 patients (PRIC). Eight days prior to the onset of symptoms, he was in contact with a friend who was SARS-CoV-2 positive. On day 7 after symptom onset and positive SARS-CoV-2 real-time polymerase chain reaction test, he was admitted to PRIC. Symptoms and signs included fatigue, muscle pain, fever (up to 39 ∞C), non-productive cough, and anosmia. Two days prior to hospital admission, he developed mild dyspnea and occasional chest pressure. Physical examination at admission showed mild respiratory distress with the following vital signs: axillary temperature 37.2 °C, heart rate 86/min, blood pressure 170/90 mm Hg, respiratory rate 20/min, peripheral oxygen saturation (SpO2) 84% on room air in upright position and 90% in lateral decubital or prone position. Arterial blood gas analysis showed moderate hypoxemia and mild hypocapnia (PaO2 6.5 kPa, PaCO2 4.4 kPa) with normal base deficit and lactate levels. Chest x-ray showed discrete inhomogeneous opacities in the right lower lobe (Fig. 1). Immediately after admission and blood sampling, the patient received 4 L/min of O2 through facemask, which resulted in fast relief of dyspnea with improvement of SpO2 to 98% and PaO2 to 10.8 kPa. According to the hospital protocol, chloroquine phosphate (total of 5 days) and azithromycin (total of 3 days) were prescribed. QTc interval and liver enzymes were regularly checked given the possible side effects of the previously mentioned drugs. After day 4 of ICU stay, the patient showed fatigue during mild physical exertion (for example, going to the bathroom) with SpO2 82%. Repeated chest x-ray showed worsening of bilateral infiltrates and small pleural effusion on the left side. From that moment, the patient was encouraged to lie in a prone position for several hours through day and night, which led to relief of symptoms and improvement of SpO2.

Fig. 1.

Fig. 1

Chest x-ray at admission.

Nevertheless, on day 6 of ICU stay, his state worsened further with aggravation of hypoxemia (with 6 L/min of O2 through facemask SpO2 fell to 82%, PaO2 to 6.2 kPa, and PaO2/FiO2 105 mm Hg). Disparity between the clinical condition (primarily in the severity of dyspnea) and oxygen blood levels was present, hence the patient was not in severe respiratory distress nor did he complain of shortness of breath to the extent it would be expected. Also, further progressive changes in radiographic findings were recorded. Figure 2 demonstrates extensive bilateral infiltrates affecting the entire lung with predominance in the lower and medial lung fields. Computed tomography (CT) showed subpleural perihilar diffuse alveolar consolidations, ground-glass opacities, and intra- and interlobular septal thickening as common CT features in COVID-19.

Fig. 2.

Fig. 2

Chest x-ray on day 6 of Intensive Care Unit stay.

Considering worsening of hypoxemia and chest radiograph, HFNC (Hi-Flow Star, Dräger, Lübeck, Germany) was initiated, with FiO2 1.0, flow 35 L/min and temperature of 37 ∞C as initial settings, which were subsequently adjusted to the aimed SpO2 >93%. When necessary, maximum HFNC flow was utilized (50 L/min). Additionally, surgical mask was used over the nose and mouth to reduce the risk of aerosol spread. The patient reported alleviated breathing approximately 30 minutes after starting HFNC, accompanied with gradual rise of SpO2 up to 92% and PaO2 to 8.7 kPa, which were even more pronounced in prone position (SpO2 up to 94%). Due to respiratory function impairment and worsening of gas exchange, intravenous methylprednisolone was applied (1 mg/kg for 3 days, tapered to 0.5 mg/kg for the next 4 days). Laboratory findings reflected elevated systemic inflammation markers (white blood cell count, serum C-reactive protein, procalcitonin, ferritin and D-dimer). Lung ultrasound was regularly performed to reduce ionizing radiation exposure, and a decrease of B-line density was recorded over time. The patient was hemodynamically stable at all times without significant signs of other organ damage. Restrictive fluid administration regimen and daily respiratory therapy were implemented.

High-flow nasal cannula was applied for a total of 15 days, and the patient was gradually weaned to facemask and subsequently to room air. The basic principle we used in weaning HFNC therapy was firstly gradual reduction of FiO2 (approximately to 0.3-0.35) and if the respiratory rate and SpO2 were satisfactory, gradual reduction of flow was performed (3). In total, supplemental oxygen therapy was needed for a total of 40 days. At 22 days of admission, nasopharyngeal swabs were confirmed negative for SARS-CoV-2. The patient was discharged home 46 days after admission fully recovered with complete regression of pulmonary infiltrates, normal parameters of gas exchange and other laboratory findings.

Discussion

Endotracheal intubation and mechanical ventilation are still the gold standard in the treatment of acute HRF but it is associated with a high complication rate and increased mortality in COVID-19 patients (4). There is a hypothesis that certain patients with COVID-19 have presented a new phenotype that differs from clinical features previously seen in hypoxemic patients. In these patients, respiratory mechanics are preserved, and hypoxemia may be attributed to pulmonary thromboembolism and loss of hypoxic pulmonary vasoconstriction (5, 6). It may be reversed by a combination of high FiO2, positive airway pressure and reduced work of breathing created by HFNC coupled with decrease of intrapulmonary shunting and increase of lung compliance provided by prone positioning (7, 8). Simultaneous use of these two treatment modalities enabled avoidance of invasive mechanical ventilation in this patient. As shown in a study from China, in COVID-19 patients with PaO2/FIO2 <300 mm Hg combining prone position with HFNC significantly improved ventilation-perfusion mismatch and proved to be a good strategy in avoiding intubation and reducing the medical staff workload (9). It must also be noted that, although recently published data suggest that stress ulcer prophylaxis might increase the risk of bacterial superinfection (10), in this patient it was not the case and the collected sputum specimens showed no pathogen growth.

As COVID-19 pandemic erupted in early 2020, a main concern was limiting the spread of this highly virulent virus. Because of that, the use of HFNC was observed with skepticism and was initially discouraged in these patients (2, 11). However, both experimental and clinical published data showed HFNC to be safe to use when all the precautionary measures are employed (12) (confirmed by the fact that none of the healthcare personnel that treated this patient were infected with SARS-CoV-2) and may greatly reduce the intubation and complications rate, as well as ICU stay (13).

References

  • 1.Mauri T, Turrini C, Eronia N, Grasselli G, Volta CA, Bellani G, et al. Physiologic effects of high-flow nasal cannula in acute hypoxemic respiratory failure. Am J Respir Crit Care Med. 2017. May 1;195(9):1207–15. 10.1164/rccm.201605-0916OC [DOI] [PubMed] [Google Scholar]
  • 2.ANZICS COVID-19 Guidelines. ANZICS Available from: https://www.anzics.com.au/coronavirus-guidelines/. Accessed June 1, 2020.
  • 3.Kim MC, Lee YJ, Park JS, Cho YJ, Yoon HI, Lee CT, et al. Simultaneous reduction of flow and fraction of inspired oxygen (FiO2) versus reduction of flow first or FiO2 first in patients ready to be weaned from high-flow nasal cannula oxygen therapy: study protocol for a randomized controlled trial (SLOWH trial). Trials. 2020. January 14;21(1):81. 10.1186/s13063-019-4019-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Weiss P, Murdoch DR. Clinical course and mortality risk of severe COVID-19. Lancet. 2020;395:1014–5. 10.1016/S0140-6736(20)30633-4 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Gattinoni L, Chiumello D, Rossi S. COVID-19 pneumonia: ARDS or not? Crit Care. 2020. April 16;24(1):154. 10.1186/s13054-020-02880-z [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Deshpande C. Thromboembolic findings in COVID-19 autopsies: pulmonary thrombosis or embolism? Ann Intern Med. 2020. September 1;173(5):394–5. 10.7326/M20-3255 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Despres C, Brunin Y, Berthier F, Pili-Floury S, Besch G. Prone positioning combined with high-flow nasal or conventional oxygen therapy in severe COVID-19 patients. Crit Care. 2020. May 26;24(1):256. 10.1186/s13054-020-03001-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Ghelichkhani P, Esmaeili M. Prone position in management of COVID-19 patients; a commentary. Arch Acad Emerg. 2020. April 11;8(1):e48. [PMC free article] [PubMed] [Google Scholar]
  • 9.Xu Q, Wang T, Qin X, Jie Y, Zha L, Lu W. Early awake prone position combined with high-flow nasal oxygen therapy in severe COVID-19: a case series. Crit Care. 2020. May 24;24(1):250. 10.1186/s13054-020-02991-7 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Muzlović I, Štubljar D. Stress ulcer prophylaxis as a risk factor for tracheal colonization and hospital-acquired pneumonia in intensive care patients: impact on latency time for pneumonia. Acta Clin Croat. 2019. March;58(1):72–86. 10.20471/acc.2019.58.01.10 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Brewster DJ, Chrimes N, Do TB, Fraser K, Groombridge CJ, Higgs A, et al. Consensus statement: Safe Airway Society principles of airway management and tracheal intubation specific to the COVID-19 adult patient group. Med J Aust. 2020. June;212(10):472–81. Epub 2020 May 1. 10.5694/mja2.50598 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.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. 10.1371/journal.pone.0035797 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Lyons C, Callaghan M. The use of high-flow nasal oxygen in COVID-19. Anaesthesia. 2020. July;75(7):843–7. 10.1111/anae.15073 [DOI] [PubMed] [Google Scholar]

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