Buscar en
Medicina Clínica (English Edition)
Toda la web
Inicio Medicina Clínica (English Edition) Benefits of early use of high-flow-nasal-cannula (HFNC) in patients with COVID-1...
Journal Information
Visits
0
Brief report
Full text access
Benefits of early use of high-flow-nasal-cannula (HFNC) in patients with COVID-19 associated pneumonia
Beneficio del empleo precoz de la oxigenoterapia nasal de alto flujo (ONAF) en pacientes con neumonía por SARS-CoV-2
Visits
...
Laura García-Pereña, Violeta Ramos Sesma, María Lucía Tornero Divieso, Alfonso Lluna Carrascosa, Sara Velasco Fuentes, Jorge Parra-Ruiz
Corresponding author
jorge.parra@grupohla.com

Corresponding author.
Servicio de Medicina Interna, Hospital HLA Inmaculada, Granada, Spain
Received 05 March 2021. Accepted 26 May 2021
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Abstract
Introduction

Severe COVID-19 is associated with hypoxemic bilateral pneumonia that leads to mechanical ventilation in a considerable proportion of patients. To the best of our knowledge, there are no recommendations about the best time to initiate high flow nasal cannula (HFNC).

Patients and methods

Retrospective study of all patients admitted for COVID-19 pneumonia who required HNFO between March 2020 and February 2021. Patients were grouped in early HNFC or late HNFC, according to the modified Kirby index.

Results

53 patients were included. Forty-four of them were included in the early HFNC and 9 in late HNFC. There were no statistically significant clinical-epidemiological differences. Early use of HFNC was associated with a decrease in the need for intubation (29.5 vs. 66.6%, p = 0.044), hospital stay (18.8 d vs. 36 d, p = 0.022) and mortality (22.7 vs. 55.5%, p = 0.061).

Conclusions

Early HFNC use is associated with a decrease in the need for intubation, mortality and overall hospital stay.

Keywords:
HNFC
Kirby index
Pneumonia
COVID-19
Resumen
Introducción

La COVID-19 grave se asocia con una neumonía bilateral hipoxemiante, que desemboca en la necesidad de ventilación mecánica en un considerable número de pacientes. Hasta la fecha no existen recomendaciones acerca del momento óptimo para el inicio de la ONAF.

Pacientes y métodos

Estudio retrospectivo de todos los pacientes ingresados por neumonía por COVID-19 y que precisaron ONAF entre marzo de 2020 y febrero de 2021. Se agruparon los pacientes en función del momento de inicio de la ONAF de acuerdo con la PaFi modificada.

Resultados

Se incluyeron 53 pacientes, en 44 se inició la ONAF precozmente y en nueve de ellos se inició tardíamente. No existieron diferencias clínico-epidemiológicas significativas. La utilización precoz de la ONAF se asoció con una disminución de la necesidad de intubación (29,5 vs. 66,6%, p = 0,044), de la estancia hospitalaria (18,8 d vs. 36 d, p = 0,022) y de la mortalidad (22,7 vs. 55,5%, p = 0,061).

Conclusiones

El empleo precoz de la ONAF se asocia con una disminución de la necesidad de intubación, de la mortalidad y de la estancia hospitalaria global.

Palabras clave:
ONAF
Índice de Kirby
Neumonía
COVID-19
Full Text
Introduction

High-flow nasal cannula (HFNC) oxygen therapy has demonstrated benefits in a number of situations where gas exchange is compromised. There are many benefits provided by HFNC therapy, the most important being the achievement of a more stable FiO2 at a higher flow rate, the reduction of air resistance by obtaining warm and properly humidified air, the reduction of dead space and the improvement of alveolar ventilation.1

On the other hand, SARS-CoV-2 infection causes bilateral hypoxemic pneumonia in some patients, which progresses rapidly, requiring increased oxygen therapy and, in up to 15-20% of patients, admission to the Intensive Care Unit (ICU) for orotracheal intubation (OTI) and connection to mechanical ventilation (MV).

Despite the known benefits of HNFC therapy in patients with respiratory failure, the initial expert recommendation was early intubation of patients with hypoxemic COVID-19 pneumonia because of the risk of aerosolization and infection,2 as well as doubts about the efficacy of HNFC therapy in these patients, recommending the use of continuous positive airway pressure (CPAP)3 if oxygenation other than Ventimask® or nasal cannula was required.

Oxygen therapy of patients with bilateral hypoxemic COVID-19 pneumonia has seen improvements in our hospital as our understanding of the pathophysiology of COVID-19 has improved, with HFNC therapy starting earlier and earlier. From an initial use in patients with SpO2 <90% with FiO2 50% (Ventimask >10 bpm) to early use in patients with a PaO2/FiO2 < 300 with FiO2 40% (Ventimask 6-8 bpm). This has led us to comparatively evaluate the outcome of early versus non-early application of HFNC therapy.

Patients and methods

Retrospective study including all patients requiring HFNC therapy as part of treatment during admission, seen in our hospital from March 2020 to February 2021. HLA Inmaculada Hospital is a private specialty hospital with 83 conventional hospital beds and six ICU beds.

For the definition of early HFNC therapy and non-early HFNC therapy, PaO2/FiO2 was used, substituting PaO2 by SpO2.4 In this way, early HFNC therapy was defined as that which began in patients without severe respiratory distress (SpO2/FiO2 > 100), and non-early HFNC therapy if started in patients with severe respiratory distress (SpO2/FiO2 ≤100).

A patient was considered to have a hyperinflammatory syndrome if they he/she met two or more of the following criteria: CRP > 100 mg/L, ferritin > 500 ng/mL, LDH > 300 IU/L and D-dimer > 1 mg/L.

Results

53 patients were included, 32 (60%) of whom were male. The mean age of the patients was 68.5 years (48-90 years), of whom 44 had some comorbidity, with HTN (19/53), obesity (14/53) and DM (6/53) being the most common.

Table 1 shows the laboratory values at the time of admission and at the time of HFNC therapy initiation.

Table 1.

Patient laboratory values on admission and at HFNC initiation.

Variable  Admission  HFNC 
CRP (mg/L)  102.6  103.6  0.907 
Ferritin (ng/mL)  697.11  838.2  0.020 
LDH (IU/L)  345.6  407.5  0.032 
DD (mg/L)  1.09  1.47  0.295 
SHI (n)  32  46  0.035 

Values are presented as mean, except SHI, which reflects the number of patients.

DD: D-dimer; LDH: lactate dehydrogenase test; HFNC: high-flow nasal cannula oxygen therapy; CRP: C-reactive protein; HIS: hyperinflammatory syndrome.

Of the total number of patients, 20 (37.7%) required admission to the ICU for OTI and MV and 15 patients (28.3%) died.

Of the 53 patients, nine (17%) had severe respiratory distress at the time of starting HFNC therapy, so it was considered that nine patients had non-early HFNC therapy, and 44 patients (83%) had early HFNC therapy.

Table 2 details the epidemiological and laboratory characteristics of patients with early HFNC therapy and patients with non-early HFNC therapy.

Table 2.

Characteristics of patients with early HFNC vs. Non-early HFNC.

  Early HFNC (n = 44)  Non-early HFNC (n = 9) 
Age  67.6  73  0.212 
Sex, male n (%)  29 (66%)  3 (33%)  0.075 
Sx up to admission (days)  6.98  8.22  0.273 
Sx up to HFNC (days)  9.4  11  0.227 
CRP (mg/L)  97.5  127.6  0.183 
Ferritin (ng/mL)  703  667  0.886 
LDH (IU/L)  335  393  0.140 
DD (mg/L)  1.12  0.9  0.719 
HIS, n (%)  36 (81.8%)  9 (100%)  0.200 
SpO2/FiO2  216  93.8  0.0001 
Immunosuppressants, n (%)  11 (25%)  1 (11.1%)  0.338 
ICU n (%)  13 (29.5%)  6 (66.6%)  0.044 
Death n (%)  10 (22.7%)  5 (55.5%)  0.061 
HFNC days  7.20  2.56  0.0001 
Admission days  15.8  37.1  0.001 

Data presented as mean, except sex (male), HIS, IS, ICU and death that show the number of patients who presented this characteristic.

DD: D-dimer; immunosuppressants: use of immunosuppressants (tocilizumab, baricitinib and/or anakinra); LDH: lactate dehydrogenase test; HFNC: high-flow nasal cannula oxygen therapy; CRP: C-reactive protein; Sx: symptoms; HIS: hyperinflammatory syndrome; ICU: Intensive care unit.

Discussion

In this study, the use of early HFNC therapy, that is, when there is a progressive increase in oxygen requirements, but before the patient develops severe respiratory distress, was associated with a statistically significant decrease in the need for ICU admission (p = 0.044) and a reduction in mortality that was very close to reaching statistical significance (p = 0.061). It was also associated with a significant reduction in days of hospitalisation, a difference that also reached statistical significance (p = 0.011).

In accordance with the WHO recommendations on the use of HFNC,2 the use of this ventilatory modality was reserved for patients with extremely high requirements, with deeply disappointing results. Therefore, following the publication of data on the safety of the HFNC in terms of the risk of infection transmission,5 we decided to start early HFNC therapy, despite the lack of clinical trials in patients with COVID-19.

Recently, some studies and reviews have been published which, like ours, demonstrate a reduction in the need for admission to the ICU for OTI and MV, mortality and overall hospital stay6,7; however, and unlike our study, they do not differentiate between the early and non-early use of HFNC therapy. Although the use of HFNC therapy, even in patients with severe respiratory distress, may be associated with some benefit, the application of HFNC therapy in the initial phases is the most effective strategy, which is consistent with what has been reflected by other authors,8 who already consider HFNC therapy as the non-invasive ventilatory modality of choice in patients with COVID-19.

Our study has some limitations, such as its retrospective nature, although given the development of the pandemic it was not possible to establish a clinical trial, so a retrospective design was the only option. However, given the limited number of professionals involved in the management of patients with COVID in our hospital, and the inclusion of all patients who underwent HFNC therapy, we believe that the biases inherent to this type of study do not exist. On the other hand, we decided not to assess the existence of dyspnoea as a criterion for the use of HFNC, given that in COVID-19 there is often a dissociation between the patient's hypoxia and dyspnoea, known as happy hypoxia in patients with COVID-19,9 and we therefore decided not to assess this aspect. Finally, although the decrease in mortality did not reach statistical significance, there was a very-close-to-significance trend (p = 0.061), with a considerable reduction in mortality (22.7 vs. 55.5%), which makes it clinically relevant. Finally, we believe that there are no confounding factors regarding the treatment which would affect the results; all patients received glucocorticoids according to the hospital's treatment protocol, methylprednisolone 1.5-2 mg/kg/d IV due to the development of respiratory failure; with respect to the use of immunosuppressants (tocilizumab, baricitinib, anakinra), there were no significant differences between the two groups (p = 0.338), although there were percentage differences (25 vs. 11%, early HFNC vs. late HFNC). We cannot rule out the possibility that, given the sample size, there may be some undetected bias, although given the magnitude of the p, we do not believe this to be the case.

It is important to note that patients with early HFNC therapy spent more time on HFNC therapy than those with late HFNC therapy (7.2 days ± 3.2 vs. 2.56 days ± 1.74, p = 0.0001), explained by the lower need for ICU admission and higher patient survival.

The results of this study suggest that the early use of HFNC therapy is associated with a decrease in the need for intubation, mortality and overall hospital stay, and its use should be implemented as soon as patients reach SpO2/FiO2 < 300 with FiO2 >40% (Ventimask at 6-8 bpm).

Funding

This paper has not received any type of funding.

Conflict of interests

The authors declare that they have no conflict of interest.

References
[1]
M. Nishimura.
High-flow nasal cannula oxygen therapy in adults: Physiological benefits, indication, clinical benefits, and adverse effects.
Respir Care, 61 (2016), pp. 529-541
[2]
World Health Organization.
Modes of transmission of virus causing COVID-19: implications for IPC precaution recommendations.
(2020),
[3]
L. Guan, L. Zhou, J.M. Le Grange, Z. Zheng, R. Chen.
Non-invasive ventilation in the treatment of early hypoxemic respiratory failure caused by COVID-19: Considering nasal CPAP as the first choice.
[4]
T.W. Rice, A.P. Wheeler, G.R. Bernard, D.L. Hayden, D.A. Schoenfeld, L.B. Ware.
Comparison of the SpO2/FIO2 ratio and the PaO2/FIO2 ratio in patients with acute lung injury or ARDS.
Chest, 132 (2007), pp. 410-417
[5]
J. Li, J.B. Fink, S. Ehrmann.
High-flow nasal cannula for COVID-19 patients: low risk of bio-aerosol dispersion.
Eur Respir J, 55 (2020), pp. 2000892
[6]
İ. Sayan, M. Altınay, A.S. Çınar, H.Ş. Türk, N. Peker, K. Şahin, et al.
Impact of HFNC application on mortality and intensive care length of stay in acute respiratory failure secondary to COVID-19 pneumonia.
Heart Lung, 50 (2021), pp. 425-429
[7]
C. Franco, N. Facciolongo, R. Tonelli, R. Dongilli, A. Vianello, L. Pisani, et al.
Feasibility and clinical impact of out-of-ICU noninvasive respiratory support in patients with COVID-19-related pneumonia.
Eur Respir J, 56 (2020), pp. 2002130
[8]
S. Raoof, S. Nava, C. Carpati, N.S. Hill.
High-Flow, Noninvasive Ventilation and Awake (Nonintubation) Proning in Patients With Coronavirus Disease 2019 With Respiratory Failure.
Chest, 158 (2020), pp. 1992-2002
[9]
S. Dhont, E. Derom, E. Van Braeckel, P. Depuydt, B.N. Lambrecht.
The pathophysiology of «happy» hypoxemia in COVID-19.
Respir Res, 21 (2020), pp. 198

Please cite this article as: García-Pereña L, Ramos Sesma V, Tornero Divieso ML, Lluna Carrascosa A, Velasco Fuentes S, Parra-Ruiz J. Beneficio del empleo precoz de la oxigenoterapia nasal de alto flujo (ONAF) en pacientes con neumonía por SARS-CoV-2. Med Clin (Barc). 2022;158:540–542.

Copyright © 2021. Elsevier España, S.L.U.. All rights reserved
Article options
Tools
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos