Next Article in Journal
Dental Emergencies in an Italian Pediatric Hospital during the COVID-19 Pandemic
Next Article in Special Issue
Can Lung Ultrasound Be the Ideal Monitoring Tool to Predict the Clinical Outcome of Mechanically Ventilated COVID-19 Patients? An Observational Study
Previous Article in Journal
A Mobile App for Triangulating Strategies in Phosphate Education Targeting Patients with Chronic Kidney Disease in Malaysia: Development, Validation, and Patient Acceptance
Previous Article in Special Issue
Combination of Multidisciplinary Therapies Successfully Treated Refractory Ventricular Arrhythmia in a STEMI Patient: Case Report and Literature Review
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Review

Current Practice of High Flow through Nasal Cannula in Exacerbated COPD Patients

Anesthesia and Intensive Care Unit, Department of Medical and Surgical Sciences, University Hospital Mater Domini, Magna Graecia University, 88100 Catanzaro, Italy
*
Author to whom correspondence should be addressed.
Healthcare 2022, 10(3), 536; https://doi.org/10.3390/healthcare10030536
Submission received: 21 February 2022 / Revised: 14 March 2022 / Accepted: 14 March 2022 / Published: 15 March 2022
(This article belongs to the Special Issue Pulmonary and Critical Care Medicine)

Abstract

:
Acute Exacerbation of Chronic Obstructive Pulmonary Disease is a form of severe Acute Respiratory Failure (ARF) requiring Conventional Oxygen Therapy (COT) in the case of absence of acidosis or the application of Non-Invasive Ventilation (NIV) in case of respiratory acidosis. In the last decade, High Flow through Nasal Cannula (HFNC) has been increasingly used, mainly in patients with hypoxemic ARF. However, some studies were also published in AECOPD patients, and some evidence emerged. In this review, after describing the mechanism underlying potential clinical benefits, we analyzed the possible clinical application of HFNC to AECOPD patients. In the case of respiratory acidosis, the gold-standard treatment remains NIV, supported by strong evidence in favor. However, HFNC may be considered as an alternative to NIV if the latter fails for intolerance. HFNC should also be considered and preferred to COT at NIV breaks and weaning. Finally, HFNC should also be preferred to COT as first-line oxygen treatment in AECOPD patients without respiratory acidosis.

1. Introduction

Chronic Obstructive Pulmonary Disease (COPD) is a common disease characterized by persistent respiratory symptoms and airflow limitation [1]. Patients’ history is characterized by episodes of exacerbation with worsening respiratory symptoms, commonly precipitated by upper respiratory infection [1].
In case of severe exacerbation, COPD patients may develop an acute respiratory failure (ARF) of varying entities, sometimes requiring hospital admission due to the deterioration of the gas exchange. While only conventional oxygen therapy (COT) may be required in case of sole hypoxemia, respiratory acidosis and carbon dioxide (CO2) retention may ensue in 20% of patients because of an excessive respiratory workload over the respiratory muscles pump capacity [2]. In these latter cases, non-invasive ventilation (NIV) plays a major role. NIV has been shown to improve gas exchange, reduce breathing difficulty and the need for intubation and decrease hospital length of stay and mortality [2]. In particular, NIV is recommended for all those patients with ARF leading to acute or acute-on-chronic respiratory acidosis (pH ≤ 7.35), whereas there is no indication if patients encounter an acute exacerbation of COPD (AECOPD) and hypercapnia without acidosis [2]. Of note, up to 64% of AECOPD patients may fail NIV mainly due to worsened respiratory function, intolerance of the interface, cardiovascular instability and neurological deterioration [3]. In these cases, intubation is required, and invasive mechanical ventilation (iMV) is instituted [3].
The High Flow through Nasal Cannula (HFNC) was introduced in clinical practice, and its role is gaining more and more importance. Several studies investigated its application also in AECOPD patients for the treatment of the hypercapnic ARF [4,5].
After a brief explanation of the rationale and possible physiologic advantages of HFNC in AECOPD patients, we aim to provide a focus on their possible current clinical application in this population of patients.

2. Potential Advantages of HFNC in AECOPD Patients

HFNC delivers heated and humidified air–oxygen mixture to the patient, with an inspiratory fraction of oxygen (FiO2) ranging from 21 to 100% and a flow up to 60 L/min through a large bore nasal cannula [6,7]. HFNC has some potential advantages for AECOPD patients, which herein are discussed [7].

2.1. Heated and Humidified Gas Delivery

In healthy subjects, the upper respiratory tract humidifies the inspired room air to full saturation of water vapor (absolute humidity = 44 mg/L) and heats at 37 °C [8]. However, the administration of not conditioned medical gases, such as during COT or NIV, affects the ciliary motion, damages the respiratory tract epithelial cell and reduces the water content of the bronchial secretions [9,10,11]. This is of particular relevance in AECOPD patients, which are characterized by the production of copious secretions that need to be expectorated [4,5]. Indeed, in the case of accumulation of the secretions in the airways, the risk of hospital and ICU acquired infections strongly increases [11]. The use of active and heated humidification may reduce this risk by limiting the inflammatory response and bronchial epithelial cell damage [12] and by ameliorating the mucociliary clearance and cough effectiveness [4,5,13,14].

2.2. Anatomical Dead Space Washout

The volume of air located in the segments of the respiratory tract is responsible for conducting air from airways opening to the alveoli, without acting in the process of gas exchange is called dead space, and it includes the upper airways, trachea, bronchi and terminal bronchioles.
In an upper airway model, HFNC was demonstrated to wash out the dead pharyngeal space from carbon dioxide (CO2) proportionally to the flow applied and the expiratory time [15]. In healthy subjects, the nasal cavity has a volume of about 40–50 mL, and it comprises at least 30% of the anatomical dead space in adults [16]. COPD patients are characterized by an incremented ratio between dead space and tidal volume [17]. The wash-out effect was advocated as one of the mechanisms to reduce the arterial partial pressure of CO2 (PaCO2) [18] and the respiratory drive after extubation [19] and at NIV discontinuation [20] as compared with COT.

2.3. “PEEP” Effect

HFNC also generates a small amount of positive end-expiratory pharyngeal pressure in healthy subjects [21,22,23] and in stable COPD or idiopathic pulmonary fibrosis [24]. The amount of generated positive pressure by HFNC depends on the flow delivered to the patient and the size of the nasal prong in relation to the nostrils [25,26]. The “PEEP” effect is produced by the expiratory resistance to the patient’s exhalation [21], which resembles the pursed-lip breathing pattern adopted by COPD patients [27]. This strategy diminishes the respiratory rate and prolongs the expiratory time, resulting in a reduction in the expiratory flow limitation and dynamic hyperinflation [27].
It is well known that the application of an external PEEP in COPD patients reduces the work of breathing in case of the presence of dynamic lung hyperinflation and intrinsic PEEP [28]. Together with the wash-out effect, the “PEEP” effect may explain the reduction in the respiratory muscle effort in both stable COPD patients [29] and in those recovering from an episode of exacerbation [19,20].

2.4. Provision of Stable Inspired Oxygen Fraction (FiO2)

Another potential advantage of HFNC is the delivery of stable inspired oxygen fraction (FiO2) to patients with ARF whenever the delivered flow exceeds the mean inspiratory peak flow of the patient [30]. Of note, in AECOPD patients, the mean inspiratory peak flow was reported to be around 70 L/min and exceed 60 L/min in about 70% of patients [31]. By delivering flow at around 60 L/min, HFNC guarantees a more stable FiO2 to AECOPD patients, as compared to COT through nasal prongs or Venturi masks.

2.5. Treatment Comfort

Among the most important determinants for treatment success, the comfort of the patient and the tolerance of the device play a major role during NIV [3,32]. The delivery of dry oxygen is perceived as uncomfortable and may generate pain related to mouth, throat and airways dryness; this is particularly true in critically ill patients [33].
Since the delivered gas admixture is heated and humidified, HFNC reduces this uncomfortable feeling as compared to both COT [20,30] and NIV [34]. In addition, nasal prongs are more tolerated than face masks for NIV, which may produce skin breakdown on the point of the pressure of the interfaces (i.e., forehead and nose) [34,35].

3. Clinical Application of HFNC in Exacerbated COPD Patients

According to the need for therapy, COPD exacerbation can be classified as mild, moderate and severe. A mild exacerbation is defined when the patient requires only treatment with short-acting beta-agonist bronchodilators (SABA), moderate if the hospitalization is required, in conjunction with SABA and/or corticosteroids therapy, severe when the exacerbation is associated with ARF [1]. The most important symptoms are dyspnea, increased sputum, cough and wheezing [1]. Within this spectrum of manifestation and degree of exacerbation severity, indications to oxygen and/or respiratory support vary.
In the case of sole hypoxemia, AECOPD patients require COT, whereas NIV is deemed if respiratory acidosis ensues. The recent guidelines strongly recommend the application of NIV whenever hypercapnic ARF with acidosis is present [2]. Moreover, a trial of NIV is also recommended if AECOPD patients would require iMV unless immediate deterioration occurs [2]. Of note, NIV was shown to improve gas exchange, reduce breathing difficulty and the need for intubation and decrease hospital length of stay and mortality [2].
While on one side, NIV provides these advantages, it is also affected by some drawbacks, such as patient–ventilator asynchrony, patient’s discomfort and intolerance to the treatment, leading to treatment failure [36,37,38,39,40,41,42,43]. Management of these issues becomes fundamental to avoid NIV failure, but it is not easy to achieve. For example, although patient–ventilator asynchrony can be partially managed by optimizing ventilator setting and/or modes of ventilation [36,37,38,39,40,41,42,43,44,45,46,47,48,49], the detection of asynchronous events is challenging if attempted by the sole ventilator waveform observation without the use of additional signals [50]. In addition, the patient’s discomfort and intolerance to the interface may be averted by adopting a rotating strategy and application of different interfaces, such as the helmet, possibly combined with specific ventilator settings [37,43,51].
In AECOPD patients, HFNC was demonstrated to reduce the retention of CO2 [52,53] and the activation of the diaphragm to a similar extent to NIV [20,54]. In addition, HFNC is well tolerated by patients [4,5]. Therefore, HFNC may have a potential role in the management of AECOPD patients, and several studies investigated the use of HFNC in this population as an alternative to NIV or to COT.

3.1. HFNC Settings in AECOPD Patients

Settings for HFNC are quite heterogeneous among all studies. Generally speaking, it would be preferred to set a flow between 35 and 60 L/min and titrate as much as tolerated by the patient. In addition, the temperature of the gas flow should be set between 34 and 37 °C, according to the patient’s tolerance. In the end, the FiO2 should be adjusted in order to obtain a SpO2 between 88 and 92% [55].

3.2. HFNC as an Alternative to NIV

Based on the aforementioned mechanisms, HFNC was used to test AECOPD patients as an alternative to NIV as first-line treatment in case of respiratory acidosis or after extubation.
The first applications in this sense were reported as case reports [56,57,58] or series [59]. In these reports, the alternative use of HFNC was deemed to be poor tolerance of the NIV interface [56,57,59] or had massive unmanageable air leaks [58], and it was successful with respect to both gas exchange and tolerance [56,57,58,59]. More recently, some prospective randomized controlled trials were published.
Cong et al. randomized 168 AECOPD patients with respiratory acidosis to receive NIV or HFNC as first-line treatment [60]. Both treatments improved gas exchanges in a similar fashion after 12 h and 5 days of treatment. In addition, the time spent under respiratory support and the hospital length of stay was similar between treatment, although HFNC guaranteed fewer complications and it was more comfortable as compared to NIV [60].
Cortegiani et al. designed a multicenter randomized controlled trial to assess the noninferiority of HFNC compared to NIV with respect to the reduction in PaCO2 in AECOPD patients with mild-to-moderate respiratory acidosis [61]. The trial randomized 80 patients; HFNC was found to be non-inferior to NIV with respect to PaCO2. However, it should be mentioned that one-third of the patients in the HFNC group were switched to NIV within 6 h from randomization mainly because of lack of gas exchange improvement [62].
Doshi et al. conducted a subgroup analysis from a randomized controlled trial to compare HFNC and NIV in AECOPD patients with respect to gas exchange [63]. The authors reported that gas exchange, ICU and total length of stay and treatment failure (i.e., intubation rate and need to switch to other treatment) were similar between HFNC and NIV [63].
The recent European Respiratory Society Guidelines still suggest firstly attempting NIV in AECOPD patients since the existing evidence is large and strong; however, if NIV fails due to poor tolerance and gas exchange are not worsening, HFNC may be attempted [55].
HFNC was also compared to NIV after extubation of COPD patients recovering from an episode of exacerbation. Zhang et al. randomized all intubated AECOPD patients admitted in the ICU to receive NIV or HFNC at extubation [64]. The authors reported that HFNC reduced the ICU length of stay; however, no differences were recorded between HFNC and NIV in terms of gas exchange, 28 days reintubation rate and mortality [64]. In 42 AECOPD patients randomized to receive NIV or HFNC after extubation, Jing et al. also reported no differences between HFNC and NIV with regard to gas exchange, vital signs and some major clinical outcomes (i.e., the time spent under iMV, need for reintubation, ICU length of stay and cause of 28 days mortality) [34].

3.3. HFNC as an Alternative to COT

In AECOPD patients, HFNC was also compared to COT as first-line oxygen treatment in the absence of respiratory acidosis, at NIV discontinuation or after extubation.
In AECOPD patients without respiratory acidosis, Kim et al. firstly demonstrated that PaCO2 significantly decreased after 1 h of HFNC applied as first-line treatment [65]. In keeping with Kim et al. [65], Pilcher et al. also showed that the application of HFNC at 35 L/min reduced the transcutaneous CO2 tension in 24 exacerbated COPD patients, as opposed to COT via nasal prongs [52].
Our group randomized 30 COPD patients recovering from an episode of severe exacerbation to receive HFNC and COT during NIV breaks [20]. HFNC and COT guaranteed similar gas exchange, although the activation of the diaphragm and respiratory rate was significantly higher during COT, as compared to both HFNC and NIV. On the opposite, HFNC and NIV were similar. In a post hoc analysis, we also found that the need to reinstitute NIV at discontinuation was lower with HFNC (27%) as compared to COT (47%) [20].
Finally, Di Mussi et al. demonstrated randomized 14 COPD patients recovering from an exacerbation episode to receive HFNC or COT after extubation [19]. In this context, HFNC was superior to COT since it significantly reduces the work of breathing and the respiratory drive [19].

4. Discussion

The evidence supporting the use of HFNC is increasing in patients with hypoxemic ARF or after extubation, whereas data on AECOPD are still weak [55]. The recent guidelines suggest a trial of NIV prior to the use of HFNC in the case of AECOPD with respiratory acidosis [55]. Indeed, the literature recommends the application of NIV in AECOPD patients with respiratory acidosis [2], whereas the certainty of the evidence for mortality and intubation in favor of HFNC is low, mainly due to imprecision and heterogeneity among trials [55]. However, HFNC may have a role in this population.
Figure 1 proposes a clinical flowchart of possible uses of HFNC and approaches to AECOPD in varying settings and timing, based on the current literature. If an AECOPD patient is admitted to the hospital, an arterial blood gas analysis is required to define the presence of respiratory acidosis. If ARF is characterized by hypoxemia without respiratory acidosis, HFNC might be preferred over COT. Clinicians every time should consider that an exacerbation without acidosis may precipitate due to the increased resistive load (i.e., bronchospasm, increased secretion volume. If respiratory acidosis occurs, NIV must be instituted, and an NIV trial must be attempted. At this point, three scenarios may occur: (1) if gas exchange and/or clinical condition improve, the patient can be weaned applying HFNC at NIV interruption; (2) if the patient does not tolerate NIV and gas exchange and/or clinical condition do not deteriorate, HFNC may be used as an alternative to NIV; (3) if gas exchange and/or clinical condition further impair, the physician should consider indications for intubation and iMV. Finally, when an intubated AECOPD patient is ready for a weaning attempt from iMV, NIV is recommended at extubation to facilitate the weaning process and to prevent the occurrence of post-extubation respiratory failure. At NIV interruption, HFNC should be again preferred over COT.
NIV is affected by some drawbacks leading to patients’ intolerance and treatment failure. Factors associated with intolerance are multiple. NIV is commonly applied in pneumatically-triggered and cycled-off Pressure Support mode through a face mask [66]. The intolerance to the interface and poor patient–ventilator interaction and synchrony are major factors leading to NIV failure [36,39,41,43]. Some strategies to reduce these drawbacks are: (1) the application of interfaces such as the helmet [35,51,67,68,69], associated with a rotating strategy [40,70,71]; (2) the use of proportional modes of ventilation, i.e., the Neurally Adjusted Ventilatory Assist (NAVA) [47], with specific settings to improve pressurization and to trigger performance [37,41,43].
Despite these tricks, NIV may encounter failure due to poor comfort and patient tolerance. In this scenario, HFNC plays its role as an alternative treatment for AECOPD patients [55]. It should be strengthened that HFNC could be applied only in case of NIV intolerance [56,57,58,59], and if the gas exchange or clinical conditions are not worsening, otherwise intubation should be considered [2].
HFNC can also be used as an alternative to COT, either in AECOPD without respiratory acidosis or during NIV interruptions when the patients are recovering from the exacerbation episode. In these cases, HFNC has the advantage of being more comfortable than COT, to humidify the airways to facilitate expectoration of the mucus [20] and to wash out the dead pharyngeal space, reducing the respiratory drive [19,20]. A recent systematic review and meta-analysis further highlighted the physiological advantages of HFNC over COT in AECOPD. In particular, HFNC reduces the respiratory rate and effort as opposed to COT, although the evidence is low [72].
Currently, NIV is also suggested as a strategy to facilitate weaning from iMV in patients with hypercapnic respiratory failure [2]. The literature indicates that the use of NIV after extubation to facilitate weaning reduces mortality, the rate of weaning failure and the incidence of ventilator-associated pneumonia [2]. However, if NIV cannot be used or is problematic, HFNC may be used after extubation [19,34,64].

5. Conclusions

HFNC is a valuable tool in the management of AECOPD patients, as an alternative to NIV in case of intolerance, at NIV interruption, after extubation and as oxygen therapy instead of COT. Further large trials are required to strengthen the evidence for their application in this population.

Author Contributions

A.B., E.G. and F.L. participated in the conception and study design. All authors were responsible for the acquisition, analysis and/or interpretation of the data. All authors participated in the manuscript draft and revised it for important intellectual content. They also approved the final manuscript version and accounted for all aspects of the work, ensuring that questions related to the accuracy and integrity of any part of the study were appropriately investigated and resolved. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

Federico Longhini received honoraria/speaking fees from Fisher and Paykel, Draeger and Intersurgical. Federico Longhini contributed to the development of a new device not discussed in the present study (European Patent number 3320941 released on 5 August 2020), and he is designed as inventor. The remaining authors have no conflict of interest to disclose.

References

  1. Vogelmeier, C.F.; Criner, G.J.; Martinez, F.J.; Anzueto, A.; Barnes, P.J.; Bourbeau, J.; Celli, B.R.; Chen, R.; Decramer, M.; Fabbri, L.M.; et al. Global strategy for the diagnosis, management, and prevention of chronic obstructive lung disease 2017 report: Gold executive summary. Eur. Respir. J. 2017, 49, 557–582. [Google Scholar] [CrossRef] [PubMed]
  2. Rochwerg, B.; Brochard, L.; Elliott, M.W.; Hess, D.; Hill, N.S.; Nava, S.; Navalesi, P.; Antonelli, M.; Brozek, J.; Conti, G.; et al. Official ers/ats clinical practice guidelines: Noninvasive ventilation for acute respiratory failure. Eur. Respir. J. 2017, 50, 1602426. [Google Scholar] [CrossRef] [PubMed]
  3. Squadrone, E.; Frigerio, P.; Fogliati, C.; Gregoretti, C.; Conti, G.; Antonelli, M.; Costa, R.; Baiardi, P.; Navalesi, P. Noninvasive vs invasive ventilation in copd patients with severe acute respiratory failure deemed to require ventilatory assistance. Intensive Care Med. 2004, 30, 1303–1310. [Google Scholar] [CrossRef] [PubMed]
  4. Pisani, L.; Astuto, M.; Prediletto, I.; Longhini, F. High flow through nasal cannula in exacerbated copd patients: A systematic review. Pulmonology 2019, 25, 348–354. [Google Scholar] [CrossRef] [PubMed]
  5. Bruni, A.; Garofalo, E.; Cammarota, G.; Murabito, P.; Astuto, M.; Navalesi, P.; Luzza, F.; Abenavoli, L.; Longhini, F. High flow through nasal cannula in stable and exacerbated chronic obstructive pulmonary disease patients. Rev. Recent Clin. Trials 2019, 14, 247–260. [Google Scholar] [CrossRef]
  6. Renda, T.; Corrado, A.; Iskandar, G.; Pelaia, G.; Abdalla, K.; Navalesi, P. High-flow nasal oxygen therapy in intensive care and anaesthesia. Br. J. Anaesth. 2018, 120, 18–27. [Google Scholar] [CrossRef] [PubMed]
  7. Pisani, L.; Vega, M.L. Use of nasal high flow in stable copd: Rationale and physiology. COPD J. Chronic Obstr. Pulm. Dis. 2017, 14, 346–350. [Google Scholar] [CrossRef] [PubMed]
  8. Plotnikow, G.A.; Accoce, M.; Navarro, E.; Tiribelli, N. Humidification and heating of inhaled gas in patients with artificial airway. A narrative review. Rev. Bras. Ter. Intensiva 2018, 30, 86–97. [Google Scholar] [CrossRef] [PubMed]
  9. Konrad, F.; Schiener, R.; Marx, T.; Georgieff, M. Ultrastructure and mucociliary transport of bronchial respiratory epithelium in intubated patients. Intensive Care Med. 1995, 21, 482–489. [Google Scholar] [CrossRef] [PubMed]
  10. Lacherade, J.C.; Auburtin, M.; Cerf, C.; Van de Louw, A.; Soufir, L.; Rebufat, Y.; Rezaiguia, S.; Ricard, J.D.; Lellouche, F.; Brun-Buisson, C.; et al. Impact of humidification systems on ventilator-associated pneumonia: A randomized multicenter trial. Am. J. Respir. Crit. Care Med. 2005, 172, 1276–1282. [Google Scholar] [CrossRef]
  11. De Pascale, G.; Ranzani, O.T.; Nseir, S.; Chastre, J.; Welte, T.; Antonelli, M.; Navalesi, P.; Garofalo, E.; Bruni, A.; Coelho, L.M.; et al. Intensive care unit patients with lower respiratory tract nosocomial infections: The enirris project. ERJ Open Res. 2017, 3, 00092-2017. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Jiang, M.; Song, J.J.; Guo, X.L.; Tang, Y.L.; Li, H.B. Airway humidification reduces the inflammatory response during mechanical ventilation. Respir. Care 2015, 60, 1720–1728. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  13. Hasani, A.; Chapman, T.H.; McCool, D.; Smith, R.E.; Dilworth, J.P.; Agnew, J.E. Domiciliary humidification improves lung mucociliary clearance in patients with bronchiectasis. Chron. Respir. Dis. 2008, 5, 81–86. [Google Scholar] [CrossRef] [PubMed]
  14. Rea, H.; McAuley, S.; Jayaram, L.; Garrett, J.; Hockey, H.; Storey, L.; O’Donnell, G.; Haru, L.; Payton, M.; O’Donnell, K. The clinical utility of long-term humidification therapy in chronic airway disease. Respir. Med. 2010, 104, 525–533. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  15. Moller, W.; Celik, G.; Feng, S.; Bartenstein, P.; Meyer, G.; Eickelberg, O.; Schmid, O.; Tatkov, S. Nasal high flow clears anatomical dead space in upper airway models. J. Appl. Physiol. 2015, 118, 1525–1532. [Google Scholar] [CrossRef] [PubMed]
  16. Jiang, Y.; Liang, Y.; Kacmarek, R.M. The principle of upper airway unidirectional flow facilitates breathing in humans. J. Appl. Physiol. 2008, 105, 854–858. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Elbehairy, A.F.; Ciavaglia, C.E.; Webb, K.A.; Guenette, J.A.; Jensen, D.; Mourad, S.M.; Neder, J.A.; O’Donnell, D.E. Pulmonary gas exchange abnormalities in mild chronic obstructive pulmonary disease. Implications for dyspnea and exercise intolerance. Am. J. Respir. Crit. Care Med. 2015, 191, 1384–1394. [Google Scholar] [CrossRef]
  18. Braunlich, J.; Seyfarth, H.J.; Wirtz, H. Nasal high-flow versus non-invasive ventilation in stable hypercapnic copd: A preliminary report. Multidiscip. Respir. Med. 2015, 10, 27. [Google Scholar] [CrossRef] [Green Version]
  19. Di Mussi, R.; Spadaro, S.; Stripoli, T.; Volta, C.A.; Trerotoli, P.; Pierucci, P.; Staffieri, F.; Bruno, F.; Camporota, L.; Grasso, S. High-flow nasal cannula oxygen therapy decreases postextubation neuroventilatory drive and work of breathing in patients with chronic obstructive pulmonary disease. Crit. Care 2018, 22, 180. [Google Scholar] [CrossRef] [Green Version]
  20. Longhini, F.; Pisani, L.; Lungu, R.; Comellini, V.; Bruni, A.; Garofalo, E.; Laura Vega, M.; Cammarota, G.; Nava, S.; Navalesi, P. High-flow oxygen therapy after noninvasive ventilation interruption in patients recovering from hypercapnic acute respiratory failure: A physiological crossover trial. Crit. Care Med. 2019, 47, e506–e511. [Google Scholar] [CrossRef]
  21. Ritchie, J.E.; Williams, A.B.; Gerard, C.; Hockey, H. Evaluation of a humidified nasal high-flow oxygen system, using oxygraphy, capnography and measurement of upper airway pressures. Anaesth. Intensive Care 2011, 39, 1103–1110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Groves, N.; Tobin, A. High flow nasal oxygen generates positive airway pressure in adult volunteers. Aust. Crit. Care 2007, 20, 126–131. [Google Scholar] [CrossRef] [PubMed]
  23. Garofalo, E.; Bruni, A.; Pelaia, C.; Cammarota, G.; Murabito, P.; Biamonte, E.; Abdalla, K.; Longhini, F.; Navalesi, P. Evaluation of a new interface combining high-flow nasal cannula and cpap. Respir. Care 2019, 64, 1231–1239. [Google Scholar] [CrossRef] [PubMed]
  24. Braunlich, J.; Beyer, D.; Mai, D.; Hammerschmidt, S.; Seyfarth, H.J.; Wirtz, H. Effects of nasal high flow on ventilation in volunteers, copd and idiopathic pulmonary fibrosis patients. Respiration 2013, 85, 319–325. [Google Scholar] [CrossRef] [PubMed]
  25. Parke, R.L.; Eccleston, M.L.; McGuinness, S.P. The effects of flow on airway pressure during nasal high-flow oxygen therapy. Respir. Care 2011, 56, 1151–1155. [Google Scholar] [CrossRef] [PubMed]
  26. Dysart, K.; Miller, T.L.; Wolfson, M.R.; Shaffer, T.H. Research in high flow therapy: Mechanisms of action. Respir. Med. 2009, 103, 1400–1405. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  27. Mundel, T.; Feng, S.; Tatkov, S.; Schneider, H. Mechanisms of nasal high flow on ventilation during wakefulness and sleep. J. Appl. Physiol. 2013, 114, 1058–1065. [Google Scholar] [CrossRef] [PubMed]
  28. Appendini, L.; Patessio, A.; Zanaboni, S.; Carone, M.; Gukov, B.; Donner, C.F.; Rossi, A. Physiologic effects of positive end-expiratory pressure and mask pressure support during exacerbations of chronic obstructive pulmonary disease. Am. J. Respir. Crit. Care Med. 1994, 149, 1069–1076. [Google Scholar] [CrossRef]
  29. Pisani, L.; Fasano, L.; Corcione, N.; Comellini, V.; Musti, M.A.; Brandao, M.; Bottone, D.; Calderini, E.; Navalesi, P.; Nava, S. Change in pulmonary mechanics and the effect on breathing pattern of high flow oxygen therapy in stable hypercapnic copd. Thorax 2017, 72, 373–375. [Google Scholar] [CrossRef] [Green Version]
  30. Maggiore, S.M.; Idone, F.A.; Vaschetto, R.; Festa, R.; Cataldo, A.; Antonicelli, F.; Montini, L.; De Gaetano, A.; Navalesi, P.; Antonelli, M. Nasal high-flow versus venturi mask oxygen therapy after extubation. Effects on oxygenation, comfort, and clinical outcome. Am. J. Respir. Crit. Care Med. 2014, 190, 282–288. [Google Scholar] [CrossRef]
  31. Sharma, G.; Mahler, D.A.; Mayorga, V.M.; Deering, K.L.; Harshaw, O.; Ganapathy, V. Prevalence of low peak inspiratory flow rate at discharge in patients hospitalized for copd exacerbation. Chronic Obstr. Pulm. Dis. 2017, 4, 217–224. [Google Scholar] [CrossRef] [PubMed]
  32. Elliott, M.W. The interface: Crucial for successful noninvasive ventilation. Eur. Respir. J. 2004, 23, 7–8. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Lellouche, F.; Maggiore, S.M.; Lyazidi, A.; Deye, N.; Taille, S.; Brochard, L. Water content of delivered gases during non-invasive ventilation in healthy subjects. Intensive Care Med. 2009, 35, 987–995. [Google Scholar] [CrossRef] [PubMed]
  34. Jing, G.; Li, J.; Hao, D.; Wang, T.; Sun, Y.; Tian, H.; Fu, Z.; Zhang, Y.; Wang, X. Comparison of high flow nasal cannula with noninvasive ventilation in chronic obstructive pulmonary disease patients with hypercapnia in preventing postextubation respiratory failure: A pilot randomized controlled trial. Res. Nurs. Health 2019, 42, 217–225. [Google Scholar] [CrossRef] [PubMed]
  35. Navalesi, P.; Costa, R.; Ceriana, P.; Carlucci, A.; Prinianakis, G.; Antonelli, M.; Conti, G.; Nava, S. Non-invasive ventilation in chronic obstructive pulmonary disease patients: Helmet versus facial mask. Intensive Care Med. 2007, 33, 74–81. [Google Scholar] [CrossRef] [PubMed]
  36. Bruni, A.; Garofalo, E.; Pelaia, C.; Messina, A.; Cammarota, G.; Murabito, P.; Corrado, S.; Vetrugno, L.; Longhini, F.; Navalesi, P. Patient-ventilator asynchrony in adult critically ill patients. Minerva Anestesiol. 2019, 85, 676–688. [Google Scholar] [CrossRef]
  37. Longhini, F.; Liu, L.; Pan, C.; Xie, J.; Cammarota, G.; Bruni, A.; Garofalo, E.; Yang, Y.; Navalesi, P.; Qiu, H. Neurally-adjusted ventilatory assist for noninvasive ventilation via a helmet in subjects with copd exacerbation: A physiologic study. Respir. Care 2019, 64, 582–589. [Google Scholar] [CrossRef]
  38. Cortegiani, A.; Garofalo, E.; Bruni, A.; Sanfilippo, F.; Longhini, F. Predatory open-access publishing in palliative and supportive care. J. Pain Symptom Manage. 2019, 57, e1–e3. [Google Scholar] [CrossRef]
  39. Garofalo, E.; Bruni, A.; Pelaia, C.; Liparota, L.; Lombardo, N.; Longhini, F.; Navalesi, P. Recognizing, quantifying and managing patient-ventilator asynchrony in invasive and noninvasive ventilation. Expert Rev. Respir. Med. 2018, 12, 557–567. [Google Scholar] [CrossRef]
  40. Vaschetto, R.; Longhini, F.; Persona, P.; Ori, C.; Stefani, G.; Liu, S.; Yi, Y.; Lu, W.; Yu, T.; Luo, X.; et al. Early extubation followed by immediate noninvasive ventilation vs. Standard extubation in hypoxemic patients: A randomized clinical trial. Intensive Care Med. 2019, 45, 62–71. [Google Scholar] [CrossRef]
  41. Longhini, F.; Pan, C.; Xie, J.; Cammarota, G.; Bruni, A.; Garofalo, E.; Yang, Y.; Navalesi, P.; Qiu, H. New setting of neurally adjusted ventilatory assist for noninvasive ventilation by facial mask: A physiologic study. Crit. Care 2017, 21, 170. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Longhini, F.; Abdalla, K.; Navalesi, P. Non-invasive ventilation in hypoxemic patients: Does the interface make a difference? Ann. Transl. Med. 2016, 4, 359. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Cammarota, G.; Longhini, F.; Perucca, R.; Ronco, C.; Colombo, D.; Messina, A.; Vaschetto, R.; Navalesi, P. New setting of neurally adjusted ventilatory assist during noninvasive ventilation through a helmet. Anesthesiology 2016, 125, 1181–1189. [Google Scholar] [CrossRef] [PubMed]
  44. Costa, R.; Navalesi, P.; Cammarota, G.; Longhini, F.; Spinazzola, G.; Cipriani, F.; Ferrone, G.; Festa, O.; Antonelli, M.; Conti, G. Remifentanil effects on respiratory drive and timing during pressure support ventilation and neurally adjusted ventilatory assist. Respir. Physiol. Neurobiol. 2017, 244, 10–16. [Google Scholar] [CrossRef] [PubMed]
  45. Liu, L.; Xia, F.; Yang, Y.; Longhini, F.; Navalesi, P.; Beck, J.; Sinderby, C.; Qiu, H. Neural versus pneumatic control of pressure support in patients with chronic obstructive pulmonary diseases at different levels of positive end expiratory pressure: A physiological study. Crit. Care 2015, 19, 244. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Longhini, F.; Scarlino, S.; Gallina, M.R.; Monzani, A.; De Franco, S.; Grassino, E.C.; Bona, G.; Ferrero, F. Comparison of neurally-adjusted ventilator assist in infants before and after extubation. Minerva Pediatr. 2018, 70, 133–140. [Google Scholar] [CrossRef] [PubMed]
  47. Navalesi, P.; Longhini, F. Neurally adjusted ventilatory assist. Curr. Opin. Crit. Care 2015, 21, 58–64. [Google Scholar] [CrossRef] [PubMed]
  48. Vaschetto, R.; Cammarota, G.; Colombo, D.; Longhini, F.; Grossi, F.; Giovanniello, A.; Della Corte, F.; Navalesi, P. Effects of propofol on patient-ventilator synchrony and interaction during pressure support ventilation and neurally adjusted ventilatory assist. Crit. Care Med. 2014, 42, 74–82. [Google Scholar] [CrossRef]
  49. Cammarota, G.; Olivieri, C.; Costa, R.; Vaschetto, R.; Colombo, D.; Turucz, E.; Longhini, F.; Della Corte, F.; Conti, G.; Navalesi, P. Noninvasive ventilation through a helmet in postextubation hypoxemic patients: Physiologic comparison between neurally adjusted ventilatory assist and pressure support ventilation. Intensive Care Med. 2011, 37, 1943–1950. [Google Scholar] [CrossRef]
  50. Longhini, F.; Colombo, D.; Pisani, L.; Idone, F.; Chun, P.; Doorduin, J.; Ling, L.; Alemani, M.; Bruni, A.; Zhaochen, J.; et al. Efficacy of ventilator waveform observation for detection of patient-ventilator asynchrony during niv: A multicentre study. ERJ Open Res. 2017, 3, 00075–02017. [Google Scholar] [CrossRef] [Green Version]
  51. Olivieri, C.; Longhini, F.; Cena, T.; Cammarota, G.; Vaschetto, R.; Messina, A.; Berni, P.; Magnani, C.; Della Corte, F.; Navalesi, P. New versus conventional helmet for delivering noninvasive ventilation: A physiologic, crossover randomized study in critically ill patients. Anesthesiology 2016, 124, 101–108. [Google Scholar] [CrossRef] [PubMed]
  52. Pilcher, J.; Eastlake, L.; Richards, M.; Power, S.; Cripps, T.; Bibby, S.; Braithwaite, I.; Weatherall, M.; Beasley, R. Physiological effects of titrated oxygen via nasal high-flow cannulae in copd exacerbations: A randomized controlled cross-over trial. Respirology 2017, 22, 1149–1155. [Google Scholar] [CrossRef] [PubMed]
  53. Braunlich, J.; Wirtz, H. Nasal high-flow in acute hypercapnic exacerbation of copd. Int. J. Chron. Obstruct. Pulmon. Dis. 2018, 13, 3895–3897. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Rittayamai, N.; Phuangchoei, P.; Tscheikuna, J.; Praphruetkit, N.; Brochard, L. Effects of high-flow nasal cannula and non-invasive ventilation on inspiratory effort in hypercapnic patients with chronic obstructive pulmonary disease: A preliminary study. Ann. Intensive Care 2019, 9, 122. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  55. Oczkowski, S.; Ergan, B.; Bos, L.; Chatwin, M.; Ferrer, M.; Gregoretti, C.; Heunks, L.; Frat, J.P.; Longhini, F.; Nava, S.; et al. Ers clinical practice guidelines: High-flow nasal cannula in acute respiratory failure. Eur. Respir. J. 2021, 53, 2101574. [Google Scholar] [CrossRef]
  56. Okuda, M.; Kashio, M.; Tanaka, N.; Matsumoto, T.; Ishihara, S.; Nozoe, T.; Fujii, T.; Okuda, Y.; Kawahara, T.; Miyata, K. Nasal high-flow oxygen therapy system for improving sleep-related hypoventilation in chronic obstructive pulmonary disease: A case report. J. Med. Case Rep. 2014, 8, 341. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Lepere, V.; Messika, J.; La Combe, B.; Ricard, J.D. High-flow nasal cannula oxygen supply as treatment in hypercapnic respiratory failure. Am. J. Emerg. Med. 2016, 34, 1914.e1–1914.e2. [Google Scholar] [CrossRef] [PubMed]
  58. Plotnikow, G.; Thille, A.W.; Vasquez, D.; Pratto, R.; Desmery, P. High-flow nasal cannula oxygen for reverting severe acute exacerbation of chronic obstructive pulmonary disease: A case report. Med. Intensiva 2017, 41, 571–572. [Google Scholar] [CrossRef]
  59. Pavlov, I.; Plamondon, P.; Delisle, S. Nasal high-flow therapy for type ii respiratory failure in copd: A report of four cases. Respir. Med. Case Rep. 2017, 20, 87–88. [Google Scholar] [CrossRef]
  60. Cong, L.; Zhou, L.; Liu, H.; Wang, J. Outcomes of high-flow nasal cannnula versus non-invasive positive pressure ventilation for patients with acute exacerbations of chronic obstructive pulmonary disease. Int. J. Clin. Exp. Med. 2019, 12, 10863–10867. [Google Scholar]
  61. Cortegiani, A.; Longhini, F.; Carlucci, A.; Scala, R.; Groff, P.; Bruni, A.; Garofalo, E.; Taliani, M.R.; Maccari, U.; Vetrugno, L.; et al. High-flow nasal therapy versus noninvasive ventilation in copd patients with mild-to-moderate hypercapnic acute respiratory failure: Study protocol for a noninferiority randomized clinical trial. Trials 2019, 20, 450. [Google Scholar] [CrossRef] [PubMed]
  62. Cortegiani, A.; Longhini, F.; Madotto, F.; Groff, P.; Scala, R.; Crimi, C.; Carlucci, A.; Bruni, A.; Garofalo, E.; Raineri, S.M.; et al. High flow nasal therapy versus noninvasive ventilation as initial ventilatory strategy in copd exacerbation: A multicenter non-inferiority randomized trial. Crit. Care 2020, 24, 692. [Google Scholar] [CrossRef] [PubMed]
  63. Doshi, P.B.; Whittle, J.S.; Dungan, G., 2nd; Volakis, L.I.; Bublewicz, M.; Kearney, J.; Miller, T.L.; Dodge, D.; Harsch, M.R.; DeBellis, R.; et al. The ventilatory effect of high velocity nasal insufflation compared to non-invasive positive-pressure ventilation in the treatment of hypercapneic respiratory failure: A subgroup analysis. Heart Lung 2020, 49, 610–615. [Google Scholar] [CrossRef] [PubMed]
  64. Zhang, J.C.; Wu, F.X.; Meng, L.L.; Zeng, C.Y.; Lu, Y.Q. A study on the effects and safety of sequential humidified high flow nasal cannula oxygenation therapy on the copd patients after extubation. Zhonghua Yi Xue Za Zhi 2018, 98, 109–112. [Google Scholar] [PubMed]
  65. Kim, E.S.; Lee, H.; Kim, S.J.; Park, J.; Lee, Y.J.; Park, J.S.; Yoon, H.I.; Lee, J.H.; Lee, C.T.; Cho, Y.J. Effectiveness of high-flow nasal cannula oxygen therapy for acute respiratory failure with hypercapnia. J. Thorac. Dis. 2018, 10, 882–888. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Crimi, C.; Noto, A.; Princi, P.; Esquinas, A.; Nava, S. A european survey of noninvasive ventilation practices. Eur. Respir. J. 2010, 36, 362–369. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  67. Olivieri, C.; Costa, R.; Spinazzola, G.; Ferrone, G.; Longhini, F.; Cammarota, G.; Conti, G.; Navalesi, P. Bench comparative evaluation of a new generation and standard helmet for delivering non-invasive ventilation. Intensive Care Med. 2013, 39, 734–738. [Google Scholar] [CrossRef] [PubMed]
  68. Vaschetto, R.; De Jong, A.; Conseil, M.; Galia, F.; Mahul, M.; Coisel, Y.; Prades, A.; Navalesi, P.; Jaber, S. Comparative evaluation of three interfaces for non-invasive ventilation: A randomized cross-over design physiologic study on healthy volunteers. Crit. Care 2014, 18, R2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Pisani, L.; Mega, C.; Vaschetto, R.; Bellone, A.; Scala, R.; Cosentini, R.; Musti, M.; Del Forno, M.; Grassi, M.; Fasano, L.; et al. Oronasal mask versus helmet in acute hypercapnic respiratory failure. Eur. Respir. J. 2015, 45, 691–699. [Google Scholar] [CrossRef] [Green Version]
  70. Antonelli, M.; Conti, G.; Pelosi, P.; Gregoretti, C.; Pennisi, M.A.; Costa, R.; Severgnini, P.; Chiaranda, M.; Proietti, R. New treatment of acute hypoxemic respiratory failure: Noninvasive pressure support ventilation delivered by helmet—A pilot controlled trial. Crit. Care Med. 2002, 30, 602–608. [Google Scholar] [CrossRef]
  71. Patel, B.K.; Wolfe, K.S.; Pohlman, A.S.; Hall, J.B.; Kress, J.P. Effect of noninvasive ventilation delivered by helmet vs face mask on the rate of endotracheal intubation in patients with acute respiratory distress syndrome: A randomized clinical trial. JAMA 2016, 315, 2435–2441. [Google Scholar] [CrossRef] [PubMed]
  72. Yang, P.L.; Yu, J.Q.; Chen, H.B. High-flow nasal cannula for acute exacerbation of chronic obstructive pulmonary disease: A systematic review and meta-analysis. Heart Lung 2021, 50, 252–261. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flowchart of possible use of HFNC in AECOPD patients. * if clinical conditions and gas exchange are not deteriorating. AECOPD, Acute Exacerbation of Chronic Obstructive Pulmonary Disease; NIV, Non-Invasive Ventilation; HFNC, High Flow through Nasal Cannula.
Figure 1. Flowchart of possible use of HFNC in AECOPD patients. * if clinical conditions and gas exchange are not deteriorating. AECOPD, Acute Exacerbation of Chronic Obstructive Pulmonary Disease; NIV, Non-Invasive Ventilation; HFNC, High Flow through Nasal Cannula.
Healthcare 10 00536 g001
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Bruni, A.; Garofalo, E.; Procopio, D.; Corrado, S.; Caroleo, A.; Biamonte, E.; Pelaia, C.; Longhini, F. Current Practice of High Flow through Nasal Cannula in Exacerbated COPD Patients. Healthcare 2022, 10, 536. https://doi.org/10.3390/healthcare10030536

AMA Style

Bruni A, Garofalo E, Procopio D, Corrado S, Caroleo A, Biamonte E, Pelaia C, Longhini F. Current Practice of High Flow through Nasal Cannula in Exacerbated COPD Patients. Healthcare. 2022; 10(3):536. https://doi.org/10.3390/healthcare10030536

Chicago/Turabian Style

Bruni, Andrea, Eugenio Garofalo, Daniela Procopio, Silvia Corrado, Antonio Caroleo, Eugenio Biamonte, Corrado Pelaia, and Federico Longhini. 2022. "Current Practice of High Flow through Nasal Cannula in Exacerbated COPD Patients" Healthcare 10, no. 3: 536. https://doi.org/10.3390/healthcare10030536

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop