Skip to main content
Download PDF

Current evidence for the effectiveness of heated and humidified high flow nasal cannula supportive therapy in adult patients with respiratory failure

Critical Care volume 20, Article number: 109 (2016) Cite this article

Abstract

High flow nasal cannula (HFNC) supportive therapy has emerged as a safe, useful therapy in patients with respiratory failure, improving oxygenation and comfort. Recently several clinical trials have analyzed the effectiveness of HFNC therapy in different clinical situations and have reported promising results. Here we review the current knowledge about HFNC therapy, from its mechanisms of action to its effects on outcomes in different clinical situations.

Background

Oxygen therapy is the main supportive treatment in hypoxemic respiratory failure and has traditionally been delivered using nasal prongs or masks. However, the maximal flow rates that these devices can deliver are limited because of the insufficient heat and humidity provided to the gas administered. It is accepted that flows up to 15 L/min can be delivered using conventional nasal prongs or masks, but this flow is far lower than the inspiratory flow of a patient with acute respiratory failure (ARF). Therefore, room air dilutes the supplemental oxygen, resulting in a significant decrease in the fraction of the inspired oxygen (FIO2) that finally reaches the alveoli.

In recent years, new devices that deliver totally conditioned gas through a nasal cannula at very high flow (up to 60 L/min) have emerged as a safe and useful supportive therapy in many clinical situations. High flow nasal cannula (HFNC) supportive therapy is one such technique that exerts its potential benefits through a variety of mechanisms. Here, we present a clinical review of the current knowledge of HFNC, from its mechanisms of action to its clinical indications in adult patients, and suggest future areas for research.

In the literature this treatment strategy has been variously described as nasal high flow and high flow oxygen therapy, but we believe that the most appropriate term is heated and humidified HFNC supportive therapy. This term reflects the features that generate the technique’s clinical effects (i.e., the delivery of warm and humidified air at high flows through a nasal cannula). Several HFNC devices are commercially available, but the technique always involves the delivery of a totally conditioned (37 °C containing 44 mg H2O/L [100 % relative humidity]) gas admixture via a wide bore and soft nasal prong at up to 60 L/min, with a fraction of inspired oxygen ranging from 0.21 to 1. In this study we also review the main clinical effects of HFNC therapy and how they are generated.

Clinical effects and mechanisms of action

Oxygenation improvement

Several mechanisms are known to contribute to oxygenation improvement, which is one of the main potential benefits of using HFNC therapy. However, the exact contributions of each mechanism have not been conclusively established and these may, in fact, vary from one patient to another.

Lower dilution of the administered gas with room air

During normal and quiet breathing, the peak inspiratory flow rate is around 30–40 L/min. During heavy workloads, a situation comparable with ARF, mean flow rates rise to more than 70 L/min [1]. Therefore, the peak inspiratory flow rate of ARF patients exceeds the flow rates supplemented by conventional oxygen devices, leading to a dilution of the gas administered and reducing the amount of oxygen that finally reaches the alveoli. Although the degree of dilution with room air depends on the mismatch between the flow administered and the patient’s inspiratory flow, it is much lower with a HFNC than with conventional oxygen devices. Thus, with the aim of reducing the entrainment of room air, it seems reasonable to try to match the flow rate of the HFNC with the patient’s peak inspiratory flow in order to maintain the FIO2 constant [2].

Positive end expiratory pressure effect

Another significant mechanism is the generation of a certain degree of positive airway pressure due to the resistance generated by the continuous administration of a high flow of gas [3–7]. In healthy volunteers breathing with their mouths closed, this pressure level may reach 12 cm of H2O at a provided flow of 100 L/min [5, 7] and it reaches its maximum at the end of expiration [3]. In a population of healthy volunteers, expiratory pressures with the mouth closed were higher than those with the mouth open at any given flow rate [5, 7]. Similarly, in ICU patients breathing with their mouths open and scheduled for weaning from mechanical ventilation, mean tracheal pressures dropped to 2 cm of H2O [8]. Therefore, major differences in the airway pressure achieved may be observed depending on the amount of flow delivered (the higher the flow, the higher the pressure), the type of breathing (with a significantly lower pressure in mouth breathers), the moment of the respiratory cycle, and the degree of respiratory failure. Electroimpedance tomography has been used to measure changes in bioimpedance caused by different lung conditions, especially those related to regional ventilation and it has been shown that variations in end-expiratory lung impedance correlate with changes in end-expiratory lung volume [9]. It has also been shown that HFNC therapy increases end-expiratory lung impedance [5, 10, 11] and is strongly correlated with airway pressure [10].

Dead space wash-out

It has been hypothesized that the continuous administration of a very high flow of gas flushes the carbon dioxide (CO2) out of the upper respiratory airway, avoiding the re-inhalation of the previous exhaled gas [12]. Although dead space was not measured, a recent in vitro experimental study using a silicone nasal cavity model demonstrated that fresh gas administered by HFNC at 30 L/min flushes the dead space in the nasal cavity and increases the FIO2 [13]. A randomized, crossover, experimental study with 13 neonatal piglets with lung injury treated with continuous positive airway pressure (CPAP; minimal leak) or a HFNC with a high or low degree of leak around the nasal prongs showed no changes in PaCO2 (arterial pressure of carbon dioxide) or PaO2 (arterial pressure of oxygen) with increasing CPAP [14]. Under both HFNC leak conditions, however, PaCO2 decreased and PaO2 increased with increasing flow until saturation. Beyond this saturation point no greater effect was observed, suggesting that all dead space had been flushed out. Therefore, this effect of nasopharyngeal dead space washout was associated more with increases in flow rates than with increases in pressure. One should bear in mind that, compared with the masks used with conventional oxygen delivery devices, nasal prongs reduce dead space. Moreover, continuous high flows delivered via a HFNC make rebreathing highly unlikely and, even if it occurs, differences in cannula size are unlikely to have any significant effect.

Effects on metabolic cost of gas conditioning and respiratory mechanics

An adult breathing with a 500-ml tidal volume and a respiratory rate (RR) of 12 breaths/min may expend approximately 156 calories/min conditioning gas [12]. If the gas is totally conditioned prior to administration, this metabolic cost can be avoided and, if no concomitant changes in cardiac output occur, oxygenation may be indirectly improved by reducing this energy requirement [12]. Moreover, the delivery of warm, humidified gas has been associated with better tolerance and comfort [8, 15, 16]; it improves the mucociliary function [17, 18], increasing mucus clearance and preventing atelectasis formation. Other results suggest that it may also improve the inspiratory effort [19]. It has been hypothesized that the mechanisms associated with this effect may be the increase in alveolar recruitment and the decrease in airway resistance. In fact, while it has been shown that airway resistance increases during nasal breathing of room air at 24 °C in 12 healthy subjects, no changes were observed during inhalation of moist air [20]. These results suggest that delivery of humidified gas can contribute to the decrease in airway resistance during HFNC therapy. Second, as a HFNC provides a certain level of positive pressure, it counteracts the collapse of the nasopharynx which occurs during normal spontaneous breathing and reduces upper airway resistance [21].

Effects on respiratory pattern

Another of the main effects of HFNC is a significant change in the respiratory pattern. Compared with conventional oxygen, during HFNC use a significant decrease in respiratory rate (RR) has been described with no changes in PaCO2 [16, 22–24], as well as reduced thoraco-abdominal asynchrony [23]. This change in RR without affecting PaCO2 may suggest that alveolar ventilation remains constant and, therefore, tidal volume should increase or dead space decrease.

Hemodynamic effects

As we noted above, HFNC increases lung volume and generates a certain level of positive pressure. It seems plausible that these changes may induce some hemodynamic effects; this issue was investigated in ten non-decompensated heart failure patients for whom sequential echocardiographies were performed at baseline, when using a HFNC at 20 L/min and 40 L/min, and post-HFNC use [25]. Since right atrial pressure has been considered as a surrogate of right ventricular preload and is most commonly estimated by inferior vena cava (IVC) diameter and the presence of inspiratory collapse [26], and since changes in the IVC diameter have been used to determine preload responsiveness in positive pressure ventilated patients [27, 28], the assessment of preload was inferred by the measurement of the degree of inspiratory collapse of the IVC. In these patients, treatment with a HFNC at 20 L/min and 40 L/min was associated with mean attributable reductions in the IVC inspiratory collapse of 20 % and 53 % from baseline, respectively. These changes were reversible after HFNC withdrawal and no other changes in ventricular function were reported, suggesting that HFNC therapy may be a useful supportive therapy in patients with acute cardiogenic pulmonary edema (ACPE), especially in those patients who do not tolerate non-invasive ventilation (NIV) but remain hypoxemic with conventional oxygen devices [29]. A recent retrospective cohort study that included 75 patients with ARF reported that, after adjusting for other clinical variables, patients with cardiogenic pulmonary edema as the cause of ARF were more likely to avoid intubation [30]. However, whether HFNC therapy can be compared to NIV or CPAP in terms of outcomes in hypoxemic ACPE patients remains uncertain.

Better comfort

In ARF patients, the HFNC is better tolerated and more comfortable than conventional oxygen devices [16, 23] and NIV [8, 31, 32]. The heated humidification, the correction of the hypoxemia, the increase in alveolar recruitment, and the fact that the nasal prongs allow trouble-free speaking and eating must play some role in the improvement in comfort perceived by the patient during HFNC therapy.

Clinical applications

Given its mechanisms of action and the effects generated, HFNC therapy has some potential benefits in different clinical indications. The most relevant studies are presented in Table 1 [10, 16, 22–25, 29, 30, 33–55].

Table 1 Most relevant studies of HFNC therapy
Full size table

Acute hypoxemic respiratory failure

Its mechanisms of action and its clinical effects make the HFNC an attractive supportive tool for use in ARF patients. The first studies in ARF patients focused on physiological variables [16, 22, 23] and reported an improvement in oxygenation with reduced RR and no changes in PaCO2. Moreover, the HFNC was better tolerated and achieved a greater level of comfort than conventional oxygen devices [16, 23]. Although greater oxygenation improvements were obtained with NIV, the HFNC was usually better tolerated [31, 32]. In addition, HFNC has been used in small cohorts of patients with ARF in the emergency department [36, 54] and even in 150 children aged under 2 years during interhospital transport [56]. The effects on oxygenation and rates of intubation reported in all these studies are similar to those found when HFNC therapy has been used in ARF patients admitted to critical care areas, suggesting that, with adequate monitoring, HFNC therapy can be safely used outside critical care areas.

Moreover, early predictors of HFNC outcome have also been described. Sztrymf et al. [23] reported that RR as well as the percentage of patients exhibiting thoraco-abdominal asynchrony as early as 30 and 15 min after the beginning of HFNC therapy were significantly higher in patients who required endotracheal intubation. The PaO2/FIO2 ratio 1 h after the beginning of HFNC therapy was significantly lower in patients requiring invasive mechanical ventilation. Similarly, in a series of 20 H1N1 patients treated with HFNC, worse PaO2/FIO2 ratios were observed in patients who required intubation after 6 h of treatment [24]. However, in addition to respiratory variables, non-pulmonary severity may also be a good predictor of HFNC failure. Indeed, in two small cohort studies including H1N1 patients or lung transplant recipients requiring readmission to the ICU due to ARF, both treated with HFNC, the presence of shock has been associated with a higher risk of mechanical ventilation (MV) [24, 33]. Accurate, early predictors of HFNC therapy success are important, since a recent propensity-score analysis associated early intubation (within the first 48 h) with better ICU survival [53]. In spite of its limitations [57], the study by Kang et al. [53] raises an important issue: the fact that intubation should not be delayed in patients treated with HFNC, as delay may worsen their prognosis. Therefore, the ability to describe accurate predictors of HFNC therapy success which can allow timely endotracheal intubation in patients who are likely to fail is a point of special interest.

Another controversial issue is whether acute respiratory distress syndrome (ARDS) patients should be treated with HFNC. Moreover, it is unclear whether patients with bilateral infiltrates treated with HFNC could be considered as having ARDS. In fact, most of the patients included in studies have bilateral infiltrates [33, 34, 55]. The Berlin definition of ARDS [58] requires a minimum of 5 cmH20 of positive end-expiratory pressure (PEEP) and it has been shown that HFNC can provide a level of PEEP which is higher at peak expiratory pressure [3, 5]. Moreover, ARDS does not begin at the time of MV onset. Therefore, it could be accepted that patients with a risk factor for ARDS, who are hypoxemic (PaO2/FIO2 ratio ≤300 mmHg) and have bilateral infiltrates not fully explained by cardiac failure or fluid overload, may be considered as ARDS patients [59]. In these patients, HFNC may achieve success rates [55] similar to those of NIV [60].

Besides the physiological improvement, one of the most important points is whether HFNC can reduce the need for further MV or mortality in ARF patients. The first results were reported in a randomized controlled trial (RCT) which included postoperative cardiac surgery patients with ARF [46]. HFNC patients were less likely to need escalation to NIV than those receiving conventional oxygen devices and also had fewer desaturations. In a recent retrospective analysis of a prospectively assessed cohort of 37 lung transplant patients readmitted to ICU due to ARF, HFNC therapy was the only variable at ICU admission associated with a decreased risk of MV in the multivariate analysis [33]. The absolute risk reduction for MV with HFNC was 29.8 % and only three patients needed to be treated with HFNC to prevent one intubation. Moreover, non-ventilated patients had an increased survival rate. More recently, the first large RCT to assess clinical outcomes with HFNC (50 L/min), conventional oxygen devices, and NIV has been published [34]. The study included 310 patients with hypoxemic ARF, defined as PaO2/FIO2 ratio ≤300 mmHg or RR >25 breaths per min (bpm) with 10 liters per min (lpm) of O2. Patients with a history of chronic respiratory disease, including chronic obstructive pulmonary disease (COPD), as well as patients with ACPE, severe neutropenia, and hypercapnia (PaCO2 > 45 mmHg) were excluded, as were patients with hemodynamic instability or on vasopressors at the time of inclusion. Moreover, patients in the NIV group were treated with NIV for a median of only 8 h during the first two days of randomization and received HFNC therapy between NIV sessions. The primary outcome—the rate of endotracheal intubation—did not differ significantly between the groups (38 % for the HFNC group vs 47 % for the conventional oxygen device group and 50 % for the NIV group, P = 0.18). This negative result may be due to the fact that the observed rate of intubation in the conventional oxygen devices was lower than expected and, therefore, the study may have been underpowered to identify differences in this endpoint. However, a post hoc adjusted analysis including the 238 patients with a PaO2/FIO2 ratio ≤200 mmHg found that HFNC reduced intubation rates (P = 0.009). In the entire cohort, HFNC therapy increased ventilator-free days, reduced 90-day mortality, and was associated with better comfort and lower dyspnea severity. In contrast, compared with HFNC patients, NIV patients presented higher 90-day mortality, probably due to the use of higher tidal volumes (Vt 9.2 ± 3.0 ml/kg).

Invasive procedures

HFNC therapy has been used during invasive procedures such as bronchoscopy [37, 38, 61, 62] or endotracheal intubation [42, 43] both to prevent the appearance of hypoxemia and to treat hypoxemic patients. Regarding its use during bronchoscopy, although HFNC seem to be more useful than conventional oxygen devices in preventing and treating hypoxemia, NIV may be superior to HFNC in patients with severe hypoxemia [37]. HFNC may also be useful during transesophageal echocardiography or digestive tract endoscopy.

Two studies have evaluated the efficacy of HFNC therapy during endotracheal intubation [42, 43] and have produced conflicting results. First, in a prospective, quasi-experimental, before-after study, Miguel-Montanes et al. [43] assessed the usefulness of HFNC during tracheal intubation of critically ill patients with mild to moderate hypoxemia who were intubated mainly for reasons other than ARF compared with a non-rebreathing bag reservoir facemask. They observed that HFNC significantly improved preoxygenation and reduced the prevalence of severe hypoxemia. In contrast, Vourc’h et al. [42] did not report any differences in a more recent RCT comparing the effectiveness of HFNC with 15 L/min of oxygen delivered through a facial mask in preventing desaturation in patients with severe ARF, defined as a PaO2/FIO2 < 300, SpO2 < 90 % and a FIO2 ≥ 0.5 or RR >30 bpm. The differences in the two studies may be due to the differences in the type of patient included. However, the preoxygenation time of 4 min used in the study by Vourc’h et al. [42] may not have been long enough to reveal significant differences in oxygenation. Moreover, more patients in the HFNC group were treated with HFNC prior to inclusion (16.1 % vs 5.3 %), suggesting that the HFNC group may have been more hypoxemic before the start of the study.

Post-extubation

Two preliminary physiological studies comparing HFNC with conventional oxygen devices using a crossover design and during a short period of time after extubation have confirmed the consistent benefit of HFNC in terms of overall comfort [39, 40] previously reported in ARF patients. Interestingly, however, both studies reported a significant improvement in quasi-objective surrogates of comfort, such as perceived dyspnea or tolerance score, when applied in a crossover design with conventional oxygen devices. Rittayamai et al. [40] observed a decrease in RR and heart rate when comparing HFNC therapy at 35 L/min vs conventional oxygen devices at 6–10 L/min in 17 patients during a 30-min period in a crossover study. In contrast, Tiruvoipati et al. [39] found no change in these physiological variables when comparing 30 L/min delivered through a HFNC or 15 L/min through high flow face mask.

Soon afterwards, the first large multicenter RCT comparing HFNC with conventional oxygen devices after extubation was published [41]. The study included patients with ARF due to pneumonia and trauma who were mechanically ventilated for a mean of almost five days before extubation. In these patients, the use of HFNC was associated with better comfort, better oxygenation, fewer desaturations and interface displacements, and a lower reintubation rate. However, the effectiveness of HFNC therapy during the extubation period in postoperative patients remains controversial; most studies on this issue have included patients after cardiothoracic surgery [44, 45, 47]. Parke et al. [47] included a non-selected population of cardiac surgery patients with mild to moderate ARF, observing that HFNC patients more frequently succeeded and could be weaned to conventional oxygen devices. In contrast, in patients randomized to conventional oxygen devices, ARF was more likely to worsen and escalation to NIV or HFNC required. Corley et al. [45] included a population of cardiac surgery patients with body mass index (BMI) ≥30 who were randomly assigned to prophylactic HFNC therapy or conventional oxygen devices after extubation. They did not observe any difference in atelectasis formation, oxygenation, respiratory rate, or dyspnea. Finally, the BiPOP study [44], a multicenter, non-inferiority RCT, compared HFNC and NIV for preventing or resolving ARF after cardiothoracic surgery. Three different types of patient were eligible: patients who failed after a spontaneous breathing trial; patients who succeeded but had a preexisting risk factor for postoperative ARF (BMI >30, left ventricular ejection fraction <40 %, and failure of previous extubation); and patients who succeeded after a spontaneous breathing trial but then failed extubation (defined as at least one of the following: PaO2/FIO2 < 300, RR >25 bpm for at least 2 h, and use of accessory respiratory muscles or paradoxical respiration). After randomizing more than 800 patients, HFNC therapy did not increase the rate of treatment failure (defined as reintubation, switch to the other study treatment, or premature treatment discontinuation at the patient’s request or due to an adverse event). Therefore, as HFNC therapy did not worsen outcomes, may be easier to administer, and requires lower nursing workload, the authors concluded that the results supported the use of HFNC in this subset of patients.

Certain questions remain unanswered, however, such as the optimal flow and the subset of patients who would benefit the most from HFNC therapy. Studies including other types of surgical patients, such as abdominal surgery (the OPERA trial) [63] and lung resection, will be published in the near future.

Critically ill tracheostomized patients

Weaning of tracheostomized patients is still a challenge. To our knowledge, only one randomized trial has included high flow therapy in the protocol [64]. This was a single-center study including 181 critically ill tracheostomized patients who were randomized to have the tracheal cuff deflated or not during spontaneous breathing trials. All patients received high-flow conditioned oxygen therapy through a direct tracheostomy connection to the maximum tolerated flow and conditioned up to 37 °C. Although that study was not specifically designed to assess the effectiveness of high flow through the trachea, the authors hypothesized that HFNC therapy may have some benefits in the weaning process of tracheostomized patients with a deflated tracheal cuff. Positive airway pressure may theoretically reduce microaspirations and, with a deflated cuff, a higher flow is conveyed through the pericannular space, allowing for better drainage of secretions.

Chronic diseases

Mucociliary clearance

COPD and bronchiectasis are both airway disorders characterized by neutrophilic airway inflammation, mucus hypersecretion and retention, and impaired mucociliary transport [65–70]. In these patients, some studies have also analyzed the effect of HFNC therapy on lung mucociliary clearance. In bronchiectasic patients, Hasani et al. [71] demonstrated that a period as short as 3 h/day of HFNC therapy at home over seven days significantly increased lung mucociliary clearance measured by radioaerosol labeling. Rea et al. [65] performed a 12-month randomized study with 108 patients diagnosed with COPD or bronchiectasis who received HFNC therapy ≥2 h per day in their home in order to examine the effects of HFNC therapy on the frequency of exacerbations, quality of life, lung function, exercise capacity, and airway inflammation. The results showed that patients on long-term HFNC therapy had significantly fewer exacerbation days, increased time to first exacerbation, and reduced exacerbation frequency compared with usual care. Quality of life scores and lung function at 3 and 12 months improved significantly with humidification therapy compared with usual care.

The preliminary results of a randomized, placebo-controlled, one-year study of 200 patients designed to evaluate the effect of HFNC therapy on patients in need of long-term oxygen therapy (86 COPD) have recently been reported [72]. The patients received between 20 and 30 L/min and, on average, HFNC therapy was used more than 7 h per day. Moreover, COPD patients treated with HFNC had fewer exacerbations and fewer hospital admissions than controls.

Sleep-related hypoventilation

Two short studies and one case-report have described the effects of HFNC therapy on nocturnal hypoventilation. Okuda et al. [73] reported a patient on HFNC therapy in whom the Apnea–Hypopnea Index decreased while oxygenation improved. HFNC therapy was continued at home without any recurrences of CO2 narcosis. Nilius et al. [74] assessed the effects of high flow nasal insufflations in 17 COPD patients with chronic hypercapnic respiratory failure, delivering a mixture of 20 L/min room air and 2 L/min O2 through a nasal cannula. High flow nasal insufflations led to a systematic reduction in RR without deterioration of the hypercapnia, suggesting that HFNC may improve efficiency of breathing and may be used as an adjunct to low flow oxygen for preventing hypercapnic respiratory failure in severely ill COPD patients. These same authors analyzed the effectiveness of HFNC therapy in 20 patients with severe COPD who were oxygen-dependent and had hypercapnic respiratory failure [75]. They found that, compared with oxygen alone, warm and humidified air at a rate of 20 L/min attenuated nocturnal hypoventilation in COPD patients with severe and hypercapnic respiratory failure.

Obstructive sleep apnea syndrome

The results of two short studies conducted in adult populations suggested that HFNC therapy could be an alternative to CPAP. The first study included 11 patients with mild to severe obstructive sleep apnea hypopnea syndrome [76]. In these patients, HFNC reduced the mean Apnea–Hypopnea Index and the respiratory arousal index. The second study analyzed the role of HFNC in ten patients with acute stroke and sleep-disordered breathing ranging from moderate to severe [77]. HFNC therapy was well tolerated and decreased the Apnea–Hypopnea Index and the oxygen desaturation index by >3 %. Moreover, the percentage of slow-wave sleep significantly increased and quality of sleep improved.

Patients with a do-not-intubate order

In patients with a do-not-intubate order, it is mandatory to provide as high a level of comfort as possible. Even though NIV might be considered as a potential supportive measure, it is less likely to be tolerated than HFNC therapy [31]. A retrospective study analyzing the efficacy of HFNC therapy in do-not-intubate hypoxemic patients admitted to the ICU [35] found that it provided adequate oxygenation and comfort and that only 18 % of patients required escalation to NIV, thus suggesting that HFNC may be an alternative to NIV in do-not-intubate patients. Two more retrospective studies included patients with cancer [78] or hematological malignancies [79]. In this subset of patients, HFNC therapy should be considered as a way of enhancing comfort in patients with do-not-intubate orders and in those who do not tolerate conventional oxygen devices or NIV.

Aerosol therapy

In patients with ARF, the use of aerosol therapy to treat bronchial hyperresponsiveness or pulmonary infections is becoming increasingly frequent. However, the efficiency of aerosol delivery with HFNC is likely to be low due to high flow rates, humidification, small delivery line diameters, and narrow flow passages in the cannula and abrupt changes in flow direction [80]. Therefore, questions that frequently arise are how to use aerosol therapy, where to implement the system, and whether it is effective.

Recently, an in vitro study analyzing albuterol (2.5 mg/3 mL) delivery using a vibrating mesh nebulizer (Aeroneb system, Aerogen Limited, Galway Business Park, Dangan, Galway, Ireland) during HFNC therapy was published [81]. The results showed that the amount of albuterol delivered was lower than the amount expected for a clinical response for the majority of flow rates and cannula size combinations. Other studies have shown that it is still possible to achieve a lung dose of 14 % even at flow rates of 30 L/min [82]. In this regard, other experimental studies have achieved significant improvements in delivery, with delivery efficiency up to 80 % at flow rates of 15 L/min [83]. Furthermore, HFNC therapy allows aerosol delivery without interruption of oxygen flow and pressure and it could be considered as an efficient delivery strategy for pulmonary aerosol medications [84].

Another interesting point to consider is the effect of the nebulizer position on aerosol drug deposition. The results of a recent in vitro study that simulated preterm infant settings showed that the mean percentage of dose delivered was greater with the nebulizer placed prior to the humidifier [80].

Interestingly, HFNC therapy can achieve stricter control of the administered FIO2 and may obtain totally conditioned gas during nebulization [85]. These two points are especially important in COPD patients.

We should note that all these studies have major limitations and that no strong evidence-based recommendations can be made. At very high flows, however, the amount of aerosol delivery is likely to be low. Moreover, the efficiency of aerosol delivery can be significantly improved by the use of moderate flows and it seems reasonable that if a vibrating mesh nebulizer is used in patients treated with a HFNC, it should be put in place prior to the humidifier.

Recommendations for use in patients with ARF

Although many aspects of HFNC therapy remain unclear, evidence supporting its use in hypoxemic ARF patients is accumulating steadily. Here, we present our recommendations for applying HFNC therapy from the onset of ARF until weaning based on the current evidence and our experience. Like many other therapies used in critically ill patients, HFNC therapy should be started as early as possible. It seems logical to start with an FIO2 of 1 with the maximum tolerated flow up to 50 L/min [34]. The fraction of inspired oxygen should be subsequently titrated according to a target SpO2. The flow delivered will try to satisfy the inspiratory demand, minimizing the entrainment of room air and thus ensuring administration of the required FIO2. Although it seems reasonable to titrate the flow according to the comfort of the patient, we can hypothesize that if these very high flows increase tidal volume, they may generate some degree of alveolar overdistension, especially in patients with preexisting lung injury. Finally, if the patient progresses well and HFNC can be withdrawn, we first decrease the FIO2 and then, when the FIO2 is <0.5, we start to decrease flow. When FIO2 is <0.5 and the flow rate is <20 L/min, HFNC can be replaced by conventional oxygen devices. We stress that all patients with HFNC must be strictly monitored, paying special attention to oxygenation, RR, respiratory pattern, and need for vasopressors since all these variables have been implicated in HFNC failure. It is equally important not to delay intubation in patients who fail, as delay may worsen their prognosis.

HFNC therapy presents certain advantages over NIV. It is probably easier to apply, it needs less equipment, and it generates lower workloads. Importantly, it is more comfortable for the patient and is better tolerated and does not seem to be inferior in terms of clinical outcomes in patients with hypoxemic respiratory failure. However, HFNC therapy may not be indicated in all patients with ARF [86]. Currently, NIV should still be considered as a first-line treatment in a variety of clinical situations, such as hypercapnic respiratory failure [87] during COPD exacerbations [88] or ACPE [89]. In fact, as HFNC therapy generates only slight increases in airway pressure at end expiration, it is unlikely to reduce the work of breathing as effectively as NIV. Therefore, NIV appears to be more effective in patients who are more severely affected. Finally, at centers with substantial experience treating hypoxemic ARF with NIV, decisions on the strategy to use should be individualized.

Future directions for research

Although evidence for the effectiveness of HFNC therapy is growing exponentially, several questions remain unanswered (Table 2). Future research should focus on identifying which patients will benefit the most from HFNC therapy. To achieve this, it might be worthwhile to perform RCT including patients with specific diseases rather than including all patients with different types of ARF, from pneumonia to ACPE to hypercapnic COPD. Selecting the right patients to treat and knowing how to use HFNC properly will improve results. In this regard, we need to identify and describe early predictors of HFNC success in order to minimize delays in intubations that could worsen patient outcomes. And it would also be desirable to establish the optimal flow rate to set up in each patient. While insufficient flow may lead to HFNC failure, excessively high flow may generate alveolar overdistension and increase the pre-existing lung injury. On the other hand, with strict patient monitoring to avoid delayed intubation in case of HFNC failure, HFNC can be used either in the emergency department [36, 54] or in hospital wards for the treatment of ARF patients [53]. However, we also need strong and robust cost-effectiveness analyses of HFNC therapy that support its use in different clinical situations. Finally, the evidence with patients with chronic respiratory diseases such as sleep-related hypoventilation, obstructive sleep apnea syndrome, or chronic cough is very limited [90]; what little is known is based on small series or case reports which are far from conclusive but which may generate hypotheses for further studies. Therefore, RCTs evaluating the efficiency of HFNC therapy in these situations are still mandatory.

Table 2 Areas of uncertainty and key questions in HFNC research
Full size table

Conclusion

Delivery of heated and humidified oxygen at high flow rates through nasal cannula is now widely used in adult patients. Its mechanisms of action and potential clinical benefits can help to improve the management of patients with either acute or chronic respiratory failure. With the evidence currently available, several questions still remain unanswered; in the absence of any general recommendations, decisions on HFNC treatment should be individualized in each particular situation. However, HFNC therapy is an innovative and powerful technique that is currently changing the management of patients with respiratory failure.

Abbreviations

ACPE:

acute cardiogenic pulmonary edema

ARDS:

acute respiratory distress syndrome

ARF:

acute respiratory failure

bpm:

beats per min

CO2 :

carbon dioxide

COPD:

chronic obstructive pulmonary disease

CPAP:

continuous positive airway pressure

FIO2 :

fraction of inspired oxygen

HFNC:

high flow nasal cannula

ICU:

intensive care unit

IVC:

inferior vena cava

lpm:

liters per min

MV:

mechanical ventilation

NIV:

non-invasive ventilation

PaCO2 :

arterial pressure of carbon dioxide

PaO2 :

arterial pressure of oxygen

PEEP:

positive end-expiratory pressure

RCT:

randomized controlled trial

RR:

respiratory rate

References

  1. Anderson NJ, Cassidy PE, Janssen LL, Dengel DR. Peak inspiratory flows of adults exercising at light, moderate and heavy workloads. J Int Soc Respir Prot. 2006;23:53–63.

  2. Masclans JR, Roca O. High-flow oxygen therapy in acute respiratory failure. Clin Pulm Med. 2012;19(3):127–30. doi:10.1097/CPM.0b013e3182514f29.

    Article  Google Scholar 

  3. Parke RL, McGuinness SP. Pressures delivered by nasal high flow oxygen during all phases of the respiratory cycle. Respir Care. 2013;58(10):1621–4. doi:10.4187/respcare.02358.

    Article  PubMed  Google Scholar 

  4. Parke R, McGuinness S, Eccleston M. Nasal high-flow therapy delivers low level positive airway pressure. Br J Anaesth. 2009;103(6):886–90. doi:10.1093/bja/aep280.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  5. Parke RL, Bloch A, McGuinness SP. Effect of very-high-flow nasal therapy on airway pressure and end-expiratory lung impedance in healthy volunteers. Respir Care. 2015;60(10):1397–403. doi:10.4187/respcare.04028.

    Article  PubMed  Google Scholar 

  6. Chatila W, Nugent T, Vance G, et al. The effects of high-flow vs low-flow oxygen on exercise in advanced obstructive airways disease. Chest. 2004;126(4):1108–15. doi:10.1378/chest.126.4.1108.

    Article  PubMed  Google Scholar 

  7. Groves N, Tobin A. High flow nasal oxygen generates positive airway pressure in adult volunteers. Aust Crit Care. 2007;20(4):126–31. doi:10.1016/j.aucc.2007.08.001.

    Article  PubMed  Google Scholar 

  8. Chanques G, Riboulet F, Molinari N, et al. Comparison of three high flow oxygen therapy delivery devices: a clinical physiological cross-over study. Minerva Anestesiol. 2013;79(12):1344–55. Available at: http://www.ncbi.nlm.nih.gov/pubmed/23857440. Accessed October 26, 2015.

    CAS  PubMed  Google Scholar 

  9. Hinz J, Hahn G, Neumann P, et al. End-expiratory lung impedance change enables bedside monitoring of end-expiratory lung volume change. Intensive Care Med. 2003;29(1):37–43. doi:10.1007/s00134-002-1555-4.

    CAS  Article  PubMed  Google Scholar 

  10. Corley A, Caruana LR, Barnett AG, et al. Oxygen delivery through high-flow nasal cannulae increase end-expiratory lung volume and reduce respiratory rate in post-cardiac surgical patients. Br J Anaesth. 2011;107(6):998–1004. doi:10.1093/bja/aer265.

    CAS  Article  PubMed  Google Scholar 

  11. Riera J, Pérez P, Cortés J, et al. Effect of high-flow nasal cannula and body position on end-expiratory lung volume: a cohort study using electrical impedance tomography. Respir Care. 2013;58(4):589–96. doi:10.4187/respcare.02086.

    Article  PubMed  Google Scholar 

  12. Dysart K, Miller TL, Wolfson MR, Shaffer TH. Research in high flow therapy: mechanisms of action. Respir Med. 2009;103(10):1400–5. doi:10.1016/j.rmed.2009.04.007.

    Article  PubMed  Google Scholar 

  13. Spence CJT, Buchmann NA, Jermy MC. Unsteady flow in the nasal cavity with high flow therapy measured by stereoscopic PIV. Exp Fluids. 2012;52(3):569–79. doi:10.1007/s00348-011-1044-z.

    CAS  Article  Google Scholar 

  14. Frizzola M, Miller TL, Rodriguez ME, et al. High-flow nasal cannula: impact on oxygenation and ventilation in an acute lung injury model. Pediatr Pulmonol. 2011;46(1):67–74. doi:10.1002/ppul.21326.

    Article  PubMed  PubMed Central  Google Scholar 

  15. Chanques G, Constantin J-M, Sauter M, et al. Discomfort associated with underhumidified high-flow oxygen therapy in critically ill patients. Intensive Care Med. 2009;35(6):996–1003. doi:10.1007/s00134-009-1456-x.

    CAS  Article  PubMed  Google Scholar 

  16. Roca O, Riera J, Torres F, Masclans JR. High-flow oxygen therapy in acute respiratory failure. Respir Care. 2010;55(4):408–13. Available at: http://www.ncbi.nlm.nih.gov/pubmed/20406507. Accessed October 26, 2015.

    PubMed  Google Scholar 

  17. Kilgour E, Rankin N, Ryan S, Pack R. Mucociliary function deteriorates in the clinical range of inspired air temperature and humidity. Intensive Care Med. 2004;30(7):1491–4. doi:10.1007/s00134-004-2235-3.

    Article  PubMed  Google Scholar 

  18. Chidekel A, Zhu Y, Wang J, et al. The effects of gas humidification with high-flow nasal cannula on cultured human airway epithelial cells. Pulm Med. 2012;2012:380686. doi:10.1155/2012/380686.

    Article  PubMed  PubMed Central  Google Scholar 

  19. Vargas F, Saint-Leger M, Boyer A, et al. Physiologic effects of high-flow nasal cannula oxygen in critical care subjects. Respir Care. 2015;60(10):1369–76. doi:10.4187/respcare.03814.

    Article  PubMed  Google Scholar 

  20. Fontanari P, Burnet H, Zattara-Hartmann MC, Jammes Y. Changes in airway resistance induced by nasal inhalation of cold dry, dry, or moist air in normal individuals. J Appl Physiol. 1996;81(4):1739–43. Available at: http://www.ncbi.nlm.nih.gov/pubmed/8904594. Accessed January 7, 2016.

    CAS  PubMed  Google Scholar 

  21. Miller MJ, DiFiore JM, Strohl KP, Martin RJ. Effects of nasal CPAP on supraglottic and total pulmonary resistance in preterm infants. J Appl Physiol. 1990;68(1):141–6. Available at: http://www.ncbi.nlm.nih.gov/pubmed/2179206. Accessed October 26, 2015.

    CAS  PubMed  Google Scholar 

  22. Sztrymf B, Messika J, Mayot T, et al. Impact of high-flow nasal cannula oxygen therapy on intensive care unit patients with acute respiratory failure: a prospective observational study. J Crit Care. 2012;27(3):324. e9-13. doi:10.1016/j.jcrc.2011.07.075.

  23. Sztrymf B, Messika J, Bertrand F, et al. Beneficial effects of humidified high flow nasal oxygen in critical care patients: a prospective pilot study. Intensive Care Med. 2011;37(11):1780–6. doi:10.1007/s00134-011-2354-6.

    CAS  Article  PubMed  Google Scholar 

  24. Rello J, Pérez M, Roca O, et al. High-flow nasal therapy in adults with severe acute respiratory infection: a cohort study in patients with 2009 influenza A/H1N1v. J Crit Care. 2012;27(5):434–9. doi:10.1016/j.jcrc.2012.04.006.

    Article  PubMed  Google Scholar 

  25. Roca O, Pérez-Terán P, Masclans JR, et al. Patients with New York Heart Association class III heart failure may benefit with high flow nasal cannula supportive therapy: high flow nasal cannula in heart failure. J Crit Care. 2013;28(5):741–6. doi:10.1016/j.jcrc.2013.02.007.

    Article  PubMed  Google Scholar 

  26. Moreno FL, Hagan AD, Holmen JR, et al. Evaluation of size and dynamics of the inferior vena cava as an index of right-sided cardiac function. Am J Cardiol. 1984;53(4):579–85. Available at: http://www.ncbi.nlm.nih.gov/pubmed/6695787. Accessed February 15, 2016.

    CAS  Article  PubMed  Google Scholar 

  27. Barbier C, Loubières Y, Schmit C, et al. Respiratory changes in inferior vena cava diameter are helpful in predicting fluid responsiveness in ventilated septic patients. Intensive Care Med. 2004;30(9):1740–6. doi:10.1007/s00134-004-2259-8.

    PubMed  Google Scholar 

  28. Feissel M, Michard F, Faller J-P, Teboul J-L. The respiratory variation in inferior vena cava diameter as a guide to fluid therapy. Intensive Care Med. 2004;30(9):1834–7. doi:10.1007/s00134-004-2233-5.

    Article  PubMed  Google Scholar 

  29. Carratalá Perales JM, Llorens P, Brouzet B, et al. High-flow therapy via nasal cannula in acute heart failure. Rev Esp Cardiol. 2011;64(8):723–5. doi:10.1016/j.recesp.2010.10.034.

    Article  PubMed  Google Scholar 

  30. Hyun Cho W, Ju Yeo H, Hoon Yoon S, et al. High-flow nasal cannula therapy for acute hypoxemic respiratory failure in adults: a retrospective analysis. Intern Med. 2015;54(18):2307–13. doi:10.2169/internalmedicine.54.4266.

    Article  PubMed  Google Scholar 

  31. Frat J-P, Brugiere B, Ragot S, et al. Sequential application of oxygen therapy via high-flow nasal cannula and noninvasive ventilation in acute respiratory failure: an observational pilot study. Respir Care. 2015;60(2):170–8. doi:10.4187/respcare.03075.

    Article  PubMed  Google Scholar 

  32. Schwabbauer N, Berg B, Blumenstock G, et al. Nasal high-flow oxygen therapy in patients with hypoxic respiratory failure: effect on functional and subjective respiratory parameters compared to conventional oxygen therapy and non-invasive ventilation (NIV). BMC Anesthesiol. 2014;14:66. doi:10.1186/1471-2253-14-66.

    Article  PubMed  PubMed Central  Google Scholar 

  33. Roca O, de Acilu MG, Caralt B, et al. Humidified high flow nasal cannula supportive therapy improves outcomes in lung transplant recipients readmitted to the intensive care unit because of acute respiratory failure. Transplantation. 2015;99(5):1092–8. doi:10.1097/TP.0000000000000460.

    Article  PubMed  Google Scholar 

  34. Frat J-P, Thille AW, Mercat A, et al. High-flow oxygen through nasal cannula in acute hypoxemic respiratory failure. N Engl J Med. 2015;372(23):2185–96. doi:10.1056/NEJMoa1503326.

    CAS  Article  PubMed  Google Scholar 

  35. Peters SG, Holets SR, Gay PC. High-flow nasal cannula therapy in do-not-intubate patients with hypoxemic respiratory distress. Respir Care. 2013;58(4):597–600. doi:10.4187/respcare.01887.

    PubMed  Google Scholar 

  36. Lenglet H, Sztrymf B, Leroy C, et al. Humidified high flow nasal oxygen during respiratory failure in the emergency department: feasibility and efficacy. Respir Care. 2012;57(11):1873–8. doi:10.4187/respcare.01575.

    Article  PubMed  Google Scholar 

  37. Simon M, Braune S, Frings D, et al. High-flow nasal cannula oxygen versus non-invasive ventilation in patients with acute hypoxaemic respiratory failure undergoing flexible bronchoscopy--a prospective randomised trial. Crit Care. 2014;18(6):712. doi:10.1186/s13054-014-0712-9.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Lucangelo U, Vassallo FG, Marras E, et al. High-flow nasal interface improves oxygenation in patients undergoing bronchoscopy. Crit Care Res Pract. 2012;2012:506382. doi:10.1155/2012/506382.

    PubMed  PubMed Central  Google Scholar 

  39. Tiruvoipati R, Lewis D, Haji K, Botha J. High-flow nasal oxygen vs high-flow face mask: a randomized crossover trial in extubated patients. J Crit Care. 2010;25(3):463–8. doi:10.1016/j.jcrc.2009.06.050.

    Article  PubMed  Google Scholar 

  40. Rittayamai N, Tscheikuna J, Rujiwit P. High-flow nasal cannula versus conventional oxygen therapy after endotracheal extubation: a randomized crossover physiologic study. Respir Care. 2014;59(4):485–90. doi:10.4187/respcare.02397.

    Article  PubMed  Google Scholar 

  41. Maggiore SM, Idone FA, Vaschetto R, et al. Nasal high-flow vs Venturi mask oxygen therapy after extubation: effects on oxygenation, comfort and clinical outcome. Am J Respir Crit Care Med. 2014;190(3):282–8. doi:10.1164/rccm.201402-0364OC.

    Article  PubMed  Google Scholar 

  42. Vourc’h M, Asfar P, Volteau C, et al. High-flow nasal cannula oxygen during endotracheal intubation in hypoxemic patients: a randomized controlled clinical trial. Intensive Care Med. 2015;41(9):1538–48. doi:10.1007/s00134-015-3796-z.

    Article  PubMed  Google Scholar 

  43. Miguel-Montanes R, Hajage D, Messika J, et al. Use of high-flow nasal cannula oxygen therapy to prevent desaturation during tracheal intubation of intensive care patients with mild-to-moderate hypoxemia. Crit Care Med. 2015;43(3):574–83. doi:10.1097/CCM.0000000000000743.

    CAS  Article  PubMed  Google Scholar 

  44. Stéphan F, Barrucand B, Petit P, et al. High-flow nasal oxygen vs noninvasive positive airway pressure in hypoxemic patients after cardiothoracic surgery. JAMA. 2015;313(23):2331–9. doi:10.1001/jama.2015.5213.

    Article  PubMed  Google Scholar 

  45. Corley A, Bull T, Spooner AJ, et al. Direct extubation onto high-flow nasal cannulae post-cardiac surgery versus standard treatment in patients with a BMI ≥30: a randomised controlled trial. Intensive Care Med. 2015;41(5):887–94. doi:10.1007/s00134-015-3765-6.

    Article  PubMed  Google Scholar 

  46. Parke RL, McGuinness SP, Eccleston ML. A preliminary randomized controlled trial to assess effectiveness of nasal high-flow oxygen in intensive care patients. Respir Care. 2011;56(3):265–70. doi:10.4187/respcare.00801.

    Article  PubMed  Google Scholar 

  47. Parke R, McGuinness S, Dixon R, Jull A. Open-label, phase II study of routine high-flow nasal oxygen therapy in cardiac surgical patients. Br J Anaesth. 2013;111(6):925–31. doi:10.1093/bja/aet262.

    CAS  Article  PubMed  Google Scholar 

  48. Jones PG, Kimona S, Doran O, et al. Randomized controlled trial of humidified high-flow nasal oxygen for acute respiratory distress in the emergency department: the HOT-ER study. Respir Care. 2015;61(3):291–9. doi:10.4187/respcare.04252.

    CAS  Article  PubMed  Google Scholar 

  49. Nagata K, Morimoto T, Fujimoto D, et al. Efficacy of high-flow nasal cannula therapy in acute hypoxemic respiratory failure: decreased use of mechanical ventilation. Respir Care. 2015;60(10):1390–6. doi:10.4187/respcare.04026.

    Article  PubMed  Google Scholar 

  50. Gaunt KA, Spilman SK, Halub ME, et al. High-flow nasal cannula in a mixed adult ICU. Respir Care. 2015;60(10):1383–9. doi:10.4187/respcare.04016.

    Article  PubMed  Google Scholar 

  51. Lemiale V, Mokart D, Mayaux J, et al. The effects of a 2-h trial of high-flow oxygen by nasal cannula versus Venturi mask in immunocompromised patients with hypoxemic acute respiratory failure: a multicenter randomized trial. Crit Care. 2015;19(1):380. doi:10.1186/s13054-015-1097-0.

    Article  PubMed  PubMed Central  Google Scholar 

  52. Mokart D, Geay C, Chow-Chine L, et al. High-flow oxygen therapy in cancer patients with acute respiratory failure. Intensive Care Med. 2015;41(11):2008–10. doi:10.1007/s00134-015-3994-8.

    Article  PubMed  Google Scholar 

  53. Kang BJ, Koh Y, Lim C-M, et al. Failure of high-flow nasal cannula therapy may delay intubation and increase mortality. Intensive Care Med. 2015;41(4):623–32. doi:10.1007/s00134-015-3693-5.

    Article  PubMed  Google Scholar 

  54. Rittayamai N, Tscheikuna J, Praphruetkit N, Kijpinyochai S. Use of high-flow nasal cannula for acute dyspnea and hypoxemia in the emergency department. Respir Care. 2015;60(10):1377–82. doi:10.4187/respcare.03837.

    Article  PubMed  Google Scholar 

  55. Messika J, Ben Ahmed K, Gaudry S, et al. Use of high-flow nasal cannula oxygen therapy in subjects with ARDS: a 1-year observational study. Respir Care. 2015;60(2):162–9. doi:10.4187/respcare.03423.

    Article  PubMed  Google Scholar 

  56. Schlapbach LJ, Schaefer J, Brady A-M, et al. High-flow nasal cannula (HFNC) support in interhospital transport of critically ill children. Intensive Care Med. 2014;40(4):592–9. doi:10.1007/s00134-014-3226-7.

    Article  PubMed  Google Scholar 

  57. Ricard J-D, Messika J, Sztrymf B, Gaudry S. Impact on outcome of delayed intubation with high-flow nasal cannula oxygen: is the device solely responsible? Intensive Care Med. 2015;41(6):1157–8. doi:10.1007/s00134-015-3766-5.

    Article  PubMed  Google Scholar 

  58. Ranieri VM, Rubenfeld GD, Thompson BT, et al. Acute respiratory distress syndrome: the Berlin Definition. JAMA. 2012;307(23):2526–33. doi:10.1001/jama.2012.5669.

    PubMed  Google Scholar 

  59. Calfee CS. ARDS in 2015: new clinical directions, new biological insights. Lancet Respir Med. 2015;3(12):912–3. doi:10.1016/S2213-2600(15)00425-7.

    Article  PubMed  Google Scholar 

  60. Antonelli M, Conti G, Esquinas A, et al. A multiple-center survey on the use in clinical practice of noninvasive ventilation as a first-line intervention for acute respiratory distress syndrome. Crit Care Med. 2007;35(1):18–25. doi:10.1097/01.CCM.0000251821.44259.F3.

    Article  PubMed  Google Scholar 

  61. Lomas C, Roca O, Álvarez A, Masclans JR. Fibroscopy in patients with hypoxemic respiratory insufficiency: Utility of the high-flow nasal cannula. Respir Med CME. 2009;2(3):121–4.

    Article  Google Scholar 

  62. Miyagi K, Haranaga S, Higa F, et al. Implementation of bronchoalveolar lavage using a high-flow nasal cannula in five cases of acute respiratory failure. Respir Investig. 2014;52(5):310–4. doi:10.1016/j.resinv.2014.06.006.

    Article  PubMed  Google Scholar 

  63. Futier E, Paugam-Burtz C, Constantin J-M, et al. The OPERA trial--comparison of early nasal high flow oxygen therapy with standard care for prevention of postoperative hypoxemia after abdominal surgery: study protocol for a multicenter randomized controlled trial. Trials. 2013;14:341. doi:10.1186/1745-6215-14-341.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Hernandez G, Pedrosa A, Ortiz R, et al. The effects of increasing effective airway diameter on weaning from mechanical ventilation in tracheostomized patients: a randomized controlled trial. Intensive Care Med. 2013;39(6):1063–70. doi:10.1007/s00134-013-2870-7.

    Article  PubMed  Google Scholar 

  65. Rea H, McAuley S, Jayaram L, et al. The clinical utility of long-term humidification therapy in chronic airway disease. Respir Med. 2010;104(4):525–33. doi:10.1016/j.rmed.2009.12.016.

    Article  PubMed  Google Scholar 

  66. Donaldson GC, Seemungal TAR, Bhowmik A, Wedzicha JA. Relationship between exacerbation frequency and lung function decline in chronic obstructive pulmonary disease. Thorax. 2002;57(10):847–52. Available at: doi:10.1136/thorax.57.10.847. Accessed October 3, 2015.

  67. Bhowmik A, Seemungal TA, Sapsford RJ, et al. Comparison of spontaneous and induced sputum for investigation of airway inflammation in chronic obstructive pulmonary disease. Thorax. 1998;53(11):953–6. Available at: http://www.ncbi.nlm.nih.gov/pubmed/10193394. Accessed October 26, 2015.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  68. Fuschillo S, De Felice A, Balzano G. Mucosal inflammation in idiopathic bronchiectasis: cellular and molecular mechanisms. Eur Respir J. 2008;31(2):396–406. doi:10.1183/09031936.00069007.

    CAS  Article  PubMed  Google Scholar 

  69. Prescott E, Lange P, Vestbo J. Chronic mucus hypersecretion in COPD and death from pulmonary infection. Eur Respir J. 1995;8(8):1333–8. Available at: http://www.ncbi.nlm.nih.gov/pubmed/7489800. Accessed October 26, 2015.

    CAS  Article  PubMed  Google Scholar 

  70. Rogers DF. Mucus pathophysiology in COPD: differences to asthma, and pharmacotherapy. Monaldi Arch Chest Dis. 2000;55(4):324–32. Available at: http://www.ncbi.nlm.nih.gov/pubmed/11057087. Accessed October 26, 2015.

    CAS  PubMed  Google Scholar 

  71. Hasani A, Chapman TH, McCool D, et al. Domiciliary humidification improves lung mucociliary clearance in patients with bronchiectasis. Chron Respir Dis. 2008;5(2):81–6. doi:10.1177/1479972307087190.

    CAS  Article  PubMed  Google Scholar 

  72. Storgaard LH, Frystyck M, Hockey H, Weinreich LM. Number of exacerbations in COPD patients on LTOT treated with a nasal high flow system. Eur Respir J. 2014 vol. 44 no. Suppl 58 P4730.

  73. Okuda M, Kashio M, Tanaka N, et al. 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. doi:10.1186/1752-1947-8-341.

    Article  PubMed  PubMed Central  Google Scholar 

  74. Nilius G, Franke K-J, Domanski U, et al. Effects of nasal insufflation on arterial gas exchange and breathing pattern in patients with chronic obstructive pulmonary disease and hypercapnic respiratory failure. Adv Exp Med Biol. 2013;755:27–34. doi:10.1007/978-94-007-4546-9_4.

    CAS  Article  PubMed  Google Scholar 

  75. Nilius G, Domansky U, Franke KJ, Rühle KH, Schneider H. Nasal High Flow Oxygen Therapy Attenuates Nocturnal Hypoventilation In COPD Patients With Hypercapnic Respiratory Failure. Am J Respir Crit Care Med. 2013;187:A3102.

  76. McGinley BM, Patil SP, Kirkness JP, et al. A nasal cannula can be used to treat obstructive sleep apnea. Am J Respir Crit Care Med. 2007;176(2):194–200. doi:10.1164/rccm.200609-1336OC.

    Article  PubMed  PubMed Central  Google Scholar 

  77. Haba-Rubio J, Andries D, Rey V, et al. Effect of transnasal insufflation on sleep disordered breathing in acute stroke: a preliminary study. Sleep Breath. 2012;16(3):759–64. doi:10.1007/s11325-011-0572-3.

    Article  PubMed  Google Scholar 

  78. Epstein AS, Hartridge-Lambert SK, Ramaker JS, et al. Humidified high-flow nasal oxygen utilization in patients with cancer at Memorial Sloan-Kettering Cancer Center. J Palliat Med. 2011;14(7):835–9. doi:10.1089/jpm.2011.0005.

    Article  PubMed  Google Scholar 

  79. Lee HY, Rhee CK, Lee JW. Feasibility of high-flow nasal cannula oxygen therapy for acute respiratory failure in patients with hematologic malignancies: a retrospective single-center study. J Crit Care. 2015;30(4):773–7. doi:10.1016/j.jcrc.2015.03.014.

    Article  PubMed  Google Scholar 

  80. Sunbul FS, Fink JB, Harwood R, et al. Comparison of HFNC, bubble CPAP and SiPAP on aerosol delivery in neonates: an in-vitro study. Pediatr Pulmonol. 2015;50(11):1099–106. doi:10.1002/ppul.23123.

    Article  PubMed  Google Scholar 

  81. Perry SA, Kesser KC, Geller DE, et al. Influences of cannula size and flow rate on aerosol drug delivery through the Vapotherm humidified high-flow nasal cannula system. Pediatr Crit Care Med. 2013;14(5):e250–6. doi:10.1097/PCC.0b013e31828a7f79.

    Article  PubMed  Google Scholar 

  82. MacLoughlin R, Power P, Wolny N, Duffy C. Evaluation of vibrating mesh nebulizer performance during nasal high flow therapy. J Aerosol Med Pulm Drug Deliv. 2013;26(2):A51.

  83. Longest PW, Walenga RL, Son Y-J, Hindle M. High-efficiency generation and delivery of aerosols through nasal cannula during noninvasive ventilation. J Aerosol Med Pulm Drug Deliv. 2013;26(5):266–79. doi:10.1089/jamp.2012.1006.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  84. Bhashyam AR, Wolf MT, Marcinkowski AL, et al. Aerosol delivery through nasal cannulas: an in vitro study. J Aerosol Med Pulm Drug Deliv. 2008;21(2):181–8. doi:10.1089/jamp.2007.0662.

    CAS  Article  PubMed  Google Scholar 

  85. Gea J, Orozco-Levi M, Gallart L. Increased inspiratory oxygen fractions (FIO2) using a conventional drug delivery nebuliser. Arch Bronconeumol. 2010;46(5):230–7. doi:10.1016/j.arbres.2010.02.002.

    Article  PubMed  Google Scholar 

  86. Vincent J-L. High-flow oxygen cannula: a very effective method to correct severe hypoxemia. J Thorac Dis. 2015;7(8):E207–8. doi:10.3978/j.issn.2072-1439.2015.07.33.

    PubMed  PubMed Central  Google Scholar 

  87. Pisani L, Corcione N, Nava S. Management of acute hypercapnic respiratory failure. Curr Opin Crit Care. 2016;22(1):45–52. doi:10.1097/MCC.0000000000000269.

    Article  PubMed  Google Scholar 

  88. Brochard L, Mancebo J, Wysocki M, et al. Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease. N Engl J Med. 1995;333(13):817–22. doi:10.1056/NEJM199509283331301.

    CAS  Article  PubMed  Google Scholar 

  89. Peter JV, Moran JL, Phillips-Hughes J, et al. Effect of non-invasive positive pressure ventilation (NIPPV) on mortality in patients with acute cardiogenic pulmonary oedema: a meta-analysis. Lancet. 2006;367(9517):1155–63. doi:10.1016/S0140-6736(06)68506-1.

    Article  PubMed  Google Scholar 

  90. Díaz Lobato S, Mayoralas Alises S. Effectiveness of high-flow oxygen therapy with warm humidification in a COPD patient with chronic cough. Arch Bronconeumol. 2011;47(8):420–1. doi:10.1016/j.arbres.2011.05.004.

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Critical Care Department, Vall d’Hebron University Hospital, Vall d’Hebron Research Institute, Barcelona, Spain

    Oriol Roca

  2. Ciber Enfermedades Respiratorias (Ciberes), Instituto de Salud Carlos III, Madrid, Spain

    Oriol Roca & Joan R. Masclans

  3. Critical Care Department, Virgen de la Salud Hospital, Toledo, Spain

    Gonzalo Hernández

  4. Respiratory Medicine Department, Ramón y Cajal University Hospital, Madrid, Spain

    Salvador Díaz-Lobato

  5. Emergency Medicine Department, Alicante General Hospital, Alicante, Spain

    José M. Carratalá

  6. Anesthesiology Department, De Cruces General Hospital, Bilbao, Spain

    Rosa M. Gutiérrez

  7. Critical Care Department, Del Mar University Hospital, IMIM (Medical Research del Mar Hospital Institute), Barcelona, Spain

    Joan R. Masclans

Authors
  1. Oriol Roca
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Gonzalo Hernández
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Salvador Díaz-Lobato
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. José M. Carratalá
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Rosa M. Gutiérrez
    View author publications

    You can also search for this author in PubMed Google Scholar

  6. Joan R. Masclans
    View author publications

    You can also search for this author in PubMed Google Scholar

Consortia

for the Spanish Multidisciplinary Group of High Flow Supportive Therapy in Adults (HiSpaFlow)

Corresponding author

Correspondence to Oriol Roca.

Additional information

Competing interests

Fisher & Paykel support a post doctoral fellow in Medical Research at the Hospital del Mar Institute. OR, GH, and JRM have had travel expenses covered by Fisher & Paykel.

Authors’ contributions

All the authors made substantial contributions to the work and drafting the work or revising it critically for important intellectual content. All the authors gave their final approval to the version submitted for publication.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Roca, O., Hernández, G., Díaz-Lobato, S. et al. Current evidence for the effectiveness of heated and humidified high flow nasal cannula supportive therapy in adult patients with respiratory failure. Crit Care 20, 109 (2016). https://doi.org/10.1186/s13054-016-1263-z

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/s13054-016-1263-z

Keywords

  • High flow nasal cannula
  • High flow oxygen therapy
  • Respiratory failure

Critical Care

ISSN: 1364-8535