Tag Archives: HFNC

Case

A 55 y/o male with a h/o EtOH abuse is intubated and admitted to the MICU for hypoxemic respiratory failure secondary to aspiration PNA.  Three days later, his vital signs have normalized, he is awake and able to follow commands, minimal secretions are noted with suctioning of his ET tube, and his SpO2 is >95% on 40% FiO2 and 5 PEEP.  He passes a 30 minute trial of spontaneous breathing with a T-piece.

Question

Following extubation, should he be given high-flow nasal oxygen to help prevent the need for reintubation?

Evidence

1. We previously reviewed the FLORALI trial, NEJM 2015 which looked at the up-front use of high-flow nasal cannula (HFNC) in patients with hypoxemic respiratory failure

1. 313 patients randomized to HFNC vs NIV
   1. HFNC did not lower need for intubation at 28 days
   2. HFNC did lower ICU and 90-day mortality
2. Interpretation of trial results complicated by significant cross-over in the use of HFNC and NIV between study arms

1. There is a growing body of literature on the use of HFNC following extubation
   1. We previously reviewed a JAMA 2015 trial looking at the use of HFNC vs NIV in 830 patients at high-risk of reintubation following cardiac surgery

1. No difference in treatment failure (defined as re-intubation, switch to other study treatment, or premature study discontinuation) between groups
2. Roughly 14% required re-intubation in each group (no difference)

• Similar dyspnea and comfort score between groups

1. 1. Nasal High-flow versus Venturi Mask Oxygen Therapy after Extubation, AJRCCM 2014, Italy

1. 105 patients with a P/F < 300 following SBT randomized to oxygen via HFNC (flow 50 L/min) or venturi mask for 48 hrs or until ICU discharge (the low P/F perhaps indicative of a group at higher risk of post extubation hypoxemia and need for reintubation)
   1. P/F ratio at 24 hrs (primary end point) significantly higher in HFNC group (287 vs 247). P/F also higher at 36 and 48 hrs in HFNC group
   2. Patient comfort significantly higher in HFNC group
   3. Significantly fewer reintubations in HFNC group (4% vs 21%) although the study was not powered for this outcome

1. 1. A new trial was just published on the use of HFNC following extubation in patients felt to be at low-risk of post-extubation hypoxemia – Effect of Post-extubation HFNC vs Conventional Oxygen Therapy on Reintubation in Low-Risk Patients, JAMA 2016, Spain

1. Methods
   1. Inclusion
      1. Pts on mechanical ventilation >12 hrs who passed an SBT and were defined as low risk of reintubation by having all of the following (few patients in our MICU would meet these criteria)
         1. Age <65
         2. Not initially intubated for CHF

• Absence of mod-severe COPD

1. APACHE II <12
2. BMI <30
3. No known airway problems and low risk of developing laryngeal edema

• Adequate cough and requiring suctioning <2xs Q8hrs
• Not difficult to wean

1. Mechanical ventilation <7 days
2. <2 co-morbidities

2. Exclusions
   1. DNR
   2. Trach
   3. Hypercapnia during SBT
3. Intervention
   1. Immediately following extubation, pts were randomized to either
      1. HFNC x 24 hrs
         1. set at 10L/min and titrated up at 5L/min intervals until pts experienced discomfort
         2. FiO2 titrated to SpO2 >92%.
      2. Conventional oxygen applied through facemask or nasal cannula titrated to SpO2 >92% x 24hrs

• Primary outcome
  1. Need for reintubation at 72 hrs

1. Results
   1. 1739 pts ready to be liberated from the vent  527 randomized (vast majority excluded as they were high risk for reintubation)
   2. Patient characteristics
      1. Age ≈51
      2. Neurologic co-morbidity 7.6% in HFNC group and 12.9% in conventional O2 group (only significant baseline difference between the two groups)
      3. Time on vent ≈ 1-2 days
      4. ≈30% admitted with primary neurologic diagnosis and ≈47% had either scheduled or urgent surgery at admission (not a typical MICU population)
   3. Outcomes

1. In multivariable analysis, HFNC was independently and inversely associated with all-cause reintubation.
2. NNT to prevent 1 reintubation = 14

1. Conclusion
   1. Among patients felt to be at low risk for reintubation, the use of HFNC following extubation vs conventional O2 reduced the need for reintubation at 72hrs with a NNT of 14

Faculty Feedback

I asked Dr. Ben Singer, Assistant Professor of Medicine in the Division of Pulmonary and Critical Care, whether he felt the JAMA trial was practice changing.  A summary of his comments:

• Important to remember that supplemental O2 is not an entirely benign therapy.  In both animal models and studies of healthy controls, high levels of FiO2 have been found to promote lung injury.  Supplemental FiO2 after extubation should therefore be used thoughtfully.
• With this in mind, it is important to note that the majority of the patients in the trial were placed on mechanical ventilation for surgical or neurologic diagnoses (only 16% had a primary respiratory reason for mechanical ventilation).  This population is likely at lower risk of lung injury from prolonged high levels of FiO2 than a patient recovering from PNA or ARDS.  This may have biased the trial toward a positive result.  Interestingly, more patients in the conventional O2 arm of the trial had ARDS (4.2% vs 1.5%) – perhaps contributing to the higher rates of reintubation seen in the control arm.
• As noted above, the patient population in the trial is not representative of patients typically cared for in the MICU.  As a result, the positive results seen with post-extubation HFNC are not necessarily generalizable to MICU patients.
• There were 7 cases of laryngeal edema necessitating reintubation in the control arm and 0 cases in the HFNC arm.  This is likely just an artifact of randomization as it is hard to imagine HFNC preventing severe laryngeal edema.  If 5 of the severe laryngeal edema patients had been randomized to the HFNC arm, the results of the trial would not have been significant.
• The curves from Fig 2  look convincing as they immediately separate during the first 24 hrs (when HFNC is being used) and then become essentially parallel suggesting a real benefit from HFNC

• Important for housestaff to recognize that this trial excluded hypercapnic patients, a group where the evidence supports the up-front use of NIV following extubation.
• Overall this was a well performed and methodologically rigorous trial.  The results are provocative but limited by the unique patient population (largely healthy neurocritical care and surgical patients).  The trial highlights the need for a large randomized trial of HFNC following extubation in a more inclusive group of MICU patients

Take-home Points

• The use of HFNC following extubation may reduce the risk of reintubation when compared to conventional O2.  Further trials are needed to clarify which patients stand to benefit most from this therapy.

Case

A 70 year-old male is brought in by ambulance from his nursing home with 2 days of fever, shortness of breath and purulent sputum production.  He is febrile, tachycardic, and tachypneic with an initial SpO2 of 86% on RA which improves to 92% with 5L NC.  On exam he is alert and oriented but appears ill with crackles at his right lung base.  A portable CXR shows a dense right-sided infiltrate.  ABG does not show any evidence of hypercarbia

Questions

What oxygen delivery device would you use to help manage his hypoxemic respiratory failure?  Is there a role for the use of a high-flow nasal cannula (HFNC)?

Physiology and recent trials

1. Common O2 delivery devices
   1. In general, maximal flow rates of common O2 delivery device are limited by the ability to effectively heat and humidify gas at high flow rates
   2. Nasal cannula
      1. O2 delivery inefficient as O2 flowing through cannula mixes significantly with entrained room air (unable to obtain delivered FiO2 >40%)
      2. High flow rates poorly tolerated as cool dry air irritates the nares
   3. Face mask (Venturi mask)
      1. Can achieve higher flow rates (6-10L/min). Room air entrained through exhalation ports limits maximal FiO2 to 50%
   4. Non-rebreather mask
      1. Includes special valves which limit entrained air allowing delivery of FiO2 near 95%
      2. Maximal flow rates of 10-15L/min
   5. NIV (BiPAP)
      1. Good evidence to support the use of NIV in acute decompensated heart failure and exacerbations of obstructive lung disease
      2. Cumbersome to set up and interface often uncomfortable for patients

• Mixed data on its efficacy in acute hypoxemic respiratory failure (AHRF)

2. HFNC
   1. Device (see picture above)
      1. Uses a special oxygen/air blender connected to a heated humidifier to saturate air with water and warm air to body temperature before delivery. This system allows for the delivery of very high flow rates (up to 60L/min)
      2. Connects to the nose with large soft prongs
         1. Potential benefits
            1. Ability to deliver heated and humidified gas at high flow rates
               1. Prevents drying of the airway and interference with mucocilliary clearance
               2. Enhances patient comfort
               3. May help moisten secretions making them easier to clear
               4. May lessen work of breathing by avoiding the bronchoconstricting effects of cold air and lessening the work needed to expectorate secretions
            2. Minimizing entrainment of room air
               1. Patients in respiratory failure often have high flow rates that exceed the flow of nasal cannulas and face-masks resulting in entrained room air which dilutes supplemental O2
               2. Flow rates in HFNC usually exceed patient-generated flows minimizing dilution of delivered oxygen

• Improved ventilator efficiency
  1. HFNC can continually flush CO2 out of nasopharynx (lowering nasopharyngeal dead space) and allowing more of the minute ventilation to participate in gas exchange
  2. PEEP effect
     1. HFNC increases nasopharyngeal and esophageal pressure approximating levels seen with nasal CPAP
     2. HFNC may therefore provide a small amount of inspiratory assistance, help counter-balance auto-PEEP, and potentially improve oxygenation
  3. Breathing pattern
     1. Some evidence that HFNC helps increase TV and lowers RR
  4. Use
     1. Greatest benefit likely in patients with significant hypoxemia that would ordinarily be given standard high-flow oxygen therapy via a face mask
     2. Avoid in patients with high breathing workloads whose ventilatory failure is worsening (these patients require closely monitored NIV vs intubation)
     3. Usually provides more oxygen and gas flow than is necessary for patients with mild hypoxemia
     4. Initial settings
        1. Initial adjustments should be to flow rate as it is the flow rate that drives the physiologic benefit. Increase flow if RR fails to drop or if breathing remains labored with initial settings
        2. Starting flow rate is usually 35-40L/min
        3. Increasing flow rate should improve FiO2 as the amount of entrained air decreases
     5. There are two recent large randomized trials investigating the use of HFNC which are worth knowing
        1. High-flow oxygen through nasal cannula in acute hypoxemic respiratory failure (FLORALI) – NEJM, 2015
           1. Methods
              1. Multicenter randomized trial in 23 ICUs throughout France and Belgium
              2. Inclusion (need to meet all 4)
                 1. RR>25, P/F < 300 while on O2 flow of 10L/min for at least 15 minutes, PaCO2<45, no history of chronic respiratory failure (ie pts with AHRF without concurrent hypercapnia)
              3. Exclusions
                 1. PaCO2>45, exacerbation of asthma or chronic respiratory failure, cardiogenic pulmonary edema, neutropenia, shock, GCS <13, contraindications to NIV, urgent need for intubation, DNR (important to exclude obstructive lung disease and decompensated CHF where there is a known benefit to NIV)
              4. Patients randomized to 3 groups
                 1. Standard O2 therapy: nonrebreather mask with flow of 10L/min or more with flow adjusted to maintain SpO2 >92% until patient recovered or was intubated
                 2. HFNC: flow rate >50L/min and FiO2 100% with FiO2 adjusted to maintain SpO2 >92%. HFNC applied for 48 hours.  In the HFNC and standard oxygen group, a trial of NIV was allowed at the discretion of the MD
                 3. NIV: pressure support adjusted to obtain a tidal volume of 7-10cc/kg PBW with initial PEEP between 2-10 cmH20. FiO2 and PEEP then adjusted to maintain SpO2 >92%.  Minimum duration of NIV was 8 hours/day for at least 2 calendar days.  NIV applied during sessions of at least 1 hour and could be resumed if RR was more than 25 and SpO2 <92%.  Between NIV, patients received HFNC
              5. Results
                 1. 2,500 patients admitted with HRF  525 eligible  313 randomized (13% of patients with HRF included in trial)
                 2. Causes of respiratory failure
                    1. CAP: 64%
                    2. HAP: 12%
                 3. Initial mean settings
                    1. Standard O2: O2 flow rate of 14L/min
                    2. HFNC: O2 flow rate of 48L/min, mean FiO2 80%
                    3. NIV: 8/5, FiO2 70%, TV 9 cc/kg
                 4. 25% in NIV group received therapy for <4hrs per day
                 5. 40 patients in the HFNC and standard O2 received BiPAP as a rescue therapy
                 6. Outcomes (statistically significant results in bold)

1. 90-day mortality
   2. Hazard ratio for death of 2.01 (1.01-3.99) when comparing standard O2 vs HFNC group and 2.5 (1.31-4.78) when comparing NIV vs HFNC
2. Intensity of respiratory discomfort and dyspnea score significantly improved in the HFNC group 1 hour after enrollment

• Conclusions
  1. The use of HFNC vs standard O2 or NIV did not prevent the primary outcome of need for intubation at 28 days
  2. HFNC was associated with several important secondary outcomes
     1. Lower ICU mortality
     2. Lower 90-day mortality
     3. Less need for intubation in patients with a P/F <200
  3. The authors and editorial wonder whether the high tidal volumes achieved with NIV may have contributed to the worse secondary outcomes seen in the NIV group

1. High-Flow nasal oxygen vs noninvasive positive airway pressure in hypoxemic patients after cardiothoracic surgery – JAMA, 2015
   1. Respiratory failure is common following cardiac surgery with NIV currently the treatment of choice. However, NIV is cumbersome, requires significant resources, and fails in 20% of patients.   Authors wondered whether HFNC may be a better choice.
   2. Methods
      1. Multicenter randomized trial in 6 ICUs throughout France.
      2. Patients (any of the following)
         1. Failure of post-op SBT
         2. Successful SBT in patients with a BMI >30, LVEF <40%, or failure of prior extubations
         3. Successful SBT followed by failed extubation (P/F <300, RR >25 for at least 2hrs, use of accessory muscles)
         4. Exclusions included OSA, tracheostomy, DNI, delirium, nausea, vomiting, altered mental status, hemodynamic instability
      3. Patients randomized to the use of HFNC or NIV

• Results
  1. 3,217 eligible, 830 randomized (80% were s/p CABG)
  2. Primary outcome of treatment failure (defined as re-intubation, switch to other study treatment, or premature study discontinuation)
     21. 9% in BiPAP vs 21.0% in HFNC (no difference)
     22. No difference in time to treatment failure (1 day in each group)
     23. Roughly 14% required re-intubation in each group (no difference)
     24. No difference in outcome among patients with a P/F < 200 (in contrast to the NEJM study).
     25. Similar dyspnea and comfort score
     26. No difference in ICU or 28 day mortality
  3. Conclusion
     1. HFNC is not inferior to NIV in preventing treatment failure in patients with or at risk for respiratory failure following cardiothoracic surgery

My thoughts

• I find the results of the FLORALI study less convincing than the associated editorial suggests they are. The significant cross-over between groups (when not on NIV, patients in the NIV group received HFNC and 40 patients not on NIV were placed on NIV as a rescue therapy) and the variable duration of NIV therapy (25% of patients received therapy for <4 hours per day) make a clean comparison between the three O2 delivery methods difficult.  If a patient is on NIV for <4 hours a day and the other 20 hours was managed with HFNC, should their outcome really be associated with NIV use?
• I also find it difficult to explain the improved 90-day mortality seen with HFNC.  It is hard to picture an interaction between any mode of non-invasive O2 delivery and mortality that does not hinge on precluding the need for mechanical ventilation which was not seen in this trial.  The authors of the trial and the editorial suggest that the high tidal volume achieved with NIV may have worsened lung injury thus leading to more time on the ventilator and increased mortality but it is hard to buy this conclusion if patients managed with NIV did not require intubation any more than patients in the other two groups nor did they have higher rates of refractory hypoxemia.  A trend of P/F ratios in all three arms over time would have been helpful.  Concerns have also been raised about the high rate of septic shock in the NIV arm (31%) vs the HFNC arm (18%)

• Important to note that 45% of patients required intubation by 28 days. This highlights the importance of closely monitoring patients with AHRF being managed with HFNC or NIV as roughly half will fail. 

• After reviewing this topic, I find the use of HFNC most appealing in patients who would normally be managed with a higher-flow face mask (venturi or nonrebreather). The ability to deliver very high flows of heated/humidified air seems to offer real physiologic and comfort benefits over typical higher flow devices.

• We recently discussed the FLORALI study at a pulmonary conference. Faculty raised the important point that for older patients with pneumonia, difficulty with secretion clearance is often what leads to initiation of mechanical ventilation.  In this group of patients, placing them on NIV may inhibit their ability to clear secretions and hasten respiratory failure.  Specifically for this reason, Dr. Wunderink (MICU director) supported the idea of using HFNC over NIV as a first line therapy for older patients with pneumonia and resulting hypoxemic respiratory failure who do not require immediate mechanical ventilation.
• For those who manage patients with hypoxemic respiratory failure (either in the ER or in the ICU), if you never find yourself initiating therapy with HFNC, you are probably underusing a helpful tool.

Take-home points

• High flow nasal cannula devices deliver heated and humidified air at very high flow rates. Potential benefits include improved patient comfort, improved secretion clearance, a small PEEP effect, and washout of nasopharyngeal dead space
• The use of HFNC may improve long-term outcomes in patients with acute hypoxemic respiratory failure although further trials are needed to validate this finding
• HFNC is not inferior to NIV in preventing treatment failure following cardiothoracic surgery

Attached

• Helpful review of HFNC from CHEST, 2015
• FLORALI trial, NEJM, 2015
• Randomized trial of HFNC following cardiothoracic surgery, JAMA, 2015

“Effect of postextubation high-flow nasal cannula vs conventional oxygen therapy on reintubation in low-risk patients,” JAMA, 2016, Spain

Question: Does HFNC reduce the need for reintubation in patients at low risk of post-extubation respiratory failure?

Study Type: Multicenter, randomized clinical trial in 7 ICUs in Spain

Study Population: Patients who passed an SBT after at least 12 hrs of mechanical ventilation were eligible if they meet the following inclusion criteria: Age <65, not initially intubated for CHF, absence of mod-severe COPD, APACHE II <12, BMI <30, no known airway problems and low risk of developing laryngeal edema, adequate cough and requiring suctioning <2xs Q8hrs, not difficult to wean, mechanical ventilation <7 days, <2 co-morbidities.  Patients were excluded if they had a tracheostomy or had evidence of hypercapnia during an SBT.

Study Groups: Patients in the intervention arm were placed on HFNC with flow set at 10L/min which was titrated up at 5L/min intervals until pts experienced discomfort.  FIO2 was titrated to keep SpO2 > 92%.  Patients in the control arm had conventional oxygen applied through a facemask or nasal cannula titrated to keep SpO2>92% for 24 hrs.

Primary Outcome: Need for reintubation at 72 hrs.

 Results: 527 patients randomized. Notable patient characteristics: primary neurologic diagnosis (29%), scheduled or urgent surgery at admission (47%), primary respiratory failure (17%).  HFNC significantly reduced the need for reintubation at 72 hours (4.9% vs 12.2%, p=0.004) with a number needed to treat to prevent one reintubation of 14.  Patients treated with HFNC also had lower rates of reintubation secondary to respiratory causes (8.3% vs 14.4%, p=0.03). There was no difference in ICU length of stay or mortality.

Caveats: Primarily neurology or surgery patients (not a typical MICU population), most common cause for reintubation in the control arm was inability to clear secretions which is perhaps a function of having so many pts with neurologic injuries.

 Take-home Point: In a cohort of mostly surgical and neurologic patients at low risk for reintubation, HFNC reduced the need for reintubation compared to conventional oxygen therapy.  It is unclear if these results are generalizable to a more typical MICU population.

“Effect of postextubation high-flow nasal cannula vs noninvasive ventilation on reintubation and postextubation respiratory failure in high-risk patients,” JAMA, 2016, Spain

 Question: Is high-flow nasal cannula non-inferior to non-invasive ventilation (NIV) in reducing rates of reintubation and postextubation respiratory failure in high risk patients?

Study Type: Multicenter, randomized, non-inferiority trial in 3 ICUs in Spain

 Study Population: Patients receiving mechanical ventilation > 12 hours were eligible for the trial if they met at least one of the following criteria: age >65, CHF as primary indication for MV, mod-severe COPD, APACHE II >12 on day of extubation, BMI >30, airway patency problems, inability to deal with respiratory secretions, difficult weaning, 2 or more co-morbidities, or MV > 7 days.  Exclusions included DNR, tracheostomies, and self-extubations.

 Study Groups: Patients in the HFNC arm were placed on HFNC with flow set at 10L/min which was titrated up at 5L/min intervals until pts experienced discomfort.  FIO2 was titrated to keep SpO2 > 92%.  Patients in the NIV arm had PEEP and IPAP adjusted to targets of RR 25, SaO2 92, and pH 7.35.  FiO2 was titrated to an SpO2 of at least 92%.  Both groups were switched to conventional O2 after 24 hrs.

 Primary Outcomes: Reintubation and postextubation respiratory failure within 72 hrs.  Non-inferiority margin set at 10%

 Results: 604 patients were randomized. Notable patient characteristics: respiratory failure as primary diagnosis (56%), surgical patients (38%), neurology patients (3%), median # of high risk factors (3).  HNFC was non-inferior to NIV (19.1% of pts required reintubation in NIV group vs 22.8% in HFNC group).  More patients in the NIV group experienced postextubation respiratory failure (26.9% HFNC vs 39.8% NIV).  Close to 50% of NIV patients were unable to tolerate therapy for the full 24 hours (median duration 14 hrs).  Other than a small reduction in ICU LOS with HFNC, secondary outcomes were similar between the two groups.

Caveats: Both HFNC and NIV were given for only 24hrs (in contrast to some other studies with longer periods of therapy), sedatives to facilitate NIV tolerance were not allowed, trial was not blinded.

 Take-home Point: In high risk patients, HFNC appears non inferior to NIV in reducing rates of reintubation and postextubation respiratory failure.