EBQ:NIPPV in COPD: Difference between revisions

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| fulltexturl= http://www.nejm.org/doi/full/10.1056/NEJM199509283331301
| fulltexturl= http://www.nejm.org/doi/full/10.1056/NEJM199509283331301
| pdfurl= http://www.nejm.org/doi/pdf/10.1056/NEJM199509283331301
| pdfurl= http://www.nejm.org/doi/pdf/10.1056/NEJM199509283331301
| status = Under Review
| status = Complete
}}
}}


==Clinical Question==
==Clinical Question==
Can NIPPV be used to avoid endotracheal intubation in acute COPD exacerbation?
Can NIPPV be used to avoid endotracheal intubation in acute [[COPD]] exacerbation?


==Conclusion==
==Conclusion==
NIPPV could avoid endotracheal intubation, the length of the hospital stay, and the in-hospital mortality rate in the selected patients.
NIPPV avoids endotracheal [[intubation]], reduces the length of the hospital stay, and reduces the in-hospital mortality rate in selected patients.


==Major Points==  
==Major Points==
*In acute COPD exacerbation, noninvasive ventilation helps avoid endotracheal [[intubation]] and complications associated with mechanical ventilation
 
*The use of [[Noninvasive Ventilation]] significantly reduced the need for [[intubation]] as compared in the standard-treatment group (5 liters/min, nasal canula)
 
*The frequency of complications was significantly lower in the [[noninvasive ventilation]] group.
 
*Hospital stay was significantly shorter for the [[noninvasive ventilation]] group compared to the standard group.


==Guidelines==
==Guidelines==
{{quote|NIV should be considered in all patients with an acute exacerbation of COPD in whom a [[respiratory acidosis]] (pH < 7.35, PaCO2 > 6 kPa [45 mm Hg]) is present. | sign=British Thoracic Society<ref>Roberts CM, Brown JL, Reinhardt AK, et al. Non-invasive ventilation in chronic obstructive pulmonary disease:management of acute type 2 respiratory failure. Clin Med.2008;8(5):517-521</ref>}}
{{quote|NIV improves [[respiratory acidosis]] (increases pH and decreases PaCO2) and decreases respiratory rate, severity of breathlessness, and length of hospital stay in patients with acute exacerbations of COPD. | sign=Global Initiative for Chronic Obstructive Lung Disease (GOLD)<ref>GOLD Science Committee Methodology and summary of new recommendations. Global strategy for diagnosis, management and prevention of COPD: 2010 update. 2010</ref>}}
{{quote|Bi-level NIV is a beneficial support strategy that decreases the risk for invasive mechanical ventilation and possibly improves survival in selected hospitalized patients with respiratory failure  | sign=ACCP, ACP-ASIM<ref>Bach PB, Brown C, Gelfand SE, et al. Management of acute exacerbations of chronic obstructive pulmonary disease: a summary and appraisal of published evidence. Ann Intern Med. 2001;134(7):600-620.</ref>}}


==Design==
==Design==
Line 30: Line 43:


==Population==
==Population==
Adult patients with known or suspected COPD (by history, exam or CXR).
Adult patients with known or suspected [[COPD]] (by history, exam or CXR).


===Inclusion Criteria===
===Inclusion Criteria===
Respiratory acidosis/elevated HCO3 with exacerbation of dyspnea lasting less than two weeks.  
[[Respiratory acidosis]]/elevated HCO3 with exacerbation of dyspnea lasting less than two weeks.  
And at least two of the following:  
And at least two of the following:  
- a respiratory rate above 30 bpm  
#a respiratory rate above 30 bpm  
- PaO2 <45 mm Hg
#PaO2 <45 mm Hg
- Arterial pH < 7.35 after 10min RA
#Arterial pH < 7.35 after 10min RA


===Exclusion Criteria===
===Exclusion Criteria===
- RR < 12 bmp or need for immediate intubation (as defined below)
*RR < 12 bmp or need for immediate intubation (as defined below)
*tracheotomy or endotracheal [[intubation]] performed before admission
*the administration of sedative drugs within the previous 12 hrs
*CNS disorder unrelated to hypercapnic encephalopathy or hypoxemia
*[[cardiac arrest]] (within previous 5 days)
*cardiogenic pulmonary edema
*kyphoscoliosis as the cause of chronic respiratory failure or a neuromuscular disorder
*upper airway obstruction or asthma
*a clear cause of decompensation requiring specific treatment (e.g., peritonitis, [[septic shock]], [[acute myocardial infarction]], [[pulmonary thromboembolism]], [[pneumothorax]], [[hemoptysis]], severe [[pneumonia]], or recent surgery or trauma); a facial deformity; or enrollment in other investigative protocols.
*Refusal to undergo endotracheal [[intubation]]


- tracheotomy or endotracheal intubation performed before admission
==Interventions==
Both groups received:
*[[subcutaneous heparin]]
*[[antibiotics]]
*bronchodilators (subcutaneous terbutaline, aerosolized and intravenous albuterol, and corticosteroids or intravenous aminophylline or both)
*electrolyte corrections


- the administration of sedative drugs within the previous 12 hrs
'''Standard group:'''
*Supp O2 to max 5L NC to keep arterial O2Sat >90%


- CNS disorder unrelated to hypercapnic encephalopathy or hypoxemia
'''NIPPV group:'''
*At least 6 hours daily of NIPPV by ARM 25 machine keep arterial O2Sat >90% ''(Duration of [[noninvasive ventilation]] was determined on the basis of clinical criteria and arterial-blood gas levels.)''


- cardiac arrest (within previous 5 days)
'''Hard criteria for intubation in either group:'''
#respiratory arrest
#respiratory pauses with loss of consciousness or gasping for air, psychomotor agitation
#making nursing care impossible and requiring sedation
#HR ≤ 50 bpm with loss of alertness
#Hemodynamic instability with systolic arterial blood pressure below 70 mm Hg.


- cardiogenic pulmonary edema;
''In NIPPV group if a criterion was present after the withdrawal of ventilatory support, it could be reintroduced. If the criterion persisted after ventilation had been resumed, intubation was performed''


- kyphoscoliosis as the cause of chronic respiratory failure or a neuromuscular disorder
==Outcomes==


- upper airway obstruction or asthma
===Primary Outcomes===
Need for endotracheal [[intubation]] and mechanical ventilation at any point in the study:


- a clear cause of decompensation requiring specific treatment (e.g., peritonitis, septic shock, acute myocardial infarction, pulmonary thromboembolism, pneumothorax, hemoptysis, severe pneumonia, or recent surgery or trauma); a facial deformity; or enrollment in other investigative protocols.  
Thirty-one of the 42 patients (74 percent) in the standard-treatment
group required endotracheal intubation, as compared with only 11 of the
43 patients (26 percent) in the noninvasive-ventilation group (P < 0.001).


- Refusal to undergo endotracheal intubation
===Secondary Outcomes===
*Complications:
**The proportion of patients with one or more complications was significantly higher in the standard-treatment group (20 of 42 patients, or 48 percent) than in the noninvasive-ventilation group (7 of 43, or 16 percent; P_ 0.001).


==Interventions==
*Duration of ventilator assistance:
**In the standard-treatment group, the 31 patients who required endotracheal intubation were ventilated for a total of 17_ 21 days.
**In the noninvasive- ventilation group, the 11 patients who underwent endotracheal intubation were intubated for a total of 25+ 17 days; the other 32 patients were ventilated with a face mask fora mean of 4 +4 days.


==Outcomes==
*Mortality rate during hospitalization:
**The proportion of patients who died in the hospital was also significantly higher in the standard-treatment group (12 of 42 patients, or 29 percent, vs. 4 of 43, or 9 percent; P_ 0.02).
**Ten of the 12 deaths in the standard-treatment group and 3 of the 4 in the noninvasive-ventilation group occurred during mechanical ventilation.
**Since the numbers of patients requiring intubation were different in the two groups, they  compared mortality rates after adjustment for endotracheal intubation, using the Mantel–Haenszel test. After adjustment, they found no significant difference, suggesting that the number of patients requiring intubation was the main factor explaining the difference in mortality


===Primary Outcomes===
==Review Questions==
<quiz display=simple>


===Secondary Outcomes===
{What is one group that was excluded from the study that might benefit from NIPPV?
|type="[]"}
-[[COPD]] patients with 1 week of shortness of breath.
+DNI patients with COPD exacerbation.
-Patients with hypoxia and hypercapnea.
-Patients greater that 65 yoa.


==Subgroup Analysis==
{If a patient in the NIPPV group met criteria for intubation at any time they were intubated immediately.
|type="[]"}
+False
-True


==Criticisms==
{Which was not a statistically significant result found in this study?
|type="[]"}
-Fewer patients in the NIPPV required intubation
-Mortality was higher in the standard treatment group
+Use of nebulizers was less in the NIPPV group.
-Hospital stay was longer in the standard treatment group


==Funding==
{What did the authors believe to be the cause for increased mortality seen in the standard treatment group?
|type="[]"}
-Shock
+Increased need for intubation
-Lack of antibiotics
-Delays in intubation


==CME==
</quiz>


==Sources==
==Sources==
<references/>
<references/>


[[Category:EBQ]][[Category:Pulm]]
[[Category:EBQ]][[Category:Pulmonary]]

Latest revision as of 16:12, 22 March 2016

Complete Journal Club Article
Brochard L et al. "Noninvasive ventilation for acute exacerbations of chronic obstructive pulmonary disease.". NEJM. 1995. 333(13):817-22.
PubMed Full text PDF

Clinical Question

Can NIPPV be used to avoid endotracheal intubation in acute COPD exacerbation?

Conclusion

NIPPV avoids endotracheal intubation, reduces the length of the hospital stay, and reduces the in-hospital mortality rate in selected patients.

Major Points

  • In acute COPD exacerbation, noninvasive ventilation helps avoid endotracheal intubation and complications associated with mechanical ventilation

Guidelines

NIV should be considered in all patients with an acute exacerbation of COPD in whom a respiratory acidosis (pH < 7.35, PaCO2 > 6 kPa [45 mm Hg]) is present.

—British Thoracic Society[1]


NIV improves respiratory acidosis (increases pH and decreases PaCO2) and decreases respiratory rate, severity of breathlessness, and length of hospital stay in patients with acute exacerbations of COPD.

—Global Initiative for Chronic Obstructive Lung Disease (GOLD)[2]

Bi-level NIV is a beneficial support strategy that decreases the risk for invasive mechanical ventilation and possibly improves survival in selected hospitalized patients with respiratory failure

—ACCP, ACP-ASIM[3]

Design

Multicenter prospective randomized trial at five hospitals

Population

Adult patients with known or suspected COPD (by history, exam or CXR).

Inclusion Criteria

Respiratory acidosis/elevated HCO3 with exacerbation of dyspnea lasting less than two weeks. And at least two of the following:

  1. a respiratory rate above 30 bpm
  2. PaO2 <45 mm Hg
  3. Arterial pH < 7.35 after 10min RA

Exclusion Criteria

  • RR < 12 bmp or need for immediate intubation (as defined below)
  • tracheotomy or endotracheal intubation performed before admission
  • the administration of sedative drugs within the previous 12 hrs
  • CNS disorder unrelated to hypercapnic encephalopathy or hypoxemia
  • cardiac arrest (within previous 5 days)
  • cardiogenic pulmonary edema
  • kyphoscoliosis as the cause of chronic respiratory failure or a neuromuscular disorder
  • upper airway obstruction or asthma
  • a clear cause of decompensation requiring specific treatment (e.g., peritonitis, septic shock, acute myocardial infarction, pulmonary thromboembolism, pneumothorax, hemoptysis, severe pneumonia, or recent surgery or trauma); a facial deformity; or enrollment in other investigative protocols.
  • Refusal to undergo endotracheal intubation

Interventions

Both groups received:

  • subcutaneous heparin
  • antibiotics
  • bronchodilators (subcutaneous terbutaline, aerosolized and intravenous albuterol, and corticosteroids or intravenous aminophylline or both)
  • electrolyte corrections

Standard group:

  • Supp O2 to max 5L NC to keep arterial O2Sat >90%

NIPPV group:

  • At least 6 hours daily of NIPPV by ARM 25 machine keep arterial O2Sat >90% (Duration of noninvasive ventilation was determined on the basis of clinical criteria and arterial-blood gas levels.)

Hard criteria for intubation in either group:

  1. respiratory arrest
  2. respiratory pauses with loss of consciousness or gasping for air, psychomotor agitation
  3. making nursing care impossible and requiring sedation
  4. HR ≤ 50 bpm with loss of alertness
  5. Hemodynamic instability with systolic arterial blood pressure below 70 mm Hg.

In NIPPV group if a criterion was present after the withdrawal of ventilatory support, it could be reintroduced. If the criterion persisted after ventilation had been resumed, intubation was performed

Outcomes

Primary Outcomes

Need for endotracheal intubation and mechanical ventilation at any point in the study:

Thirty-one of the 42 patients (74 percent) in the standard-treatment group required endotracheal intubation, as compared with only 11 of the 43 patients (26 percent) in the noninvasive-ventilation group (P < 0.001).

Secondary Outcomes

  • Complications:
    • The proportion of patients with one or more complications was significantly higher in the standard-treatment group (20 of 42 patients, or 48 percent) than in the noninvasive-ventilation group (7 of 43, or 16 percent; P_ 0.001).
  • Duration of ventilator assistance:
    • In the standard-treatment group, the 31 patients who required endotracheal intubation were ventilated for a total of 17_ 21 days.
    • In the noninvasive- ventilation group, the 11 patients who underwent endotracheal intubation were intubated for a total of 25+ 17 days; the other 32 patients were ventilated with a face mask fora mean of 4 +4 days.
  • Mortality rate during hospitalization:
    • The proportion of patients who died in the hospital was also significantly higher in the standard-treatment group (12 of 42 patients, or 29 percent, vs. 4 of 43, or 9 percent; P_ 0.02).
    • Ten of the 12 deaths in the standard-treatment group and 3 of the 4 in the noninvasive-ventilation group occurred during mechanical ventilation.
    • Since the numbers of patients requiring intubation were different in the two groups, they compared mortality rates after adjustment for endotracheal intubation, using the Mantel–Haenszel test. After adjustment, they found no significant difference, suggesting that the number of patients requiring intubation was the main factor explaining the difference in mortality

Review Questions

1 What is one group that was excluded from the study that might benefit from NIPPV?

COPD patients with 1 week of shortness of breath.
DNI patients with COPD exacerbation.
Patients with hypoxia and hypercapnea.
Patients greater that 65 yoa.

2 If a patient in the NIPPV group met criteria for intubation at any time they were intubated immediately.

False
True

3 Which was not a statistically significant result found in this study?

Fewer patients in the NIPPV required intubation
Mortality was higher in the standard treatment group
Use of nebulizers was less in the NIPPV group.
Hospital stay was longer in the standard treatment group

4 What did the authors believe to be the cause for increased mortality seen in the standard treatment group?

Shock
Increased need for intubation
Lack of antibiotics
Delays in intubation


Sources

  1. Roberts CM, Brown JL, Reinhardt AK, et al. Non-invasive ventilation in chronic obstructive pulmonary disease:management of acute type 2 respiratory failure. Clin Med.2008;8(5):517-521
  2. GOLD Science Committee Methodology and summary of new recommendations. Global strategy for diagnosis, management and prevention of COPD: 2010 update. 2010
  3. Bach PB, Brown C, Gelfand SE, et al. Management of acute exacerbations of chronic obstructive pulmonary disease: a summary and appraisal of published evidence. Ann Intern Med. 2001;134(7):600-620.