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NIV in COPD
Dr. Muhammed Nishadh
Dept. of Respiratory Medicine
KIMS Hospital, Trivandrum
REFERENCE
British Thoracic Society
Working for Healthier Lungs
Introduction
• NIV has an important role in the management
of acute type II respiratory failure in COPD
patients.
• Reduction in mortality of approximately 50%
demonstrated in studies.
• NIV reduces intubation rate and mortality in
COPD patients with decompensated
respiratory acidosis (pH<7.35 and PaCO2
>6kPa OR 45 mm Hg).
• Reduces the need for ICU shift from ward
• Reduces hospital costs
Selection of patients for NIV
• NIV should be considered for all COPD patients with a
persisting respiratory acidosis (PaCO2>6kPa OR 45 mm
Hg, pH <7.35 ≥7.26) after a maximum of one hour of
standard medical therapy [A]
• Patients with a pH <7.26 may benefit from NIV but
such patients have a higher risk of treatment failure
and should be managed in a high dependency or ICU
setting [A]
• Patients should be stratified into management groups
depending on their pre-morbid state, reversibility of
acute illness, relative contraindications to ventilatory
support and the patient’s wishes [C]
Standard medical therapy includes:
– Controlled oxygen to maintain SaO2 88-92%
– Nebulised salbutamol 2.5-5mg
– Nebulised ipratroprium 500μg
– Prednisolone 30mg
– Antibiotic agent (when indicated)
– All given within the first hour
Inclusion Criteria for NIV(Clinical
criteria)
• Sick but not moribund
• *Able to protect airway
• *Conscious and cooperative
• No excessive respiratory secretions
• Potential for recovery to quality of life
acceptable to the patient
• Patient’s wishes considered
• Consider NIV if unconscious and endo-tracheal
intubation deemed inappropriate or NIV is to
be provided in a critical care setting.
• Studies support the use of NIV in patients
who are in a state of coma secondary to
hypercapnoea and who respond rapidly to
this treatment
Exclusion criteria for NIV
• facial burns/trauma/recent facial or upper
airway surgery
• vomiting
• fixed upper airway obstruction
• undrained pneumothorax
• upper gastrointestinal surgery
• inability to protect the airway
• copious respiratory secretions
Exclusion criteria for NIV (contd)
• life threatening hypoxaemia
• haemodynamically unstable requiring
inotropes/pressors (unless in a critical care
unit)
• severe co-morbidity
• confusion/agitation
• bowel obstruction
• patient declines treatment
• NIV is not the treatment of choice for patients
in heart failure or who have radiological
consolidation
• It is sometimes used if escalation to intubation
and ventilation is deemed inappropriate.
NIV settings:
• A low starting IPAP enhances patient compliance
but should be quickly adjusted upwards to
achieve therapeutic effect [C]
• Initial settings [A]:
– IPAP 10cms H2O titrated rapidly in 2-5 cms increments
at a rate of approximately 5cms H2O each 10 minutes
– usual pressure target of 20cms H2O or until a
therapeutic response is achieved or patient
tolerability has been reached.
– EPAP 4-5cms H2O is recommended
• Initial IPAP of 10cms H2O and EPAP of 4-5cms
H2O are recommended.
• These settings are well tolerated by a wide
range of patients.
• Allows acclimatization of the patient to the
machine but may not significantly improve gas
exchange.
• The therapeutic IPAP for many patients is
20cms H2O.
• A 4-5cms EPAP setting reduces CO2 re-
breathing and assists triggering of the
ventilator when using BiPAP.
• Further increases in EPAP are not
recommended without obtaining expert
advice.
• Oxygen when required should be entrained
into the circuit and the flow adjusted to help
achieve SpO2 of 88-92% [C]
• Bronchodilators should preferably be
administered off NIV.
• They may be administered on NIV and when
so should be entrained between the
expiration port and face mask.
• Delivery of both oxygen and nebulised
solutions is affected by NIV pressure settings
[B]
• If a naso-gastric tube is in place, a fine bore
tube is preferred to minimize mask leakage
[C]
Monitoring
• Monitoring should include continuous pulse
oximetry and ECG monitoring for the first 12
hours and respiratory rate, pulse, blood pressure
and assessments of consciousness regularly [B]
• ABG should be taken as a minimum at 1, 4 and 12
hours after the initiation of NIV [A]
• These should be used to assist in both formulating
a management plan and, within the first 4 hours
of NIV, the decision as to the appropriateness of
escalating to intubation [A]
• Frequent clinical monitoring of acutely ill
patients is recommended every 15 minutes in
the first hour; every 30 minutes in the 1-4
hour period and hourly in the 4-12 hour
period.
• Synchrony of ventilation should be checked
frequently.
• Compliance with NIV, patient-ventilator
synchrony and mask comfort are key factors in
determining outcome and should be checked
regularly [C]
• Staff involved in the care and monitoring of
NIV patients should be appropriately trained
and experienced [B]
Escalation
• A decision to proceed to invasive mechanical
ventilation should normally be taken within 4
hours of initiation of NIV [A]
• Intubation where appropriate is the
management of choice in late (>48hrs) NIV
failures [B]
Treatment Duration
• Patients who benefit from NIV during the first
hours of treatment should receive NIV for as
long as possible during the first 24 hours [A]
• Treatment should last until the acute cause
has resolved, commonly 2-3 days [C]
• In patients in whom NIV is successful (pH
≥7.35 achieved, resolution of underlying cause
and symptoms, respiratory rate normalized) it
is appropriate to start a weaning plan [C]
Weaning
• Treatment reduction should affect day time
ventilation periods first [C].
• After withdrawal of ventilatory support in the
day a further night of NIV is recommended [C]
• The weaning strategy should be documented
in the nursing and medical records [C]
4 day weaning strategy:
• A proposed weaning strategy is to continue
NIV for 16 hours (including 6-8 hours
overnight) on day 2, and 12 hours on day 3
(including 6-8 hours overnight).
• NIV may be discontinued on day 4 unless
continuation is clinically indicated, for
example, two hours in the morning, two hours
in the afternoon and six hours or more
overnight.
THANK YOU

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NIV in COPD

  • 1. NIV in COPD Dr. Muhammed Nishadh Dept. of Respiratory Medicine KIMS Hospital, Trivandrum
  • 3. Introduction • NIV has an important role in the management of acute type II respiratory failure in COPD patients. • Reduction in mortality of approximately 50% demonstrated in studies.
  • 4. • NIV reduces intubation rate and mortality in COPD patients with decompensated respiratory acidosis (pH<7.35 and PaCO2 >6kPa OR 45 mm Hg). • Reduces the need for ICU shift from ward • Reduces hospital costs
  • 5. Selection of patients for NIV • NIV should be considered for all COPD patients with a persisting respiratory acidosis (PaCO2>6kPa OR 45 mm Hg, pH <7.35 ≥7.26) after a maximum of one hour of standard medical therapy [A] • Patients with a pH <7.26 may benefit from NIV but such patients have a higher risk of treatment failure and should be managed in a high dependency or ICU setting [A] • Patients should be stratified into management groups depending on their pre-morbid state, reversibility of acute illness, relative contraindications to ventilatory support and the patient’s wishes [C]
  • 6. Standard medical therapy includes: – Controlled oxygen to maintain SaO2 88-92% – Nebulised salbutamol 2.5-5mg – Nebulised ipratroprium 500μg – Prednisolone 30mg – Antibiotic agent (when indicated) – All given within the first hour
  • 7. Inclusion Criteria for NIV(Clinical criteria) • Sick but not moribund • *Able to protect airway • *Conscious and cooperative • No excessive respiratory secretions • Potential for recovery to quality of life acceptable to the patient • Patient’s wishes considered
  • 8. • Consider NIV if unconscious and endo-tracheal intubation deemed inappropriate or NIV is to be provided in a critical care setting. • Studies support the use of NIV in patients who are in a state of coma secondary to hypercapnoea and who respond rapidly to this treatment
  • 9. Exclusion criteria for NIV • facial burns/trauma/recent facial or upper airway surgery • vomiting • fixed upper airway obstruction • undrained pneumothorax • upper gastrointestinal surgery • inability to protect the airway • copious respiratory secretions
  • 10. Exclusion criteria for NIV (contd) • life threatening hypoxaemia • haemodynamically unstable requiring inotropes/pressors (unless in a critical care unit) • severe co-morbidity • confusion/agitation • bowel obstruction • patient declines treatment
  • 11. • NIV is not the treatment of choice for patients in heart failure or who have radiological consolidation • It is sometimes used if escalation to intubation and ventilation is deemed inappropriate.
  • 12. NIV settings: • A low starting IPAP enhances patient compliance but should be quickly adjusted upwards to achieve therapeutic effect [C] • Initial settings [A]: – IPAP 10cms H2O titrated rapidly in 2-5 cms increments at a rate of approximately 5cms H2O each 10 minutes – usual pressure target of 20cms H2O or until a therapeutic response is achieved or patient tolerability has been reached. – EPAP 4-5cms H2O is recommended
  • 13. • Initial IPAP of 10cms H2O and EPAP of 4-5cms H2O are recommended. • These settings are well tolerated by a wide range of patients. • Allows acclimatization of the patient to the machine but may not significantly improve gas exchange.
  • 14. • The therapeutic IPAP for many patients is 20cms H2O. • A 4-5cms EPAP setting reduces CO2 re- breathing and assists triggering of the ventilator when using BiPAP. • Further increases in EPAP are not recommended without obtaining expert advice.
  • 15. • Oxygen when required should be entrained into the circuit and the flow adjusted to help achieve SpO2 of 88-92% [C] • Bronchodilators should preferably be administered off NIV. • They may be administered on NIV and when so should be entrained between the expiration port and face mask.
  • 16. • Delivery of both oxygen and nebulised solutions is affected by NIV pressure settings [B] • If a naso-gastric tube is in place, a fine bore tube is preferred to minimize mask leakage [C]
  • 17. Monitoring • Monitoring should include continuous pulse oximetry and ECG monitoring for the first 12 hours and respiratory rate, pulse, blood pressure and assessments of consciousness regularly [B] • ABG should be taken as a minimum at 1, 4 and 12 hours after the initiation of NIV [A] • These should be used to assist in both formulating a management plan and, within the first 4 hours of NIV, the decision as to the appropriateness of escalating to intubation [A]
  • 18. • Frequent clinical monitoring of acutely ill patients is recommended every 15 minutes in the first hour; every 30 minutes in the 1-4 hour period and hourly in the 4-12 hour period. • Synchrony of ventilation should be checked frequently.
  • 19. • Compliance with NIV, patient-ventilator synchrony and mask comfort are key factors in determining outcome and should be checked regularly [C] • Staff involved in the care and monitoring of NIV patients should be appropriately trained and experienced [B]
  • 20. Escalation • A decision to proceed to invasive mechanical ventilation should normally be taken within 4 hours of initiation of NIV [A] • Intubation where appropriate is the management of choice in late (>48hrs) NIV failures [B]
  • 21. Treatment Duration • Patients who benefit from NIV during the first hours of treatment should receive NIV for as long as possible during the first 24 hours [A] • Treatment should last until the acute cause has resolved, commonly 2-3 days [C] • In patients in whom NIV is successful (pH ≥7.35 achieved, resolution of underlying cause and symptoms, respiratory rate normalized) it is appropriate to start a weaning plan [C]
  • 22. Weaning • Treatment reduction should affect day time ventilation periods first [C]. • After withdrawal of ventilatory support in the day a further night of NIV is recommended [C] • The weaning strategy should be documented in the nursing and medical records [C]
  • 23. 4 day weaning strategy: • A proposed weaning strategy is to continue NIV for 16 hours (including 6-8 hours overnight) on day 2, and 12 hours on day 3 (including 6-8 hours overnight). • NIV may be discontinued on day 4 unless continuation is clinically indicated, for example, two hours in the morning, two hours in the afternoon and six hours or more overnight.