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Hypoxia and oxygen therapy
Historical considerations
ī‚— Carl Wilhelm Scheele – 1773
Discovered O2
ī‚— John Pristley – 1774
Was the first to publish
a paper on O2
ī‚— Antoine Lavoisier – 1777
Coined the term “O2”
Oxygen:
ī‚— Colourless
ī‚— Odourless
ī‚— Tasteless
ī‚— Transparent gas
ī‚— Slightly heavier than air
ī‚— Constitues 20-21% of atmospheric air
ī‚— Essential for life
Importance of O2 in cell chemistry
ī‚— Required in aerobic metabolism for:
1. Production of high energy phosphate compounds
(ATP)
2. Dehydrogenation of flavo proteins
3. Biotransformation of drugs
4. Oxidation of certain other substrates..
Definations:
ī‚— Hypoxia: low level of oxygen at tissue level
ī‚— Hypoxemia: low levels of oxygen in blood
ī‚— Partial pressure: the pressure exerted on a surface by
the molecules of individual gases.
The partial pressure of oxygen can be calculated
for a given atmospheric pressure, by multiplying
concentration of a gas by the atmospheric or
barometric pressure.
Eg: 760 mm Hg 21% = 160 mm Hg
Oxygen cascade
ī‚— Oxygen cascade refers to the progressive decrease in
the partial pressure of oxygen from the ambient air
to the cellular level.
PO2 in inspired air 150-160 mm Hg
PO2 in alveolar gas (PAO2) 100- 110 mm Hg
PO2 in arterial blood (PaO2) 98 mm Hg
PO2 in Capillary blood 50-80 mm Hg
PO2 in tissues 30- 50 mm Hg
PO2 in cell mitochondria 10- 20 mmHg
Factors affecting oxygenation at various levels in
O2 cascade:
Partial pressure Affected by:
Inspired oxygen
PiO2
Barometric pressure
PB
Oxygen concentration
FiO2
Alveolar gas
PAO2
Oxygen consumption
VO2
Alveolar ventilation
VA
Arterial blood
PaO2
Dead space ventilation
Increased V/Q
Shunt
Decreased V/Q
Cellular PO2 Cardiac output
CO
Hemoglobin
Hb
Oxygen therapy
Goals of oxygen therapy:
1. Correcting Hypoxemia
īƒˇBy raising Alveolar & Blood levels of Oxygen
īƒˇEasiest objective to attain & measure
2. Decreasing symptoms of Hypoxemia
īƒˇSupplemental O2 can help relieve symptoms of
hypoxia
ī‚ĸLessen dyspnoea/work of breathing
ī‚ĸImprove mental function
3. Minimizing Cardiopulmonary workload
īƒˇ Cardiopulmonary system will compensate for
Hypoxemia by:
ī‚ĸ Increasing ventilation to get more O2 in the lungs & to the
Blood
ī‚ĸ Increased work of breathing
ī‚ĸ Increasing Cardiac Output to get more oxygenated blood to
tissues
ī‚ĸ Hard on the heart, especially if diseased
īƒˇ Hypoxia causes Pulmonary vasoconstritcion &
Pulmonary Hypertension
ī‚ĸ These cause an increased workload on the right side of heart
ī‚ĸ Over time the right heart will become more muscular & then
eventually fail (Cor Pulmonale)
ī‚— Supplemental o2 can relieve hypoxemia & relieve
pulmonary vasoconstriction &
Hypertension, reducing right ventricular
workload!!
ī‚— At our institution, minimal acceptable saturation
for post surgical patients who are cared for in non
critical setup is 92%
Assessing the need for oxygen therapy
3 basic ways:
Laboratory measures – invasive or noninvasive
PAO2, PaO2, SaO2, SpO2 monitoring
Clinical Problem or condition
postoperative patients, pneumonia, atelectasis,
pulmonary edema, etcâ€Ļ
Symptoms of hypoxemia
Eg: tachycardia, tachypnoea, hypertension,
cyanosis, dyspnoea, disorientation, clubbing, etc
Methods of oxygen administration
ī‚— Method selection depends upon required
concentration of oxygen.
ī‚— However, during oxygen therapy the relative dangers
of hypoxia and O2 toxicity should be kept in mind.
Criteria for selecting the method:
1. Patient’s GCS and patient’s comfort
2. Level & range of FiO2 required
3. Extent of humidification required
Classification of O2 therapy devices
Oxygen
delivery
systems
Low flow
systems
High flow
systems
Low flow O2 delivery system
ī‚— Flow does not meet inspiratory demand
ī‚— Oxygen is diluted with air on inspiration
ī‚— These devices have limited reservoir to store
oxygen and are unable to deliver consistent
inspired oxygen concentrations in settings of
varying respiratory rates & tidal volumes.
Nasal prongs:
Simple face masks:
High flow O2 delivery system:
ī‚— Supplies given FiO2 at flow rates higher than
inspiratory demand.
ī‚— They are suitable for delivering consistent and
predictable concentrations of oxygen.
ī‚— Uses entrainment of air to maintain oxygen supply.
ī‚— Eg: venturi mask, non rebreathing mask, puritan
face mask.
Air Entrainment system
ī‚ĄAmount of air entrained varies directly
with:
īƒˇport size
īƒˇVelocity
ī‚ĄThe more air
entrained:
īƒˇHigher flow
īƒˇLower FiO2
Venturi mask:
Non rebreathing mask with reservoir mask:
Indications for O2 therapy:
ī‚— Arterial PO2 < 60 mmHg or SaO2 < 90%
ī‚— Cardiac & respiratory arrest
ī‚— Respiratory failure
ī‚— Cardiac failure or myocardial infarction
ī‚— Shock of any cause
ī‚— Increased metabolic demands (eg. Burns, multiple
injuries, severe sepsis)
ī‚— Post operative state
ī‚— Carbon monoxide poisoning.
Hypoxia
ī‚— HYPOXIA: A condition in which the oxygen
available is inadequate at the tissue level
ī‚— Five types of hypoxia:
ī‚Ą Anemic
ī‚Ą Hypoxemic
ī‚Ą Histotoxic
ī‚Ą Circulatory
ī‚Ą Hypermetabolic
Anemic Hypoxia
ī‚— Having a decreased carrying capacity for oxygen, the pt
with decreased or abnormal Hb
ī‚— Anemia
ī‚— Carbon monoxide poisoning
ī‚— Methemoglobinemia
ī‚— Sickle Cell Anemia
ī‚— Treatment involves blood transfusions, hyperbaric
chamber, bone marrow transplant
Hypoxemic Hypoxia
ī‚— Low PAO2 due to the atmosphere
ī‚— Hypoventilation – PCO2 is rising
ī‚— Diffusion Defects
ī‚— The PaO2 will be lower in all cases, but the PCO2 may or
may not be increased.
ī‚— Treatment: Compensatory actions to reduce inequalities,
supplemental oxygen
Histotoxic Hypoxia
ī‚— Inability for tissues to utilize oxygen available
ī‚— Cyanide Poisoning will inhibit cellular metabolism
from occuring; the cells can not process the O2
ī‚— Treatment: Reversal of poisoning, supplemental
oxygen and/or ventilation
Circulatory Hypoxia
ī‚— A decrease in cardiac output results in a low BP and a
prolonged systemic transit time
ī‚— The PaO2 can be high, but because of the time it takes
to get to the tissues, the pt is hypoxic
ī‚— Cardiovascular instability or failure
ī‚— Shock
ī‚— Arrhythmias
ī‚— Treatment include increasing cardiac output with use
of cardiovascular drugs and therapy, supplemental
oxygen
Hypermetabolic Hypoxia
ī‚— In some disease states the body requires a slight
increase in metabolism (i.e. – wound healing
requires 5% increase)
ī‚— Extensive burns and some cancers will cause large
increases metabolism to the point that supplemental
O2 is required
ī‚— Treatment: Supplemental O2 or FiO2
Approach to selecting appropriate O2 delivery
system:
Purpose (Objective)
īƒˇ Increase FiO2 to correct hypoxemia
īƒˇ minimize symptoms of hypoxemia
īƒˇ Minimize Cardiopulmonary workload
Patient
īƒˇ Cause & severity of hypoxemia
īƒˇ Age
īƒˇ Neuro status/orientation
īƒˇ Airway in place/protected
īƒˇ Regular rate & rhythm (minute Ventilation)
Equipment Performance
The more critical, the greater need for high stable FiO2
īƒˇ Becomes more difficult the more critical due to pt varying pattern
ī‚Ą Pt Categories
īƒˇEmergency
ī‚ĸ Highest FiO2 possible
ī‚ĸ Highest PaO2 possible
īƒˇCritical Adult
ī‚ĸ >60% O2
ī‚ĸ PaO2 >60mmHg
ī‚ĸ SpO2 >90%
īƒˇStable adult, acute illness, mild hypoxemia
ī‚ĸ Low to moderate FiO2
ī‚ĸ Response to therapy, not precise concentrations
īƒˇChronic dz adult, acute on chronic illness
ī‚ĸEnsure adequate oxygenation without depressing
Ventilation
â€ĸ SpO2 85-90%
â€ĸ PaO2 50-60mmHg
â€ĸ Use ventilating mask to control FiO2 precision
â€ĸ Assess response to therapy!!
â€ĸ If not maintainable on Cannula, use masks
ī‚—Pt may remove mask frequently due to
â€ĸ Discomfort
â€ĸ Convenience
â€ĸ Change in mental status
ī‚—Encourage Cannula use between mask use if
mask must come off for periods
Precautions & Hazards
ī‚Ą O2 Toxicity
īƒˇPrimarily affects Lungs & CNS
īƒˇ2 determining factors of O2 toxicity
ī‚ĸ PO2
ī‚ĸ Time of exposure
ī‚ĸ i.e., higher the PO2 & exposure time the greater the
toxicity.
īƒˇCNS effects occur with Hyperbaric Pressures
īƒˇPulmonary effects can occur @ clinical PO2 levels
ī‚ĸ Patchy infiltrates on x-ray, prominent in lower lung
fields
ī‚ĸ Major alveolar injury
īƒˇPathophysiology
ī‚ĸHigh PO2 damages capillary endothelium
ī‚ĸFollowed by interstitial edema & AC
membrane thickening
ī‚ĸType I cells are destroyed (cells that create
new lung tissue, gas exchange cells)
ī‚ĸType II cells proliferate (trigger inflamatory
response)
ī‚ĸ Exudative phase
â€ĸ Alveolar fluid buildup (from inflamatory response)
leads to
ī‚— low ventilation/perfusion ratio (shunting)
ī‚— hypoxemia
ī‚— Hyaline membranes form @ alveolar level
â€ĸ Proteinaceous eosinophilic (basic) material
â€ĸ Composed of cellular debris & condensed plasma
proteins.
ī‚— Pulmonary fibrosis develop
ī‚— Pulmonary Hypertension develops
Treatment:
ī‚ĸ Try to keep pt alive while reducing FiO2
īƒˇCause:
ī‚ĸ Overproduction of O2 free radicals
â€ĸ Byproducts of cellular metabolism
â€ĸ Toxic in excessive amounts
â€ĸ Normally antioxidants & other special enzymes dispose of excess
free radicals
â€ĸ Neutrophils (WBC’s) & macrophages flood the infiltrate the tissue
& mediate inflammation response, leading to more free radicals
How much is too much?
ī‚ĸ>50% for very extended times
ī‚ĸ>PO2 the less time it takes
īƒˇGoal of ideal oxygen therapy:
ī‚ĸUse the lowest FiO2 possible to maintain
adequate tissue oxygenation
Other side effects
Growing lungs are more sensitive to O2
Retinopathy of Prematurity (ROP), more later
Bronchopulmonary Dysplasia (BPD), chronic lung
dz, Absorption Atelectasis, Fire hazards, etc
Depression of Ventilation
īļ Hypercarbic drive is blunted
High PCO2 no longer stimulates pt to
increase Ventilation
īļSuppression of hypoxic drive
The only stimulus left to increase Ventilation
is due to hypoxia
īļ When you add to much O2, (remove the hypoxia) you
effectively remove the neurological stimulus to breathe.
(peripheral chemoreceptor’s)
â€ĸ Hypoventilation occurs
īļ CO2 continues to elevate to sedative levels
â€ĸ Pt stops breathing until hypoxic again
â€ĸ If CO2 is too high, they will remain sedated & causes
Cardiopulmonary arrest
â€ĸ Never withhold O2 therapy from a
Hypoxic pt (PaO2)
Take home message!!
ī‚— Oxygen is a drug, prescribe it as other
drugs, ie, amount, device and time should be
specified.
ī‚— If patient’s SpO2 is not good with nasal
cannula, consider changing the device instead
of increasing flow rate.
ī‚— Overzealous use of oxygen is often without
justification & consideration of toxic effects of
oxygen therapy. So think before such
unaccounted for use of oxygen.
Bibliography:
i. Anaesthesia for medical students .
ii. The ICU book ; by Paul Marino
Hypoxia and oxygen therapy

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Hypoxia and oxygen therapy

  • 2. Historical considerations ī‚— Carl Wilhelm Scheele – 1773 Discovered O2 ī‚— John Pristley – 1774 Was the first to publish a paper on O2 ī‚— Antoine Lavoisier – 1777 Coined the term “O2”
  • 3. Oxygen: ī‚— Colourless ī‚— Odourless ī‚— Tasteless ī‚— Transparent gas ī‚— Slightly heavier than air ī‚— Constitues 20-21% of atmospheric air ī‚— Essential for life
  • 4. Importance of O2 in cell chemistry ī‚— Required in aerobic metabolism for: 1. Production of high energy phosphate compounds (ATP) 2. Dehydrogenation of flavo proteins 3. Biotransformation of drugs 4. Oxidation of certain other substrates..
  • 5. Definations: ī‚— Hypoxia: low level of oxygen at tissue level ī‚— Hypoxemia: low levels of oxygen in blood ī‚— Partial pressure: the pressure exerted on a surface by the molecules of individual gases. The partial pressure of oxygen can be calculated for a given atmospheric pressure, by multiplying concentration of a gas by the atmospheric or barometric pressure. Eg: 760 mm Hg 21% = 160 mm Hg
  • 6. Oxygen cascade ī‚— Oxygen cascade refers to the progressive decrease in the partial pressure of oxygen from the ambient air to the cellular level. PO2 in inspired air 150-160 mm Hg PO2 in alveolar gas (PAO2) 100- 110 mm Hg PO2 in arterial blood (PaO2) 98 mm Hg PO2 in Capillary blood 50-80 mm Hg PO2 in tissues 30- 50 mm Hg PO2 in cell mitochondria 10- 20 mmHg
  • 7. Factors affecting oxygenation at various levels in O2 cascade: Partial pressure Affected by: Inspired oxygen PiO2 Barometric pressure PB Oxygen concentration FiO2 Alveolar gas PAO2 Oxygen consumption VO2 Alveolar ventilation VA Arterial blood PaO2 Dead space ventilation Increased V/Q Shunt Decreased V/Q Cellular PO2 Cardiac output CO Hemoglobin Hb
  • 8. Oxygen therapy Goals of oxygen therapy: 1. Correcting Hypoxemia īƒˇBy raising Alveolar & Blood levels of Oxygen īƒˇEasiest objective to attain & measure 2. Decreasing symptoms of Hypoxemia īƒˇSupplemental O2 can help relieve symptoms of hypoxia ī‚ĸLessen dyspnoea/work of breathing ī‚ĸImprove mental function
  • 9. 3. Minimizing Cardiopulmonary workload īƒˇ Cardiopulmonary system will compensate for Hypoxemia by: ī‚ĸ Increasing ventilation to get more O2 in the lungs & to the Blood ī‚ĸ Increased work of breathing ī‚ĸ Increasing Cardiac Output to get more oxygenated blood to tissues ī‚ĸ Hard on the heart, especially if diseased īƒˇ Hypoxia causes Pulmonary vasoconstritcion & Pulmonary Hypertension ī‚ĸ These cause an increased workload on the right side of heart ī‚ĸ Over time the right heart will become more muscular & then eventually fail (Cor Pulmonale)
  • 10. ī‚— Supplemental o2 can relieve hypoxemia & relieve pulmonary vasoconstriction & Hypertension, reducing right ventricular workload!! ī‚— At our institution, minimal acceptable saturation for post surgical patients who are cared for in non critical setup is 92%
  • 11. Assessing the need for oxygen therapy 3 basic ways: Laboratory measures – invasive or noninvasive PAO2, PaO2, SaO2, SpO2 monitoring Clinical Problem or condition postoperative patients, pneumonia, atelectasis, pulmonary edema, etcâ€Ļ Symptoms of hypoxemia Eg: tachycardia, tachypnoea, hypertension, cyanosis, dyspnoea, disorientation, clubbing, etc
  • 12. Methods of oxygen administration ī‚— Method selection depends upon required concentration of oxygen. ī‚— However, during oxygen therapy the relative dangers of hypoxia and O2 toxicity should be kept in mind. Criteria for selecting the method: 1. Patient’s GCS and patient’s comfort 2. Level & range of FiO2 required 3. Extent of humidification required
  • 13. Classification of O2 therapy devices Oxygen delivery systems Low flow systems High flow systems
  • 14. Low flow O2 delivery system ī‚— Flow does not meet inspiratory demand ī‚— Oxygen is diluted with air on inspiration ī‚— These devices have limited reservoir to store oxygen and are unable to deliver consistent inspired oxygen concentrations in settings of varying respiratory rates & tidal volumes.
  • 17. High flow O2 delivery system: ī‚— Supplies given FiO2 at flow rates higher than inspiratory demand. ī‚— They are suitable for delivering consistent and predictable concentrations of oxygen. ī‚— Uses entrainment of air to maintain oxygen supply. ī‚— Eg: venturi mask, non rebreathing mask, puritan face mask.
  • 18. Air Entrainment system ī‚ĄAmount of air entrained varies directly with: īƒˇport size īƒˇVelocity ī‚ĄThe more air entrained: īƒˇHigher flow īƒˇLower FiO2
  • 20. Non rebreathing mask with reservoir mask:
  • 21. Indications for O2 therapy: ī‚— Arterial PO2 < 60 mmHg or SaO2 < 90% ī‚— Cardiac & respiratory arrest ī‚— Respiratory failure ī‚— Cardiac failure or myocardial infarction ī‚— Shock of any cause ī‚— Increased metabolic demands (eg. Burns, multiple injuries, severe sepsis) ī‚— Post operative state ī‚— Carbon monoxide poisoning.
  • 22. Hypoxia ī‚— HYPOXIA: A condition in which the oxygen available is inadequate at the tissue level ī‚— Five types of hypoxia: ī‚Ą Anemic ī‚Ą Hypoxemic ī‚Ą Histotoxic ī‚Ą Circulatory ī‚Ą Hypermetabolic
  • 23. Anemic Hypoxia ī‚— Having a decreased carrying capacity for oxygen, the pt with decreased or abnormal Hb ī‚— Anemia ī‚— Carbon monoxide poisoning ī‚— Methemoglobinemia ī‚— Sickle Cell Anemia ī‚— Treatment involves blood transfusions, hyperbaric chamber, bone marrow transplant
  • 24. Hypoxemic Hypoxia ī‚— Low PAO2 due to the atmosphere ī‚— Hypoventilation – PCO2 is rising ī‚— Diffusion Defects ī‚— The PaO2 will be lower in all cases, but the PCO2 may or may not be increased. ī‚— Treatment: Compensatory actions to reduce inequalities, supplemental oxygen
  • 25. Histotoxic Hypoxia ī‚— Inability for tissues to utilize oxygen available ī‚— Cyanide Poisoning will inhibit cellular metabolism from occuring; the cells can not process the O2 ī‚— Treatment: Reversal of poisoning, supplemental oxygen and/or ventilation
  • 26. Circulatory Hypoxia ī‚— A decrease in cardiac output results in a low BP and a prolonged systemic transit time ī‚— The PaO2 can be high, but because of the time it takes to get to the tissues, the pt is hypoxic ī‚— Cardiovascular instability or failure ī‚— Shock ī‚— Arrhythmias ī‚— Treatment include increasing cardiac output with use of cardiovascular drugs and therapy, supplemental oxygen
  • 27. Hypermetabolic Hypoxia ī‚— In some disease states the body requires a slight increase in metabolism (i.e. – wound healing requires 5% increase) ī‚— Extensive burns and some cancers will cause large increases metabolism to the point that supplemental O2 is required ī‚— Treatment: Supplemental O2 or FiO2
  • 28. Approach to selecting appropriate O2 delivery system: Purpose (Objective) īƒˇ Increase FiO2 to correct hypoxemia īƒˇ minimize symptoms of hypoxemia īƒˇ Minimize Cardiopulmonary workload Patient īƒˇ Cause & severity of hypoxemia īƒˇ Age īƒˇ Neuro status/orientation īƒˇ Airway in place/protected īƒˇ Regular rate & rhythm (minute Ventilation) Equipment Performance The more critical, the greater need for high stable FiO2 īƒˇ Becomes more difficult the more critical due to pt varying pattern
  • 29. ī‚Ą Pt Categories īƒˇEmergency ī‚ĸ Highest FiO2 possible ī‚ĸ Highest PaO2 possible īƒˇCritical Adult ī‚ĸ >60% O2 ī‚ĸ PaO2 >60mmHg ī‚ĸ SpO2 >90% īƒˇStable adult, acute illness, mild hypoxemia ī‚ĸ Low to moderate FiO2 ī‚ĸ Response to therapy, not precise concentrations
  • 30. īƒˇChronic dz adult, acute on chronic illness ī‚ĸEnsure adequate oxygenation without depressing Ventilation â€ĸ SpO2 85-90% â€ĸ PaO2 50-60mmHg â€ĸ Use ventilating mask to control FiO2 precision
  • 31. â€ĸ Assess response to therapy!! â€ĸ If not maintainable on Cannula, use masks ī‚—Pt may remove mask frequently due to â€ĸ Discomfort â€ĸ Convenience â€ĸ Change in mental status ī‚—Encourage Cannula use between mask use if mask must come off for periods
  • 32. Precautions & Hazards ī‚Ą O2 Toxicity īƒˇPrimarily affects Lungs & CNS īƒˇ2 determining factors of O2 toxicity ī‚ĸ PO2 ī‚ĸ Time of exposure ī‚ĸ i.e., higher the PO2 & exposure time the greater the toxicity. īƒˇCNS effects occur with Hyperbaric Pressures īƒˇPulmonary effects can occur @ clinical PO2 levels ī‚ĸ Patchy infiltrates on x-ray, prominent in lower lung fields ī‚ĸ Major alveolar injury
  • 33. īƒˇPathophysiology ī‚ĸHigh PO2 damages capillary endothelium ī‚ĸFollowed by interstitial edema & AC membrane thickening ī‚ĸType I cells are destroyed (cells that create new lung tissue, gas exchange cells) ī‚ĸType II cells proliferate (trigger inflamatory response)
  • 34. ī‚ĸ Exudative phase â€ĸ Alveolar fluid buildup (from inflamatory response) leads to ī‚— low ventilation/perfusion ratio (shunting) ī‚— hypoxemia ī‚— Hyaline membranes form @ alveolar level â€ĸ Proteinaceous eosinophilic (basic) material â€ĸ Composed of cellular debris & condensed plasma proteins. ī‚— Pulmonary fibrosis develop ī‚— Pulmonary Hypertension develops
  • 35. Treatment: ī‚ĸ Try to keep pt alive while reducing FiO2 īƒˇCause: ī‚ĸ Overproduction of O2 free radicals â€ĸ Byproducts of cellular metabolism â€ĸ Toxic in excessive amounts â€ĸ Normally antioxidants & other special enzymes dispose of excess free radicals â€ĸ Neutrophils (WBC’s) & macrophages flood the infiltrate the tissue & mediate inflammation response, leading to more free radicals
  • 36. How much is too much? ī‚ĸ>50% for very extended times ī‚ĸ>PO2 the less time it takes īƒˇGoal of ideal oxygen therapy: ī‚ĸUse the lowest FiO2 possible to maintain adequate tissue oxygenation
  • 37. Other side effects Growing lungs are more sensitive to O2 Retinopathy of Prematurity (ROP), more later Bronchopulmonary Dysplasia (BPD), chronic lung dz, Absorption Atelectasis, Fire hazards, etc Depression of Ventilation īļ Hypercarbic drive is blunted High PCO2 no longer stimulates pt to increase Ventilation īļSuppression of hypoxic drive The only stimulus left to increase Ventilation is due to hypoxia
  • 38. īļ When you add to much O2, (remove the hypoxia) you effectively remove the neurological stimulus to breathe. (peripheral chemoreceptor’s) â€ĸ Hypoventilation occurs īļ CO2 continues to elevate to sedative levels â€ĸ Pt stops breathing until hypoxic again â€ĸ If CO2 is too high, they will remain sedated & causes Cardiopulmonary arrest â€ĸ Never withhold O2 therapy from a Hypoxic pt (PaO2)
  • 39. Take home message!! ī‚— Oxygen is a drug, prescribe it as other drugs, ie, amount, device and time should be specified. ī‚— If patient’s SpO2 is not good with nasal cannula, consider changing the device instead of increasing flow rate. ī‚— Overzealous use of oxygen is often without justification & consideration of toxic effects of oxygen therapy. So think before such unaccounted for use of oxygen.
  • 40. Bibliography: i. Anaesthesia for medical students . ii. The ICU book ; by Paul Marino