Oxygenation & Gas Exchange

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Last updated 10:40 PM on 9/22/26
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98 Terms

1
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What is pulmonary edema?

  • Fluid builds up in the alveoli and interstitial spaces of the lungs.

  • This interferes with normal oxygen and carbon dioxide exchange.

  • The most common cause is left-sided heart failure.

  • The extra fluid makes it harder for oxygen to move into the blood.


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What would you hear with pulmonary edema?

  • Rales/crackles on auscultation.

  • Crackles occur because fluid is present in the lungs.

  • Other findings:

    • Shortness of breath

    • Tachypnea

    • Hypoxemia

    • Frothy secretions


3
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What is a pleural effusion?

  • Fluid collects in the pleural space around the lungs.

  • The fluid takes up space and limits normal lung expansion.

  • The patient may develop:

    • Dyspnea

    • Cough

    • Inspiratory chest pain


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What would you hear with a pleural effusion?

  • Diminished or absent breath sounds over the affected area.

  • Fluid around the lung prevents normal transmission of breath sounds.

  • Patient may also have:

    • Dyspnea

    • Cough

    • Inspiratory chest pain


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What is atelectasis?

  • Partial or complete collapse of the lung.

  • The alveoli become deflated.

  • The most common cause is airway obstruction from retained secretions/exudates.

  • Common after surgery or with hypoventilation.


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What are the signs and symptoms of atelectasis?


  • Rapidly developing atelectasis:

    • Sudden dyspnea

    • Pain

    • Cyanosis

  • Slowly developing atelectasis:

    • May be asymptomatic

    • Mild shortness of breath

    • Cough

  • Breath sounds may be diminished or absent.


7
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What is the V/Q ratio?

  • V = ventilation, or air reaching the alveoli.

  • Q = perfusion, or blood reaching the alveoli.

  • It compares the amount of air reaching the alveoli with blood flow.

  • Normal V/Q is about 0.80.

  • Approximately 4 L of air : 5 L of blood.


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What causes a high V/Q ratio?

  • More ventilation or less perfusion.

  • There is air reaching the alveoli, but not enough blood to pick up oxygen.

  • Called dead space.

  • Example: pulmonary embolism, where blood flow is decreased.


9
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What causes a low V/Q ratio?

  • Less ventilation or more perfusion.

  • Blood reaches the alveoli, but there is not enough air for gas exchange.

  • Called a shunt.

  • Example: asthma, where ventilation is decreased.


10
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What are the 2 types of acute respiratory failure?


  • Hypoxemic respiratory failure

    • Problem getting oxygen into the blood.

    • PaO₂ is low.

  • Hypercapnic respiratory failure

    • Problem removing CO₂ from the blood.

    • PaCO₂ is elevated.

  • A patient can have both hypoxemia and hypercapnia.


11
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What is hypoxemic respiratory failure?

  • Also called lung failure.

  • The lungs cannot adequately transfer oxygen into the blood.

  • PaO₂ <60 mmHg.

  • PaCO₂ is usually normal or low.

  • Caused by problems such as:

    • V/Q mismatch

    • Pulmonary edema

    • Atelectasis

    • Right-to-left shunt


12
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What is hypercapnic respiratory failure?

  • Also called ventilation failure.

  • The patient cannot adequately remove CO₂.

  • PaCO₂ becomes elevated.

  • CO₂ buildup causes respiratory acidosis.

  • Often occurs from inadequate ventilation or respiratory pump failure.


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What causes hypercapnic respiratory failure?

  • Decreased respiratory drive

  • Respiratory muscle weakness

  • Increased dead space

  • Sedative medications

  • Spinal cord injury

  • Quadriplegia

  • End-stage COPD

  • Increased CO₂ production from conditions such as:

    • Fever

    • Sepsis

    • Burns


14
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What ABG findings indicate hypercapnic respiratory failure?

  • PaCO₂ >45 mmHg

  • pH <7.35

  • This indicates respiratory acidosis.

  • Remember:

    • CO₂ ↑

    • Acid ↑

    • pH ↓


15
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What ABG findings indicate hypoxemic respiratory failure?

  • PaO₂ <60 mmHg

  • PaCO₂ is usually normal or decreased.

  • The primary problem is inadequate oxygen transfer.

  • Severe untreated hypoxemia can lead to tissue hypoxia and cell injury.


16
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What are signs and symptoms of hypoxemia?

  • SpO₂ <90% on room air

  • Irritability

  • Confusion

  • Tachypnea

  • Tachycardia

  • Dysrhythmias

  • Cyanosis is a late sign

  • Severity depends on how low the oxygen level is and how long it has been low.


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What are signs and symptoms of hypercapnia?

  • Headache

  • Behavior changes

  • Flushed skin

  • Nausea/vomiting

  • Asterixis

  • Myoclonus

  • Seizures

  • Decreased LOC

  • Severe cases can progress to coma/obtundation.


18
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What manifestations can occur with both types of respiratory failure?

  • Shortness of breath

  • Tachypnea

  • Increased work of breathing

  • Changes in mental status

  • Confusion

  • Tachycardia

  • The exact symptoms depend on the cause and severity of respiratory failure.


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What is the priority when treating acute respiratory failure?

  • Restore respiratory and hemodynamic stability.

  • Perform frequent respiratory assessments.

  • Improve oxygenation.

  • Support ventilation when needed.

  • Identify and treat the underlying cause.


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What is the progression of oxygen support in ARF?

  • Start with the least invasive method appropriate for the patient:

    1. Nasal cannula

    2. Face mask

    3. Non-rebreather

    4. CPAP/BiPAP

    5. Intubation + mechanical ventilation

  • Goal is generally SpO₂ >90%.


21
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What medications may be used to treat ARF?

  • Albuterol: bronchodilator

  • Ipratropium: bronchodilator

  • Methylprednisolone/dexamethasone: decrease inflammation

  • Furosemide: removes excess fluid

  • Morphine: may help pain/air hunger

  • Treatment also depends on the underlying cause.


22
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What is the purpose of furosemide in respiratory failure?

  • Furosemide is a diuretic.

  • Promotes removal of excess fluid.

  • Useful when hypervolemia/pulmonary edema contributes to impaired gas exchange.

  • Removing excess fluid can improve oxygenation.


23
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How do you know gas exchange is improving?

  • PaO₂ increases

  • PaCO₂ decreases when CO₂ retention is present

  • SpO₂ improves

  • Work of breathing decreases

  • Respiratory status improves

  • Mental status may improve as oxygenation improves.


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What is ARDS?

  • Severe inflammatory injury of the lungs.

  • Capillaries become damaged and leak fluid into the alveoli.

  • The lungs become stiff with decreased compliance.

  • Oxygen cannot move easily into the blood.

  • Severe cases can cause life-threatening hypoxemia.


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What is the most common cause of ARDS?

  • Sepsis is the most common cause listed in the PowerPoint.

  • Other triggers can include:

    • Infection

    • Trauma

    • Severe inflammatory injury

  • The inflammatory response damages the alveolar-capillary membrane.


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When does ARDS usually develop?

  • Usually develops within 3 days of the infection, trauma, or other insult.

  • Nearly always develops within 7 days.

  • Respiratory symptoms progressively worsen.


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What are the signs and symptoms of ARDS?

  • Progressive dyspnea

  • Tachypnea

  • Hypoxemia

  • Cough

  • Chest discomfort

  • Anxiety/restlessness

  • Tachycardia

  • Hypotension

  • Accessory muscle use

  • Decreased lung compliance

  • Pulmonary edema

  • Cyanosis is a late finding.


28
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What is refractory hypoxemia in ARDS?

  • Severe hypoxemia that does not improve adequately despite high levels of oxygen.

  • The patient may remain hypoxemic even when receiving 100% oxygen.

  • This indicates severe impairment of gas exchange


29
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What ABG findings are concerning in ARDS?

  • SaO₂ <90%

  • PaO₂ <60 mmHg

  • pH <7.3

  • These findings indicate significant oxygenation problems and possible acid-base disturbance.


30
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What diagnostics are used for ARDS?

  • ABG

  • Chest X-ray

  • CT scan

  • CBC

  • Electrolytes

  • BUN/creatinine

  • Blood and sputum cultures

  • ECG to help exclude cardiac causes

  • BUN/creatinine are important because AKI can progress to MODS.


31
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What nursing interventions are important for ARDS?

  • Monitor VS frequently

  • Assess oxygenation

  • Assess lung and heart sounds

  • Monitor LOC

  • Maintain oxygen therapy

  • Suction as needed

  • Monitor ETT placement if intubated

  • Assess skin and perfusion

  • Position appropriately

  • Prone severe ARDS >12 hours/day when indicated.


32
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Why is prone positioning used for severe ARDS?

  • Decreases compression of the lungs.

  • Improves ventilation.

  • Improves gas exchange.

  • Helps distribute ventilation to better-perfused areas of the lungs.

  • Severe ARDS patients may be prone >12 hours/day.


33
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What interventions decrease oxygen consumption in ARDS

  • Provide adequate pain control.

  • Give sedation/anxiolytics when indicated.

  • Reduce anxiety and agitation.

  • Mechanical ventilation decreases the patient's work of breathing.

  • Prevent shivering and excessive activity when appropriate.

  • Goal: reduce the body's oxygen demand.


34
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What is CPAP?

  • Provides one continuous pressure during inspiration and expiration.

  • Helps prevent alveolar collapse.

  • Improves oxygenation.

  • Decreases work of breathing.

  • Requires an intact respiratory drive and adequate tidal volume.

  • Commonly used for sleep apnea.


35
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What is BiPAP?

  • Provides two pressure levels:

    • Higher inspiratory pressure

    • Lower expiratory pressure

  • Helps provide ventilatory assistance.

  • Especially useful for patients with hypercapnia.

  • Example setting: 10/5 means IPAP 10 and EPAP 5.


36
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What is the main difference between CPAP and BiPAP?

  • CPAP: one continuous pressure, mainly supports oxygenation.

  • BiPAP: two pressures, supports ventilation and oxygenation.

  • BiPAP is useful when the patient needs help removing CO₂.

  • CPAP is not appropriate for significant hypercapnia.


37
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When is noninvasive ventilation contraindicated?

  • Unable to protect the airway

  • Altered mental status with aspiration risk

  • Severe hemodynamic instability

  • Facial trauma

  • Unable to tolerate the mask

  • Severe respiratory failure requiring invasive ventilation

  • Very low pH may indicate need for intubation.


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When should a patient be intubated?

  • RR >30–35 or <8

  • Severe accessory muscle use

  • Paradoxical breathing

  • Respiratory muscle exhaustion

  • GCS <8 with respiratory failure

  • Hemodynamic instability from hypoxia/hypercapnia

  • Failure of noninvasive ventilation

  • Unable to protect the airway

  • Persistent abnormal ABGs


39
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What ABGs may indicate need for intubation?

  • Hypoxemic: PaO₂ <60 despite FiO₂ >0.60

  • Hypercapnic: PaCO₂ >50 with pH <7.25

  • Persistent abnormalities despite noninvasive support are concerning.


40
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💉 Rapid Sequence Intubation - What is the correct medication order for RSI?

  • 1. Fentanyl

    • Pain medication

  • 2. Etomidate

    • Sedation/induction

  • 3. Succinylcholine or rocuronium

    • Paralytic

  • The patient should receive analgesia and sedation before paralysis.


41
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Why must sedation be given before the paralytic?

  • Paralytics cause muscle paralysis only.

  • They do not provide pain relief or sedation.

  • Giving a paralytic before adequate sedation could leave the patient unable to move or breathe while still aware.

  • Therefore:
    Pain → Sedation → Paralysis.


42
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What should the nurse monitor during RSI?

  • SpO₂

  • Blood pressure

  • Heart rate and rhythm

  • Oxygenation

  • Airway status

  • Medication sequence

  • Have a BVM at the bedside.

  • Monitor for hypoxemia, dysrhythmias, aspiration, and other complications.


43
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Where is an endotracheal tube placed?


  • Inserted through the mouth into the trachea.

  • Provides a secure airway.

  • Allows connection to mechanical ventilation.

  • Used when the patient cannot maintain adequate ventilation or oxygenation independently.


44
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How is ETT placement confirmed?

  • End-tidal CO₂

  • Bilateral breath sounds

  • Physical assessment

  • Chest X-ray confirms final tube position.

  • The nurse should continuously monitor for displacement.


45
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What is the purpose of the ETT cuff?

  • Creates a seal inside the trachea.

  • Prevents air from leaking around the tube.

  • Helps ensure the ventilator's tidal volume reaches the lungs.

  • Helps reduce aspiration of secretions around the tube.


46
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Can a patient with an inflated ETT cuff eat, drink, or talk?


  • No.

  • The patient cannot normally talk with the ETT in place.

  • Oral eating and drinking are not allowed.

  • Nutrition is provided through tube feeding when appropriate.


47
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What are the benefits of mechanical ventilation?

  • Improves oxygenation.

  • Improves CO₂ removal.

  • Corrects respiratory acidosis.

  • Decreases work of breathing.

  • Allows respiratory muscles to rest.

  • Provides a secure airway and helps prevent aspiration.


48
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What is FiO₂?

  • Fraction of inspired oxygen.

  • Indicates the percentage of oxygen delivered by the ventilator.

  • Room air = 21% oxygen.

  • Ventilator settings can range from 21% to 100%.


49
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What is PEEP?

  • Positive end-expiratory pressure.

  • Pressure remains in the lungs at the end of expiration.

  • Helps keep alveoli open.

  • Improves oxygenation and prevents alveolar collapse.


50
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What is tidal volume?

  • The amount of air delivered to the patient with each ventilator breath.

  • Helps determine how much air enters the lungs with each breath.


51
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What does the ventilator rate control?

  • The minimum number of breaths delivered by the ventilator each minute.

  • The patient may breathe above the set rate.

  • Respiratory rate contributes to total minute ventilation.


52
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Ventilator Modes - What is Assist-Control (A/C)?

  • The ventilator provides a set minimum number of breaths.

  • It assists each patient-initiated breath.

  • If the patient does not breathe enough, the ventilator provides the set breaths.

  • Provides substantial ventilatory support.


53
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What is SIMV?

  • Synchronized intermittent mandatory ventilation.

  • Provides a set number of mandatory breaths.

  • The patient can breathe spontaneously between mandatory breaths.

  • Allows more patient participation in breathing.


54
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What is pressure support ventilation?

  • Supports spontaneous breaths initiated by the patient.

  • A preset inspiratory pressure helps make each breath easier.

  • Commonly used during weaning/extubation readiness trials.

  • Patient must be able to initiate breaths.


55
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Ventilator Alarms - What causes a low-pressure ventilator alarm?

  • Usually indicates a leak or disconnection.

  • Possible causes:

    • ETT displacement

    • Disconnected tubing

    • Leak in the ventilator circuit

  • Assess the patient first and provide manual ventilation if needed.


56
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What causes a high-pressure ventilator alarm?


  • Indicates increased resistance to airflow.

  • Possible causes:

    • Kinked tubing

    • Secretions

    • Mucus plug

    • Coughing

    • Pulmonary edema

    • Pneumothorax

  • Always assess the patient first.


57
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What complications can occur with mechanical ventilation?

  • Barotrauma

  • Pneumothorax

  • Subcutaneous emphysema

  • Fluid retention

  • Hemodynamic compromise

  • Oxygen toxicity

  • Aspiration

  • GI ulceration

  • Ventilator-associated pneumonia


58
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How can mechanical ventilation cause fluid retention?


  • Positive pressure can decrease cardiac output.

  • This can activate the RAAS, causing sodium and water retention.

  • Monitor:

    • I&O

    • Daily weight

    • Breath sounds

    • Secretions

  • Watch for worsening fluid overload.


59
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What is oxygen toxicity?

  • Lung injury caused by prolonged exposure to high oxygen concentrations.

  • Risk increases with FiO₂ >50% for 24–48 hours.

  • Monitor for:

    • Restlessness

    • Dyspnea

    • Tachypnea

    • Tachycardia

    • Crackles

    • Cyanosis


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How does mechanical ventilation cause hemodynamic compromise?

  • Increased intrathoracic pressure decreases venous return.

  • Less venous return can decrease cardiac output.

  • Monitor for:

    • Hypotension

    • Tachycardia

    • UO ≤30 mL/hr

    • Cool/clammy skin

    • Decreased pulses

    • Decreased LOC


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How can the nurse reduce aspiration risk?

  • Keep the HOB at least 30°.

  • Monitor enteral feeding according to facility policy.

  • Assess feeding tolerance.

  • Monitor for signs of aspiration.

  • Proper positioning helps reduce aspiration risk.


62
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How is GI ulceration monitored/prevented?

  • Monitor GI drainage.

  • Check stool for occult blood.

  • Medications may include:

    • Sucralfate

    • H2 blockers

    • PPIs for appropriate high-risk patients


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What is ventilator-associated pneumonia (VAP)?


  • Pneumonia associated with mechanical ventilation.

  • The ETT bypasses the normal upper-airway defenses.

  • Bacteria can enter directly into the lower respiratory tract.

  • Airway colonization can occur within about 48 hours.


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How can VAP be prevented?

  • Strict hand hygiene

  • Use gloves appropriately

  • Maintain proper airway care

  • Keep HOB elevated

  • Follow infection-control practices.

  • Prevent aspiration when possible.

  • Acid-suppression therapy may be used for appropriate high-risk patients.


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Weaning From the Ventilator - What indicates a patient may be ready for weaning?

What indicates a patient may be ready for weaning?

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What is a spontaneous breathing trial (SBT)?

  • A trial to determine whether the patient can breathe with less ventilator support.

  • May use:

    • Pressure support

    • T-piece

  • Helps determine readiness for extubation.


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What findings indicate a patient is NOT ready for extubation?

  • Tachycardia

  • Tachypnea

  • Respiratory distress

  • Increased work of breathing

  • Restlessness/anxiety

  • Decreased LOC

  • Worsening ABGs

  • Inability to maintain adequate oxygenation


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What findings support readiness for extubation?

  • RR <35/min

  • HR <140/min

  • SpO₂ >90%

  • SBP 90–180 mmHg

  • No increased work of breathing

  • Awake and alert

  • Follows commands

  • Adequate oxygenation and stable ABGs


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What are the immediate nursing interventions after extubation?


  • Place patient in semi-Fowler's/high-Fowler's.

  • Apply humidified oxygen as ordered.

  • Closely monitor respiratory status.

  • Assess for fatigue and respiratory distress.

  • Monitor oxygen saturation and vital signs.

  • Obtain ABG as ordered, often within 1–2 hours.


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What complications should be monitored after extubation?

  • Respiratory fatigue

  • Laryngospasm

  • Stridor

  • Airway obstruction

  • Laryngeal edema

  • Excessive secretions

  • Respiratory failure

  • Need for emergency reintubation


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Why is the patient kept NPO after extubation?

  • Extubation can cause swallowing problems.

  • Patient needs a swallow assessment before eating/drinking.

  • Helps prevent aspiration.

  • Speech therapy may evaluate swallowing if needed.


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What is the basic pathophysiology of cystic fibrosis?

  • CF is caused by an abnormal protein involved in mucus and salt/water movement.

  • Produces thick, sticky mucus.

  • Thick mucus blocks airways.

  • Leads to infection, scarring, and impaired gas exchange.


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What are common respiratory manifestations of CF?

  • Chronic cough

  • Recurrent respiratory infections

  • Wheezing

  • Shortness of breath

  • Declining FEV₁

  • Thick secretions that are difficult to clear

  • Progressive lung damage


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What are advanced respiratory complications of CF?

  • Pneumothorax

  • Hemoptysis

  • Severe lung damage

  • Hypoxemic respiratory failure

    • PaO₂ <60

  • Hypercapnic respiratory failure

    • PaCO₂ >50

  • Possible need for lung transplant


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What gastrointestinal/nutritional problems occur with CF?

  • Thick mucus can block pancreatic ducts.

  • Causes maldigestion and malabsorption.

  • Can cause:

    • Low BMI

    • Poor growth

    • Steatorrhea

    • Fat-soluble vitamin deficiencies

  • Vitamins A, D, E, K are especially affected.


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How is cystic fibrosis diagnosed?


  • Genetic testing

  • Sweat chloride testing

  • Nutritional assessment

  • Chest X-ray

  • Clinical findings

  • Diagnosis is based on a combination of findings, not one test alone.


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What sweat chloride result supports CF?

  • Sweat chloride ≥60 mmol/L supports the diagnosis.

  • CF causes increased sodium and chloride in sweat.

  • The sweat test is interpreted along with other clinical/genetic findings.


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What is the goal of CF treatment?

  • There is currently no cure.

  • Treatment focuses on:

    • Maintaining lung function

    • Clearing mucus

    • Preventing/treating infection

    • Maintaining nutrition

    • Preventing complications


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What medications are used to treat CF?

  • Bronchodilators → open airways

  • Mucolytics → thin mucus

  • Inhaled corticosteroids → decrease inflammation

  • Antibiotics → treat/prevent infection

  • CFTR modulators → target the abnormal CFTR protein

  • Pancreatic enzymes → improve digestion


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What is the correct order of CF airway treatments?

  • 1. Bronchodilator

    • Opens the airways.

  • 2. Mucolytic

    • Thins mucus.

  • 3. Airway clearance

    • Removes mucus.

  • 4. Inhaled corticosteroid

    • Decreases inflammation.


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Why is the bronchodilator given first in CF?

  • Example: albuterol

  • Opens the airways.

  • This allows the medications given afterward to reach deeper into the lungs.

  • It also makes airway clearance easier.


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What are mucolytics and why are they given?

  • Mucolytics thin and loosen thick mucus.

  • Examples:

    • Dornase alfa

    • Hypertonic saline

  • Given after the bronchodilator.

  • Makes secretions easier to remove.


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What is airway clearance therapy in CF?

  • Helps physically remove loosened mucus from the lungs.

  • Examples:

    • Chest physiotherapy

    • HFCWO vest

    • Flutter/Acapella

    • PEP

    • Postural drainage

    • Coughing


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How often should airway clearance therapy be performed?

  • Usually 2–4 times per day.

  • It should be performed consistently to prevent mucus buildup.

  • Avoid performing airway clearance right before or after meals to reduce nausea/vomiting.


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Why are inhaled corticosteroids used in CF?


  • Example: budesonide

  • Decreases airway inflammation.

  • Given after airway clearance in the treatment sequence listed in the PowerPoint.


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What nutrition is recommended for a patient with CF?

  • High-calorie diet

  • High-protein diet

  • Supports increased energy needs.

  • Helps maintain growth and body weight.

  • Pancreatic enzymes are used when pancreatic insufficiency is present.


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When should pancreatic enzymes be taken?

  • Take pancrelipase with meals and snacks.

  • The PowerPoint specifies within 30 minutes of meals/snacks.

  • Helps digest and absorb nutrients.

  • Especially important when pancreatic ducts are blocked by thick mucus.


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Which vitamins should CF patients receive?

  • Fat-soluble vitamins:

    • Vitamin A

    • Vitamin D

    • Vitamin E

    • Vitamin K

  • These may be poorly absorbed because of pancreatic insufficiency.


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What CF patient education is important?

  • Teach airway-clearance techniques.

  • Teach proper medication/breathing-treatment use.

  • Encourage immunizations.

  • Encourage high-protein/high-calorie nutrition.

  • Take pancreatic enzymes with meals/snacks.

  • Take vitamins A, D, E, K.

  • Maintain hydration and adequate salt during hot weather.

  • Genetic counseling/testing may be discussed when planning pregnancy.


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What are the key ARF numbers to remember?

  • Hypoxemic: PaO₂ <60

  • Hypercapnic: PaCO₂ >45

  • Hypercapnic respiratory acidosis: pH <7.35

  • SpO₂ concerning for hypoxemia: <90%


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What is the easiest way to remember hypoxemic vs hypercapnic?

  • Hypoxemic = LOW O₂

    • Problem getting oxygen into blood.

  • Hypercapnic = HIGH CO₂

    • Problem removing CO₂.

  • Hypoxemic = oxygenation problem

  • Hypercapnic = ventilation problem


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What is the easiest way to remember CPAP vs BiPAP?

  • CPAP = 1 pressure

    • Mainly oxygenation.

  • BiPAP = 2 pressures

    • Helps ventilation and oxygenation.

  • Think: BiPAP helps blow off CO₂.


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What is the RSI sequence to memorize?

  • Fentanyl → Etomidate → Paralytic

  • Pain → Sedation → Paralysis

  • Paralytic does NOT provide sedation or pain relief.

  • Never paralyze before adequate sedation.


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What is the CF treatment sequence to memorize?

  • 1. Albuterol → open

  • 2. Mucolytic → thin

  • 3. Airway clearance → remove

  • 4. Steroid → decrease inflammation


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What are the major ventilator alarm differences?

  • Low pressure = leak/disconnection

    • Displaced ETT

    • Disconnected tubing

  • High pressure = obstruction/resistance

    • Kink

    • Secretions

    • Mucus plug

    • Coughing

    • Pulmonary edema

    • Pneumothorax


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What are the major signs of respiratory failure?

  • Early:

    • Restlessness

    • Anxiety

    • Tachypnea

    • Tachycardia

    • Changes in mental status

  • Late/severe:

    • Cyanosis

    • Severe hypoxemia

    • Decreased LOC

    • Respiratory exhaustion

    • Possible respiratory arrest


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What are the most concerning signs of worsening respiratory failure?

  • Worsening hypoxemia despite oxygen

  • Increasing work of breathing

  • Severe tachypnea or respiratory fatigue

  • Decreasing LOC

  • Cyanosis

  • Worsening ABGs

  • Failure of CPAP/BiPAP

  • Hemodynamic instability


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What is the overall escalation from respiratory support to ventilation?

  • Oxygen → CPAP/BiPAP → Intubation → Mechanical ventilation

  • Escalate when the patient cannot maintain adequate oxygenation/ventilation.

  • Persistent abnormal ABGs, respiratory distress, altered LOC, or NIV failure can indicate need for intubation.