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Acute Respiratory Distress
Syndrome (ARDS)
ARDS
• Acute respiratory distress syndrome (ARDS) is characterised
by non-cardiac pulmonary oedema and progressive
refractory hypoxaemia
• It is widely recognised as a severe form of acute respiratory
failure.
ETIOLOGY
Etiologies can be pulmonary or Non pulmonary.
These include:
• Pneumonia, sepsis, aspiration
• Shock (any cause)
• Trauma
• Metabolic, hematologic(eg DIC) and immunologic disorders.
• Inhaled agents, smoke, high concentration of oxygen, corrosive substances.
• Major surgery
• Fat or air embolism
PATHOPHYSIOLOGY
Clinical Manifestations
• Dyspnoea, tachypnoea and anxiety are early manifestations
• Progressive respiratory distress develops, with increasing respiratory
rate, intercostal retractions and use of accessory muscles of
respiration
• Cyanosis develops that may not improve with oxygen administration.
• Breath sounds are initially clear, but crackles (rales) and rhonchi
develop later.
• As respiratory failure progresses, mental status changes such as
agitation, confusion and lethargy occur.
Diagnostic Evaluation
• The hallmark sign for ARDS is a shunt; hypoxemia remains despite
increasing oxygen therapy.
• ABG
• Chest X-ray exhibits bilateral infiltrates.
• Pulmonary artery catheter readings: pulmonary artery wedge
pressure >18 mm Hg.
• CT SCAN
• PFT
Management
• The underlying cause for ARDS must be determined so appropriate
treatment can be initiated.
• Ventilatory support with PEEP will be instituted. PEEP keeps the
alveoli open, thereby improving gas exchange. Therefore, a lower
oxygen concentration (Fio2) can be used to maintain satisfactory
oxygenation.
• Fluid management must be maintained. The patient may be
hypovolemic due to the movement of fluid into the interstitium of the
lung.
• inotropic medications
Management
• Corticosteroids are used infrequently due to the controversy
regarding benefits of usage.
• Treatment of any infections with appropriate antibiotics
• A Swan–Ganz line may be placed to monitor pulmonary artery
pressures and cardiac output.
• Adequate nutrition should be initiated early and maintained
• Enteral or parenteral feeding is necessary to maintain nutritional
status and prevent tissue catabolism.
Managemnt…
• Low-molecular-weight heparin may be ordered to prevent
thrombophlebitis and possible pulmonary embolus or disseminated
intravascular coagulation, a possible complication of ARDS
Complications
• Infections, such as pneumonia, sepsis.
• Respiratory complications, such as pulmonary emboli, barotrauma,
oxygen toxicity, subcutaneous emphysema, or pulmonary fibrosis.
• GI complications, such as stress ulcer, ileus.
• Cardiac complications, such as decreased cardiac output and
dysrhythmias.
• Renal failure, disseminated intravascular coagulation
NURSING MANAGEMENT
Nursing Diagnoses
• Impaired gas exchange related to effects of near drowning evidenced
by increased respiration rate and decreasing oxygen saturations.
• Anxiety related to hypoxaemia evidenced by decreasing oxygen
saturations.
• Risk of decreased cardiac output related to mechanical ventilation
evidenced by decreasing blood pressure and increasing heart rate.
• Risk of injury related to endotracheal intubation evidenced by
haemoptysis.
Planning
■■ Obtain all necessary supplies and radiology in preparation for
intubation and mechanical ventilation.
■■ Explain the purpose and procedure of intubation.
■■ Provide an opportunity to express fears related to intubation and
mechanical ventilation; answer questions and provide reassurance.
■■ Discuss communication strategies while intubated; obtain a magic
slate.
Expected outcomes
• Breathe effectively with the mechanical ventilator.
• Demonstrate improved oxygen saturation, ETCO2 and ABG values
• Express fears related to intubation and mechanical ventilation.
• Demonstrate reduced anxiety levels (relaxed facial expression, ability
to rest).
• Maintain adequate cardiac output and tissue perfusion.
• Tolerate endotracheal intubation and mechanical ventilation without
evidence of infection or barotrauma.
Nursing Interventions
• Monitor oxygen saturation and ETCO2 levels every 30 to 60 minutes
initially after mechanical ventilation is commenced; report changes to
the doctor.
• Obtain ABGs as ordered or indicated; monitor and report results.
• Suction via endotracheal tube as needed to maintain clear airways.
• Provide periods of uninterrupted rest.
• Monitor vital signs every 1 to 2 hours.
• Assess skin colour, capillary refill and the presence of oedema every 4
hours.
Nursing management…
• Monitor urine output hourly; report output of less than 30 mL per
hour.
• Assess lung sounds and chest excursion every 1 to 2 hours

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ARDS-1.pptx

  • 2. ARDS • Acute respiratory distress syndrome (ARDS) is characterised by non-cardiac pulmonary oedema and progressive refractory hypoxaemia • It is widely recognised as a severe form of acute respiratory failure.
  • 3. ETIOLOGY Etiologies can be pulmonary or Non pulmonary. These include: • Pneumonia, sepsis, aspiration • Shock (any cause) • Trauma • Metabolic, hematologic(eg DIC) and immunologic disorders. • Inhaled agents, smoke, high concentration of oxygen, corrosive substances. • Major surgery • Fat or air embolism
  • 5. Clinical Manifestations • Dyspnoea, tachypnoea and anxiety are early manifestations • Progressive respiratory distress develops, with increasing respiratory rate, intercostal retractions and use of accessory muscles of respiration • Cyanosis develops that may not improve with oxygen administration. • Breath sounds are initially clear, but crackles (rales) and rhonchi develop later. • As respiratory failure progresses, mental status changes such as agitation, confusion and lethargy occur.
  • 6. Diagnostic Evaluation • The hallmark sign for ARDS is a shunt; hypoxemia remains despite increasing oxygen therapy. • ABG • Chest X-ray exhibits bilateral infiltrates. • Pulmonary artery catheter readings: pulmonary artery wedge pressure >18 mm Hg. • CT SCAN • PFT
  • 7. Management • The underlying cause for ARDS must be determined so appropriate treatment can be initiated. • Ventilatory support with PEEP will be instituted. PEEP keeps the alveoli open, thereby improving gas exchange. Therefore, a lower oxygen concentration (Fio2) can be used to maintain satisfactory oxygenation. • Fluid management must be maintained. The patient may be hypovolemic due to the movement of fluid into the interstitium of the lung. • inotropic medications
  • 8. Management • Corticosteroids are used infrequently due to the controversy regarding benefits of usage. • Treatment of any infections with appropriate antibiotics • A Swan–Ganz line may be placed to monitor pulmonary artery pressures and cardiac output. • Adequate nutrition should be initiated early and maintained • Enteral or parenteral feeding is necessary to maintain nutritional status and prevent tissue catabolism.
  • 9. Managemnt… • Low-molecular-weight heparin may be ordered to prevent thrombophlebitis and possible pulmonary embolus or disseminated intravascular coagulation, a possible complication of ARDS
  • 10. Complications • Infections, such as pneumonia, sepsis. • Respiratory complications, such as pulmonary emboli, barotrauma, oxygen toxicity, subcutaneous emphysema, or pulmonary fibrosis. • GI complications, such as stress ulcer, ileus. • Cardiac complications, such as decreased cardiac output and dysrhythmias. • Renal failure, disseminated intravascular coagulation
  • 12. Nursing Diagnoses • Impaired gas exchange related to effects of near drowning evidenced by increased respiration rate and decreasing oxygen saturations. • Anxiety related to hypoxaemia evidenced by decreasing oxygen saturations. • Risk of decreased cardiac output related to mechanical ventilation evidenced by decreasing blood pressure and increasing heart rate. • Risk of injury related to endotracheal intubation evidenced by haemoptysis.
  • 13. Planning ■■ Obtain all necessary supplies and radiology in preparation for intubation and mechanical ventilation. ■■ Explain the purpose and procedure of intubation. ■■ Provide an opportunity to express fears related to intubation and mechanical ventilation; answer questions and provide reassurance. ■■ Discuss communication strategies while intubated; obtain a magic slate.
  • 14. Expected outcomes • Breathe effectively with the mechanical ventilator. • Demonstrate improved oxygen saturation, ETCO2 and ABG values • Express fears related to intubation and mechanical ventilation. • Demonstrate reduced anxiety levels (relaxed facial expression, ability to rest). • Maintain adequate cardiac output and tissue perfusion. • Tolerate endotracheal intubation and mechanical ventilation without evidence of infection or barotrauma.
  • 15. Nursing Interventions • Monitor oxygen saturation and ETCO2 levels every 30 to 60 minutes initially after mechanical ventilation is commenced; report changes to the doctor. • Obtain ABGs as ordered or indicated; monitor and report results. • Suction via endotracheal tube as needed to maintain clear airways. • Provide periods of uninterrupted rest. • Monitor vital signs every 1 to 2 hours. • Assess skin colour, capillary refill and the presence of oedema every 4 hours.
  • 16. Nursing management… • Monitor urine output hourly; report output of less than 30 mL per hour. • Assess lung sounds and chest excursion every 1 to 2 hours