ARDS/Mechanical Ventilation
Pathophysiology:
Scattered, nonhomogeneous alveolar damage that leads to oxygenation (V/Q mismatch) problems
Diagnosis:
- Onset: within one week of a known clinical insult, or new or worsening respiratory symptoms
- Imaging: bilateral infiltrates on CXR not fully explained by effusions, nodules, or lung collapse
- Origin: respiratory failure not fully explained by cardiac failure or fluid overload. An objective assessment (eg ECHO) is required to exclude pulmonary edema if no ARDS risk factors are present
- Oxygenation: (on ventilator settings that include PEEP or CPAP >5cm H2O)
- Mild ARDS: PaO2/FiO2 ratio 200-300 mmHg
- Moderate ARDS: PaO2/FiO2 ratio 100-200 mmHg
- Severe ARDS: PaO2/FiO2 ratio <100 mmHg
Etiology:
- Direct lung injury: Pneumonia, aspiration, pulmonary contusion, fat emboli, near-drowning, inhalational injury, post lung transplantation, or hematopoietic stem cell transplant
- Indirect lung injury: Sepsis, severe trauma, shock, drug overdose, DIC, pancreatitis, cardiopulmonary bypass, transfusion of blood products (TRALI)
Management:
- Mechanical ventilation:
- Goal: Maintain adequate gas exchange until the inflammation and edema subside and minimize ventilator-induced lung injury
- ARDSnet protocol (ARMA Trial): low tidal volume (4-6 ml/kg) and low airway pressure (Pplat <30 mmHg)
- Additional therapeutic considerations
- "Conservative" fluid management: FACTT trial showed that it improves oxygenation and shortens the duration of mechanical ventilation and intensive care but does not improve 60 day mortality. Goal CVP <4, PCWP <8. Excluded patients with hypotension, pressures, HD, oliguric renal failure.
- Early neuromuscular blockade in severe ARDS: ACURASYS trial (single randomized trial) showed the use of cisatracurium in patients with severe ARDS resulted in a reduction in 90 day mortality and an increase in ventilator free days. ROSE trial did not reproduce this mortality benefit.
- Prone positioning PROSEVA randomized trial showed a reduction in mortality in patients with severe ARDS; recommended for patients with P/F < 100, consider if P/F < 150
- ECMO and high frequency oscillatory ventilation: further studies are required to evaluate high frequency oscillatory ventilation and extra-corporeal membrane oxygenation. There are no consensus guidelines but consider in P/F <80.
- Steroids should NOT be initiated in late ARDS (14 days or longer). The impact of earlier steroid therapy on mortality is uncertain, as the DEXA-ARDS trial showed reduced mortality and improved liberation from the vent but previous studies were less clear.
- Recombinant surfactant does not improve survival or ventilator free days
- Low-dose nitric oxide temporarily improves oxygenation but not mortality
- Overall care
- Identify and treat underlying causes
- Ensure adequate nutrition (preferably enteral)
- Provide GI and DVT prophylaxis
- Prevent and treat nosocomial infections early
Indications for intubation
- Is there failure of airway maintenance or protection?
- Upper airway obstruction, airway protection
- Is there a failure of oxygenation or ventilation?
- Uncorrectable hypoxemia (pO2 <70 mmHg on 100% O2 NRB)
- Hypercapnea (pCO2 >55 mmHg) with acidosis [clinical judgement for pCO2 in COPD]
- Ineffective respiration (max inspiratory force <25 cm H2O)
- Does the anticipated clinical course require intubation?
- Fatigue (RR>35 with increasing pCO2)
Initial ventilator settings
- ARDS
- Initial TV 6ml/kg PBW (range 4-8 ml/kg)
- Ventilator rate 14-22 breaths per minute
- Initial PEEP of 5 cm H2O, up to 24 cm H2O
- Non-ARDS
- Initial TV between 6-8 ml/kg PBW reasonable,
- Ventilator rate 12-16 breaths per minute
- PEEP between 3-5 cm H2O
Ware LB, Matthay MA. The acute respiratory distress syndrome. N Engl J Med 2000; 342:1334-49.
https://www.uptodate.com/contents/acute-respiratory-distress-syndrome-clinical-features-diagnosis-and-complications-in-adults
https://www.uptodate.com/contents/ventilator-management-strategies-for-adults-with-acute-respiratory-distress-syndrome
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