Skip to main content

Table 3 Type of assessment and criteria for performing a spontaneous breathing test

From: Rationale, study design, and analysis plan of the Alveolar Recruitment for ARDS Trial (ART): Study protocol for a randomized controlled trial

Clinical assessment

Improvement of acute process (ARDS and associated conditions) leading to intubation and mechanical ventilation

 

Patient is alert and cooperative

 

Chest pain is controlled

 

Adequate cough (moderate to high strength)

 

Absence of excessive tracheobronchial secretion

 

No signs of respiratory distress:

 

 Nostril flaring

 

 Use of accessory muscles of respiration (suprasternal and/or intercostal retraction)

 

 Paradoxical movements of the chest/abdomen

Objective measurements

Respiratory stability: oxygenation

 

 PEEP ≤10 cmH2O

 

 Support pressure ≤10 cmH2O

 

 PaO2/FiO2 ≥250 (consider weaning if ≥150)

 

 SpO2 > 90% under FiO2 ≤40%

 

Respiratory stability: function

 

 Respiratory rate ≤35 breaths/min 

 

 Minute volume  < 10 L/min

 

 Respiratory rate/tidal volume (L)  < 105 breath/min/L

 

 No significant respiratory acidosis (pH ≥7.25) 

 

Cardiovascular stability

 

 Heart rate <140 bpm

 

 Systolic blood pressure  > 90 and <160 mmHg

 

 Without vasoconstrictor/inotropic drugs (or low doses) 

 

Neurological stability

 

 Patient alert and cooperative - SAS 4 (acceptable: slightly drowsy patient (SAS 3) slightly agitated (SAS 5))