Average Volume Assured Pressure Support (AVAPS) for 24-Hour Use
AVAPS is appropriate for 24-hour use in patients with chronic respiratory failure requiring continuous noninvasive ventilation, particularly when transitioning from nocturnal-only support to around-the-clock ventilation. 1
Clinical Context for 24-Hour AVAPS Use
The primary indication for 24-hour noninvasive ventilation occurs when patients progress from nocturnal hypoventilation to constant daytime hypoventilation, requiring continuous ventilatory support. 1 This transition is indicated when:
- Waking PaCO₂ exceeds 50 mm Hg 1
- Hemoglobin saturation remains ≤92% while awake 1
- Progressive respiratory muscle weakness prevents adequate spontaneous ventilation throughout the day 1
AVAPS vs. Standard BiPAP for Extended Use
Efficacy Evidence
AVAPS demonstrates comparable or superior efficacy to standard BiPAP S/T mode for continuous use:
- More rapid CO₂ clearance: AVAPS achieves significantly better improvement in pH at 6 hours (p=0.027) and 24 hours (p=0.032), and better pCO₂ reduction at 6 hours (p=0.012) and 24 hours (p=0.013) compared to BiPAP S/T 2
- Faster neurological recovery: In patients with hypercapnic encephalopathy, AVAPS produces statistically significant improvements in Glasgow Coma Scale scores (p=0.00001) and pCO₂ (p=0.03) compared to standard BiPAP 3
- Shorter hospital stays: AVAPS is associated with reduced duration of hospitalization (p=0.003) 2
Mechanism of Advantage
The key advantage of AVAPS for 24-hour use is its automatic adjustment of inspiratory pressure to maintain target tidal volume (typically 6-8 mL/kg) despite changing pulmonary mechanics throughout day and night. 4, 5 This addresses the limitation of fixed-pressure BiPAP, which cannot adapt to variations in:
- Patient position changes (sitting vs. lying)
- Sleep-wake transitions
- Fluctuating respiratory muscle strength
- Changes in lung compliance 4
Practical Implementation for 24-Hour Support
Initial Settings
When initiating 24-hour AVAPS:
- Maximum IPAP: Start at 20 cm H₂O, titrate up to 30 cm H₂O as needed 5
- Minimum IPAP: Set at 5 cm H₂O higher than EPAP 5
- Target tidal volume: 6-8 mL/kg ideal body weight 1, 5
- EPAP: Typically 4-8 cm H₂O, adjusted to eliminate upper airway obstruction 1
- Backup rate: Set equal to or slightly less than spontaneous sleeping respiratory rate (minimum 10 breaths/minute) 6
Daytime Delivery Methods
For daytime continuous support, multiple interfaces can be used:
- Mouthpiece intermittent positive pressure ventilation: Most commonly used technique, allowing eating and speaking without interruption; successfully used in patients with mean FVC of 0.6 L (5% predicted) for >8 years 1
- Nasal mask: Can be alternated with full-face mask to reduce skin breakdown 1
- Full-face mask: For patients unable to use mouthpiece or nasal interface 1
Monitoring Requirements
Because most bilevel machines lack built-in alarms, additional monitoring is essential for 24-hour use:
- Pulse oximetry: Continuous monitoring recommended, especially during initial 24 hours 1
- Target SpO₂: Maintain between 85-90% 1
- Arterial blood gas analysis: Measure at baseline, 1 hour, 4-6 hours, then as clinically indicated 1
- Clinical assessment: Regular evaluation of respiratory rate, accessory muscle use, patient comfort, and coordination with ventilator 1
Limitations and Caveats
Evidence Quality
While AVAPS shows clinical benefits, important limitations exist:
- No mortality benefit demonstrated: Studies show no significant difference in ICU mortality, hospital mortality, 6-month, or 1-year mortality between AVAPS and BiPAP S/T 5
- No difference in intubation rates: Need for invasive mechanical ventilation is similar between modes (p=0.338) 2
- Small sample sizes: Most chronic respiratory failure studies involve limited patient numbers 4, 7
- Equivalent long-term outcomes: No significant differences in PaCO₂, PaO₂, sleep efficiency, or compliance when comparing AVAPS to PS-NIV for chronic respiratory failure 7
Clinical Pitfalls
Mask displacement risk: In fragile patients requiring 24-hour support, mask displacement can rapidly lead to severe hypoxemia and hypercapnia; continuous monitoring is critical 1
Higher pressure requirements: AVAPS typically requires significantly higher maximum IPAP levels compared to fixed BiPAP (p<0.001 across all time points), which may increase risk of air leaks and patient discomfort 5
Not a substitute for intubation: When patients meet criteria for invasive ventilation (progressive deterioration despite optimized NIV, inability to protect airway, hemodynamic instability), AVAPS should not delay definitive airway management 1
Algorithm for 24-Hour AVAPS Implementation
Confirm indication: Waking PaCO₂ >50 mm Hg or SpO₂ ≤92% while awake despite nocturnal NIV 1
Assess contraindications: Rule out inability to protect airway, hemodynamic instability, uncontrolled arrhythmias, or facial trauma 1
Select interface: Start with mouthpiece for daytime if patient can coordinate; use nasal or full-face mask as backup 1
Initiate AVAPS settings: Maximum IPAP 20 cm H₂O, minimum IPAP 5 cm H₂O above EPAP, target TV 6-8 mL/kg, backup rate ≥10/min 1, 6, 5
Monitor response: ABG at 1 hour and 4-6 hours; continuous pulse oximetry for 24 hours 1
Titrate pressures: Increase maximum IPAP by 1-2 cm H₂O increments every 5 minutes if TV remains below target or hypoventilation persists 1
Schedule reassessment: Periodic follow-up appropriate to disease stage, monitoring for progression requiring tracheostomy 1