Is average volume pressure support (AVPS) suitable for 24-hour use?

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Last updated: December 25, 2025View editorial policy

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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

  1. Confirm indication: Waking PaCO₂ >50 mm Hg or SpO₂ ≤92% while awake despite nocturnal NIV 1

  2. Assess contraindications: Rule out inability to protect airway, hemodynamic instability, uncontrolled arrhythmias, or facial trauma 1

  3. Select interface: Start with mouthpiece for daytime if patient can coordinate; use nasal or full-face mask as backup 1

  4. 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

  5. Monitor response: ABG at 1 hour and 4-6 hours; continuous pulse oximetry for 24 hours 1

  6. Titrate pressures: Increase maximum IPAP by 1-2 cm H₂O increments every 5 minutes if TV remains below target or hypoventilation persists 1

  7. Schedule reassessment: Periodic follow-up appropriate to disease stage, monitoring for progression requiring tracheostomy 1

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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