Clinical studies on target volume during pressure-preset ventilation
Study | Year | Design | Cohort | Target volume setting | Main target volume outcomes* |
Storre et al7 † | 2006 | 6-week cross-over RCT (n=10) | OHS‡ | 7 ml/kg IBW (n=5), 10 ml/kg IBW (n=5) |
|
Janssens et al10 † | 2009 | 1-day cross-over RCT (n=12) | OHS¶ | 7.5±0.8 ml/kg body weight |
|
Ambrogio et al11 † | 2009 | 1-day cross-over RCT (n=28) | Mixed¶ | 8 ml/kg IBW or 110% of baseline VT |
|
Crisafulli et al12 † | 2009 | 5-day cross-over RCT (n=9) | COPD‡ | 8 ml/kg IBW |
|
Oscroft et al13 § | 2010 | 8-week cross-over RCT (n=24) | COPD¶ | 11.0±3.9 l/min (minute volume) |
|
Murphy et al14 † | 2012 | 3-month RCT (n=46) | OHS‡ | Individual adjustments aimed at achieving control of nocturnal hypoventilation while abolishing obstructive events |
|
↵* Compared with conventional pressure-preset non-invasive positive pressure ventilation (NPPV).
↵† Mode for target volume: average volume assured pressure support.
↵‡ Patients naive to any form of NPPV.
↵§ Mode for target volume: intelligent volume assured pressure support.
↵¶ Patients already established on pressure-preset NPPV.
COPD, chronic obstructive pulmonary disease; ESS, Epworth Sleepiness Score; IBW, ideal body weight; OHS, obesity hypoventilation syndrome; PaCO2, arterial partial pressure of carbon dioxide; PtcCO2, transcutaneous partial pressure of carbon dioxide; RCT, randomised controlled trial; VT, tidal volume.