Abstract
BACKGROUND: In the intensive care unit we have observed that patients have different adherence to 2 commonly used positive-expiratory-pressure (PEP) therapy devices: the PEP bottle and the PEP mask. The reason for this difference is not clear.
METHODS: In a randomized prospective study, we made continuous recordings of airway pressure and airflow, with 20 healthy volunteers, with the PEP bottle and the PEP mask. The measurement sequence consisted of 3 sessions of 10 breaths with the PEP bottle and the PEP mask, in a randomized crossover design. A rest period of 15 min separated the PEP bottle and PEP mask measurements.
RESULTS: With the PEP bottle the expiratory phase began with a zero-flow period of 0.39 s, during which airway pressure rose 11.9 cm H2O. With the PEP bottle the mean expiratory pressure was 11.7 cm H2O, and end-expiratory pressure was 9.5 cm H2O. With the PEP mask the initial expiratory zero-flow period was almost nonexistent (0.04 s) and without any change in airway pressure. With the PEP mask the shape of the expiratory pressure curve was different; mean expiratory pressure was 8.6 cm H2O, and end-expiratory pressure was zero. With the PEP bottle the inspiration also began with a zero-flow period of 0.43 s, during which airway pressure decreased 9.6 cm H2O from the end-expiratory airway pressure. With the PEP mask the initial inspiratory zero-flow period was only 0.01 s and there was no concomitant change in airway pressure.
CONCLUSIONS: The PEP bottle and the PEP mask showed major differences in the relationship between airflow and airway pressure. These findings might explain the observed differences in patient adherence to these therapies.
- positive expiratory pressure
- PEP
- airflow
- airway pressure
- Borg scale
- chest physiotherapy
- flow resistor
- threshold resistor
Footnotes
- Correspondence: Maria Sehlin RPT MSc, Department of Community Medicine and Rehabilitation, Physiotherapy, Operationscentrum, Umeå University Hospital, S-901 85 Umeå, Sweden. E-mail: maria.sehlin{at}vll.se.
This research was supported by grants from the Swedish Association of Registered Physiotherapists. The authors report no other conflicts of interest.
Maria Sehlin RPT MSc presented a version of this paper at the meeting of the Scandinavian Society of Anaesthesiology and Intensive Care Medicine, held July 2, 2005, in Reykjavik, Iceland, and at the Swedish Association of Registered Physiotherapists Congress, held October 28, 2005, in Stockholm, Sweden.
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