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European Respiratory Journal 17:100-107 (2001)
© 2001 ERS Journals Ltd


In vitro assessment of equipment and software to assess tidal breathing parameters in infants

G. Schmalisch1, B. Foitzik1, R.R. Wauer1 and J. Stocks2

1 Dept of Neonatology (Charité), Humboldt University Berlin, Germany and 2 Portex Anaesthesia, Intensive Therapy and Respiratory Medicine Unit, Institute of Child Health, London, UK

CORRESPONDENCE: G. Schmalisch, Dept of Neonatology (Charité), Humboldt University Berlin, Schumannstraße 20/21, D-10098, Berlin, Germany. Fax: 49 3028025824

This work, was supported by the German Ministry for Research and Technology, project "Perinatal Lung" (grant 01 ZZ 9511) and Deutsche Forschungsgemeinschaft (Schm 1160/1-2).

The aim of this in vitro study was to compare the measurement accuracy of two currently available devices for measuring tidal breathing in infants.

A mechanical model pump was used to generate flow profiles which simulated those observed in infants. A range of flows was applied simultaneously to two different devices, namely the commercially available SensorMedics 2600 (SM 2600) and more recently developed, custom-made equipment based on the flow-through technique (FTT). Automatically derived values from both devices were compared with one another and with manual calculations of printouts of the same breaths.

There were no differences in the raw flow signal obtained from the two devices, nor between values calculated automatically or manually from the FTT. Similarly, the deviations between the FTT and SM 2600 were <3% for tidal volume, respiratory frequency and minute ventilation. However, when comparing either with manually calculated values or those derived automatically from the FTT, there was a systematic and highly significant underestimation of shape-dependent parameters, such as the time to peak tidal expiratory flow as a proportion of tidal expiratory time (tPTEF/tE), derived by the SM 2600. The lower the applied flow, the higher the observed deviations, the underestimation being up to 60% when flows simulating those observed in preterm neonates were applied.

These errors appear to result from differences in signal processing such as the algorithms used for breath detection and can only be detected if appropriate nonsinusoidal flow profiles representing those seen in infants are used to evaluate equipment.

Keywords: equipment, flow-through technique, infants, respiratory function tests, software, validation




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