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Validation of a Transcutaneous CO2 Monitor in Adult Patients with Chronic Respiratory Failure

Home mechanical ventilation is usually started in hospital as arterial blood gas sampling is deemed necessary to monitor CO2 and O2 adequately during institution of ventilatory support. A non-invasive device to reliably measure CO2 transcutaneously would alleviate the need for high care settings for measurement and open the possibility for home registration.

Objectives: In this study we investigated whether the TOSCA® transcutaneous CO2 (PtcCO2) measurements, performed continuously during the night, reliably reflect arterial CO2 (PaCO2) measurements in adults with chronic respiratory failure.

Methods: Paired measurements were taken in 15 patients hospitalised to evaluate their blood gas exchange. Outcomes were compared 30 min, 2, 4, 6 and 8 h after attaching the sensor to the earlobe. A maximum difference of 1.0 kPa and 95% limits of agreement (LOA) of 1 kPa between CO2 pressure measurements, following the analysis by Bland and Altman, were determined as acceptable.

Results: Mean PtcCO2 was 0.4 kPa higher (LOA –0.48 to 1.27 kPa) than mean PaCO2 after 30 min. These figures were 0.6 kPa higher (LOA –0.60 to 1.80 kPa) after 4 h, with a maximum of 0.72 kPa (LOA 0.35 to 1.79 kPa) after 8 h. The corresponding values for changes in PtcCO2 versus PaCO2 were not significant (ANOVA).

Conclusions: PtcCO2 measurement, using TOSCA, is a valid method showing an acceptable agreement with PaCO2 during 8 h of continuous measurement. Therefore, this device can be used to monitor CO2 adequately during chronic ventilatory support.

Authors : A. Hazenberga, J.G. Zijlstrab, H.A.M. Kerstjensc, P.J. Wijkstraa, c
Source: Respiration
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