Real-time human respiration carbon dioxide measurement device for cardiorespiratory assessment

The development of a human respiration carbon dioxide (CO ₂ ) measurement device to evaluate cardiorespiratory status inside and outside a hospital setting has proven to be a challenging area of research over the few last decades. Hence, we report a real-time, user operable CO ₂ measurement device using an infrared CO ₂ sensor (Arduino Mega2560) and a thin film transistor (TFT, 3.5″), incorporated with low pass (cut-off frequency, 10 Hz) and moving average (span, 8) filters. The proposed device measures features such as partial end-tidal carbon dioxide (EtCO ₂ ), respiratory rate (RR), inspired carbon dioxide (ICO ₂ ), and a newly proposed feature - Hjorth activity - that annotates data with the date and time from a real-time clock, and is stored onto a secure digital (SD) card. Further, it was tested on 22 healthy subjects and the performance (reliability, validity and relationship) of each feature was established using (1) an intraclass correlation coefficient (ICC), (2) standard error measurement (SEM), (3) smallest detectable difference (SDD), (4) Bland-Altman plot, and (5) Pearson's correlation (r). The SEM, SDD, and ICC values for inter- and intra-rater reliability were less than 5% and more than 0.8, respectively. Further, the Bland-Altman plot demonstrates that mean differences ±standard deviations for a set limit were 0.30 ±0.77 mmHg, -0.34 ±1.41 mmHg and 0.21 ±0.64 breath per minute (bpm) for CO ₂ , EtCO ₂ and RR. The findings revealed that the developed device is highly reliable, providing valid measurements for CO ₂ , EtCO ₂ , ICO ₂ and RR, and can be used in clinical settings for cardiorespiratory assessment. This research also demonstrates that EtCO ₂ and RR (r, -0.696) are negatively correlated while EtCO ₂ and activity (r, 0.846) are positively correlated. Thus, simultaneous measurement of these features may possibly assist physicians in understanding the subject's cardiopulmonary status. In future, the proposed device will be tested with asthmatic patients for use as an early screening tool outside a hospital setting.