Objectives: To evaluate the performance of a newly developed single br
eath CO2 analysis station in measuring the airway deadspace in a lung
model (study 1), and then to quantify the bias and precision of the ph
ysiologic deadspace measurement in a surfactant-depleted animal model
(study 2). Design: A prospective bench validation of a new technique o
f airway deadspace measurement using a criterion standard (study 1); a
prospective, animal cohort study comparing a new technique of physiol
ogic deadspace measurement with a reference method (Bohr-Enghoff metho
d) (study 2). Setting: A bench laboratory and animal laboratory in a u
niversity-affiliated medical center. Subjects: A lung model (study 1),
and adult sheep with induced surfactant deficiency (saline ravage) (s
tudy 2). Methods: The single breath CO2 analysis station consists of a
mainstream capnometer, a variable orifice pneumotachometer, a signal
processor, and computer software with capability for both on and off l
ine data analysis. Study 1: We evaluated the accuracy of the airway de
adspace calculation using a plexiglass lung model. The capnometer and
pneumotachometer were placed at the ventilator Y-piece with polyvinyl
chloride tubing added to simulate increased airway deadspace. Segments
of tubing were sequentially removed during each testing session to si
mulate decreasing deadspace. The calculated airway deadspace was deriv
ed from the single breath CO2 plot and compared with the actual tubing
volume using least-squares linear regression and paired t-tests. Stud
y 2: The accuracy of the physiologic deadspace measurement was examine
d in a saline-lavaged animal model by comparing the physiologic deadsp
ace calculated from the single breath CO2 analysis station with values
obtained using the Enghoff modification of the Bohr equation: deadspa
ce/tidal volume ratio = (PaCO2 - mixed expired PCO2)/PaCO2. Measuremen
ts and Main Results: Study 1: Thirty six measurements of calculated ai
rway deadspace were made and compared with actual circuit deadspace du
ring four different testing conditions. Measured airway deadspace corr
elated significantly with actual circuit deadspace (r(2) = .99). The p
roportional error of the method was -0.8% with a 95% confidence interv
al from -3.6% to 1.9%. Study 2: A total of 27 pairs of measurements in
four different animals were available for analysis. The derived physi
ologic deadspace/tidal volume ratio significantly correlated with the
value obtained using the Bohr Enghoff method (r(2) = .84). The bias an
d precision of our physiologic deadspace calculation were .02 and .02,
respectively, and the mean percent difference for the physiologic dea
dspace calculated from the single breath CO2 analysis station was 2.4%
. Conclusions: Our initial experience with the single breath CO2 analy
sis station indicates that this device can reliably provide on line ev
aluation of the single-breath CO2 waveform. In particular, estimation
of the airway and physiologic deadspace under a variety of testing con
ditions was consistently within 5% of actual values. We feel that with
further application and refinement of the technique, single breath CO
2 analysis may provide a noninvasive, on-line monitor of changes in pu
lmonary blood flow.