Chest
Volume 132, Issue 3, September 2007, Pages 977-983
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ORIGINAL RESEARCH
EXERCISE TESTING
Mixed-Expired and End-Tidal CO2 Distinguish Between Ventilation and Perfusion Defects During Exercise Testing in Patients With Lung and Heart Diseases

https://doi.org/10.1378/chest.07-0619Get rights and content

Background

Mismatching of ventilation to perfusion is found in patients with COPD, left ventricular failure (LVF), and pulmonary vascular diseases. Such mismatching may be due to ventilation or perfusion defects or both. Our primary hypothesis was that pressures of mixed-expired CO2 pressure (Peco2), end-tidal Pco2 pressure (Petco2), and their ratios would differ between groups during exercise testing, depending on whether the ventilation/perfusion ( V˙/ Q˙) abnormality was dominantly caused by airways or perfusion defects.

Methods

We administered incremental cycle ergometry tests to 25 normal subjects and three groups of 25 patients, each group with uncomplicated COPD, LVF, or primary pulmonary arterial hypertension (PAH). We compared Peco2, Petco2, and their ratios at rest, unloaded pedaling, anaerobic threshold, and peak exercise.

Results

Although each patient group had mean peak O2 uptake of approximately 50% of predicted normal, the levels and patterns of change for each group for Peco2, Petco2, and their ratios were surprisingly distinctive. As hypothesized, the COPD group always had markedly lower Peco2/Petco2 ratios than all other groups (p < 0.001). In addition, patients with LVF had slightly lower Peco2/Petco2 ratios at heavy exercise than normal subjects (p < 0.05). At all times, except for COPD group Petco2 at peak exercise, each group had significantly lower Petco2 and Peco2 than normal subjects (p < 0.001). In patients with PAH, the Petco2 decline with exercise was distinctive.

Conclusions

The levels and changes in Peco2, Petco2, and their ratios during cardiopulmonary exercise testing are distinctive and explained by the differing pathophysiologies of V˙/ Q˙ mismatching in these disorders.

Section snippets

Subjects

The study was approved by our institutional review board. From our recent files, the authors screened and selected cardiopulmonary exercise test results obtained with informed consent from 25 adults in each of the following four groups: normal, COPD, LVF, and PAH. All normal subjects were considered healthy. All COPD patients had FEV1/FVC ratios < 50% and low or reduced gas transfer index; none had asthma. All LVF patients were New York Heart Association class III or IV left ventricular

Results

Demographics of the subjects are noted in Table 1. Although age and sex distributions were dissimilar, generally reflecting age and sex distributions seen in the respective disease states, disease severities (percentage of predicted peak V˙o2), peak V˙e, and peak V˙co2 for the three disease groups were not significantly different. However, FEV1/VC, Dlco, and breathing reserve were significantly lower and residual volume/total lung capacity significantly higher in the COPD group

Discussion

Discerning the dominant disorder in patients with dyspnea can sometimes be difficult. As previously found in several studies, V˙/ Q˙ inequalities, increased Vd/Vt, and/or decreased Peco2 and Petco2 occur at rest and during exercise in COPD,678910 LVF,1112131415 and PAH.161718 The major hypothesis and finding of this study was that V˙/ Q˙ mismatch caused by airway defects could be differentiated from that of perfusion defects using noninvasive measures of Peco2 and Petco2.

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      Moreover, assessment of partial pressure of end-tidal CO2 can be utilized to differentiate whether V/Q mismatch is caused by airway defects as opposed to perfusion defects. This can be particularly helpful in establishing the dominant mechanism of V/Q mismatch in HF patients with several comorbidities such as pulmonary artery hypertension or chronic obstructive pulmonary disease (47). Ventilatory pattern analysis during symptom-limited CPX allows for the identification of a periodic breathing pattern at rest and during exercise (48).

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    This work was performed at Los Angeles Biomedical Research Institute, Harbor-UCLA Medical Center.

    James E. Hansen has received consultation fees from MET-Test, LLC, and salary support from St. Jude Medical. Dr. Ulubay received support from the Turkish Scientific Research Institute (Tubitak). Dr. Chow reports no conflict of interest. Dr. Sun has received salary support from St. Jude Medical. Dr. Wasserman has received consultation fees from MET-Test, LLC, and salary support from St. Jude Medical.

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