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Phasic venous return abnormality in chronic pulmonary diseases: pulsed Doppler echocardiography study
S Izumi1, K Moriyama, S Kobayashi
1Fourth Department of Internal Medicine, Shimane Medical University, Izumo.
Internal Medicine (Tokyo, Japan)
|June 1, 1994
Summary
Chronic pulmonary diseases alter venous return by affecting superior vena cava (SVC) flow patterns. Reduced lung function and increased pulmonary vascular resistance correlate with abnormal SVC flow, impacting venous return.
Area of Science:
- Cardiology
- Pulmonology
- Medical Imaging
Background:
- Venous return is crucial for cardiac function.
- Chronic pulmonary diseases can significantly impact hemodynamics.
- Understanding venous return alterations is vital for managing these conditions.
Purpose of the Study:
- To investigate the characteristics of venous return in patients with chronic pulmonary diseases.
- To identify factors influencing these venous return features.
- To correlate venous flow patterns with lung function and pulmonary vascular resistance.
Main Methods:
- Analysis of respiration-related variation in superior vena cava (SVC) flow using pulsed Doppler echocardiography.
- Comparison of flow patterns between 85 patients with chronic pulmonary diseases and 54 healthy controls.
- Assessment of forced expiratory volume in 1 second (FEV1.0%) and vital capacity (VC).
Main Results:
- Healthy subjects exhibited a typical "type I" SVC flow pattern.
- Patients with pulmonary diseases showed "type I" or an abnormal "type II" pattern (wave disappearance).
- Type II pattern was more frequent in patients with reduced FEV1.0% and %VC, linked to elevated right atrial pressure and positive pleural pressure.
- Increased A wave velocity correlated with pulmonary vascular resistance.
Conclusions:
- Venous return in chronic pulmonary disease is influenced by ventilatory disturbances and pulmonary vascular resistance.
- Abnormal SVC flow patterns (type II) are associated with decreased lung function and elevated right atrial pressure.
- Echocardiography can reveal significant alterations in venous return dynamics in pulmonary disease.