Examination of pulmonary diffusion and perfusion
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Pulmonary perfusion = delivery of deoxygenated blood to the alveoli and removal of oxygenated blood.
- pulmonary perfusion disorders can cause restrictive or obstructive lung diseases, e.g. pulmonary hypertension or hypotension, pulmonary artery embolism, etc.)
- reduced perfusion → transfer of reduced amounts of O2 and CO2 by blood → pulmonary hypertension → enlargement of the right heart.
Pulmonary diffusion = diffusion of O2 and CO2 acrossthe alveolo-capillary membrane (basement membrane of pneumocytes + basement membrane of capillary endothelium + endothelial cells)
- pulmonary diffusion disorders can be caused by a reduction in the diffusion area: e.g.inflammation (and subsequent thickening of the alveolo-capillary membrane), edema (exudation of blood plasma into the interstitium), interstitial lung fibrosis (fibrous tissue moves the alveoli away from the capillaries), anemias , etc.
- reduced diffusion → mainly reduced pO2
Methods of measuring pulmonary perfusion[edit | edit source]
Ventilation-perfusion scan[edit | edit source]
It is a combination of a perfusion scan and a ventilation scan. This type of examination is suitable for suspected pulmonary embolism or a disorder of the lung parenchyma
- perfusion scan - principle: administration of a radioactive substance (Technetium) into a vein (or so-called Tc macroaggregates with human albumin) → we monitor the blood flow through the lungs → we detect embolizations, etc.
- ventilation scan principle: the examined patient inhales a radioactive substance (e.g. Technetium, Krypton, Xenon) → we monitor the distribution of air in the lungs → we detect embolization
- evaluation:
- visual (we observe inhomogeneities in the lungs)
- quantitative determination of the relative perfusion of the right and left lung or lung segments (correction for different absorption of gamma radiation )
- creating a final protocol (images, values, verbal evaluation)
Pulmonary angiography[edit | edit source]
For more information see Angiography.
principle: application of x-ray contrast material into a vein → display of blood flow on x-ray
CT[edit | edit source]
For more information see CT.
PET[edit | edit source]
For more information see PET.
Chest X-ray[edit | edit source]
For more information see Chest X-ray.
Examination of pulmonary diffusion[edit | edit source]
Single breath method[edit | edit source]
- especially when pulmonary emphysema and lung parenchymal disorders are suspected.
- the examinee inhales a test mixture of gases (with a low concentration of CO and inert gas - e.g. helium or methane) from the device and holds his breath for about 10 seconds. We will then perform an analysis of the expired air. Due to the dilution of the inert gas in the residual volume of the lungs, its concentration in the exhaled air is lower. The same dilution factor also applies to the CO concentration, thanks to which we determine the original and subsequent alveolar concentration. The given values (including the length of breath holding) are used to calculate the so-called transfer factor ( (also called the „Krogh factor“)
- result:
- transfer factor below normal → emphysema, disorders of the lung parenchyma (pulmonary vasculitis, granulomatosis, interstitial pulmonary fibrosis)
- transfer factor above normal → left-right shunts, intrapulmonary bleeding (CO in the alveoli also binds hemoglobin)
- result:
Links[edit | edit source]
External links[edit | edit source]
- astronuklfyzika.cz
- pats.atsjournals.org
- www.upol.cz
- www.nlm.nih.gov/medlineplus
- www.nationaljewish.org
References[edit | edit source]
- NEČAS, Emanuel. Pathological Physiology of Organ Systems I. 1. edition. Karolinum, 2003. 760 pp. ISBN 80-246-0675-5.