Ventilation-perfusion mismatch pathophysiology

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Template:Ventilation-perfusion mismatch

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Aida Javanbakht, M.D.

Overview

Any discrepancy between pulmonary blood flow and ventilation is called V/Q mismatch. Ideally ventilation and perfusion should be equal with a V/Q ratio of 1, but the normal lung varies due to a higher perfusion at the base of the lung than the apex of the lung. This causes a higher V/Q ratio at the apex compared to the base. The average V/Q ratio in a normal lung is about 0.8, with about 4 liters of oxygen and 5 liters of blood entering the lung per minute. Diseased lung can cause a V/Q mismatch due to decreased blood flow or oxygenation. This results in hypoxemia, and there are many causes of it.

Pathogenesis

V/Q mismatch is one of the most common reasons of hypoxemia in patients with lung diseases like obstructive lung diseases, pulmonary vascular diseases, and interstitial diseases . An increased V/Q mismatch is caused by a decrease in blood flow to the lung, for example a pulmonary embolism. A decreased V/Q mismatch is caused by a decrease in ventilation or an airway obstruction, for example Asthma. A V/Q mismatch due to a perfusion defect will improve with 100% oxygen therapy.

In normal condition when there is a low ventilation, the body tries to keep this ratio in a normal range by restricting the perfusion in that specific area of the lung. This unique mechanism is called hypoxic pulmonary vasoconstriction. If this process continues for a long time it can cause pulmonary hypertension .

Associated Conditions

Some conditions that cause decrease in V/Q are:

Some conditions that cause increase in V/Q are:

Genetics

The association between V/Q mismatch and genetic depends on the etiology of the mismatch. For example ORMDL3 and GSDML genes play a role in causing asthma .

Gross Pathology

The gross pathology depends on the exact reason for the V/Q mismatch.

Microscopic Pathology

The microscopic pathology depends on the exact reason for the V/Q mismatch. For example in asthma there are extracellular Charcot-Leyden crystals and increased mucosal goblet cells.

  1. Bita Hajian, Jan De Backer, Wim Vos, Wouter H. van Geffen, Paul De Winter, Omar Usmani, Tony Cahn, Huib Am Kerstjens, Massimo Pistolesi & Wilfried De Backer (2018). "Changes in ventilation-perfusion during and after an COPD exacerbation: an assessment using fluid dynamic modeling". International journal of chronic obstructive pulmonary disease. 13: 833–842. doi:10.2147/COPD.S153295. PMID 29563783.
  2. Krishnan Parameswaran, Andrew C. Knight, Niall P. Keaney, E. David Williams & Ian K. Taylor (2007). "Ventilation and perfusion lung scintigraphy of allergen-induced airway responses in atopic asthmatic subjects". Canadian respiratory journal. 14 (5): 285–291. doi:10.1155/2007/474202. PMID 17703244. Unknown parameter |month= ignored (help)
  3. Johan Petersson & Robb W. Glenny (2014). "Gas exchange and ventilation-perfusion relationships in the lung". The European respiratory journal. 44 (4): 1023–1041. doi:10.1183/09031936.00037014. PMID 25063240. Unknown parameter |month= ignored (help)
  4. Johan Petersson & Robb W. Glenny (2014). "Gas exchange and ventilation-perfusion relationships in the lung". The European respiratory journal. 44 (4): 1023–1041. doi:10.1183/09031936.00037014. PMID 25063240. Unknown parameter |month= ignored (help)
  5. Bita Hajian, Jan De Backer, Wim Vos, Wouter H. van Geffen, Paul De Winter, Omar Usmani, Tony Cahn, Huib Am Kerstjens, Massimo Pistolesi & Wilfried De Backer (2018). "Changes in ventilation-perfusion during and after an COPD exacerbation: an assessment using fluid dynamic modeling". International journal of chronic obstructive pulmonary disease. 13: 833–842. doi:10.2147/COPD.S153295. PMID 29563783.