Ventilation-perfusion mismatch pathophysiology: Difference between revisions

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==Overview==
==Overview==
Any discrepancy between pulmonary blood flow and [[ventilation]] is called V/Q mismatch. Ideally [[Ventilation (physiology)|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 lung|base of the lung]] than the [[Apex of lung|apex of the lung]]. This causes a higher V/Q ratio at the apex compared to the base.<ref>{{Cite journal
Any discrepancy between pulmonary blood flow and [[ventilation]] is called V/Q mismatch. Ideally [[Ventilation (physiology)|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 lung|base of the lung]] than the [[Apex of lung|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.
| author = [[Malay Sarkar]], [[N. Niranjan]] & [[P. K. Banyal]]
| title = Mechanisms of hypoxemia
| journal = [[Lung India : official organ of Indian Chest Society]]
| volume = 34
| issue = 1
| pages = 47–60
| year = 2017
| month = January-February
| doi = 10.4103/0970-2113.197116
| pmid = 28144061
}}</ref> 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==
==Pathogenesis==
Line 26: Line 15:
==Associated Conditions==
==Associated Conditions==
Some conditions that cause decrease in V/Q are:  
Some conditions that cause decrease in V/Q are:  
* [[Chronic Bronchitis]]<ref>{{Cite journal
* [[Chronic Bronchitis]]
| author = [[Johan Petersson]] & [[Robb W. Glenny]]
* [[Asthma]]
| title = Gas exchange and ventilation-perfusion relationships in the lung
* [[Foreign body aspiration]]
| journal = [[The European respiratory journal]]
| volume = 44
| issue = 4
| pages = 1023–1041
| year = 2014
| month = October
| doi = 10.1183/09031936.00037014
| pmid = 25063240
}}</ref><ref>{{Cite journal
| author = [[Kelvin Hsu]], [[Jonathan P. Williamson]], [[Matthew J. Peters]] & [[Alvin J. Ing]]
| title = Endoscopic Lung Volume Reduction in COPD: Improvements in Gas Transfer Capacity Are Associated With Improvements in Ventilation and Perfusion Matching
| journal = [[Journal of bronchology & interventional pulmonology]]
| volume = 25
| issue = 1
| pages = 48–53
| year = 2018
| month = January
| doi = 10.1097/LBR.0000000000000445
| pmid = 29261579
}}</ref>
* [[Asthma]]<ref>{{Cite journal
| author = [[Krishnan Parameswaran]], [[Andrew C. Knight]], [[Niall P. Keaney]], [[E. David Williams]] & [[Ian K. Taylor]]
| title = Ventilation and perfusion lung scintigraphy of allergen-induced airway responses in atopic asthmatic subjects
| journal = [[Canadian respiratory journal]]
| volume = 14
| issue = 5
| pages = 285–291
| year = 2007
| month = July-August
| doi = 10.1155/2007/474202
| pmid = 17703244
}}</ref>
* [[Foreign body aspiration]]<ref>{{Cite journal
| author = [[Natan Cramer]], [[Roger S.. Taylor]] & [[Melissa M.. Tavarez]]
| title = Foreign Body Aspiration
| year = 2018
| month = January
| pmid = 30285375
}}</ref>
* [[Hepatopulmonary syndrome]]
* [[Hepatopulmonary syndrome]]
* [[ARDS]]
* [[ARDS]]
* Bronchiectasis<ref>{{Cite journal
* [[Bronchiectasis]]
| author = [[Malay Sarkar]], [[N. Niranjan]] & [[P. K. Banyal]]
* [[Interstitial Lung disease]]
| title = Mechanisms of hypoxemia
* [[Cystic Fibrosis]]
| journal = [[Lung India : official organ of Indian Chest Society]]
* [[Pulmonary Hypertension]]
| volume = 34
| issue = 1
| pages = 47–60
| year = 2017
| month = January-February
| doi = 10.4103/0970-2113.197116
| pmid = 28144061
}}</ref>
* Interstitial Lung disease<ref>{{Cite journal
| author = [[Malay Sarkar]], [[N. Niranjan]] & [[P. K. Banyal]]
| title = Mechanisms of hypoxemia
| journal = [[Lung India : official organ of Indian Chest Society]]
| volume = 34
| issue = 1
| pages = 47–60
| year = 2017
| month = January-February
| doi = 10.4103/0970-2113.197116
| pmid = 28144061
}}</ref>
* Cystic Fibrosis<ref>{{Cite journal
| author = [[Malay Sarkar]], [[N. Niranjan]] & [[P. K. Banyal]]
| title = Mechanisms of hypoxemia
| journal = [[Lung India : official organ of Indian Chest Society]]
| volume = 34
| issue = 1
| pages = 47–60
| year = 2017
| month = January-February
| doi = 10.4103/0970-2113.197116
| pmid = 28144061
}}</ref>
* Pulmonary Hypertension<ref>{{Cite journal
| author = [[Malay Sarkar]], [[N. Niranjan]] & [[P. K. Banyal]]
| title = Mechanisms of hypoxemia
| journal = [[Lung India : official organ of Indian Chest Society]]
| volume = 34
| issue = 1
| pages = 47–60
| year = 2017
| month = January-February
| doi = 10.4103/0970-2113.197116
| pmid = 28144061
}}</ref>
Some conditions that cause increase in V/Q are:
Some conditions that cause increase in V/Q are:
* [[Pulmonary embolism]]<ref>{{Cite journal
* [[Pulmonary embolism]]
| author = [[Johan Petersson]] & [[Robb W. Glenny]]
* [[Emphysema]]
| title = Gas exchange and ventilation-perfusion relationships in the lung
| journal = [[The European respiratory journal]]
| volume = 44
| issue = 4
| pages = 1023–1041
| year = 2014
| month = October
| doi = 10.1183/09031936.00037014
| pmid = 25063240
}}</ref>
* [[Emphysema]]<ref>{{Cite journal
| author = [[Johan Petersson]] & [[Robb W. Glenny]]
| title = Gas exchange and ventilation-perfusion relationships in the lung
| journal = [[The European respiratory journal]]
| volume = 44
| issue = 4
| pages = 1023–1041
| year = 2014
| month = October
| doi = 10.1183/09031936.00037014
| pmid = 25063240
}}</ref>


==Genetics==
==Genetics==

Revision as of 22:33, 25 November 2018


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.