Multiple inert gas elimination technique

The multiple inert gas elimination technique (MIGET) is a medical technique used mainly in pulmonology that involves measuring the concentrations of various infused, inert gases in mixed venous blood, arterial blood, and expired gas of a subject. The technique quantifies true shunt, physiological dead space ventilation, ventilation versus blood flow (VA/Q) ratios, and diffusion limitation.

Background

Hypoxemia is generally attributed to one of four processes: hypoventilation, shunt (right to left), diffusion limitation, and ventilation/perfusion (VA/Q) inequality.[1] Moreover, there are also "extrapulmonary" factors that can contribute to fluctuations in arterial PO2.

There are several measures of hypoxemia that can be assessed, but there are various limitations associated with each. It was for this reason that the MIGET was developed, to overcome the shortcomings of previous methods.[2][3][4][5]

Theoretical basis

Steady-state gas exchange in the lungs obeys the principles of conservation of mass.[6] This leads to the ventilation/perfusion equation for oxygen:

and for carbon dioxide:

where:

  • denotes the end-capillary concentration of the gas (mL/dL),
  • denotes the mixed venous concentration of the gas (mL/dL),
  • denotes the inspired partial pressure of the gas (mmHg), and
  • denotes the alveolar partial pressure of the gas (mmHg)
  • denotes the ratio of alveolar ventilation to cardiac output

For the purposes of utilizing the MIGET, the equations have been generalized for an inert gas (IG):

where:

  • solubility is the ratio of concentration to partial pressure expressed in mL of gas dissolved per dL of blood per mmHg of the gas in blood

Assuming diffusion equilibration is complete for the inert gas, dropping the subscript IG, and substituting the blood-gas partition coefficient (λ) renders:

Rearranging:

where:

  • denotes the mixed venous partial pressure of the gas (mmHg)
  • denotes the end-capillary partial pressure of the gas (mmHg)

This equation is the foundation for the MIGET, and it demonstrates that the fraction of inert gas not eliminated from the blood via the lung is a function of the partition coefficient and the VA/Q ratio. This equation operates under the presumption that the lung is perfectly homogenous. In this model, retention (R) is measured from the ratio . Stated mathematically:

From this equation, we can measure the levels of each inert gas retained in the blood. The relationship between retention (R) and can be summarized as follows: As for a given λ increases, R decreases; however, this relationship between and R is the most obvious at values of between ten times higher and lower than a gas's λ. Beyond this, however, it is possible to measure the concentrations of the inert gases in the expired gas from the subject. The ratio of the mixed expired concentration to the mixed venous concentration has been termed excretion (E) and describes the ventilation to regions of varying . When taken together:

where:

  • VIG denotes volume of an inert gas eliminated per minute (mL/min)
  • denotes minute ventilation (mL/min)
  • denotes cardiac output (mL/min)

When observing a collection of alveoli in which PO2 and PCO2 are uniform, local alveolar ventilation and local blood flow define :

From these equations it can be deduced that to have knowledge of either retention or excretion implies knowledge of the other. Moreover, a similar understanding exists for the relationship between the distribution of blood flow and the distribution of ventilation.[6]

Limitations

The data produced by the MIGET is an approximation of the distribution of ratios across the entire lung. It has been estimated that nearly 100,000 gas exchange units exist in the human lung;[7] this could lead to a theoretical maximum of VA/Q compartments as high as 100,000, in that case.

References

  1. West, JB (2008). Pulmonary Pathophysiology - The Essentials. Baltimore, MD: Lippincott Williams & Wilkins.
  2. Wagner, PD; Saltzman, HA; West, JB (1974). "Measurement of continuous distributions of ventilation-perfusion ratios: theory". J Appl Physiol. 36 (5): 588–599. doi:10.1152/jappl.1974.36.5.588. PMID 4826323.
  3. Wagner, PD; Naumann, PF; Laravuso, RB (1974). "Simulatenous measurement of eight foreign gases in blood by gas chromatography". J Appl Physiol. 36 (5): 600–605. doi:10.1152/jappl.1974.36.5.600. PMID 4151148.
  4. Wagner, PD; Laravuso, RB; Uhl, RR; West, JB (1974). "Continuous distributions of ventilation-perfusion ratios in normal subjects breathing air and 100% O2". J Clin Invest. 54 (1): 54–68. doi:10.1172/jci107750. PMC 301524. PMID 4601004.
  5. Evans, JW; Wagner, PD (1977). "Limits on VA/Q distributions from analysis or experimental inert gas elimination". J Appl Physiol. 42 (6): 889–898. doi:10.1152/jappl.1977.42.6.889. PMID 195926.
  6. Wagner, PD (2008). "The multiple inert gas elimination technique (MIGET)". Intensive Care Med. 34 (6): 994–1001. doi:10.1007/s00134-008-1108-6. PMID 18421437. S2CID 6593155.
  7. Young, I; Mazzone, RW; Wagner, PD (1980). "Identification of functional lung unit in the dog by graded vascular embolization". J Appl Physiol Respirat Environ Exercise Physiol. 49 (1): 132–141. doi:10.1152/jappl.1980.49.1.132. PMID 7399985.
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