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LETTER |
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Slope of Phase III Is Being Overinterpreted
To the Editor: In 1975, Paiva (2) reported the results of an analysis of a two-compartment model of ventilation. The model included different volume expansions and different time courses of emptying of the two compartments, and Paiva computed gas concentrations and slopes of phase III for a multibreath washout of a test gas. He noted that the slopes of phase III, normalized by mean concentration in the expired gas (SN), increased nearly linearly with breath number for several breaths and approached an asymptotic value at large breath numbers. Later, Paiva and Engel (3) analyzed the diffusional transport at a branch with different flows in the branches. The analysis revealed a diffusional pendelluft between the branches that contributed to gas mixing. Paiva et al. (4) noted that this mechanism produced a value of SN that was relatively large for the first breath and quickly reached a limiting value. They denoted this mechanism in which diffusional transport occurs between convective pathways as diffusion-convection-dependent inhomogeneity (dcdi) to distinguish it from convection-dependent inhomogeneity (cdi), in which transport occurs only along pathways. They argued that these two mechanisms were distinguishable in plots of SN vs. breath number (n) by virtue of the following characteristics: the contribution of dcdi is large for breath 1, increases slightly during the next few breaths, and remains constant for higher breath numbers, whereas the contribution of cdi continues to increase with n. A small but persistent stream of papers has followed. Differences between plots of SN vs. n for gases with different diffusivities and changes in these differences with changes in gravity or posture have been interpreted according to these ideas.Recently, I was asked to review a paper from this school. In my review, I expressed my concern that data on SN were being overinterpreted. Rather than lying in the bushes as a reviewer, it seems better to express these concerns publicly, and that is the purpose of this letter.
My belief that plots of SN vs. n are
being overinterpreted is based on the results of more modeling. A
slightly extended, but still extremely simplified, model of nonuniform
ventilation illustrates this point. The model is a compartmental model
with different volume expansions and different time courses of emptying for the compartments. The model is described as follows. Total lung
volume, nondimensionalized by end-inspiratory lung volume, is denoted
as VL. In the washout maneuver, each breath extends from
VL = 1/2 to VL = 1. The lung
is divided into m compartments with equal volumes at
VL = 1. The volume of the ith compartment, nondimensionalized by its end-inspiratory volume, is denoted
Vi. The nondimensionalized compartmental volumes
are assumed to be quadratic functions of VL.
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(1) |
ai = m/2,
bi = m, and
ci = 0. Because of the
constraint on Vi, only two of these three
equations are independent.
At the beginning of the washout maneuver, the concentration of the test
gas in the lung is uniform and taken to be 1. The concentration in the
ith compartment at the end of the nth
inspiration, denoted Ci(n), is the
concentration during the previous breath
Ci(n
1) times the volume
ratio ai; the concentration in the expired gas,
denoted C(VL,n), is the sum over compartments of
the product of Ci(n) and the
contribution of the ith compartment to expired volume,
(1/m)dVi/dVL; and the slope of phase III, denoted S(n), is the
derivative of C(VL,n) with respect to expired
volume. The mean concentration in the expired gas, denoted
(n), is the value of C(VL,n)
midway through the expiration at VL = 3/4.
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(2) |
(n). This is a simplified
model in which dead space is neglected and diffusion is ignored, except
that the compartments are assumed to be well mixed. It is the same as
Paiva's earlier model (2) but generalized to m
compartments.
Two three-compartment models, described by the two sets of parameter
values shown in Table 1, are denoted
models A and B. Plots of
Vi vs. VL for these models are shown
in Fig. 1, and plots of
SN vs. n are shown in Fig.
2. The plot of SN
vs. n for model A is like the plots for humans
reported by Crawford et al. (1), and the plot for
model B is like the plots for rats reported by Verbanck et
al. (5). The human data have been interpreted as showing a
dominant cdi mechanism, and the rat data have been
interpreted as showing a dominant dcdi mechanism. Of course,
the values of SN shown in Fig. 2 are entirely
the result of the cdi mechanism because the dcdi
mechanism is not included in the model.
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In a two-compartment model, ventilation and course of emptying in the two compartments are completely coupled; the values of the parameters for the second compartment are entirely determined by the values for the first, and only two of the six coefficients in Eq. 1 can be chosen independently. A three-compartment model allows a little more freedom. Four of the nine parameters of that model can be chosen independently. With the different distributions of ventilation and time courses of emptying that are allowed in a multicompartment model, a wide variety of plots of SN vs. n can be obtained, and these include plots that have been interpreted as signatures of the dcdi mechanism.
My objective here is not to propose an alternative model for interpreting the slope of phase III or to claim that diffusion, including the dcdi mechanism, does not play a role in determining the slope of phase III. There is ample evidence that diffusion plays a role in gas transport, and the physical basis for the dcdi mechanism is clearly sound. Dr. Paiva has made a determined effort to use accurate models of the geometry of the acinus. However, assumptions about the distribution of ventilation are still required in the model. In addition, the slope of phase III not only depends on the distribution of ventilation, it also depends on the distribution of time constants and the correlation between ventilation and time constants. The distribution of ventilation at the small scale at which most of the nonuniformity occurs has not been described thoroughly. Less is known about the time course of emptying and the correlation between ventilation and time course. The mechanisms that lie behind nonuniform ventilation and time of emptying are unknown. My objective is only to state that, at this point, I do not think we have an adequate foundation for interpreting plots of SN vs. n.
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REFERENCES |
|---|
1.
Crawford, ABH,
Makowski M,
Paiva M,
and
Engel LA.
Convection- and diffusion-dependent ventilation maldistribution in normal subjects.
J Appl Physiol
59:
838-846,
1985
2.
Paiva, M.
Two new pulmonary function indexes suggested by a simple mathematical model.
Respiration
32:
389-403,
1975[Web of Science][Medline].
3.
Paiva, M,
and
Engel LA.
Pulmonary interdependence of gas transport.
J Appl Physiol
47:
296-305,
1979
4.
Paiva, M,
Van Muylem A,
and
Engel LA.
The slope of phase III in multibreath N2 washout and washin.
Bull Eur Physiopath Respir
18:
273-280,
1982[Web of Science][Medline].
5.
Verbanck, S,
Gonzalez N,
Peces-Barba G,
and
Paiva M.
Multiple-breath washout experiments in rat lungs.
J Appl Physiol
71:
847-854,
1991
|
Theodore A. Wilson, Department of Aerospace Engineering and Mechanics University of Minnesota Minneapolis, Minnesota 55455 |
Only experiments and new intra-acinar morphometrical data
in humans will tell whether the "slope of phase III is being
overinterpreted" . . . Or not To the Editor:
The letter of Ted Wilson helps to shed light on the interpretation of
the phase III slope, and I would like to make a suggestion along his
lines. Nevertheless, his letter also requires a clarification and two corrections.
Clarification.
Traditionally, the slope of phase III or alveolar plateau refers to
vital capacity (VC) single-breath washouts (SBW). Usually, the measured
gas is nitrogen, after a VC inspiration of oxygen followed by a VC
expiration at constant flow. We will only be concerned here with the
slope of phase III during multiple-breath washouts (MBW). The
traditional end-expired volume at each breath is functional residual
capacity. This point is important, as it was shown (5)
that almost all the phase III slope of a VC SBW is due to
inhomogeneities occurring near residual volume and total lung capacity.
MBW involves mechanisms acting only in the range of normal breathing.
Corrections.
The MBW in humans has not "been interpreted as showing a dominant
cdi mechanism" (1-4, 10) and "the plot
of SN vs. n for model A"
is not "like the plots for humans reported by Crawford et al.
(1)." The basis for computation of dcdi and
cdi contributions is that, contrary to cdi, the
back-extrapolation to breath 0 of SN
should not be zero for dcdi models. This is clearly shown in Fig. 6 of Crawford et al. (1) and Fig. 3 of Verbanck et
al. (10).
Suggestion.
Even if Dr. Wilson states that his objective "is not to propose an
alternative model for interpreting the slope of phase III," the
interest of extending to three compartments the two-compartment model
published in 1975 (6) can only be evaluated by comparison with experiments. Unfortunately, Dr. Wilson simulated experiments with
20 successive inspirations up to TLC that were never performed (they
may not be feasible, even in trained subjects). I suggest that he use
the three-compartmental model to simulate the slopes from 1-liter
inspiration from FRC and to compute the model parameters from
parametric fitting on the published data. Then, using the same
parameters, he can evaluate the predictive power of the model by
checking whether the simulated slopes with increasing tidal volume or
end-expiratory lung volume are in agreement with experiments (3,
4). My guess is that the number of compartments has to be
increased to four, five, or more. Perhaps I have a too negative preconception of models of data because my research has been focused on
models of systems (7).
Discussion.
Whatever the number of compartments characterized by the curves of Fig.
1 and obtained from experimental data, the physiological meaning of
these curves is of interest. Because MBW performed in microgravity were
identical to those performed on the ground (8), the
mechanical characteristics of the compartments are gravity-independent.
Furthermore, because 1 s of end-inspiratory apnea significantly
changes the normalized slopes (2), the curves of Fig. 1 should correspond to inhomogeneous properties of lung periphery.
However, I think that different time constants, as suggested by Dr.
Wilson, are not relevant for the model, because, in those zones, time
constants are much smaller than the breathing period. Obviously,
inhomogeneous elastic properties (compliances) in the lung periphery
may play a role, and we fully agree that "the distribution of
ventilation at the small scale at which most of the nonuniformity
occurs has not been described thoroughly." New imaging techniques may
be decisive in this field.
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REPLY
Conclusion. I am confident that 1) both cdi and dcdi mechanisms are important in describing ventilation inhomogeneities in the human lung, 2) the models we have been using are realistic, and 3) the slope of phase III is not being overinterpreted. I think that a consensus on the subject will come more from experiments and new intra-acinar morphometrical data in humans than from new modeling.
I thank Ted Wilson for his letter and for not "lying in the bushes" as a reviewer.| |
REFERENCES |
|---|
1.
Crawford, ABH,
Makowska M,
Paiva M,
and
Engel LA.
Convection- and diffusion-dependent ventilation maldistribution in normal subjects.
J Appl Physiol
59:
838-846,
1985.
2.
Crawford, ABH,
Makowska M,
Kelly S,
and
Engel LA.
Effect of breath holding on ventilation maldistribution during tidal breathing in normal subjects.
J Appl Physiol
61:
2108-2115,
1986
3.
Crawford, ABH,
Makowska M,
and
Engel LA.
Effect of tidal volume on ventilation maldistribution.
Respir Physiol
66:
11-25,
1986[Web of Science][Medline].
4.
Crawford, ABH,
Cotton DJ,
Paiva M,
and
Engel LA.
Effect of lung volume on ventilation distribution.
J Appl Physiol
66:
2502-2510,
1989
5.
Dutrieue, B,
Lauzon AM,
Verbanck S,
Elliott AR,
West JB,
Paiva M,
and
Prisk GK.
Helium and sulfurhexafluoride bolus washin in short-term microgravity.
J Appl Physiol
86:
1594-1602,
1999
6.
Paiva, M.
Two new pulmonary function indexes suggested by a simple mathematical model.
Respiration
32:
389-403,
1975.
7.
Paiva, M,
and
Engel LA.
Theoretical studies of gas mixing and ventilation distribution in the lung.
Physiol Rev
67:
750-796,
1987
8.
Prisk, GK,
Elliott AR,
Guy HJB,
Verbanck S,
Paiva M,
and
West JB.
Multiple-breath washin of helium and sulfur hexafluoride in sustained microgravity.
J Appl Physiol
84:
244-252,
1998
9.
Verbanck, S,
Weibel ER,
and
Paiva M.
Simulation of washout experiments in postmortem rat lungs.
J Appl Physiol
75:
441-451,
1993
10.
Verbanck, S,
Schuermans D,
Van Muylem A,
Paiva M,
Noppen M,
and
Vinken W.
Ventilation distribution during histamine provocation.
J Appl Physiol
83:
1531-1537,
1997
|
Manuel Paiva, Biomedical Physics Laboratory Université Libre de Bruxelles B-1070 Brussels, Belgium |
This article has been cited by other articles:
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M. J. Rodriguez-Nieto, G. Peces-Barba, N. Gonzalez Mangado, M. Paiva, and S. Verbanck Similar ventilation distribution in normal subjects prone and supine during tidal breathing J Appl Physiol, February 1, 2002; 92(2): 622 - 626. [Abstract] [Full Text] [PDF] |
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