Journal of Applied Physiology Journal of Neurophysiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 94: 1084-1091, 2003. First published November 15, 2002; doi:10.1152/japplphysiol.00256.2002
8750-7587/03 $5.00
This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
94/3/1084    most recent
00256.2002v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (4)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Singh, B.
Right arrow Articles by Finucane, K. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Singh, B.
Right arrow Articles by Finucane, K. E.
Vol. 94, Issue 3, 1084-1091, March 2003

Breath-by-breath measurement of the volume displaced by diaphragm motion

Bhajan Singh1,2, Janine A. Panizza1, and Kevin E. Finucane1

1 Department of Pulmonary Physiology, Sir Charles Gairdner Hospital, and 2 Department of Physiology, University of Western Australia, Nedlands, Western Australia 6009, Australia


    ABSTRACT
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

To develop an accurate method to measure the volume displaced by diaphragm motion (Delta Vdi) breath by breath, we compared Delta Vdi measured by a previously evaluated biplanar radiographic method (Singh B, Eastwood PR, and Finucane KE. J Appl Physiol 91: 1913-1923, 2001) at several lung volumes during vital capacity inspirations in 10 healthy and nine hyperinflated subjects with 1) Delta Vdi measured from the same chest X-rays by two previously described uniplanar methods (Petroll WM, Knight H, and Rochester DF. J Appl Physiol 69: 2175-2182, 1990; Verschakelen JA, Deschepper K, and Demendts M. J Appl Physiol 72: 1536-1540, 1992) and a proposed method that considered actual cross-sectional shape of the rib cage and spinal volume (Delta VdiS); and 2) Delta VdiS measured by lateral fluoroscopy in the same 10 healthy subjects. Relative to biplanar Delta Vdi, Delta VdiS values from lateral chest X-rays and fluoroscopy were not different, whereas Delta Vdi values of Petroll et al. and Verschakelen et al. were increased by (means ± SD) 1.98 ± 1.59 and 1.16 ± 0.82 liters, respectively (both P < 0.001). During quiet breathing, Delta VdiS by lateral fluoroscopy was 66 ± 16% of tidal volume and similar to that between functional residual capacity and one-half inspiratory capacity by the biplanar radiographic method. We conclude that accurate breath-by-breath measurements of Delta Vdi can be made by using lateral fluoroscopy.

respiratory muscles; respiratory mechanics; fluoroscopy


    INTRODUCTION
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

OUR LABORATORY HAS RECENTLY described a radiographic method for measuring inspired volume attributable to diaphragm motion (Delta Vdi) using matched posteroanterior (PA) and lateral chest X-rays (CXRs) to quantify the change in subphrenic volume during inspirations from residual volume (RV) (9, 10). Delta Vdi and the change in lung volume attributable to expansion of the pulmonary rib cage, measured independently, closely approximated inspired volume in healthy controls and subjects with hyperinflation due to emphysema (9). These results suggest that Delta Vdi measured with the biplanar method is accurate and defines the volume contribution of the diaphragm to inspiration.

Breath-by-breath measurements of Delta Vdi would allow measurement of work and power output of the diaphragm and may improve assessment of diaphragm function. Measurement of Delta Vdi during breathing cannot be made by using CXRs but may be possible with the use of fluoroscopy, if Delta Vdi could be accurately measured from a single plane. Two such methods have been proposed. Petroll et al. (7) measured Delta Vdi in dogs using anteroposterior fluoroscopy and modeling the subphrenic space and dome of the diaphragm as a truncated cone with a circular cross section and an oblate spheroid, respectively. Verschakelen et al. (11) measured Delta Vdi in humans using lateral fluoroscopy to measure sagittal rib cage diameter and the surface area swept by the diaphragm during inspiration, modeling the cross-sectional shape of the abdominal rib cage as a rectangle. The cross-sectional shape of the rib cage used in these models differed substantially from shapes based on studies in humans (4, 8), and neither method corrected the volume swept by the diaphragm for the volume occupied by the spine and paraspinal tissues (Vsp). For these reasons, the methods of Petroll et al. (7) and Verschakelen et al. (11) are likely to give inaccurate estimates of Delta Vdi in humans. The accuracy of the biplanar method previously reported by us depends in part on the validity of the geometric shape used to calculate the cross-sectional area of the abdominal rib cage from the coronal and sagittal diameters measured from the PA and lateral CXRs, respectively. We adopted the shape described by Pierce et al. (8) for the pulmonary rib cage. To the extent that this shape may not apply to the abdominal rib cage, our measurements would also be inaccurate.

The aim of this study was to develop a fluoroscopic method for measuring Delta Vdi breath by breath, which was accurate in both healthy and hyperinflated subjects. To assess the relative accuracy of various models for estimating the cross-sectional area of the abdominal rib cage, we compared estimated and measured cross-sectional areas of thoracic computed tomography (CT) scans. The accuracy of methods for estimating Delta Vdi from a single radiographic plane and lateral fluoroscopy was assessed by comparing results with those obtained, in the same subjects, with the previously validated biplanar method. Methods used to estimate Delta Vdi from a single plane were those described by Petroll et al. (7), Verschakelen et al. (11), and a new method that incorporated our findings on the cross-sectional shape of the abdominal rib cage and considered the Vsp. We found that the cross-sectional shape of the abdominal rib cage was accurately modeled as one-third the way between an ellipse and a rectangle, as described by Pierce et al. (8) for the pulmonary rib cage, and that the shape of the rib cage changed little with lung volume. We hypothesized that Delta Vdi would be 1) overestimated by the methods of Petroll et al. (7) and of Verschakelen et al. (11) because these methods assumed thoracic shapes that overestimated the actual cross-sectional area of the abdominal rib cage and did not consider the volume occupied by spinal tissues, and 2) most accurately estimated by the proposed new method. Our findings confirmed these hypotheses.


    METHODS
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

Rib cage shape. To examine the accuracy of various models used to estimate the cross-sectional area of the rib cage (4, 7, 8, 11), CT images of the thorax close to relaxed total lung capacity (TLC) were obtained in 25 healthy subjects and 22 with pulmonary hyperinflation due to emphysema (Table 1). The CT scans were obtained for clinical purposes with consent of the subjects. The internal cross-sectional area of the rib cage at the levels of the xiphoid process (abdominal rib cage) and the carina (pulmonary rib cage) were 1) measured by planimetry and 2) calculated by using the major sagittal and coronal diameters of the rib cage. The following geometric models were used: circles, ellipse, rectangle, a rectangle bounded by two semicircles ("athletic track") as described by Chihara et al. (4), and one-third the way between an ellipse and a rectangle as defined by Pierce et al. (8). Separate cross-sectional areas were calculated for circles with diameters equal to the major coronal and sagittal diameters of the rib cage. All measurements were made by using a digitizing palette (Accugrid, Numonics, Montgomeryville, PA).

                              
View this table:
[in this window]
[in a new window]
 
Table 1.   Characteristics of subjects used to model cross-sectional shape of the rib cage and to measure Delta Vdi

Radiographic measurements of Delta Vdi. Delta Vdi was measured by the biplanar method (9) in 10 healthy subjects and nine subjects with emphysema and severe pulmonary hyperinflation (Table 1). These results were then used to assess the accuracy of Delta Vdi estimated by various uniplanar methods using the same CXRs. Subphrenic volume and the Vsp were estimated from PA and lateral CXRs taken at active RV, functional residual capacity (FRC), one-half inspiratory capacity (1/2IC), and TLC during a slow vital capacity (VC) inspiration in the erect posture. At each lung volume, Delta Vdi was also measured with the method described by Petroll et al. (7) applied to the right subphrenum on the PA CXRs and to the lateral CXRs, the method of Verschakelen et al. (11), and a new method described below (Delta VdiS). Informed consent was obtained from each subject, and ethical approval was granted by the Committee for Human Rights, University of Western Australia.

Delta VdiS. Lateral CXR images at RV, FRC, and 1/2IC were superimposed on images at FRC, 1/2IC, and TLC, respectively, using the images of vertebral bodies and radiopaque ball bearings adhered to the posterior chest wall. The subphrenic space at the lower lung volume was defined by the silhouette of the right hemidiaphragm, a straight line joining the anterior and posterior costophrenic angles at the higher lung volume, a straight line joining the anterior costophrenic angles at each lung volume, and the posterior limit of the lung (Fig. 1A). This volume was divided into a dome (Vdome,L) and a frustrum (Vfr), the latter being represented by the area between the lines joining the anterior and posterior costophrenic angles at each volume (Fig. 1A). The subphrenic space at the higher lung volume was taken as the dome of the diaphragm (Vdome,H). The Vsp within the volume swept by the diaphragm was defined by the silhouettes of the diaphragm at each lung volume, the anterior margin of the vertebral bodies, and the posterior limit of the lung (Fig. 1A). The Delta Vdi was calculated by using the following equation
&Dgr;Vdi<SUB>S</SUB> = V<SUB>dome,L</SUB> + V<SUB>fr</SUB> − V<SUB>dome,H</SUB> − V<SUB>sp</SUB> (1)
This equation can be represented as follows (see APPENDIX)
&Dgr;Vdi<SUB>S</SUB><IT>=D</IT><SUB>dome,L</SUB><IT> · A</IT><SUB>dome,L</SUB><IT>+</IT>0.6(<IT>D</IT><SUB>dome,L</SUB><IT>+D</IT><SUB>dome,H</SUB>) (2)

×<IT>A</IT><SUB>fr</SUB><IT>−D</IT><SUB>dome,H</SUB><IT> · A</IT><SUB>dome,H</SUB><IT>−</IT>0.25<IT>&pgr;D</IT><SUB>sp</SUB><IT> · A</IT><SUB>sp</SUB>
where Ddome,L and Ddome,H are the length or sagittal diameter of the base of the dome at the lower and higher lung volume, respectively; Adome and Afr are the areas projected by the dome and frustrum in the sagittal plane, respectively; Adome,H and Adome,L are the Adome at higher and lower lung volume, respectively; Dsp is the sagittal width of the volume of spinal tissues at the level of Ddome,L; and Asp is the area of spinal tissues projected in the sagittal plane (Fig. 1A). Equation 2 is derived in the APPENDIX; it assumes that the ratio of coronal to sagittal diameters does not change with lung volume and that the cross-sectional shape of the spinal tissues is circular.


View larger version (24K):
[in this window]
[in a new window]
 
Fig. 1.   A: schematic illustration of proposed uniplanar method for measuring the volume displaced by diaphragm motion (Delta VdiS) from a lateral chest X-ray (CXR) or fluoroscopy. The silhouette of the diaphragm dome, sagittal diameter of the rib cage at the base of the diaphragm dome, and the anterior and posterior walls of the rib cage are represented by solid lines at the lower (L) lung volume and dashed lines at the higher (H) lung volume. Delta VdiS was the difference in volume between (DomeL + frustrum) and (DomeH + spine), which are represented by the respective areas bcdb, abdea, ahea, and abcha. The sagittal diameter of spinal tissues was taken as distance bg. B: where the anterior costophrenic angle at the higher volume is cephalad to the costophrenic angle at the lower volume, the volume represented by area fdd'f was excluded from analysis, and DomeL is represented by area bcd'b and frustrum by area abd'a. See text for details.

Cephalic movement of the anterior chest wall during inspiration resulted in the anterior costophrenic angle at the higher lung volume being cephalad of the anterior costophrenic angle at the lower volume in 17 of the 46 volume pairs measured. To avoid overestimation of Delta VdiS in this circumstance, the anterior limit of Vdome,L was defined by its intersection with the straight line joining the anterior and posterior costophrenic angles at the higher volume (Fig. 1B).

Fluoroscopic measurement of Delta VdiS. To assess the accuracy of Delta Vdi estimated from lateral fluoroscopy, Delta VdiS was measured by fluoroscopy in the 10 healthy subjects in whom Delta Vdi had been measured with the biplanar radiographic method. The diaphragm and lower rib cage were imaged by lateral fluoroscopy, with a field of vision 16 in. in diameter (Toshiba CAS 8000 DSA, Tokyo, Japan) at a frame rate of 15 per second. Images and time of day were stored by using a super VHS video recorder and cassette [Mitsubishi, HS-E82(A) and Fuji, Pro]. Radiopaque ball bearings adhered to the chest wall allowed alignment of images at different lung volumes. Each subject was seated with the left chest wall as close as possible to the image intensifier with the arms elevated and with hands resting on the head. Two sequences of two to four tidal breaths followed by an exhalation to RV and an inspiration to TLC were imaged. Inspiratory flow and volume were measured with a pneumotachograph and recorded continuously on computer (Powerlab, ADInstruments, Sydney, Australia). Posture was maintained constant; no attempt was made to control chest wall configuration. Radiation exposure was varied to optimize contrast of the diaphragm silhouette and bony landmarks and was estimated at ~0.1 mSv.

Fluoroscopic images at end expiration and end inspiration during quiet breathing and at RV, FRC, 1/2IC, and TLC during VC inspirations were identified by interpolating images on video frames and inspired volume. Images of the diaphragm and bony landmarks were traced onto transparent paper. Distortion and magnification of the images were defined by using a precise grid with radiopaque lines at 1-cm intervals placed at the same distance from the image intensifier as the right midclavicular line. The distorted image of the grid, also on transparent paper, was used to replot the position of the diaphragm and chest wall on Cartesian coordinates, thereby correcting for distortion and magnification. Delta VdiS was then measured from the replotted images by using the method described above.

Data analysis and statistics. All data are expressed as means ± SD. Characteristics of healthy and hyperinflated subjects were compared by using the Student's t-test. Paired t-tests and the methods of Bland and Altman (2) were used to examine the relationships between 1) measured and calculated rib cage cross-sectional area and 2) biplanar and uniplanar Delta Vdi. Significance was defined as P < 0.05.


    RESULTS
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

Cross-sectional shape of the rib cage. The measured cross-sectional areas of the abdominal and pulmonary rib cage are compared with those calculated using the major sagittal and or coronal diameters and various models of thoracic shape, in Fig. 2. In both healthy and hyperinflated subjects, the cross-sectional areas of the rib cage were underestimated when modeled as an ellipse, overestimated when modeled as a rectangle, and either under- or overestimated when modeled as a circle, depending on whether the major sagittal or coronal diameter was taken to be the diameter of the circle. The cross-sectional areas of the abdominal and pulmonary rib cages were most accurately calculated when modeled as one-third the way between an ellipse and a rectangle or as an "athletic track" (Figs. 2 and 3). The ratios of the major coronal-to-sagittal diameters of the abdominal rib cage were 1.44 ± 0.11 in healthy subjects and 1.36 ± 0.13 in hyperinflated subjects. These results were similar to those obtained with the biplanar method, where the ratios were 1.5 ± 0.08 at RV and 1.36 ± 0.06 at TLC in controls and 1.38 ± 0.13 at RV and TLC in emphysematous subjects (9).


View larger version (15K):
[in this window]
[in a new window]
 
Fig. 2.   Difference between calculated cross-sectional (CS) area of the abdominal and pulmonary rib cages with the use of a variety of geometric models and actual CS area measured by digitizer, expressed as a percentage of the measured value, in 25 healthy and 22 hyperinflated subjects. Values are means ± SD. Significant difference from measured CS area: * P < 0.01, dagger  P < 0.001 (paired t-test).



View larger version (16K):
[in this window]
[in a new window]
 
Fig. 3.   Bland and Altman comparison of the calculated and measured CS areas of the abdominal (A) and pulmonary (B) rib cages in 25 healthy and 22 hyperinflated subjects. CS area was calculated geometrically from the major coronal and sagittal diameters of the rib cage and assuming a shape of one-third the way between an ellipse and a rectangle and was measured from computed tomograms by digitizer. The solid lines are the mean difference, and the dashed lines are the limits of the 95% confidence intervals.

Delta Vdi. Delta Vdi estimated by the methods of Petroll et al. (7) using PA CXRs, and of Verschakelen et al. (11) using lateral CXRs, exceeded biplanar Delta Vdi by 1.98 ± 1.59 and 1.16 ± 0.82 liters, respectively (both P < 0.001). These overestimates increased with volume, and, in many cases, Delta Vdi exceeded inspired volume (Table 2, Fig. 4). Delta Vdi by the method of Petroll et al. (7) applied to lateral CXRs was reduced (-0.47 ± 0.33 liter, P < 0.001) relative to biplanar Delta Vdi (Table 2, Fig. 4). There was no difference between biplanar Delta Vdi and Delta VdiS measured from lateral CXRs in the healthy and hyperinflated subjects (mean difference 0.06 ± 0.24 liter, P = 0.08) or from lateral fluoroscopy in healthy subjects (mean difference 0.06 ± 0.28 liter, P = 0.30) (Table 2, Fig. 4). If the Vsp had not been considered, Delta VdiS measured from lateral CXRs would have exceeded biplanar Delta Vdi by 0.29 ± 0.27 liter (P < 0.001) and 0.15 ± 0.29 liter (P = 0.03) in healthy and hyperinflated subjects, respectively. Delta Vdi measured fluoroscopically during tidal breathing was 0.66 ± 0.16 relative to tidal volume. Delta Vdi/tidal volume had a coefficient of variation within subjects of 11.6 ± 5.7% (Fig. 5), and the mean value was similar to the ratio of Delta Vdi to the volume inspired between FRC and 1/2IC during VC inspirations in the six subjects, in whom this information was obtained with the biplanar method (0.71 ± 0.14 vs. 0.68 ± 0.12, P = 0.66).

                              
View this table:
[in this window]
[in a new window]
 
Table 2.   Ratio of Delta Vdi to inspired volume for breaths between RV and FRC, between RV and 1/2IC, and between RV and TLC, measured using the biplanar and several uniplanar methods



View larger version (21K):
[in this window]
[in a new window]
 
Fig. 4.   Bland and Altman comparisons of the volume displaced by diaphragm motion (Delta Vdi) in 10 healthy and 9 hyperinflated subjects for breaths between residual volume (RV) and functional residual capacity, RV and one-half inspired capacity, and RV and total lung capacity, measured from matched posteroanterior (PA) and lateral (LAT) CXRs (biplanar Delta Vdi) and the uniplanar methods of Petroll et al. (7) applied to PA [Delta VdiPetroll(PA CXR); A] and LAT CXRs [Delta VdiPetroll(LAT CXR); B] separately, Verschakelen et al. (11) applied to LAT CXRs [Delta VdiVerschakelen(LAT CXR); C], and our proposed method (Delta VdiS) applied to LAT CXRs [Delta VdiS(LAT CXR); D]. In 10 healthy subjects, biplanar Delta Vdi was compared with our proposed method applied to LAT fluoroscopy [Delta VdiS(LAT Fluoroscopy); E]. The solid lines are the mean difference, and the dashed lines are the limits of the 95% confidence intervals.



View larger version (10K):
[in this window]
[in a new window]
 
Fig. 5.   The volume contribution of the diaphragm to tidal volume (Delta VdiS/VT) measured by LAT fluoroscopy in 10 healthy subjects using our proposed method. The dashed line is the mean value for the group.


    DISCUSSION
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

This study found that the Delta Vdi in healthy and hyperinflated subjects was measured accurately from lateral CXRs by considering excursion of the diaphragm, sagittal diameter, and cross-sectional shape of the abdominal rib cage and the Vsp. The method enabled accurate breath-by-breath measurements of Delta Vdi in healthy subjects by using fluoroscopy. Previously published methods for measuring Delta Vdi by fluoroscopy (7, 11) were found to be inaccurate.

Assumptions and limitations. The accuracy of measuring Delta Vdi from a single radiographic plane or from fluoroscopy was examined by comparing, in the same subjects, the results of three uniplanar methods with those of a biplanar method using matched PA and lateral CXRs. The validity of our conclusions relies on the accuracy of our biplanar method (9). Although there is no direct validation of this method, several lines of evidence support its accuracy. First, in healthy subjects at all inspired volumes and in emphysema subjects at intermediate and high lung volumes, the sum of Delta Vdi and the change in lung volume attributable to expansion of the pulmonary rib cage, both measured independently by the biplanar method, accurately estimated inspired volume measured by pneumotachograph (9). Second, the model of the cross-sectional shape of the rib cage used to quantify subphrenic volume was validated in healthy and hyperinflated subjects in this study (Figs. 2 and 3). Third, the method assumes that the coronal and sagittal planes determining the radiographic silhouette of the diaphragm remain constant at different lung volumes so that the change in position of the silhouette represents the overall change in diaphragm position. These planes do move slightly as lung volume increases (5, 13). However, the movements are unlikely to significantly influence biplanar estimates of Delta Vdi, because our previous results showed that changes in the length of the diaphragm over the VC measured radiographically (9) were consistent with changes in length of the entire diaphragm measured by MRI (5).

The method used by us for measuring Delta Vdi from a single plane entails a number of assumptions. First, we assumed that the cross-sectional shape of the abdominal rib cage remained constant during inspirations from RV and that spinal tissues had a circular rather than an elliptical cross section, as assumed in the previous biplanar study (9). The ratio of major coronal to sagittal rib cage diameters, obtained during active inspirations from RV to TLC in the erect posture with the use of biplanar CXRs (9), decreased by ~10% in healthy subjects and did not change in those with emphysema. The constant ratio of 1.4 assumed in the expression used to estimate Delta Vdi from uniplanar images (APPENDIX) was within the range of values found in healthy and emphysematous subjects and unlikely to lead to errors of significant magnitude. The finding that, for inspirations between RV and TLC, Delta Vdi measured by the uniplanar and biplanar methods were not different supported this conclusion. This finding also suggests that our assumption of a circular cross section of spinal tissues did not cause significant error. On biplanar CXRs, we found no consistent relationship between the coronal and sagittal diameters of spinal tissues and, therefore, adopted the more simple assumption of a circular cross section. Second, we assumed that the change in position of the right hemidiaphragm silhouette in the imaging plane is representative of the overall change in position of the diaphragm. Excursion of the right hemidiaphragm usually exceeds that of the left (3, 5, 9, 10, 13), and this could lead to an overestimation of Delta Vdi. The error is likely to be small in healthy subjects in whom the mean difference in shortening of the hemidiaphragms over the VC was only ~1% (9). In subjects with hyperinflation, the mean difference was ~14%, and the corresponding overestimation of Delta Vdi over the VC would approximate 90 ml. Third, we assumed that the position of the costophrenic angles around the circumference of the rib cage could be represented by a straight line between the anterior and posterior costophrenic angles (Fig. 1). Whitelaw (13) and Gauthier et al. (5) have shown that, in the supine posture, the lateral costophrenic angle lies slightly above this line at low lung volumes and slightly below it at high lung volumes. However, the departure of the costophrenic angles from a straight line around the circumference of the rib cage is small, and we expect the error associated with this assumption to be small. Regarding the assumption that the anterior costophrenic angle moves along a straight line during inspiration, examination of the lateral CXRs showed that this assumption was reasonable for the volume increments used. For larger volume changes, e.g., VC inspirations, departures from this assumption are common, resulting in overestimation of Delta Vdi.

Delta Vdi as measured in this study could underestimate the total contribution of the diaphragm to inspired volume because it does not include the effect of diaphragm tension in expanding and elevating the rib cage, but this indirect contribution is believed to be small (6, 9, 12). Diaphragm motion during inspiration is not simply a function of diaphragm action but also of rib cage and abdominal muscle activities and elastances and of the mechanical coupling between the diaphragm and chest wall (6). As measured in this study, Delta Vdi reflects the volume change of the lung attributable to diaphragm motion, including motion due both to active shortening and to the mechanical properties of the chest wall. Where there is paradox of the pulmonary rib cage, Delta Vdi reflects the volume change of the lung and pulmonary rib cage; such behavior was observed in two healthy subjects between RV and FRC.

Implications. The ability to measure Delta Vdi breath by breath is likely to be of clinical value. Aliverti et al. (1) have shown that, in humans during exercise, the diaphragm contracts nearly isotonically and acts mainly to generate inspiratory flow, whereas the increased pressures required to displace the rib cage and abdomen are developed largely by rib cage and abdominal muscles, respectively. These findings suggest that the contribution of the diaphragm to inspiration depends not only on its ability to develop tension, but also on its capacity to shorten and displace volume. Using biplanar measurements of Delta Vdi, we have previously shown that decreases in VC in asbestos-related pleural fibrosis were due mainly to reduced expansion of the lower rib cage with relative preservation of Delta Vdi (10) and revealed mechanisms by which the function of the diaphragm as a volume pump was preserved in emphysema, despite severe pulmonary hyperinflation (9). The ability to measure Delta Vdi from a single plane using fluoroscopy enables dynamic study of the pump function of the diaphragm.

Delta Vdi was not accurately measured by the methods of Petroll et al. (7) or by those of Vershakelen et al. (11) (Table 2, Fig. 4). Our data show that this was due, first, to significant departures of actual cross-sectional shape of the abdominal rib cage in humans from the circular and rectangular shapes, respectively, assumed in these models (Fig. 2) and, second, to failure to consider the volume occupied by spinal and paraspinal tissues. The geometric model of Vershakelen et al. (11) assumes that the cross-sectional shape of the abdominal rib cage was rectangular with coronal dimensions 1.8 times the sagittal diameter; our data show that this ratio was inappropriately high.

In contrast to these methods, Delta Vdi measured from lateral CXRs and fluoroscopy, using a method that considered excursion of the diaphragm, actual shape of the abdominal rib cage, and the volume occupied by spinal and paraspinal tissues, did not differ from that measured by the biplanar method (Table 2, Fig. 4), despite the assumptions and limitations discussed above. Delta Vdi during tidal breaths in 10 healthy subjects was relatively consistent from breath to breath (Fig. 5), and the ratio of Delta Vdi to inspired volume was similar to that during slow inspirations between FRC and 1/2IC. These findings suggest that this method allows accurate dynamic measurements of Delta Vdi. In combination with measurements of transdiaphragmatic pressure and the duration of inspiration, fluoroscopic measurements of Delta Vdi may allow breath-by-breath estimation of work and power output of the diaphragm and enable a clearer understanding of the role of the diaphragm in pathogenesis of breathlessness, exercise limitation, and the development of respiratory failure in chronic obstructive lung disease.


    APPENDIX
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

Derivation of Proposed Method for Estimating Delta Vdi From a Lateral Radiographic/Fluoroscopic Image (Delta VdiS)

Subphrenic volume was divided into Vdome,L and Vfr and Vdome,H as described in METHODS and Fig. 1. If the domes were elliptical in cross section, their volumes (Vdome,ellipse) could be calculated from the equation
V<SUB>dome,ellipse</SUB><IT>=</IT>0.67<IT>&pgr; · </IT>0.5<IT>D</IT><SUB>Sag</SUB><IT> · </IT>0.5<IT>D</IT><SUB>Cor</SUB><IT> · H</IT><SUB>dome</SUB> (3)
where DSag and DCor are the sagittal and coronal rib cage diameters at the base of the domes, respectively, and Hdome is the height of the domes. The Adome can be calculated from the equation
A<SUB>dome</SUB><IT>=</IT>0.5<IT>&pgr; · </IT>0.5<IT>D</IT><SUB>Sag</SUB><IT> · H</IT><SUB>dome</SUB> (4)
Combining Eqs. 3 and 4
V<SUB>dome,ellipse</SUB><IT>=</IT>0.67<IT>D</IT><SUB>Cor</SUB><IT> · A</IT><SUB>dome</SUB> (5)
We found that, in health and hyperinflation, the ratio of DCor to DSag was ~1.4. Therefore
V<SUB>dome,ellipse</SUB><IT>≈</IT>0.93<IT>D</IT><SUB>Sag</SUB><IT> · A</IT><SUB>dome</SUB> (6)
Because the cross-sectional area of the rib cage is best approximated by a shape one-third the way between an ellipse and a rectangle (Figs. 2 and 3), and this area is 1.091 times the area of an ellipse of the same dimensions
V<SUB>dome</SUB><IT>≈D</IT><SUB>Sag</SUB><IT> · A</IT><SUB>dome</SUB> (7)
The Vfr can be calculated by dividing it into multiple horizontal slices with a cross-sectional shape one-third the way between an ellipse and a rectangle. The volume of each slice (Vslice) can be calculated as follows
V<SUB>slice</SUB><IT>=H</IT><SUB>slice</SUB>[0.25<IT>&pgr;D</IT><SUB>Sag</SUB><IT> · D</IT><SUB>Cor</SUB><IT>+</IT>0.33 (8)

(<IT>D</IT><SUB>Sag</SUB><IT> · D</IT><SUB>Cor</SUB><IT>−</IT>0.25<IT>&pgr;D</IT><SUB>Sag</SUB><IT> · D</IT><SUB>Cor</SUB>)]
where Hslice is the height of each slice. This can be simplified to
V<SUB>slice</SUB><IT>=</IT>0.857<IT>H</IT><SUB>slice</SUB><IT> · D</IT><SUB>Sag</SUB><IT> · D</IT><SUB>Cor</SUB> (9)
Assuming that a straight line can represent the lateral walls of the frustrum, Vfr can be approximated by the following equation
V<SUB>fr</SUB> ≈ 0.857 mean <IT>D</IT><SUB>Sag</SUB><IT> · </IT>mean <IT>D</IT><SUB>Cor</SUB><IT> · H</IT><SUB>fr</SUB> (10)
where Hfr is the height of the frustrum. The area of each slice of the frustrum projected in the sagittal plane (Aslice) is
A<SUB>slice</SUB><IT>=D</IT><SUB>Sag</SUB><IT> · H</IT><SUB>slice</SUB> (11)
and the Afr is approximated by
A<SUB>fr</SUB> ≈ mean <IT>D</IT><SUB>Sag</SUB><IT> · H</IT><SUB>fr</SUB> (12)
Combining Eqs. 10 and 12
V<SUB>fr</SUB><IT>≈</IT>0.857<IT> · </IT>mean <IT>D</IT><SUB>Cor</SUB><IT> · A</IT><SUB>fr</SUB> (13)
As the ratio of DCor to DSag is ~1.4, the equation can be expressed as
V<SUB>fr</SUB> ≈ 1.2 mean <IT>D</IT><SUB>Sag</SUB><IT> · A</IT><SUB>fr</SUB> (14)
or
V<SUB>fr</SUB><IT>≈</IT>0.6(<IT>D</IT><SUB>dome,L</SUB><IT>+D</IT><SUB>dome,H</SUB>)<IT>A</IT><SUB>fr</SUB> (15)
The Vsp within the volume swept by the diaphragm can be estimated by assuming that this volume is cylindrical, i.e.
V<SUB>sp</SUB><IT>=</IT>0.25<IT>&pgr; · D</IT><SUP>2</SUP><SUB>sp</SUB><IT> · H</IT><SUB>sp</SUB> (16)
where Dsp is the diameter of the spinal column, and Hsp is the height of spinal mass. The Asp is
A<SUB>sp</SUB><IT>=D</IT><SUB>sp</SUB><IT> · H</IT><SUB>sp</SUB> (17)
Combining Eqs. 16 and 17
V<SUB>sp</SUB><IT>=</IT>0.25<IT>&pgr;D</IT><SUB>sp</SUB><IT> · A</IT><SUB>sp</SUB> (18)
The Delta Vdi can be calculated from the equation
&Dgr;Vdi = V<SUB>dome,L</SUB> − V<SUB>dome,H</SUB> + V<SUB>fr</SUB> − V<SUB>sp</SUB> (19)
Combining Eqs. 7, 15, 18, and 19
&Dgr;Vdi<IT>≈D</IT><SUB>dome,L</SUB><IT> · A</IT><SUB>dome,L</SUB><IT>−D</IT><SUB>dome,H</SUB><IT> · A</IT><SUB>dome,H</SUB><IT>+</IT> (20)

0.6(<IT>D</IT><SUB>dome,L</SUB><IT>+D</IT><SUB>dome,H</SUB>)<IT>A</IT><SUB>fr</SUB><IT>−</IT>0.25<IT>&pgr;D</IT><SUB>sp</SUB><IT> · A</IT><SUB>sp</SUB>


    ACKNOWLEDGEMENTS

The authors thank P. R. Eastwood and W. J. Noffsinger for technical assistance, Y. M. Lam for statistical advice, M. Crabbe for assistance with radiography, N. Hicks for assistance with fluoroscopy, and the Departments of Radiology and Radiotherapy, Sir Charles Gairdner Hospital, for access to equipment and materials.


    FOOTNOTES

This study was supported by grants from the Medical Research Fund of Western Australia and the Sir Charles Gairdner Hospital Research Fund. B. Singh is the recipient of an Australian Lung Foundation/Boehringer Ingelheim Chronic Airflow Limitation Research Fellowship.

Address for reprint requests and other correspondence: B. Singh, Dept. of Pulmonary Physiology, Sir Charles Gairdner Hospital, Hospital Ave., Nedlands, WA 6009, Australia (E-mail: Bhajan.Singh{at}health.wa.gov.au).

The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

First published November 15, 2002;10.1152/japplphysiol.00256.2002

Received 27 March 2002; accepted in final form 7 November 2002.


    REFERENCES
TOP
ABSTRACT
INTRODUCTION
METHODS
RESULTS
DISCUSSION
APPENDIX
REFERENCES

1.   Aliverti, A, Cala SJ, Duranti R, Ferrigno G, Kenyon CM, Pedotti A, Scano G, Sliwinski P, Macklem PT, and Yan S. Human respiratory muscle actions and control during exercise. J Appl Physiol 83: 1256-1269, 1997[Abstract/Free Full Text].

2.   Bland, JM, and Altman DG. Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 1: 307-310, 1986[ISI][Medline].

3.   Cassart, M, Pettiaux N, Gevenois PA, Paiva M, and Estenne M. Effect of chronic hyperinflation on diaphragm length and surface area. Am J Respir Crit Care Med 156: 504-508, 1997[Abstract/Free Full Text].

4.   Chihara, K, Kenyon CM, and Macklem PT. Human rib cage distortability. J Appl Physiol 81: 437-447, 1996[Abstract/Free Full Text].

5.   Gauthier, AP, Verbanck S, Estenne M, Segebarth C, Macklem PT, and Paiva M. Three-dimensional reconstruction of the in vivo human diaphragm shape at different lung volumes. J Appl Physiol 76: 495-506, 1994[Abstract/Free Full Text].

6.   Kenyon, CM, Cala SJ, Yan S, Aliverti A, Scano G, Duranti R, Pedotti A, and Macklem PT. Rib cage mechanics during quiet breathing and exercise in humans. J Appl Physiol 83: 1242-1255, 1997[Abstract/Free Full Text].

7.   Petroll, WM, Knight H, and Rochester DF. A model approach to assess diaphragmatic volume displacement. J Appl Physiol 69: 2175-2182, 1990[Abstract/Free Full Text].

8.   Pierce, RJ, Brown DJ, Holmes M, Cumming G, and Denison DM. Estimation of lung volumes from chest x-rays using shape information. Thorax 34: 726-734, 1979[Abstract].

9.   Singh, B, Eastwood PR, and Finucane KE. The volume displaced by diaphragm motion in emphysema. J Appl Physiol 91: 1913-1923, 2001[Abstract/Free Full Text].

10.   Singh, B, Eastwood PR, Finucane KE, Panizza JA, and Musk AW. Effect of asbestos-related pleural fibrosis on excursion of the lower chest wall and diaphragm. Am J Respir Crit Care Med 160: 1507-1515, 1999[Abstract/Free Full Text].

11.   Verschakelen, JA, Deschepper K, and Demendts M. Relationship between axial motion and volume displacement of the diaphragm during VC maneuvers. J Appl Physiol 72: 1536-1540, 1992[Abstract/Free Full Text].

12.   Ward, ME, Ward JW, and Macklem PT. Analysis of human chest wall motion using a two-compartment rib cage model. J Appl Physiol 72: 1338-1347, 1992[Abstract/Free Full Text].

13.   Whitelaw, WA. Shape and size of the human diaphragm in vivo. J Appl Physiol 62: 180-187, 1987[Abstract/Free Full Text].


J APPL PHYSIOL 94(3):1084-1091
8750-7587/03 $5.00 Copyright © 2003 the American Physiological Society



This article has been cited by other articles:


Home page
Eur Respir JHome page
F. Bellemare and A. Jeanneret
Sex differences in thoracic adaptation to pulmonary hyperinflation in cystic fibrosis
Eur. Respir. J., January 1, 2007; 29(1): 98 - 107.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
K. E. Finucane, J. A. Panizza, and B. Singh
Efficiency of the normal human diaphragm with hyperinflation
J Appl Physiol, October 1, 2005; 99(4): 1402 - 1411.
[Abstract] [Full Text] [PDF]


This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
94/3/1084    most recent
00256.2002v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (4)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Singh, B.
Right arrow Articles by Finucane, K. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Singh, B.
Right arrow Articles by Finucane, K. E.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online