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The following is the abstract of the article discussed in the subsequent letter:
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ABSTRACT |
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Matthie, J., B. Zarowitz, A. De Lorenzo, A. Andreoli, K. Katzarski, G. Pan, and P. Withers. Analytic
assessment of the various bioimpedance methods used to estimate body
water. J. Appl. Physiol. 84(5): 1801-1816, 1998.
Knowledge of patient fluid distribution would be useful
clinically. Both single-frequency (SF) and impedance modeling
approaches are proposed. The high intercorrelation between body water
compartments makes determining the best approach difficult. This study
was conducted to evaluate the merits of an SF approach. Mathematical
simulation was performed to determine the effect of tissue change on
resistance and reactance. Dilution results were reanalyzed, and
resistance and parallel reactance were used to predict the
intracellular water for two groups. Results indicated that the amount
of intracellular and extracellular water conduction at any SF can vary
with tissue change, and reactance at any SF is affected by all tissue
parameters. Modeling provided a good prediction of dilution
intracellular and extracellular water, but an SF method did not.
Intracellular, extracellular, and total body water were equally
predicted at all frequencies by SF resistance and parallel reactance.
Extracellular and intracellular water are best measured through
modeling, because only at the zero and infinite frequencies are the
results sensitive only to extracellular and intracellular water. At all
other frequencies there are other effects.
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LETTER |
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Bioimpedance Measurement of Extracellular Water
To the Editor: The paper by Matthie and others (1) purports to demonstrate the superiority of the Xitron multifrequency bioimpedance analyzer over single-frequency bioimpedance for measurement of extracellular water (ECW). The paper uses the same eight human subjects and data, which this group, in a paper by Patel et al., including Zarowitz but not Matthie, reported previously (2). The paper by Matthie et al. (1), which does not include Patel as co-author, is heavily math oriented but does not reproduce exactly the source data, including individual values for deuterium and bromide dilution in the paper by Patel et al. (2). For example, in Table 1 in the paper by Matthie et al. (1), listing descriptive characteristics of eight cardiac surgery patients, the data differ from the values in Table 1 of the paper by Patel et al. (2). In the paper by Patel et al., the patients' age is 68 ± 6.8 yr; in the paper by Matthie et al. (1), patients' age is 68.77 ± 6.77 yr. In the paper by Patel et al. (2), patients' weight is 90 ± 24 kg. In the paper by Matthie et al. (1), it is 90.94 ± 24.14 kg. Were other data modified?In my letter to the editor (3) discussing the paper by Patel et al. (2), I suggested that in their subjects with normal body composition, ECW was a sufficiently constant fraction of total body water (TBW) that, using their own dilution data, it could be calculated from TBW as accurately as the bioimpedance measurement. The authors were given the opportunity to respond and chose not to do so. The important point, available evidence suggests, is that neither single- nor multiple-frequency bioimpedance analysis has been shown to reliably measure documented excess ECW in patients with clinical evidence of fluid overload (4).
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REFERENCES |
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1.
Matthie, J.,
B. Zarowitz,
A. De Lorenzo,
A. Audreoli,
K. Katzarski,
G. Pan,
and
P. Withers.
Analytic assessment of the various bioimpedance methods used to estimate body water.
J. Appl. Physiol.
84:
1801-1816,
1998
2.
Patel, R. V.,
E. L. Peterson,
N. Silverman,
and
B. J. Zarowitz.
Estimation of total body and extracellular water in post-coronary artery bypass graft surgical patients using single and multiple frequency bioimpedance.
Crit. Care. Med.
24:
1824-1828,
1996[Medline].
3.
Schloerb, P. R.
Extracellular water measured by bioimpedance.
Crit. Care Med.
25:
894-895,
1997[Medline].
4.
Schloerb, P. R.,
J. Forster,
R. Delcore,
and
J. D. Kindscher.
Bioimpedance in the clinical evaluation of liver disease.
Am. J. Clin. Nutr.
64:
510S-514S,
1996
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Paul R. Schloerb, Department of Surgery University of Kansas Medical Center Kansas City, Kansas 66160 |
To the Editor: The points raised by Schloerb in his letter are
addressed in the order they were introduced. That previously reported
data had been reanalyzed was fully disclosed and extensively discussed
in our paper (6). That there is variation in the dilution method is an
important information to disseminate, and these data provided the
opportunity to do so. A new method cannot be validated if the reference
method it is being compared against changes dramatically. In addition,
we reported entirely new statistics.
Indeed, the mean age of the patients was 68.13 not 68.77 yr. Evidently,
the two decimal places for SD, which was 6.77, were typed twice when
Table 1 containing descriptive information was created (6). As their
patients' descriptive information, Patel et al. (7) used the prestudy
weight rounded up, in this case, to the nearest whole number, rather
than weights postsurgery after 4 h of equilibration of deuterium and bromide.
Schloerb suggests that there is no need to measure ECW with impedance
because it cannot detect fluid overload and, for healthy subjects, ECW
does not vary; thus it can be determined by assuming it to be a fixed
percentage of TBW. We believe that it is important to measure both ECW
and intracellular water (ICW) because the ECW/ICW ratio is health, age,
gender, and activity dependent. The argument by Schloerb et al. (8) was
that a wrist to ankle measurement is not sensitive to ascites or fluid
accumulation in the trunk. This cannot be disputed (5, 11), but
Schloerb et al. (8) reported near-exact predictions of fluid overload in the trunk by using segmental impedance measurements. Segmental measurements of ECW have recently been used to successfully determine the net fluid balance in 30 surgery patients (9). As Zarowitz and
Matthie discussed (11), the impedance method is not ready to be used
routinely in surgery or intensive care, but an outright dismissal of
such a promising and needed technology appears uninformed. Albeit
impedance spectroscopy (that is, fitting impedance spectral data to a
physical model) is an engineering- and physics-based method, it is a
powerful assessment technique used in many fields of science. De
Lorenzo has recently published a review for the field of human body
composition (1).
Impedance spectroscopy has yielded numerous promising results for
characterization of ECW. Most subjects do not have ascites, and body
water tends to be consistently distributed (1, 5, 11).
Therefore, strong relationships between impedance and
dilution-determined water volumes have emerged in populations
including, but not limited to, cardiac surgery patients (6). Ho et al.
(3) used impedance spectroscopy to accurately predict a deuterium TBW
before and after hemodialysis. Because TBW was predicted as ECW + ICW
(1), and dialysis patients tend to have an expanded ECW, this study serves as a validation for ECW and ICW. Van Marken Litchtenbelt (10)
discovered that growth hormone-deficient patients have an enlarged ECW
compared with ICW compartment. For impedance spectroscopy to accurately
predict ICW, which is technically far more difficult to predict than
ECW, it must be predicting ECW accurately. Katzarski et al. (4)
discovered that hypertensive hemodialysis patients had significantly
larger ECW volumes than did controls and normotensive patients. It is
well known that much of the hypertension in dialysis patients is caused
by fluid overload (that is, ECW). For seriously ill intensive care
patients with severe wasting, Finn et al. (2) reported an excellent
relationship between the impedance and bromide dilution-determined ECW
and its change at four time points over 21 days. Normally, if a
parameter is not being measured physically, it will not accurately
reflect differences between subjects or accurately predict change.
To summarize, the error caused by an inappropriate electrode placement
is different than that caused by not properly interpreting the
measurement. Our investigation was designed to evaluate the latter (6).
The most widely used physical model of biological tissue consists of
four variables (1), and this model cannot be computed with impedance
measured at one frequency (6). On the other hand, through mathematical
modeling, the different parameters of the tissue (e.g., ECW and ICW)
can be independently predicted. Impedance spectroscopy has profound
implications for the medical field.
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FOOTNOTES |
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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. §1734 solely to indicate this fact.
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REFERENCES |
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1.
De Lorenzo, A.,
A. Andreoli,
J. Matthie,
and
P. Withers.
Predicting body cell mass with bioimpedance by using theoretical methods: a technological review.
J. Appl. Physiol.
82:
1542-1558,
1997
2.
Finn, P. J.,
L. D. Plank,
M. A. Clark,
A. B. Connolly,
and
G. Hill.
Progressive dehydration and proteolysis in critically ill patients.
Lancet
347:
654-656,
1996[Medline].
3.
Ho, L. T.,
R. Kushner,
D. A. Schoeller,
R. Gudivaka,
and
D. M. Spiegel.
Bioimpedance analysis of total body water in hemodialysis patients.
Kidney Int.
46:
1438-1442,
1994[Medline].
4.
Katzarski, K., B. Charra, G. Laurent, F. Lopot, J. C. Filho, J. Nisell,
and J. Bergstrom. Multifrequency bioimpedance in assessment of dry
weight in haemodialysis. Nephrol. Dial. Transplant 11, Suppl. 2: 20-23, 1996.
5.
Matthie, J. R.,
and
P. O. Withers.
Segmental vs. whole body multifrequency impedance measurements (Letter).
J. Appl. Physiol.
79:
2177-2179,
1995
6.
Matthie, J.,
B. Zarowitz,
A. De Lorenzo,
A. Andreoli,
K. Katzarski,
G. Pan,
and
P. Withers.
Analytic assessment of the various bioimpedance methods used to estimate body water.
J. Appl. Physiol.
84:
1801-1816,
1998.
7.
Patel, R. V.,
E. L. Peterson,
N. Silverman,
and
B. J. Zarowitz.
Estimation of total body and extracellular water in post-coronary artery bypass graft surgical patients using single and multiple frequency bioimpedance.
Crit. Care Med.
24:
1824-1828,
1996.
8.
Schloerb, P. R.,
J. Forster,
R. Delcore,
and
J. D. Kindsches.
Bioimpedance in the clinical evaluation of liver disease.
Am. J. Clin. Nutr.
64:
5105-5145,
1996.
9.
Tatara, T.,
and
K. S. Tsukaki.
Segmental bioelectrical impedance analysis improves the prediction for extracellular water volume changes during abdominal surgery.
Crit. Care Med.
26:
470-476,
1998[Medline].
10.
Van Marken Lichtenbelt, W. D.,
Y. E. M. Snel,
R.-J. M. Brummer,
and
H. P. F. Koppeschar.
Deuterium and bromide dilution, and bioimpedance spectrometry independently show that growth hormone-deficient adults have an enlarged extracellular water compartment related to intracellular water.
J. Clin. Endocrinol. Metab.
82:
907-911,
1997
11.
Zarowitz, B., and J. Matthie. Bioimpedance and the estimation of
net fluid balance in critical care patients: problems and possibilities
(Editorial). Crit. Care Med. In press.
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Jim Matthie, George Pan, Paul Withers, Xitron Technologies, Inc. San Diego, California 92121 | |||||
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Barbara Zarowitz, Ambulatory Pharmacy Administration Henry Ford Health System Bingham Farms, Michigan 48025 | |||||
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Antonio de Lorenzo, Angela Andreoli, Department of Physiology University of Rome "Tor Vergata" 1-00173 Rome, Italy | |||||
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Krassimir Katzarski, Division of Renal Medicine Karolinska Institute, Huddinge University Hospital S-14186 Huddinge, Sweden |
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