Lp. Malmberg et al., Intraindividual variability of infant whole-body plethysmographic measurements: Effects of age and disease, PEDIAT PULM, 28(5), 1999, pp. 356-362
The intraindividual variability of whole-body plethysmographic measurements
was studied in a large series of consecutive infants (N = 144), divided in
to two groups: a group of infants born very prematurely (PM, N = 63), with
(N = 28) or without (N = 35) a history of bronchopulmonary dysplasia (BPD),
and a group of infants with persistent respiratory symptoms (PRS, N = 81),
i.e., wheezing (N = 53) or cough (N = 28). The intraindividual variability
was determined within each test and between tests, separated by a 10-min i
nterval.
In both study groups, the between-test variability was significantly larger
than that within tests. Expressed as the median coefficient of variation (
CV), the between-test repeatabilities in the PRS group were 8.0% for thorac
ic gas volume (TGV), 17.5% for airway resistance (Raw), and 18.4% for speci
fic airway conductance (sGaw), and in the PM group, 8.9% for TGV, 20.4% for
Raw, and 20.7% for sGaw. However, the individual range of CVs was large, r
anging from 3 to 19% for TGV and from 5 to 55% for sGaw. With respect to TG
V, the difference between the groups was statistically significant (P = 0.0
3). In infants with a history of BPD, there was also a significant negative
age dependency in CVs of sGaw (r = -0.50, P = 0.009), showing larger varia
tion among younger individuals. The presenting symptom (wheezing or cough)
in the PRS group did not influence the measurement variability significantl
y, and neither did the degree of bronchial obstruction.
We conclude that on a group basis, the repeatability of infant body plethys
mographic measurements may be satisfactory for scientific studies demonstra
ting pharmacodynamic effects; however, the intraindividual measurement vari
ability should be reported for each test conditions and for infant groups i
n each study. Due to the large range in individual variation and the influe
nce of age and disease processes on the variation, for an individual child
there is only questionable benefit from a given measurement, unless the int
rasubject, between-test variability is assessed individually before interve
ntions, such as a bronchodilation test. Pediatr Pulmonol. 1999; 28:356-362.
(C) 1999 Wiley-Liss, Inc.