Assessment of variable obstruction by forced expiratory volume in 1 second, forced oscillometry, and interrupter technique
Alfredo Boccaccino, M.D.,* Diego G. Peroni, M.D.,# Angelo Pietrobelli, M.D.,#Giorgio Piacentini, M.D.,# Alessandro Bodini, M.D.,# Atanasio Chatzimichail, M.D.,§Enrico Spinosa, M.D.,* and Attilio L. Boner, M.D.# (Italy and Greece)
ABSTRACT The aim of this study was to evaluate the presence and the degree of reversible airflow obstruction as detected by forcedexpiratory volume in 1 second (FEV1), forced oscillometry (FOT), and interrupter technique (resistance measured by theinterrupter technique [Rint]) in mild asthmatic children compared with controls. FOT, Rint, and FEV1 were evaluated beforeand after albuterol (200 g) administered by metered-dose inhaler and spacer in 28 asthmatic children (mean age Ϯ SD, 9.1 Ϯ1.9 years) and in 20 healthy children (mean age Ϯ SD, 8.5 Ϯ 2.1 years). No correlation was found between FEV1, FOT, andRint values either before or after albuterol. FOT and Rint values were highly correlated pre- and postbronchodilatation. Animprovement in FEV Ն
12% after albuterol was observed in 11 (39%) asthmatic subjects. As suggested using the cutoff valueat R Ն 29%, significant bronchodilatation wasobserved in 20 (71%) children with FOT and using a reduction Ն0.20 kPaor 2 cm of H2O, 22 (78%) subjects showed significant bronchodilatation with Rint. No significant changes were observed afteralbuterol in controls. FOT and Rint techniques showed a greater sensitivity in detecting reversibility of bronchoconstriction inmild asthmatic patients. Prospective studies are needed to clarify the possible advantages of these findings in mild–moderateasthmatic children.
(Allergy Asthma Proc 28:331–335, 2007; doi: 10.2500/aap.2007.28.2963)
Key words: Asthma, children, FEV1, forced expiratory volume, forced oscillometry, interrupter technique, pulmo- nary function test, spirometry The detection of reversible airflow limitation is a and interrupter technique (resistance measured by the
major criteria for asthma diagnosis in children.1
interrupter technique [Rint]), may be used to measure
In the evaluation of asthmatic children it is inappro-
respiratory resistance (Rrs) even in younger and not
priate to relate only to clinical perception of airway
collaborative children.7,8 Few studies evaluated FOT
obstruction because it may persist despite therapy in
and Rint as tools in the detection of bronchial obstruc-
apparently asymptomatic patients.2,3 Therefore, air-
tion and its reversibility in asthmatic children.9–11 Re-
way obstruction frequently might go undetected in
cently, cutoff values of postbronchodilator changes in
apparently healthy children who have a history of
rs were defined to discriminate children with a neg-
persistent wheezing or asthma if lung function test are
ative or positive response to albuterol.9 However, the
not performed.4,5 Measurement of forced expiratory
concordance in FEV1 and Rrs in establishing reversibil-
volume in 1 second (FEV1) and its improvement after
ity of airway obstruction is not always present.10 In this
2-agonist is considered the “gold standard” for the
study we performed lung function tests (FEV1, FOT,
assessment of airway obstruction and its reversibili-
and Rint) in children with mild asthma and in normal
ty.1,6 Other techniques that use the “respiratory tidal
children, as controls, to evaluate the presence and the
volume” and demand only passive cooperation and no
degree of reversible airflow obstruction as detected by
forced maneuvers, such as forced oscillometry (FOT)
From the Department of Pediatrics, Ospedale “G. Rummo,” Benevento, Italy, #De-partment of Pediatrics, University of Verona, Verona, Italy, and §Clinic of Pediatrics,Subjects Democrition University, Alexandropolis, GreeceAddress correspondence to Diego Peroni, M.D., Department of Pediatrics, Verona
Twenty-eight asthmatic children (13 boys and 15
University, Policlinic GB. Rossi, P.le Scuro 10, 37134 Verona, Italy,
girls), 5–13 years old (mean age Ϯ SD, 9.1 Ϯ 1.9 years)
E-mail address: [email protected] reprint requests to Attilio Boner, M.D., Department of Pediatrics, Verona
were studied. They were all well-known asthmatic
University, Policlinico GB. Rossi, P.le Scuro 10, 37134 Verona, Italy
children according to the American Thoracic Society
E-mail address: [email protected]
(ATS) definition.12 Only children complaining of mild
Copyright 2007, OceanSide Publications, Inc., U.S.A.
wheeze and/or cough without any other symptoms at
the physician’s evaluation were consecutively enrolled
available with Pulmowin software. These measure-
into the study. Twenty normal subjects (12 boys and 8
ments were recorded and coefficients of variation were
girls) 5–14 years old (mean age Ϯ SD, 8.5 Ϯ 2.1) were
enrolled as controls. Parents and guardians gave writ-ten inform consent to the study protocol, which was
approved by the local Hospital Ethical Committee.
Rint was measured as previously described.7,23
Briefly, children were instructed to sit upright, while
Study Design
breathing quietly, and a minimum number of 6 correct
Baseline measurements were obtained in all children.
tracings (maximum number 10) were obtained in all
FOT (Oscilink V; SensorMedics, Yorba Linda, CA) and
children by the same operator. Shutter closure was
Rint (MicroRint; Micromedical, Rochester, U.K.) mea-
programmed at maximal inspiration of tidal flow to
surements were performed before flow volume curves
avoid problems related with airway collapse during
to avoid the influence of deep inspiration.13 Albuterol
expiration.24 Thus, Rint values were obtained at or
(200 g) was administrated via metered-dose inhaler
close to midinspiration, minimizing the breath-to-
and spacer 20 minutes before all postbronchodilator
breath variation in inflation level and, hence, on Raw.
Timing of the shutter closure was shown on the dis-
were withheld for at least 8 and 24 hours, respectively,
play. The mean value of six consecutive, technically
before the reversibility tests were performed.
satisfactory measurements (identical pressure and flowcurves) was saved as the results. Tracings were in-
Spirometry
spected immediately after the measurement and ac-
Forced expiratory flow–volume curves were re-
cepted or rejected according to Bridge et al.7
corded using Oscilink and Pulmowin software (Sen-sorMedics). Spirometric tests were done according to
Statistical Analyses
ATS criteria: at least three acceptable forced expiratory
All analyses were performed using the statistical
curves were recorded and the curve with the highest
program SAS release 6.10 (SAS Institute, Inc., Cary,
NC). Descriptive analyses are presented as mean Ϯ SD.
1 and forced vital capacity was selected.14
Reference values were used according to Quanjer.15
Pre- and postbronchodilator administration values andasthmatic versus control data were analyzed using Stu-
dent’s t-test. Pearson’s coefficients of correlation wereused to compare parametric variables. To test the
FOT impedance measurements (Zrs) were performed
agreement between methods of clinical measurements,
by Oscilink spirometer impedancemeter using Pul-
a Bland and Altman analysis was performed.25 Signif-
mowin software as previously described.16,17 Pressure
icance levels were based on two-tail tests and ␣ was set
and flow calibrations were done before each new pa-
tient. Children’s positions were monitored carefully. Briefly, the FOT method used in our study used the
frequency range of 4 –32. The signals were filtered for
low- (Ͻ3 Hz) and high-frequency components to elim-
Pulmonary function tests at baseline and postbron-
inate errors caused by the presence of breathing noise18
chodilator for asthmatic children and controls are re-
and processed by computer using Fourier analysis.
Low frequencies are suited most for studying vis-coelastic respiratory properties after bronchoconstric-
Asthmatic Children
tion/bronchodilatation.19 We selected the low frequen-
Evaluation of baseline lung function showed high
cies (R6 and R12) according to previous studies, which
significant differences between asthmatic subjects and
indicated high sensitivity in distinguishing normal ver-
controls in FEV1 (p Ͻ 0.0001), in FOT values (R6 and
sus asthmatic children.20 Furthermore, Rrs use at low
R12, all p Ͻ 0.0001; R16, p ϭ 0.001; and R24, p ϭ 0.02,
frequencies (i.e., 6 –10) rather than high frequencies
respectively), and in Rint values (p Ͻ 0.0001).
(i.e., 24 –32) is accepted widely in the evaluation of the
FEV1 significantly increased, whereas Rrs (R6, R12,
effect of bronchoconstricting agents.18,21 Particular at-
R16, and R24) and Rint showed a highly significant
tention was given to monitor resting ventilation, ex-
reduction postbronchodilator in asthmatic children
cluding data with coughing, hyperventilation, irregu-
(for all, p Ͻ 0.0001). At baseline Pearson’s correlation
lar breathing, apnea, or leaks through mouthpiece.
test showed no correlation between FEV1 and Rrs at R6,
Measurements were repeated on an average of three to
R12, R16, and R24 as expected by the slope of the FOT
five times until three consecutive tests gave adequate
curve. Furthermore, no correlation was found between
reproducibility.22 This was done based on the two
FEV1 and Rint. Prebronchodilatator Rint and Rrs at low
graphs (Rrs versus frequency and Xrs versus frequency)
frequencies were highly correlated (R6, r ϭ 0.67, p Ͻ
Table 1 Pulmonary function test results Asthmatic Subjects Normal Subjects Prebroncho- Postbroncho- p* Prebroncho- Postbroncho- p* Data are shown as mean Ϯ SD. *p for student’s unpaired t-test prebronchodilator versus postbronchodilator administration.
0.0001; R12 r ϭ 0.53, p ϭ 0.004, respectively), while at
given frequencies (R6, r ϭ 0.62 and p ϭ 0.005; R12, r ϭ
high frequencies (R16 and R24) we did not find any
0.56 and p ϭ 0.01; R16, r ϭ 0.61 and p ϭ 0.006; and R24,
r ϭ 0.64 and p ϭ 0.003).
cutoff value suggested by ATS for a significant bron-
DISCUSSION
chodilatation,14 was observed in only 11 (39%) asth-
The gold standard for the diagnosis of airway ob-
matic subjects. Using the cutoff of Ն29% at R6,26 sig-
struction is represented by evaluation of lung function
nificant bronchodilatation was observed in 20 (71%)
with forced expiratory maneuvers performed before
children. Twenty-two (78%) subjects showed signifi-
and after bronchodilator administration.1,6,14 No single
cant bronchodilatation with Rint, using the cutoff re-
test by itself can be considered completely adequate for
duction of Ն0.20 kPa or 2 cm of H2O.27 Postbronchodi-
assessing variable obstruction associated with persis-
latator data showed no correlation between FEV1and
tent asthma.4 Furthermore, previous studies have
Rrs at any given frequencies (R6, R12, R16, and R24). The
shown a difficult relationship between asthma symp-
correlations between Rint and Rrs were instead highly
toms and objective measures of airway obstruction
significant (R6, r ϭ 0.76, p Ͻ 0.0001; R12, r ϭ 0.65, p Ͻ
0.0001; R16, r ϭ 0.45; p ϭ 0.01; and R24, r ϭ 0.69, p Ͻ
In this study, the patients, despite complaining of
only minimal symptoms (cough and/or mild wheeze),
The Delta (⌬), i.e., the difference between post- and
presented with reduced FEV1 and significantly in-
prebroncodilator values, was also evaluated. The
creased FOT and Rint values. This is in agreement with
⌬FEV1 and ⌬Rrs at any given frequency (R6, R12, R16,
previous findings suggesting that asthma disease ac-
and R24) were not correlated. We found a significant
tivity can not always be completely revealed by history
⌬Rint and ⌬Rrs at R6 (r ϭ 0.56
and clinical examination alone both in populations and
and p ϭ 0.002) and R12, (r ϭ 0.42 and p ϭ 0.02), but
in clinical studies.29,30 Failure to perform lung function
not at R16 and R24. The Bland-Altman analysis
tests in asthmatic children, even when they are asymp-
showed no significant correlation between the ana-
tomatic, may result in underdiagnosis of airflow ob-
struction5 with consequent loss of elastic recoil andchronic hyperinflation if obstruction is prolonged.31 In
Controls
our study FOT and Rint evaluation detected reversibil-
Prebronchodilator data showed no correlation be-
ity of airflow limitations in a greater number of mild
tween FEV1, Rint, and Rrs at any given frequency.
asthmatic children than that depicted by FEV1. Using
Instead, Rint was highly correlated with R6 (r ϭ 0.85
established cutoff values,14,23,24 a significant bron-
and p Ͻ 0.0001), R12 (r ϭ 0.80 and p Ͻ 0.0001), R16 (r ϭ
chodilatation was documented only in 39% of our sub-
0.79 and p Ͻ 0.0001), and R24 (r ϭ 0.77 and p Ͻ 0.0001).
jects with FEV1 but in 71% using FOT and in 78% with
Postbronchodilator analysis showed no correlation be-
tween FEV1 and Rint. FEV1 presented a negative cor-
Discrepancies between FEV1 and FOT results were
relation with Rrs at low frequencies R6 (r ϭ Ϫ0.54 and
found in other studies,10,32 showing that FOT and Rint
p ϭ 0.01) and R12 (r ϭ Ϫ0.48 and p ϭ 0.03), whereas no
were not significantly correlated to FEV1 in detecting
correlation was found at high frequencies (R16 and
bronchodilatation after albuterol use in children. Our
R24). Rint was significantly correlated with Rrs at any
results are according to previous studies in adults
showing that Rint and FOT have higher capacity than
5. Bye MR, Kerstein D, and Barsh E. The importance of spirometry
spirometry in detecting reversible bronchial obstruc-
in the assessment of childhood asthma. Am J Dis Child 146:977–
tion.33,34 The reduced sensitivity of FEV
6. Dickman ML, Schmidt CD, and Gardner RM. Spirometric stan-
plained by the fact that forced expiratory maneuvers
dards for normal children and adolescents (ages 5 years
are effort dependent and require a deep inhalation that
through 18 years). Am Rev Respir Dis 104:680 – 687, 1971.
in asthmatic patients may be associated with broncho-
7. Bridge PD, Rangantathan S, and McKenzie SA. Measurement of
constriction.13,35 This could limit the effect of broncho-
airway resistance using the interrupter technique in preschool
dilator, and, on the other hand, FOT and Rint are
children in the ambulatory setting. Eur Respir J 13:792–796,1999.
performed during tidal volume breathing and are ef-
8. Nielsen KG, and Bisgaard H. Lung function response to cold air
fort independent. These techniques at low frequencies
challenge in asthmatic and healthy children of 2–5 years of age.
measure resistance mainly determined by the patency
Am J Respir Crit Care Med 161:1805–1809, 2000.
of the peripheral airways,11,36 where obstruction could
9. Delacourt C, Lorino H, Herve-Guillot M, et al. Use of forced
oscillation technique to assess airway obstruction and revers-
be even less related to symptoms’ perception.37
ibility in children. Am J Respir Crit Care Med 161:730 –736,
Therefore, FOT and Rint seem to be particularly
promising in clinical pediatric practice.7–11 They
10. Lebecque P, and Stanescu D. Respiratory resistance by the
present the advantages of being rapid to perform and
forced oscillation technique in asthmatic children and cystic
require minimal cooperation. For these reasons they
fibrosis patients. Eur Respir J 10:891– 895, 1997.
11. Delacourt C, Lorino H, Fuhrman C, et al. Comparison of the
can be performed in preschool children7,38,39 and in
forced oscillation technique and the interrupter technique for
infants,40 in whom detection of airflow limitation may
assessing airway obstruction and its reversibility in children.
be more difficult. Obviously, evaluation of
Am J Respir Crit Care Med 164:965–972, 2001.
struction and its reversibility are central keys for early
12. American Thoracic Society Committee on Diagnostic Standards
diagnosis and early treatment of children with asth-
for Non-tuberculosis Respiratory Diseases. Definition and clas-sifications of chronic bronchitis, asthma, and pulmonary em-
ma.41 Moreover, Rint has been found useful in detect-
physema. Am Rev Respir Dis 85:762–768, 1962.
ing airways responsiveness to methacholine42 and cold
13. Pellegrino R, Sterk PJ, Sont JK, and Brusasco V. Assessing the
air43 in young children, further increasing the applica-
effect of deep inhalation on airway caliber: A novel approach to
tion of the method in the evaluation of young asth-
lung function in bronchial asthma and COPD. Eur Respir J
14. American Thoracic Society. Standardization of spirometry—
In conclusion, our results confirm and further expand
1994 update. Am J Respir Crit Care Med 152:1107–1136, 1995.
the concept that FOT and Rint, particularly with the
15. Quanjer P, Borsboom GJ, Brunekreef B, et al. Spirometric refer-
evaluation of the bronchodilator response, should be en-
ence values for withe European children and adolescents: Pol-
couraged in asthmatic patiens. FOT and Rint should be
gar revisited. Pediatr Pulmonol 19:135–142, 1995.
used to add sensitivity to classic lung function measure-
16. Van de Woestijne KP, Desager KN, Duiverman EJ, and Marchal
F. Recommendations for measurement of respiratory input im-
ments particularly in asthmatic children with normal or
pedance by means of the forced oscillation method. Eur Respir
near normal FEV1. The good correlation between FOT
and Rint suggests that both techniques offer useful infor-
17. Lorino A, Atlan G, Lorino H, et al. Influence of posture on
mechanical parameters derived from respiratory impedance.
asthmatic children. The clinical meaning of changes in
18. Duiverman EJ, Neijens HJ, Van der Snee-van Smaalen M, and
Kerrebijn KF. Comparison of forced oscillometry and forced
spective studies performed in patients with low correla-
expirations for measuring dose-related responses to inhaled
tion between symptoms severity and traditional lung
histamine in asthmatic children. Bull Eur Physiopathol Respir
19. Klug B, and Bisgaard H. Specific airway resistance, interrupter
resistance, and respiratory impedance in healthy children aged2–7 years. Pediatr Pulmonol 25:322–331, 1998. REFERENCES
20. Van Noord JA, Clement J, Van de Woestijne KP, and Demedts
1. Warner JO, and Naspitz CK. Third international pediatric con-
M. Total respiratory resistance and reactance as a measurement
sensus statement on the management of childhood asthma:
of response to bronchial challenge with histamine. Am Rev
International pediatric asthma consensus group. Pediatr Pulmo-
21. Bohadana AB, Peslin R, Megherbi SE, et al. Dose-response slope
2. Weng TR, and Levison H. Pulmonary function in children with
of forced oscillation and forced expiratory parameters in bron-
asthma at acute attack and symptom free status. Am Rev Respir
chial challenge testing. Eur Respir J 13:295–300, 1999.
22. Van de Woestijne KP, Desager KN, Duiverman EJ, and Marchal
3. Cooper DM, Cutz E, and Levison H. Occult pulmonary abnor-
F. Recommendations for measurement of respiratory input im-
malities in asymptomatic asthmatic children. Chest 71:361,
pedance by means of the forced oscillation method. Eur Respir
4. Ferguson AC. Persisting airway obstruction in asymptomatic
23. Lombardi E, Sly P, Concutelli G, et al. Reference values of
children with asthma with normal peak expiratory flow rates. J
interrupter respiratory resistance in healthy preschool white
Allergy Clin Immunol 82:19 –22, 1988.
children. Thorax 56:691– 695, 2001.
24. Chowienczyk PJ, Lawson CP, Lane S, et al. A flow interruption
asthma by isocapnic hyperpnoea of cold air. Eur Respir J 10:
device for measurement of airway resistance. Eur Respir J
35. Milanese M, Mondino C, Tosca M, et al. Modulation of airway
25. Bland JM, and Altman DG. Statistical methods for assessing
caliber by deep inhalation in children. J Appl Physiol 88:1259 –
agreement between two methods of clinical measurements.
36. Lebecque P, Desmond K, Swartebroeckx Y, et al. Measurement
26. Nielsen KJ, and Bisgaard H. Discriminative capacity of bron-
of respiratory system resistance by forced oscillation in normal
chodilator response measured with three different lung func-
children: A comparison with spirometric values. Pediatr Pul-
tion techniques in asthmatic and healthy children aged 2 to 5
years. Am J Respir Crit Care Med 164:554 –559, 2001.
37. Kraft M. The distal airways: Are they important in asthma? Eur
27. McKenzie SA, Bridge PD, and Healy MJ. Airway resistance and
atopy in preschool children with wheeze and cough. Eur Respir
38. Hellinckx J, Cauberghs M, De Boeck K, and Demedts M. Eval-
uation of impulse oscillation system: Comparison with forced
28. Teeter JG, and Bleecker ER. Relationship between airway ob-
oscillation technique and body plethysmography. Eur Respir J
struction and respiratory symptoms in adult asthmatics. Chest
39. Pao CS, and McKenzie SA. Randomized controlled trial of
29. Siersted HC, Boldsen J, Hansen HS, et al. Population based
fluticasone in preschool children with intermittent wheeze.
study of risk factors for underdiagnosis of asthma in adoles-
Am J Respir Crit Care Med 166:945–949, 2002.
cence: Odense schoolchild study. BMJ 316:651– 657, 1998.
40. Malmberg LP, Mieskonen S, Pelkonen A, et al. Lung function
30. Shingo S, Zhang J, and Reiss TF. Correlation of airways obstruc-
tion and patient-reported endpoints in clinical studies. Eur Re-
measured by the oscillometric method in prematurely born
children with chronic lung disease. Eur Respir J 16:598 – 603,
31. Kraemer R, Meister B, Schaad UB, Rossi E. Reversibility of lung
function abnormalities in children with perennial asthma. J Pe-
41. Martinati LC, and Boner AL. Clinical diagnosis of wheezing in
early childhood. Allergy 50:701–710, 1995.
32. Mazurek H, Marchal F, Derelle J, et al. Specificity and sensitiv-
42. Beydon N, Trang-Pham H, Bernard A, and Gaultier C. Mea-
ity of respiratory impedance in assessing reversibility of airway
surements of resistance by the interrupter technique and of
obstruction in children. Chest 107:1996 –1002, 1995.
transcutaneous partial pressure of oxygen in young children
33. Snashall PD, Parker S, Phil M, et al. Use of an impedance meter
during methacholine challenge. Pediatr Pulmonol 31:238 –246,
for measuring airway responsiveness to histamine. Chest 99:
43. Nielsen KS, and Bisgaard H. Lung function response to cold air
34. Schmekel B, and Smith H-J. The diagnostic capacity of forced
challenge in asthmatic and healthy children of 2–5 years of age.
oscillations and forced expiration techniques in identifying
Am J Respir Crit Care Med 161:1805–1809, 2000.
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