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Abstract
Correspondence The objective of the present study was to evaluate incentive spirom- Key words
V.F. Parreira eters using volume- (Coach and Voldyne) and flow-oriented (Triflo II • Incentive spirometry
Dona Cecília, 500, Apto. 1504 and Respirex) devices. Sixteen healthy subjects, 24 ± 4 years, 62 ± 12 • Respiratory inductive
30220-070 Belo Horizonte, MG
kg, were studied. Respiratory variables were obtained by respiratory plethysmography
Brasil • Physiotherapy
Fax: +55-31-3499-4790
inductive plethysmography, with subjects in a semi-reclined position
• Volume-oriented spirometer
E-mail: parreira@ufmg.br (45º). Tidal volume, respiratory frequency, minute ventilation, in-
• Flow-oriented spirometer
spiratory duty cycle, mean inspiratory flow, and thoracoabdominal
Research partially supported by motion were measured. Statistical analysis was performed with Kol-
CNPq. mogorov-Smirnov test, t-test and ANOVA. Comparison between the
Coach and Voldyne devices showed that larger values of tidal volume
(1035 ± 268 vs 947 ± 268 ml, P = 0.02) and minute ventilation (9.07
± 3.61 vs 7.49 ± 2.58 l/min, P = 0.01) were reached with Voldyne,
Received March 16, 2004
Accepted February 10, 2005
whereas no significant differences in respiratory frequency were
observed (7.85 ± 1.24 vs 8.57 ± 1.89 bpm). Comparison between flow-
oriented devices showed larger values of inspiratory duty cycle and
lower mean inspiratory flow with Triflo II (0.35 ± 0.05 vs 0.32 ± 0.05
ml/s, P = 0.00, and 531 ± 137 vs 606 ± 167 ml/s, P = 0.00, respective-
ly). Abdominal motion was larger (P < 0.05) during the use of volume-
oriented devices compared to flow-oriented devices (52 ± 11% for
Coach and 50 ± 9% for Voldyne; 43 ± 13% for Triflo II and 44 ± 14%
for Respirex). We observed that significantly higher tidal volume
associated with low respiratory frequency was reached with Voldyne,
and that there was a larger abdominal displacement with volume-
oriented devices.
respiratory disease were studied: 9 women the nose clipped, for 30 to 60 s, and the
and 7 men aged 24 ± 4 years (mean ± SD), electrical spirometer output was recorded
age range: 21-38 years, weight 62 ± 12 kg, with a computer and used to calibrate the
height 1.68 ± 0.10 m, body mass index: respiratory inductive plethysmographic sum
21.96 ± 2.41 kg/m2. A pulmonary function signal for absolute volume in ml (24). The
test was performed with a hand-held spirom- spirometer was calibrated with a 3-liter sy-
eter (Vitalograph 2120, Vitalograph Ltd., ringe (Hans Rudolph Inc., Kansas City, MO,
Buckingham, England). The mean values of USA) using computer software (RespiPanel
the spirometric variables, reported as per- 4.0, Nims) and signals were recorded with a
cent of predicted according to Knudson val- digital acquisition system (RespiEvents 5.2,
ues (22) were: FVC = 98.8 ± 8.6%, FEV1 = Nims). Transcutaneous oxygen saturation
100.1 ± 7.4%, FEV1/FVC = 101.6 ± 6.8%, (SpO2) and pulse rate were recorded by pulse
PEF = 104 ± 15.6%, FEF 25-75% = 94.5 ± oximetry (Datex-Ohmeda Inc., Louisville,
20.8%. Subjects had never seen or used IS CO, USA) using a finger probe.
before and received instructions about the
procedure and how to use the devices just Procedure
before the measurements. All subjects re-
ceived the same instructions as follows: in- Subjects lay comfortably in bed in a semi-
spire deeply and slowly through the mouth- reclined position (45º), avoiding any shift of
piece of the spirometer, trying to displace the the body during recording. Respitrace® and
abdomen beyond the rib cage, and expire. the finger sensor of the pulse oximeter were
Subjects gave written informed consent to then applied. Four incentive spirometers were
participate in the study, which was approved used: two of them volume-oriented devices
by the University Ethics Research Commit- (Coach, DHD Medical Products, Canasota,
tee. NY, USA, and Voldyne, Hudson RCI,
Temecula, CA, USA), with a predetermined
Signals and recording equipment volume of 1500 ml, and two flow-oriented
devices (Triflo II, Hudson RCI, and Respirex,
Respiratory variables were obtained by DHD Medical Products), set at a flow rate of
respiratory inductive plethysmography (Res- 900 ml/s. The choice of these devices was
pitrace®, Nims, Miami, FL, USA). Teflon- based on the fact that these incentive spirom-
coated inductance coils of appropriate size eters are commonly used in our clinical set-
were placed around the rib cage and abdo- tings. The target of volume-oriented IS was
men; the upper edge of the rib cage band was chosen as a function of the tidal volume of
placed at the level of the axilla and the approximately 400 ml described in the lit-
abdominal band at the level of umbilicus. erature for young adults (25). According to
Signals were calibrated using qualitative di- Bendixen et al. (26), sigh volume corre-
agnostic calibration (23) during natural sponds to 2 or 3 times the tidal volume. Our
breathing; this is a two-step procedure choice was based on this consideration (3 x
whereby the rib cage and abdominal electri- 400 ml = 1200 ml). However, for the Coach
cal gains of the respiratory inductive plethys- and Voldyne devices it is easier to visualize
mography amplifiers are correctly partitioned 1500 ml. For flow-oriented IS, the literature
during tidal breathing and subsequently com- recommends to raise the first two balls of the
pared to the output of a spirometer to attain Triflo II device corresponding to 900 ml/s
equivalence. The subject then breathed into (14,27). To have equivalence between flow-
a spirometer via a mouthpiece (Vitatrace, oriented devices we chose the same flow
Pro Médico, Rio de Janeiro, RJ, Brazil) with level for the Respirex device.
After calibration, 5-min baseline periods pared by one-sample t-test. Data regarding
were recorded and then the test with the first transcutaneous oxygen saturation (SpO2) and
incentive spirometer was performed. The pulse rate before and after IS were compared
following sequence was used: 1st baseline by the Student t-test for paired samples. The
period, 1st device, 2nd baseline, 2nd device, level of significance (α) was set at 0.05 for
3rd baseline, 3rd device, 4th baseline, 4th all tests.
device, and the 5th and last baseline period.
At least 5 min of recording was allowed for Results
each baseline period. For each IS period 1
min or at least 8 breaths were recorded. A Data were obtained during the five base-
custom-made random number generator pro- line and four IS periods for all 16 subjects.
gram was used to assign the order in which Four of them repeated one of the IS periods
the incentive spirometers would be used for (two subjects with Triflo II, one with Respirex
each subject. Just before and after each IS and one with Coach). A total of 689 respira-
trial SpO2 and pulse rate were recorded. tory cycles of IS periods were analyzed, with
a mean (± SD) of 43 ± 5 cycles per subject.
Measurements With respect to the five baseline periods, a
total of 1224 respiratory cycles were ana-
For the baseline periods, only tidal vol- lyzed, with a mean of 76 ± 13 cycles per
ume was analyzed. For each IS period, all subject. For baseline data the mean was cal-
individual values for tidal volume (Vt), res- culated from 1-min measurements corre-
piratory frequency (f), minute ventilation, sponding to the last minute of each baseline
inspiratory duty cycle (Ti/Ttot), mean in- period (approximately 15 breaths).
spiratory flow (Vt/Ti), and rib cage motion
contribution to Vt (%RC/Vt) were obtained Baseline tidal volume
directly via the digital acquisition system, on
a breath by breath basis. The abdominal The following Vt values (mean ± SD)
motion contribution to Vt was calculated were obtained during the five baseline peri-
breath by breath (%AB/Vt = 100 - %RC/Vt). ods: baseline 1 (277 ± 106 ml), baseline 2
(296 ± 145 ml), baseline 3 (270 ± 118 ml),
Statistical analysis baseline 4 (286 ± 117 ml), and baseline 5
(274 ± 94 ml). There were no significant
Data are reported as means ± SD. Statis- differences in tidal volume between the five
tical analysis was performed with the Statis- baseline periods (F = 0.40; P = 0.80).
tical Package for Social Sciences (SPSS 10.0,
Chicago, IL, USA). Distribution analysis was Comparison of Coach and Voldyne
performed using the Kolmogorov-Smirnov (volume-oriented incentive spirometers)
test. ANOVA for repeated measures was
performed, followed by the Tukey-Kramer Table 1 shows the data obtained with
post hoc test (Vt for baseline data and f, Ti/ volume-oriented incentive spirometers with
Ttot, %RC/Vt, and %AB/Vt for the IS peri- a required volume of 1500 ml. Comparison
ods). The data obtained for all respiratory showed that higher tidal volume and minute
variables with two volume-oriented and two ventilation values were reached with Voldyne
flow-oriented spirometers were compared (P < 0.05). Mean inspiratory flow was lower
by independent sample t-test. The volume and inspiratory duty cycle was longer when
and flow required by the incentive spirom- Coach was used (P < 0.05). With respect to
eters and those actually measured were com- respiratory frequency, rib cage and abdomi-
nal motion contribution to Vt, there were no Table 1. Data obtained with volume-oriented in-
significant differences between spirometers. centive spirometers for healthy subjects.
Re yne
Vo a c h
Tr ex
II
Tr ex
II
ir
ir
Co
sp
Co
ld
eters (Respirex: t = -6.99; P = 0.00; Triflo II: (Respirex and Triflo II). *P < 0.05
%RC %AB (ANOVA).
t = -10.71; P = 0.00).
the volume-oriented device. Mang and Ober- Our results showed that SpO2 was sig-
mayer (21), using a test lung model, tested nificantly increased after IS in all but one IS
six different models of incentive spirometers device. With healthy subjects these SpO2
(Coach, Voldyne and Triflo II between them) values were not clinically significant despite
and observed that Triflo II imposed the high- being statistically different. Monitoring of
est breathing work. This finding is similar to SpO2 during the use of IS should be recom-
that obtained in the present study, which mended when working with patients at risk
demonstrated a higher rib cage motion with for PPC.
Triflo II and Respirex (flow-oriented de- Limitations of the present study can be
vices). the fact that we studied healthy subjects and
In the devices evaluated by us, the actu- that a relation between this experimental
ally measured volume for volume-oriented situation and clinical situations involving
incentive spirometers and flow for flow- patients cannot be directly established. How-
oriented devices differed significantly from ever, studies on the influence of body posi-
those indicated by the manufacturers (about tion during incentive spirometry in normal
40%). The tidal volume measured differed subjects and patients submitted to surgery
significantly between the volume-oriented obtained similar results (20,30).
devices even though the subjects reached the Another limitation could be a possible
same levels on the cylinders. This fact might influence of different settings of volume and
be related to leak or friction on the cylinder. flow devices on results related to thoracoab-
This difference was also reported by Mang dominal motion. Although this was not an
et al. (29) in a study about incentive spirom- aim in this study, we observed close tidal
eters. The largest difference was observed volume measured using volume- or flow-
with flow-oriented devices (25-50% above oriented incentive spirometers. In view of
the flow declared by the manufacturers) but these considerations, we believe that the dif-
a difference was also observed with volume- ferences observed in thoracoabdominal mo-
oriented devices (± 10%). These results ob- tion between volume and flow IS were not
served by us and others show that there is a related to targets but to the characteristics of
source of error when this therapy is used and each device.
could help to explain inconsistent results Our results showed that a larger tidal
published in the literature evaluating the ef- volume associated with a low respiratory
ficacy of IS. This matter deserves further frequency, resulting in higher minute venti-
investigation. lation, was reached when subjects used Vol-
In our study, we analyzed the use of IS by dyne, a volume-oriented incentive spirom-
subjects without previous knowledge of the eter. Abdominal motion during the use of
technique, a fact that can influence the per- incentive spirometers was higher with vol-
formance obtained during the measurements. ume-oriented devices. In all devices, the ac-
However, our purpose with this inclusion tually measured volume or flow differed
criterion was to simulate the clinical context, significantly from those indicated by the
in which the patients are not necessarily manufacturers.
familiar with IS.
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