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1 onary function was assessed with a hand-held spirometer.
2 e recorded with a pneomatotachograph-coupled spirometer.
3  disappearance of oxygen from a water-sealed spirometer.
4  flow pattern, and collected in a water-seal spirometer.
5 erestimated VO2 measured with a water-sealed spirometer.
6 pe that is frequently used by volume-sensing spirometers.
7 in the intervention group received incentive spirometers.
8  lower lung function values than heated-wire spirometers.
9 ounter, and then compared against each field spirometer and syringe.
10        Subjects with IPF were given handheld spirometers and instruction on how to self-administer sp
11 rrently used to test the performance of both spirometers and peak expiratory flow (PEF) meters, but f
12 ng system consisting of a testing chamber, a spirometer, and a calibration syringe to evaluate the re
13 oking, age at completed full-time education, spirometer, and including study center as random effect.
14 were rotated to obtain data for each syringe-spirometer combination.
15                               Variance among spirometers exceeded variance among syringes.
16 or measurement bias given the replacement of spirometer in long-term population studies, we built spi
17  a population cohort study, used heated-wire spirometers in 1991 and 2002 and then ultrasonic spirome
18 ometers in 1991 and 2002 and then ultrasonic spirometers in 2010 revealing measurement bias in health
19 connected to the side port of a "bag-in-box" spirometer, making measurements independent of inspired
20                We conclude that variation in spirometers may limit the reliability of epidemiologic f
21 y of epidemiologic findings, even when these spirometers meet ATS specifications.
22                                            A spirometer occasionally changed its volume readout by ap
23                We used multiple rolling-seal spirometer/personal computer systems.
24         In healthy never smokers, ultrasonic spirometers record lower lung function values than heate
25         We provide a novel method to address spirometer replacement in cohort studies.
26 d deviation (SD), 28.7) mL/year while, after spirometer replacement, uncorrected, corrected by fixed
27 d volume were determined from the PT and the spirometer, respectively.
28 er in long-term population studies, we built spirometer-specific reference equations from healthy nev
29  Compared with baseline reference equations, spirometer-specific reference equations predicted lower
30  measured simultaneously with a water-sealed spirometer (spirometry VO2).
31 field testing season, a laboratory reference spirometer system was calibrated against a water-displac
32 thropomorphic, and socioeconomic factors and spirometer/technician effects.
33 thout and with spirometric gating by using a spirometer to trigger scanning at 90% of vital capacity
34 r not only anthropometric variables but also spirometer type.
35 index, calendar month, caste, and individual spirometer used.
36 s as a function of explicit variables (e.g., spirometer volume, generator output rate, wash-in half-t

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