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Table 1 Quality of Spirometry Performance and Reporting

From: Effects of a 12-month multi-faceted mentoring intervention on knowledge, quality, and usage of spirometry in primary care: a before-and-after study

Criterion

Pre-Intervention

During Intervention

Mean difference

Odds Ratio

p-value

Total spirometries

210

208

-

-

-

Mean No. of blows per spirometry

3.8 (3.5, 4.1)

3.7 (3.4, 4.0)

−0.08 (−0.25, 0.09)

-

0.37

Mean No. of acceptablea blows per spirometry

1.9 (1.3, 2.5)

2.1 (1.5, 2.7)

0.22 (−0.07, 0.50)

-

0.16

Probability of spirometries with ≥3 acceptable blows

0.36 (0.16, 0.63)

0.49 (0.27, 0.72)

-

1.7 (1.1, 2.6)

0.03

Probability of spirometries with ≥2 repeatable blowsb

0.85 (0.74, 0.92)

0.93 (0.85, 0.97)

-

2.2 (1.0, 4.6)

0.05

Probability of blows with a poor start

0.06

0.05

-

0.74 (0.35, 1.6)

0.58

Probability of blows with an unsatisfactory exhalation

0.39

0.35

-

0.84 (0.62, 1.1)

0.30

Probability of blows with significant artifact

0.13

0.14

-

1.2 (0.86, 1.6)

0.34

Probability of reporting correct FVCc

0.71 (0.57, 0.85)

0.78 (0.66, 0.90)

-

1.43 (0.72, 2.9)

0.35

Probability of reporting correct FEV1c

0.73 (0.61, 0.85)

0.79 (0.68, 0.89)

-

1.4 (0.62, 3.0)

0.45

Probability of documenting inadequate spirometryd

0.08 (0, 0.18)

0.12 (0, 0.18)

-

1.4 (0.73, 2.8)

0.46

Probability of identifying appropriate reason for inadequate spirometrye, f

0.02 (0, 0.07)

0.06 (0, 0.13)

-

2.4 (0.67, 8.8)

0.20

Probability that spirometer was calibrated before test

0.96 (0.68, 1.0)

0.97 (0.77, 1.0)

-

1.4 (1.1, 1.9)

0.01

Probability that spirometry met both acceptability and repeatability criteria

0.32 (0.14, 0.58)

0.45 (0.25, 0.67)

-

1.7 (1.0, 3.0)

<0.05

  1. 95 % confidence intervals are provided in brackets
  2. CI denotes confidence interval
  3. a“acceptable” was defined by the absence of a poor start [i.e. an extrapolated volume < 5 % of FVC or 150 mL (whichever was greater)], a satisfactory exhalation [defined by reaching a plateau in the volume–time curve, with no change in volume (<0.025 L) for ≥ 1 s], and absence of any significant artifact (including evidence of cough during the first second of exhalation, glottis closure that influences the measurement, early termination or cut-off, submaximal effort, leak, or an obstructed mouthpiece) [22]
  4. bamong spirometries with at least 2 acceptable blows (a spirometry was considered “repeatable” when the two largest FVC values and the two largest FEV1 values were each within 150 mL of each other) [22]
  5. camong spirometries with at least 1 acceptable blow
  6. dTechnician comments were searched for documentation that the test was inadequate (among spirometries which did not meet ATS criteria of at least 3 acceptable and 2 repeatable blows) [22]
  7. eTechnician comments were searched for documentation of the reason that the test was inadequate (among spirometries which did not meet ATS criteria of at least 3 acceptable and 2 repeatable blows) [22]
  8. fFor this outcome, applying the bootstrap method to estimate standard errors failed to converge in one-third of the replications. Therefore, results are reported using robust standard errors