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Table 4 Summary of Beneficial Transition Probabilities for Spirometrically-defined States at Any Time Over Approximately 5 Years, Albuquerque, New Mexico, 2001–2015, Lovelace Smokers’ Cohort

From: Spirometric variability in smokers: transitions in COPD diagnosis in a five-year longitudinal study

 

Normal spirometry at any time

COPD GOLD Stage I at any time

GOLD Unclassified at any time

COPD GOLD Stage II+ at any time

All smokers, irrespective of spirometric disease at baseline (n = 1553)

All beneficial transitionsa

87 %

16 %

39 %

22 %

 Resolution of diseasea

NA

16 %

35 %

4 %

Smokers with normal spirometry at baseline (n = 956)*

All beneficial transitionsa

89 %

26 %

64 %

64 %

 Resolution of diseasea

NA

26 %

57 %

29 %

Smokers with abnormal spirometry at baseline (n = 597)

All beneficial transitionsa

55 %

12 %

33 %

20 %

 Resolution of diseasea

NA

12 %

29 %

2 %

  1. Abbreviations COPD Chronic Obstructive Pulmonary Disease, GOLD Global Initiative for Chronic Obstructive Lung Disease
  2. aA beneficial transition, our primary outcome variable, was defined by either a decrease in spirometric state severity, including resolution, or continued maintenance of normal spirometric state at any time during longitudinal follow-up. Resolution of disease state, our secondary outcome variable, was defined by change of spirometrically-defined diseased states to normal spirometry state at any time during longitudinal follow-up
  3. *reflect transitions for new onset disease
  4. Additional data are provided in Fig. 1 in the main text and Additional file 1: Figures SE1 and SE2, including data on change in severity of individual spirometric disease states
  5. Probabilities for beneficial transition and for resolution of disease were significantly different between groups with ‘normal’ and ‘abnormal spirometry at baseline’ (P < 0.001 for both analyses), using SAS Proc GENMOD
  6. A similar table using the statistically defined NHANES-III lower limits of normal for FEV1/FVC ratio to define obstruction is presented in the Additional file 1: Table SE2