TABLE 1

Nontuberculous mycobacterial pulmonary disease (NTM-PD) among adults ≥35 years of age, with and without obstructive lung disease in Ontario, Canada, 2001–2013

NTM-PDTotal Ontario populationNo obstructive lung diseaseCOPDAsthma
Subjects6 290 6035 436 773543 119406 712
Primary analysis
 Cases9658439845381850
 Incidence (95% CI)#13.33 (13.07–13.60)6.63 (6.44–6.83)143.26 (139.12–147.49)52.83 (50.45–55.30)
 Unadjusted HR (95% CI)Not applicable1.00 (ref.)20.03 (19.19–20.91)8.47 (7.99–8.98)
 Age- and sex-adjusted HR (95% CI)Not applicable1.00 (ref.)12.51 (11.94–13.10)7.74 (7.30–8.21)
 Fully adjusted HR (95% CI)Not applicable1.00 (ref.)8.73 (8.29–9.18)5.14 (4.83–5.47)
Sensitivity analysis
 CasesNot applicable535036501564
 Incidence (95% CI)#Not applicable8.01 (7.80–8.23)128.54 (124.40–132.77)48.12 (45.77–50.57)
 Unadjusted HR (95% CI)Not applicable1.00 (ref.)15.45 (14.79–16.13)7.27 (6.84–7.72)
 Age- and sex-adjusted HR (95% CI)Not applicable1.00 (ref.)9.15 (8.73–9.59)6.58 (6.19–6.99)
 Fully adjusted HR (95% CI)Not applicable1.00 (ref.)6.01 (5.71–6.33)4.26 (3.99–4.55)
  • Because some patients with chronic obstructive pulmonary disease (COPD) also had asthma and some patients with asthma also had COPD, these two groups were not mutually exclusive. Primary analysis: NTM-PD was assigned to COPD or asthma if NTM-PD was diagnosed at any time after the diagnosis of COPD or asthma. Sensitivity analysis: NTM-PD was assigned to COPD or asthma if NTM-PD diagnosed ≥1 year after the diagnosis of COPD or asthma. Asthma was defined as fulfilling the diagnostic definition of asthma, regardless of co-existing COPD. COPD was defined as fulfilling the diagnostic definition of COPD, regardless of co-existing asthma. Hazard ratios (HRs) were calculated by Cox proportional hazards regression. #: calculated per 100 000 person-years with Poisson 95% confidence intervals; : controlling for age, sex, income, rurality and comorbidities that may be associated with NTM-PD (bronchiectasis, chronic kidney disease, diabetes mellitus, gastro-oesophageal reflux disease, HIV infection, lung cancer, rheumatoid arthritis, transplantation (haematopoietic stem cell or solid organ) and prior culture-proven tuberculosis) modelled in a time-varying fashion.