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Table 2 Odds/Risk of long-term adverse outcomes based on CIDs in the first 6 months of the TORCH study (ITT population)

From: Long-term outcomes following first short-term clinically important deterioration in COPD

Outcome

CID+ population (N = 2870)

CID- population (N = 2422)

CID+ vs CID-, OR (95% CI)

≥100 mL decrease in FEV1a, n (%)

2004 (70)

1296 (54)

2.00 (1.78, 2.24)*

≥200 mL decrease in FEV1a, n (%)

1696 (59)

1018 (42)

1.97 (1.77, 2.20)*

≥4-unit increase in SGRQa, n (%)

1516 (67)

930 (53)

1.82 (1.60, 2.07)*

≥8-unit increase in SGRQa, n (%)

1342 (59)

827 (47)

1.65 (1.45, 1.88)*

Moderate-to-severe COPD exacerbationb, n (%)

2082 (73)

1450 (60)

1.61c (1.50, 1.72)*

Hospitalization eventsb, n (%)

797 (28)

491 (20)

1.55c (1.38, 1.73)*

Risk (HR) of all-cause mortalityb, n (%)

237 (8)

160 (7)

1.41c (1.15, 1.72)*

  1. *P < 0.001, arisk of deterioration at 36-months assessed from the pre-randomization period; brisk of a new exacerbation or all-cause death assessed from Week 24; cdata report HR (95% CI)
  2. CID clinically important deterioration, CID+ presence of a CID within 6 months of enrollment into the study, CID- absence of a CID within 6 months of enrollment into the study, FEV1 forced expiratory volume in 1 s, HR hazard ratio, ITT intent-to-treat, OR odds ratio, SGRQ St George’s Respiratory Questionnaire, TORCH TOwards a Revolution in COPD Health