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Table 4 Construct validity: E-RS and wheeze Spearman correlations with SGRQ and clinical assessments

From: Reliability, validity and responsiveness of E-RS:COPD in patients with spirometric asthma-COPD overlap

 

Baseline week (Day − 7 to Day − 1)

Final treatment week (Day 21 to Day 28)

SGRQ: Total

SGRQ: Activity

SGRQ: Impacts

SGRQ: Symptoms

Rescue medication use

Morning PEF

FEV1

FEV1% predicted

SGRQ: Total

SGRQ: Activity

SGRQ: Impacts

SGRQ: Symptoms

Rescue medication use

Morning PEF

FEV1

FEV1% predicted

N

326

328

329

327

336

338

338

338

321

324

325

325

326

327

327

327

RS-Total

0.46

0.43

0.36

0.39

0.33

−0.30

−0.18

−0.17

0.52

0.54

0.40

0.43

0.40

−0.27

− 0.18

− 0.17

RS-Cough and Sputum

0.32

0.29

0.22

0.35

0.26

−0.23

−0.11

− 0.11

0.38

0.36

0.29

0.44

0.34

− 0.16

− 0.11

− 0.10

RS-Chest Symptoms

0.37

0.32

0.3

0.33

0.29

− 0.19

−0.06

− 0.05

0.45

0.43

0.37

0.39

0.32

−0.18

− 0.09

− 0.08

RS-Breathlessness

0.48

0.48

0.38

0.35

0.33

−0.33

−0.24

− 0.22

0.53

0.59

0.42

0.38

0.40

−0.31

−0.23

− 0.23

Wheeze

0.38

0.33

0.29

0.41

0.33

−0.12

0.01

−0.11

0.42

0.38

0.34

0.43

0.32

−0.12

−0.04

− 0.06

  1. Weak, moderate and strong correlations were defined as r ≤ 0.4 (unmarked), r > 0.4 (bold) and r > 0.7 (none present in this table), respectively
  2. E-RS Evaluating Respiratory Symptoms in chronic obstructive pulmonary disease, FEV1 forced expiratory volume in 1 s, PEF peak expiratory flow, RS respiratory symptoms, SGRQ St George’s Respiratory Questionnaire