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Table 1 Main sociodemographic characteristics at inclusion and clinical profile of COPD patients prescribed with FSC

From: Real-life use of fluticasone propionate/salmeterol in patients with chronic obstructive pulmonary disease: a French observational study

 

GPs

N patients (n = 352)

Pulmonologists

N patients (n = 358)

Age in years, mean (SD)

61.6 (11.4)

352

65.3 (11.5)

358

Male, N (%)

227 (64.5%)

352

269 (75.1%)

358

Professional status, N (%)

 

352

 

357

  Working

122 (34.7%)

 

57 (16.0%)

 

  Retired

186 (52.8%)

 

246 (68.9%)

 

  Other

44 (12.5%)

 

54 (15.1%)

 

BMI (kg/m 2 ), N (%)

 

349

 

358

  Underweight (<18)

10 (2.9%)

 

25 (7.0%)

 

  Normal (18–25)

131 (37.5%)

 

138 (38.5%)

 

  Overweight (25–30)

133 (38.1%)

 

121 (33.8%)

 

  Obese (≥ 30)

75 (21.5%)

 

74 (20.7%)

 

Current smoker, N (%)

195 (55.4%)

352

127 (35.6%)

357

Pulmonary hypertension, N (%)

12 (3.5%)

343

32 (9.2%)

348

≥1 cardiovascular comorbidity, N (%)

116 (33.0%)

352

138 (38.5%)

358

  Heart failure

44 (12.5%)

 

43 (12.0%)

 

  Coronary heart disease

35 (9.9%)

 

62 (17.3%)

 

  Peripheral artery disease

48 (13.6%)

 

45 (12.6%)

 

  Other1

35 (9.9%)

 

55 (15.4%)

 

COPD severity (investigator), N (%)

 

352

 

358

  Mild

49 (13.9%)

 

14 (3.9%)

 

  Moderate

197 (56.0%)

 

151 (42.2%)

 

  Severe

100 (28.4%)

 

152 (42.4%)

 

  Very severe

6 (1.7%)

 

41 (11.5%)

 

COPD severity (GOLD 2006), N (%)

 

137

 

323

  Grade 1 (mild)

31 (22.6%)

 

16 (5.0%)

 

  Grade 2 (moderate)

62 (45.3%)

 

183 (56.6%)

 

  Grade 3 (severe)

13 (9.5%)

 

38 (11.8%)

 

  Grade 4 (very severe)

31 (22.6%)

 

86 (26.6%)

 

COPD severity (GOLD 2011), N (%) 2

 

136

 

319

  Group A: Low risk, less symptoms

20 (14.7%)

 

71 (22.3%)

 

  Group B: Low risk, more symptoms

15 (11.0%)

 

72 (22.6%)

 

  Group C: High risk, less symptoms

45 (33.1%)

 

52 (16.3%)

 

  Group D: High risk, more symptoms

56 (41.2%)

 

124 (38.9%)

 

Median time in years since diagnosis (range)

5.0 (0–40)

347

4.0 (0–30)

352

FEV 1 , mean (SD) 3

    

  % predicted

60.5 (22.8)

145

53.6 (16.7)

334

Arterial blood gas (mmHg), mean (SD)

    

  PaO2

72.4 (12.8)

79

70.0 (11.7)

221

  PaCO2

42.1 (6.2)

66

41.2 (6.0)

218

Dyspnea (MRC grade), N (%)

 

349

 

353

  1 (strenuous exercise)

58 (16.6%)

 

24 (6.8%)

 

  2 (walking upstairs or uphill)

146 (41.8%)

 

114 (32.3%)

 

  3 (walking on the flat)

96 (27.5%)

 

103 (29.2%)

 

  4 (walking slowly)

35 (10.0%)

 

77 (21.8%)

 

  5 (daily activities)

14 (4.0%)

 

35 (9.9%)

 

Chronic symptoms, N (%) 4

    

  Daily expectorations

261 (74.6%)

350

232 (65.4%)

355

  Daily cough

307 (87.7%)

350

287 (81.1%)

354

  Daily expectorations + cough

245 (70.0%)

350

224 (63.3%)

354

Quality of life (CCQ) score, median 5

 

304

 

336

  Symptoms

3.3

 

2.8

 

  Functional status

2.5

 

2.3

 

  Mental status

2.0

 

2.0

 

  Total

2.7

 

2.4

 

History of repeated exacerbations, N (%) 6

222 (63.1%)

352

106 (29.6%)

358

  1. 1Excluding vascular (hypertension) and metabolic conditions (diabetes, hypercholesterolemia).
  2. 2A: GOLD 1–2 and < 1 exacerbation/year, MRC < 2; B: GOLD 1–2 and < 1 exacerbation/year, MRC ≥ 2; C: GOLD 3–4 and/or ≥ 2 exacerbations/year, MRC < 2; D: GOLD 3–4 and/or ≥ 2 exacerbations/year, MRC ≥ 2 [15].
  3. 3An additional 8 GP patients had FEV1 results which were aberrant and were excluded from the analysis; for one pulmonologist patient only FEV1 (L) was available (% FEV1 was missing).
  4. 4During the 3 months prior to initiation.
  5. 5During 7 days prior to initiation; score on a scale of 0 to 6 where 6 is the worst score.
  6. 6During the 12 months prior to initiation; exacerbation was defined as at least two of the following separated by at least 7 days over the last year: an emergency department visit, hospitalization, or a course of oral corticosteroids or antibiotics for respiratory problems.