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Table 6 Characteristics of patients with severe asthma exacerbations

From: Efficacy and safety of ipratropium bromide/albuterol compared with albuterol in patients with moderate-to-severe asthma: a randomized controlled trial

 

CVT-MDI

ALB-HFA

 

Patient 10868

Patient 11356

Patient 11473

Patient 12410

Patient 12454

Patient 10853

Patient 11752

Patient 11803

Patient 12055

Age (years), gender, race

52, Female, Caucasian

69, Female, Caucasian

64, Female, Hawaiian/PI

36, Female, Caucasian

59, Male, Caucasian

45, Female, Afr Amer

35, Male, Afr Amer

49, Female, Caucasian

74, Female, Caucasian

BMI (kg/m2)

33.2

32.5

22.5

48.2

28.6

41.4

N/A

N/A

29.0

Exacerbation - start day, phase

Day 3, Ph 1

Day 2, Ph 1

Day 29, Ph 1

Day 24, Ph 1

Day 15, Ph 1

Day 19, Ph 2

Day 29, Ph 2

Day 11, Ph 2

Day 22, Ph 2

Exacerbation in prior year

None

Yes, 2 months prior

None

Yes, 6 months prior

Yes, 2.5 months prior

None

N/A

Yes, 6 months prior

None

Baseline FEV1 % predicted

56.3 %

36.4 %

41.4 %

71.3 %

64.9 %

52.3 %

46.8 %

63.7 %

72.5 %

Background and concomitant asthma medications (daily dose)

Advair 500/100 μg; Alb 180 μg, d/c;

Symbicort 640/18 μg;

Advair 1000/100 μg; Alb 180 μg, d/c;

Advair 250/50 μg; Singulair 10 mg; Zyrtec; Flonase;

Advair 1000/100 μg; Singulair 10 mg;

Advair 1000/100 μg

Advair 1000/100 μg; Singulair 10 mg; Alb 180 μg, d/c; Zyrtec D; Nasonex;

Flovent 440 μg, Combivent 84/480 μg, Alb 180 μg, d/c Flonase

Xopenex 2.5 mg, Pulmicort 360 μg, Alb, d/c

Respiratory infection reported preceding exacerbation

No

No

No

No

No

Yes

Yes

No

No

Use of rescue medication (No. of puffs) 3 days before and day of exacerbation

−3 days: 2

−3 days: 2

−3 days: 4

−3 days: 0

−3 days: 5

−3 days: 2

−3 days: 6

−3 days: 6

−3 days: 4

−2 days: 4

−2 days: 3

−2 days: 8

−2 days: 2

−2 days: 4

−2 days: 0

−2 days: 8

−2 days:6

−2 days: 4

−1 day: 2

−1 day: 3

−1 day: 4

−1 day: 2

−1 day: 5

−1 day: 6

−1 day: 6

−1 day: 6

−1 day: 4

0: 4

0: 6

0: 0

0: 2

0: 7

0: 4

0: N/A

0: 6

0: 6

PEF (L/min) 3 days before and day of exacerbation (best of day)

−3 days: 365

−3 days: 189

−3 days: 155

−3 days: 381

−3 dy: 371

−3 days: 254

−3 days: 388

−3 days: 392

−3 days: 339

−2 days: 359

−2 days: 160

−2 days: 172

−2 dy: 392

−2 days: 399

−2 days: 227

−2 days: 298

−2 days: 395

−2 days: 334

−1 day: 353

−1 day: 180

−1 day: 129

−1 day: 426

−1 day: 337

−1 day: 180

−1 day: 307

−1 day: 406

−1 day: 305

0: 350

0: 181

0: 104

0: 368

0: 353

0: 194

0: 284

0: 374

0: 281

Duration of exacerbation

17 days

9 days

4 days

9 days

7 days

9 days

13 days

81 days

11 days

PEF (L/min) 3 days after end of exacerbation

+1 day: 356

+1 day: 154

N/A

+1 day: 368

+1 day: 492

+1 day: 310

N/A

+1 day: 326

N/A

+2 days: 311

+2 days: 155

+2 days: 402

+2 days: 486

+2 days: 347

+2 days: 344

+3 days: 361

+3 days: 153

+3 days: 384

+3 days: 536

+3 days: 271

+3 days: 314

  1. Afr Am African American, ALB-HFA albuterol hydrofluoroalkaline, Alb albuterol, BMI body mass index, CVT-MDI ipratropium bromide/albuterol sulfate metered-dose inhaler, d/c discontinued, FEV 1 forced expiratory volume in 1 s, FVC forced vital capacity, ICS inhaled corticosteroids, LABA long-acting β2-agonist, PEF peak expiratory flow, ph phase, PI pacific islander