Ref. no. | Patient numbers and characteristics | Study design | Intervention1-a | Dose of salbutamol via CFC-MDI | Dose of salbutamol via CFC-free device | Outcome measures | Interpretation of result | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Efficacy1-b | Potency | |||||||||||||||
(a) Trials comparing salbutamol delivered via Airomir (HFC-MDI) and CFC-MDI | ||||||||||||||||
8 | 25 moderately asthmatic adults | DB crossover R, PC | Single dose on separate days | 100 or 200 μg | 100, 200 or 300 μg | FEV1 | HFC-MDI = CFC-MDI | HFC-MDI = CFC-MDI | ||||||||
9 | 44 mild to moderately asthmatic children | DB crossover R | Single dose | 200 μg (Volumatic® spacer device) | 200 μg (Volumatic® spacer device) | FEV1, VC | HFC-MDI = CFC-MDI | |||||||||
10 | 24 moderately asthmatic adults | SB crossover R, PC | Cumulative dosing | 100–1600 μg | 100–1600 μg | FEV1 | HFC-MDI = CFC-MDI | HFC-MDI = CFC-MDI | ||||||||
11 | 24 mild to moderately asthmatic adults | SB crossover R | Cumulative dosing | 100–1600 μg | 100–1600 μg | FEV1, FVC, FEF25–75% | HFC-MDI = CFC-MDI | HFC-MDI = CFC-MDI | ||||||||
12 | 565 moderately asthmatic adults | DB parallel R, PC | 12 weeks | 200 μg qid | 200 μg qid | FEV1 | HFC-MDI = CFC-MDI | |||||||||
13 | 63 asthmatic children | Open parallel R | 4 weeks | 200 μg qid | 200 μg qid | FEV1 | HFC-MDI = CFC-MDI | |||||||||
(b) Trials comparing salbutamol delivered via Evohaler (HFC-MDI) and CFC-MDI | ||||||||||||||||
14 | 20 mild to moderately asthmatic adults | DB crossover R, PC | Single dose on separate days | 100 μg, 200 μg | 100 μg, 200 μg | FEV1 | HFC-MDI = CFC-MDI | |||||||||
15 | 24 asthmatic adults | DB crossover R, PC | Single dose | 200 μg (spacer device) | 200 μg (spacer device) | Histamine PD20, FEV1 | HFC-MDI = CFC-MDI | |||||||||
16 | 25 asthmatic children | DB crossover R, PC | Single dose | 200 μg (spacer device) | 200 μg (spacer device) | Histamine PD20, FEV1 | HFC-MDI = CFC-MDI | |||||||||
17 | 423 mild to moderately asthmatic adults | DB parallel R | 4 weeks | 400 μg per day | 400 μg per day | Total daily dose, PEFR, FEV1 | HFC-MDI = CFC-MDI | |||||||||
(c) Trials comparing salbutamol delivered via Rotahaler (ROT) and CFC-MDI | ||||||||||||||||
18 | 20 adults | DB crossover R, PC | Single dose on separate days | 200 μg | 200, 400, 600 μg | FEV1, FVC | ROT = CFC-MDI | |||||||||
19 | 10 acutely asthmatic adults | DB crossover R | Single dose on separate days | 200 μg | 50, 100, 200, 400 μg | PEFR | ROT = CFC-MDI | |||||||||
20 | 10 moderately asthmatic adults | DB crossover R, PC | Single dose on separate days | 200 μg | 200, 400 μg | FEV1, VC | ROT = CFC-MDI | |||||||||
21 | 22 moderate to severely asthmatic adults | DB crossover PC | Single dose on separate days | 200 μg | 400 μg | PEFR | ROT = CFC-MDI | |||||||||
22 | 9 moderate to severely asthmatic adults | crossover R | Single dose on separate days | 400 μg | 400 μg | FEV1, PEFR, FVC | ROT < CFC-MDI (FEV1) | ROT < CFC-MDI | ||||||||
23 | 44 mildly asthmatic adults | DB crossover R, PC | Single dose on separate days | 200 μg | 200 μg | FEV1 | ROT = CFC-MDI | |||||||||
24 | 14 adults | crossover R | Cumulative dosing | 100–1500 μg | 100–1500 μg | FEV1, FVC | ROT = CFC-MDI | ROT = CFC-MDI | ||||||||
25 | 7 adults | open crossover R | Cumulative dosing | 100–4400 μg | 200–9000 μg | FEV1, FVC | ROT = CFC-MDI | ROT = CFC-MDI | ||||||||
26 | 25 children | DB crossover R, PC | Cumulative dosing | 100–200 μg | 100–400 μg | FEV1, FVC, FEF25–75% | ROT = CFC-MDI | ROT = CFC-MDI | ||||||||
27 | 27 severely asthmatic adults | Open parallel R | Cumulative dosing | 3600 μg total (spacer device) | 3600 μg total | FEV1 | ROT = CFC-MDI | ROT = CFC-MDI | ||||||||
24 | 12 adults | Open crossover R | 1 month | 674 μg/day | 790 μg/day | Total daily dose, PEFR | ROT = CFC-MDI | |||||||||
26 | 185 mild to moderately asthmatic children | DB parallel R | 3 months | 200 μg qid | 200 μg qid | FEV1, FVC, FEF25–75% | ROT = CFC-MDI | |||||||||
28 | 38 adults | DB sequential | 3 months | 720 μg/day | 660 μg/day | Total daily dose, PEFR, FEV1 | ROT = CFC-MDI | |||||||||
29 | 43 moderately asthmatic children | DB crossover R | 1 month | 320 μg/day | 660 μg/day | Total daily dose, PEFR | ROT > CFC-MDI (PEFR) | |||||||||
(d) Trials comparing salbutamol delivered via Diskhaler (DISK) and CFC-MDI | ||||||||||||||||
30 | 41 adults | DB crossover R, PC | Single dose on separate days | 200 μg | 400 μg | FEV1 | DISK = CFC-MDI | |||||||||
31 | 11 mildly asthmatic adults | DB crossover | Single dose on separate days | 200 μg | 400 μg | FEV1, VC, FRC, FEV1PC20 | DISK = CFC-MDI | |||||||||
32 | 9 moderately asthmatic adults | Open crossover R | Single dose on separate days | 400 μg | 400 μg | FEV1, urinary salbutamol | DISK = CFC-MDI (FEV1) | DISK = CFC-MDI | ||||||||
DISK > CFC-MDI (urinary excretion) | ||||||||||||||||
(e) Trials comparing salbutamol delivered via Accuhaler and CFC-MDI | ||||||||||||||||
33 | 24 mild to moderately asthmatic adults | DB crossover R, PC | Single dose on separate days | 200 μg | 200 μg | FEV1, PEFR | Accuhaler = CFC-MDI | |||||||||
34 | 30 mild to moderately asthmatic | DB crossover | Single dose on separate days | 200 μg | 200 μg | FEV1, PC20 | Accuhaler = CFC-MDI | |||||||||
(f) Trials comparing salbutamol delivered via Clickhaler (CLICK) and CFC-MDI | ||||||||||||||||
35 | 16 mild, moderate and severely asthmatic adults | DB crossover R, PC | Single dose on separate days | 200 μg | 200 μg | FEV1 | CLICK = CFC-MDI | |||||||||
36 | 85 mild to moderately asthmatic children | Crossover | Single dose on separate days | 100 μg (spacer device) | 100 μg | FEV1, FVC, PEFR | CLICK = CFC-MDI | |||||||||
37 | 62 mild to moderately asthmatics | DB crossover R | Cumulative dosing | 100–400 μg | 100–400 μg | FEV1, FVC, PEFR | CLICK = CFC-MDI | CLICK = CFC-MDI |
↵1-a Time refers to duration of treatment per group.
↵1-b Comparative efficacy at the doses used in each study.
SB = single blind; DB = double blind; R = randomised; PC = placebo controlled; VC = vital capacity; FVC = forced vital capacity; FEF25–75% = forced expiratory flow between 25% and 75% of FVC; Vmax50 = 50% maximum instantaneous forced expiratory flow; FRC = functional residual capacity; VTG = volume of trapped gas; Rrs = respiratory system resistance; sGaw = specific airway resistance; (=) = equieffective (or potent); more (>) and less (<) effective (potent); tending to be more (=) or less (=) effective (potent).