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. 2015 Jul 14;2015(7):CD010337. doi: 10.1002/14651858.CD010337.pub2

5. Outcomes in Cochrane reviews ‐ lung function.

Intervention/comparison Outcome Number of participants (number of studies) Results: treatment effect (95% CI) unless otherwise stated Interpretation of result1 Evaluation1
Pharmacological interventions
Antibiotics (long term) vs. placebo
(Evans 2007)
FEV1 % predicted at end of trial 27 (1, children)
17 (1, adults)
MD ‐1.05% (‐6.93 to 4.83), P value = 0.7 NSD No evidence of benefit
FEV1 (unit not reported) 59 (3) Not pooled but all reported no difference (values not reported) NSD No evidence of benefit
Antibiotics (short term) vs. placebo
(Wurzel 2011)
Tobramycin vs. placebo: FEV1 % predicted change from baseline 74 (1, adults) MD and CI not reported, tobramycin ‐2.2%; placebo 1.5%, P value = 0.41 NSD No evidence of benefit
ICS vs. placebo/no treatment
(Kapur 2009)
Short‐term follow‐up < 6 months: FEV1 L change from baseline 101 (3, adults) MD 0.09 L (0.03 to 0.15), P value = 0.002
Effect based on 1 study without placebo comparison
Statistically significant difference Evidence of statistical benefit
LABA/ICS combination vs. ICS
(Goyal 2014)
FEV1 mL change from baseline 40 (1) MD ‐14.00 mL (‐84.14 to 56.14), P value not reported NSD No evidence of benefit
Inhaled hyperosmolar vs. placebo or ITS
(Hart 2014)
Mannitol vs. placebo: FEV1 % predicted change from baseline 17 (1) MD 2.70% (‐8.53 to 13.93), P value not reported NSD No evidence of benefit
Mannitol vs. placebo
FEV1 L: at end of trial
343 (1) MD 0.03 L (‐0.10 to 0.16), P value not reported NSD No evidence of benefit
Mannitol vs. placebo FEV1: change (unit not reported) 12 (1) Not reported NSD No evidence of benefit
HTS vs. ITS: FEV1 % predicted change from baseline 30 (1) MD 13.30% (CI not reported), P value < 0.01
Favoured HTS
Statistically significant difference Evidence of clinically relevant benefit
HTS vs. ITS: FEV1 L at end of trial 40 (1) MD 0.19 L (‐0.37 to 0.75), P value = 0.5 NSD No evidence of benefit
Mucolytics vs. placebo
(Wilkinson 2014)
Bromhexine vs. placebo: FEV1 mL at end of trial 88 (1) MD 184.00 mL (‐149.75 to 517.75), P value not reported NSD No evidence of benefit
RhDNase 5 mg vs. placebo: FEV1 L % change from baseline 40 (1) MD 2.10% (‐2.90 to 7.10), P value not reported NSD No evidence of benefit
RhDNase 2.5 mg vs. placebo: FEV1 L % change from baseline 237 (2) n = 197, MD ‐1.9% decline, P value < 0.05, favoured placebo;
n = 40, MD 2.10% (‐4.05 to ‐8.25), P value not reported
Statistically significant difference (1 trial)
NSD (1 trial)
Unclear
Erdosteine vs. nothing: FEV1 mL change from baseline 30 (1) MD 200 mL (40 to 360), P value not reported Statistically significant difference Evidence of clinically relevant benefit
Erdosteine vs. nothing: FEV1 % predicted change from baseline 30 (1) MD 4.50% (‐3.11 to 12.11), P value not reported NSD No evidence of benefit
Non‐pharmacological interventions
Physical therapy: IMT vs. no intervention or sham treatment
(Bradley 2002)
Outcome not reported in trial
Nurse‐led vs. doctor‐led care
(French 2003)
FEV1 % predicted at end of trial 80 (1) MD 2.37 (‐7.37 to 12.11), P value not reported NSD No evidence of benefit
ACTs vs no treatment
(Lee 2013)
FEV1 L at end of trial 38 (3, adults) Median difference 0.0 L, P value = 0.7 (1 study, no values for other 2 studies) NSD No evidence of benefit
FEV1 (unit not reported) at end of trial 9 (1, children) Difference 8.86% (values not reported), P value not reported, favoured ACT Statistically significant difference Unclear

1. No minimum clinically important difference for FEV1 in bronchiectasis. Reference values from American Thoracic Society/European Respiratory Society recommendations as follows: change of at least 100 mL or change of ≥ 20% in short‐term trials (of weeks of duration) and ≥ 15% in long‐term trials (≥ 1 year) (Pellegrino 2005).

Abbreviations: ACT: airway clearance technique; CI: confidence interval; FEV1: forced expiratory volume in 1 second; HTS: hypertonic saline; ICS: inhaled corticosteroids; IMT: inspiratory muscle training; ITS: isotonic saline; LABA: long‐acting beta2‐agonist; n: number of participants; MD: mean difference; NSD: no statistically significant difference; RhDNase: recombinant human deoxyribonuclease I; vs: versus.