Cochrane · systematic review · CD012102

Long‐acting inhaled bronchodilators for cystic fibrosis

Smith, S, Edwards, CT · Cochrane Database of Systematic Reviews · 2017 · Cochrane Library

SoF tableOnly the outcomes this review put in its Summary of Findings table are listed (the Cochrane Handbook caps them at about seven per comparison). Its other analyses are not shown here.
Questions
11
current version
GRADE rated
7
No studies
4
Included studies
NR
No studies 4 · 36.4%Ungraded 0 · 0%Very low 1 · 9.1%Low 2 · 18.2%Moderate 3 · 27.3%High 1 · 9.1%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

Questions and results

Beta‐2 agonists versus placebo

Population: adults and children with cystic fibrosis
5 questions
OutcomeEffectEvidenceStatus / GRADE
FEV1: change from baseline
Beta‐2 agonists vs placebo
no estimate extracted1 study · 16 participantsVery low
Downgraded: risk of bias, imprecision, indirectness
Participant‐reported outcomes: quality of life (measured by CFQ‐R)
Beta‐2 agonists vs placebo
no estimate extractedNRNo studies
Adverse events after tiotropium 5.0 µg
Beta‐2 agonists vs placebo
no estimate extractedNRNo studies
Pulmonary exacerbations
Beta‐2 agonists vs placebo
no estimate extractedNRNo studies
Other measures of lung function
Beta‐2 agonists vs placebo
no estimate extractedNRNo studies

LAMAs versus placebo

Population: adults and children with cystic fibrosis
6 questions
OutcomeEffectEvidenceStatus / GRADE
FEV1: mean change from baseline (L)
LAMAs vs placebo
no estimate extracted1 study · 34 participantsLow
Downgraded: risk of bias, imprecision, indirectness
Participant‐reported outcomes: quality of life (measured by CFQ‐R)
LAMAs vs placebo
no estimate extracted2 studies · 974 participantsLow
Downgraded: risk of bias, imprecision, indirectness
Adverse events after tiotropium 5.0 µg
LAMAs vs placebo
RR 0.96 [0.88, 1.04]2 studies · 807 participantsHigh
Pulmonary exacerbations: participants reporting ≥1 pulmonary exacerbation during the trial period after tiotropium 5 µg
LAMAs vs placebo
RR 0.6 [0.32, 1.12]2 studies · 805 participantsModerate
Downgraded: risk of bias, imprecision, indirectness
Other measures of lung function: mean change from baseline in FEV1 AUC0-4h (% predicted) after tiotropium 5.0 µg
LAMAs vs placebo
no estimate extracted2 studies · 770 participantsModerate
Downgraded: risk of bias, imprecision, indirectness
Other measures of lung function: mean change from baseline in trough FEV1 (% predicted) after tiotropium 5.0 µg
LAMAs vs placebo
no estimate extracted2 studies · 772 participantsModerate
Downgraded: risk of bias, imprecision, indirectness