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Search review questions

Each row is one question a systematic review asked: who, what, compared with what, and which outcome, with the effect it found and how certain that is. Words match anywhere in the field.

Limit to evidence status or GRADE (optional)

2,325 questions in 216 reviews · Airways

current versions
No studies 249 · 10.7%Ungraded 107 · 4.6%Very low 276 · 11.9%Low 751 · 32.3%Moderate 718 · 30.9%High 224 · 9.6%

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.

QuestionEffectEvidenceStatus / GRADE
Supportive intervention vs control
2.3 N deemed adherent (≥ four hours/night) · adults with obstructive sleep apnoea
Educational, supportive and behavioural interventions to improve usage of continuous positive airway… (2020) · Cochrane
OR 1.68 [1.08, 2.6]2 studies · 376 participantsLow
Supportive intervention vs control
2.4 Withdrawals · adults with obstructive sleep apnoea
Educational, supportive and behavioural interventions to improve usage of continuous positive airway… (2020) · Cochrane
OR 1.27 [0.97, 1.66]11 studies · 1702 participantsLow
Sublingual immunotherapy vs control
Exacerbation requiring ED or hospital visit Weighted mean duration of studies: 31 weeks · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
OR 0.35 [0.1, 1.2]2 studies · 108 participantsVery low
Sublingual immunotherapy vs control
Quality of life · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
no estimate extractedNRNo studies
Sublingual immunotherapy vs control
Serious adverse events Weighted mean duration of studies: 56 weeks · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
no estimate extracted29 studies · 4810 participantsModerate
Sublingual immunotherapy vs control
Exacerbation requiring OCS Weighted mean duration of studies: 58 weeks · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
OR 0.75 [0.45, 1.24]5 studies · 1364 participantsVery low
Sublingual immunotherapy vs control
All adverse events Weighted mean duration of studies: 62 weeks** · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
OR 1.99 [1.49, 2.67]27 studies · 4251 participantsHigh
Sublingual immunotherapy vs control
Bronchial provocation · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
no estimate extracted5 studies · 200 participantsLow
Sublingual immunotherapy vs control
ICS use · adults and children with asthma
Sublingual immunotherapy for asthma (2020) · Cochrane
no estimate extracted3 studies · 778 participantsLow
Pulmonary rehabilitation/exercise training vs no intervention
Time/change in time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted3 studies · 190 participantsLow
Intervention NR
Time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 411 participantsLow
Intervention NR
Time in moderate‐intensity physical activity · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 35 participantsLow
Intervention NR
Change in time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted2 studies · 131 participantsModerate
Intervention NR
Time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 426 participantsModerate
Pulmonary rehabilitation/exercise training vs no intervention
Time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted2 studies · 275 participantsModerate
Pulmonary rehabilitation/exercise training vs no intervention
Time in moderate intensity physical activity · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 97 participantsModerate
Intervention NR
Change in time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 58 participantsLow
Intervention NR
Time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 40 participantsLow
Intervention NR
Time in moderate‐intensity physical activity · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 97 participantsModerate
Intervention NR
Change in time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 280 participantsModerate
Intervention NR
Change in time in moderate intensity physical activity · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 43 participantsLow
Intervention NR
Time in MVPA · people with COPD, clinical stability
Interventions for promoting physical activity in people with chronic obstructive pulmonary disease (COPD) (2020) · Cochrane
no estimate extracted1 study · 26 participantsModerate
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Exacerbation rate (participants with one or more) study duration: 12 months · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
RR 0.46 [0.26, 0.81]1 study · 100 participantsLow
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Pneumonia and other serious adverse events · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extractedNRNo studies
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Quality of life · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extractedNRNo studies
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Lung function indices · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extractedNRNo studies
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Acute respiratory infections study duration: 12 months · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
RR 0.96 [0.67, 1.39]1 study · 100 participantsVery low
PPI plus usual care vs usual care alone or chronic obstructive pulmonary disease
Disease‐specific adverse events · chronic obstructive pulmonary disease
Proton pump inhibitors for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extractedNRNo studies
Atorvastatin vs placebo
Asthma exacerbations requiring hospitalisation or a course of steroids · people with asthma
Statins for asthma (2020) · Cochrane
no estimate extractedNRNo studies
Atorvastatin vs placebo
Health‐related quality of life · people with asthma
Statins for asthma (2020) · Cochrane
no estimate extractedNRNo studies
Atorvastatin vs placebo
Lung function: change in morning PEF · people with asthma
Statins for asthma (2020) · Cochrane
MD 12.321 study · 60 participantsVery low
Atorvastatin vs placebo
Lung function: change in FEV1 (pre) · people with asthma
Statins for asthma (2020) · Cochrane
MD 0.131 study · 60 participantsVery low
Atorvastatin vs placebo
Lung function: change in FEV1 (post) · people with asthma
Statins for asthma (2020) · Cochrane
MD 0.111 study · 60 participantsVery low
Atorvastatin vs placebo
Serious adverse events or adverse events · people with asthma
Statins for asthma (2020) · Cochrane
no estimate extractedNRNo studies
Atorvastatin vs placebo
Asthma control: change in ACQ · people with asthma
Statins for asthma (2020) · Cochrane
MD 0.411 study · 60 participantsVery low
Mepolizumab 100 mg vs placebo
Rate of moderate or severe exacerbations Eosinophilic phenotype · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.81 [0.71, 0.93]2 studies · 911 participantsHigh
Mepolizumab 300 mg vs placebo
Rate of moderate or severe exacerbations Eosinophilic phenotype · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.86 [0.7, 1.06]1 study · 451 participantsModerate
Mepolizumab 300 mg vs placebo
Time to first moderate or severe exacerbation Eosinophilic phenotype · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Hazard ratio 0.77 [0.6, 0.99]1 study · 451 participantsModerate
Mepolizumab 300 mg vs placebo
Rate of exacerbations with ED visit or hospitalisations Eosinophilic phenotype · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.83 [0.51, 1.35]1 study · 451 participantsModerate
Mepolizumab 300 mg vs placebo
Serious adverse events · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Odds ratio 0.84 [0.56, 1.27]1 study · 451 participantsModerate
Mepolizumab 300 mg vs placebo
Health‐related quality of life: change in SGRQ total score Scale: 0 to 100 (lower is better) Eosinophilic phenotype · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extracted1 study · 451 participantsModerate
Mepolizumab 750 mg vs placebo
Number of participants experiencing an exacerbation within 6 months · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Odds ratio 0.43 [0.06, 2.97]1 study · 18 participantsLow
Mepolizumab 750 mg vs placebo
Number of participants experiencing an exacerbation in 4‐month · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Odds ratio 9 [0.75, 108.31]1 study · 18 participantsLow
Mepolizumab 750 mg vs placebo
Serious adverse events · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Odds ratio 3 [0.22, 40.93]1 study · 18 participantsLow
Mepolizumab 750 mg vs placebo
Heath‐related quality of life (CRQ at 6 months) · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extracted1 study · 18 participantsLow
Mepolizumab 750 mg vs placebo
Lung function (FEV₁) (litres post‐bronchodilator) at 6 months · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
no estimate extracted1 study · 18 participantsLow
Mepolizumab 100 mg vs placebo
Rate of moderate or severe exacerbations All participants · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.92 [0.82, 1.03]2 studies · 1285 participantsModerate
Benralizumab 10 mg vs placebo
Rate of moderate or severe exacerbations Eosinophils ≥ 220/μL · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.85 [0.71, 1.02]1 study · 765 participantsModerate
Benralizumab 10 mg vs placebo
Rate of moderate or severe exacerbations Eosinophils < 220/μL · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 1.04 [0.82, 1.32]1 study · 365 participantsModerate
Benralizumab 10 mg vs placebo
Rate of severe exacerbations requiring hospitalisation Eosinophils ≥ 220/μL · individuals with COPD
Anti‐IL‐5 therapies for chronic obstructive pulmonary disease (2020) · Cochrane
Rate ratio 0.68 [0.49, 0.94]1 study · 765 participantsModerate