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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
Selexipag vs placebo
Mortality · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted2 studies · 1199 participantsModerate
Selexipag vs placebo
mPAP the higher the mPAP, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted1 study · 43 participantsModerate
Selexipag vs placebo
PVR (the higher the PVR, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted1 study · 43 participantsModerate
Selexipag vs placebo
Cardiac index (the lower the cardiac index, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted1 study · 43 participantsModerate
Selexipag vs placebo
RAP (the lower the RAP, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted1 study · 43 participantsModerate
Selexipag vs placebo
Dyspnoea (lower scores indicates more severe breathlessness) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted1 study · 43 participantsModerate
Selexipag vs placebo
Headache+ · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted2 studies · 1199 participantsHigh
Prostacyclin vs control
6MWD · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted13 studies · 2283 participantsLow
Prostacyclin vs control
Mortality · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
OR 0.6 [0.38, 0.94]15 studies · 2554 participantsModerate
Prostacyclin vs control
mPAP (the higher the mPAP, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted8 studies · 1132 participantsLow
Prostacyclin vs control
PVR (the higher the PVR, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted7 studies · 658 participantsModerate
Prostacyclin vs control
Cardiac index (the lower the cardiac index, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted6 studies · 868 participantsLow
Prostacyclin vs control
RAP (the lower the RAP, the worse the pulmonary hypertension) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted6 studies · 1060 participantsModerate
Prostacyclin vs control
Dyspnoea (lower scores indicates more severe breathlessness) · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted8 studies · 1521 participantsLow
Prostacyclin vs control
Quality of life · pulmonary arterial hypertension
Prostacyclin for pulmonary arterial hypertension (2019) · Cochrane
no estimate extracted3 studies · 271 participantsModerate
Once‐daily LABA/LAMA in a combined inhaler vs placebo
All‐cause mortality (3‐week to 1‐year · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
OR 1.88 [0.81, 4.36]18 studies · 8752 participantsLow
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Serious adverse events (3‐week to 1‐year · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
OR 1.06 [0.88, 1.28]22 studies · 10536 participantsHigh
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Acute exacerbations of COPD (4‐week to 24‐week · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
OR 0.53 [0.36, 0.78]3 studies · 1127 participantsModerate
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Difference vs placebo in adjusted SGRQ score (HRQoL) Scale 0‐100, lower on the scale is better. (12‐week to 1‐year · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
no estimate extracted8 studies · 4952 participantsHigh
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Difference vs placebo in adjusted trough FEV1 at EOT (3‐week to 1‐year · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
no estimate extracted13 studies · 6598 participantsModerate
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Difference vs placebo in adjusted peak FEV1 (3‐week to 6‐month · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
no estimate extracted7 studies · 4188 participantsModerate
Once‐daily LABA/LAMA in a combined inhaler vs placebo
Adverse events (3‐week to 1‐year · Adults with COPD
Once daily long‐acting beta2‐agonists and long‐acting muscarinic antagonists in a combined inhaler versus… (2019) · Cochrane
OR 0.95 [0.86, 1.04]17 studies · 8235 participantsHigh
Macrolide+tetracycline vs macrolide
Quality of life, measured by CRQ (dyspnoea, fatigue, emotional function, and mastery subscales) · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extracted1 study · 187 participantsVery low
Quinolone vs macrolide
All‐cause mortality · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extracted1 study · 50 participantsUngraded
Quinolone vs macrolide
Quality of life Drug resistance/microbial sensitivity Serious adverse events Lung function Hospitalisations Adverse events/side effects Number of participants colonised with P aeruginosa · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extractedNRNo studies
Macrolide vs tetracycline
Number of participants experiencing one or more exacerbations Macrolide versus tetracycline · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
OR 0.44 [0.14, 1.38]1 study · 50 participantsLow
Macrolide vs tetracycline
All‐cause mortality · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extracted1 study · 50 participantsUngraded
Macrolide vs tetracycline
Quality of life Drug resistance/microbial sensitivity Serious adverse events Lung function Hospitalisations Adverse events/side effects Number of participants colonised with P aeruginosa · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extractedNRNo studies
Macrolide+tetracycline vs macrolide
All‐cause serious adverse events 60 weeks (end of study) · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
OR 1 [0.52, 1.93]1 study · 198 participantsVery low
Macrolide+tetracycline vs macrolide
Lung function (trough FEV1) Change from baseline to 12 weeks (end of active treatment) · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extracted1 study · 182 participantsVery low
Macrolide+tetracycline vs macrolide
All‐cause mortality 60 weeks (end of study) · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
OR 1.63 [0.38, 7.02]1 study · 198 participantsVery low
Macrolide+tetracycline vs macrolide
Number of people experiencing one or more exacerbations, Drug resistance/microbial sensitivity (as reported by trialists), including emergence of atypical bacteria, Number of participants colonised with Pseudomonas aeruginosa · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extractedNRNo studies
Quinolone vs tetracycline
Number of participants experiencing one or more exacerbations Quinolone versus tetracycline · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
OR 0.44 [0.14, 1.38]1 study · 50 participantsLow
Quinolone vs tetracycline
All‐cause mortality · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extracted1 study · 50 participantsUngraded
Quinolone vs tetracycline
Quality of life Drug resistance/microbial sensitivity Serious adverse events Lung function Hospitalisations Adverse events/side effects Number of participants colonised with P aeruginosa · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
no estimate extractedNRNo studies
Quinolone vs macrolide
Number of participants experiencing one or more exacerbations Quinolone versus macrolide · chronic obstructive pulmonary disease
Head‐to‐head oral prophylactic antibiotic therapy for chronic obstructive pulmonary disease (2019) · Cochrane
OR 1 [0.32, 3.1]1 study · 50 participantsLow
Speech and language therapy vs healthy lifestyle advice
Health‐related quality of life · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
MD 1.53 [0.21, 2.85]1 study · 71 participantsLow
Speech and language therapy vs healthy lifestyle advice
Serious adverse events · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 75 participantsLow
Speech and language therapy vs healthy lifestyle advice
Objective cough counts (over 24‐hour period) · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 71 participantsLow
Speech and language therapy vs healthy lifestyle advice
Symptoms · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 87 participantsLow
Speech and language therapy vs healthy lifestyle advice
Clinical improvement (as defined by trialists) · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
OR 48.13 [13.53, 171.25]1 study · 87 participantsVery low
Speech and language therapy vs healthy lifestyle advice
Subjective measures of cough (e.g. VAS/numerical cough scale score) · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 71 participantsLow
Speech and language therapy vs healthy lifestyle advice
Cough reflex sensitivity (as measured by cough challenge: capsaicin concentration required to provoke 5 coughs) · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 49 participantsLow
Speech and language therapy vs healthy lifestyle advice
Adverse events · participants with chronic cough
Speech and language therapy for management of chronic cough (2019) · Cochrane
no estimate extracted1 study · 75 participantsLow
Inhaled corticosteroids vs placebo
Lung function (spirometry indices) ‐ FEV1 (in L, end study minus baseline values) · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
no estimate extracted2 studies · 156 participantsLow
Inhaled corticosteroids vs placebo
Number of participants improved · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
OR 0.57 [0.24, 1.34]1 study · 86 participantsLow
Inhaled corticosteroids vs placebo
Lung function (spirometry indices) ‐ FVC (in L, end study minus baseline values) · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
no estimate extracted2 studies · 156 participantsLow
Inhaled corticosteroids vs placebo
Lung function (other indices) ‐ diffusion capacity % predicted (end of study) · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
no estimate extracted1 study · 57 participantsLow
Inhaled corticosteroids vs placebo
Lung function (other indices) ‐ RV % predicted (end of study values) · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
no estimate extracted1 study · 57 participantsLow
Inhaled corticosteroids vs placebo
Lung function (other indices) ‐ TLC % predicted (end of study values) · people with bronchiectasis
Inhaled corticosteroids for bronchiectasis (2018) · Cochrane
no estimate extracted1 study · 57 participantsLow