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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)

1,080 questions in 109 reviews · Acute Respiratory Infections

current versions
No studies 132 · 12.2%Ungraded 90 · 8.3%Very low 169 · 15.6%Low 306 · 28.3%Moderate 287 · 26.6%High 96 · 8.9%

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
Heliox vs placebo or no treatment
Change in croup score at 60 minutes · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extracted1 study · 47 participantsLow
Heliox vs placebo or no treatment
Change in respiratory rate at 60 minutes · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extracted1 study · 47 participantsLow
Heliox vs placebo or no treatment
Change in heart rate at 60 minutes · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs placebo or no treatment
Proportion of children hospitalised · children with croup
Heliox for croup in children (2021) · Cochrane
OR 0.46 [0.04, 5.41]1 study · 47 participantsLow
Heliox vs placebo or no treatment
Duration of hospitalisation · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs placebo or no treatment
Proportion of children intubated · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs placebo or no treatment
Duration of intubation · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs placebo or no treatment
Proportion of children re‐presenting for medical care for ongoing croup symptoms (return to care) · children with croup
Heliox for croup in children (2021) · Cochrane
OR 0.95 [0.12, 7.41]1 study · 47 participantsLow
Heliox vs placebo or no treatment
Adverse events · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Change in respiratory rate at 20 minutes · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extracted1 study · 15 participantsLow
Heliox vs oxygen 30%
Change in heart rate at 20 minutes · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extracted1 study · 15 participantsLow
Heliox vs oxygen 30%
Proportion of children hospitalised · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Duration of hospitalisation · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Proportion of children intubated · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Duration of intubation · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Proportion of children re‐presenting for medical care for ongoing croup symptoms · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Heliox vs oxygen 30%
Adverse events · children with croup
Heliox for croup in children (2021) · Cochrane
no estimate extractedNRNo studies
Antibiotic therapy vs placebo compared to placebo
Clinical cure (symptomatic and clinical recovery by the end of treatment) · children, aged 2 to 59 months, with WHO‐defined non‐severe pneumonia and wheeze
Antibiotic therapy versus no antibiotic therapy for children aged 2 to 59 months with WHO‐defined non‐severe… (2021) · Cochrane
RR 1.02 [0.96, 1.08]1 study · 456 participantsModerate
Antibiotic therapy vs placebo compared to placebo
Treatment failure (development of more severe signs and symptoms by the end of treatment) · children, aged 2 to 59 months, with WHO‐defined non‐severe pneumonia and wheeze
Antibiotic therapy versus no antibiotic therapy for children aged 2 to 59 months with WHO‐defined non‐severe… (2021) · Cochrane
RR 0.8 [0.68, 0.94]3 studies · 3222 participantsLow
Antibiotic therapy vs placebo compared to placebo
Relapse (children who were 'cured' but developed symptoms within 14‐day · children, aged 2 to 59 months, with WHO‐defined non‐severe pneumonia and wheeze
Antibiotic therapy versus no antibiotic therapy for children aged 2 to 59 months with WHO‐defined non‐severe… (2021) · Cochrane
RR 1 [0.74, 1.34]3 studies · 2795 participantsLow
Antibiotic therapy vs placebo compared to placebo
Treatment harms (adverse events or side effects associated with antibiotic therapy within 14‐day · children, aged 2 to 59 months, with WHO‐defined non‐severe pneumonia and wheeze
Antibiotic therapy versus no antibiotic therapy for children aged 2 to 59 months with WHO‐defined non‐severe… (2021) · Cochrane
RR 0.81 [0.6, 1.09]3 studies · 3253 participantsLow
Vitamin C vs placebo
Incidence of pneumonia Defined as patient admitted to hospital with a diagnosis of pneumonia Dose: 2 g per day · school‐aged children (6 to 15 years) and marine corps recruits (mean age 18.5 years)
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
RR 0.15 [0.02, 1.2]1 study · 674 participantsVery low
Vitamin C vs placebo
Prevalance of pneumonia · school‐aged children (6 to 15 years) and marine corps recruits (mean age 18.5 years)
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRNo studies
Vitamin C vs placebo
Mortality due to pneumonia · school‐aged children (6 to 15 years) and marine corps recruits (mean age 18.5 years)
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRNo studies
Vitamin C vs placebo
Adverse effects (urticaria) Defined as participants reporting urticaria (hives) Dose: 2 g per day · school‐aged children (6 to 15 years) and marine corps recruits (mean age 18.5 years)
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
RR 3.11 [0.13, 76.03]1 study · 674 participantsVery low
Vitamin C vs placebo
Duration of illness Defined as number of days until illness improved Dose: 200 mg daily · children under 5 years of age
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRVery low
Vitamin C vs placebo
Clinical cure rate · children under 5 years of age
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRNo studies
Vitamin C vs placebo
Mortality due to pneumonia · children under 5 years of age
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRNo studies
Vitamin C vs placebo
Adverse effects · children under 5 years of age
Vitamin C supplementation for prevention and treatment of pneumonia (2021) · Cochrane
no estimate extractedNRNo studies
Intervention NR
Mortality during the · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 0.94 [0.81, 1.09]3 studies · 1274 participantsLow
Intervention NR
Any hearing loss defined as 40 dB or more not detected by the better ear during the · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 1.04 [0.8, 1.34]2 studies · 901 participantsLow
Intervention NR
Any neurological sequelae other than hearing loss defined as health consequences of the infection that involve the central nervous system during the · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 1.56 [0.98, 2.5]3 studies · 1274 participantsLow
Intervention NR
Adverse events during the · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
no estimate extracted3 studies · 1274 participantsVery low
Intervention NR
Severe hearing loss defined as a threshold of 60 dB or more in the better ear or requiring bilateral hearing aid during the · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 0.96 [0.67, 1.36]2 studies · 901 participantsLow
Intervention NR
Short‐term neurological sequelae other than hearing loss defined as sequelae present up to 6 weeks after hospital discharge · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 1.99 [1.4, 2.81]2 studies · 1096 participantsLow
Intervention NR
Long‐term neurological sequelae other than hearing loss defined as sequelae present between 6 weeks after hospital discharge and the last time point reported in the study · children with acute bacterial meningitis
Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane
RR 2.32 [1.34, 4.04]2 studies · 901 participantsLow
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Length of hospital stay ‐ actual · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
no estimate extracted2 studies · 810 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Length of hospital stay (theoretical) · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
no estimate extracted2 studies · 810 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Duration of time requiring non‐oral fluid therapy (time to resume full oral feeding) · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
no estimate extracted2 studies · 810 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Successful insertion of intravenous fluid/enteral tube fluid at first attempt · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
RR 1.52 [1.36, 1.69]1 study · 617 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Change in modality of fluid therapy · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
RR 0.52 [0.38, 0.71]1 study · 759 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Local complications (overall): IV line bruising, soreness, infection, epistaxis, nasal trauma, others · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
RR 0.65 [0.42, 1]1 study · 678 participantsModerate
Summary of findings table ‐ Enteral tube feeding vs intravenous fluids
Parental satisfaction · health problem or population
Parenteral versus enteral fluid therapy for children hospitalised with bronchiolitis (2021) · Cochrane
no estimate extracted1 study · 759 participantsModerate
Palivizumab vs placebo, no intervention or standard care
Hospitalisation due to RSV infection · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 0.44 [0.3, 0.64]5 studies · 3343 participantsHigh
Palivizumab vs placebo, no intervention or standard care
Mortality · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 0.69 [0.42, 1.15]5 studies · 3343 participantsModerate
Palivizumab vs placebo, no intervention or standard care
Adverse events · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 1.09 [0.85, 1.39]3 studies · 2831 participantsModerate
Palivizumab vs placebo, no intervention or standard care
Hospitalisation due to respiratory‐related illness · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 0.78 [0.62, 0.97]5 studies · 3343 participantsModerate
Palivizumab vs placebo, no intervention or standard care
RSV infection · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 0.33 [0.2, 0.55]3 studies · 554 participantsLow
Palivizumab vs placebo, no intervention or standard care
Number of wheezing days · children (0 to 24 months)
Palivizumab for preventing severe respiratory syncytial virus (RSV) infection in children (2021) · Cochrane
RR 0.39 [0.35, 0.44]1 study · 429 participantsHigh
Cefepime vs ceftazidime
All‐cause mortality Maximum · neonates and children with hospital‐acquired pneumonia
Antibiotics for hospital‐acquired pneumonia in neonates and children (2021) · Cochrane
RR 0.14 [0.01, 2.55]1 study · 30 participantsVery low