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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.
1,080 questions in 109 reviews · Acute Respiratory Infections
current versionsNo 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.
| Question | Effect | Evidence | Status / 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 extracted | 1 study · 47 participants | Low |
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 extracted | 1 study · 47 participants | Low |
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 extracted | NR | No 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 participants | Low |
Heliox vs placebo or no treatment Duration of hospitalisation · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs placebo or no treatment Proportion of children intubated · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs placebo or no treatment Duration of intubation · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No 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 participants | Low |
Heliox vs placebo or no treatment Adverse events · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs oxygen 30% Change in respiratory rate at 20 minutes · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | 1 study · 15 participants | Low |
Heliox vs oxygen 30% Change in heart rate at 20 minutes · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | 1 study · 15 participants | Low |
Heliox vs oxygen 30% Proportion of children hospitalised · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs oxygen 30% Duration of hospitalisation · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs oxygen 30% Proportion of children intubated · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No studies |
Heliox vs oxygen 30% Duration of intubation · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No 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 extracted | NR | No studies |
Heliox vs oxygen 30% Adverse events · children with croup Heliox for croup in children (2021) · Cochrane | no estimate extracted | NR | No 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 participants | Moderate |
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 participants | Low |
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 participants | Low |
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 participants | Low |
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 participants | Very 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 extracted | NR | No 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 extracted | NR | No 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 participants | Very 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 extracted | NR | Very 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 extracted | NR | No 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 extracted | NR | No 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 extracted | NR | No 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 participants | Low |
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 participants | Low |
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 participants | Low |
Intervention NR Adverse events during the · children with acute bacterial meningitis Non‐corticosteroid adjuvant therapies for acute bacterial meningitis (2021) · Cochrane | no estimate extracted | 3 studies · 1274 participants | Very 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 participants | Low |
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 participants | Low |
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 participants | Low |
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 extracted | 2 studies · 810 participants | Moderate |
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 extracted | 2 studies · 810 participants | Moderate |
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 extracted | 2 studies · 810 participants | Moderate |
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 participants | Moderate |
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 participants | Moderate |
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 participants | Moderate |
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 extracted | 1 study · 759 participants | Moderate |
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 participants | High |
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 participants | Moderate |
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 participants | Moderate |
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 participants | Moderate |
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 participants | Low |
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 participants | High |
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 participants | Very low |