Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Noyola et al, 2000, USA | 1530 pts, age 1-19 y during two consecutive confirmed influenza seasons at an urban children’s hospital | Retrospective case control study. RIT used to detect influenza A virus. RIT +ve as case control group and -ve as control group. Blood cultures used to confirm the results | Antibiotic prescription,. Duration of antibiotic treatment | In admitted pts: RIT +ve 43% vs 64% RIT -ve. p-0.04 Discharged pts RIT +ve 20% vs 53% RIT -ve p=0.04. RIT +ve 3.5 vs 5.4 days -ve p=0.03 | Retrospective study Relied on electronic database for identifying pts who had RIT, then their medical records, so possible selection bias. Underlying diseases and their severity influencing the investigations not explained. |
Bonner et al, 2003, USA | 391 pts 2 month to 21 years during one confirmed influenza season at tertiary care urban hospital. Data/results for the sub group of 241 pts aged 2-36 months analysed and available as well. | Prospective Randomised Control Trial. One group, for which physicians were aware (PA) of RIT results and the other group for which they were unaware (PUA) of results for influenza A and B | CBC requesting | PA 0% vs 13% PUA (p<0.001) | Single influenza season results. Results not confirmed by blood cultures |
Blood cultures | PA 0% vs 11% PUA (p<0.001) | ||||
CXR | PA 7% vs 26% PUA (p=001) | ||||
Financial costs of investigations | PA $15 vs $92 PUA (p<0.001) | ||||
Antibiotic usage | PA 7% vs 26% PUA (p<0.001) | ||||
Length of emergency department stay | PA 25 vs 49 min PUA (p<0.001) | ||||
Benito-Fernández et al, 2006, USA | 206 pts aged 0-36 months during two confirmed seasons at a tertiary care children’s hospital | Prospective observational study. RIT (influenza A & B) for all febrile pts, grouped by results into RIT +ve and RIT eve groups (all pts <3 months old had RIT whether febrile or not | Blood tests (CBC, CRP, blood cultures) | RIT +ve 33% vs 100% RIT -ve (p <0.01) | No randomisation. No follow up of -ve RIT patients (presumably no follow up of the positives either). No confirmatory tests by viral culture done. |
Urine analysis | RIT +ve 80% vs 100% RIT -ve (p <0.01) | ||||
Lumbar puncture | RIT +ve 1.3% vs 21% RIT -ve (p<0.01) | ||||
CXR | RIT +ve 14% vs 32% RIT -ve (p <0.01) | ||||
Emergency department stay | RIT +ve 116 vs 192 min RIT -ve (p<0.01) | ||||
Observation ward admission | RIT +ve 8.3% vs 21% RIT-ve (p<0.01) | ||||
In-patient admission | RIT +ve 2.3% vs 16.4% RIT -ve (p<0.01) | ||||
Antibiotic treatment | RIT +ve 0% vs 38% RIT -ve (p<0.01) | ||||
Poehling et al, 2006, USA | 486 pts < 5 years during two consecutive influenza seasons at a university hospital paediatric emergency department | Prospective Randomised Control Trial. TG underwent RIT with results available to the clinician. CG had no RIT. Both groups had formal viral cultures or PCR lab testing for influenza. | Any diagnostic test done | TG 39% vs 52% CT p=0.03 | No follow up. Convenience sample. |
CXR | TG 23% vs 33% CT p=0.06 | ||||
Blood count/cultures | TG 10% vs 18% CT p=0.05 | ||||
Iyer et al, 2006, USA | 700 pts 2-24 months during 2 influenza seasons at an urban tertiary care hospital | Prospective Quasi- Randomised Control Trial Intervention group (POCT) underwent RIT for influenza with available results. CG (ST): no RIT results available | Blood cultures | Reduction in POCT by 22.6% p=0.05 | Convenience sample. Pneumococcus immunisation status & its effects on pts not considered. No follow-up |
Urine analysis | OR 0.45 vs 0.67 p=0.002 | ||||
Urine culture | OR 0.46 vs 0.67 p=0.005 | ||||
Abanses et al, 2006, USA | 1007 patients aged 3-36 months during one influenza season at an urban children's hospital emergency department | Prospective randomized controlled trial. Febrile patients were randomised at triage into an intervention group (TT) having RIT for influenza A and B with available results or a non-intervention group (SP) for which the physician decided the need for further testing. | RSV testing | TT 7% vs 18% SP (RR 2.5) | Failure of randomisation in TT group due to their non-adherence to their devised protocol so taken as convenience sample. Single influenza season results. |
CXR | TT 20% vs 26% SP (RR 1.3) | ||||
CBC | TT 2.5% vs 29% SP (RR 12) | ||||
Blood cultures | TT 2.5% vs 31% SP (RR 5.7) | ||||
Urine analysis | TT 4.9% vs 28% SP (RR 9.2) | ||||
Emergency department length of stay | TT 156 vs 195 min SP | ||||
Total medical cost per patient | TT $393 vs $666 SP | ||||
Sharma et al, 2002, USA | 72 patients aged 2-24 months during two consecutive influenza seasons at an urban children's hospital emergency department. | Retrospective observational study. Influenza A virus detection by RIT in two groups: those who had RIT results available (early detection; ED) and those who had diagnosis after discharge (late detection; LD). | Ceftriaxone use | ED 2% vs 24% LD p=0.006 | Selection bias. Small sample size. Retrospective study relying on electronic database, so some patients could be missed if difference in tests and conditions. Physician's discretion to do RIT. |
CBC performed | ED 17% vs 44% LD p=0.02 | ||||
Urine analysis performed | ED 2% vs 24% LD p=0.006 |