Hong‐yun 2007.
Methods | Randomized | |
Participants | Adults (no age mentioned) Hospitalized CAP | |
Interventions | Atypical: iv gatifloxacin (400 mg) Non‐atypical: iv cefuroxime (2 G) | |
Outcomes | Success: clinical and bacteriological Adverse reactions |
|
Notes | Data extracted from abstract, no correspondence | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | High risk | Not described |
Allocation concealment (selection bias) | Unclear risk | Not described |
Incomplete outcome data (attrition bias) Mortality | Unclear risk | Not described |
Incomplete outcome data (attrition bias) Failure | Unclear risk | Not described |
Selective reporting (reporting bias) | Unclear risk | Not described |
Other bias | Unclear risk | Not enough data |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not enough data |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Not enough data |