Poropat 2015.
Methods | Randomised clinical trial | |
Participants | Country: Croatia Number randomised: 43 Postrandomisation dropouts: 0 (0%) Revised sample size: 43 Average age: not stated Women: not stated Acute interstitial oedematous pancreatitis: not stated Necrotising pancreatitis: not stated Mild pancreatitis: not stated Moderate pancreatitis: not stated Severe pancreatitis: not stated Persistent organ failure: not stated Infected pancreatitis: not stated Inclusion criteria
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Interventions | Group 1: antibiotics (n = 23): imipenem 500 mg IV 3 times daily for 10 days Group 2: no intervention (n = 24) | |
Outcomes | Mortality, serious adverse events, adverse events, infected pancreatic necrosis, and organ failure Follow‐up: not stated (probably until discharge) |
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Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Comment: this information was not available. |
Allocation concealment (selection bias) | Unclear risk | Comment: this information was not available. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Comment: this information was not available. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Comment: this information was not available. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Comment: there were no postrandomisation dropouts. |
Selective reporting (reporting bias) | Low risk | Comment: mortality and adverse events were reported. |
For profit‐bias | Unclear risk | Comment: this information was not available. |
Other bias | Low risk | Comment: no other risk of bias |