| Methods |
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| Participants |
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| Interventions | RRT modality
Treatment group
Co‐interventions
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| Outcomes | Primary outcome
Secondary outcome
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| Notes |
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| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Insufficient information to permit judgement; Quote: "All patients were divided randomly into two groups" |
| Allocation concealment (selection bias) | Unclear risk | Insufficient information to permit judgement |
| Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Insufficient information to permit judgement |
| Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcome measurement was unlikely to be influenced by lack of blinding (for kidney recovery was unclear risk but for death was low risk) |
| Incomplete outcome data (attrition bias) All outcomes | High risk | > 20% of included patients not reported |
| Selective reporting (reporting bias) | Low risk | Published report included survival and recovery of kidney function |
| Other bias | Unclear risk | Insufficient information to permit judgement |
AIDS ‐ acquired immune deficiency syndrome; AKI ‐ acute kidney injury; BUN ‐ blood urea nitrogen; CKD ‐ chronic kidney disease; CrCl ‐ creatinine clearance; CRRT ‐ continuous renal replacement therapy; CVVH ‐ continuous venovenous haemofiltration; CVVHDF ‐ continuous venovenous haemodiafiltration; (e)GFR ‐ (estimated) glomerular filtration rate; GN ‐ glomerulonephritis; HF ‐ haemofiltration; ICU ‐ intensive care unit; IHD intermittent haemodialysis; M/F ‐ male/female; NGAL ‐ plasma neutrophil gelatinase‐associated lipocalin; RCT ‐ randomised controlled trial; RRT ‐ renal replacement therapy; SCr ‐ serum creatinine; SD ‐ standard deviation; UF ‐ ultrafiltration