Blight 1998.
Methods | Randomized controlled trial | |
Participants | 769 ICU patients with a CVC containing crystalloids, PN, lipid or drugs. ICU, Australia | |
Interventions | Administration set changes at 72 or 120 hours | |
Outcomes |
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Notes | Exclusions: CVCs inserted by other institutions Central catheters: 100% PN: mixed (proportion unknown) Loss to follow‐up: 36% | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Adequate random sequence generation method; computer generated |
Allocation concealment (selection bias) | Unclear risk | Not discussed Quote: "Randomised on day 3/5 by an independent person" (abstract) |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Not discussed, not feasible because of research design |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Not discussed, not feasible because of research design |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Minimal information discussed, "independent microbiologist" for primary and secondary outcomes |
Incomplete outcome data (attrition bias) All outcomes | High risk | Large dropout rate resulting around 30% of tips not cultured; 437/1206 The rate of attrition was similar in both groups |
Selective reporting (reporting bias) | Unclear risk | Conference abstract only, never published No pre‐protocol Lumen culture performed but not reported |