Ikuta 2004 (A).
| Study characteristics | ||
| Methods | Randomised controlled trial Run‐in period: April 2001‐February 2002 Published 2004 Number of centres and location: not specified |
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| Participants | Twenty‐three participants were assessed in part A of this study. Inclusion criteria: first‐time elective CABG Exclusion criteria: previous cardiac surgery, renal or liver dysfunction, and preoperative coagulopathy |
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| Interventions | Intervention: Heparin‐coated CPB circuit Control: Uncoated circuit. |
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| Outcomes |
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| Notes | ||
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | Forty‐five patients undergoing CABG were randomly assigned to PMEA‐coated (group P, n = 15), heparin‐coated (group H, n = 15), and noncoated (group N, n = 15) circuit groups. |
| Allocation concealment (selection bias) | Unclear risk | No details given |
| Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | No details given |
| Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No details given |
| Incomplete outcome data (attrition bias) All outcomes | Low risk | All data included in analysis |
| Selective reporting (reporting bias) | Low risk | No reporting bias apparent |
| Other bias | Unclear risk | Not clearly stated |