Methods | Randomised trial | |
Participants | 1632 participants (858 intervention, 774 control) Mean age: 81 years Male:female proportion: 33.3% male Inclusion criteria: patients ≥ 70 years of age admitted to general medical service Exclusion criteria: admitted to intensive care units/other speciality units, electively; length of stay < 2 days |
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Interventions |
Intervention team members: attending geriatrician, trained nursing,
social workers, physiotherapists Intervention team organisation: comprehensive assessment, at least weekly MDT meetings, assessment tools, protocols, ward environment, outpatient follow‐up Control: general inpatient unit, where younger and older patients resided together |
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Outcomes | Alive and in own home Death Re‐admission Activities of daily living Length of stay Resource use Trial conclusions: resulted in reduced length of stay and in cost savings |
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Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated random numbers |
Allocation concealment (selection bias) | Low risk | Sequentially numbered opaque sealed envelopes |
Blinding of participants and personnel (performance bias) | High risk | Blinding of participants not possible, blinding of services not possible |
Blinding of outcome assessment (detection bias) for objective outcome measures | Low risk | Objective outcome measures (e.g. living at home) unlikely to be influenced by lack of blinding |
Blinding of outcome assessment (detection bias) for subjective outcome measures | Unclear risk | No details of outcome assessors given |
Incomplete outcome data (attrition bias) All outcomes | Low risk | No missing data reported |
Selective reporting (reporting bias) | Unclear risk | No protocol available |
Other bias | Low risk | Little evidence of contamination of control group |