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Risk of bias in included studies<br />

The studies identified were heterogeneous in quality (Figure 3).<br />

All employed some method of individual patient randomisation,<br />

however reporting of key issues such as allocation concealment<br />

varied. Outcome <strong>assessment</strong> was seldom blinded. This is less significant<br />

<strong>for</strong> hard outcomes such as death or institutionalisation,<br />

but becomes more important <strong>for</strong> outcomes such as activities of<br />

daily living or cognition.<br />

Figure 3. ’Risk of bias’ graph: review authors’ judgements about each risk of bias item presented as<br />

percentages across all included studies.<br />

We extracted data from published in<strong>for</strong>mation only. We did not<br />

contact trialists <strong>for</strong> additional data. Reporting of outcomes was<br />

variable. Different reporting mechanisms were used <strong>for</strong> description<br />

of some data (<strong>for</strong> example, activities of daily living, which could be<br />

reported as a categorical or variable outcome). For this reason, we<br />

did not combine some outcomes <strong>for</strong> meta-analysis. Data quality<br />

was also variable with some trialists reporting data with standard<br />

deviations, some reporting interquartile ranges and some reporting<br />

standard errors.<br />

We noted attrition in some trials (Collard 1985; Harris 1991) <strong>for</strong><br />

functional outcomes. In some cases (Collard 1985) this exceeded<br />

25%. We felt that the possibility of attrition bias might be introduced<br />

<strong>for</strong> outcomes that could be unduly influenced by an un-<br />

<strong>Comprehensive</strong> <strong>geriatric</strong> <strong>assessment</strong> <strong>for</strong> <strong>older</strong> <strong>adults</strong> <strong>admitted</strong> <strong>to</strong> hospital (Review)<br />

Copyright © 2011 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.<br />

blinded trial design. Results from this trial have been included <strong>for</strong><br />

the outcome of dependence, however the results must be interpreted<br />

with some caution.<br />

Effects of interventions<br />

Comparison 1: <strong>Comprehensive</strong> <strong>geriatric</strong> <strong>assessment</strong><br />

(CGA) versus usual care<br />

The first primary outcome summarises data from 22 trials of<br />

10,315 participants comparing CGA with usual care (e.g. on a<br />

general medical ward). We analysed this using the main subgrouping<br />

of CGA wards and CGA teams versus usual care. Subgroup<br />

8

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