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Physical fitness training for stroke patients (Review) - Update Software

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Case fatality<br />

Number of deaths was reported in four trials.<br />

In the Katz-Leurer 2003 trial one participant had died in the cardiorespiratory<br />

<strong>training</strong> group (1/42) compared with one participant<br />

in the control group (1/39) at the end of the scheduled follow-up<br />

period (Analysis 2.1). Fewer deaths were observed in the<br />

time between baseline assessment and the end of the intervention<br />

in the intensive mixed <strong>training</strong> group of the Langhammer 2007<br />

trial (1/32 ) than in the usual rehabilitation group (4/35) (Analysis<br />

5.1). Three trials reported the number of deaths that occurred<br />

between end of intervention and end of the scheduled follow-up<br />

period in <strong>stroke</strong> survivors receiving mixed <strong>training</strong> (Cooke 2010;<br />

Duncan 2003; Langhammer 2007). Mixed <strong>training</strong> in <strong>stroke</strong> survivors<br />

compared with the usual rehabilitation programme did not<br />

increase the probability of death after completion of the <strong>training</strong><br />

intervention (OR 0.27, 95% CI 0.05 to 1.37) (Analysis 6.1).<br />

Death or dependence<br />

The composite outcome of death or dependence was not reported<br />

by any trial.<br />

Disability<br />

Cardiorespiratory <strong>training</strong><br />

Few trials of cardiorespiratory <strong>training</strong> shared the same outcome<br />

measures and there<strong>for</strong>e few data were available <strong>for</strong> meta-analyses.<br />

Two trials with a total of 110 participants (Cuviello-Palmer 1988;<br />

Katz-Leurer 2003) used the Functional Independence Measure<br />

(FIM) to assess disability outcomes after usual care and found no<br />

significant difference between <strong>fitness</strong> <strong>training</strong> and standard rehabilitation<br />

at the end of the intervention (SMD 0.17, 95% CI -<br />

0.29 to 0.63) (Analysis 1.1). Similarly, Bateman 2001 did not find<br />

any improvement in the FIM score after <strong>training</strong>, at the end of<br />

the intervention during usual care (SMD 0.23, 95% CI -0.32 to<br />

0.78) (Analysis 1.1). In the Bateman 2001 trial, however, the procedures<br />

<strong>for</strong> obtaining FIM data at end of intervention were not<br />

uni<strong>for</strong>m and there was a high proportion of missing data (38%).<br />

Mudge 2009 assessed participants after usual care using the <strong>Physical</strong><br />

Activity and Disability scale but found that cardiorespiratory<br />

<strong>training</strong> was not significantly better than a control ’non-exercise’<br />

intervention at the end of the <strong>training</strong> period (MD 19.90, 95%<br />

CI -17.58 to 57.38) (Analysis 2.4), but confidence intervals were<br />

wide.<br />

At the end of follow-up three individual trials used different scales<br />

(Rivermead Mobility Index; Nottingham Extended ADLs; <strong>Physical</strong><br />

Activity and Disability Scale; Frenchay Activities Index) to assess<br />

functional activities and disability outcomes during (Bateman<br />

2001) and after usual care (Katz-Leurer 2003; Mudge 2009). We<br />

were not able to combine the results as the functional scales included<br />

in these trials cover slightly different domains and because<br />

one trial (Bateman 2001), which had a considerable proportion<br />

of missing data (21%), reported results from more than one single<br />

scale. No <strong>training</strong> effect was evident in each individual analysis.<br />

Resistance <strong>training</strong><br />

Ouellette 2004 assessed participants’ functional abilities and disability<br />

outcomes by means of the Late Life Function and Disability<br />

Instrument (LLFD). This scale, however, has not been validated<br />

in <strong>stroke</strong> survivors and we have not included it in the analyses.<br />

The remaining trials either did not measure disability outcomes or<br />

used subscales or specific dimensions of existing functional scales<br />

(Inaba 1973; Winstein 2004), which we did not deem suitable <strong>for</strong><br />

inclusion.<br />

Mixed <strong>training</strong><br />

Four trials (Duncan 1998; Duncan 2003; Langhammer 2007;<br />

Mead 2007) assessed the effects of mixed <strong>training</strong> at the end of<br />

the treatment phase or at follow-up using a variety of scales which<br />

measured disability outcomes (Lawton IADL, Barthel Index, FIM,<br />

Notthingham Extended ADLs, Rivermead Mobility Index, Stroke<br />

Impact Scale). We were able to pool only Lawton IADL results<br />

and Barthel Index and FIM scores in combination. There were no<br />

significant <strong>training</strong> effects at the end of intervention (Analysis 5.2;<br />

Analysis 5.4) or at follow-up (Analysis 6.3). It is worth noting that<br />

two trials included in the analyses (Duncan 1998; Duncan 2003)<br />

were confounded by increased <strong>training</strong> time and one trial by the<br />

fact that the Barthel Index scores reached ceiling level in five out of<br />

20 participants at baseline and 10 out of 20 participants at followup<br />

(Duncan 1998).<br />

Results of the remaining rating scales, reported by individual trials,<br />

did not show any significant effect of mixed <strong>training</strong> at either the<br />

end of intervention or at follow-up.<br />

Effect of <strong>training</strong> on secondary outcomes<br />

Adverse events<br />

<strong>Physical</strong> <strong>fitness</strong> <strong>training</strong> <strong>for</strong> <strong>stroke</strong> <strong>patients</strong> (<strong>Review</strong>)<br />

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

Adverse events were not reported systematically in the included<br />

trials.<br />

Mead 2007 reported 11 falls in eight of 32 <strong>patients</strong> in the exercise<br />

group and five falls in four of 34 <strong>patients</strong> in the control group (P<br />

= ns). None of these falls occurred within <strong>training</strong> sessions.<br />

Eight of the 32 included trials provided some comments on the<br />

patient tolerance of the <strong>training</strong> programme and did not report<br />

any adverse events such as falls, fractures, or injuries arising during<br />

the intervention.<br />

Considering all included trials, four participants (three participants<br />

receiving the <strong>training</strong> intervention and one control) were<br />

reported to have suffered a cerebrovascular event between baseline<br />

and the end of the <strong>training</strong> intervention.<br />

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