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