national-clinical-guidelines-for-stroke-fourth-edition
national-clinical-guidelines-for-stroke-fourth-edition
national-clinical-guidelines-for-stroke-fourth-edition
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● where appropriate refer the person with <strong>stroke</strong> on to community organisations<br />
(statutory and non-statutory) that can support the patient in fulfilling their wanted<br />
roles.<br />
B Local commissioners should ensure that community integration and participation <strong>for</strong><br />
disabled people is facilitated through:<br />
7.3.2 Sources<br />
● ensuring a suitable community transport system that is accessible and available<br />
● organising and supporting venues <strong>for</strong> social and leisure activities able to<br />
accommodate disabled people, especially people with communication and<br />
cognitive problems<br />
● organising and supporting social networks <strong>for</strong> disabled people (eg through<br />
voluntary groups)<br />
● making sure appropriate <strong>stroke</strong> specialist and generic voluntary sector services and<br />
peer support (eg communication support groups, <strong>stroke</strong> clubs, self-help groups<br />
and communication partner schemes) are available and that in<strong>for</strong>mation and<br />
signposting to them are given.<br />
A–B Consensus; National Stroke Strategy quality markers 13 and 15<br />
7.4 Support (practical and emotional)<br />
Many people need considerable care from others after <strong>stroke</strong>, both <strong>for</strong> personal<br />
activities such as washing and dressing, and more so <strong>for</strong> domestic and community<br />
activities. Provision of this support is rarely the responsibility of the healthcare<br />
system, but healthcare teams do have a responsibility to identify and specify the<br />
support needs of each patient, and to help organise this support from the responsible<br />
organisations.<br />
Evidence to recommendations<br />
There is evidence of unmet need in nearly 50% of <strong>stroke</strong> survivors, between 1 and 5 years<br />
after <strong>stroke</strong>. This includes problems related to mobility, falls, fatigue, pain, emotion,<br />
memory, reading and concentration (McKevitt et al 2011). Services should ensure that<br />
mechanisms are in place to identify and address such issues. The research evidence to<br />
in<strong>for</strong>m service development and delivery in this area is limited. One approach has been<br />
to employ and train healthcare workers or volunteers (eg a <strong>stroke</strong> liaison worker) to<br />
provide education and social support (including counselling) and liaison with services<br />
<strong>for</strong> people with <strong>stroke</strong> and carers. A meta-analysis of trials of such interventions reported<br />
that these were associated with significant reductions in disability and death in patients<br />
with mild to moderate disability (Ellis et al 2010). There is no trial evidence that they<br />
improve subjective health status or activities of daily living.<br />
7.4.1 Recommendations<br />
7 Long-term management<br />
A Patients and their carers should have their individual practical and emotional support<br />
needs identified:<br />
© Royal College of Physicians 2012 127