05.03.2013 Views

national-clinical-guidelines-for-stroke-fourth-edition

national-clinical-guidelines-for-stroke-fourth-edition

national-clinical-guidelines-for-stroke-fourth-edition

SHOW MORE
SHOW LESS

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

● 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

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!