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SMASAC Working Group Post Polio Syndrome - Scottish Health On ...

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<strong>Scottish</strong> Medicines and Scientific Advisory Committee <strong>Working</strong> <strong>Group</strong><br />

<strong>Post</strong> <strong>Polio</strong> <strong>Syndrome</strong>/Late Effects of <strong>Polio</strong><br />

Referral to a lymphoedema specialist is advised so self management advice<br />

and support can be given. However, access to services is varied and<br />

lymphoedema clinic provision is not standardised in Scotland.<br />

A course of intensive treatment may be required if the swelling is severe and<br />

persistent, the limb shape is distorted, or the skin is in a poor condition.<br />

Further referral to relevant services such as the vascular specialist may be<br />

indicated for some people.<br />

The lymphoedema needs of people with PPS/LEOP should be kept in mind<br />

by <strong>SMASAC</strong> as part of its current scoping work on the condition.<br />

2.8 Orthotic services<br />

Concern about the availability and standard of orthotic services has been a<br />

key feature of many of the group’s discussions. The SPPN conducted a<br />

review of some of its members’ experiences of orthotic services which<br />

provided anecdotal evidence that these were often less than ideal. This has<br />

been supplemented by personal testimonies from some of the group’s<br />

members and their acquaintances. Similarly, BPF conducted a review of<br />

patient experiences of using the NHS orthotics service in part to inform the<br />

NHS Orthotics Panel and help gather information that could help to improve<br />

the service to BPF members and to orthotics users generally. Specific<br />

objectives were to explore:<br />

• What orthoses are used.<br />

• How the process works for users, in terms of waiting times,<br />

consistency of the team that treats them, etc.<br />

• How users feel the service should be improve.<br />

A summary of the findings of the review is included at Annex E.<br />

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