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  5. Module 1 - Spinal Cord Injury and Seating
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Module 1 - Spinal Cord Injury and Seating

An overview of spinal cord injuries

It is estimated that the prevalent population of people in Australia with a spinal cord injury (SCI) is approximately 9,000-10,000 people. SCI is caused by both trauma and by disease processes (non-traumatic SCI) such as spinal cord infection and infarction. Typically people who acquire a traumatic SCI are young and male, whilst non-traumatic SCIs occur more often in later life and with a more even gender split.

Persisting SCI impacts on every aspect of a person's life: health status, physiological, active community participation, psychological, social, reproductive, economic, employment, educational and recreation.

An SCI will affect people in variable ways, depending on the level of the spinal cord lesion and the completeness of the injury. Generally all people with SCI have some degree of motor or sensory loss and a disrupted autonomic nervous system. This has a profound effect on a person's health, function and physiology. The most important factors predicting functional outcome are the neurological level and degree of completeness of spinal cord lesion. However, a range of other medical and non-medical factors can influence outcome, including age, body shape and weight, associated injuries, pre-existing disease, spasticity and contractures, living arrangements and family support, level of education and financial resources. As the neurological level becomes lower, functional independence should increase. Functional goals are based on sequential organisation of spinal segments and capacity of spared muscle groups to perform specific activities of daily living, qualified by other factors such as those listed above.

When working with clients to establish wheeled mobility goals, it is essential to understand the individual impact of a person's SCI and other health issues associated with co-morbid conditions and with ageing. Pre-morbid lifestyle and interests, personality characteristics and coping style, degree of social support and economic circumstances will all be important factors influencing adjustment and eventual outcome. Within the learning modules is information about establishing and assessing a client's health status.

For people who require wheeled mobility, the effective prescription and use of a wheelchair enables and empowers them to participate in life and interact in their community. Many clients with a spinal cord injury will spend most of their waking hours in their wheelchair; each client is unique and has highly individual and, over time, changing needs. It is no longer acceptable, if it every was, to prescribe a wheelchair and seating system without careful consideration of the client's goals and postural, pressure, functional, safety and environmental needs.

A correctly prescribed wheelchair and seating system will optimise function, address the impact of environmental factors, correct and prevent postural and pressure issues and meet a client's community participation needs. The short and long term consequences of an incorrectly prescribed system can be profound, as are the safety issues associated with wheelchair use. It is equally important to consider how a client perceives their wheelchair, and the psychological issues of self- and societal perception of wheelchair use when working with the client in setting goals.

Further information about SCI is available in the resources section of this site. It is strongly recommended that health professionals gain a good understanding of the risk factors for developing a pressure ulcer, the impact this condition has on clients, how to reduce risks and implement treatment options.

Spinal Cord Injury - A Consumer's Perspective

The following account describes the changing nature of seating and wheeled mobility requirements over time for a person living with SCI. Medical complications and ageing have further impacted on this man's functional, postural and pressure care needs. It is a high priority for him to be safe and properly positioned in his power wheelchair so he can drive it and use other assistive technology in his environment. He recognises the importance of effective communication and trust between himself and the therapist to achieve positive outcomes. This perspective concurs with the client-centred approach and the need for the systematic assessment and intervention processes described in the study modules.

We would like to thank David for sharing his perspective with us.

"My name is David. I am 51 years old and sustained a spinal injury in 1977 in a sporting-related accident. At the time I was 19 and thought I was 'bullet proof' & that nothing could hurt me permanently.

My accident was a big awakening and after 12 weeks of acute care for my body to adjust, then I started to realise that injury was nothing like a broken leg and that this paralysis was permanent.

Initially, my level of disability was classified as a "C5-6" complete quadriplegic. But in 1993 I had a fall in my wheelchair which caused further trauma to my neck and a fracture of my hip that did not heal well, resulting in poor posture.  To complicate things further, I then developed a spinal cord syrinx which caused a deterioration of my injury to a C4 quadriplegic. I have had to adapt my life around the continuing changes to my body shape over the years which in turn have affected my sitting arrangement in the wheelchair.

With my original accident in 1977, it didn't take too long for me to realise how important the health professionals and clinicians would be in my rehabilitation and ongoing care. Associated with this was the ongoing role of the seating clinic and how it would require a long term relationship for advice and guidance with regards to caring for my skin in particular.

The seating clinicians helped overcome problems with pressure sores and this in turn gave me confidence of not having to worry about spending long periods of time in my chair and the consequences of a pressure ulcer, such as long periods in bed for pressure management and not being able to work.

When being assessed by clinicians, I found it important that my thoughts and suggestions were taken into account. Having confidence in the staff, especially on a professional level, means a lot to me because there were times when I have had to trust their recommendations and professional judgement.

The time spent working through seating and wheelchair issues over the years has reinforced how important it is to be treated as an individual. I used mouth sticks to access my phone and computer on my wheelchair tray. Small things make such a difference especially when it comes to pressure care and sitting posture that allows me to do things in my home and my work."

This web page is managed and authorised by Greater Metropolitan Clinical Taskforce. Last updated: 16 March, 2009

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