A spinal cord injury (SCI) is an injury which affects the spinal cord – whether acute and traumatic or the result of degenerative disease. The spinal cord is housed within a canal running through the vertebrae, the bones of the spinal column. As the spinal cord is the conduit for nerve function between the brain and the rest of the body, an injury to the spinal cord affects motor control and sensation, as well as some of the unconscious processes of the autonomic nervous system.

The more severe an injury to the spinal cord, the more function is affected. Where damage to the spinal cord is complete, a person loses all nerve function below the point of injury. This causes total loss of movement and sensation. The higher up the spinal cord the injury occurs, the more of the body is affected, as function between the brain and the point of injury is largely preserved, and function from the point of injury downward is impaired or lost.

Common causes of spinal cord injuries

The causes of spinal cord injuries can either be from traumatic external events, or from intrinsic changes within the body. An external event causing spinal cord injury must be severe enough to cause damage to the spine and spinal cord, which is normally well protected within the vertebral canal.

Road traffic accidents, sports injuries, and falling from a height are potential culprits. As the kind of activities which can cause traumatic spinal injury tend to be those undertaken by a certain demographic, people who suffer traumatic spinal cord injuries tend therefore to be younger and more frequently male compared to the general population.[i] Intrinsic factors causing spinal cord injuries may be degenerative neurological diseases or conditions where body processes cause damage to the spinal cord, such as spinal stenosis or tumours.

Bone density after spinal cord injury

Bone mineral density is the term used to describe how strong our bones are. It refers literally to the density of the tissues that make up our bones. Bones comprise a matrix of an overlapping network of structural supports, made mainly of collagen and calcium.

This framework supports further organic and mineral deposits, mainly calcium which gives the bones their strength. When we have more mineral deposits per area of bone tissue, our bones have greater mass per volume; they are denser, and therefore stronger.

We can begin to lose bone density for several reasons, and some people are more at risk than others. Reduced bone density means lower levels of mineral deposits on the underlying matrix, but also affects the structural architecture within the bones. SCI is a significant independent risk factor for reduced bone density.

One of the main factors influencing our bone density is the amount of weight bearing exercise we take; weight-bearing exercise improves bone density. This is the factor most influenced by a spinal cord injury, or any condition which significantly impacts a person’s ability to weight-bear. An SCI which substantially impacts our motor control can mean total or partial loss of movement and mobility, and so our capacity for weight-bearing exercise after an SCI may be minimal.

Without weight-bearing, our bones very quickly lose density, at a rate of approximately 1% per week, continuing for several years after the injury until bone density is severely reduced.[ii] Bones become very brittle and fragile, and are easily broken.

Osteopenia is the term for mildly reduced bone density. Osteoporosis is the term used for severely reduced bone density. People may also refer to ‘brittle bones’, or bone fragility.

Fracture risk after spinal cord injury

Fragility fractures are common in people with bone mineral density loss following an SCI. Reduced bone mineral density means that fractures can happen easily through various mechanisms. A person with very severe bone density loss – with profound osteoporosis – can develop fractures simply through the pressure of their own body weight or from minimal movement.

Compression fractures in the spine – especially unstable wedge or ‘burst’ type fractures can have their own independent impact on the spinal cord and may change the nature of an existing spinal cord injury.[iii]

New fractures caused by traumatic injury are naturally less common in people who have very limited movement after an SCI – the usual external causes of traumatic fracture, i.e. falls and accidents, are less likely in people whose independent movement is very restricted. Where someone with a high and relatively complete spinal cord injury has traumatic, rather than fragility, fractures from injuries, that may raise questions about the nature of the care they receive.

Osteoporosis and fractures

The more we lose bone density, the more prone we are to fractures. As mineral deposits throughout the structure of our bones thin out, the bones become fragile and friable. The more fragile our bones are, the more prone to breaking they are. It takes less and less impact to cause fractures, and fractures are more likely to be complex and to heal poorly.

The factors which make us more at risk of reduced bone density and fractures include:

  • Sex – being female, especially post-menopause, increases bone density loss.
  • Low body mass index – partly as a predictor of malnutrition, partly because bones are physically less protected in people with very low levels of body fat. Having adequate fat reserves is also linked to production of some of the hormones that regulate bone density. On the other hand, obesity is linked to lower bone strength adjusted for body weight so maintaining a healthy BMI is optimal.[iv]
  • Diet – Poor nutrition and nutritional absorption leads to deficiencies in bone health-specific nutrients, including calcium. Alcohol consumption and smoking cigarettes are also linked to osteoporosis.
  • Vitamin D deficiency – made by our skin in the sunshine, and also part of a healthy diet, vitamin D is essential for the body’s uptake and use of calcium in bone-building.
  • Being sedentary – as weight-bearing exercise is one of the best ways to maintain or improve bone density, people whose mobility is profoundly reduced by SCI are particularly affected by this risk factor.

A history of fractures is also an indicator of future risk, as is a family history of osteoporosis. Many other diseases are linked to osteoporosis risk through various mechanisms, including inflammatory and autoimmune diseases, cardiovascular disease, and diabetes.[v]

The coccyx, or tailbone

The coccyx, or ‘tailbone’ is at the very end of the spinal column – as the name suggests, it’s where our tails would be if we had them! It’s an important part of the spine as it supports mobility and is partly responsible for our sitting balance. Due to its position, size and shape, damage to the coccyx isn’t uncommon. An injury to the coccyx can cause some serious problems.

Coccyx injuries associated with spinal cord injuries contribute significantly to pain and subsequent functional and mobility problems relating to the injury.[vi] Good management, early recognition, and effective physiotherapy can help reduce the impact of a coccyx injury in many people, although those with an existing SCI may have some restrictions to rehabilitation of coccyx injuries.

Can a broken tailbone cause paralysis?

The nerves responsible for motor control and sensation diverge from the spinal column above the level of the coccyx, so damage solely to the coccyx should not be able to cause paralysis.

Symptoms of an injury to the coccyx can include pain and tenderness in the area; bruising; discomfort associated with sitting, and pain on moving the bowels, which can contribute to constipation or other problems with continence. A coccyx injury can also make sex painful.

Can a broken tailbone cause problems with continence?

A broken tailbone or other painful coccyx injury can cause problems with continence. Although the nerves responsible for sensation or control of the bowels and bladder may be preserved, problems with pain, mobility, and pelvic floor dysfunction can be caused by coccyx damage and pain.[vii]

There are various different points across the coccyx where fractures can occur, and the position and severity of the fracture predicts the type of impact that the fracture has. The position can influence continence problems and challenges with both male and female sexual function.[viii]

Constipation is a common occurrence in people with coccyx injuries, and is often related to increased pain when using the toilet. A healthy diet with plenty of fluids and fibre can help improve gut health and make bowel movements easier. Stool softeners or other medication may be necessary too.

Painkillers given for spinal injuries can also cause severe constipation; opioid painkillers are the most likely to cause constipation, and these include codeine, tramadol, and morphine.

Constipation can cause serious problems for people with spinal cord injury, including bowel perforation and autonomic dysreflexia, so it’s important to manage bowel function carefully. There are lots of different products and methods available for managing continence and bowel habits after an SCI.

What are Bone Spurs, and why do they form?

A bone spur or ‘osteophyte’ is a growth of bone that protrudes from an existing bony structure. They can grow on any part of bone but are typically found in areas of movement, i.e. near joints and on or within the spinal column. They can occur without causing any problems, and may only be discovered as an incidental finding, for example when having an x-ray for an unrelated reason.

When bone spurs grow enough to rub against other bones and joints, or where they cause pressure on nerves or other tissues, they can begin to cause symptoms, which range in severity. Symptoms can include pain in and around joints, and where bone spurs affect nerves, they can cause pain, weakness, and odd sensations like pins and needles or areas of numbness.

Bone spurs that grow in areas with less protective tissue, like on the fingers, may cause lumps and bumps which can damage the tissues and skin and create wounds. Bone spurs can affect mobility and quality of life through pain and by restricting range of motion in some joints.

Bone spurs can affect anyone, but risk factors include malnutrition, advancing age, being female, and having existing osteoarthritis.[ix] Osteophytes which are causing problems, particularly when they are compressing nerves, may be surgically removed (resected), but considering surgery always requires a pragmatic risk-benefit analysis, particularly people with existing conditions which might increase their risk from surgery and general anaesthetic.

Protecting bone health after a spinal cord injury

As with many medical conditions, there are a number of different factors which can impact a person’s bone health, irrespective of whether that person also has a spinal cord injury. Some of these risk factors are unchangeable, for example, being post-menopause (although HRT may modify risk to some degree[x]). Other risk factors may be modifiable – for example, having low vitamin D levels has a significant impact on bone density, and is an easily treatable condition.

Medical imaging specifically for evaluating bone health is increasingly sophisticated, and can guide treatment plans to help maintain good bone health. There are also emerging treatments which aim to maintain bone density by mechanical-loading physiotherapy which mimics normal weight-bearing, or vibration stimulation therapies.[xi]

There are a number of pharmacological treatments which can slow deterioration or even improve bone density, and the medical professionals who help look after a person with an SCI should consider the potential benefits of these treatments.[xii] While someone with severe limitations to their independent mobility, i.e. someone who is tetraplegic may be at very low risk of traumatic injury from external factors, their potential for severe osteoporosis and fragility fractures should not be underestimated. Bisphosphonate medications, calcium and vitamin D supplements have been used in preventing bone density loss after spinal cord injury, with good results.[xiii]

Living with a spinal cord injury takes many adjustments to a person’s lifestyle and circumstances, and it’s important to do everything possible to reduce the impact of subsequent conditions relating to the injury. This should include managing bone and joint health.[xiv] Anyone with questions about protecting their bone health with reduced mobility should consult their GP as there may be options for improving or protecting their existing bone mineral density.

 

 

[i] Kang, Y., Ding, H., Zhou, H., Wei, Z., Liu, L., Pan, D., & Feng, S. (2018). Epidemiology of worldwide spinal cord injury: a literature review. Journal of Neurorestoratology, 6(1), 3.

[ii] Bauman WA, Cardozo CP. (2015) Osteoporosis in individuals with spinal cord injury. Journal of Injury, Function, and Rehabilitation, 7(2), 188–201

[iii] McCARTHY, J., & Davis, A. (2016). Diagnosis and management of vertebral compression fractures. American family physician, 94(1), 44-50.

[iv] Frotzler, A., Krebs, J., Göhring, A. et al. Osteoporosis in the lower extremities in chronic spinal cord injury. Spinal Cord 58, 441–448 (2020). https://doi.org/10.1038/s41393-019-0383-0

[v] Pouresmaeili, F., Kamalidehghan, B., Kamarehei, M., & Goh, Y. M. (2018). A comprehensive overview on osteoporosis and its risk factors. Therapeutics and clinical risk management, 14, 2029.

[vi] Tekin, L., Yilmaz, B., Alaca, R., Ozçakar, L.., & Dinçer, K. (2010). Coccyx fractures in patients with spinal cord injury. European Journal of Physical and Rehabilitation Medicine, 46(1), 43-46.

[vii] Dean, L. M., Syed, M. I., Jan, S. A., Patel, N. A., Shaikh, A., Morar, K., & Shah, O. (2006). Coccygeoplasty: treatment for fractures of the coccyx. Journal of vascular and interventional radiology, 17(5), 909-912.

[viii] Wright, J. L., Nathens, A. B., Rivara, F. P., MacKenzie, E. J., & Wessells, H. (2006). Specific fracture configurations predict sexual and excretory dysfunction in men and women 1 year after pelvic fracture. The Journal of urology, 176(4), 1540-1545.

[ix] Wong, S. H. J., Chiu, K. Y., & Yan, C. H. (2016). osteophytes. Journal of orthopaedic surgery, 24(3), 403-410.

[x] Wu, F., Ames, R., Clearwater, J., Evans, M. C., Gamble, G., & Reid, I. R. (2002). Prospective 10‐year study of the determinants of bone density and bone loss in normal postmenopausal women, including the effect of hormone replacement therapy. Clinical endocrinology, 56(6), 703-711.

[xi] Battaglino, R. A., Lazzari, A. A., Garshick, E., & Morse, L. R. (2012). Spinal cord injury-induced osteoporosis: pathogenesis and emerging therapies. Current osteoporosis reports, 10(4), 278–285. https://doi.org/10.1007/s11914-012-0117-0

[xii] Bouxsein, M. L., Eastell, R., Lui, L. Y., Wu, L. A., de Papp, A. E., Grauer, A., … & FNIH Bone Quality Project. (2019). Change in bone density and reduction in fracture risk: a meta‐regression of published trials. Journal of bone and mineral research, 34(4), 632-642.

[xiii] Ashe, M. C., Craven, C., Eng, J. J., Krassioukov, A., & the SCIRE Research Team (2007). Prevention and Treatment of Bone Loss after a Spinal Cord Injury: A Systematic Review. Topics in spinal cord injury rehabilitation, 13(1), 123–145. https://doi.org/10.1310/sci1301-123

[xiv] Frotzler, A., Krebs, J., Göhring, A. et al. (2020) Osteoporosis in the lower extremities in chronic spinal cord injury. Spinal Cord 58, 441–448. https://doi.org/10.1038/s41393-019-0383-0

 

Improvements in health and social care mean that people are living longer than ever before. This is especially true for people with spinal cord injuries (SCI), as advances in medicine and medical technology mean that conditions which would previously have significantly shortened someone’s expected lifespan are now simply a facet of a long life.

There are naturally additional challenges for those of us living with spinal cord injuries as we age; aging and SCI are each independent risk factors for a wide range of conditions. Some of the conditions which are more common in people with spinal cord injuries are exacerbated or hastened as those people age. Additionally, SCI can also be a trigger for some of the processes which are usually associated with aging.

Life Expectancy for People with Spinal Cord Injury

A spinal cord injury cannot easily be generalised, as there is no one-size-fits-all; variations in the point of injury and completeness of the injury have a huge impact on the result of the injury. Therefore, the life expectancy of someone with a spinal cord injury is as variable as that of anyone else.[i] In addition, the data we have becomes outdated with every new advance in medical and surgical SCI management. Long-term studies into survival rates and life expectancy after SCI show remarkable improvement corresponding to advances in medicine and formal care, but the life expectancy of someone with an SCI is still lower than that of the general population.[ii]

Life expectancy after SCI correlates strongly to the level of neurological impairment.[iii] That said, some of the most likely causes of death in people with SCI are related to conditions that can often be well managed with good rehab, medical and nursing care.

Top Causes of Death in Spinal Cord Patients

The largest population studies into causes of death in people who have lived with spinal cord injuries, rather than those whose cause of death relates to the immediate cause of their spinal cord injury, have found that the largest proportion of deaths are due to respiratory complications.

High spinal cord injuries vastly increase a person’s risk of developing respiratory tract infections, so that risk needs to be carefully managed.[iv] After that, the most common causes of death are cardiovascular disease and cancer; similar to people without SCI, although causes of death for people with SCI do correlate closely to underlying problems relating to that injury.[v]

Staying healthy with an SCI, especially with a risk of respiratory complications – people who can’t breathe or cough without mechanical assistance, for example – takes extra care and management. An effective, specialised and holistic care package can significantly reduce the risk of some of the complications of living with an SCI, with knock-on effects on morbidity, mortality, and quality of life.[vi]

Effects of Ageing in the Vertebral Column

Aging can affect the bones of the spinal column in several ways. As we age, we are more likely to develop changes in our musculoskeletal system. This includes those that affect the bones, like osteoporosis; the bones and joints, like osteoarthritis, and the changes in muscle density and general tone that come with age and accompany reductions in mobility and exercise tolerance.

Conditions associated with aging also include spinal stenosis and vertebral compression fractures which can cause damage or compression to the spinal cord.

How Ageing Affects the Spinal Cord

The changes that affect the bony processes of the spine can have an impact on the spinal cord. Spinal stenosis, a condition where the canal encasing the spinal cord begins to narrow, can create pressure on the spinal cord, causing damage and triggering some symptoms of spinal cord injury.

Degenerative neurological conditions, while rare, also tend to increase in incidence with age. While these are often only associated with changes in the brain, some also affect the nerves in the spinal cord and sometimes the peripheral nervous system. Multiple sclerosis is one of the more common neurological conditions that can affect the brain and spinal cord and have an impact on sensation and movement.

Body Changes when Ageing with Spinal Cord Injury

Our bodies change as we get older – for many of us, our skin and other tissues lose elasticity and begin to sag. Our muscles often lose tone, and our bones can become more brittle with lower bone density. There’s a strong genetic element to the impact of aging; some very elderly people stay extremely fit and well, whereas other people show many of the physical signs of aging relatively early in life.

When we have a spinal cord injury that affects our mobility and sensation, the changes of aging can seem to be accelerated. Our bodies benefit immensely from exercise, and without the ability to move independently we begin to lose muscle tone, bone density, and flexibility almost immediately. Passive physiotherapy can help maintain flexibility, but the impact of simply being unable to exercise brings on some of those changes that we usually associate with aging.[vii]

Functional and Psychological Ageing

Longevity is easy to measure; quality of life is not necessarily so simple. Aging with a spinal cord injury means huge changes to lifestyle and expectations of work, family position, leisure interests, and effectively every part of a person’s life needs some adjustment. In the immediate to short-term, the psychological impact of a new spinal cord injury can be incredibly taxing.

Any new major diagnosis, especially one with a traumatic origin, can trigger strain on a person’s mental health. The level, acuteness and completeness of the injury again can influence a person’s emotional response. There are few diagnoses as all-encompassing as being told you now have permanent total quadriplegia, perhaps that you will be dependent some or all of the time on a mechanical ventilator, and that you’ll need support with almost all of your usual activities of daily living.

That said, the long-term impact of SCI on mental health seems to resolve to a level that may be surprising to those who experienced profound grief and feelings of loss at the first stages of their condition. In fact, the general quality of life and sense of wellbeing in older people living with spinal cord injury is overwhelmingly both high and stable.[viii]

Musculoskeletal Changes in Spinal Cord Injury

Chiropractor showing spinal cord bones to aged man for orthopedic diagnosis and physical recovery. Chiropractic assistant with human skeleton explaining spine injury to retired patient

Chiropractor showing spinal cord bones to aged man for orthopedic diagnosis and physical recovery. Chiropractic assistant with human skeleton explaining spine injury to retired patient

Musculoskeletal changes can cause problems with the vertebrae and spinal cord – spinal stenosis, arthritic changes, and osteoporosis are some of the more common conditions that can affect the spinal cord. Spinal cord injury also causes significant musculoskeletal changes. A complete SCI means a lack of motor control and sensation from the point of injury downwards, and the loss of mobility means the loss of muscle mass and tone, and the loss of the benefits of exercise and weight-bearing. As these conditions tend to worsen with age even in those without SCI, the impact of SCI has the effect of profoundly accelerating these aspects usually associated with age.[ix]

Cardiovascular Changes in Spinal Cord Injury

A spinal cord injury can cause changes in the autonomic nervous system which can affect cardiovascular health. Changes in the activity of the sympathetic nervous system can trigger arrhythmias, hypotension, and chronic risk of autonomic dysreflexia, which in turn can cause arrhythmias, profound hypo- and hyper-tension, and cardiac arrest. As well as those risks intrinsic to SCI, immobility and loss of exercise is an independent risk factor for cardiovascular diseases like stroke and coronary artery disease.[x]

Respiratory complications

Respiratory problems are the most common and potentially serious of the sequelae of SCI. People with SCI, depending on the level and completeness of injury, may have lost some or all of their ability to breathe independently. People can become fully or partly dependent on mechanical ventilation, an independent risk factor for respiratory tract infection. People who cannot control their breathing and who cannot cough effectively find it harder to clear their lungs and are more prone to aspiration pneumonia. This risk is further increased for those who still take oral diet and fluids, but who have a compromised swallow reflex.

The risk of respiratory complications can increase with age for some people as any preserved motor function and musculature can weaken, exacerbating existing risk. Respiratory tract infections are the most common cause of death for people with SCI, but this risk can be reduced with effective medical and nursing care. The care of a person who is fully or partially dependent on mechanical ventilation requires specialist knowledge and experience. A dedicated care team – which can include training a close family member who wishes to be involved with ventilator care or have some knowledge of what to do if issues arise – can reduce the risk of problems and ventilator-associated infection.

Urinary and Bowel complications

Problems with continence, bowel and bladder function are common in people with SCI who lost control and sensation relating to those systems. While incontinence can cause serious problems with the skin, mental and physical health, urinary retention and severe constipation are both relatively common in people with SCI and have serious consequences, including bowel perforation and autonomic dysreflexia.

SCI can also impact the upper gastrointestinal system, with reduced motility increasing the likelihood of acute bowel issues.[xi]

Pressure Ulcers

Pressure ulcers, formerly known as ‘bed sores’ and moisture lesions are a huge risk for people with reduced mobility, and particularly so for those who are unable to sense the discomfort of staying too long in a position that puts pressure on some of the delicate tissues that take our weight.

pressure ulcers

Pressure ulcers are most commonly seen on the buttocks and back of the heels, but any part of the body where bony pressure is exerted on the tissues

below can develop pressure ulcers. Without good care they can become very serious, sometimes even exposing bone and causing significant risk of infection, fluid loss, autonomic dysreflexia and a range of adverse outcomes associated with open wounds.

Moisture lesions are areas of damage to the skin and underlying tissues causes by having urine or faeces, or even sweat, held against the skin for any length of time. It can begin as irritation but can degrade into open wounds, usually in the moist folds around the groin. Moisture also increases the risk of fungal as well as bacterial infections. Good nursing care and continence management can reduce this risk.

Ageing Well with Spinal Cord Injury

Although there are significant extra challenges to aging for people with spinal cord injuries, most people can expect to experience good quality of life, and there are solutions to many of the long-term risks associated with SCI.

If you’re living with an SCI, there will be changes in your care needs and lifestyle as you get older. You may have to have reassessments for your practical care needs if there are changes to your mobility, your respiratory needs, or any of the other areas where you need additional support. Housing, environment, and equipment may also need reassessment as needs change.

Some of the conditions associated with aging are unrelated to SCI, but having an SCI may pose additional challenges for people who do develop unrelated conditions. For example, cancer treatments can have significant side effects, some of which may be particularly difficult to manage for people with SCI.

As many health conditions become more common as we age, anyone with mobility and access needs can find particular challenges in their ongoing care. Regular trips to hospitals or clinics may already be a routine part of the life of someone with extra health needs due to an SCI. This is likely to increase for those of us who develop additional health conditions. Modern healthcare facilities are designed with accessibility in mind, but just getting around can become more difficult for people with SCI as they age.

With the right adjustments, a person with an SCI can expect good longevity and – perhaps more important – good quality of life. A care package designed for the individual which incorporates a team of specially trained and dedicated carers means that a person’s care needs can be met safely and effectively, allowing that person to live well and with a good expected lifespan, with support and adjustments for their extra needs.

[i] Chamberlain, J. D., Meier, S., Mader, L., Von Groote, P. M., & Brinkhof, M. W. (2015). Mortality and longevity after a spinal cord injury: systematic review and meta-analysis. Neuroepidemiology, 44(3), 182-198.

[ii] Savic, G., DeVivo, M. J., Frankel, H. L., Jamous, M. A., Soni, B. M., & Charlifue, S. (2017). Long-term survival after traumatic spinal cord injury: a 70-year British study. Spinal cord, 55(7), 651-658.

[iii] Middleton, J. W., Dayton, A., Walsh, J., Rutkowski, S. B., Leong, G., & Duong, S. (2012). Life expectancy after spinal cord injury: a 50-year study. Spinal cord, 50(11), 803-811.

[iv] Berlowitz, D. J., Wadsworth, B., & Ross, J. (2016). Respiratory problems and management in people with spinal cord injury. Breathe, 12(4), 328-340.

[v] Cao, Y., DiPiro, N., & Krause, J. S. (2019). Health factors and spinal cord injury: a prospective study of risk of cause-specific mortality. Spinal Cord, 57(7), 594-602.

[vi] Xia, Y., Wang, J., & Wang, P. (2022). Systematic Nursing Interventions Combined with Continuity of Care in Patients with a Spinal Fracture Complicated with a Spinal Cord Injury and Its Effect on Recovery and Satisfaction. Evidence-Based Complementary and Alternative Medicine, 2022.

[vii] Liem, N. R., McColl, M. A., King, W., & Smith, K. M. (2004). Aging with a spinal cord injury: factors associated with the need for more help with activities of daily living. Archives of physical medicine and rehabilitation, 85(10), 1567-1577.

[viii] Sakakibara, B. M., Hitzig, S. L., Miller, W. C., & Eng, J. J. (2012). An evidence-based review on the influence of aging with a spinal cord injury on subjective quality of life. Spinal cord, 50(8), 570-578.

[ix] Biering‐Sørensen, B., Kristensen, I. B., Kjær, M., & Biering‐Sørensen, F. (2009). Muscle after spinal cord injury. Muscle & Nerve: Official Journal of the American Association of Electrodiagnostic Medicine, 40(4), 499-519.

[x] Partida, E., Mironets, E., Hou, S., & Tom, V. J. (2016). Cardiovascular dysfunction following spinal cord injury. Neural Regeneration Research, 11(2), 189.

[xi] Ebert, E. (2012). Gastrointestinal involvement in spinal cord injury: a clinical perspective. Journal of Gastrointestinal & Liver Diseases, 21(1).

The spinal cord – the bundle of nerves that extends down from the brain and branches off to supply nerve function to every part of the body – runs through a canal in the middle of the spine. Each vertebra – bone of the spine – has a hole in it and together they form a long, protective passageway for the spinal cord.

Sometimes, this passageway can become narrower than it should be, and this can put pressure on the nerves of the spinal cord, which can cause a range of problems. This narrowing is known as spinal stenosis.

What causes spinal stenosis?

  • Arthritis: The most common cause of spinal stenosis is changes in the bones caused by arthritis. Rubbing and deterioration caused by arthritis can cause thickened, raised areas of bone known as bone spurs which can cause pressure on the spinal cord.
  • normal vs stenosis spinal cord

    Illustration showing spinal canal stenosis lumbar vertebra with intervertebral disc and herniated nucleus pulposus

    Injury: An injury that affects the bones of the spine can cause movement or inflammatory changes that affect the width of the spinal canal. Surgery on the spine for any reason also increases the risk of developing spinal stenosis in future.

  • Tumours: Tumours can be cancerous or benign growth; either way, they can invade the spinal canal and put pressure on the cord.
  • Paget’s Disease: Bones are just like other tissues of the body in that they are broken down and renewed. In people with Paget’s disease, the cells are broken down faster than they’re renewed, which causes thinning of the bones, making them very fragile. These weak, fragile bones gradually change shape, sometimes causing movement and pressure within the spinal column itself, or changes in the way the spine curves.
  • Hypertrophy of the ligaments: This means a thickening and hardening of the ligaments, and when it affects the ligaments of the spinal column it can cause narrowing of the spinal canal.

Types of Spinal Stenosis

Spinal stenosis affects either the vertebrae that make up the neck – known as the cervical or c-spine, or the vertebrae at the lumbar or l-spine. Some people have stenosis in both of these areas of the spine.

spinal stenosis

Cervical

The cervical spine is the part of the spine that makes up the neck, and comprises the top seven vertebrae below the skull.

Lumbar

The lumbar spine is the 5 vertebrae that make up the lower back above the sacrum.

imaging of spinal stenosis

Symptoms of spinal stenosis

Symptoms of cervical spinal stenosis include:

  • Neck pain
  • Numbness
  • Odd sensations like pins and needles or tingling in the one or more limbs
  • Back pain
  • Changes to gait and balance

Symptoms of lumbar spinal stenosis include:

  • Cramping pain in one or both legs
  • Lower back pain

Spinal stenosis can sometimes cause problems with bladder or bowel control, and occasionally with sexual function. The pain associated with spinal stenosis can become very severe, and can have a significant negative impact on a person’s life, mobility, fitness, and general health.

The majority of cases of spinal stenosis are caused by arthritis or other chronic degenerative bone disease. In these cases it begins slowly so there can be a fairly significant narrowing of the spinal canal before symptoms are really noticeable. When they do begin they usually develop gradually and worsen over time.

Spinal stenosis that is caused by injury can start much more quickly if the injury leads to long-term narrowing of the spinal canal. When someone has an injury involving the spine, there are short-term inflammatory processes which can cause compression on the spinal cord but don’t necessarily mean there will be long-term spinal stenosis.

Spinal stenosis caused by a tumour can also cause symptoms to develop more quickly than stenosis caused by chronic deterioration.

Diagnosing spinal stenosis

A person’s symptoms and risk factors for spinal stenosis will be considered when they first present, normally at their GP. A physical examination, usually to demonstrate the movement of the spine and any accompanying symptoms, will also help to suggest a diagnosis.[i]

An absolute diagnosis can be confirmed with the use of medical imaging. The type of imaging requested can depend on whether there is any suspicion of certain other conditions or causes. Tests can include:

  • X-rays – these give a good picture of the bones, and so can be used to spot any changes in bone structure that might cause pressure on the spinal cord.
  • CT (computed tomography) scans – these give a more detailed picture of the structures around the spinal cord, and can show problems like herniated discs and tumours.
  • MRI (magnetic resonance imaging) scans – these give a very detailed picture of the tissues of the body, and can give doctors a lot of detail about any changes in the bones and the soft tissues. MRI scans can indicate areas of damage or inflammation, tumours and other problems.

A doctor might also request blood tests which can include measuring inflammatory markers and markers for autoimmune causes of arthritis.

How bad can spinal stenosis get?

The symptoms of spinal stenosis, such as pain, numbness, mobility problems, and problems with continence, can become very severe. The impact of these kind of symptoms can have a profound effect on someone’s life. Reduced mobility can cause other problems with the muscles, bones and joints.

Problems with bowel and bladder control, particularly combined with reduced mobility, can also be associated with a risk of other problems like pressure damage, moisture lesions, and have a serious impact on a person’s mental health and quality of life.

Chronic pain can be difficult to manage, and even more difficult to live with. Spinal stenosis can seriously affect a person’s quality of life, and ultimately their independence.

Risk Factors for Spinal Stenosis

Most people who develop spinal stenosis do so because of long-term degenerative changes in the bones of the spine, most often caused by arthritis. Arthritis is usually – but not always – associated with the processes of aging, which means that spinal stenosis tends to affect people more as they age. It also affects women more than it affects men, which may be for a range of reasons, including under-diagnosis in men.[ii]

People who have had previous surgery on their spine are more likely to develop spinal stenosis, and it is also more common in people who are overweight or obese.[iii]

People who have curvature of the spine (kyphosis or scoliosis) or other structural changes are also more likely to experience problems from compression of the spinal cord. Rarely, people can be born with unusually narrow spinal canals, and may have problems with pain and movement from a very young age.

Stages of Spinal Stenosis

Once spinal stenosis has developed, it will gradually get worse without treatment.

Treatment depends on the cause, but where spinal stenosis is caused by chronic irreversible degenerative bone disease like osteoarthritis, treatment is only likely to slow progression or manage symptoms.

Spinal Stenosis Treatment

The treatment for spinal stenosis depends on the cause. Most causes of spinal stenosis are not reversible, i.e. cannot be completely removed by treatment. Treatment, therefore, usually focuses on slowing progression, alleviating symptoms, and reducing the risk of complications or side-effects.[iv]

Conservative (non-surgical) treatment

  • Medication – anti-inflammatory medication can help reduce compression on the spinal cord and also independently reduce pain. Chronic severe pain can also be managed with stronger pain medication, and there are specialist teams of healthcare professionals whose job is to help people manage chronic pain. Sometimes medications that are usually used for depression or to prevent seizures are also used to manage chronic pain.[v]
  • Injections – some medicines are best given as injections, and steroid injections at the site can be very effective, and usually only need to be given every few months.

steroid injection into spinal cord

  • Physiotherapy – physiotherapy is an important part of the treatment of spinal stenosis and some of its associated symptoms. Exercises can help to strengthen the muscles supporting the spine, and to maintain good movement and flexibility. Physiotherapy can also help with problems with gait and balance that can arise in people with spinal stenosis and related conditions.[vi]

Surgery for spinal stenosis

Surgery can widen the spinal canal somewhat, but the effectiveness can depend on the cause of the spinal stenosis.[vii] Surgery for spinal stenosis is something of a last resort, and generally only considered when more conservative treatment has been unsuccessful.

Surgery to widen the spinal canal is performed under a general anaesthetic and it can take some months to fully recover. The surgery is performed on the lamina – this is the arched back section of each vertebra. This can take the form of:

  • Laminectomy – where the lamina of the affected vertebra or vertebrae is removed, creating more space around the spinal cord. This may be replaced with specially designed surgical metalware which bridges the gap created and maintains strength in the backbone.
  • Laminotomy – this is where a small amount of interior arch the lamina is removed, creating a wider spinal canal but leaving the outer part of the vertebra intact.
  • Laminoplasty – This is only used in the bones of the c-spine; one side of the lamina is ‘hinged’, opened outwards a few degrees and metalware is used to maintain that position.

If the spinal stenosis is cause by a tumour then removal of the tumour may cure the spinal stenosis. Sometimes tumours around the spine are associated with other areas of thickening and cell overgrowth so some people may have continuing symptoms.

Exercise

Professional physiotherapy can be incredibly beneficial in spinal stenosis, strengthening the muscles around the spinal column, maintaining mobility, and managing pain. Referral to a physiotherapist means that treatment and exercise can be tailored to the individual and adjusted over time. There are also some useful exercises to try at home, but a personal physiotherapy plan from a professional is the ideal, especially if there are other complications or conditions affecting a person’s ability to exercise.

Good exercises for most people with spinal stenosis usually focus on maintaining or improving range of motion, so stretching and bending – within an individual’s limits – will make up some of an exercise plan.

Some people with spinal stenosis find that they’re most comfortable bent slightly forward, so cycling, whether on a stationary exercise bike or outdoors, can be a comfortable way of increasing strength.

Swimming is good low impact exercise and can be a comfortable way of improving symptoms and increasing strength and fitness.

Exercise classes that focus on slow, core-strengthening exercises like Pilates or yoga can be helpful, and a gym membership that includes access to a personal trainer with experience in supporting people with spinal problems is ideal.

Exercises to avoid

Everyone has different limits, and while exercise is very beneficial to most people with spinal stenosis, very high impact exercises like running on pavements can cause more pain than they relieve.

Living with Spinal Stenosis

Spinal stenosis is fairly common, so if you’re living with the condition, you’re not alone. There are lots of treatment options, and there are teams of healthcare professionals who specialise in conditions relating to the spine and nerves, to chronic pain, and to improving symptoms with physical therapy and other treatment.

There are also support groups for people living with conditions affecting their usual ability, and the internet is a good place to start to look for online, national, or local organisations or groups.

Whatever your symptoms, there will be some choices for helping to manage them. It’s always okay to ask for support, and it’s a good idea to keep your GP or specialist in the loop if symptoms change, as there might be other ways to manage them.

As with any chronic disease, looking after yourself is key. Maintaining a healthy lifestyle is good for both mental and physical health, and if you’re able to be proactive in gaining treatment, there is help at hand. If you’re unable to easily advocate for yourself, it might be important to ask a family member or friend to help support you with accessing healthcare services.

Maintaining your quality of life is key, and that might require a multi-pronged treatment plan. It’s also important to acknowledge other symptoms that can accompany spinal stenosis – these can include depression, sleeplessness, loneliness and reduced mobility. If you’re able to talk about these problems, there’s always a way to try and make things better.

 

[i] Haig, A. J., & Tomkins, C. C. (2010). Diagnosis and management of lumbar spinal stenosis. Jama, 303(1), 71-72.

[ii] Sekiguchi, M., Yonemoto, K., Kakuma, T., Nikaido, T., Watanabe, K., Kato, K., … & Konno, S. I. (2015). Relationship between lumbar spinal stenosis and psychosocial factors: a multicenter cross-sectional study (DISTO project). European Spine Journal, 24(10), 2288-2294.

[iii] Wang, C., Chang, H., Gao, X., Xu, J., & Meng, X. (2019). Risk factors of degenerative lumbar scoliosis in patients with lumbar spinal canal stenosis. Medicine, 98(38). https://doi.org/10.1097/MD.0000000000017177

[iv] Melancia, J. L., Francisco, A. F., & Antunes, J. L. (2014). Spinal stenosis. Handbook of clinical neurology, 119, 541-549.

[v] Hylands-White, N., Duarte, R. V., & Raphael, J. H. (2017). An overview of treatment approaches for chronic pain management. Rheumatology international, 37(1), 29-42.

[vi] Özden, F., Tümtürk, İ., Yuvakgil, Z., & Sarı, Z. (2022). The effectiveness of physical exercise in patients with lumbar spinal stenosis: a systematic review. Sport Sciences for Health, 1-12.

[vii] Wei, F. L., Zhou, C. P., Liu, R., Zhu, K. L., Du, M. R., Gao, H. R., … & Qian, J. X. (2021). Management for lumbar spinal stenosis: a network meta-analysis and systematic review. International Journal of Surgery, 85, 19-28.

Epilepsy is the most common cause of seizures; it is a condition where sudden ‘storms’ of electrical activity in the brain have an impact on the body. Seizures can also have other causes, however, and can be triggered by several of the conditions which affect the central nervous system.

charles edouard brown sequard scaled

The idea of spinal cord injury (SCI) independently causing spinal cord seizures was described by Charles-Édouard Brown-Séquard, the 19th Century physician for whom the manifestation of a single-sided spinal cord injury is named. However, this does not tend to appear in modern literature; the animal experiments through which he demonstrated seizures associated with acquired SCI were largely debunked.[i] Seizures which were thought to be of a spinal cord origin[ii] found in medical literature from the 1960s[iii] have not translated into modern medical practice. Seizures are usually described according to the area of the brain from which they arise and their symptoms, which often inherently involve motor activity affecting the spinal cord, but which do not specifically arise from the spinal cord.

What are seizures?

Seizures often used to be known as ‘fits’, but the word became associated with historically negative views of the people who experience seizures, so the more accurate term ‘seizures’ is preferred. The term ‘fit’ or describing someone as ‘fitting’ when they experience a seizure is still in use in some areas and among some groups of people. There are different types of seizure, and it’s helpful to categorise them according to the area of the brain they start in and how they affect the body.

Different types of seizure may be described as:

  • Absence seizures: these are more common in children than adults, and appear as a ‘blank’ episode. This typically occurs without any obvious physical features except for a short period of what looks like ‘daydreaming’, but where the person is not responsive. Absence seizures used to be known as ‘petit-mal’ seizures.
  • Focal onset seizures: these are seizures that only affect one area of the brain, although they can develop into other types of seizures with a broader impact. They are further divided according to how much they affect a person’s awareness; in a focal aware seizure the person stays awake and knows what it is happening, whereas in a focal impaired awareness seizure, the person affected has changes in their levels of consciousness and comprehension.
  • Myoclonic seizures: these are typified by jerking muscle movements and may be accompanied by other types of seizure at the same time.
  • Tonic and atonic seizures: a tonic seizure is one where a person’s muscles become very, uncontrollably stiff, and an atonic seizure is one where the muscles suddenly relax. Both of these types of seizure typically cause a person to fall down, during which time they may injure themselves.
  • Tonic clonic seizures: previously called ‘grand mal’ seizures, they are typified by a loss of consciousness, falling down with classic jerking and shaking of the muscles with repetitive alternating tonic and atonic episodes. They are usually associated with a classic, archetypal picture of epilepsy, and media portrayals of epilepsy usually centre on this kind of seizure as the symptoms are very visible.

Afterwards, the person who experienced the seizure may continue to have some symptoms, and this time is known as the ‘postictal’ period. It can last any length of time from a few seconds to several days. The symptoms can include confusion, drowsiness, and reduced levels of consciousness. Headaches, nausea and fatigue often follow seizures.

The nature of a person’s postictal symptoms depend on the type and severity of the seizure, and the part of their brain that’s affected.[iv] Other existing conditions can affect the way a person presents in the postictal period and can also have overlapping symptoms which can make diagnosis more difficult. For example, urinary tract infections, can cause seizures in some people and the symptoms may mimic postictal-type symptoms.

What causes spinal cord seizures?

Although seizures are usually caused by epilepsy, or sometimes some serious acute systemic illness, occasionally seizures can arise from other conditions that affect the central nervous system. These can include transverse myelitis, multiple sclerosis, and sometimes toxicity. A rare condition known as spinal muscular atrophy associated with progressive myoclonic epilepsy (SMA-PME) is caused by a faulty genetic mutation where the affected person experiences epileptic seizures and progressive spinal muscular atrophy.[v]

spinal muscular atrophy

An episode of spinal cord injury independently causing seizures is almost unique in medical literature[vi], but spinal cord injury can indirectly cause seizures primarily as a secondary symptom of autonomic dysreflexia.

As seizures are generally related to a specific area of the brain experiencing abnormal bursts of electrical activity, they are intrinsically linked to nerve activity throughout the central nervous system – i.e. the brain and spinal cord, and also impact the peripheral nervous system, hence the symptoms of muscle twitching and jerking movements.

Who is at risk of spinal cord seizures?

Spinal cord seizures are rare, but where they occur they affect people with those central nervous system conditions that are known to be linked with seizures, mainly transverse myelitis and multiple sclerosis. Some conditions that affect the spinal cord can also cause movement disorders which can result in seizure-like activity. Spinal cord-mediated seizures have also historically been associated with contrast dye administration for medical imaging in persons with specific rare circulatory disorders[vii] or conditions affecting the blood-brain barrier.[viii] Modern use of contrast dye is very safe and managed by experienced practitioners.

People who have spinal cord injuries or serious neurological conditions with a profound effect on movement and sensation can be liable to experience a condition known as autonomic dysreflexia (AD) where the body’s autonomic nervous system mounts a systemic reaction to a stimulus.

One of the symptoms of autonomic dysreflexia can be seizures, so people with spinal cord injuries and anybody involved in their care or who are close to them can benefit from an awareness of this potentially serious condition. Knowing how to identify and manage AD can help save the life of someone with a spinal cord injury.

Seizure treatment

The immediate treatment of a seizure depends on the symptoms and how long it lasts. In the short-term, the main thing is to make sure that the person having a seizure is safe and won’t hurt themselves if they’re experiencing muscle jerking and weakness. Protecting the head is the most important consideration, and the risk of injury can be reduced with cushions, pillows, or rolled-up coats against any nearby sharp corners of furniture.

Sometimes people having a seizure can accidentally bite the inside of their mouth, but there isn’t any easy way to prevent this and you should not put anything inside the mouth of someone having a seizure. It’s quite common for people having tonic clonic seizures to lose control of their bladder during a seizure, which may be embarrassing afterwards, and when this happens it’s important to try and preserve that person’s privacy and dignity as much as possible.

A first seizure or seizure without an obvious manageable cause will usually be investigated and local healthcare providers may have specific clinics for investigating first seizures (sometimes known as a ‘first fit clinic’). Investigations may include blood tests, medical imaging of the brain, and an encephalograph (EEG). Sometimes a person may have one seizure without a clear cause and never have another, but more than one seizure will usually mean that ongoing treatment will need to be considered.

encelphalograph

Brainwave EEG or Electroencephalograph Examination in a Clinic

If a seizure happens to someone who has never had one before, it’s important to get urgent medical attention. It’s also important to get medical help for a seizure that lasts more than five minutes. Sometimes seizure activity can affect a person’s breathing, and if they appear to stop breathing properly that should be treated as a medical emergency, and anyone at the scene should get help and begin first aid as needed. If in doubt: get help.

In the longer-term, people who have seizures may be treated with medication. The cause of the seizure and the severity and frequency at which they occur influences the kind of preventative treatment given for seizures. Typical antiepileptic drugs may be tried for recurrent seizures; these include carbamazepine, sodium valproate and lamotrigine, among others. Antiepileptic drugs need to be taken exactly as described and not stopped without advice from a doctor.

Can a spinal cord injury cause seizures?

An injury that affects nerve pathways could cause something akin to seizure activity, but SCI is not usually independently associated with seizures, unless there is involvement of the brain stem or there is a secondary complication, for example autonomic dysreflexia.

autonomic dysreflexia

Autonomic dysreflexia (AD) is a condition that can occur in people with spinal cord injury where there is some physical problem that a person is unable to sense due to their spinal cord injury affecting sensation, but which stimulates the autonomic nervous system. It can occur due to physical injuries like pressure damage, to constipation or urinary retention, infection, and even sometimes dysmenorrhea or sexual stimulation.

AD causes a rise in blood pressure and systemic effects, which sometimes include seizures.[ix] AD can become very serious, very quickly and it’s important to be aware of signs of AD if you’re involved in the care of someone with a spinal cord injury or another condition that means significant loss of sensation or motor control. Signs of AD can include sudden profuse sweating, reddening of the face, confusion or anxiety, bradycardia (a slow heart rate) and sometimes breathing problems and seizures. Sometimes AD can be managed simply by managing the underlying cause, but medical help should be sought as AD can lead to serious adverse events including strokes.

Seizures in multiple sclerosis

Multiple sclerosis (MS) is an autoimmune condition that affects the central nervous system. A person’s own immune system begins to attack the myelin sheath, the protective process of the nerves. MS is chronic and may or may not be progressive. Changes in the function of the central nervous system can cause lots of different symptoms, and seizures – usually focal motor seizures – can be experienced as a result of the changes in MS.[x] People with MS are more likely to experience seizures than the general population.

Seizures in transverse myelitis

Transverse myelitis is another condition affecting the nervous system, where sections of the spinal cord become inflamed and fail to function normally. It can happen as a result of other conditions like MS or infections affecting the central nervous system. Transverse myelitis can affect anyone, of any age and background, and can sometimes be the first indication of other conditions. The symptoms include pain, weakness, and reduced sensory function.

The changes in nerve function caused by transverse myelitis can occasionally trigger seizures.[xi]

Living with seizures

People who are prone to seizures with any underlying cause may need to take extra care with some normal day-to-day activities. This can include anything where a sudden loss of control or function could cause harm to themselves or others, such as driving, bathing, and swimming.

People who have seizures associated with neurological conditions may need extra care for their combined conditions. A care package designed to support someone who has seizures should be made up of care workers who have had special training in managing seizures, what to do if there’s a problem and when to get help. The close friends and relatives of someone who has seizures may also wish to learn more about what to do in an emergency.

Medication used to prevent seizures is usually considered a ‘critical’ medication, as maintaining regular timing of administration may be crucial. Antiepileptic medicine can be given in many forms, and liquid preparations are available for people who are unable to swallow tablets or who are fed by percutaneous endoscopic gastrostomy (PEG).

Around 1 in 10 people will experience a seizure at some point in their lives, and at least 50 million people worldwide have epilepsy.[xii] Specialist medical, nursing, and allied health professional teams may be involved in the care of someone who has seizures, and there are lots of local or online support groups and resources to help people living with seizures.

[i] Koehler, P. (1994). Brown-Séquard’s spinal epilepsy. Medical History, 38(2), 189-203.

[ii] Castaigne, P., Cambier, J., & Brunet, P. (1968). Spinal sensory-motor seizures. The Lancet, 291(7538), 357.

[iii] Ekbom, K. A., Westerberg, C. E., & Osterman, P. O. (1968). Focal sensory-motor seizures of spinal origin. The Lancet, 291(7533), 67.

[iv] Pottkämper, J. C., Hofmeijer, J., van Waarde, J. A., & van Putten, M. J. (2020). The postictal state—What do we know?. Epilepsia, 61(6), 1045-1061.

[v] Topaloglu, H., & Melki, J. (2016). Spinal muscular atrophy associated with progressive myoclonus epilepsy. Epileptic Disorders, 18(s2), S128-S134.

[vi] Meythaler, J. M., Tuel, S. M., & Cross, L. L. (1991). Spinal cord seizures: a possible cause of isolated myoclonic activity in traumatic spinal cord injury. Spinal Cord, 29(8), 557-560.

[vii] Willison, H. J., Kendall, B. E., Trend, P., Thomas, P. K., Symon, L., & Thrush, D. (1990). Spinal arteriovenous malformation unmasked during intravenous urography. Journal of Neurology, Neurosurgery, and Psychiatry, 53(2), 175.

[viii] Rüber, T., David, B., Lüchters, G., Nass, R. D., Friedman, A., Surges, R., … & Elger, C. E. (2018). Evidence for peri-ictal blood–brain barrier dysfunction in patients with epilepsy. Brain, 141(10), 2952-2965.

[ix] Hartman, K. C., Vadivelu, S., & Hueschen, L. A. (2021). Seizures: A Rare Presentation of Autonomic Dysreflexia in a Young Adult with Complete Spinal Cord Injury. The Journal of emergency medicine, 61(5), 529-532.

[x] Gupta, K., Burchiel, K.J. Atypical facial pain in multiple sclerosis caused by spinal cord seizures: a case report and review of the literature. J Med Case Reports

[xi] Cherrick, A. A., & Ellenberg, M. (1986). Spinal cord seizures in transverse myelopathy: report of two cases. Archives of physical medicine and rehabilitation, 67(2), 129-131. https://doi.org/10.1016/0003-9993(86)90125-5

[xii] World Health Organization (2022) Factsheets: Epilepsy. WHO.

Paralysis as a symptom of spinal cord injury (SCI) specifically refers to lack of motor control causing reduced ability to move one’s body – this is, of course, inextricably linked to sensation and an injury to the spinal cord that severs motor control will also affect sensory perception.[i] When talking about paralysis it is useful to describe the region or regions of the body affected as well as the severity or ‘completeness’ of the impact.

Degrees of paralysis

The cause, and in the case of SCI, the completeness of the injury, informs the severity of the motor control loss.[ii] Someone with a complete spinal cord injury – that is, an injury severe enough to completely discontinue nerve function – will lose all sensation and control below the point of injury. An injury that disrupts nerve function in only one part of a cross section of spinal cord will have a different effect, with the impact depending on the region of the spinal cord cross-section affected. Someone with injury to one or the other side of the spinal cord may have paralysis on one side only, with little or no impact on the other side of their body. Injuries to the front, back, or central core of the spinal cord have, in turn, various other effects.

  • Anterior cord syndrome is usually typified by weakness with preserved, though reduced, motor control.[iii]
  • Brown-Sequard syndrome describes the impact of a left- or right-sided SCI; an injury only affecting the nerve bundle at one side of the spinal cord may only affect that side.[iv]
  • Posterior cord syndrome is rarer and primarily affects sensation and proprioception (the innate awareness of the body’s position and movement).[v]
  • Central cord syndrome is the most common SCI associated with degenerative spinal changes and aging as well as traumatic injury, and its effects can range from minimal loss of fine movement control to paralysis.[vi]

Regions of paralysis

The definition of paralysis can be applied to any part of the body that has lost movement, but is usually broadly labelled by its impact on the limbs. The regions of paralysis are predicted by the region of impact of injury.[vii] However, paralysis extends beyond deliberate limb movement to affect more innate functions like breathing, continence, and the sexual organs.

Tetraplegia/quadriplegia

Tetraplegia describes a condition where all four limbs are affected. High SCI in the C1-C4 vertebral levels will have a significantly impaired or total loss of nerve pathways below that point. That affects not only the sensation and motor control for limbs and other voluntary movements, but involuntary motor control as well, including conscious and unconscious breathing control, and the functions of the pelvic organs. People with SCI affecting the lower cervical vertebrae – C5-C8 – may have degrees of preserved nerve function to parts of the arms and hands, so it can be more useful to describe the actual preserved function for an individual.

Formerly, tetraplegia was more commonly referred to as quadriplegia. Both prefixes mean ‘four’, as in the four limbs affected; the difference is etymological rather than medical, to maintain consistently Greek, rather than Latin and Greek combined, word-roots for conditions of paralysis.

complete vs incomplete spinal cord injuries

Paraplegia

Paraplegia refers to paralysis of the lower limbs, i.e. lack of motor control of the legs. People with paraplegia also experience impact on the nervous system relating to the pelvic organs, so bowel and bladder problems including constipation, incontinence, and urinary retention are common. Paralysis affecting the lower limbs also affects the nerves of the reproductive system, so sexual function is affected.

Paraplegia can be caused by an SCI that occurs below the level that would affect the upper limbs. People with an SCI at the levels of the high thoracic vertebra – T1-T5 – usually have preserved function of the arms and hands, but some impact on the muscles of the chest and abdomen. People with lower thoracic SCI – T6-T12 – may still have some impact on back and abdominal muscles, but retain normal function above that point. With intact upper limb function and no concerns about breathing, self-care is usually a lot more straightforward.

Right or Left Hemiplegia

Damage affecting only the right or left side of the spinal cord is less common. If only those nerves affecting one side of the body are damaged, then the paralysis would only affect that sided of the body, from the point of injury down. More commonly, a spinal cord injury that affected one side would not be that precise, and there may be some degree of global impact.

Monoplegia

Monoplegia describes paralysis of only one limb, and can be the result of injury to the brain, spinal cord, or damage to the peripheral nervous system relating to that limb. Cerebral palsy is the most common cause of monoplegia.

Lower spinal cord injuries

nerve root

Nerve root anatomical structure labeled cross section, vector illustration educational diagram. Medical information with root scheme. Human spine health guide as informative poster. Graphical example.

Injuries to the lower spinal cord may have a lesser impact on lower limb function; different nerve pairs supply sensation and motor control to different areas of the legs. People with SCI affecting the lumbar or sacral spinal cord, depending on the level of injury, may retain good control over the muscles of the leg but are likely to have reduced control over their bowels and bladder.

Sexual function is likely to be altered with any spinal cord injury; this may mean lack of sensation or control, erectile dysfunction, vaginal dryness, and other issues arising from the impact of SCI and paralysis.

As well as paralysis stemming from spinal cord injury, damage to a nerve root after it diverges from the spinal cord can cause regions of paralysis, though this will apply to a specific area rather than the classic signs of spinal cord injury, i.e. an injury affecting a single nerve will not affect other areas of nerve function.

 

Does a fractured spine always mean paralysis?

A vertebral fracture – damage to the bones of the spine – does not necessarily affect the spinal cord. The spinal cord is the conduit for movement and sensation signals, and so only when the spinal cord is damaged do you get paralysis. A vertebral fracture or traumatic injury affecting the spine can, however, cause damage to the spinal cord, whether it is an acute traumatic injury or a degenerative, progressive condition.

Other causes of paralysis

Spinal cord injury is just one of the possible causes of paralysis[viii]; other causes include:

  • Stroke: particularly a one-sided loss of motor control.
  • Brain injury: the brain and spinal cord form the continuous central nervous system and a brain injury can have a range of impact, including paralysis which can be regional or widespread.
  • Degenerative diseases affecting the nerves, like motor neurone disease or Huntington’s disease.
  • Autoimmune conditions which affect the nerves, such as Guillain-Barre syndrome or multiple sclerosis.

Risks associated with paralysis

Being unable to move independently is associated with a number of significant health conditions and outcomes.[ix] Without control over movement, a person is at risk of:

  • Pressure damage to the skin and underlying tissues.[x]
  • Moisture damage to the skin, from sweat and incontinence, plus an increased risk of fungal skin infections.
  • Obesity, coupled with muscle degeneration.
  • Depression – becoming paralysed triggers a number of huge lifestyle changes which can be overwhelming and can contribute to significant mental health problems. A life-changing injury, alongside permanent disability, changes in lifestyle and which can affect family life, recreational activities, and work or education, takes time and support to come to terms with.

Higher spinal cord injuries which affect the muscles involved with breathing have their own risks and are associated with higher incidence of serious illness.

  • Pneumonia – alongside an inability to cough and clear mucous, and which may be exacerbated by inability to change position and poor sitting balance.
  • Aspiration – an impaired swallow means that food or fluid can enter the respiratory tract and cause aspiration pneumonia.
  • Difficulty managing complex care needs – some people with high spinal cord injuries have tracheostomies, and some need part- or full-time mechanical ventilation. Some people with high spinal cord injuries need to have their nutrition and hydration needs met through an alternative to the oral route – usually a percutaneous endoscopic gastrostomy (PEG). While this can all be well-managed with a trained care team, it does inevitably mean that activities take a little more planning and organisation than for people without complex care needs.

Some of the risks associated with paralysis can often be prevented, or at least reduced, by provision of good care. Pressure or moisture damage can be minimised with regular positional changes, good continence care, and appropriate pressure-relieving equipment like mattresses and cushions. A team of specialised carers can support people living with paralysis to stay healthy and active.

There is a range of solutions to problems with urinary or faecal incontinence, constipation and urinary retention, and they are tailored to the individual. Problems associated with immobility can be reduced with an appropriate healthy diet, physiotherapy and management of other issues. A person with reduced physical function should also be able to continue having a healthy sex life, although the impact of a spinal cord injury means that there usually have to be some adjustments – and a little imagination – in the way people have sex.

depression

Depressed Man with Problems holding hand over his Face and Crying, occupied by Mind Blowing Thoughts

Depression and other mental health problems can be associated with trauma, injury, immobility, a changing body and changing abilities, feelings of self-worth, and changes to position in society, the workplace, and the home. There is no right or wrong way to feel after a life-changing injury or with changing care needs for any reason. It may take time to realise that a person with extra care needs is as valued and valuable as anyone else in society, and that a person’s potential does not have to be linked to their physical abilities. Feelings of depression and other negative emotions can be transient or can last a long time and become a serious problem. Asking for help when struggling with mental health is a positive, responsible action, and there is lots of support available.[xi]

Living with paralysis after a spinal cord injury

The world has almost always been designed by, and for, able-bodied people. In more recent years, efforts have been made to create a more accessible and inclusive infrastructure, but living with any level of paralysis will require some adaptation. Equipment is better than ever, with an overwhelming number of devices aimed at improving quality of life for people with complex restrictions and extra care needs.

While it requires practical, physical, and emotional solutions to adapting to life with any degree of paralysis, the kind of care a person receives has a huge influence on their quality of life and abilities. The aim of good nursing care teams is to make for any deficits in self-caring abilities; if carers can ‘fill the gaps’, then a person with complex care needs can continue to live a full and fulfilling life. Everyone – from the fittest, most physically able people to those with the most severe disabilities – requires some sort of support to live, and care packages are not designed to reduce independence, but rather to facilitate independence with support.[xii]

A care package designed to support people with paralysis will be built to respect an individual’s wishes and with their lifestyle and values in mind, while meeting their functional needs. Care packages can be built to support people in their own home, out and about, and even going on holiday. For someone with ongoing care needs, a care team can become familiar and valued, promoting and facilitating the kind of life the individual wants to lead. Health and social care services, specialist care providers, and in-person or online professional or peer support groups can help with the social and practical side of life with these kind of new care needs, and people with spinal cord injuries causing paralysis can expect their care providers to help them live the lives they want.

[i] Alizadeh, A., Dyck, S. M., & Karimi-Abdolrezaee, S. (2019). Traumatic spinal cord injury: an overview of pathophysiology, models and acute injury mechanisms. Frontiers in neurology, 10, 282.

[ii] Bryden, A., Kilgore, K. L., & Nemunaitis, G. A. (2018). Advanced assessment of the upper limb in tetraplegia: a three-tiered approach to characterizing paralysis. Topics in Spinal Cord Injury Rehabilitation, 24(3), 206-216.

[iii] Pearl, N. A., & Dubensky, L. (2020). Anterior cord syndrome.

[iv] Shams, S., & Arain, A. (2021). Brown Sequard Syndrome. In StatPearls [Internet]. StatPearls Publishing.

[v] McKinley, W., Hills, A., & Sima, A. (2021). Posterior cord syndrome: Demographics and rehabilitation outcomes. The Journal of Spinal Cord Medicine, 44(2), 241-246.

[vi] Avila, M. J., & Hurlbert, R. J. (2021). Central Cord Syndrome Redefined. Neurosurgery Clinics, 32(3), 353-363.

[vii] Kirshblum, S. C., Burns, S. P., Biering-Sorensen, F., Donovan, W., Graves, D. E., Jha, A., … & Waring, W. (2011). International standards for neurological classification of spinal cord injury (revised 2011). The journal of spinal cord medicine, 34(6), 535-546.

[viii] Armour, B. S., Courtney-Long, E. A., Fox, M. H., Fredine, H., & Cahill, A. (2016). Prevalence and causes of paralysis—United States, 2013. American journal of public health, 106(10), 1855-1857.

[ix] Sezer, N., Akkuş, S., & Uğurlu, F. G. (2015). Chronic complications of spinal cord injury. World journal of orthopedics, 6(1), 24.

[x] Cowan, L. J., Ahn, H., Flores, M., Yarrow, J., Barks, L. S., Garvan, C., … & Stechmiller, J. (2019). Pressure ulcer prevalence by level of paralysis in patients with spinal cord injury in long-term care. Advances in Skin & Wound Care, 32(3), 122-130.

[xi] Post, M. W. M., & van Leeuwen, C. M. (2012). Psychosocial issues in spinal cord injury: a review. Spinal cord, 50(5), 382-389.

[xii] Barclay, L., McDonald, R., & Lentin, P. (2015). Social and community participation following spinal cord injury: a critical review. International Journal of Rehabilitation Research, 38(1), 1-19.

High spinal cord injuries (SCI) can have a profound impact on respiratory function, leaving people vulnerable to breathing problems and recurrent chest infections and pneumonia. Some people with high SCI are dependent on mechanical ventilation to help them breathe for all or part of their daily lives.

The higher a spinal cord injury, the more impact it has on the life and ability of the affected person. The spinal cord is a long bundle of nerves which run continuously through a canal within the vertebrae – the bones of the spine. Pairs of nerves branch off from the spinal cord, extending to the left and right of each vertebra and branching off further to form a network nervous system throughout the body.

Each of these pairs of nerves supplies nerve function – impulses that control movement and sensation – to specific areas of the body depending on the level of the nerve. This means that an injury high up the spinal cord will affect more of the body, as there will be dysfunction of the nerves below that point.

The completeness of an SCI also predicts the impact on function – an injury with total or near-total destruction of the nerve pathways will have a more profound effect on a person’s body and life than one which affects, for example, one side of the spinal cord or a specific portion of the bundle of nerves.[i]

What is a C-spine injury?

The C-spine is the cervical spine, roughly the portion of the spinal column that makes up the neck. The cervical spine comprises the top seven vertebrae, labelled from the top (closest to the skull) downwards: C-1 to C-7. These correspond to 8 spinal cord segments, each of which describes a single pair of nerves, with the C8 nerves diverging from the spinal cord just under the C7 vertebra.[ii]

Film x-ray c-spine (Lateral view): Cervical level spine

A spinal injury high in the neck – the cervical spine or C-spine – might affect all four limbs and body functions including movement and sensation, respiratory health, digestive health and continence, sexual function and more. A lower injury, in the lumbar or thoracic spine, might only affect the lower limbs and aspects of continence and sexual function, leaving respiratory function and arm and hand control intact. Spinal injuries can be acute, such as in a traumatic accident like a car crash, or can be a result of chronic conditions, infections, degenerative changes, congenital and genetic conditions, and more.[iii]

How does a C-spine injury affect breathing?

Respiratory dysfunction is the most common cause of serious illness and mortality in people with spinal cord injuries, and higher spinal cord injuries can have a profound impact on respiratory function.[iv]

When the nerves that convey impulses to and from the brain to the body are damaged, a person can lose some or all sensation and conscious control over the parts of their body that rely on those nerves and related muscles. Some unconscious functions can also be affected, meaning that some of the body’s innate actions are disrupted. Sleep-disordered breathing and autonomic dysfunction contribute to breathing problems in people with spinal cord injury.[v]

The muscles responsible for breathing control include the diaphragm – the flat muscle directly beneath the lungs; the abdominal muscles; and the intercostal muscles – the muscles between each rib. With reduced control over these muscles, breathing is affected. The impact of this loss of muscle control can range from a person being completely unable to make useful respiratory effort and becoming dependent on mechanical ventilation to being unable to cough strongly enough to clear secretions from the throat, through to having a reduced vital lung capacity or weakened cough.[vi][vii]

People who are unable to clear fluid from the back of the throat can become very prone to chest infections, and mechanical devices are available to help clear the lungs, including mechanical cough assist devices, and suction for upper airways secretions.

 

Having an impaired swallow also poses a significant risk to the lungs, as any food or fluid that enters the lungs instead of the stomach can cause very severe aspiration pneumonia.[viii] Aspiration pneumonia most commonly begins in the right lower lobe of the lungs, as the anatomy of the airways mean that any aspirated fluids have a more direct route to the right lung.

Some people with a reduced swallow after a spinal cord injury will need alternative ways of maintaining their nutritional and hydration needs in the short- or long-term. This could be through an NG or nasogastric tube – a tube passed through a nostril directly into the stomach, or through a PEG (percutaneous endoscopic gastrostomy) – a tube fitted to the stomach through the abdominal wall. Either of these routes can be used to administer a special liquid food mix and fluids directly into the stomach. A PEG is particularly likely for people who have tracheostomies.

Levels of spinal cord injury impact on respiratory function

The completeness or incompleteness of a spinal cord injury, and where incomplete, the portion of the spinal cord affected, can mean significant differences in the elements of respiratory function that are preserved on an individual basis.

For the sake of clarity, further discussion of SCI levels assumes a complete or near-complete spinal cord injury. It is also important to remember that the chronic impact of a spinal cord injury isn’t always possible to predict during the acute stages of a spinal cord injury where spinal shock is present.

  • C1-C3: Any spinal cord injury at this level will have a profound impact on breathing. Without a pathway to the nerves controlling the respiratory muscles, a person will have very little control over their breathing, especially those important functions like coughing. With loss of control over the muscles of the abdomen, the diaphragm and the rib cage, breathing will be shallow, with a reduced lung volume for each breath and inability to clear matter from the chest and throat through deep breathing and coughing. People with C1-C3 spinal cord injuries are likely to need mechanical ventilation for some or all of the time. Complex care needs like mechanical ventilation and tracheostomy care can often be met at home; having a comprehensive package of care can support people in living independent lives.
  • C4: a C4 injury will mean impaired diaphragm function, reduced ability to fill the lungs to vital capacity, and a reduced cough. People with a C4 injury may need mechanical ventilation overnight and may find that their breathing can be impaired by something as simple as poor positioning. A cough assist device can help clear the lungs of any secretions, food or fluid.
  • C5: someone with an injury at C5 may be able to breathe independently but will have a reduced lung capacity with less effective breathing and cough.
  • C6-C7: C7 is the lowest of the cervical vertebrae, and someone with an injury at C6 or below is likely to be able to breathe independently. While some respiratory function is preserved, reduced strength and muscle control does mean that someone with a C6-C7 injury may still have a weaker cough and some reduction in lung volume for each breath. Someone with a C6 – C7 injury is likely to still have some impaired diaphragmatic control, using accessory muscles of the back and chest more than someone without SCI.

A number of other predictors for respiratory impact from lower cervical spinal injuries – those at C5 or lower – have been identified, including pre-existing respiratory disease and whether the person has sustained an injury directly affecting the respiratory system.[ix]

Acute traumatic spinal cord injuries have historically been overwhelmingly incurred by younger people, especially men, although this trend is shifting towards an older at-risk demographic.[x] This means that pre-existing respiratory disease is relatively rare. However, lung conditions can develop subsequently and can also be exacerbated by, or precipitated by, spinal cord injuries.

Other spinal conditions that can affect breathing

Any condition that affects a person’s control over their breathing can cause respiratory problems too. This includes other degenerative conditions that affect the cervical spine, such as cervical stenosis and cervical spondylosis. Chronic neurological conditions which involve progressively worsening nerve function can also affect breathing as they reach severe stages.[xi]

Spinal cord function can be affected by a wide range of conditions relating to the spinal column, muscles or nerves, including:

  • Cervical spondylosis: a very common condition caused by age-related osteoarthritic-type changes in the vertebrae, severe cervical spondylosis can cause pressure on or restrict the spinal cord. The most common symptom is neck pain, but in extreme cases cervical spondylosis can begin to affect the nerves of the spinal cord, sometimes affecting breathing.[xii]
  • Cervical stenosis: a narrowing of the spinal canal can put pressure on the nerves of the spinal cord, affecting control over the muscles of respiration.[xiii]
  • Myositis and related muscle-wasting conditions like dermatomyositis: any condition which can affect the tone of the muscles related to breathing can cause breathing problems and increase the tendency for chest infections and other respiratory complications. These kinds of diseases can also affect related functions such as swallowing, contributing to further problems with the lungs.[xiv]
  • Poliomyelitis and post-polio syndrome: polio can cause extreme muscle weakness or even paralysis, and while survival rates are good and the acute symptoms resolve, post-polio syndrome can last a lifetime and is typified by muscle weakness and fatigue which affect the breathing, as well as more specific respiratory symptoms like sleep apnoea and a tendency for chest infections as a secondary complication of muscle weakness.[xv]
  • MS: the progressive muscle weakness people with MS experience may, in severe cases, cause weakness of the chest muscles which can affect respiratory effort and make a person more likely to develop respiratory problems. [xvi]

Living with respiratory needs after acute or chronic spinal cord injury

The impact of a spinal injury can vary hugely from one person to the next. The physical impact: the completeness of the injury, the level of impact, and whether the problems are caused by chronic neurodegenerative diseases or acute injury can mean that no two spinal cord injuries are quite the same. The individual person affected can also make a difference, and their psychological and social needs when living with a damaged spinal cord inform their care needs as much as any physical challenges.

Methods for managing problematic respiratory function after a spinal cord injury are increasingly sophisticated and improve both the quality and quantity of life for those living with spinal cord injury. Portable mechanical ventilation as well as larger home devices, home oxygen and equipment are more readily available than ever. Nurses and professional carers who are highly trained in specific complex and respiratory care in the home are also changing the lives of people living in the community with complex care needs.

Close up patient doing hand stretching exercise on massage table

 

Someone with a condition or injury affecting their high cervical spine is likely to need support with lots of their physical needs, including physiotherapy, access to outside activities, meeting nutrition, hydration and continence needs, and any of the usual activities of daily living that can become a challenge after a spinal cord injury.

Particular challenges for people with affected respiratory function can include finding ways to get out and about when reliant on mechanical ventilation, preventing and managing chest infections, using cough assist devices, tracheostomy management, and respiratory function and support when asleep.

Family members may be able and willing to help meet some of these needs, but someone with complex care needs can access full-time care packages to cover all physical and support with emotional and social needs too. A good care package supports independence and allows a person to continue to live the kind of life they want, seamlessly making up for self-care deficits and needs.

Mechanical ventilation

Some people with c-spine damage will need to use a mechanical ventilator for some or all of the time to support their respiratory effort and maintain adequate ventilation. Although essential and lifesaving, mechanical ventilation carries its own risks, including an increased risk of chest infections – although this risk is already inherent in anyone who needs respiratory support – and risk of mechanical failure. However, equipment and care is now specialised and sophisticated and with the right support, mechanical ventilation at home can enable, rather than hinder, a desirable lifestyle.

____________________________________________________________________

[i] Anderson, D. K., & Hall, E. D. (1993). Pathophysiology of spinal cord trauma. Annals of emergency medicine, 22(6), 987-992.

[ii] Diaz, E., & Morales, H. (2016, October). Spinal cord anatomy and clinical syndromes. In Seminars in Ultrasound, CT and MRI (Vol. 37, No. 5, pp. 360-371). WB Saunders.

[iii] McDonald, J. W., & Sadowsky, C. (2002). Spinal-cord injury. The Lancet, 359(9304), 417-425.

[iv] Zimmer, M. B., Nantwi, K., & Goshgarian, H. G. (2007). Effect of spinal cord injury on the respiratory system: basic research and current clinical treatment options. The journal of spinal cord medicine, 30(4), 319-330.

[v][v] Berlowitz, D. J., Wadsworth, B., & Ross, J. (2016). Respiratory problems and management in people with spinal cord injury. Breathe (Sheffield, England), 12(4), 328–340. https://doi.org/10.1183/20734735.012616

[vi] Benditt, J. O. (2006). The neuromuscular respiratory system: physiology, pathophysiology, and a respiratory care approach to patients. Respiratory care, 51(8), 829-839.

[vii][vii] Winslow, C., & Rozovsky, J. (2003). Effect of spinal cord injury on the respiratory system. American journal of physical medicine & rehabilitation, 82(10), 803-814.

[viii] Mandell, L. A., & Niederman, M. S. (2019). Aspiration pneumonia. New England Journal of Medicine, 380(7), 651-663.

[ix] Sampol, J., González-Viejo, M. Á., Gómez, A., Martí, S., Pallero, M., Rodríguez, E., … & Ferrer, J. (2020). Predictors of respiratory complications in patients with C5–T5 spinal cord injuries. Spinal cord, 58(12), 1249-1254.

[x] Aarabi, B., Albrecht, J. S., Simard, J. M., Chryssikos, T., Schwartzbauer, G., Sansur, C. A., … & Scarboro, M. (2021). Trends in demographics and markers of injury severity in traumatic cervical spinal cord injury. Journal of neurotrauma, 38(6), 756-764.

[xi] Gilchrist J. M. (2002). Overview of neuromuscular disorders affecting respiratory function. Seminars in respiratory and critical care medicine, 23(3), 191–200. https://doi.org/10.1055/s-2002-33027

[xii] Yu, E., Romero, N., Miles, T., Hsu, S. L., & Kondrashov, D. (2016). Dyspnea as the Presenting Symptom of Cervical Spondylotic Myelopathy. Surgery journal (New York, N.Y.), 2(4), e147–e150. https://doi.org/10.1055/s-0036-1597664

[xiii] Fahad, E. M., Hashm, Z. M., & Nema, I. M. (2020). Cervical spinal stenosis and risk of pulmonary dysfunction. International journal of critical illness and injury science, 10(1), 16–19. https://doi.org/10.4103/IJCIIS.IJCIIS_83_19

[xiv] Rowen, A. J., & Reichel, J. (1983). Dermatomyositis with lung involvement, successfully treated with azathioprine. Respiration, 44(2), 143-146.

[xv] Bach, J. R., & Alba, A. S. (1991). Pulmonary dysfunction and sleep disordered breathing as post-polio sequelae: evaluation and management. Orthopedics, 14(12), 1329-1337.

[xvi] Tantucci, C., Massucci, M., Piperno, R., Betti, L., Grassi, V., & Sorbini, C. A. (1994). Control of breathing and respiratory muscle strength in patients with multiple sclerosis. Chest, 105(4), 1163-1170.

Bowel management, particularly addressing challenges like constipation and incontinence, is one of the most important considerations after a spinal cord injury (SCI). The primary and secondary consequences of bowel problems can be profound and have a severe impact on physical and mental health.

How can a back injury affect the bowels?

Injury to the spinal cord can profoundly affect all nerve function between the brain and nerves below the point of injury. There is loss of control and sensation, meaning that the injured person has no voluntary control over movement, and also loss of some of the intrinsic nervous system activity of the bowels. Losing sensation also means loss of that feeling of pressure in the bowels, which is what helps us know when to go to the toilet; knowing when to perform bowel care is a large part of managing continence for people with or without an SCI. A spinal cord injury also has an intrinsic effect on muscle and anal tone.

The point at which the spinal cord is affected has a significant impact on the nature and severity of the impact on the bowel. The higher the injury, the more impact on physical function, movement, and sensation. Aside from SCI, acute neurological events or chronic neurodegenerative conditions can result in similar bowel management challenges.

The completeness of the spinal cord injury also affects the impact of the injury on the bowel. The nerves which form a feedback loop conveying sensation and impulses for movement between the brain and the bowel, as well as some reflexive action, can be severed or damaged in a way that means that there is no control beyond that point. The damage can be partial, affecting only a portion of the bundle of nerves which comprise the spinal cord, and so some sensation, control, or tone may be retained.

Bowel problems after a spinal cord injury

There are three main contributing factors to bowel management difficulties after a spinal cord injury:

  • An SCI damages our ability to sense our need to go to the toilet, meaning that we can become incontinent, passing stool before we’re prepared. An SCI can also affect our ability to control the complex voluntary mechanisms controlling bowel movements. We need intact spinal cord nerves to allow us to tense and relax our abdominal muscles, to deliberately increase muscular pressure within the abdomen, to relax the anal sphincter and to push stool out.
  • An SCI that affects our mobility and motor control can make it harder to manage the physical practicalities of managing continence, including simply getting to the toilet or managing continence care. The extent of effect of the SCI might mean that the right management techniques are different from person to person depending on their levels of physical mobility and independence as well as the type of care input they have from others. Someone with intact movement and sensation in their upper body may be able to independently manage complex bowel management after a spinal cord injury, whereas someone with a high spinal cord injury affecting movement will need a different management plan with more input from carers.
  • The involuntary side of the digestive process is also affected by spinal cord injury. This affects peristalsis, the movement which conveys matter through the digestive system. This affects the speed of the bowel – the rate at which the contents of the digestive system move from one end to the other. It also affects every reflex part of the process, which can include aspects like the reflexive opening – or tightening – of the anal sphincter after different forms of stimulation. The level of the SCI affects the nature of the bowel dysfunction, and a dysfunctional bowel caused by damage or disease affecting the nerves is known as a neurogenic bowel.

The Neurogenic Bowel

The area of impact of spinal cord injury affects the type of bowel dysfunction a person experiences.[i] Neurogenic bowel can also be caused by other conditions which affect the nerves of the bowel, including multiple sclerosis and stroke.

Neurogenic bowel can be grouped into two broad categories – upper motor neurone bowel and lower motor neurone bowel.[ii]

Upper motor neurone bowel syndrome, or hyper-reflexive bowel, is caused by injury above the conus medullaris – it is characterised by increased tone to the walls of the bowel and anus. Gut motility is reasonable but without voluntary control of a highly toned anal sphincter, bowel evacuation can be a challenge, and upper motor neurone bowel is associated with faecal retention and constipation. People with upper motor neurone bowel can have good results from bowel evacuation techniques which employ stimulation to promote reflex opening of the anal sphincter.

Lower motor neurone bowel, or a reflexive bowel, results from injury at the conus medullaris and/or cauda equina. People with lower motor neurone bowel have disruption to the peristaltic action of the gut triggered by higher spinal cord activity, and so gut motility is poor and stool passage time is slow, meaning constipation can be a significant problem. Lower motor neurone bowel also results in an atonic, flaccid anal sphincter and so incontinence is more likely and more difficult to manage.

The level of higher spinal injuries has an impact on a person’s voluntary bowel motility, as reduced physical movement and an inability to deliberately increase intraabdominal pressures through diaphragm control, Valsalva-type manoeuvres, or positional changes create more challenges.

Complications of bowel problems after a spinal cord injury

Continence requires careful management for people with injury to the spinal cord, and the repercussions of poor bowel management can be profound.

  • Severe constipation – a build-up of hard stool in the bowel can cause serious problems without effective intervention, leading to faecal impaction, bowel perforation, and potentially serious illness.
  • Damage to skin – incontinence is a huge risk factor for damage to the skin and underlying tissues, causing moisture lesions and contributing to pressure damage, fungal infections and bacterial skin infections.
  • Autonomic dysreflexia – in people with cervical or high thoracic spine injuries, autonomic dysreflexia is a potentially severe complication of bodily stress which can result from various problems including constipation or tissue damage.[iii]
  • Impact on daily life – if constipation, incontinence, or a lengthy and complex bowel management regime are a problem, that can have a significant impact on quality of life and a person’s ability to continue any of their usual activities. Social and family life, work and mental and physical health can suffer.

Some of the interventions used for bowel management after nervous system damage can carry their own risks as well as benefits; some of the ‘last resort’ type treatments can include surgical interventions.

Managing bowel problems after a spinal injury

Specialist care teams will always recommend the safest, least invasive methods of bowel management first, but it can take some trial and error to find an effective and acceptable method for an individual. Managing constipation and continence after SCI requires a two-pronged approach – firstly, to ensure that stool is moving through the bowel at a reasonable rate to avoid constipation, and secondly to enable effective and safe emptying of stool from the bowel.

The first – maintaining healthy bowel motility – can often be effectively managed with a healthy diet and some oral medications including stool softeners and various forms of laxative. Other non-invasive techniques like abdominal massage and positional changes can help stool propulsion.

Evacuating the bowel can be more difficult at times, as it’s important to find the right balance between constipation and the possibility of incontinence, and this depends largely on the level and completeness of the injury, or the severity of other conditions causing spinal cord damage. People with reflexive bowel emptying may always require some incontinence pads and other products, and to plan for the possibility of incontinence, but a good bowel care routine can make a huge difference. Planning bowel evacuation procedures to follow patterns of peristalsis and likely timing of the need to remove stool from the rectum can help prevent accidents. Bowel management for people with spinal injuries can involve one or more of the following[iv]:

  • Diet and adequate fluid intake – a healthy diet can have a significant impact on gut motility and stool volume. For people with neurogenic bowel, a healthy diet and adequate fluid intake alone will not be enough to ensure effective bowel emptying, but can help reduce the risk of constipation and make management a little easier.
  • Abdominal massage – this can be effective in supporting passage of stool through the gut and raising the pressure within the abdomen to improve expulsion of stool.[v]

  • Positioning – just the pressure of stool in the rectum can trigger anal opening for some people, and so sitting on a toilet, upright and with hips and knees bent can help move stool towards, or sometimes through, the anus.
  • Digital stimulation – using a gloved, lubricated finger inserted a few centimetres into the anus, then swirled around for around 30 seconds can stimulate reflex anal relaxation and result in a bowel movement. However, this reflex is not present in people with lower motor neurone bowel.
  • Manual evacuation – a gloved, lubricated finger can be inserted into the anus to manually remove stool using a scooping motion.
  • Suppositories – there are various types of suppository, which work to soften the stool or stimulate the bowel, with varying efficacy. Glycerin suppositories work by lubricating the rectum and anus and softening the stool, so can be useful for evacuating hardened stool in the rectum. Bisacodyl suppositories work by increasing bowel contractions approximately half an hour after insertion, but are associated with more risk of incontinence as their duration of action is not entirely predictable.
  • Enemas – another way of delivering small amounts of stimulant in liquid form into the rectum, enemas can have good results for managing bowel evacuation. Larger volume enemas can be effective in some circumstances but carry more risk of bowel damage, poor retention, and, occasionally, autonomic dysreflexia.
  • Trans-anal bowel irrigation – the introduction of a set volume of warm water through a balloon-cuffed rectal catheter increases the volume and fluidity of bowel contents, literally washing out the bowel.

 

If severe constipation is still a problem despite trials of simple and minimally invasive methods of management, some surgical interventions may be considered. These can include implanted sacral nerve root stimulation devices or a MACE – an irrigation tube implanted to flush the large bowel from the appendix.[vi] A colostomy or ileostomy are sometimes considered a last resort, but have had good results in improving quality of life for people with spinal cord injuries.[vii]

Care and support

Management of continence and constipation is one of the most important considerations after a spinal cord injury and can have a profound impact on physical and mental health and quality of life. People with spinal cord injuries who retain good use of their arms and hands may be able to perform bowel evacuation procedures independently, whereas others will need support from carers. An effective care package is one designed to work around the individual, actually enabling supported independence and covering any self-care deficits to enhance quality of life.

Bowel habits are traditionally a sensitive, even taboo subject so it’s very natural for many people to feel shy or embarrassed about having new bowel care needs and incontinence. Support groups, acceptance and openness, disability activists and social media personalities with SCI have helped make this an acceptable topic for frank discussion. The impact of continued constipation, incontinence, and the other potential problems associated with bowel dysfunction cannot be understated. Quality of life and mental health are paramount after a spinal cord injury, and poor continence management is associated with poor quality of life and mental health outcomes.[viii]

Bowel care needs a holistic and person-centred approach. The method needs to be effective, preventing constipation and incontinence; practical and practicable in terms of care input and availability of an appropriate setting and equipment; and acceptable to the individual. Effective care includes monitoring, essential for early identification and management of emerging problems. Abdominal distention, autonomic dysreflexia, new patterns of incontinence and constipation can all indicate problems that need to be addressed.

_____________________________________________________________________________________________

[i] Hughes M. (2014). Bowel management in spinal cord injury patients. Clinics in colon and rectal surgery, 27(3), 113–115. https://doi.org/10.1055/s-0034-1383904

[ii] Krassioukov, A., Eng, J. J., Claxton, G., Sakakibara, B. M., & Shum, S. (2010). Neurogenic bowel management after spinal cord injury: a systematic review of the evidence. Spinal cord, 48(10), 718-733.

[iii] Cragg, J., & Krassioukov, A. (2012). Autonomic dysreflexia. Cmaj, 184(1), 66-66.

[iv] Krassioukov, A., Eng, J. J., Claxton, G., Sakakibara, B. M., & Shum, S. (2010). Neurogenic bowel management after spinal cord injury: a systematic review of the evidence. Spinal cord, 48(10), 718-733.

[v] Ebert, E. (2012). Gastrointestinal involvement in spinal cord injury: a clinical perspective. Journal of Gastrointestinal & Liver Diseases, 21(1).

[vi] Hughes M. (2014). Bowel management in spinal cord injury patients. Clinics in colon and rectal surgery, 27(3), 113–115. https://doi.org/10.1055/s-0034-1383904

[vii] Hocevar, B., & Gray, M. (2008). Intestinal diversion (colostomy or ileostomy) in patients with severe bowel dysfunction following spinal cord injury. Journal of Wound Ostomy & Continence Nursing, 35(2), 159-166.

[viii] Gurcay, E., Bal, A., Eksioglu, E., & Cakci, A. (2010). Quality of life in patients with spinal cord injury. International Journal of Rehabilitation Research, 33(4), 356-358.

Sometimes, traditional imaging with x-ray or CT scan does not find a clear physical cause for the spinal cord injury symptoms the patient is experiencing – no injuries to the vertebrae or other obvious physical damage around the spine. This is known as ‘spinal injury without radiographic abnormalities’, or ‘SCIWORA’. Sometimes the terms ‘neuroimaging’ or ‘imaging’ may be used in place of ‘radiographic’.

Someone presenting to hospital with acute symptoms that suggest a spinal cord injury may be experiencing loss of movement, bladder and bowel control, sensation, and possibly problems breathing independently. A spinal cord injury (SCI) is most likely to occur following some traumatic incident – a car accident, for example, or a fall from a height. There may be some bruising or obvious signs of trauma, or it may be only the physical changes that suggest an SCI. A suspected spinal cord injury is always a medical emergency and must receive paramedic and hospital treatment immediately.

In general, spinal cord injuries are suspected when someone presents with some of the many symptoms of a spinal cord injury, and this is confirmed by medical imaging. X-rays and computed tomography (CT) scans are common, non-invasive ways of confirming and investigating a spinal injury.

Although an x-ray or CT scan may not show any damage to the bones and tissues around the suspected injury, medical imaging has improved since the first distinction between SCI with and without radiographic abnormalities, and a magnetic resonance imaging  (MRI) scan will almost always show damage even when only the spinal cord has been injured.

Common diagnostic use of MRI scans as a medical imaging option has led to discussion within the medical community over whether the term ‘without radiological abnormalities’ is still appropriate, now that a pure spinal cord injury can, in fact, be radiologically identified.[i]

X-Ray vs. MRI scan of spinal cord injury

SCIWORA is very rare in adulthood – this is because the bones and processes of the adult spinal column are much more fixed and inflexible than in childhood. This means that a spinal cord injury in an adult is almost always accompanied by damage to the bones and surrounding structures – in other words, a spinal cord injury with surrounding injuries that are visible on traditional medical imaging such as CT scans.

Who is likely to sustain a spinal injury without radiographic abnormalities?

SCIWORA is much more common in childhood and extremely uncommon in people over the age of 18. SCIWORA actually accounts for something between 15% and 42%[ii] of spinal cord injuries in people aged 18 and under – this wide range is because the incidence of SCIWORA among children and adolescents with SCI varies greatly according to the age of the child. In general, the younger the child who suffers a spinal cord injury, the more likely it is to be unaccompanied by bone injuries, and SCIWORA is much more common again in children younger than 8[iii].

The main reason for the higher risk for children is thought to be the fact that young children’s spinal ligaments and intravertebral discs are flexible and elastic, and so provide less protection to the spinal cord. A back trauma – a car injury or sports injury, for example – sustained by someone with a very elastic spine can cause damage to the spinal column without significantly damaging any part of the backbone or cartilage.

Where adults experience a SCIWORA, they are more likely to have a non-traumatic underlying cause, such as degenerative changes causing pressure on the spinal cord or problems with blood supply, such as venous congestion.[iv]

The age of the child can also influence the area of the spinal cord damaged, with younger children more likely to have injuries higher up the spine than older children and adolescents[v]. This is thought to be due to a combination of a very elastic spine, weak neck muscles and the large head to body ratio of younger children. It is not hard to imagine the damage sustained by someone with a large, heavy head on a flexible, elastic spine during a car accident or other traumatic event, and younger children are therefore more likely to sustain very serious injuries with more significant long-term effects.[vi]

What are the results of an SCIWORA?

As with any spinal cord injury, the effects vary widely, and depend largely on the area of the injury and how much of the spinal cord is damaged at that point. As younger children tend to have higher spinal injuries, they are more likely to have profound changes to their ongoing ability.

SCIWORA is also seen, on occasion, to be recurrent. The likelihood of this depends on the mechanism of injury – it is thought to be more common where the spinal cord was damaged in such a way as to make it, or rather the surrounding bones and tissues, less stable in the long term.[vii] Anyone who has sustained an SCI is likely to have a significant hospital stay and so a recurrent SCI is likely to be during a period of close clinical monitoring and can be managed appropriately.

Can people recover from a SCIWORA?

All spinal cord injuries are different, so there is no answer that applies to everyone. Recovery potential varies case to case, and the only people who can really give an answer are the healthcare specialists involved in the immediate care of the person with an SCI.

People with a total or near total SCIWORA – in other words whose spinal cord nerves are too damaged to relay a useful amount of information – will almost always need significant extra support for life, and higher injuries in the neck or C-spine may mean that that person is dependent on support for all of their normal activities of daily living. Injuries to the high spinal cord can mean that a person becomes dependent on a ventilator for breathing and coughing.

Where there is less damage to the spinal cord, the injuries may be transient, and sometimes a full recovery can be made. A partial spinal cord injury may leave people with only minimal altered movement, control, or sensation. The effects of a partial spinal cord injury can affect one or both sides of the body, and can be very varied. Someone with a partial SCI may still have very profound support needs, or they may be only very slightly affected – people with the least severe spinal cord injuries may simply have slightly altered sensation, or may need to take extra care of their bladder or bowel control.

Spinal Cord Injury Without Radiographic Abnormalities

The full effects of SCIWORA can sometimes take up to 4 days to be fully realised, and anyone with a suspected spinal cord injury will be monitored very closely in hospital for some time. Immobilisation of the spine is one of the most important early treatments for anyone with a suspected SCI. As with any SCI, people with a SCIWORA which has significantly affected their ability to live independently may benefit from a stay in a neurological rehabilitation facility, where they can receive intensive physiotherapy, occupational therapy, and plan for the ongoing changes in their life. This period of time is also sometimes essential to ensure that an appropriate care package can be put in place for them going home, and adjustments to their home can be made.

Living with a SCIWORA

A serious spinal cord injury sustained in childhood is, naturally, an incredibly emotive thing – a child sustaining any trauma or serious illness will affect the whole family and may feel like a tragedy. There will be, of course, massive adjustments to make, but there’s more than one way to live a life, and the world is scattered with happy, successful people living with even the most profound injuries and continued care needs.

The professionals involved in the care and rehabilitation of people with spinal cord and neurological injuries should be able to point individuals and families affected by SCI towards support groups and resources to help them adjust to the changes. The internet can also be an incredibly useful tool in finding local or online support networks and advice about living with a SCIWORA. Parents and families of children with spinal cord injuries can also expect individualised support through what is bound to be an uncertain time. One of the most common concerns parents of young children with SCI have is over how much the child can understand, and how much they should be told. There’s no easy answer to this, but it’s something that the healthcare professionals involved in the care of children of all ages with SCI are very experienced in.

Even if they had exactly the same injury and effect, there are clearly huge differences in the types of support that children and adults need after an SCI. There are similarities too – anyone may need personal care, continence care, and the support of a team experienced in, for example, ventilator and tracheostomy care. The differences may include the type of activity that a care team will support the person through – whether schooling or work, family activities as a dependent child or as an independent adult, and a care team needs to be able to adapt to the changes anyone experiences through childhood and adolescence.

The dynamics of a family where someone has sustained an SCI, who now needs long-term support and has new restrictions in their activity and ability, can be complex and changeable. The roles and involvement that families take in the support of a person with extra needs is very varied. Parents may take a very active role in the support of a child with complex needs, or may be more comfortable with professional help always at hand. There is no right or wrong here – no standard amount of involvement that a care team expects from the family, only the love and attention that the child has always needed.

Care after a SCIWORA

A severe spinal cord injury sustained at any time of life will mean that some degree of extra medical, nursing, and social support is needed from that point onwards. The level and severity of injury is the main thing that should influence the sort of support someone gets – everyone should have the support they need to live their live the way they want to, and there are many resources with advice on funding and arranging levels of support.

The level of care someone might need after a spinal injury is wide-ranging. Someone may be able to live entirely independently, with or without physical aids to support mobility or continence issues. Others may require a team of carers who are trained in the management of ventilators, pressure area care and supporting people who require assistance with almost every physical need.

A dedicated care team is not just there to make up for new deficits in a person’s ability to care for themselves – they are there to enable that person to live the life they want. With an effective care team, some people with even the most profound injuries and needs can maintain a social life, a family life, a career, and – a question heard often by care providers – can go away on holidays, even while needing full-time support.

Total Community Care is a care provider with a difference – we help all our clients select their care team, giving them and their nearest and dearest complete control over the people they choose to give them support and care. That care team is able to support the client throughout their life, meaning that all care can continue to be given by the people they’ve chosen and grown to know and trust. TCC can create bespoke care packages for a minimum of around 70 hours a week, including 24-hour care packages with both waking and sleeping nights.

We specialise in spinal cord injury and neurological needs so our teams can be highly trained in their specialty. We work hard to have a highly specialised, happy and well supported workforce, meaning our teams provide the very best quality of care and support. We believe that quality of life after a neurological injury begins with having choice over the people who support you.

IMPORTANT NOTE

Total Community Care can only provide packages of care for individuals who are 18 years old and above. We are unable to provide packages of care for children.

Like to know more?

[i] https://doi.org/10.1016/j.clineuro.2008.02.004

[ii] https://online.boneandjoint.org.uk/doi/full/10.1007/s11832-016-0740-x

[iii] https://thejns.org/view/journals/j-neurosurg/57/1/article-p114.xml

[iv]https://journals.lww.com/jtrauma/Abstract/2008/07000/The_Adult_Spinal_Cord_Injury_Without_Radiographic.14.aspx

[v] https://www.hindawi.com/journals/aorth/2018/7060654/

[vi]https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4262055/#:~:text=High%2Denergy%20injuries%20are%20often,Launay%20et%20al.

[vii] https://journals.lww.com/jtrauma/Abstract/1989/05000/Spinal_Cord_Injury_without_Radiographic.21.aspx

Spinal cord injuries (SCI) classically affect function – movement, control and sensation – of all parts of the body which use the nerves at and below the level of injury. This means that, although the brain’s communication with some parts of the body may be permanently and partially or completely obstructed, there is not necessarily any effect on pure brain function.

In some instances, a traumatic incident which results in SCI may also cause traumatic brain injury (TBI); the number of people who suffer both injuries seems to be increasing[i]. There is also a risk of brain injury without obvious evidence on medical scans – ‘occult brain injury’[ii] being overlooked or underdiagnosed, and symptoms being ascribed purely to the spinal cord injury.

However, even when an acute injury is clearly below the level of the brain and there was no direct injury to the head, some people do find that they develop degrees of memory loss, altered thought processes, and ‘brain fog’. The effects of a spinal cord injury can, therefore, have short- or long-term effects on certain cognitive function[iii].

Many people who experience spinal cord injury have no cognitive symptoms at all, and lead full, rewarding lives with adjustments for any new physical needs. Indeed, people with cognitive impairment should also be able to expect to lead the kind of life they want to with adjustments and support for any changes in their ability.

Symptoms like memory loss, cognitive impairment, and fatigue may have a profound effect on a person’s contentment and quality of life. There are many incredible adjustments that can be made to enable a person to engage in normal activities despite physical restrictions and even very complex care needs. However, overcoming cognitive and psychological barriers can be even more complicated.

The association between spinal cord injury and cognitive impairment is often overlooked. Perhaps this is because the effects on other parts of the body can be so profound; advice and management after a spinal cord injury focuses on maximising independence and quality of life by managing physical changes and restrictions. A failure to recognise and understand the cognitive changes that sometimes accompany a spinal cord injury can make people living with these symptoms feel very isolated; understanding a condition makes it easier to live with that condition.

How do Spinal Cord Injuries Affect Brain Function?

The likely reasons for changes in brain function after a spinal cord injury are complex and multifaceted. Someone who sustains a spinal cord injury with no direct effect on the brain might still notice some symptoms relating to their thought processes and memory. Some of the factors that are thought to cause cognitive symptoms include:

  • Inflammatory changes triggered by spinal cord injury which can affect the entire central nervous system.
  • Management of chronic post-SCI symptoms[iv] with strong painkillers, antidepressants, or other medications which might cause drowsiness, memory problems or mood changes.
  • Damage from reduced oxygen supply, either from respiratory arrest at the time of the injury or subsequent difficult airway or ventilation management.
  • The mental health impact of a traumatic injury or when adapting to life with a spinal cord injury.

Inflammatory Complications

Spinal cord injury causes inflammation which can affect the whole nervous system – this includes the brain, and the brain can be very sensitive to inflammation and pressure. The effects of spinal cord injury on the brain have been studied in animal models[v], and have a strong correlation to apparent changes in mood and problem-solving processes.

Using animal models to study mood and thought patterns comes with obvious restrictions; without verbal and other forms of communication which are inherently and exclusively human, effective assessment of the impact on higher brain processes is difficult.

What the studies do show, however, is that a precise injury below the level of the spinal cord that should directly affect the brain does cause changes in processing and behaviour, and that this seems to be related to an inflammatory process which can affect the whole nervous system.

The Effect of Medications

A spinal cord injury can have a profound and widespread effect on physical health, and polypharmacy[vi] – the use of a high number of different types of medication – is very common after an SCI. Some of the medications commonly used long-term for people with a spinal cord injury can have a significant impact on the way a person feels.

Any medicines that affect sleep patterns and mood can cause changes in the way a person functions. Medicines that make people drowsy particularly cause feelings of fatigue, and difficulty concentrating, and even changes in word-finding and simple problem-solving abilities.

The sheer number of medications people typically take after an SCI is associated with a high risk of side-effects[vii]. Medications commonly prescribed for symptoms after a spinal cord injury which can cause apparent changes in brain function include:

Opiates: Many medications for pain can affect mental clarity and cause extreme fatigue and problems concentrating. Opioid medicines[viii] in particular come in a range of forms, long- and short-acting, and are associated with drowsiness and ‘brain fog’.

Anti-convulsants: These are commonly used in the management of pain following spinal cord injury. Gabapentin and Pregabalin have been proved to be especially effective in decreasing neuropathic pain and other secondary outcomes in people with spinal cord injuries.

Anti-convulsant medications have side effects that produce symptoms commonly associated with brain injury and cognitive impairment: patients given Gabapentin are significantly more likely to experience dizziness, somnolence and, less frequently, ataxia including slurred speech, gait disturbance, stumbling and lack of coordination. However, these symptoms appear to be transient.

Anti-depressants: Common antidepressants and medications to help stabilise the mood include:

  • Selective Serotonin Reuptake Inhibitors (SSRIs) such as citalopram, fluoxetine, and sertraline.
  • Tricylic drugs – like amitriptyline and clomipramine.
  • Serotonin and Norepinephrine Reuptake Inhibitors (SNRIs) such venlafaxine and duloxetine.
  • Benzodiazepines – often used for anxiety or to help with sleeping problems, diazepam, temazepam, and lorazepam are all common benzodiazepines.

Nearly all medications prescribed specifically for mood and mental health conditions have reported side effects including fatigue and concentration difficulty. The side effects of these drugs, however, often closely mimic some of the symptoms commonly associated with the depression and mood disorders they are intended to treat. Weighing up the risks and benefits of taking antidepressant medication is sometimes a matter of trial and error; although the side effects of drugs used in mental health medicine can be significant, antidepressants can also be lifesaving.

Anti-spasmodics: Spasticity affects roughly two thirds of patients with spinal cord injury. This is characterised by exaggerated tendon stretch reflexes and involuntary muscle spasms.

Antispasmodics (also commonly called anticholinergics) and muscle relaxants can be used to reduce the effects of spasticity after spinal cord injury.

Commonly used antispasmodic medications include temazepam, clorazepate, baclofen, phenobarbital, tizanidine, cyclobenzaprine and metaxalone.

Use of antispasmodic medication in the treatment of post trauma spinal cord injury patients has a negative impact on neurological and functional outcomes at and after discharge. Antispasmodic medications work to reduce spasticity by inhibiting neural networks and neural activity. Recovery from acute SCI and other injuries to the central nervous system is determined by neural plasticity which depends upon neural activity.

While spasticity affects two thirds of patients with spinal cord injury only a minority of those report that it appreciably effects their quality of life and it seems that clinicians may prescribe medications for signs of spasticity without consideration of the long term reduction in neurological functioning.[ix]

Hypoxic Brain Injury

A high spinal cord injury can have a serious and severe impact on a person’s ability to breathe independently. A period of reduced ventilation or respiratory arrest following a spinal cord injury – for example, if there is any delay in medical care – can cause profound brain injury as a secondary result of a spinal cord injury.

Acute hypoxic brain injury – damage to the brain caused by a lack of oxygen supply – may resolve fully or partially, but extended periods with a lack of oxygen to the brain can cause irreversible damage. This secondary effect can cause changes in mood, behaviour, even personality.

As a direct secondary effect, the link between high spinal cord injury and lack of oxygen to the brain seems straightforward. There are also other mechanisms which might be considered a ‘tertiary’ effect of SCI on the brain – for example, the longer-term changes in nervous system control in people with injuries above T1 – the top vertebra of the thoracic spine – are associated with low blood pressure (hypotension) and a slow heart rate (bradycardia). Some association has been shown between these kind of cardiovascular findings and impaired cognitive function[x].

Mental Health Problems

Whether or not a spinal cord injury has physical effects on the brain, the impact of any serious life-changing event can have a significant impact on mental health. People with acute or chronic mental illness, particularly major depression, consistently show worse results in tests for memory and cognitive function than they do when they have good, stable mental health. This is irrespective of any other health problems, but the high rates of depression experienced among people with spinal cord injury mean that the effects of mental illness on cognitive function are likely to have a considerable impact on some people with spinal cord injury.

Autonomic Dysreflexia

Autonomic Dysreflexia (AD) describes a situation where the body’s unconscious nervous system has an exaggerated and uncontrolled reflex response to a problem, a damaging or irritating stimulus. This response can cause very elevated blood pressure (hypertension) leading to seizures, stroke and cardiac arrest.

Individuals with a spinal core injury are at high risk of AD: the direct risk caused by the nerve damage of their initial injury. This means they have the potential to experience serious physical problems without any sensation or ‘early warning signs.’ Indirectly, they are at higher risk of AD because of the results of their neurological injury – a higher likelihood of bowel or bladder dysfunction, for example.

AD can cause delirium and other symptoms associated with neurological functioning. This should, however, be able to be resolved by the quick and effective identification and treatment that is critical to deal with AD.

Symptoms of AD should be treated as a medical emergency. Having a care package with a dedicated team who can provide continuity of care – a partnership with an individual, a family, and carers – means that everyone involved in a person’s care is in a good position to spot signs of AD.

Avoidance and treatment of AD relies upon good nursing care: monitoring the patient’s symptoms, bowel and bladder emptying, skin and pressure care – support with positional changes and identifying early signs of high blood pressure and heart rate.

Living with Cognitive Impairment

People do report symptoms like brain fog and memory problems after spinal cord injuries, and there are certainly reasons why that might happen. However, it is important to remember that for many people, an injury that only affects the spinal cord does not cause cognitive symptoms.

This is reassuring for many, but also a sign that people who are experiencing memory or mood problems should report their symptoms to their doctors, as there may be ways of improving the symptoms or further investigating the cause. There are many potential chronic post-SCI complications[xi][xii] which can cause or exacerbate cognitive dysfunction, and careful management with continued input from specialist neurological rehabilitation teams is important.

Anyone with a significant spinal cord injury, especially higher injuries affecting breathing, can benefit from a comprehensive care package with a team of nurses and healthcare assistants who have had specialist training in the care of people with complex care needs after a spinal cord injury. Care and input from family members can also be helpful for some people.

Having the option of full professional support, however, can help everybody maintain the kind of relationships they value the most. The resilience of family and close social circles after traumatic, life-changing injuries cannot be valued highly enough[xiii] and professional carers understand and bolster those support networks.

Like to know more?

[i] Hagen, E. M., Eide, G. E., Rekand, T., Gilhus, N. E., & Gronning, M. (2010). Traumatic spinal cord injury and concomitant brain injury: a cohort study. Acta Neurologica Scandinavica122, 51-57. https://doi.org/10.1111/j.1600-0404.2010.01376.x

[ii] Macciocchi, S., Seel, R. T., Thompson, N., Byams, R., & Bowman, B. (2008). Spinal cord injury and co-occurring traumatic brain injury: assessment and incidence. Archives of physical medicine and rehabilitation89(7), 1350-1357. https://doi.org/10.1016/j.apmr.2007.11.055

[iii] Heled, E., Tal, K., & Zeilig, G. (2020). Does lack of brain injury mean lack of cognitive impairment in traumatic spinal cord injury?. The Journal of Spinal Cord Medicine, 1-8. https://doi.org/10.1080/10790268.2020.1847564

[iv] Sezer, N., Akkuş, S., & Uğurlu, F. G. (2015). Chronic complications of spinal cord injury. World journal of orthopedics6(1), 24–33. https://doi.org/10.5312/wjo.v6.i1.24

[v] Wu, J., Zhao, Z., Sabirzhanov, B., Stoica, B. A., Kumar, A., Luo, T., Skovira, J., & Faden, A. I. (2014). Spinal cord injury causes brain inflammation associated with cognitive and affective changes: role of cell cycle pathways. The Journal of neuroscience : the official journal of the Society for Neuroscience34(33), 10989–11006. https://doi.org/10.1523/JNEUROSCI.5110-13.2014

[vi] Cadel, L., C. Everall, A., Hitzig, S. L., Packer, T. L., Patel, T., Lofters, A., & Guilcher, S. J. (2020). Spinal cord injury and polypharmacy: a scoping review. Disability and rehabilitation42(26), 3858-3870. https://doi.org/10.1080/09638288.2019.1610085

[vii] Kitzman, P., Cecil, D., & Kolpek, J. H. (2017). The risks of polypharmacy following spinal cord injury. The Journal of Spinal Cord Medicine40(2), 147-153. https://doi.org/10.1179/2045772314Y.0000000235

[viii] Cardenas, D. D., & Jensen, M. P. (2006). Treatments for chronic pain in persons with spinal cord injury: A survey study. The journal of spinal cord medicine29(2), 109–117. https://doi.org/10.1080/10790268.2006.11753864

[ix] Theriault, E. R., Huang, V., Whiteneck, G., Dijkers, M. P., & Harel, N. Y. (2018). Antispasmodic medications may be associated with reduced recovery during inpatient rehabilitation after traumatic spinal cord injury. The journal of spinal cord medicine41(1), 63–71. https://doi.org/10.1080/10790268.2016.1245010

[x] Wecht, J. M., & Bauman, W. A. (2013). Decentralized cardiovascular autonomic control and cognitive deficits in persons with spinal cord injury. The journal of spinal cord medicine36(2), 74-81.

https://doi.org/10.1179/2045772312Y.0000000056

[xii] Jensen, M. P., Kuehn, C. M., Amtmann, D., & Cardenas, D. D. (2007). Symptom burden in persons with spinal cord injury. Archives of physical medicine and rehabilitation, 88(5), 638–645. https://doi.org/10.1016/j.apmr.2007.02.002

[xiii]Simpson, G., & Jones, K. (2013). How important is resilience among family members supporting relatives with traumatic brain injury or spinal cord injury?. Clinical rehabilitation27(4), 367-377. https://doi.org/10.1177%2F0269215512457961

 

 

 

 

 

The scope of impact a spinal cord injury (SCI) has on the body can be incredibly widespread and varied, affecting almost all of the functions and processes of the body below the level of the injury. The physical effects and the events leading to the SCI can also have a significant psychosocial impact on both the person affected and the people around them.

An SCI can have a huge impact on a person’s social role, and their position within a home, workplace, social group and society – but, with adjustment and support, people living with the effects of a spinal cord injury can live as valuable and valued a life as anyone can hope for.

Reduced mobility or paralysis

The level of impact a spinal cord injury has on physical function depends on the position of the injury and how complete it is – i.e. whether it affects only part of the spinal cord or whether communication from the brain to the nerves beyond that point is totally or near-totally broken.

As sensation and movement are restricted below the level of SCI, the higher the injury, the more impact it has. The impact of a spinal cord injury is therefore on a spectrum; very high spinal cord injuries – C1 to C4 – mean a person has near-total paralysis below the neck and will have severe respiratory involvement, meaning that a person’s breathing becomes dependent on a mechanical ventilator and they lose control and sensation below that level.

The lowest levels of spinal cord injury might have some effect on continence, sexual function and lower limb sensation, but may be manageable without significant changes or support.

Becoming dependent on mobility aids can feel very restrictive at first, but there is a huge range of equipment and support to enable people to stay mobile and involved.

Tissue damage

The reduction in sensation and mobility that can come with a SCI bring with them a risk of tissue damage – pressure sores (‘bed sores’) can develop without regular positional changes, and a lack of sensation in the areas at risk mean that significant damage can occur before anyone is aware of it.

Pressure-relieving equipment – airflow mattresses and cushions can help, and a care plan for regular positional changes, checks and skin care is essential. Problems with continence, personal care, and sweating can also lead to excoriated skin, moisture lesions, fungal infections, and complications of broken skin such as bacterial infections and difficult-to-heal wounds.

Orthostatic hypotension

The common feeling of dizziness when you sit or stand up too fast is caused by dropping blood pressure, and is known as orthostatic hypotension (OH). It can be exacerbated in someone with an SCI – the body’s natural response to the drop in blood pressure when we stand up is to constrict blood vessels in the legs, encouraging venous return and reducing the space within the circulatory system.

In people with spinal cord injuries, this natural response is often impaired or sluggish, and so drops in blood pressure with positional changes can be problematic. Changing position slowly can help, as can staying hydrated. Some medications can also make OH worse so if it’s a problem, it’s important to see a doctor.

Autonomic dysreflexia

People with spinal cord injuries at T6 or above and their families and carers should be aware of the symptoms and risks of autonomic dysreflexia (AD). AD is characterised by a sudden, uncontrolled rise in blood pressure as a response to some stressor. A very slow – or sometimes very fast – heartbeat often accompanies this blood pressure change, and autonomic dysreflexia can make someone very unwell very quickly.

The cause is often as simple but potentially serious as constipation or urinary retention – someone with impaired sensation may be unable to recognise a problem until the autonomic nervous system creates an exaggerated systemic (whole body) response. This response, if untreated, can cause serious illness, seizures, and cardiac arrhythmias. Suspected AD is a medical emergency.

AD is not always predictable, but the most common triggers for AD can be prevented through good nursing care, close management of bowel and bladder dysfunction and prevention of wounds or tissue damage.

Neuropathic pain

There are different types and locations of pain someone might experience after an SCI. Nerve pain, or neuropathic pain, can occur even when the spinal cord injury means that that area of the body doesn’t experience any other kind of pain or sensation. Neuropathic pain is often described as feeling sharp, hot, ‘electric’, or like being stuck with a needle.

Pain after an SCI can be complex, multifaceted and difficult to manage, and specialist pain team intervention can be helpful. Some people find medications beneficial; others try complementary therapies or a combination of both. There are lots of different ways to manage pain, and it’s important to seek help if pain is a problem.

Sexual dysfunction

Problems with sexual function are common after SCI at almost all levels, and it can affect anyone. A lack of sensation and control of movement can diminish anyone’s interest in sex, and people may also be struggling with all the other physical and emotional issues surrounding life with an SCI.

An SCI can change a person’s self-image and confidence in their body. Having reduced sexual desire after a spinal cord injury is very normal, and it may pass; there are lots of ways to enjoy sexual contact even after a profound injury. It may simply take time, care, and adjustment – and spinal care specialists can give good advice for these common problems.

Spinal cord injuries can also affect fertility, particularly for men – not only through impaired sexual function and desire, but through changes in sperm count and difficulty in getting or maintaining an erection and ejaculating. Spinal cord injuries in women can sometimes causes changes in their menstrual cycle, but unless there are other injuries affecting the reproductive system, it is usually possible to get pregnant, and carry a pregnancy to term and birth.

People with spinal cord injuries are likely to experience specific challenges in pregnancy and when giving birth, but with some extra input and adjustment, there’s no reason not to expect a happy, healthy pregnancy and baby.

Continence (bladder and bowel function)

Bladder function is very commonly altered after an SCI and tends to follow one of two patterns of dysfunction – hyperreflexive or non-reflex bladder. People with injuries above T12 commonly have a hyperreflexive bladder condition; a bladder that is overactive, uncontrolled and unpredictable. Incontinence and moisture must be carefully managed to prevent excoriated skin and moisture lesions.

People with injuries at or below T12 may have a non-reflexive bladder – a bladder prone to urinary retention and flaccidity. People with urinary retention may have to have a long-term urinary catheter, or to intermittently catheterise. Good catheter care is important to prevent urinary tract infections (UTIs). Urinary retention can occur in people with spinal cord injuries at any level.

Bowel function is also affected by SCI. This is in part due to reduced gut motility after an injury, and changes in activity and diet. Bowel function is also affected by a loss of sensation, reduced awareness of a full bowel, and inability to empty the bowels through sphincter control and the ability to bear down. This can lead to constipation or impaction and needs to be very carefully managed.

Diet and the use of laxatives can help to regulate bowel movements. A flaccid bowel and lack of ability to empty the bowels can mean that a person with SCI needs help with manually removing stools. Conversely, some people with SCI experience overactive or uncontrollable bowel movements and require very careful continence care to prevent skin damage.

In people with injuries at T6 or higher, autonomic dysreflexia can be triggered by urinary retention, UTIs, moisture damage and skin breakdown, constipation and a distended rectum, bowel infections, haemorrhoids, and other conditions of the bowel or bladder. Incontinence can seriously affect self-esteem and self-image, and it’s a very sensitive subject to many people. Continence care is one of the most crucial roles of anyone caring for someone with SCI.

Breathing problems

The level and completeness of a spinal cord injury determine the amount of physical impact it has. A high spinal cord injury – at levels C1 to C4 – can significantly affect the respiratory system: a person’s ability to breathe and speak independently. Someone with a complete high SCI may always be tracheostomy and ventilator-dependent.

Someone with a slightly lower injury may only need a ventilator some of the time or not at all. Even a C5 or C6 level injury, affecting all the nerves below that point, will have some impact on a person’s diaphragmatic control, so they may need a cough-assist device at times. People with extra respiratory needs after an SCI may become prone to chest infections, so careful management and monitoring of changes in their condition is essential.

Mental health

The physical impact of a spinal cord injury means that some adjustments must be made. The position of the injury largely determines how much of their previous function a person retains, and the higher and more complete the injury, the more impact on their previous function – and the more impact on their lifestyle and, potentially, mental health.

The way in which the injury occurred may be traumatic in itself, and people who have had serious accidents often suffer from some degree of post-traumatic stress disorder. After a serious physically and mentally traumatic event resulting in an SCI, people also usually have to endure an extended hospital stay.

The effects of a stay in an intensive care setting are well-documented; ‘ICU psychosis’ or ‘ICU delirium’ is a common phenomenon, a form of delirium where a combination of a serious illness and the necessary intensive treatment in a highly medicalised and alien environment causes the patient to be confused, disorientated, and agitated. This is an acute condition, but the effects of an extended hospital stay can stay with a person for a long time.

In the longer-term, the physical changes and needs that come with a moderate to severe spinal cord injury mean that substantial lifestyle changes are almost always necessary. Significantly reduced independent mobility can limit much of the activity a person previously enjoyed, and severe injuries often make it impossible to continue to work, to look after family members in the same way, and to attend certain settings and activities.

Becoming dependent on others for physical needs such as washing and dressing, continence care, and possibly eating, drinking, even breathing, takes a period of emotional adjustment for most people. Reliance on mechanical ventilation can also be very restricting and can cause anxiety.

A spinal cord injury can also impact on personal relationships – and again, the higher the injury, the more physical effect it has, and the more impact on a person’s lifestyle. A high spinal injury may mean the loss of the relationships within a workplace. It may mean that a person becomes unable to care for children or other family members in the same way.

Spinal cord injuries can also change the balance within a partnership, with altered physical needs including sexual dysfunction, sensation and movement meaning that significant adjustments are needed to fulfil a couple’s romantic and sexual needs.

In short, any of the physical and social changes that come with a spinal cord injury of any degree can cause huge and restrictive changes to a person’s lifestyle. The psychological impact of this can be profound.

It is important to remember, however, that many people with even very profound high spinal cord injuries continue to lead full and happy lives, and there is no need to go through it alone. The world is becoming more inclusive and accessible all the time, and online and in-person (pandemic permitting) support groups are available.

At Total Community Care, our goal is to provide tailored care packages that enable people with extra care needs to continue their everyday lives. Some people need more support than others. Consequently, our care plans are individualised to ensure that support is designed to facilitate a person’s desired activities and lifestyle, with our minimum care requirements set around no less than 70 hours per week.

Like to know more?

References

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