Reflex Sympathetic Dystrophy
- Persistent burning pain
- Sensitivity to touch and/or cold
- Changes in skin color (to red or even a shade of purple)
- Swelling
- Changes in skin temperature
- Changes in hair and nail growth
The pain of RSD is often intense. Patients tend to exhibit a touch-me-not reaction of vigilance and alarm to the mild touch of others or even to the wind blowing on the affected body part. As such, patients often limit activity and hold the affected part in a rigid and motionless manner. In addition to being impairing, the persistent sense of vigilance and alarm naturally leads to emotional distress.
RSD is an old term for the condition and is no longer the preferred term. Instead, healthcare providers use the term complex regional pain syndrome I. Nonetheless, some people continue to use the term RSD.
There is no known cause of RSD. It likely involves the sympathetic nervous system. The sympathetic nervous system affects immune system functioning. As such, the sympathetic nervous system likely has something to do with the immune system response of inflammation that causes the swelling, changes in skin color, and high sensitivity to touch or mild pressure. The cause of RSD also involves the central nervous system – the brain and spinal cord. Among other functions, the central nervous system processes signals sent from the peripheral nerves in the affected body part. Because of the high sensitivity to touch and cold that occurs, the amplification of these signals suggests that there is some type of problem in the information processing function of the central nervous system.
Despite having no known cause, RSD often starts with surgeries or injuries – even mild injuries -- to the affected body part. Obviously, however, there must be more to the picture when it comes to causes of RSD, as most surgeries and mild injuries do not typically lead to RSD.
Is there a cure for reflex sympathetic dystrophy (RSD)?
The course of RSD can vary across different individuals. Conventional wisdom in the healthcare community is that RSD can be cured if caught early, but will become chronic if it continues for too long. This notion comes from anecdotal evidence that RSD can sometimes be cured through early interventions. However, there are no well-designed, published research data that clearly supports this view.
RSD can progress beyond the original affected body part. It can come to affect other limbs or indeed the whole body. Central sensitization likely plays a role in this progression.1 Central sensitization is a highly reactive state of the nervous system, which amplifies pain. Like RSD itself, it can cause sensitivity to touch, but also fatigue, poor sleep, anxiety, and sometimes depression. It can occur with any pain disorder, including RSD. It is important to address in treatment when it occurs.
Typically, RSD is a chronic pain disorder. Chronic conditions are health conditions that have no cure and which tend to last indefinitely. Healthcare for chronic conditions focuses on reducing symptoms and reducing the impact that the condition has on the patient’s life. The goal is to still live well despite having the condition.
Therapies & Procedures
Common treatments for RSD are anti-inflammatory medications, corticosteroid medications, antidepressant medications, anticonvulsant medications, bisphosohonates, calcitonin, physical therapy, nerve blocks, neural blockades, spinal cord stimulation, and chronic pain rehabilitation programs.
Recent published reviews of research express concern about how there are no well-designed studies of the effectiveness for any of these common treatments.2, 3 Despite how often they are pursued, their effectiveness are all unproven. Both reviews indicate that there are limited data to suggest bisphosphonates can be helpful. Quisel, et al., suggest that calcitonin and chronic pain rehabilitation program are likely to be helpful. They also report that spinal cord stimulation shows some promise but should only be pursued after considerable consultation due the invasiveness of the procedure.
References
1. Janig, W. & Baron, R. (2002). Complex regional pain syndrome is a disease of the central nervous system. Clinical Autonomic Research, 12, 150-164.
2. Quisel, A., Gill, J. A., & Witherell, P. (2005). Complex regional pain syndrome: Which treatments show promise? Journal of Family Practice, 54, 599-603.
3. Tran, D. Q., Duong, S., Bertini, P., & Finlayson, R. J. (2010). Complex regional pain syndrome: A review of the evidence. Canadian Journal of Anethesia, 57, 149-166.
Date of publication: April 27, 2012
Date of last modification: October 26, 2015