Condition

Complex Regional Pain Syndrome (CRPS) Treatment in Tallahassee, FL

CRPS is one of the most complex and debilitating pain conditions — but it is also one where early, targeted interventional treatment can make a significant difference. A thorough evaluation is the critical first step.

Overview

What Is Complex Regional Pain Syndrome?

Complex regional pain syndrome (CRPS) — formerly known as reflex sympathetic dystrophy (RSD) — is a chronic pain condition characterized by severe, burning pain that is disproportionate to any original injury, along with changes in skin color, temperature, sweating, and texture, swelling, and extreme sensitivity to touch or temperature. It most commonly affects an arm, hand, leg, or foot, and can spread over time to involve a larger area of the body.

CRPS Type 1 occurs without a confirmed underlying nerve injury — often developing after a fracture, surgery, or soft tissue injury. CRPS Type 2 (causalgia) involves a confirmed peripheral nerve injury. Both types involve abnormal activation of the sympathetic nervous system and a process of central sensitization in which the nervous system becomes hypersensitized to pain signals. Early diagnosis and treatment are critical — CRPS tends to become harder to treat the longer it remains unaddressed.

Causes

What Causes It

CRPS most commonly develops after an injury, surgery, stroke, or immobilization — but the hallmark of the condition is that the pain response is far greater than the original event would explain. A minor ankle sprain, a Colles fracture, or a routine surgical procedure can trigger a cascade of abnormal sympathetic activity and neuroinflammation that becomes self-sustaining. The exact reason why some people develop CRPS in response to an injury while others do not is not fully understood, but it involves an interaction between the peripheral nervous system, the sympathetic nervous system, and central pain processing pathways. Genetics, immune function, and psychological factors may all play a role.

Evaluation

How We Evaluate It

CRPS is a clinical diagnosis based on history, physical examination, and the Budapest Criteria — a standardized set of signs and symptoms used to confirm the diagnosis. We conduct a detailed history of the original injury or triggering event, the progression of symptoms, and all treatments that have been tried. Physical examination assesses the characteristic features of CRPS including allodynia, temperature asymmetry, skin changes, edema, and motor dysfunction. Electrodiagnostic testing, imaging, and laboratory studies may be ordered to rule out other conditions and identify any underlying nerve injury. An accurate diagnosis is essential before any treatment plan is developed.

Treatment

How We Treat CRPS

CRPS requires a multidisciplinary approach that addresses both the sympathetic nervous system component and the central sensitization driving the ongoing pain. Sympathetic nerve blocks — lumbar sympathetic blocks for lower extremity CRPS and stellate ganglion blocks for upper extremity CRPS — interrupt the abnormal sympathetic activity that perpetuates the pain cycle and can provide meaningful diagnostic and therapeutic benefit. For patients who respond to sympathetic blockade or who have not achieved adequate long-term relief, neuromodulation offers more durable options. Dorsal root ganglion stimulation is FDA-approved for CRPS and causalgia and provides highly targeted stimulation to the specific spinal level responsible for the painful area — making it particularly effective for focal CRPS affecting the foot, knee, hip, or hand. Spinal cord stimulation is well-established for broader CRPS distributions, and peripheral nerve stimulation may be appropriate for specific nerve-territory involvement. For patients with severe, refractory CRPS, intrathecal drug delivery can provide superior pain control alongside other interventional approaches.

CRPS is a condition where the timing of treatment matters. Patients who receive appropriate interventional care early in the course of the disease tend to have better outcomes than those who wait. If you or your provider suspect CRPS, a prompt consultation is strongly encouraged.

Frequently Asked Questions

Common Questions

Complex regional pain syndrome (CRPS) is a chronic pain condition characterized by severe, burning pain that is disproportionate to any original injury, along with changes in skin color, temperature, and texture, swelling, and extreme sensitivity to touch or temperature. It most commonly affects an arm, hand, leg, or foot, and can spread over time. CRPS Type 1 occurs without confirmed nerve injury, while CRPS Type 2 (formerly called causalgia) involves a confirmed peripheral nerve injury. Both types involve dysfunction of the sympathetic nervous system and central sensitization.
CRPS often develops after an injury, surgery, stroke, or heart attack — but the severity of the pain is typically far greater than would be expected from the original event. In some cases it develops after a seemingly minor injury such as a sprain or fracture. The exact mechanism is not fully understood, but it involves abnormal activation of the sympathetic nervous system and an exaggerated inflammatory response that becomes self-sustaining. Early diagnosis and treatment are important because CRPS can be more difficult to treat the longer it is allowed to progress.
CRPS typically produces severe, constant burning or aching pain in the affected limb. The skin may become hypersensitive — even a light touch, a breeze, or a change in temperature can trigger intense pain (allodynia). The affected area may show changes in skin color (red, blue, or purple), skin temperature (warmer or cooler than the unaffected side), sweating patterns, and texture. Swelling, stiffness, and changes in nail and hair growth are also common. The pain often feels out of proportion to any visible injury.
CRPS is best managed with a multidisciplinary approach that addresses the sympathetic nervous system involvement, the central sensitization component, and the functional impairment. Sympathetic nerve blocks — including lumbar sympathetic blocks for lower extremity CRPS and stellate ganglion blocks for upper extremity CRPS — can interrupt the abnormal sympathetic activity driving the pain. Spinal cord stimulation and dorsal root ganglion stimulation are highly effective neuromodulation options for carefully selected patients. Peripheral nerve stimulation and intrathecal drug delivery are additional interventional options depending on the distribution and severity of symptoms.
Both spinal cord stimulation and dorsal root ganglion stimulation have strong evidence for the treatment of CRPS. DRG stimulation in particular is FDA-approved for CRPS and causalgia and offers highly targeted stimulation to the specific spinal level responsible for the painful area — making it particularly useful for focal CRPS affecting the foot, knee, hip, or hand. SCS provides broader coverage and is well-established for CRPS affecting larger regions. A trial period for either therapy allows patients to evaluate their response before any permanent decision is made.
Sympathetic nerve blocks target the sympathetic nervous system — the part of the autonomic nervous system that is abnormally activated in CRPS. A lumbar sympathetic block is used for lower extremity CRPS, delivering medication alongside the sympathetic chain in the lower back to interrupt the abnormal pain signaling. A stellate ganglion block is used for upper extremity CRPS, targeting the sympathetic ganglion in the neck. These blocks can provide meaningful relief and are often used as part of a broader treatment plan that includes physical therapy and neuromodulation.

CRPS Requires Prompt, Specialized Evaluation.

Early intervention leads to better outcomes. Our clinical team will evaluate your symptoms and determine the most appropriate treatment path for your specific situation.