eMedicine Specialties > Neurology > Headache and Pain
Reflex Sympathetic Dystrophy: Follow-up
Updated: Apr 18, 2006
Follow-up
Further Inpatient Care
- In CRPS type 1/RSD, inpatient care typically is reserved for patients with refractory pain or infections of the atrophic limb, patients requiring surgery, and sometimes patients requiring procedures.
Further Outpatient Care
- Patients with CRPS type 1/RSD should receive care in a pain clinic in which appropriate evaluation and treatment can minimize discomfort and degree of disability.
Transfer
- Patients should be referred to a pain clinic as soon as CRPS type 1 is suspected on clinical grounds.
Deterrence/Prevention
- Early treatment of pain appears to decrease the frequency of chronic disease and later complications.
Complications
- Osteoporosis
- Limitation of active movement in joints
- Infections
- Nodular fasciitis of the palmar or plantar skin
Prognosis
- Approximately 80% of the patients with CRPS type 1/RSD have complete spontaneous relief of signs and symptoms within 18 months; however, no criteria have been established to predict from the very beginning who will have a spontaneous cure and who will not. Some of the patients whose symptoms do not resolve spontaneously still may be cured by treatment.
- Of patients who develop refractory CRPS type 1/RSD, 50-80% have disability secondary to pain and/or limited range of motion. The main disabilities are limitations in activities of daily living (ADL).
- Long duration of symptoms and signs, the presence of trophic changes, and the presence of primarily cold RSD are associated with higher chances of poor outcome and disability.
Patient Education
- Patients should be informed that, even while wearing a cast, they will undergo mild passive range of motion exercises. After the cast is removed, physical therapy and occupational therapy should be started early, and some ADLs should be resumed as soon as possible following the recommendations of the physical therapist and occupational therapist.
Miscellaneous
Medicolegal Pitfalls
- Underestimating symptoms that suggest CRPS type 1/RSD is risky, because they sometimes could be associated with emotional load or depression. Patients' complaints should always be taken seriously and appropriate referral performed.
Special Concerns
- Diagnosis is based on the clinical picture, with additional information regarding the presence of SMP or autonomic dysfunction provided by carefully performed and interpreted supplemental tests.
- The diagnosis of conversion disorder or malingering should be a diagnosis of exclusion made only after careful evaluation by a pain specialist.
- Opinions that CRPS type 1/RSD occurs mainly in people with psychiatric problems, although never proven, have done patients a lot of harm because their complaints often are not taken seriously.
More on Reflex Sympathetic Dystrophy |
| Overview: Reflex Sympathetic Dystrophy |
| Differential Diagnoses & Workup: Reflex Sympathetic Dystrophy |
| Treatment & Medication: Reflex Sympathetic Dystrophy |
Follow-up: Reflex Sympathetic Dystrophy |
| References |
| « Previous Page |
References
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Further Reading
Keywords
acute peripheral trophoneurosis, algodystrophy, causalgia, chronic traumatic edema, mimocausalgia, neurovascular posttraumatic painful syndrome, neurovascular reflex dystrophy, neurovascular reflex sympathetic dystrophy, posttraumatic chronic edema, posttraumatic osteoporosis, posttraumatic pain syndrome, posttraumatic sympathetic dystrophy, RSD, shoulder-hand syndrome, spreading neuralgia, Sudeck atrophy, sympathalgia, thermalgia, traumatic angiospasm, traumatic vasospasm, complex regional pain syndrome type 1
Follow-up: Reflex Sympathetic Dystrophy