eMedicine Specialties > Neurology > Neuro-vascular Diseases
Dissection Syndromes: Follow-up
Updated: Dec 15, 2008
Follow-up
Further Inpatient Care
Pursue physical therapy, occupational therapy, speech therapy, and/or swallowing evaluation in appropriate patients.
Further Outpatient Care
- Advise patients to avoid high-risk physical activities (eg, contact sports, yoga, chiropractic neck manipulation) to minimize the risk of recurrent dissection.
- Transfer to a neurorehabilitation facility when appropriate.
Complications
The risk of recurrent dissection is approximately 1% per year. Recurrent dissections are more likely to occur in previously unaffected vessels than at the sites of previous dissections.
Prognosis
- In extracranial carotid dissections, 50% of patients have no residual neurologic deficits, 20% have mild deficits, and 25% have moderate-to-severe residual deficits.
- In intracranial carotid dissections, one half of survivors have moderate-to-severe residual deficits.
- Of patients with extracranial vertebral dissections, 80-85% have mild neurologic deficits or are neurologically normal at the follow-up point. Moderate-to-severe deficits are found in 10%.
- The morbidity and mortality rates for intracranial vertebrobasilar dissection are not well defined but tend to be higher due to increased occurrence of subarachnoid hemorrhage and brainstem infarction.
Miscellaneous
Medicolegal Pitfalls
Failure to consider the diagnosis, especially in a young patient
I would like to thank Jeffrey L. Saver, MD, for his thoughtful review of this article.
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References
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Further Reading
Keywords
alpha-1-antitrypsin deficiency, basilar artery dissection, cervical dissection, connective tissue disorders, cystic medial necrosis, Ehlers-Danlos syndrome, extracranial internal carotid artery dissection, extracranial vertebral artery dissection, intracranial internal carotid artery dissection, intracranial vertebral artery dissection, Marfan syndrome, meningovascular syphilis, middle cerebral artery dissection, moyamoya disease, type 1 collagen point mutation, dissection syndromes
Follow-up: Dissection Syndromes