Autonomic Dysreflexia
"Autonomic Dysreflexia" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A syndrome associated with damage to the spinal cord above the mid thoracic level (see SPINAL CORD INJURIES) characterized by a marked increase in the sympathetic response to minor stimuli such as bladder or rectal distention. Manifestations include HYPERTENSION; TACHYCARDIA (or reflex bradycardia); FEVER; FLUSHING; and HYPERHIDROSIS. Extreme hypertension may be associated with a STROKE. (From Adams et al., Principles of Neurology, 6th ed, pp538 and 1232; J Spinal Cord Med 1997;20(3):355-60)
| Descriptor ID |
D020211
|
| MeSH Number(s) |
C10.177.090 C10.900.850.250
|
| Concept/Terms |
Autonomic Dysreflexia- Autonomic Dysreflexia
- Autonomic Dysreflexias
- Dysreflexias, Autonomic
- Hyperreflexia, Autonomic
- Spinal Autonomic Dysreflexia
- Autonomic Dysreflexia, Spinal
- Autonomic Dysreflexias, Spinal
- Dysreflexia, Spinal Autonomic
- Dysreflexias, Spinal Autonomic
- Spinal Autonomic Dysreflexias
- Autonomic Hyperreflexia
- Autonomic Hyperreflexias
- Hyperreflexias, Autonomic
- Dysreflexia, Autonomic
|
Below are MeSH descriptors whose meaning is more general than "Autonomic Dysreflexia".
Below are MeSH descriptors whose meaning is more specific than "Autonomic Dysreflexia".
This graph shows the total number of publications written about "Autonomic Dysreflexia" by people in UAMS Profiles by year, and whether "Autonomic Dysreflexia" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2020 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
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Below are the most recent publications written about "Autonomic Dysreflexia" by people in Profiles over the past ten years.
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White WD, Mansfield JT, Gosai EV, Groah SL. Vertebral insufficiency fractures as a cause of autonomic dysreflexia in a patient with chronic tetraplegia: A case report. J Spinal Cord Med. 2022 Sep; 45(5):769-772.