A report on an unusual presentation of autonomic dysreflexia

A 48-year-old male with complete tetraplegia C6 presented with sweating and flushing of the right half of the face and neck that recurred when lying in supine and left lateral positions. The symptoms subsided immediately upon sitting upright or lying in a right lateral position. The symptoms were as...

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Main Authors: Suhaida, S.S., Julia, P.E.
Format: Article
Published: Malaysian Medical Association 2012
Subjects:
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author Suhaida, S.S.
Julia, P.E.
author_facet Suhaida, S.S.
Julia, P.E.
author_sort Suhaida, S.S.
collection UM
description A 48-year-old male with complete tetraplegia C6 presented with sweating and flushing of the right half of the face and neck that recurred when lying in supine and left lateral positions. The symptoms subsided immediately upon sitting upright or lying in a right lateral position. The symptoms were associated with occasional mild head discomfort rather than headache and were accompanied by marked elevation of blood pressure, which was 190-200/120-130 mmHg compared to his previous baseline blood pressure of 80-90/50-70 mmHg, and he had a heart rate of 60-70 beats per minute. We believe that post-traumatic syringomyelia, found upon further investigation, was the cause of the Autonomic dysreflexia (AD) in this patient. He was advised to avoid the positions causing the symptoms and the progression of symptoms was monitored regularly. AD might not have been diagnosed in this patient because of the atypical and unusual presentations. Therefore, knowledge and a heightened level of awareness of this possible complication are important when treating individuals with spinal cord injury (SCI).
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spelling um.eprints-99142019-03-01T06:13:46Z http://eprints.um.edu.my/9914/ A report on an unusual presentation of autonomic dysreflexia Suhaida, S.S. Julia, P.E. R Medicine A 48-year-old male with complete tetraplegia C6 presented with sweating and flushing of the right half of the face and neck that recurred when lying in supine and left lateral positions. The symptoms subsided immediately upon sitting upright or lying in a right lateral position. The symptoms were associated with occasional mild head discomfort rather than headache and were accompanied by marked elevation of blood pressure, which was 190-200/120-130 mmHg compared to his previous baseline blood pressure of 80-90/50-70 mmHg, and he had a heart rate of 60-70 beats per minute. We believe that post-traumatic syringomyelia, found upon further investigation, was the cause of the Autonomic dysreflexia (AD) in this patient. He was advised to avoid the positions causing the symptoms and the progression of symptoms was monitored regularly. AD might not have been diagnosed in this patient because of the atypical and unusual presentations. Therefore, knowledge and a heightened level of awareness of this possible complication are important when treating individuals with spinal cord injury (SCI). Malaysian Medical Association 2012 Article PeerReviewed Suhaida, S.S. and Julia, P.E. (2012) A report on an unusual presentation of autonomic dysreflexia. Medical Journal of Malaysia, 67 (6). pp. 616-617. ISSN 0300-5283,
spellingShingle R Medicine
Suhaida, S.S.
Julia, P.E.
A report on an unusual presentation of autonomic dysreflexia
title A report on an unusual presentation of autonomic dysreflexia
title_full A report on an unusual presentation of autonomic dysreflexia
title_fullStr A report on an unusual presentation of autonomic dysreflexia
title_full_unstemmed A report on an unusual presentation of autonomic dysreflexia
title_short A report on an unusual presentation of autonomic dysreflexia
title_sort report on an unusual presentation of autonomic dysreflexia
topic R Medicine
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AT juliape areportonanunusualpresentationofautonomicdysreflexia
AT suhaidass reportonanunusualpresentationofautonomicdysreflexia
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