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autonomic dysreflexia/cefalàlgia
L'enllaç es desa al porta-retalls
Pàgina 1 des de 65 resultats
Headache Attributed to Autonomic Dysreflexia: Clinical Presentation, Pathophysiology, and Treatment.
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A patient presenting with marked elevation in blood pressure and concurrent headache often presents a diagnostic challenge for even the most seasoned clinician. When marked hypertension and headache occur in a patient with a history of upper spinal cord injury, the patient should be presumed to have
Headache attributed to autonomic dysreflexia: an underrecognized clinical entity.
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OBJECTIVE
The recognition and the management of headache attributed to autonomic dysreflexia after spinal cord injury (SCI) are challenging issues. Given this, I systematically reviewed the literature to establish the features of the headache attributed to autonomic dysreflexia after
Autonomic dysreflexia presenting as a severe headache.
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Hypertension, bradycardia, and severe headache have been associated with autonomic dysreflexia. Autonomic dysreflexia affects those with spinal transection above the level of T6 after plastic changes of the afferent pathways. This restructuring in the presence of noxious stimuli below the level of
Charcot joint of the spine, a cause of autonomic dysreflexia in spinal cord injured patients.
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METHODS
Case report of two subjects.
OBJECTIVE
Charcot joints of the spine as a cause of Autonomic Dysreflexia in spinal cord lesions.
METHODS
Stoke Mandeville Hospital, UK.
METHODS
Two patients with long standing spinal cord lesions developed symptoms of headaches and sweating associated with
Seizures and cortical blindness after meglumine (hypaque) administration: a variant of autonomic dysreflexia.
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Autonomic dysreflexia (AD) is a syndrome that consists of facial flushing, excessive sweating, nasal congestion, throbbing headache and paroxysmal hypertension which may occur in response to bladder distension in patients with spinal cord lesions above the T6 level. We report the case of a C2
Autonomic Dysreflexia Resulting in Seizure After Colonoscopy in a Patient With Spinal Cord Injury.
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There are many potential procedural risks associated with colonoscopy. We present a case of autonomic dysreflexia complicated by seizure after colonoscopy in a patient with a spinal cord injury. Autonomic dysreflexia is a disorder characterized by hypertension, bradycardia, headache, and diaphoresis
Autonomic dysreflexia in a tetraplegic patient due to a blocked urethral catheter: spinal cord injury patients with lesions above T-6 require prompt treatment of an obstructed urinary catheter to prevent life-threatening complications of autonomic dysreflexia.
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BACKGROUND
The Manchester Triage System is commonly used as the triage system in emergency departments of the UK. As per the Manchester Triage System, patients presenting with retention of urine to the accident and emergency department are categorized to yellow, which denotes that the ideal maximum
Autonomic hyperreflexia: a mortal danger for spinal cord-damaged women in labor.
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Reproductive care of women with spinal cord damage demands knowledge of such women's reproductive potential and the specific complications to which these women are prone during pregnancy and childbirth, especially autonomic hyperreflexia. Fertility in cord-damaged women of reproductive age is
Infarct of the right basal ganglia in a male spinal cord injury patient: adverse effect of autonomic dysreflexia.
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Autonomic dysreflexia is a clinical emergency that occurs in individuals with spinal cord injury at level T-6 and above. We present a 58-year-old male patient with paraplegia who developed a severe, recurrent, throbbing headache during the night, which was relieved by emptying the urinary bladder by
Autonomic dysreflexia and telehealth.
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With the rapid expansion of telehealth lines in the United States and the establishment of provincially funded lines in Canada, a growing number of people use this convenient approach to establish their initial health needs and to pursue self-care. Telehealth providers, for the most part, rely on
Charcot arthropathy in relation to autonomic dysreflexia in spinal cord injury: case report and review of the literature.
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Charcot spinal arthropathy has been described as a late complication of spinal cord injury. In patients with these injuries in whom the spine below the level of injury is insensate, joint trauma can progress until spinal instability ensues. The authors describe the case of a 50-year-old man with
Reversible posterior leukoencephalopathy in a patient with autonomic dysreflexia: a case report.
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METHODS
Case report.
OBJECTIVE
To report a case of reversible posterior leukoencephalopathy (RPL) in a patient with traumatic cervical spinal cord injury.
METHODS
Neurologic inpatient Unit, Lahey Clinic, Burlington, MA, USA.
METHODS
A 55-year-old woman with a residual spastic quadriparesis from a
Delayed complications of discontinuation of intrathecal baclofen therapy: resurgence of dyssynergic voiding, which triggered off autonomic dysreflexia and hydronephrosis.
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METHODS
Case report.
OBJECTIVE
To report insidious development of autonomic dysreflexia and hydronephrosis due to dyssynergic voiding following discontinuation of intrathecal baclofen therapy.
METHODS
Regional Spinal Injuries Centre, Southport, UK.
METHODS
A male patient with paraplegia at T-5
Headaches in patients with traumatic lesions of the cervical spinal cord.
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We established the occurrence of headache in a group of 20 patients with traumatic transections of the cervical spinal cord. All but two patients had complete sensory lesions at levels varying from C2-3 to C7-8. Only three patients claimed to have no headaches at all although one of them had nuchal
Fatal cerebral hemorrhage in a tetraplegic patient due to autonomic dysreflexia triggered by delay in emptying urinary bladder after unsuccessful intermittent catheterization by carer: lessons learned.
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UNASSIGNED
Over-distension of urinary bladder in a high spinal cord injury patient is a triggering factor for autonomic dysreflexia. Removing triggering factors is vital to prevent autonomic dysreflexia.
UNASSIGNED
A 36-year-old tetraplegic patient, who was managed by intermittent catheterizations
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