Management of Paroxysmal Sympathetic Hypertension
The management of paroxysmal sympathetic hypertension requires combined alpha and beta-blockade or central alpha-agonists such as clonidine as first-line therapy, often supplemented with anxiolytic and/or antidepressant agents. 1
Diagnostic Approach
Clinical Presentation
- Episodic, severe BP surges with sympathetic activation
- Associated symptoms:
- Tachycardia
- Hypertension (often severe)
- Diaphoresis (excessive sweating)
- Tachypnea
- Occasionally fever and dystonic postures
- Episodes may occur spontaneously or be triggered by stimulation
Differential Diagnosis
- Pheochromocytoma (must be excluded)
- Paroxysmal sympathetic hyperactivity following brain injury
- Pseudopheochromocytoma (psychological basis)
- Sympathetic hyperreactivity from substance use
Diagnostic Workup
- 24-hour ambulatory BP monitoring to document paroxysms
- Plasma and urinary catecholamines and metanephrines to exclude pheochromocytoma
- Brain imaging if neurological symptoms present
- Toxicology screening if substance use suspected
- Psychological assessment for underlying emotional trauma or repressive coping style
Treatment Algorithm
1. Pharmacological Management
First-line therapy:
Specific agents:
2. Etiology-Specific Management
For Brain Injury-Related PSH:
- Use PSH-Assessment Measure (PSH-AM) tool for diagnosis and monitoring 4, 5
- Reduce environmental stimulation
- Consider benzodiazepines before specific antihypertensive treatment 2
For Substance-Induced Sympathetic Hyperreactivity:
- Benzodiazepines as first-line therapy
- Phentolamine for alpha-blockade
- Clonidine for central sympatholysis
- Avoid beta-blockers alone (may worsen hypertension) 2
For Pseudopheochromocytoma (Psychological Basis):
- Combined pharmacological and psychological approach:
3. Monitoring and Follow-up
- Regular BP monitoring (home and ambulatory)
- Titrate medications based on frequency and severity of episodes
- Assess for medication side effects
- Follow-up psychological support if indicated
Treatment Efficacy and Outcomes
Studies have shown that with appropriate treatment:
- 62% of patients with pseudopheochromocytoma can achieve complete elimination of paroxysms 3
- Some cases can be cured with psychotherapy alone 3
- Early diagnosis and treatment improve long-term outcomes 5
Common Pitfalls and Caveats
Misdiagnosis: 98% of patients with paroxysmal hypertension do not have pheochromocytoma, yet this remains the primary suspected diagnosis 1
Underdiagnosis: PSH is frequently underrecognized, especially in ICU settings, leading to delayed treatment 4, 5
Beta-blocker monotherapy: Using beta-blockers alone can worsen hypertension in sympathetic hyperactivity; always combine with alpha-blockade 2
Overlooking psychological factors: Many patients deny stress connection initially, but careful psychological assessment often reveals underlying emotional trauma or repressive coping 3
Medication selection: In cases of sympathomimetic substance use, benzodiazepines should be used before specific antihypertensive treatment 2
The management approach should be tailored based on the identified cause of paroxysmal sympathetic hypertension, with combined pharmacological therapy addressing both the sympathetic overactivity and any underlying psychological factors.