Orthostatic Vital Signs Assessment and Management
Proper Measurement Technique
Measure blood pressure after 5 minutes of supine rest, then at 1 minute and 3 minutes after standing, maintaining the arm at heart level throughout all measurements. 1
Patient Preparation
- Fast for 3 hours before testing 2, 3
- Avoid nicotine, caffeine, theine, or taurine-containing drinks on the day of examination 2, 3
- Perform testing in a temperature-controlled environment (21-23°C) 2, 3
- Use a validated blood pressure device with appropriate cuff size based on arm circumference 1, 2
Measurement Protocol
- Baseline: Measure BP and heart rate after 5 minutes in supine position (preferred for sensitivity, though sitting is more practical in clinical settings) 1
- Standing measurements: Measure BP and HR at 1 minute and 3 minutes after standing 1, 2
- Keep the patient's back and arm supported during supine/sitting measurements, with BP cuff at heart level 1
- Maintain arm at heart level during all standing measurements 1, 2
- At first visit, measure BP in both arms; if systolic BP differs by >10 mmHg, use the arm with higher BP for all subsequent measurements 1, 2
- Record heart rate and check for arrhythmias during assessment 1
Diagnostic Criteria for Orthostatic Hypotension
Classical orthostatic hypotension is diagnosed when systolic BP drops ≥20 mmHg OR diastolic BP drops ≥10 mmHg OR systolic BP falls to <90 mmHg within 3 minutes of standing. 2, 3
Special Diagnostic Thresholds
- In patients with supine hypertension, use a threshold of ≥30 mmHg systolic drop 2, 3
- Initial orthostatic hypotension: BP decrease >40 mmHg systolic and/or >20 mmHg diastolic within 15 seconds of standing 2, 3
- Delayed orthostatic hypotension: BP drop meeting criteria but occurring beyond 3 minutes of standing 2, 3
Pattern Recognition
- Classical OH shows a "concave" BP curve immediately after standing 4, 3
- Delayed OH has a more variable pattern of BP and HR decrease 4, 2
- In neurogenic OH, heart rate increase is blunted (usually <10 beats per minute) due to impaired autonomic HR control 2
- Supine BP is commonly elevated in neurogenic OH 4
Clinical Assessment
Key Symptoms to Assess
- Dizziness, lightheadedness, visual disturbances, weakness, and fatigue 3
- Syncope, presyncope, palpitations, dyspnea, and chest pain 3
- Shoulder and neck pain ("coat hanger syndrome") 5
Medication Review
Review for causative medications including: 3
- Diuretics, vasodilators, alpha-blockers, antihypertensives
- Tricyclic antidepressants, phenothiazines
- Alcohol
Initial Laboratory Testing
- Complete blood count (rule out anemia) 3
- Serum electrolytes (assess for disturbances) 3
- Serum creatinine with eGFR (evaluate renal function) 3
- Fasting blood glucose (screen for diabetes) 3
- Thyroid-stimulating hormone (rule out thyroid dysfunction) 3
- 12-lead ECG (rule out arrhythmias, conduction abnormalities, structural heart disease) 3
Advanced Testing
- Consider 24-hour ambulatory BP monitoring to detect patterns of BP variability 2
- Head-up tilt-table testing if standard orthostatic vital signs are nondiagnostic or to assess treatment response in autonomic disorders 6, 5
- Echocardiography only if cardiac cause is suspected with clinical evidence of cardiac disease (diagnostic yield is low otherwise) 2
Etiologic Classification
Neurogenic Causes
- Primary autonomic failure: Parkinson's disease, multiple system atrophy, pure autonomic failure 2, 3
- Secondary autonomic neuropathies: Diabetes mellitus, amyloidosis, autoimmune disorders 2, 3
Non-Neurogenic Causes
- Hypovolemia (dehydration, blood loss) 3, 6
- Medications (most common reversible cause) 3
- Cardiac causes 3
- Endocrine causes 3
Management Approach
Initial Steps
- Correct reversible causes and discontinue responsible medications when possible 6
- Assess orthostatic hypotension before starting or intensifying BP-lowering medication, particularly in older patients 1
Nonpharmacologic Treatment (Offer to All Patients)
- Dietary modifications (increase salt and fluid intake) 5
- Compression garments (support stockings) 7, 6
- Physical countermaneuvers 5
- Avoid triggering environments 5
- Fluid expansion and lifestyle alterations 7
Pharmacologic Treatment
For patients who do not respond adequately to nonpharmacologic treatment, midodrine is FDA-approved and proven beneficial for symptomatic orthostatic hypotension. 7
Midodrine (First-Line)
- FDA-approved indication: Treatment of symptomatic orthostatic hypotension in patients whose lives are considerably impaired despite standard clinical care 7
- Mechanism: Alpha1-agonist that increases vascular tone and elevates BP 7
- Effect: Elevates standing systolic BP by approximately 15-30 mmHg at 1 hour after a 10 mg dose, with effect persisting 2-3 hours 7
- Dosing: Typically 10 mg three times daily, with last dose not later than 6 PM 7
- Critical warning: Can cause marked elevation of supine BP (>200 mmHg systolic); patients with pre-existing sustained supine hypertension above 180/110 mmHg were excluded from trials 7
- Continuation criteria: Should only be continued for patients who report significant symptomatic improvement 7
Alternative Pharmacologic Options
- Fludrocortisone (improves symptoms but has concerning long-term effects) 5
- Droxidopa (first-line alternative) 5
- Pyridostigmine (proven beneficial) 6
Treatment Goals
- Improve hypotension without excessive supine hypertension 6
- Relieve orthostatic symptoms 6
- Improve standing time and quality of life 6, 5
- Reduce fall risk 5
Important Clinical Pearls
- Symptoms depend more on the absolute BP level than the magnitude of the fall 2
- If symptoms suggest OH but initial testing is negative, extend standing time beyond 3 minutes to assess for delayed OH 2
- Continuous BP measurement devices are more accurate than interval devices for diagnosis 2
- BP cannot be measured reliably in atrial fibrillation using standard instruments 1
- Midodrine is removed by dialysis in patients undergoing hemodialysis 7
- OH prevalence is approximately 10% in all hypertensive adults and up to 50% in older institutionalized adults 2
- OH is associated with up to 50% increase in relative risk of all-cause mortality 5