Laboratory Testing and Monitoring in Hypertension
Essential Initial Laboratory Tests
All patients with newly diagnosed hypertension should undergo a core panel of laboratory tests to assess cardiovascular risk, screen for secondary causes, and detect hypertension-mediated organ damage (HMOD). 1
Routine Initial Tests (Mandatory)
- Serum creatinine and estimated glomerular filtration rate (eGFR): Assess kidney function and cardiovascular risk 1
- Serum electrolytes (sodium and potassium): Screen for secondary hypertension (primary aldosteronism, Cushing's disease) and establish baseline before initiating therapy 1
- Fasting blood glucose and HbA1c (if glucose elevated): Assess cardiovascular risk and identify diabetes as a comorbidity 1
- Lipid profile: Total cholesterol, LDL-cholesterol, HDL-cholesterol, and triglycerides to assess cardiovascular risk 1
- Urinalysis with dipstick: Screen for proteinuria and hematuria 1
- Urinary albumin-to-creatinine ratio: Assess HMOD and cardiovascular risk 1
- 12-lead ECG: Detect atrial fibrillation, left ventricular hypertrophy, and ischemic heart disease 1
- Hemoglobin/hematocrit: Screen for polycythemia as a secondary cause 1
- Serum calcium: Screen for hyperparathyroidism 1
- Thyroid-stimulating hormone (TSH): Screen for thyroid disease as a secondary cause 1
Optional Tests for HMOD Assessment
These tests should be considered based on clinical context to visualize organ damage, which can motivate treatment adherence and overcome clinical inertia 1:
- Echocardiography: Assess for left ventricular hypertrophy, systolic/diastolic dysfunction, and previous myocardial infarction 1
- Carotid or femoral artery ultrasound: Detect atherosclerotic plaques 1
- Coronary artery calcium scoring by cardiac CT: Assess atherosclerotic burden 1
- Arterial stiffness measurement (carotid-femoral or brachial-ankle pulse wave velocity): Assess vascular HMOD 1
- High-sensitivity cardiac troponin and/or NT-proBNP: Detect subclinical cardiac damage 1
- Ankle-brachial index: Screen for peripheral artery disease 1
- Fundoscopy: Assess hypertensive retinopathy, particularly important in hypertensive emergencies 1
Monitoring During Antihypertensive Therapy
Timing of Follow-up Testing
- Recheck serum potassium and creatinine 2-4 weeks after initiating or uptitrating ACE inhibitors, ARBs, or diuretics to detect hyperkalemia, hypokalemia, or acute kidney injury 2, 3
- Reassess blood pressure within 2-4 weeks after any medication adjustment 2, 3
- Achieve target blood pressure within 3 months of initiating or modifying therapy 2, 3
Ongoing Monitoring in Patients with CKD
For patients with moderate-to-severe chronic kidney disease (eGFR <60 mL/min/1.73m²), repeat measurements of serum creatinine, eGFR, and urinary albumin-to-creatinine ratio at least annually. 1
Screening for Secondary Hypertension
Consider additional testing when clinical features suggest secondary causes 1:
- Primary aldosteronism: Aldosterone-renin ratio (screen if resistant hypertension, hypokalemia, or adrenal incidentaloma) 1
- Pheochromocytoma: Plasma free metanephrines (screen if paroxysmal hypertension, sweating, palpitations, headaches) 1
- Cushing syndrome: Late-night salivary cortisol or 24-hour urinary free cortisol (screen if central obesity, striae, proximal muscle weakness) 1
- Renovascular hypertension: Renal artery duplex ultrasound, CT angiography, or MR angiography (screen if resistant hypertension, acute rise in creatinine with ACE inhibitor/ARB, or abdominal bruit) 1
- Obstructive sleep apnea: Home sleep apnea testing or polysomnography (screen if snoring, daytime sleepiness, neck circumference >40 cm) 1
Common Pitfalls to Avoid
- Do not omit baseline testing before initiating therapy, as 36% of patients in real-world practice receive no laboratory monitoring within 6 months of starting antihypertensive medication 4
- Do not delay treatment intensification while waiting for laboratory results in patients with stage 2 hypertension (≥160/100 mmHg), as prompt action reduces cardiovascular risk 2
- Do not assume normal renal function without testing, as 6.7% of patients without comorbidities and 26.3% of multi-comorbid patients have renal dysfunction at hypertension diagnosis 5
- Do not overlook electrolyte abnormalities, which occur in 9.8% of patients without comorbidities and 20.5% of multi-comorbid patients 5
Frequency of Laboratory Abnormalities
Real-world data demonstrate that clinically significant abnormalities are common at hypertension diagnosis 5:
- Renal dysfunction: 6.7% in patients without comorbidities, 26.3% in multi-comorbid patients
- Electrolyte abnormalities: 9.8% in patients without comorbidities, 20.5% in multi-comorbid patients
- Diabetes: 13.4% in patients without comorbidities, 38.8% in multi-comorbid patients
These findings underscore the importance of comprehensive baseline testing, particularly in older patients and those with multiple comorbidities 5.