What lab tests and medications are recommended to monitor and treat a patient with hypertension?

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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.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Guideline

Adding Antihypertensive Medication to Amlodipine Twice Daily

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Guideline

Optimizing Antihypertensive Therapy with Diuretics

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2026

Research

Frequency of laboratory testing and associated abnormalities in patients with hypertension.

Journal of clinical hypertension (Greenwich, Conn.), 2020

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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