Hypertension: Diagnosis and Management in Adults
Blood Pressure Diagnostic Thresholds
Hypertension is defined as systolic blood pressure ≥130 mmHg or diastolic blood pressure ≥80 mmHg based on the 2017 ACC/AHA guideline, which lowered the threshold from the traditional 140/90 mmHg. 1, 2
Blood Pressure Categories (ACC/AHA Classification)
- Normal: <120/<80 mmHg 1
- Elevated: 120–129/<80 mmHg 1
- Stage 1 Hypertension: 130–139/80–89 mmHg 1, 2
- Stage 2 Hypertension: ≥140/≥90 mmHg 1, 2
Diagnostic Confirmation Requirements
- The diagnosis requires an average of ≥2 readings obtained on ≥2 separate occasions using proper technique: seated with back supported, feet flat on floor, arm at heart level after 5 minutes of quiet rest. 1, 3, 4
- Out-of-office blood pressure monitoring (home or 24-hour ambulatory) must be used to confirm the diagnosis before initiating medication to exclude white-coat hypertension and identify masked hypertension. 1, 3, 2, 5
- Home BP ≥135/85 mmHg or 24-hour ambulatory BP ≥130/80 mmHg confirms true hypertension when office readings are elevated. 1
Blood Pressure Treatment Targets
For most adults with hypertension, the target blood pressure is <130/80 mmHg. 1, 2, 6
Population-Specific Targets
- General adult population (<65 years): <130/80 mmHg 1
- Adults ≥65 years (ambulatory, community-dwelling): Systolic <130 mmHg if tolerated 1, 2
- Diabetes mellitus: <130/80 mmHg 1, 3
- Chronic kidney disease (stage 3+ or albuminuria ≥300 mg/day): <130/80 mmHg 1, 3
- Stable ischemic heart disease or post-MI: <130/80 mmHg 1
- High-risk patients: Avoid lowering diastolic pressure below 60–70 mmHg; optimal diastolic range is 70–79 mmHg 1
Lifestyle Modifications (First-Line for All)
All individuals with blood pressure ≥120/70 mmHg should adopt comprehensive lifestyle measures before or alongside pharmacologic therapy. 1, 3, 6
Evidence-Based Lifestyle Interventions
- Sodium restriction to <1,500 mg/day 1
- DASH dietary pattern (high in fruits, vegetables, whole grains, low-fat dairy, low in saturated fat) 1, 3, 6
- Weight reduction to achieve BMI <25 kg/m² 1, 6
- Aerobic exercise 90–150 minutes per week 1, 6
- Potassium supplementation 3,500–5,000 mg/day when not contraindicated 1, 6
- Alcohol moderation (≤2 drinks/day for men, ≤1 drink/day for women) 1, 6
- Smoking cessation 1, 6
When to Initiate Pharmacologic Therapy
Stage 1 Hypertension (130–139/80–89 mmHg)
Begin antihypertensive medication when the patient has established cardiovascular disease OR a 10-year ASCVD risk ≥10% calculated with the ACC/AHA Pooled Cohort Equations. 1, 2
- Virtually all adults ≥70 years and most ≥65 years have 10-year ASCVD risk ≥10% and therefore meet the threshold for treatment at Stage 1 levels. 1
- If 10-year ASCVD risk is <10% and no high-risk conditions exist, continue lifestyle modification alone and reassess annually. 1
Stage 2 Hypertension (≥140/≥90 mmHg)
Initiate lifestyle measures AND pharmacologic therapy simultaneously; do not delay treatment beyond 3 months. 1
- Start with a two-drug combination from different first-line classes, preferably as a single-pill formulation. 1, 2
High-Risk Conditions Requiring Earlier Treatment
Medication is indicated regardless of risk score when any of the following are present:
- Established cardiovascular disease 1
- Diabetes mellitus 1, 3
- Chronic kidney disease (stage 3+ or albuminuria ≥300 mg/day) 1, 3
- Hypertension-mediated organ damage (left ventricular hypertrophy, retinopathy, microalbuminuria) 1
- Familial hypercholesterolemia 1
First-Line Pharmacologic Therapy
The four first-line drug classes are thiazide/thiazide-like diuretics, ACE inhibitors, angiotensin receptor blockers (ARBs), and long-acting dihydropyridine calcium-channel blockers (CCBs). 1, 6, 7, 5
Optimal First-Line Agent for General Population
Chlorthalidone 12.5–25 mg once daily is the optimal first-line agent for uncomplicated hypertension because it provides superior cardiovascular outcomes demonstrated in the ALLHAT trial of >50,000 participants. 1, 8
- In ALLHAT, chlorthalidone reduced heart failure incidence by 38% compared with amlodipine and stroke incidence by 15% compared with lisinopril. 1
- Chlorthalidone is preferred over hydrochlorothiazide due to its 40–60 hour half-life providing 24-hour BP control and stronger outcome evidence. 1, 3
- Start at 12.5 mg daily, titrate to 25 mg after 4 weeks if needed; doses >25 mg increase metabolic side effects without additional BP benefit. 1
Population-Specific First-Line Choices
Black Patients Without Heart Failure or CKD
Initiate therapy with a thiazide diuretic (chlorthalidone preferred) or calcium-channel blocker. 1
- ACE inhibitors and ARBs are 30–36% less effective for stroke prevention in Black patients due to lower renin activity. 1
- ARBs may be better tolerated than ACE inhibitors (less cough, angioedema) but confer no additional cardiovascular benefit. 1
Diabetes Mellitus
Prefer an ACE inhibitor or ARB as initial therapy to protect renal function. 1, 3
- When albuminuria ≥300 mg/day is present, ACE inhibitor or ARB is mandatory to slow kidney disease progression. 1
Chronic Kidney Disease (Stage 3+ or Albuminuria)
ACE inhibitor or ARB is first-line to decelerate eGFR decline and reduce proteinuria. 1
- Thiazide diuretics remain effective even when eGFR <30 mL/min/1.73 m² and should not be avoided solely because of reduced kidney function. 1
Post-Myocardial Infarction or Stable Ischemic Heart Disease
Combine a β-blocker with an ACE inhibitor or ARB as foundational therapy. 1
- β-blockers should be continued for ≥3 years post-MI; extending therapy beyond 3 years is reasonable for ongoing hypertension control. 1
- If angina persists and BP remains uncontrolled, add a dihydropyridine CCB (e.g., amlodipine). 1
Heart Failure with Reduced Ejection Fraction
Use a three-drug regimen: ACE inhibitor or ARB + β-blocker + diuretic. 1
Combination Therapy Strategy
Stage 1 Hypertension
Start with single-agent monotherapy and titrate upward before adding a second drug from a different class. 1
- Reassess monthly until BP <130/80 mmHg is achieved. 1
Stage 2 Hypertension
Begin with a two-drug combination from different first-line classes, preferably as a single-pill formulation. 1, 2
Preferred Two-Drug Combinations
Thiazide diuretic + (ACE inhibitor or ARB) 1
Calcium-channel blocker + (ACE inhibitor or ARB) 1
Single-pill combinations markedly improve medication adherence and persistence compared with separate pills. 1
Combination therapy using two submaximal doses from different classes yields larger BP reductions with fewer adverse effects than maximal dosing of a single agent. 1
Escalation to Triple Therapy
If BP remains uncontrolled after 3 months on a two-drug regimen, escalate to triple therapy (ACE inhibitor/ARB + CCB + thiazide diuretic), preferably as a single-pill combination. 1
Agents NOT Recommended as First-Line
β-Blockers
β-blockers should not be used as first-line therapy in uncomplicated hypertension, especially in patients >60 years, because they are ≈36% less effective than CCBs and ≈30% less effective than thiazides for stroke prevention. 1
- Reserve β-blockers for compelling indications: post-MI, heart failure with reduced ejection fraction, angina, or heart rate control. 1
Alpha-Blockers
Alpha-blockers are not first-line because they are less effective for cardiovascular disease prevention than thiazide diuretics. 1
- In ALLHAT, doxazosin was associated with an 80% higher rate of heart failure compared with chlorthalidone. 1
Monitoring and Follow-Up
Visit Schedule
- After initiating or adjusting therapy, review patients monthly until the BP target is achieved, then every 3–5 months for maintenance. 1, 2
- Dose adjustments should be spaced ≥4 weeks apart to allow full BP response. 1
Laboratory Monitoring
- Baseline: Serum creatinine, eGFR, potassium, sodium, fasting glucose, lipid panel, urine albumin 1
- When ACE inhibitors, ARBs, or diuretics are prescribed: Repeat creatinine, eGFR, and potassium within 1–2 weeks of initiation, after each dose increase, and annually thereafter. 1, 3
- An increase in serum creatinine up to 50% above baseline or to 3 mg/dL (whichever is greater) is acceptable. 1
Out-of-Office Monitoring
Systematic use of home BP monitoring is essential to assess treatment response, detect white-coat effect, and identify masked uncontrolled hypertension. 1, 2
Resistant Hypertension
Resistant hypertension is defined as BP ≥130/80 mmHg despite ≥3 antihypertensive agents at optimal doses (including a diuretic), or BP <130/80 mmHg requiring ≥4 agents. 1, 2
Systematic Approach
- Confirm true resistance by excluding white-coat effect with out-of-office monitoring and assessing adherence. 1, 2
- Identify contributing lifestyle factors: obesity, excess alcohol, high sodium intake, NSAIDs, obstructive sleep apnea. 1, 2
- Screen for secondary causes: primary aldosteronism, CKD, renal artery stenosis, pheochromocytoma, Cushing syndrome, coarctation. 1, 2
- Optimize diuretic therapy: use loop diuretics in CKD. 1, 2
- Add a mineralocorticoid-receptor antagonist (e.g., spironolactone). 1, 2, 5
- Refer to a hypertension specialist if uncontrolled after 6 months. 1, 2
Special Populations
Pregnancy
Women who become pregnant while hypertensive must be switched immediately to methyldopa, extended-release nifedipine, or labetalol. 1, 2
- ACE inhibitors, ARBs, and direct renin inhibitors are absolutely contraindicated in pregnancy due to fetal toxicity. 1, 2
Older Adults (≥85 Years)
Continue BP-lowering treatment lifelong if well tolerated; asymptomatic orthostatic hypotension should not prompt withdrawal. 1
- For older adults with high comorbidity burden or limited life expectancy, individualized clinical judgment and team-based risk-benefit assessment are reasonable. 1, 2
Critical Pitfalls to Avoid
- Delaying combination therapy in Stage 2 hypertension (≥140/90 mmHg) increases cardiovascular risk. 1
- Using β-blockers as first-line agents in patients >60 years without a compelling indication leads to inferior stroke prevention. 1
- Excessive diastolic lowering below 60 mmHg in high-risk patients may increase adverse cardiovascular events. 1
- Combining an ACE inhibitor with an ARB (or adding a direct renin inhibitor) should be avoided due to lack of benefit and higher adverse-event risk (hyperkalemia, acute kidney injury). 1
- Continuing ACE inhibitors or ARBs during pregnancy is contraindicated because of fetal toxicity. 1, 2
- Failing to employ out-of-office BP monitoring can miss white-coat or masked hypertension, compromising management. 1, 2
- Relying on a single office measurement for diagnosis; improper technique can falsely raise readings by 10–30 mmHg. 1
- Initiating medication immediately in low-risk individuals with BP 130–139/70–89 mmHg leads to overtreatment. 1