Current Hypertension Management Guidelines
Blood Pressure Diagnostic Thresholds
The ACC/AHA 2017 guideline defines hypertension as ≥130/80 mmHg, while the 2024 European Society of Cardiology and WHO retain the traditional ≥140/90 mmHg threshold. 1 This creates an international divergence, with the lower ACC/AHA threshold increasing U.S. prevalence from 32% to 46% of adults. 1
ACC/AHA Classification:
- Normal: <120/80 mmHg 1
- Elevated: 120–129/<80 mmHg 1
- Stage 1: 130–139/80–89 mmHg 1
- Stage 2: ≥140/90 mmHg 1
Diagnostic Confirmation:
- Diagnosis requires the average of ≥2 readings on ≥2 separate occasions 1
- Confirm with out-of-office monitoring before starting medication (home BP ≥135/85 mmHg or 24-hour ambulatory ≥130/80 mmHg) to exclude white-coat hypertension 1, 2
Blood Pressure Treatment Targets
For most adults, target <130/80 mmHg based on ACC/AHA guidelines, which show a ≈25% reduction in cardiovascular events and ≈27% reduction in all-cause mortality at this goal. 1
Specific Population Targets:
- General adults <65 years: <130/80 mmHg (Class I, Level A) 1
- Adults ≥65 years (ambulatory, non-institutionalized): systolic <130 mmHg if tolerated 1
- Diabetes mellitus: <130/80 mmHg 1
- Chronic kidney disease: <130/80 mmHg 1
- Stable ischemic heart disease: <130/80 mmHg 1
- Post-stroke/TIA: <130/80 mmHg may be reasonable 1
Critical Diastolic Consideration:
In high-risk patients, do not lower diastolic below 60–70 mmHg; optimal diastolic range is 70–79 mmHg to avoid compromising coronary perfusion. 1
Lifestyle Modifications
All individuals with BP ≥120/70 mmHg should adopt lifestyle measures immediately, not sequentially after failed pharmacotherapy. 1 This includes:
- Weight management (target BMI <25 kg/m²) 1
- DASH diet (rich in fruits, vegetables, low-fat dairy) 1
- Sodium restriction (<2.3 g/day, ideally <1.5 g/day) 1
- Regular aerobic activity (≥150 min/week moderate intensity) 1
- Alcohol moderation (≤2 drinks/day men, ≤1 drink/day women) 1
- Smoking cessation 1
When to Initiate Pharmacologic Therapy
Stage 1 Hypertension (130–139/80–89 mmHg):
Start medication when:
- 10-year ASCVD risk ≥10% (calculated via ACC/AHA Pooled Cohort Equations) 1, 2
- Established cardiovascular disease 1
- Diabetes mellitus 1
- Chronic kidney disease 1
- Hypertension-mediated organ damage 1
If none of the above apply, continue lifestyle measures for 3 months; add medication if BP remains ≥130/80 mmHg. 1
Stage 2 Hypertension (≥140/90 mmHg):
Initiate lifestyle measures AND pharmacologic therapy simultaneously; do not delay beyond 3 months. 1, 2 Virtually all adults ≥70 years and most ≥65 years have 10-year ASCVD risk ≥10% and therefore meet treatment threshold even at Stage 1 levels. 1
First-Line Pharmacologic Agents
Four drug classes are endorsed as first-line therapy: thiazide/thiazide-like diuretics, ACE inhibitors, ARBs, and long-acting dihydropyridine calcium-channel blockers (CCBs). 1 All produce comparable office BP reductions of ≈9/5 mmHg and ambulatory reductions of ≈5/3 mmHg as monotherapy. 1
Optimal First-Line Choice for General Population:
Thiazide-like diuretics (especially chlorthalidone 12.5–25 mg daily) are the optimal first-line agent because the ALLHAT trial (>50,000 participants) demonstrated superior prevention of heart failure (38% reduction vs. amlodipine) and stroke (15% reduction vs. lisinopril). 1 Chlorthalidone's 40–60 hour half-life provides 24-hour BP control. 1
Monotherapy vs. Combination Strategy
Stage 1 Hypertension:
Start with single-agent monotherapy (chlorthalidone 12.5 mg or amlodipine 5 mg) and titrate upward before adding a second class. 1 Reassess monthly until target 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 Single-pill combinations markedly improve adherence and persistence. 1 Two submaximal doses from different classes yield larger BP reductions with fewer adverse effects than maximal dosing of a single agent. 1
Preferred Two-Drug Combinations:
- ACE inhibitor or ARB + thiazide-like diuretic (optimal for general population) 1
- ACE inhibitor or ARB + long-acting dihydropyridine CCB (when thiazides contraindicated) 1
Population-Specific Recommendations
Black Patients (Without Heart Failure or CKD):
Initiate with thiazide diuretic or CCB rather than ACE inhibitor/ARB, because renin-angiotensin system blockers are ≈30–36% less effective for stroke prevention in this group due to lower renin activity. 1 ARBs may cause less cough and angioedema than ACE inhibitors but provide no additional cardiovascular benefit. 1
Diabetes Mellitus:
Prefer ACE inhibitor or ARB as initial therapy to preserve renal function, especially when albuminuria ≥300 mg/day is present. 1 Target <130/80 mmHg. 1
Chronic Kidney Disease (Stage 3+ or Albuminuria):
ACE inhibitor or ARB is first-line to decelerate eGFR decline and reduce proteinuria. 1 Target <130/80 mmHg. 1 An increase in creatinine up to 50% above baseline or to 3 mg/dL (whichever is greater) is acceptable. 1
Post-Myocardial Infarction or Stable Ischemic Heart Disease:
Combine β-blocker with ACE inhibitor or ARB as foundational therapy. 1 If angina persists and BP remains uncontrolled, add a dihydropyridine CCB. 1 Continue β-blocker for ≥3 years post-MI. 1 Target <130/80 mmHg. 1
Heart Failure with Reduced Ejection Fraction:
Use three-drug regimen: ACE inhibitor or ARB + β-blocker + diuretic. 1
Pregnancy:
Switch to methyldopa, extended-release nifedipine, or labetalol. 1 ACE inhibitors, ARBs, and direct renin inhibitors are absolutely contraindicated due to fetal toxicity. 1
Older Adults (≥85 years):
Continue BP-lowering therapy lifelong if well tolerated; asymptomatic orthostatic hypotension alone should not prompt withdrawal. 1 For frail patients or those with limited life expectancy, individualized clinical judgment is reasonable, but treatment may be deferred until BP exceeds 140/90 mmHg. 1
Escalation to Triple Therapy
If BP remains ≥140/90 mmHg despite dual therapy at optimal doses, add a third agent to create the standard triple regimen: ACE inhibitor or ARB + CCB + thiazide-like diuretic, preferably as a single-pill combination. 1, 2 Prior to adding the third agent, optimize the doses of the first two drugs. 2
Resistant Hypertension (≥130/80 mmHg on ≥3 agents including a diuretic):
- Confirm true resistance with out-of-office monitoring and assess adherence 1
- Identify contributing factors (obesity, excess alcohol, high sodium, NSAIDs, obstructive sleep apnea) 1
- Screen for secondary causes (primary aldosteronism, renal artery stenosis, pheochromocytoma) 1
- Optimize diuretic therapy; use loop diuretics in CKD 1
- Add mineralocorticoid-receptor antagonist (spironolactone) 1
- Refer to hypertension specialist if uncontrolled after 6 months 1
Monitoring and Follow-Up
After initiating or adjusting therapy, review patients monthly until BP target is achieved, then every 3–5 months for maintenance. 1 Dose adjustments should be spaced ≥4 weeks apart to allow full BP response. 1
Baseline Laboratory Evaluation:
When Prescribing ACE Inhibitors, ARBs, or Diuretics:
Repeat creatinine, eGFR, and potassium within 1–2 weeks of initiation, after each dose increase, and annually thereafter. 1, 3
Out-of-Office Monitoring:
Home or ambulatory BP monitoring is essential to assess treatment response, detect white-coat effect, and identify masked uncontrolled hypertension. 1
Critical Agents to Avoid as First-Line
β-Blockers:
Should not be used as first-line 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 for compelling indications (angina, post-MI, HFrEF, atrial fibrillation). 1
α-Blockers:
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
Hydrochlorothiazide <25 mg Daily:
Discouraged as monotherapy because such low doses are unproven or less effective in outcome trials. 1
Contraindicated Combinations
Never combine an ACE inhibitor with an ARB (or add aliskiren) because dual renin-angiotensin system blockade increases risk of hyperkalemia and acute kidney injury without added cardiovascular benefit. 1, 2, 3
Common Pitfalls to Avoid
- Delaying combination therapy in Stage 2 hypertension increases cardiovascular risk 1
- Using β-blockers as first-line in patients >60 years without compelling indication leads to inferior stroke prevention 1
- Excessive diastolic lowering below 60 mmHg in high-risk patients may increase adverse cardiovascular events 1
- Failing to employ out-of-office BP monitoring can miss white-coat or masked hypertension 1
- Assuming treatment failure before confirming medication adherence, as non-adherence is the most common cause of apparent resistance 2
- Continuing ACE inhibitors or ARBs during pregnancy is contraindicated due to fetal toxicity 1