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Updated October 2025
Guideline Brief

Hypertension Management 2024–2025: Guideline Updates and Therapeutic Sequencing

Recent European and North American updates converge on earlier initiation of combination therapy, strong use of out-of-office BP, and structured sequencing: ACEi/ARB + CCB or thiazide-like diuretic as the default, with clear roles for β‑blockers, mineralocorticoid receptor antagonists, and device therapy in resistant cases. Targets generally <130/80 mm Hg for most, with some societies retaining <140/90 mm Hg standard targets. Nuanced initiation thresholds for very old adults appear in ESH 2023, whereas ESC 2024 promotes uniform thresholds.

Clinical question
What are the current (2023–2025) evidence-based recommendations for diagnosing, treating, and sequencing pharmacotherapy in adult hypertension, and how do recent guidelines differ?
HypertensionGuidelinesTherapeuticsPrimary CareCardiology
Key points
Earlier, combination-first pharmacotherapy
ESC 2024 endorses prompt lifestyle + pharmacologic therapy at ≥140/90 mm Hg for all ages, reflecting data that age is not a major effect modifier up to ~85 years. Single-pill combinations are preferred to accelerate control [1].
ESH nuance for very old adults
ESH 2023 permits initiating pharmacotherapy at SBP ≥160 mm Hg (Class I) in adults ≥80 years, with consideration at 140–160 mm Hg (Class II), and allows a lifestyle-only trial in low-risk grade 1 hypertension before drugs [4], [1].
Out-of-office BP emphasized
ESH 2023 strongly emphasizes ambulatory and home BP monitoring to confirm diagnosis and guide therapy, reducing white-coat and masked hypertension misclassification [6].
Therapeutic sequencing clarified
Default initial therapy is ACEi/ARB + CCB or thiazide-like diuretic; add the third class if needed, then spironolactone for resistant hypertension, with β‑blockers positioned earlier when compelling indications exist [4], [9].
Targets and pragmatism
Most modern societies aim for <130/80 mm Hg in many adults, while some (e.g., AAFP) recommend a standard <140/90 mm Hg target, underscoring shared decision-making and tolerability [8].
Evidence highlights
≥140/90 mm Hg for lifestyle + drugs [1]
Universal start threshold (ESC 2024)
Often at SBP ≥160 mm Hg; consider 140–160 mm Hg [4]
Very old (≥80 y) ESH 2023 start
ACEi/ARB, CCB, thiazide-like diuretic; β‑blockers restored role [4], [9]
First-line classes
Diagnosis and Risk Stratification
Confirming Hypertension and Establishing Targets
Use standardized techniques, confirm with out-of-office readings, and individualize targets based on age, comorbidity, and treatment tolerance.
1
Standardize measurement and confirm with out-of-office BP
Use repeat seated office measurements, then confirm with HBPM or 24-hour ABPM to exclude white-coat and detect masked hypertension, as emphasized in ESH 2023 [6], [4].
2
Set initial targets
Aim for <130/80 mm Hg when tolerated for most non-frail adults per contemporary practice trends; recognize that some groups (e.g., AAFP) endorse <140/90 mm Hg as a standard target, particularly in primary care contexts [8].
3
Decide when to start medications
ESC 2024: Start drugs at ≥140/90 mm Hg regardless of age/CVD risk and pair with lifestyle (Class I) [1]. ESH 2023: start at ≥140/90 mm Hg for most, but in ≥80 years, Class I at SBP ≥160 mm Hg, with consideration at 140–160 mm Hg; low-risk grade 1 may try lifestyle first for several months [4], [1].
Therapeutic Sequencing
Stepwise Pharmacotherapy: From First-Line to Resistant Hypertension
Prioritize combination therapy early, expand to triple therapy, and use mineralocorticoid receptor antagonism before device therapy.
1
Start with 2-drug single-pill therapy
Preferred: ACEi/ARB + DHP-CCB or ACEi/ARB + thiazide-like diuretic (chlorthalidone or indapamide). Single-pill combinations improve adherence and speed BP control [4], [1].
2
Escalate to triple therapy
If uncontrolled, add the third class to form ACEi/ARB + CCB + thiazide-like diuretic before switching classes [4].
3
Resistant hypertension (≥3 drugs including a diuretic, uncontrolled)
Add spironolactone 12.5–50 mg as the preferred fourth agent (monitor K+ and renal function). Consider chlorthalidone/indapamide optimization and evaluate for secondary causes. For persistent true resistance, consider renal denervation in select patients, acknowledging evolving evidence and guideline positioning [4], [5].
4
Role of β‑blockers
β‑blockers are restored as therapeutic options in ESH 2023, particularly for coronary disease, heart failure with reduced EF, arrhythmias, pregnancy, or sympathetic overactivity; they may be earlier-line in those indications [9], [4].
Nonpharmacologic Therapy
Lifestyle and Adherence Optimization
Initiate lifestyle measures for all patients at diagnosis and throughout care; they potentiate medications and reduce pill burden.
Lifestyle interventions
Weight reduction and physical activity; even modest loss lowers BP [11].
DASH-style diet, sodium restriction, and moderation of alcohol [11].
Sleep hygiene and OSA screening when suggestive; treat OSA to aid control.
Smoking cessation and stress reduction to lower overall CVD risk.
Adherence and simplification
Use single-pill combinations when possible to improve persistence [4], [1].
Align dosing with routines; address cost and side effects proactively.
Employ home BP logs and digital reminders; verify technique [6].
Special Populations and Considerations
Tailoring Therapy
Adjust agents, thresholds, and targets based on comorbidity, age, and physiologic context.
Very old adults (≥80 years)
ESC 2024: treat at ≥140/90 mm Hg similar to younger adults [1].
ESH 2023: initiate at SBP ≥160 mm Hg (Class I); consider 140–160 mm Hg based on frailty, orthostasis, and preferences [4].
Prioritize tolerance, orthostatic BP checks, and renal/electrolyte monitoring.
Compelling indications
CAD, HFrEF, arrhythmias, pregnancy: β‑blockers often indicated [9], [4].
CKD/proteinuria: ACEi/ARB foundational; diuretic intensity often needed [4].
Diabetes: standard first-line classes; monitor for orthostasis and albuminuria.
Emerging/advanced therapies
RNA-based therapeutics targeting the renin–angiotensin system (e.g., AGT knockdown) show promise for infrequent dosing; phase II data awaited [2].
Interventional approaches (e.g., renal denervation) are expanding for true resistant cases in specialized centers [5].
Targets and Monitoring
Follow-Up and Treatment Targets
Frequency and intensity of follow-up should match risk and BP level.
Follow-up cadence
Reassess every 4–6 weeks until control; sooner for stage 2 or high risk.
Use home BP averages to guide titration; confirm control with ABPM when uncertain [6].
Targets and de-intensification
Aim <130/80 mm Hg if tolerated; ensure diastolic not pushed too low in CAD.
AAFP supports a standard <140/90 mm Hg target; individualize per frailty and adverse effects [8].
Consider cautious de-intensification if orthostatic symptoms or adverse events emerge.
References
Source material
Primary literature that informs this article.
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