Managing Hypertension
Guides JNC/ACC hypertension management with staging, treatment algorithms, and monitoring schedules.
Why This Skill Exists
Hypertension affects approximately 116 million U.S. adults and is the leading modifiable risk factor for cardiovascular disease, stroke, heart failure, and chronic kidney disease. The 2017 ACC/AHA guideline redefined hypertension thresholds (≥130/80 mmHg), replacing the prior JNC 8 threshold of ≥140/90 mmHg, which significantly expanded the population requiring intervention. Uncontrolled hypertension accounts for an estimated 500,000 deaths annually in the United States.
Primary care clinicians manage the overwhelming majority of hypertensive patients, yet control rates remain below 50% nationally. Common errors include reliance on single office readings, failure to rule out white-coat hypertension, inadequate titration intervals, and missed secondary causes. This skill enforces the ACC/AHA stepwise approach to diagnosis, staging, treatment selection, and monitoring to drive blood pressure to target with minimal adverse effects.
Checkpoint A: Pre-Draft Intake (Mandatory)
- What is the patient's most recent office BP (average of ≥2 readings, seated, ≥1 minute apart)? Default: [REQUIRED]
- Has ambulatory blood pressure monitoring (ABPM) or home BP monitoring (HBPM) been performed? Default: no
- What is the patient's 10-year ASCVD risk score (Pooled Cohort Equations)? Default: calculate
- Does the patient have established clinical ASCVD, heart failure, CKD, or diabetes? Default: no
- What antihypertensives is the patient currently taking with doses? Default: none
- Has secondary hypertension been considered or ruled out? Default: not yet assessed
- What is the patient's baseline creatinine, potassium, and eGFR? Default: pending labs
- Is the patient pregnant or planning pregnancy? Default: no
Documents to Request
- Office BP log with at least 2 readings per visit over 2-3 visits
- ABPM or HBPM data if available (≥12 readings over ≥4 days)
- Current medication list including NSAIDs, decongestants, oral contraceptives
- Baseline metabolic panel (BMP) with creatinine, potassium, sodium, glucose
- Lipid panel and fasting glucose or A1c for ASCVD risk calculation
- ECG (12-lead) for LVH assessment if not done within past year
- Urinalysis with albumin-to-creatinine ratio
- Prior echocardiogram report if history of LVH or heart failure
Step 1: Accurate Diagnosis and Staging
Confirm hypertension diagnosis per 2017 ACC/AHA criteria:
| BP Category |
Systolic (mmHg) |
Diastolic (mmHg) |
Action |
| Normal |
<120 |
and <80 |
Reassess in 1 year |
| Elevated |
120-129 |
and <80 |
Lifestyle modifications; reassess 3-6 months |
| Stage 1 HTN |
130-139 |
or 80-89 |
Lifestyle + meds if ASCVD risk ≥10% or known CVD/CKD/DM |
| Stage 2 HTN |
≥140 |
or ≥90 |
Lifestyle + medication (two-drug combo if BP ≥20/10 above target) |
| Hypertensive Crisis |
>180 |
and/or >120 |
Immediate evaluation for end-organ damage |
Confirm with out-of-office readings if feasible. ABPM is the gold standard; HBPM (average of morning and evening readings over 7 days, discard day 1) is acceptable. White-coat hypertension: office BP elevated but ABPM daytime average <135/85.
Step 2: Secondary Hypertension Screening
Screen for secondary causes when any of the following are present:
- Age of onset <30 or >55 with no prior history
- Resistant hypertension (uncontrolled on ≥3 drugs including a diuretic at optimal dose)
- Sudden loss of BP control in previously well-managed patient
- Hypokalemia (K+ <3.5) not explained by diuretics
- Renal bruit or asymmetric kidney size
| Suspected Cause |
Screening Test |
Prevalence |
| Primary aldosteronism |
Aldosterone-to-renin ratio (ARR) |
5-10% of HTN |
| Renal artery stenosis |
Renal duplex ultrasound or CT angiography |
1-5% |
| Pheochromocytoma |
Plasma free metanephrines |
<1% |
| Cushing syndrome |
24-hour urine free cortisol or overnight dexamethasone suppression |
<1% |
| Obstructive sleep apnea |
STOP-BANG questionnaire → polysomnography |
30-50% of resistant HTN |
| Thyroid disease |
TSH |
1-3% |
Step 3: First-Line Pharmacotherapy
Select initial therapy per ACC/AHA compelling indications:
| Compelling Indication |
Preferred Agent(s) |
Rationale |
| No compelling indication |
ACEi, ARB, CCB, or thiazide-type diuretic |
All four classes equivalent as first-line |
| CKD with albuminuria |
ACEi or ARB |
Renoprotective; reduce proteinuria |
| Diabetes mellitus |
ACEi or ARB |
Renoprotective independent of BP lowering |
| Heart failure (HFrEF) |
ACEi/ARB + beta-blocker + diuretic |
Guideline-directed medical therapy |
| Post-MI / CAD |
ACEi + beta-blocker |
Cardioprotective |
| Black patients (no CKD/HF) |
CCB or thiazide-type diuretic |
Better efficacy per ALLHAT |
| Pregnancy |
Labetalol, nifedipine, or methyldopa |
ACEi/ARB CONTRAINDICATED |
Starting doses: Lisinopril 10mg daily, amlodipine 5mg daily, chlorthalidone 12.5mg daily. Titrate at 4-week intervals.
Step 4: Combination Therapy and Titration
If BP remains above target on single agent at adequate dose:
Dual therapy: Combine agents from two different classes; preferred combinations:
- ACEi/ARB + CCB (e.g., lisinopril 20mg + amlodipine 5mg)
- ACEi/ARB + thiazide-type diuretic (e.g., losartan 100mg + HCTZ 25mg)
- Avoid: ACEi + ARB combination (hyperkalemia, renal risk per ONTARGET trial)
Triple therapy: Add third class if dual therapy insufficient after 4 weeks at max tolerated doses
- Standard triple: ACEi/ARB + CCB + thiazide-type diuretic
Resistant hypertension (uncontrolled on ≥3 drugs including diuretic):
- Confirm adherence (pill counts, pharmacy refill data)
- Optimize diuretic (switch HCTZ to chlorthalidone 25mg or indapamide 1.25mg)
- Add spironolactone 25-50mg (per PATHWAY-2 trial) as fourth agent
- Check for secondary causes if not previously done
Step 5: Monitoring and Follow-Up Schedule
| Phase |
Visit Interval |
Labs |
Actions |
| Initial titration |
Every 2-4 weeks |
BMP at 2 weeks after starting ACEi/ARB/diuretic |
Titrate to target |
| Stable on therapy |
Every 3-6 months |
BMP annually; lipids per ASCVD risk |
Assess adherence, side effects |
| Well-controlled ≥1 year |
Every 6-12 months |
Annual BMP, UACR |
Consider step-down if sustained control |
| Resistant HTN |
Every 2-4 weeks |
BMP, aldosterone/renin if indicated |
Specialist referral if uncontrolled on 4 drugs |
BP targets per ACC/AHA 2017:
- General: <130/80 mmHg (if can be achieved without undue treatment burden)
- Age ≥65, non-institutionalized: <130 systolic (per SPRINT trial); individualize if frail
- CKD: <130/80 mmHg
- Diabetes: <130/80 mmHg
Checkpoint B: Post-Draft Alignment (Mandatory)
- Is BP staging documented with the method of measurement (office, ABPM, HBPM)?
- Has ASCVD risk been calculated and documented to justify treatment threshold?
- Are medication selections aligned with compelling indications and contraindications?
- Is the titration plan documented with specific dose escalation timeline and lab monitoring?
- Has secondary hypertension been considered with screening rationale documented?
Quality Audit
Guidelines
- Never start ACEi and ARB simultaneously—dual RAAS blockade increases hyperkalemia and acute kidney injury risk
- Always check potassium and creatinine within 1-2 weeks of starting or uptitrating ACEi, ARB, or diuretic
- White-coat hypertension affects 15-30% of patients with elevated office BP; confirm with out-of-office readings before initiating pharmacotherapy
- Chlorthalidone is preferred over HCTZ due to longer half-life, proven cardiovascular outcomes (ALLHAT), and superior 24-hour BP control
- ACEi/ARB must be discontinued immediately if pregnancy is confirmed or planned—teratogenic effects include renal agenesis and oligohydramnios
- Beta-blockers are NOT first-line for uncomplicated hypertension per ACC/AHA 2017; reserve for compelling indications (post-MI, HFrEF, rate control)
- Orthostatic hypotension must be assessed in elderly patients at each visit: check standing BP at 1 and 3 minutes after rising
- Document all BP readings in a structured log to enable trend analysis across visits
1---2name: managing-hypertension3description: Guides JNC/ACC hypertension management with staging, treatment algorithms, and monitoring schedules. Use when managing blood pressure, titrating antihypertensives, or creating hypertension care plans.4---5
6# Managing Hypertension
7
8Guides JNC/ACC hypertension management with staging, treatment algorithms, and monitoring schedules.
9
10## Why This Skill Exists
11
12Hypertension affects approximately 116 million U.S. adults and is the leading modifiable risk factor for cardiovascular disease, stroke, heart failure, and chronic kidney disease. The 2017 ACC/AHA guideline redefined hypertension thresholds (≥130/80 mmHg), replacing the prior JNC 8 threshold of ≥140/90 mmHg, which significantly expanded the population requiring intervention. Uncontrolled hypertension accounts for an estimated 500,000 deaths annually in the United States.
13
14Primary care clinicians manage the overwhelming majority of hypertensive patients, yet control rates remain below 50% nationally. Common errors include reliance on single office readings, failure to rule out white-coat hypertension, inadequate titration intervals, and missed secondary causes. This skill enforces the ACC/AHA stepwise approach to diagnosis, staging, treatment selection, and monitoring to drive blood pressure to target with minimal adverse effects.
15
16---
17
18## Checkpoint A: Pre-Draft Intake (Mandatory)
19
201. What is the patient's most recent office BP (average of ≥2 readings, seated, ≥1 minute apart)? **Default: [REQUIRED]**
212. Has ambulatory blood pressure monitoring (ABPM) or home BP monitoring (HBPM) been performed? **Default: no**
223. What is the patient's 10-year ASCVD risk score (Pooled Cohort Equations)? **Default: calculate**
234. Does the patient have established clinical ASCVD, heart failure, CKD, or diabetes? **Default: no**
245. What antihypertensives is the patient currently taking with doses? **Default: none**
256. Has secondary hypertension been considered or ruled out? **Default: not yet assessed**
267. What is the patient's baseline creatinine, potassium, and eGFR? **Default: pending labs**
278. Is the patient pregnant or planning pregnancy? **Default: no**
28
29### Documents to Request
30
31- Office BP log with at least 2 readings per visit over 2-3 visits
32- ABPM or HBPM data if available (≥12 readings over ≥4 days)
33- Current medication list including NSAIDs, decongestants, oral contraceptives
34- Baseline metabolic panel (BMP) with creatinine, potassium, sodium, glucose
35- Lipid panel and fasting glucose or A1c for ASCVD risk calculation
36- ECG (12-lead) for LVH assessment if not done within past year
37- Urinalysis with albumin-to-creatinine ratio
38- Prior echocardiogram report if history of LVH or heart failure
39
40---
41
42## Step 1: Accurate Diagnosis and Staging
43
44Confirm hypertension diagnosis per 2017 ACC/AHA criteria:
45
46| BP Category | Systolic (mmHg) | Diastolic (mmHg) | Action |
47|---|---|---|---|
48| Normal | <120 | and <80 | Reassess in 1 year |
49| Elevated | 120-129 | and <80 | Lifestyle modifications; reassess 3-6 months |
50| Stage 1 HTN | 130-139 | or 80-89 | Lifestyle + meds if ASCVD risk ≥10% or known CVD/CKD/DM |
51| Stage 2 HTN | ≥140 | or ≥90 | Lifestyle + medication (two-drug combo if BP ≥20/10 above target) |
52| Hypertensive Crisis | >180 | and/or >120 | Immediate evaluation for end-organ damage |
53
54Confirm with out-of-office readings if feasible. ABPM is the gold standard; HBPM (average of morning and evening readings over 7 days, discard day 1) is acceptable. White-coat hypertension: office BP elevated but ABPM daytime average <135/85.
55
56---
57
58## Step 2: Secondary Hypertension Screening
59
60Screen for secondary causes when any of the following are present:
61
62- Age of onset <30 or >55 with no prior history
63- Resistant hypertension (uncontrolled on ≥3 drugs including a diuretic at optimal dose)
64- Sudden loss of BP control in previously well-managed patient
65- Hypokalemia (K+ <3.5) not explained by diuretics
66- Renal bruit or asymmetric kidney size
67
68| Suspected Cause | Screening Test | Prevalence |
69|---|---|---|
70| Primary aldosteronism | Aldosterone-to-renin ratio (ARR) | 5-10% of HTN |
71| Renal artery stenosis | Renal duplex ultrasound or CT angiography | 1-5% |
72| Pheochromocytoma | Plasma free metanephrines | <1% |
73| Cushing syndrome | 24-hour urine free cortisol or overnight dexamethasone suppression | <1% |
74| Obstructive sleep apnea | STOP-BANG questionnaire → polysomnography | 30-50% of resistant HTN |
75| Thyroid disease | TSH | 1-3% |
76
77---
78
79## Step 3: First-Line Pharmacotherapy
80
81Select initial therapy per ACC/AHA compelling indications:
82
83| Compelling Indication | Preferred Agent(s) | Rationale |
84|---|---|---|
85| No compelling indication | ACEi, ARB, CCB, or thiazide-type diuretic | All four classes equivalent as first-line |
86| CKD with albuminuria | ACEi or ARB | Renoprotective; reduce proteinuria |
87| Diabetes mellitus | ACEi or ARB | Renoprotective independent of BP lowering |
88| Heart failure (HFrEF) | ACEi/ARB + beta-blocker + diuretic | Guideline-directed medical therapy |
89| Post-MI / CAD | ACEi + beta-blocker | Cardioprotective |
90| Black patients (no CKD/HF) | CCB or thiazide-type diuretic | Better efficacy per ALLHAT |
91| Pregnancy | Labetalol, nifedipine, or methyldopa | ACEi/ARB CONTRAINDICATED |
92
93Starting doses: Lisinopril 10mg daily, amlodipine 5mg daily, chlorthalidone 12.5mg daily. Titrate at 4-week intervals.
94
95---
96
97## Step 4: Combination Therapy and Titration
98
99If BP remains above target on single agent at adequate dose:
100
1011. **Dual therapy**: Combine agents from two different classes; preferred combinations:
102 - ACEi/ARB + CCB (e.g., lisinopril 20mg + amlodipine 5mg)
103 - ACEi/ARB + thiazide-type diuretic (e.g., losartan 100mg + HCTZ 25mg)
104 - Avoid: ACEi + ARB combination (hyperkalemia, renal risk per ONTARGET trial)
105
1062. **Triple therapy**: Add third class if dual therapy insufficient after 4 weeks at max tolerated doses
107 - Standard triple: ACEi/ARB + CCB + thiazide-type diuretic
108
1093. **Resistant hypertension** (uncontrolled on ≥3 drugs including diuretic):
110 - Confirm adherence (pill counts, pharmacy refill data)
111 - Optimize diuretic (switch HCTZ to chlorthalidone 25mg or indapamide 1.25mg)
112 - Add spironolactone 25-50mg (per PATHWAY-2 trial) as fourth agent
113 - Check for secondary causes if not previously done
114
115---
116
117## Step 5: Monitoring and Follow-Up Schedule
118
119| Phase | Visit Interval | Labs | Actions |
120|---|---|---|---|
121| Initial titration | Every 2-4 weeks | BMP at 2 weeks after starting ACEi/ARB/diuretic | Titrate to target |
122| Stable on therapy | Every 3-6 months | BMP annually; lipids per ASCVD risk | Assess adherence, side effects |
123| Well-controlled ≥1 year | Every 6-12 months | Annual BMP, UACR | Consider step-down if sustained control |
124| Resistant HTN | Every 2-4 weeks | BMP, aldosterone/renin if indicated | Specialist referral if uncontrolled on 4 drugs |
125
126BP targets per ACC/AHA 2017:
127- General: <130/80 mmHg (if can be achieved without undue treatment burden)
128- Age ≥65, non-institutionalized: <130 systolic (per SPRINT trial); individualize if frail
129- CKD: <130/80 mmHg
130- Diabetes: <130/80 mmHg
131
132---
133
134## Checkpoint B: Post-Draft Alignment (Mandatory)
135
1361. Is BP staging documented with the method of measurement (office, ABPM, HBPM)?
1372. Has ASCVD risk been calculated and documented to justify treatment threshold?
1383. Are medication selections aligned with compelling indications and contraindications?
1394. Is the titration plan documented with specific dose escalation timeline and lab monitoring?
1405. Has secondary hypertension been considered with screening rationale documented?
141
142---
143
144## Quality Audit
145
146- [ ] BP measured correctly: seated ≥5 minutes, supported arm at heart level, appropriate cuff size
147- [ ] At least 2 readings averaged, ≥1 minute apart
148- [ ] BP stage documented per 2017 ACC/AHA classification
149- [ ] Out-of-office confirmation obtained or plan documented
150- [ ] 10-year ASCVD risk calculated and recorded
151- [ ] Secondary hypertension screening considered and documented
152- [ ] First-line agent selected per compelling indications
153- [ ] ACEi/ARB contraindicated medications checked (pregnancy, bilateral RAS, angioedema history)
154- [ ] BMP checked within 2 weeks of ACEi/ARB/diuretic initiation
155- [ ] Creatinine rise ≤30% from baseline on ACEi/ARB (>30% = hold and investigate)
156- [ ] Lifestyle modifications counseled: DASH diet, sodium <2300mg/day, exercise 150 min/week, weight loss, alcohol moderation
157- [ ] Follow-up interval documented per titration phase
158- [ ] Adherence assessment performed at each visit
159- [ ] Home BP monitoring instructions provided with target values
160
161---
162
163## Guidelines
164
165- Never start ACEi and ARB simultaneously—dual RAAS blockade increases hyperkalemia and acute kidney injury risk
166- Always check potassium and creatinine within 1-2 weeks of starting or uptitrating ACEi, ARB, or diuretic
167- White-coat hypertension affects 15-30% of patients with elevated office BP; confirm with out-of-office readings before initiating pharmacotherapy
168- Chlorthalidone is preferred over HCTZ due to longer half-life, proven cardiovascular outcomes (ALLHAT), and superior 24-hour BP control
169- ACEi/ARB must be discontinued immediately if pregnancy is confirmed or planned—teratogenic effects include renal agenesis and oligohydramnios
170- Beta-blockers are NOT first-line for uncomplicated hypertension per ACC/AHA 2017; reserve for compelling indications (post-MI, HFrEF, rate control)
171- Orthostatic hypotension must be assessed in elderly patients at each visit: check standing BP at 1 and 3 minutes after rising
172- Document all BP readings in a structured log to enable trend analysis across visits