Hypertension
The following is based on NICE guidance 136, Hypertension in Adults: Diagnosis & Management. The threshold for diagnosis of hypertension is 140/90 (Office blood pressure) or 135/85 mmHg (Ambulatory BP Monitoring or Home BP Monitoring).
Sections on this page:
- Types of measurement
- Monitoring blood pressure
- Staging of hypertension
- Targets for BP control
- Drug management of hypertension
Types of measurement
Pros and cons of the various BP measurement modalities are discussed below
Office Blood Pressure Measurement (OBPM) |
|
Equipment required |
Electronic or calibrated analogue sphygmomanometer.
Direct manual measurement is not recommended unless the patient has an arrhythmia (e.g. atrial fibrillation). More information can be found here. |
Technique |
|
Pros |
Easily accessed at short notice Cheap/free Gives an instant result in front of the patient |
Cons |
Susceptible to white-coat effect Crude measure of patient’s true blood pressure Is rarely performed in a “relaxed temperate setting”, with 5 minutes rest beforehand |
Notes |
OBPM can generally be relied upon if normal (masked hypertension is rare), should not be relied upon for the diagnosis of hypertension
NICE guidance recommends confirming hypertension with either Home or 24h Ambulatory BP measurement. |
Ambulatory Blood Pressure Measurement (ABPM) |
|
Equipment required |
24h Ambulatory monitor + recording device |
Technique |
Performed in secondary care usually. Referral details available here. |
Pros |
|
Cons |
|
Notes |
Some GP practices may also have ABPM monitors that they can loan out to patients, mitigating some of the cons listed above. Some patient groups should have ABPM in order to assess their nocturnal dipping status: diabetes, CKD, sleep apnoea, endocrine hypertension and autonomic dysfunction. |
Home Blood Pressure Measurement (HBPM) |
|
Equipment required |
Automated BP Monitor; the BIHS keeps a list of approved validated monitors, which can be purchased from as little as £15. The Omron M2 is a cheap and basic option. |
Technique |
We have developed a HBPM information sheet and monitoring form for patients to use, which includes details on optimal technique: see here. |
Pros |
Cheap Gives accurate results (if done correctly, on a par with ABPM) Not susceptible to the white coat effect & identifies masked hypertension Suitable for long term monitoring |
Cons |
Patient has to fund initial cost of purchase Relies on patient motivation and use of optimal technique for accurate monitoring Patients can fail to record enough readings to allow accurate interpretation Does not assess for nocturnal ‘dipping’ |
Notes |
This is the recommended modality for monitoring of hypertension, but does require patient engagement |
Monitoring blood pressure
HBPM is the recommended method, due to its low cost and accuracy. In patients who cannot perform HBPM accurately, or who cannot afford a monitor, OBPM can be used, but is not advised if HBPM is possible.
ABPM can be used when the patient has persistently high OBPM readings despite increases to their antihypertensive medication regimen, as the white coat effect may be masking adequate BP control.
Telemonitoring (e.g. Scale-up BP) is also an option in most NHS Lothian GP practices. See here for details.
Staging of Hypertension
Management of hypertension should always incorporate non-drug management, as this is likely to have a much greater reduction on the patient’s overall cardiovascular risk. Recommend lifestyle modification for all patients.
Recommended introduction of drug and non-drug management according to severity:
Stage |
Systolic BP (mmHg) |
Diastolic BP (mmHg) |
Recommendation |
I |
140–159 |
90–99 |
Lifestyle advice only (reassess at appropriate interval) Consider drug treatment if:
Also consider drug treatment for patients aged >80 with SBP >150. |
II |
160–179 |
100–119 |
Lifestyle advice Drug treatment |
III |
180+ |
120+ |
Lifestyle advice Drug treatment In addition, look for end-organ damage/secondary hypertension and consider referral to specialist care |
NB: for ABPM/HBPM the targets are 5mmHg lower, i.e. 135 instead of 140
Targets for BP control
The following are taken from NICE guidance 2019-2020:
Patient group |
Target BP (mmHg) NB: for ABPM/HBPM the targets are 5mmHg lower, i.e. 135 instead of 140 |
Adults <80 years |
140/90 |
Adults ³80 years |
150/90 |
Type 1 diabetic patients |
135/85
If 2+ features of metabolic syndrome or albuminuria, target is 130/80 |
Chronic kidney disease patients |
140/90
If proteinuria present, target is 130/80 |
Stroke patients |
Systolic BP <130 |
Drug management of Hypertension
The recommended order in which medications are started is in the flowchart below (reproduced from NICE guidance 136).
NB:
- Patients with type 1 diabetes should also be started on ACEi/ARB for first line therapy.
- Amiloride can be used in place of spironolactone if better tolerated
Link to Lothian Hypertension guidance is available. Short notes on the drugs recommended in the Lothian Joint Formulary are below.
Lisinopril |
|
Type/class |
ACE inhibitor |
Dosage |
Start: 10mg daily Increase: Double dosage (10mg, 20mg, 40mg) Max: 40mg daily |
Pharmacokinetic issues |
Bioavailability: 25% Half-life: 12h Eliminated unchanged in urine |
Common Adverse Drug Reactions |
Postural hypotension, dizziness, cough, hyperkalaemia; less commonly angioedema (more so in black patients) |
Significant Interactions |
Spironolactone/amiloride – hyperkalaemia Lithium – increased lithium levels NSAIDs – renal impairment |
Notes |
First-dose hypotension uncommon Due to the above increased risk of angioedema, some guidelines advise using ARBs preferentially in black patients Recheck creatinine after initiation/dosage increase (a rise in creatinine of up to 25% is acceptable) |
Alternatives |
Ramipril (2.5mg/day, titrate to max. 10mg/day) Candesartan |
Candesartan |
|
Type/class |
Angiotensin Receptor Blocker |
Dosage |
Start: 8mg daily (4mg if risk of renal injury) Increase: Double dosage (8mg, 16mg, 32mg) Max: 32mg daily |
Pharmacokinetic issues |
Bioavailability: 15% Half-life: 9h Elimination: 33% renal / 66% stool |
Common Adverse Drug Reactions |
Abdominal/back pain, dizziness |
Significant Interactions |
Spironolactone/amiloride – hyperkalaemia Lithium – increased lithium levels NSAIDs – renal impairment |
Notes |
First-dose hypotension uncommon Recheck creatinine after initiation/dosage increase (a rise in creatinine of up to 25% is acceptable) |
Alternatives |
ACE inhibitors Losartan (25mg/day, titrate to max. 100mg/day) |
Amlodipine |
|
Type/class |
Calcium channel blocker (dihydropyridine) |
Dosage |
Start: 5mg daily Max: 10mg daily |
Pharmacokinetic issues |
Bioavailability: 65-80% Half-life: 35-50h Elimination: 60% renal |
Common Adverse Drug Reactions |
Leg swelling (common reason for discontinuation) GI disturbance Flushing Rash Dizziness |
Significant Interactions |
P450 Inducing medication – lower drug levels of amlodipine P450 Inhibiting medication – higher drug levels of amlodipine Simvastatin – increased level of simvastatin
|
Notes |
If stopped because of leg swelling, consider Lercanidipine Some formulations are scored, allowing reduction to 2.5mg daily if this is better tolerated |
Alternatives |
Lercanidipine (start 10mg/day; titrate to max. 20mg/day) Diltiazem/verapamil |
Indapamide |
|
Type/class |
Thiazide-like diuretic |
Dosage |
Dose is 2.5mg once daily, or 1.5mg of the modified-release preparation Choose lowest-cost formulation |
Pharmacokinetic issues |
Bioavailability: 100% Half-life: 14-18h Elimination: 70% renal; 23% GI tract |
Common Adverse Drug Reactions |
Dry mouth GI disturbance Hypokalaemia Erectile dysfunction Rash |
Significant Interactions |
Amiodarone – arrhythmia Lithium – Lithium toxicity |
Notes |
NICE guidance recommends thiazide-like diuretics (Indapamide) over thiazides (Bendroflumethiazide) Choose lowest-cost formulation |
Alternatives |
Bendroflumethiazide |
Bendroflumethiazide |
|
Type/class |
Thiazide diuretic |
Dosage |
Start: 2.5mg daily Increase: 2.5mg increments Max: 10mg daily |
Pharmacokinetic issues |
Bioavailability: 100% Half-life: 3.5h Elimination: 30% urine; 70% metabolised |
Common Adverse Drug Reactions |
Dry mouth GI disturbance Hypokalaemia Erectile dysfunction |
Significant Interactions |
Amiodarone – arrhythmia Lithium – Lithium toxicity |
Notes |
|
Alternatives |
Indapamide |
Spironolactone |
|
Type/class |
Potassium-sparing diuretic |
Dosage |
Start: 25mg daily Increase: 25mg increments Max: 100mg daily |
Pharmacokinetic issues |
Bioavailability: 75% Half-life: 1.4h Elimination: Hepatic urine/bile |
Common Adverse Drug Reactions |
Hyperkalaemia Renal impairment Headache Weakness GI disturbance Erectile dysfunction Gynaecomastia |
Significant Interactions |
Ciclosporin – hyperkalaemia Lithium – Lithium toxicity Digoxin – Digoxin toxicity |
Notes |
Frail elderly patients can start at 12.5mg daily |
Alternatives |
Amiloride (starting dose 10mg daily, max. 20mg daily), Eplerenone |
Bisoprolol |
|
Type/class |
Beta-adrenoceptor antagonist |
Dosage |
Start: 1.25 – 2.5mg daily (lower dose in elderly) Increase: 2.5mg increments Max: 20mg daily (10mg in heart failure) |
Pharmacokinetic issues |
Bioavailability: 90% Half-life: 10-12h Elimination: 50% hepatic / 50% renal |
Common Adverse Drug Reactions |
Dizziness Headache Sleep disturbance Bradycardia Cool/numb peripheries GI disturbance Weakness |
Significant Interactions |
Verapamil/Diltiazem – heart block Theophylline/Aminophylline – bronchospasm Mefloquine – bradycardia |
Notes |
|
Alternatives |
Atenolol, Carvedilol, Metoprolol |
Doxazosin |
|
Type/class |
Alpha-1-adrenoceptor antagonist |
Dosage |
Start: 1mg daily Increase: Double every 1-2 weeks Max: 16mg daily |
Pharmacokinetic issues |
Bioavailability: 66% Half-life: 22h Elimination: Hepatic |
Common Adverse Drug Reactions |
Postural hypotension (particularly on initiating therapy) Weakness Chest pain Oedema Flu-like illness |
Significant Interactions |
Sildenafil – hypotension
|
Notes |
Alpha-blockers should generally be used as a last resort. |
Alternatives |
Prazosin, Terazosin |