Introduction
Epidemiology
- Incidence: 1000.00 cases per 100,000 person-years
- Peak incidence: 50-60 years
- Sex ratio: 1:1
<1 | 1-5 | 6+ | 16+ | 30+ | 40+ | 50+ | 60+ | 70+ | 80+ |
Aetiology
Secondary hypertension may be caused by a wide variety of endocrine, renal and other causes. The table below lists some of the conditions that may cause secondary hypertension
Renal disease | Endocrine disorders | Other causes |
---|---|---|
• Glomerulonephritis • Chronic pyelonephritis • Adult polycystic kidney disease • Renal artery stenosis | • Primary hyperaldosteronism • Phaeochromocytoma • Cushing's syndrome • Liddle's syndrome • Congenital adrenal hyperplasia (11-beta hydroxylase deficiency) • Acromegaly | • Glucocorticoids • NSAIDs • Pregnancy • Coarctation of the aorta • Combined oral contraceptive pill |
Clinical features
- headaches
- visual disturbance
- seizures
In terms of signs hypertension is obviously usually detected when checking someones blood pressure. For diagnosing longstanding blood pressure there has been a move in recent years to using 24 hour blood pressure monitors. These avoid cases of so called 'white coat' hypertension where a patients blood pressure rises when they are in a clinical setting, for example a GP surgery. Studies have shown that readings from 24 hour blood pressure monitors correlate better with clinical outcomes and hence should be used to guide decisions about treatment.
It also also important when assessing a patient with newly diagnosed hypertension to ensure they do not have any end-organ damage:
- fundoscopy: to check for hypertensive retinopathy
- urine dipstick: to check for renal disease, either as a cause or consequence of hypertension
- ECG: to check for left ventricular hypertrophy or ischaemic heart disease
Investigations
Following diagnosis patients typically have the following tests:
- urea and electrolytes: check for renal disease, either as a cause or consequence of hypertension
- HbA1c: check for co-existing diabetes mellitus, another important risk factor for cardiovascular disease
- lipids: check for hyperlipidaemia, again another important risk factor for cardiovascular disease
- ECG
- urine dipstick
Diagnosis
- classifying hypertension into stages
- recommending the use of ambulatory blood pressure monitoring (ABPM) and home blood pressure monitoring (HBPM)
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Why were these guidelines needed?
It has long been recognised by doctors that there is a subgroup of patients whose blood pressure climbs 20 mmHg whenever they enter a clinical setting, so called 'white coat hypertension'. If we just rely on clinic readings then such patients may be diagnosed as having hypertension when, the vast majority of the time, their blood pressure is normal.
This has led to the use of both ambulatory blood pressure monitoring (ABPM) and home blood pressure monitoring (HBPM) to confirm the diagnosis of hypertension. These techniques allow a more accurate assessment of a patients' overall blood pressure. Not only does this help prevent overdiagnosis of hypertension - ABPM has been shown to be a more accurate predictor of cardiovascular events than clinic readings.
Blood pressure classification
This becomes relevant later in some of the management decisions that NICE advocate.
Stage | Criteria |
---|---|
Stage 1 hypertension | Clinic BP >= 140/90 mmHg and subsequent ABPM daytime average or HBPM average BP >= 135/85 mmHg |
Stage 2 hypertension | Clinic BP >= 160/100 mmHg and subsequent ABPM daytime average or HBPM average BP >= 150/95 mmHg |
Severe hypertension | Clinic systolic BP >= 180 mmHg, or clinic diastolic BP >= 110 mmHg |
Diagnosing hypertension
Firstly, NICE recommend measuring blood pressure in both arms when considering a diagnosis of hypertension.
If the difference in readings between arms is more than 20 mmHg then the measurements should be repeated. If the difference remains > 20 mmHg then subsequent blood pressures should be recorded from the arm with the higher reading.
It should of course be remember that there are pathological causes of unequal blood pressure readings from the arms, such as supravalvular aortic stenosis. It is therefore prudent to listen to the heart sounds if a difference exists and further investigation if a very large difference is noted.
NICE also recommend taking a second reading during the consultation, if the first reading is > 140/90 mmHg. The lower reading of the two should determine further management.
NICE suggest offering ABPM or HBPM to any patient with a blood pressure >= 140/90 mmHg.
If however the blood pressure is >= 180/110 mmHg:
- immediate treatment should be considered
- if there are signs of papilloedema or retinal haemorrhages NICE recommend same day assessment by a specialist
- NICE also recommend referral if a phaeochromocytoma is suspected (labile or postural hypotension, headache, palpitations, pallor and diaphoresis)
Ambulatory blood pressure monitoring (ABPM)
- at least 2 measurements per hour during the person's usual waking hours (for example, between 08:00 and 22:00)
- use the average value of at least 14 measurements
If ABPM is not tolerated or declined HBPM should be offered.
Home blood pressure monitoring (HBPM)
- for each BP recording, two consecutive measurements need to be taken, at least 1 minute apart and with the person seated
- BP should be recorded twice daily, ideally in the morning and evening
- BP should be recorded for at least 4 days, ideally for 7 days
- discard the measurements taken on the first day and use the average value of all the remaining measurements
Interpreting the results
ABPM/HBPM >= 135/85 mmHg (i.e. stage 1 hypertension)
- treat if < 80 years of age AND any of the following apply; target organ damage, established cardiovascular disease, renal disease, diabetes or a 10-year cardiovascular risk equivalent to 20% or greater
ABPM/HBPM >= 150/95 mmHg (i.e. stage 2 hypertension)
- offer drug treatment regardless of age
Management
- lowering the threshold for treating stage 1 hypertension in patients < 80 years from 20% to 10%
- angiotensin receptor blockers can be used instead of ACE-inhibitors where indicated
- if a patient is already taking an ACE-inhibitor or angiotensin receptor blocker, then a calcium channel blocker OR a thiazide-like diuretic can be used. Previously only a calcium channel blocker was recommended
Managing hypertension
Lifestyle advice should not be forgotten and is frequently tested in exams:
- a low salt diet is recommended, aiming for less than 6g/day, ideally 3g/day. The average adult in the UK consumes around 8-12g/day of salt. A recent BMJ paper* showed that lowering salt intake can have a significant effect on blood pressure. For example, reducing salt intake by 6g/day can lower systolic blood pressure by 10mmHg
- caffeine intake should be reduced
- the other general bits of advice remain: stop smoking, drink less alcohol, eat a balanced diet rich in fruit and vegetables, exercise more, lose weight
ABPM/HBPM >= 135/85 mmHg (i.e. stage 1 hypertension)
- treat if < 80 years of age AND any of the following apply; target organ damage, established cardiovascular disease, renal disease, diabetes or a 10-year cardiovascular risk equivalent to 10% or greater
- in 2019, NICE made a further recommendation, suggesting that we should 'consider antihypertensive drug treatment in addition to lifestyle advice for adults aged under 60 with stage 1 hypertension and an estimated 10-year risk below 10%. '. This seems to be due to evidence that QRISK may underestimate the lifetime probability of developing cardiovascular disease
ABPM/HBPM >= 150/95 mmHg (i.e. stage 2 hypertension)
- offer drug treatment regardless of age
For patients < 40 years consider specialist referral to exclude secondary causes.
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Step 1 treatment
- patients < 55-years-old or a background of type 2 diabetes mellitus: ACE inhibitor or a Angiotensin receptor blocker (ACE-i or ARB): (A)
- angiotensin receptor blockers should be used where ACE inhibitors are not tolerated (e.g. due to a cough)
- patients >= 55-years-old or of black African or African–Caribbean origin: Calcium channel blocker (C)
- ACE inhibitors have reduced efficacy in patients of black African or African–Caribbean origin are therefore not used first-line
Step 2 treatment
- if already taking an ACE-i or ARB add a Calcium channel blocker or a thiazide-like Diuretic
- if already taking a Calcium channel blocker add an ACE-i or ARB or a thiazide-like Diuretic
- for patients of black African or African–Caribbean origin taking a calcium channel blocker for hypertension, if they require a second agent consider an angiotensin receptor blocker in preference to an ACE inhibitor
- (A + C) or (A + D) or (C + A) or (C + D)
Step 3 treatment
- add a third drug to make, i.e.:
- if already taking an (A + C) then add a D
- if already (A + D) then add a C
- (A + C + D)
Step 4 treatment
- NICE define step 4 as resistant hypertension and suggest either adding a 4th drug (as below) or seeking specialist advice
- first, check for:
- confirm elevated clinic BP with ABPM or HBPM
- assess for postural hypotension.
- discuss adherence
- if potassium < 4.5 mmol/l add low-dose spironolactone
- if potassium > 4.5 mmol/l add an alpha- or beta-blocker
Patients who fail to respond to step 4 measures should be referred to a specialist. NICE recommend:
If blood pressure remains uncontrolled with the optimal or maximum tolerated doses of four drugs, seek expert advice if it has not yet been obtained.
Blood pressure targets
Clinic BP | ABPM / HBPM | |
---|---|---|
Age < 80 years | 140/90 mmHg | 135/85 mmHg |
Age > 80 years | 150/90 mmHg | 145/85 mmHg |
New drugs
Direct renin inhibitors
- e.g. Aliskiren (branded as Rasilez)
- by inhibiting renin blocks the conversion of angiotensinogen to angiotensin I
- no trials have looked at mortality data yet. Trials have only investigated fall in blood pressure. Initial trials suggest aliskiren reduces blood pressure to a similar extent as angiotensin converting enzyme (ACE) inhibitors or angiotensin-II receptor antagonists
- adverse effects were uncommon in trials although diarrhoea was occasionally seen
- only current role would seem to be in patients who are intolerant of more established antihypertensive drugs
*BMJ 2013;346:f1325