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Table 55.6

Causes of Secondary Hypertension

CauseClues/investigation
Intrinsic renal disease

Family history of heritable renal disease (e.g. polycystic kidney disease)

Abnormal urine stick test and microscopy Raised creatinine

Abnormal kidneys on ultrasound Discuss further investigation with nephrologist if intrinsic renal disease suspected

Primary hyperaldosteronism

Low plasma potassium

High plasma aldosterone with suppressed plasma renin

Cushing syndrome

Truncal obesity, thin skin with purple abdominal striae, proximal myopathy (unable to rise from chair without using arms)

Increased urinary free cortisol excretion

Pheochromocytoma (see Chapter94)

Paroxysmal headache, sweating or palpitation

Hypertensive crisis following anaesthesia or administration of contrast

Family history of pheochromocytoma Increased urinary catecholamine excretion

Coarctation of aorta

Radiofemoral delay

Coarctation demonstrated by echocardiography/MRI

Renal artery stenosis

May be due to fibromuscular dysplasia (age <50 with no family history of hypertension) or, more commonly, to atherosclerosis (age >50 with other atherosclerotic arterial disease)

Refractory hypertension

Deteriorating blood pressure control in compliant, long-standing hypertensive patients

Rise in creatinine on treatment with ACE inhibitor

Renal impairment with minimal proteinuria Low plasma sodium and potassium (due to secondary hyperaldosteronism)

Difference in kidney size >1.5cm on ultrasound

Other causesMany causes including drugs, obstructive sleep apnoea, acromegaly

ACE, angiotensin-converting enzyme.