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Clinical approach to young hypertension - bimjonline.com

Review Article Brunei Int Med J. 2013; 9 (2): 81-92. Clinical approach to young hypertension Norlela SUKOR. Endocrine Unit, Department of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Malaysia ABSTRACT. hypertension affects approximately 30% of the population worldwide. It is a serious disease, expensive to treat, and can lead to long-term morbidity and mortality. young hypertension , defined as hyperten- sion occurring in patients aged 40 or younger, is now seen more frequently. A correct and holistic ap- proach in the evaluation of patients with suspected young hypertension is essential, as the underlying cause is demonstrable in more than half of the cases.

Clinical approach to young hypertension Norlela SUKOR Endocrine Unit, Department of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Malaysia

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Transcription of Clinical approach to young hypertension - bimjonline.com

1 Review Article Brunei Int Med J. 2013; 9 (2): 81-92. Clinical approach to young hypertension Norlela SUKOR. Endocrine Unit, Department of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Malaysia ABSTRACT. hypertension affects approximately 30% of the population worldwide. It is a serious disease, expensive to treat, and can lead to long-term morbidity and mortality. young hypertension , defined as hyperten- sion occurring in patients aged 40 or younger, is now seen more frequently. A correct and holistic ap- proach in the evaluation of patients with suspected young hypertension is essential, as the underlying cause is demonstrable in more than half of the cases.

2 Among these causes include primary aldosteron- ism, phaeochromocytoma, Cushing's syndrome, renal parenchymal disease and renal artery stenosis. The detection of these causes is important as it provides an opportunity to convert an incurable disease into a potentially curable disease, hence avoiding the long-term sequelae and complications of hyper- tension. Keywords: young hypertension , secondary hypertension , primary aldosteronism, phaeochromocytoma, Cushing's syndrome INTRODUCTION. hypertension is a major long-term health hypertension in the young can be condition, and is the leading cause of prema- been attributed to some underlying causes.

3 Ture death among adults throughout the This view stems from the study by Platt, who world. It is now established that hypertension demonstrated secondary causes in 75% of 64. 1. detected at young age is not uncommon. hypertensive patients under the age of 40. young hypertension is defined as hyperten- In another study looking at 127 young hyper- sion diagnosed in patients at the age of less tensive patients, an identifiable cause was 2. than 40 years. The challenges faced by clini- found in 57%. The incidence of secondary cians include how to distinguish young or sec- hypertension is variably estimated between 3.

4 Ondary hypertension from essential hyperten- five and 10%. The detection of a secondary sion. cause is of important as it provides an oppor- Correspondence author: Norlela SUKOR tunity to convert an incurable disease into a Endocrine Unit, Department of Medicine, potentially curable disease. Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, 56000 Cheras, Kuala Lumpur, Malaysia. Tel: +60391456087, Fax: +60391456679. E mail: A number of rare causes of secondary SUKOR. Brunei Int Med J. 2013; 9 (2): 82. hypertension have been identified.

5 However, minute resting in a seated position, and keep- this review will focus only on the more com- ing the upper arm at heart level) can lead to mon secondary causes and the diagnostic false diagnoses of hypertension . Once the approach . diagnosis is confirmed, evaluation of second- ary causes should be pursued. Ambulatory General Clinical approach blood pressure monitoring may be useful in Before instituting laborious evaluations in a certain patients due to diurnal variation. young patient with hypertension , the clinician must be certain that the blood pressure read- A detailed medical history and review ings obtained are indicative of the patient's of systems should be obtained, complement- blood pressure level.

6 It is crucial to establish ed with a careful and complete physical ex- that the blood pressure measurement meth- aminations. These will provide information ods are valid and accurate as per established and guidance to the diagnostic approach . Ta- 4. guidelines. Lack of attention to proper ble 1 illustrates some of the causes of sec- measurement techniques (including using an ondary hypertension and the relevant history appropriate arm-cuff size, allowing a full 5- and Clinical findings. minute resting in a seated position, and keep- Table 1. Causes of secondary hypertension .)

7 System Diseases Important history Clinical findings Difficult to control blood pressure, hypertension with hypokalaemia, Muscle or body weakness Primary aldosteronism family history of intracerebral haemorrhage Headaches, palpitation and/or Significant postural drop or Phaeochromocytoma sweating fluctuating blood pressure Easy bruising, unable to stand up Cushingoid appearance, facial plethora, from a squatting position, weight thin skin, reddish Cushing's syndrome gain, fracture due to osteoporosis purple striae, proximal myopathy Increasing in ring and/or shoe size, Frontal bossing, thickening of the nose, Endocrine Acromegaly enlargement of extremities or visual macroglossia, prognathism disturbance, headache Weight loss, palpitation, irritability Goiter, exophthalmos Hyperthyroidism or Cold intolerance, tiredness and Dry skin, ccoarse, brittle, straw like hair, Hypothyroidism weight gain goitre Polyuria, kidney stones, bone/joint Muscle weakness, depression Hyperparathyroidism pain, depression, epigastric pain Other mineralocorticoid hyperten- sion (.)

8 Apparent mineralocorti- hypertension with hypokalaemia Muscle or body weakness coid excess, Liddle's syndrome). Reduced urine output, facial or lower Renal Renal parenchymal disease limb swelling, hypertension , Facial or lower limb oedema, anaemia haematuria Difficult to control blood pressure, Renal bruit Renal artery stenosis sudden deterioration in kidney func- tion Haematuria or flank pain or recurrent Ballotable kidneys Polycystic kidneys urinary infections Systolic murmur at left infra-clavicular Cardiovascular Coarctation of aorta hypertension , chest pain area, blood pressure difference >20.

9 MmHg between arms and legs Small joint pain, mouth ulcers, Malar rash, small joints polyarthropathy, Others Systemic lupus erythematosus rashes oral ulcers, alopecia Obstructive sleep apnoea Snoring or fall asleep during daytime Morbid obesity Drug abuse or taking over-the- Cushingoid appearance (if exogenous Exogenous drug use counter medications drug contain steroids). SUKOR. Brunei Int Med J. 2013; 9 (2): 83. Table 2: Reported effects of drugs on the aldosterone/renin ratio. Medications Renin Aldosterone Effects No effect Non-dihydropyridine calcium channel blocker (verapamil) Minimal Minimal No effect Alpha blockers Nil Nil No effect Hydralazine (with verapamil) Minimal Minimal No effect False negative effect Diuretics (including spironolactone and amiloride) Increased markedly Increased False negative ACE inhibitors Increased Decreased False negative Angiotensin receptor blockers Increased Decreased False negative (probably similar to ACEI).

10 Minoxidil Increased Minimal False negative Dihydropyridine calcium channel blocker (Amlodipine) Minimal increased Minimal decreased False negative False positive effect -blockers Decreased Minimal decreased False positive -methyldopa Decreased Minimal decreased False positive Clonidine Decreased Minimal decreased False positive Primary Aldosteronism appropriate interpretation of results. Primary Aldosteronism (PA) is characterised by overproduction of aldosterone by the ad- Many factors can affect the ARR result renal cortex which causes salt and water re- and compromise its sensitivity and specificity.


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