dr. m. sofi md; frcp (london); frcpedin; fecsedin
TRANSCRIPT
HYPERTENSION
DR. M. SofiMD; FRCP (London); FRCPEdin; FECSEdin
Hypertension is defined as a systolic blood pressure (SBP) of 140 mm Hg or more, or a diastolic blood pressure (DBP) of 90 mm Hg or more, or taking antihypertensive medication.
Classification of BP for adults aged 18 years or older: Normal: Systolic lower than 120 mm Hg, diastolic lower than
80 mm Hg Prehypertension: Systolic 120-139 mm Hg, diastolic 80-89 mm Hg Stage 1: Systolic 140-159 mm Hg, diastolic 90-99 mm Hg Stage 2: Systolic 160 mm Hg or greater, diastolic 100 mm Hg
or greater
HYPERTENSION
Classification: Defining normal blood pressure, prehypertension, hypertension (stages I and II), and isolated systolic hypertension.
Classification Systolic pressure
Diastolic pressure
mmHg mmHg
Normal 90–119 60–79
Prehypertension 120–139 81–89
Stage 1 140–159 90–99
Stage 2 ≥160 ≥100
Isolated systolic hypertension
≥140 <90
Stage 1 140–159 90–99
Source: American Heart Association (2003).
Malignant (accelerated) hypertension: Characterized by severe hypertension (e.g. systolic >200 mm Hg, diastolic >130 mm Hg) accompanied by encephalopathy or nephropathy, or by papilloedema and/or angiopathic haemolytic anaemia.
Suspected Pheochromocytoma: Consider if there is labile or postural hypotension, headache, palpitations, pallor and profuse sweating.
Hypertensive crisis: (SBP) ≥180 mm Hg or a (DBP) ≥120 mm Hg is considered a 'hypertensive crisis'. Immediate reduction in BP is required only in patients with acute end-organ damage.
Systolic or diastolic pressure: Framingham study and the Multiple Risk Factor Intervention Trial (MRFIT) study
indicates that systolic pressure is the most important determinant of cardiovascular risk.
Other considerations
The evaluation of hypertension involves: Accurate measuring of BP Focused medical history Physical examination Routine laboratory studies. A 12-lead electrocardiogram.
Confirmation of an elevated blood pressure (at 3 separate occasions); detailed history should extract the following information:
1. Extent of end-organ damage (e.g., heart, brain, kidneys, eyes)
2. Assessment of patients’ cardiovascular risk status
3. Exclusion of secondary causes of hypertension
EVALUATION: HYPERTENSION
Assessment end organ damage:
Heart: left ventricular hypertrophy, angina/previous myocardial infarction, previous coronary revascularization, and heart failure
Brain: stroke or transient ischemic attack dementia
Chronic kidney disease
Peripheral arterial disease
Retinopathy
EVALUATION: HYPERTENSION
Age – Advancing age is associated with HTN
Obesity – Obesity and weight gain are major risk factors.
Family history – HTN is about twice as common in subjects who have one or two hypertensive.
Race – HTN tends to be more common, be more severe, occur earlier in life, in blacks.
Reduced nephron number –may predispose to hypertension.
High Sodium intake (e.g., >3000 mg/day) increases the risk for hypertension
Excessive alcohol consumption
Physical inactivity – may increases the risk for hypertension
Diabetes and dyslipidemia
Personality traits and depression
Hypovitaminosis D
Risk factors for primary (essential) hypertension
Hypertension: component of metabolic syndrome
Tobacco use, cigarettes, including chewing tobacco
Elevated LDL cholesterol (or total cholesterol ≥240 mg/dL) or low HDL cholesterol: component of metabolic syndrome
Diabetes mellitus: component of metabolic syndrome
Obesity (BMI ≥30 kg/m2): component of metabolic syndrome
Age greater than 55 years for men or greater than 65 years for women:
Estimated glomerular filtration rate less than 60 mL/min
Microalbuminuria Family history of
premature cardiovascular disease (men < 55 years; women < 65 years)
Lack of exercise
Cardiovascular risk factors
One or more of these criteria qualifies as hypertension:
A 24-hour average of 130/80 mmHg or above
Daytime (awake) average of 135/85 mmHg or above
Nighttime (asleep) average of 120/70 mmHg or above
PRIMARY (ESSENTIAL) HYPERTENSION:
The pathogenesis of primary hypertension (formerly called "essential" hypertension) is poorly understood but is most likely the result of
Genetic and environmental factors that have multiple compounding effects on cardiovascular and renal structure and function.
Diagnosis of HTN is made using ambulatory blood pressure monitoring (ABPM) or home blood pressure monitoring.
Prescription or over-the-counter medications:
Oral contraceptives, particularly those containing higher doses of estrogen,
NSAIDs, particularly chronic use
Antidepressants, including tricyclic antidepressants and SSRI’s
Glucocorticoids Decongestants
pseudoephedrine
Weight loss medications Erythropoietin Cyclosporin Stimulants:
methylphenidate and amphetamines
Illicit drug: Drugs such as methamphetamines and cocaine can raise blood pressure
SECONDARY OR CONTRIBUTING CAUSES OF HYPERTENSION
Secondary hypertension is commonly caused by renal disease or pregnancy.
Renal disease - approximately 75% are from intrinsic renal disease: glomerulonephritis, polyarteritis nodosa, systemic sclerosis, chronic pyelonephritis, or polycystic kidneys.
Approximately 25% are due to renovascular disease - most frequently atheromatous (e.g. elderly cigarette smokers with peripheral vascular disease) or fibromuscular dysplasia (more common in younger females).
SECONDARY OR CONTRIBUTING CAUSES OF HYPERTENSION
Endocrine disease: Cushing's syndrome Conn's syndrome Pheochromocytoma Acromegaly Hyperparathyroidism
CoarctationPre-eclampsia and
hypertension in pregnancy.
Drugs and toxins, e.g. alcohol, cocaine, ciclosporin, tacrolimus, erythropoietin, adrenergic medications, decongestants containing ephedrine and herbal remedies containing licorice.
SECONDARY OR CONTRIBUTING CAUSES OF HYPERTENSION
Medical history
• Duration and classification of hypertension
• Patient history of CVD
• Family history
• Symptoms suggesting causes of hypertension
• Lifestyle factors
• Current and previous medications
• Duration and classification of hypertension
Physical examination
• BP readings (2 or more), including the standing position
• Verification in contralateral arm
• Height, weight, and waist circumference
• Funduscopic examination for hypertensive retinopathy
• Exam. neck, heart, lungs, A/S for target organ damage
• BP readings (2 or more), including the standing position
Medical history and physical examination
LVH: is a common and early finding in patients with hypertension.
LVH is associated with a higher incidence of subsequent heart failure, myocardial infarction, sudden death, and stroke
Heart failure: both systolic (reduced ejection fraction) and diastolic (preserved ejection fraction), increases with the degree of blood pressure elevation.
Ischemic stroke: HTN is the most common and most important risk factor for ischemic stroke, the incidence of which can be markedly reduced by effective antihypertensive therapy
COMPLICATIONS OF HYPERTENSION
Hypertension is the most important risk factor for the development of intracerebral hemorrhage.
Hypertension is a leading risk factor for IHD, including myocardial infarction and coronary interventions.
Chronic kidney disease and end-stage renal disease.
It can both directly cause kidney disease, which is called hypertensive nephrosclerosis, and accelerate the progression of a variety of other renal diseases
COMPLICATIONS OF HYPERTENSION
Electrolytes and serum creatinine (to calculate the estimated glomerular filtration rate)
Fasting glucose Urinalysis Lipid profile (total and
HDL-cholesterol, triglycerides)
Electrocardiogram (ECG)
Additional tests may be indicated in certain settings:
Increased albuminuria is increasingly recognized as an independent risk factor for cardiovascular disease.
Echocardiography is a more sensitive means of identifying the presence of left ventricular hypertrophy (LVH) than an ECG
Laboratory testing
GENERAL CLINICAL CLUES:
Severe or resistant hypertension
Acute rise in BP in a patient with previously stable HT.
Age < 30 years in non-obese, patients with a negative F/H and no other risk factors.
Malignant or accelerated HT (e.g., patients with severe hypertension and signs of end-organ damage such as retinal hemorrhages or papilledema, heart failure, neurologic disturbance, or acute kidney injury).
Proven age of onset before puberty
Evaluation of secondary hypertension: Not cost effective for a complete evaluation for secondary HT in every pt. Important to be aware of the clinical clues that suggest secondary HTN
CLINICAL CLUES FOR RENOVASCULAR HYPERTENSION
Onset of severe HTN(blood pressure ≥180 mmHg systolic and/or 120 mmHg diastolic) after the age of 55 years
Unexplained deterioration of kidney function during antihypertensive therapy
Severe hypertension in patients with diffuse atherosclerosis
Severe hypertension in a patient with an unexplained atrophic kidney
A systolic-diastolic abdominal bruit that lateralizes to one side.
Evaluation of secondary hypertension:
Identifiable Hypertension and Screening TestsCondition Screening Test
Chronic kidney disease Estimated glomerular filtration rate
Coarctation of the aorta Computed tomography angiography
Cushing syndrome; other states of glucocorticoid excess
Dexamethasone suppression test
Drug-induced/drug-related HTN Drug screening
Pheochromocytoma 24-hour urinary metanephrine and normetanephrine
Primary aldosteronism, other states of mineralocorticoid excess
24-hour urinary aldosterone level, specific mineralocorticoid tests
Renovascular hypertension Doppler flow U/S, MR Angiography, computed tomography angiography
Sleep apnea Sleep study with oxygen saturation (ESS)
Thyroid/parathyroid disease Thyroid stimulating hormone level, serum parathyroid hormone level
Less aggressive targeting of blood pressures and treatment-initiation thresholds for elderly patients and for those younger than age 60 years with diabetes and kidney disease
Initial therapy in most patients (ACE) inhibitors, angiotensin receptor blockers [ARBs], calcium channel blockers, or diuretics are recommended).
Initiate therapy in 60 years with BP levels at 150/90 mm Hg or greater
In younger than 60 years as well as those older than 18 years with either chronic kidney disease (CKD) or diabetes, the BP treatment initiation and goals should be 140/90 mm Hg.
In nonblack hypertensive patients, begin treatment with either a thiazide-type diuretic, CCB, ACE inhibitor, or ARB
Treatment Guidelines:
In hypertensive black patients, initiate therapy with a thiazide-type diuretic or CCB
Regardless of race or DM, in 18 years or older with CKD, therapy should consist of an ACE inhibitor or ARB
Do not use an ACE inhibitor together with an ARB in the same patient
If goal is not achieved within 1/12, increase the dose or add an agent from another of the recommended drug
If 2-drug therapy is unsuccessful, add a third agent from the recommended drug classes.
If goal BP cannot be reached with 3/12 use agents from other drug classes and/or refer the patients to a hypertension specialist
Treatment Guidelines:
Treatment should be started in all patients (any age) with stage 2 hypertension. Treat isolated systolic hypertension in the same way Initial Drug Choices
If the patient is young (≤55 years) and non-black, start with:• (A) angiotensin-converting enzyme (ACE) inhibitor or low-cost angiotensin-II receptor antagonist (AIIRA).• A beta-blocker may be appropriate in younger adults if an ACE is not tolerated, in women who may become pregnant or if there is evidence of increased sympathetic drive.
If the patient is aged >55 years or a black person of African or Caribbean family origin, use:• (C) calcium-channel blocker (CCB).
Stage 2 Drug Choices
• (A+C) ACE inhibitor or AIIRA with CCB.• Use an ACE/AIIRA and a thiazide-like diuretic (D) if CCB is not tolerated (or if there is any evidence of heart failure).• If initially started on a beta-blocker, add a CCB rather than a thiazide-like diuretic second-line (reduce diabetic risk).
• Consider an AIIRA rather than an ACE with a CCB in black (African or Caribbean) patients
Treatment should be started in all patients (any age) with stage 2 hypertension. Treat isolated systolic hypertension in the same way Stage 3 Drug Choices
• (A+C+D) ACE inhibitor or AIIRA and a CCB and a thiazide-like diuretic (chlortalidone or indapamide).
Stage 4 Drug Choices
• (A+C+D) ACE inhibitor or AIIRA and a CCB and a thiazide-like diuretic plus a further diuretic (higher-dose thiazide-like diuretic or spironolactone, depending on potassium). If the higher-dose diuretic is not tolerated, consider an alpha- or beta-blocker, or seek expert advice.
The combination of an ACE inhibitor with an AIIRA is not recommended for the treatment of hypertension
Treatment targets People aged <80 years: clinic <140/90 mm Hg, ABPM/HBPM <135/85 mm Hg.People aged ≥80 years: clinic <150/90 mm Hg, ABPM/HBPM <145/85 mm Hg.
Urgent treatment needed: Accelerated
hypertension, severe hypertension (>220/>120 mm Hg) or impending complications (e.g. (TIA), (LV) failure).
Possible underlying cause: low K+, Na+ elevated (possible Conn's syndrome); elevated creatinine, proteinuria or haematuria; rapidly worsening or resistant hypertension (i.e. needs >3 drugs); young age: patient aged <20 years, or <30 years needing treatment.
Therapeutic problems: Multiple drug
intolerance or contra-indications, persistent noncompliance or treatment refusal (the reluctant hypertensive).
Special situations: hypertension in pregnancy, unusual BP variability.
Indications for specialist referral