HYPERTENSIVE CRISIS

MOHAMMED R ARAFAH MBBS FACP FRCPC FACC PROFESSOR OF CARDIOLOGY

Proposed new definition of hypertension

is a progressive cardiovascular syndrome arising from complex and interrelated etiologies. Early markers of the syndrome are often present before blood-pressure elevation is sustained; therefore, hypertension cannot be classified solely by discreet blood-pressure thresholds. Progression is strongly associated with function and structural cardiac and vascular abnormalities that damage the heart, kidneys, brain, vasculature and other organs and lead to premature morbidity and death.
ASH Writing Group 2005

Joint National Committee VII

Blood Pressure Classification

BP Classification SBP mmHg DBP mmHg

Normal Prehypertension
Stage 1 Hypertension Stage 2 Hypertension

<120 120139 140159

and or or

<80 8089 9099

>160

or

>100

Joint National Committee VII

Hypertensive Urgencies and Emergencies

Patients with marked BP elevations and acute TOD (e.g., encephalopathy, myocardial infarction, unstable angina, pulmonary edema, eclampsia, stroke, head trauma, life-threatening arterial bleeding, or aortic dissection) require hospitalization and parenteral drug therapy. Patients with markedly elevated BP but without acute TOD usually do not require hospitalization, but should receive immediate combination oral antihypertensive therapy.

Target Organ Damage

Stroke Atherosclerosis* Vasoconstriction Vascular hypertrophy Endothelial dysfunction LV hypertrophy Fibrosis Remodeling Apoptosis

Hypertension

Heart failure MI

DEATH

GFR Proteinuria Aldosterone release Glomerular sclerosis

Renal failure

*preclinical data LV = left ventricular; MI = myocardial infarction; GFR = glomerular filtration rate
Adapted from Willenheimer R et al Eur Heart J 1999; 20(14): 9971008, Dahlf B J Hum Hypertens 1995; 9(suppl 5): S37S44, Daugherty A et al J Clin Invest 2000; 105(11): 16051612, Fyhrquist F et al J Hum Hypertens 1995; 9(suppl 5): S19S24, Booz GW, Baker KM Heart Fail Rev 1998; 3: 125130, Beers MH, Berkow R, eds. The Merck Manual of Diagnosis and Therapy. 17th ed. Whitehouse Station, NJ: Merck Research Laboratories 1999: 16821704, Anderson S Exp Nephrol 1996; 4(suppl 1): 3440, Fogo AB Am J Kidney Dis 2000; 35(2): 179188

Joint National Committee VII

Target Organ Damage

Heart Left ventricular hypertrophy Angina or prior myocardial infarction Prior coronary revascularization Heart failure

Brain Stroke or transient ischemic attack

Chronic kidney disease

Peripheral arterial disease Retinopathy

Progression From Hypertension to CHF

Obesity Diabetes

LVH

Systolic dysfunctio n

Hypertension
Smoking Dyslipidemia Diabetes
Diastolic dysfunctio n

CH F

MI

Normal LV structure and function

LV remodelling

Subclinical LV dysfunction

Overt heart failure

Vasan RS et al. Arch Intern Med 1996

Increasing Systolic BP Linked to EndStage Renal Disease Risk: MRFIT

Adjusted Relative Risk

6 5 4 3 2 1 0 <117 117-123 124-130 131-140 1 1

P<.001 P=.009

P<.001

2.2

1.5

>140

Systolic BP (mm Hg)

Klag et al. N Engl J Med. 1996;334:13-18.

MANAGMENT
In

hypertensive urgencies critically elevated BP should be lowered rapidly (within 15-30minutes reduction of MBP by 25%, aim DBP 100-110, SBP 160 mm Hg) . Avoid sudden drop of BP which lead to reduction of perfusion to vital organs (brain, heart,. etc).
hypertensive emergencies critically elevated BP should be lowered gradually within hours (aim DBP 100-110 mm Hg, SBP 160 mm Hg).

In

Joint National Committee VII

Benefits of Lowering BP

Average Percent Reduction Stroke incidence Myocardial infarction 3540% 2025%

Heart failure

50%

Joint National Committee VII

Patient Evaluation

Evaluation of patients with documented HTN has three objectives: 1. Assess lifestyle and identify other CV risk factors or concomitant disorders that affects prognosis and guides treatment. 2. Reveal identifiable causes of high BP.

3. Assess the presence or absence of target organ damage and CVD.

Joint National Committee VII

CVD Risk Factors

Hypertension* Cigarette smoking Obesity* (BMI >30 kg/m2) Physical inactivity Dyslipidemia* Diabetes mellitus* Microalbuminuria or estimated GFR <60 ml/min Age (older than 55 for men, 65 for women) Family history of premature CVD (men under age 55 or women under age 65)
*Components of the metabolic syndrome.

Joint National Committee VII

Identifiable Causes of Hypertension

Sleep apnea

Drug-induced or related causes Chronic kidney disease Primary aldosteronism Renovascular disease Chronic steroid therapy and Cushings syndrome Pheochromocytoma Coarctation of the aorta Thyroid or parathyroid disease

Joint National Committee VII

Laboratory Tests

Routine Tests Electrocardiogram Urinalysis Blood glucose, and hematocrit Serum potassium, creatinine, or the corresponding estimated GFR, and calcium Lipid profile, after 9- to 12-hour fast, that includes high-density and low-density lipoprotein cholesterol, and triglycerides Optional tests Measurement of urinary albumin excretion or albumin/creatinine ratio More extensive testing for identifiable causes is not generally indicated unless BP control is not achieved

Joint National Committee VII

Goals of Therapy
Reduce CVD and renal morbidity and mortality.
Treat to BP <140/90 mmHg or BP <130/80 mmHg in patients with diabetes or chronic kidney disease.

Achieve SBP goal especially in persons >50 years of age.

Joint National Committee VII

Causes of Resistant Hypertension

Improper BP measurement

Excess sodium intake Inadequate diuretic therapy Medication Inadequate doses Drug actions and interactions (e.g., nonsteroidal anti-inflammatory drugs (NSAIDs), illicit drugs, sympathomimetics, oral contraceptives) Over-the-counter (OTC) drugs and herbal supplements Identifiable causes of HTN

Risk of a major cardiovascular event reduced by 30% in the HOT Study

105 0 5 10 Optimal DBP reduction in the HOT Study 100 95 90 85 Achieved DBP 80 mm Hg

15
20 25 30 % risk reduction

Risk of a major cardiovascular event reduced by 22% in the HOT Study

170 0 5 10 15 20 25 Optimal SBP reduction in the HOT Study 160 150 140 Achieved SBP mm Hg 130

30 % risk reduction