| Hypertension | |
|---|---|
| Classification and external resources | |
Automated arm blood pressure meter showing arterial hypertension (shown a systolic blood pressure 158 mmHg, diastolic blood pressure 99 mmHg and heart rate of 80 beats per minute). |
|
| ICD-10 | I10,I11,I12, I13,I15 |
| ICD-9 | 401 |
| OMIM | 145500 |
| DiseasesDB | 6330 |
| MedlinePlus | 000468 |
| eMedicine | med/1106 ped/1097 emerg/267 |
| MeSH | D006973 |
Hypertension (HTN) or high blood pressure, sometimes arterial hypertension, is a chronic medical condition in which the blood pressure in the arteries is elevated. This requires the heart to work harder than normal to circulate blood through the blood vessels. Blood pressure involves two measurements, systolic and diastolic, which depend on whether the heart muscle is contracting (systole) or relaxed (diastole) between beats. Normal blood pressure is at or below 120/80 mmHg. High blood pressure is said to be present if it is persistently above 140/90 mmHg.
Hypertension is classified as either primary (essential) hypertension or secondary hypertension; about 90–95% of cases are categorized as "primary hypertension" which means high blood pressure with no obvious underlying medical cause.[1] The remaining 5–10% of cases (secondary hypertension) are caused by other conditions that affect the kidneys, arteries, heart or endocrine system.
Persistent hypertension is a major risk factor for stroke, myocardial infarction (heart attacks), heart failure and aneurysms of the arteries (e.g. aortic aneurysm), and is a cause of chronic kidney disease. Even moderate elevation of arterial blood pressure is associated with a shortened life expectancy. Dietary and lifestyle changes can improve blood pressure control and decrease the risk of associated health complications, although drug treatment is often necessary in patients for whom lifestyle changes prove ineffective or insufficient.
Contents |
| Classification (JNC7)[2] | Systolic pressure | Diastolic pressure | ||
|---|---|---|---|---|
| mmHg | kPa | mmHg | kPa | |
| Normal | 90–119 | 12–15.9 | 60–79 | 8.0–10.5 |
| Prehypertension | 120–139 | 16.0–18.5 | 80–89 | 10.7–11.9 |
| Stage 1 hypertension | 140–159 | 18.7–21.2 | 90–99 | 12.0–13.2 |
| Stage 2 hypertension | ≥160 | ≥21.3 | ≥100 | ≥13.3 |
| Isolated systolic hypertension |
≥140 | ≥18.7 | <90 | <12.0 |
Hypertension is defined as a systolic and/or a diastolic blood pressure measurement consistently higher than an accepted normal value (currently 139 mmHg systolic, 89 mmHg diastolic: see table — Classification (JNC7)) in people aged 18 years or older. Lower thresholds are used (135 mmHg systolic or 85 mmHg diastolic) if measurements are derived from 24-hour ambulatory or home monitoring [3]. The presence of other cardiovascular risk factors is taken into account when decisions are made regarding drug treatment. Recent international hypertension guidelines have also created categories below the hypertensive range to indicate a continuum of risk with higher blood pressures in the normal range. JNC7 (2003)[2] uses the term prehypertension for blood pressure in the range 120-139 mmHg systolic and/or 80-89 mmHg diastolic, while ESH-ESC Guidelines (2007)[4] and BHS IV (2004)[5] use optimal, normal and high normal categories to subdivide pressures below 140 mmHg systolic and 90 mmHg diastolic. Hypertension is also sub-classified: JNC7 distinguishes hypertension stage I, hypertension stage II, and isolated systolic hypertension. Isolated systolic hypertension refers to elevated systolic pressure with normal diastolic pressure and is common in the elderly[2]. The ESH-ESC Guidelines (2007)[4] and BHS IV (2004)[5], additionally define a third stage (stage III hypertension) for people with systolic blood pressure exceeding 179 mmHg or a diastolic pressure over 109 mmHg. Hypertension is classified as "resistant" if medications do not reduce blood pressure to normal levels.[2]
Hypertension is usually not accompanied by any symptoms, and its identification is usually through screening, or when seeking healthcare for an unrelated problem. A proportion of people with high blood pressure reports headaches (particularly at the back of the head and in the morning), as well as lightheadedness, vertigo, tinnitus (buzzing or hissing in the ears), altered vision or fainting episodes.[6]
On physical examination, hypertension itself can mainly be detected through ophthalmoscopy, which allows visualisation of the blood vessels in the retina. Hypertension can cause a number of changes that may indicate the risk of complications, and may reflect the state of blood vessels elsewhere in the body.[7] Classically, the severity of the hypertensive retinopathy changes is graded from grade I–IV, although the milder types may be difficult to distinguish from each other.[7] Ophthalmoscopy findings may also indicate how long a person has been hypertensive.[6]
Some additional signs and symptoms suggest that the hypertension is caused by disorders in hormone regulation. Hypertension combined with obesity distributed on the trunk of the body, accumulated fat on the back of the neck ("buffalo hump"), wide purple marks on the abdomen (abdominal striae), or the recent onset of diabetes suggests that an individual has a hormone disorder known as Cushing's syndrome. Hypertension caused by other hormone disorders such as hyperthyroidism, hypothyroidism, or growth hormone excess will be accompanied by additional symptoms specific to these disorders. For example, hyperthyrodism can cause weight loss, tremors, heart rate abnormalities, reddening of the palms, and increased sweating.[8] Signs and symptoms associated with growth hormone excess include coarsening of facial features, protrusion of the lower jaw, enlargement of the tongue,[9] excessive hair growth, darkening of the skin color, and excessive sweating.[10]:499. Other hormone disorders like hyperaldosteronism may cause less specific symptoms such as numbness, excessive urination, excessive sweating, electrolyte imbalances and dehydration, and elevated blood alkalinity.[11] and also cause mental pressure.
Severely elevated blood pressure (systolic over 180 or diastolic over 110) is conventionally referred to as a "hypertensive crisis", as blood pressures above these levels are known to confer a high risk of complications. People with blood pressures in this range may have no symptoms, but are more likely to report headaches and dizziness.[6] Most people with severe hypertension are known to have elevated blood pressure, but additional triggers may have led to a sudden rise.[12] This situation is referred to as a "hypertensive urgency", as treatment is unequivocally required to reduce the blood pressure to safer levels within several days.[12]
A "hypertensive emergency", previously "malignant hypertension", is said to be present where there is evidence of direct damage to one or more organs as a result of the severely elevated blood presure. In these situations, rapid reduction of the blood pressure is mandated to stop ongoing organ damage.[12] Hypertensive encephalopathy, caused by brain swelling and dysfunction, is characterised by headaches and an altered level of consciousness (confusion or drowsiness). Chest pain may indicate heart muscle damage (which may progress to myocardial infarction) or sometimes aortic dissection, the tearing of the inner wall of the aorta. Breathlessness, cough, and the expectoration of blood-stained sputum are characteristic signs of pulmonary edema, the swelling of lung tissue due to inability of the left ventricle of the heart to circulate blood from the lungs into the arterial system.[12] Rapid deterioration of kidney function (acute kidney injury) and microangiopathic hemolytic anemia (destruction of blood cells) may also occur.[12]
Hypertension in pregnant women is one symptom of pre-eclampsia. Pre-eclampsia can progress to a life-threatening condition called eclampsia, which is the development of protein in the urine, generalized swelling, and severe seizures. Other symptoms indicating that brain function is becoming impaired may precede these seizures such as nausea, vomiting, headaches, and vision loss.[13]
In addition, the systemic vascular resistance and blood pressure decrease during pregnancy. The body must compensate by increasing cardiac output and blood volume to provide sufficient circulation in the utero-placental arterial bed.[14]
Some signs and symptoms are especially important in newborns and infants such as failure to thrive, seizures, irritability, lack of energy, and difficulty breathing.[15] In children, hypertension can cause headache, fatigue, blurred vision, nosebleeds, and facial paralysis.[15]
Even with the above clinical symptoms, the true incidence of pediatric hypertension is not known. In adults, hypertension has been defined due to the adverse effects caused by hypertension. However, in children, similar studies have not been performed thoroughly to link any adverse effects with the increase in blood pressure. Therefore, the prevalence of pediatric hypertension remains unknown due to the lack of scientific knowledge.[16]
Hypertension is the most important risk factor for death in industrialized countries.[17] It increases hardening of the arteries[18] thus predisposes individuals to heart disease,[19] peripheral vascular disease,[20] and strokes.[21] Types of heart disease that may occur include: myocardial infarction,[21] heart failure,[22] and left ventricular hypertrophy[23]
Other complications include:
Primary (essential) hypertension is the most common form of hypertension, accounting for 90–95% of all cases of hypertension.[1] In almost all contemporary societies, blood pressure rises with aging and the risk of becoming hypertensive in later life is considerable [26]. Hypertension results from a complex interaction of genes and environmental factors. Numerous common genes with small effects on blood pressure have been identified [27] as well as some rare genes with large effects on blood pressure [28] but the genetic basis of hypertension is still poorly understood. Several environmental factors influence blood pressure. Lifestyle factors that lower blood pressure, include reduced dietary salt intake [29], increased consumption of fruits and low fat products (Dietary Approaches to Stop Hypertension (DASH diet)), exercise,[30] weight loss [31] reduced alcohol intake,[32]. The possible role of other factors such as stress[33], caffeine consumption[34], and vitamin D deficiency [35] are less clear cut. Insulin resistance, which is a component of syndrome X (or the metabolic syndrome), is also thought to contribute to hypertension.[36] Recent studies have also implicated events in early life (for example low birth weight, maternal smoking and lack of breast feeding) as risk factors for adult essential hypertension [37], although the mechanisms linking these exposures to adult hypertension remain obscure.
Secondary hypertension by definition results from an identifiable cause. This type is important to recognize since it's treated differently to essential hypertension, by treating the underlying cause of the elevated blood pressure. Hypertension results in the compromise or imbalance of the pathophysiological mechanisms, such as the hormone-regulating endocrine system, that regulate blood plasma volume and heart function. Many conditions cause hypertension. Some are common, well-recognized secondary causes such as renovascular hypertension and Cushing's syndrome,[38] which is a condition where the adrenal glands overproduce the hormone cortisol.[38] Hypertension is also caused by other conditions that cause hormone changes, such as hyperthyroidism, hypothyroidism, and certain tumors of the adrenal medulla (e.g., pheochromocytoma). Other common causes of secondary hypertension include kidney disease, obesity/metabolic disorder, pre-eclampsia during pregnancy, the congenital defect known as coarctation of the aorta, and certain prescription and illegal drugs.
Most of the mechanisms associated with secondary hypertension are generally fully understood. However, those associated with essential (primary) hypertension are far less understood. What is known is that cardiac output is raised early in the disease course, with total peripheral resistance (TPR) normal; over time cardiac output drops to normal levels but TPR is increased. Three theories have been proposed to explain this:
It is also known that hypertension is highly heritable and polygenic (caused by more than one gene) and a few candidate genes have been postulated in the etiology of this condition.[41]
Recently, work related to the association between essential hypertension and sustained endothelial damage has gained popularity among hypertension scientists. It remains unclear, however, whether endothelial changes precede the development of hypertension or whether such changes are mainly due to longstanding elevated blood pressures.
| System | Tests |
|---|---|
| Renal | Microscopic urinalysis, proteinuria, serum BUN (blood urea nitrogen) and/or creatinine |
| Endocrine | Serum sodium, potassium, calcium, TSH (thyroid-stimulating hormone). |
| Metabolic | Fasting blood glucose, total cholesterol, HDL and LDL cholesterol, triglycerides |
| Other | Hematocrit, electrocardiogram, and chest radiograph |
| Sources: Harrison's principles of internal medicine[42] others[43][44][45][46][47][48] | |
Hypertension is generally diagnosed on the basis of a persistently high blood pressure. Traditionally,[3] this requires three separate sphygmomanometer measurements at one monthly intervals.[49] Initial assessment of the hypertensive patient should include a complete history and physical examination. With the availability of 24-hour ambulatory blood pressure monitors and home blood pressure machines, the importance of not wrongly diagnosing those who have white coat hypertension has led to a change in protocol advice in the United Kingdom, with best practice of now following up a single raised clinic reading with ambulatory measurement, or less ideally with home blood pressure monitoring over the course of 7 days.[3]
Once the diagnosis of hypertension has been made, physicians will attempt to identify the underlying cause based on risk factors and other symptoms, if present. Secondary hypertension is more common in preadolescent children, with most cases caused by renal disease. Primary or essential hypertension is more common in adolescents and has multiple risk factors, including obesity and a family history of hypertension.[50] Laboratory tests can also be performed to identify possible causes of secondary hypertension, and to determine whether hypertension has caused damage to the heart, eyes, and kidneys. Additional tests for diabetes and high cholesterol levels are usually performed because these conditions are additional risk factors for the development of heart disease and require treatment.[1] Typical tests are classified as seen in the table at the right.
Creatinine (renal function) testing is done to assess the presence of kidney disease, which can be either the cause or the result of hypertension. In addition, creatinine testing provides a baseline measurement of kidney function that can be used to monitor for side effects of certain antihypertensive drugs on kidney function. Additionally, testing of urine samples for protein is used as a secondary indicator of kidney disease. Glucose testing is done to determine if diabetes mellitus is present. Electrocardiogram (EKG/ECG) testing is done to check for evidence that the heart is under strain from high blood pressure. It may also show whether there is thickening of the heart muscle (left ventricular hypertrophy) or whether the heart has experienced a prior minor disturbance such as a silent heart attack. A chest X-ray may be performed to look for signs of heart enlargement or damage to heart tissue.
Much of the disease burden of high blood pressure is experienced by people who are not hypertensive[51]. Consequently, population strategies are required to reduce the consequences of high blood pressure and reduce the need for antihypertensive drug therapy. Lifestyle changes are recommended to lower blood pressure, before starting drug therapy. The 2004 British Hypertension Society guidelines[52] proposed the following lifestyle changes consistent with those outlined by the US National High BP Education Program in 2002[53] for the primary prevention of hypertension:
Effective lifestyle modification may lower blood pressure as much an individual antihypertensive drug. Combinations of two or more lifestyle modifications can achieve even better results [54].
The first line of treatment for hypertension is identical to the recommended preventive lifestyle changes [55] and includes: dietary changes[56] physical exercise, and weight loss. These have all been shown to significantly reduce blood pressure in people with hypertension.[57] If hypertension is high enough to justify immediate use of medications, lifestyle changes are still recommended in conjunction with medication. Drug prescription should take into account the patient's absolute cardiovascular risk (including risk of myocardial infarction and stroke) as well as blood pressure readings, in order to gain a more accurate picture of the patient's cardiovascular profile.[58] Different programs aimed to reduce psychological stress such as biofeedback, relaxation or meditation are advertised to reduce hypertension. However, in general claims of efficacy are not supported by scientific studies, which have been in general of low quality.[59][60][61]
Regarding dietary changes, a low sodium diet is beneficial. A long term (more than 4 weeks) low sodium diet in Caucasians is effective in reducing blood pressure, both in people with hypertension and in people with normal blood pressure.[62] Also, the DASH diet (Dietary Approaches to Stop Hypertension) is a diet promoted by the National Heart, Lung, and Blood Institute (part of the NIH, a United States government organization) to control hypertension. A major feature of the plan is limiting intake of sodium,[63] and it also generally encourages the consumption of nuts, whole grains, fish, poultry, fruits and vegetables while lowering the consumption of red meats, sweets, and sugar. It is also "rich in potassium, magnesium, and calcium, as well as protein".
Several classes of medications, collectively referred to as antihypertensive drugs, are currently available for treating hypertension. Reduction of the blood pressure by 5 mmHg can decrease the risk of stroke by 34%, of ischaemic heart disease by 21%, and reduce the likelihood of dementia, heart failure, and mortality from cardiovascular disease.[64] The aim of treatment should be to reduce blood pressure to <140/90 mmHg for most individuals, and lower for individuals with diabetes or kidney disease (some medical professionals recommend keeping levels below 120/80 mmHg).[65] If the blood pressure goal is not met, a change in treatment should be made as therapeutic inertia is a clear impediment to blood pressure control.[66] Comorbidity also plays a role in determining target blood pressure, with lower BP targets applying to patients with end-organ damage or proteinuria.[58]
Often multiple medications are needed to be combined to achieve the goal blood pressure. Guidelines on the choice of first line agent and how to best to step up treatment with multiple agents for various subgroups of patients have changed over time and differ between countries.
In the UK low dose thiazide-based diuretic were previously thought the best first line agent,[67] but latest guidelines emphasise calcium channel blockers (CCB) in preference for patients over the age of 55 years or if of African or Caribbean family origin, with angiotensin converting enzyme inhibitors (ACE-I) used first line for younger patients.[68] Preferred dual therapy is generally CCB with an ACE-I, and triple therapy with addition of a thiazide-like diuretic. If a fourth agent is needed then additional diuretics of spironolactone or a higher-dose of a thiazide-like diuretics. Additional agents that may be considered are alpha blockers or beta blockers.[68] Angiotensin II receptor antagonists are suggested as preferable to ACE-I for black people of African or Caribbean family origin, and are an alternative for patients who are unable to tolerate ACE-I. Beta-blockers may be also be considered first line in younger people, and women of child-bearing potential.[68]
Tablets containing fixed combinations of two classes of drugs are available and whilst convenient for the patient, may be best reserved for patients who have been established on the individual components.[69]
Some examples of common combined prescription drug include:
Combinations of an ACE-inhibitor or angiotensin II–receptor antagonist, a diuretic and an NSAID (including selective COX-2 inhibitors and non-prescribed drugs such as ibuprofen) should be avoided whenever possible due to a high documented risk of acute renal failure. The combination is known colloquially as a "triple whammy" in the Australian health industry.[55]
Treating moderate to severe high blood pressure decreases death rates in those under 80 years of age.[71] In those over 80 years old there was a decrease in morbidity but no decrease in mortality.[71] The recommended BP goal is advised as <140/90 mm Hg with thiazide diuretics being the first line medication in America,[72] but in the revised UK guidelines calcium-channel blockers are advocated with targets of clinic readings <150/90, or <145/85 on ambulatory or home blood pressure monitoring.[68]
Guidelines for treating resistant hypertension have been published in the UK[73] and US.[74]
In the year 2000 it is estimated that nearly one billion people or ~26% of the adult population had hypertension worldwide.[75] It was common in both developed (333 million ) and undeveloped (639 million) countries.[75] However rates vary markedly in different regions with rates as low as 3.4% (men) and 6.8% (women) in rural India and as high as 68.9% (men) and 72.5% (women) in Poland.[76]
In 1995 it is estimated that 43 million people in the United States had hypertension or were taking antihypertensive medication, almost 24% of the adult population.[77] The prevalence of hypertension in the United States is increasing and reached 29% in 2004.[78][79] It is more common in blacks and native Americans and less in whites and Mexican Americans, rates increase with age, and is greater in the southeastern United States. Hypertension is more prevalent in men (though menopause tends to decrease this difference) and those of low socioeconomic status.[1]
Over 90–95% of adult hypertension is essential hypertension.[1] One of the most common causes of secondary hypertension is primary aldosteronism.[44]
The prevalence of high blood pressure in the young is increasing.[80] Most childhood hypertension, particularly in preadolescents, is secondary to an underlying disorder. Kidney disease is the most common (60–70%) cause of hypertension in children. Adolescents usually have primary or essential hypertension, which accounts for 85–95% of cases.[81]
Modern understanding of the cardiovascular system began with the work of physician William Harvey (1578–1657), who described the circulation of blood in his book "De motu cordis". The English clergyman Stephen Hales made the first measurement of blood pressure in 1733,[82] in horses.[83] Descriptions of hypertension as a disease came among others from Thomas Young in 1808 and especially Richard Bright in 1836.[82] The first report of elevated blood pressure in a patient without evidence of kidney disease was made by Frederick Akbar Mahomed (1849–1884).[84] However hypertension as a clinical entity came into being in 1896 with the invention of the cuff-based sphygmomanometer by Scipione Riva-Rocci in 1896.[85] This allowed blood pressure to be measured in the clinic. In 1905, Nikolai Korotkoff improved the technique by describing the Korotkoff sounds that are heard when the artery is ausculated with a stethoscope while the sphygmomanometer cuff is deflated.[83]
The concept of essential hypertension ('hypertonie essential') was introduced in 1925 by the physiologist Otto Frank to describe elevated blood pressure for which no cause could be found. In 1928, the term malignant hypertension was coined by physicians from the Mayo Clinic to describe a syndrome of very high blood pressure, severe retinopathy and adequate kidney function which usually resulted in death within a year from strokes, heart failure or kidney failure.[86] A prominent sufferer of severe hypertension was Franklin D. Roosevelt.[87] However, while the menace of severe or malignant hypertension was well recognised, the risks of more moderate elevations of blood pressure were uncertain and the benefits of treatment doubtful. Consequently, hypertension was often classified into "malignant" and "benign". In 1931, John Hay, Professor of Medicine at Liverpool University, wrote that "there is some truth in the saying that the greatest danger to a man with a high blood pressure lies in its discovery, because then some fool is certain to try and reduce it".[88][89] This view was echoed by the eminent US cardiologist Paul Dudley White in 1937, who suggested that "hypertension may be an important compensatory mechanism which should not be tampered with, even were it certain that we could control it".[90] Charles Friedberg's 1949 classic textbook "Diseases of the Heart",[91] stated that "people with 'mild benign' hypertension... [defined as blood pressures up to levels of 210/100 mm Hg]... need not be treated".[89] However the tide of medical opinion was turning: it was increasingly recognised in the 1950s that "benign" hypertension was not harmless.[92] Over the next decade increasing evidence accumulated from actuarial reports[83][93] and longitudinal studies, such as the Framingham Heart Study,[94] that "benign" hypertension increased death and cardiovascular disease, and that these risks increased in a graded manner with increasing blood pressure across the whole spectrum of population blood pressures. Subsequently the National Institutes of Health also sponsored other population studies, which additionally showed that African Americans had a higher burden of hypertension and its complications.[95]
Historically the treatment for what was called the "hard pulse disease" consisted in reducing the quantity of blood by blood letting or the application of leeches.[82] This was advocated by The Yellow Emperor of China, Cornelius Celsus, Galen, and Hipocrates. [82]
In the 19th and 20th centuries, before effective pharmacological treatment for hypertension became possible, three treatment modalities were used, all with numerous side-effects: strict sodium restriction (for example the rice diet [82]), sympathectomy (surgical ablation of parts of the sympathetic nervous system), and pyrogen therapy (injection of substances that caused a fever, indirectly reducing blood pressure).[82][95] The first chemical for hypertension, sodium thiocyanate, was used in 1900 but had many side effects and was unpopular.[82] Several other agents were developed after the Second World War, the most popular and reasonably effective of which were tetramethylammonium chloride and its derivative hexamethonium, hydralazine and reserpine (derived from the medicinal plant Rauwolfia serpentina). A major breakthrough was achieved with the discovery of the first well-tolerated orally available agents. The first was chlorothiazide, the first thiazide diuretic and developed from the antibiotic sulfanilamide, which became available in 1958;[82][96] it increased salt excretion while preventing fluid accumulation. A randomized controlled trial sponsored by the Veterans Administration comparing hydrochlorothiazide plus reserpine plus hydralazine versus placebo had to be stopped early in a high blood pressure group because those not receiving treatment developed many more complications and it was deemed unethical to withhold treatment from them. The study continued in people with lower blood pressures and showed that treatment even in people with mild hypertension more than halved the risk of cardiovascular death.[97] These studies prompted public health campaigns to increase public awareness of hypertension and promoted the measurement and treatment of high blood pressure. These measures appear to have contributed at least in part to the observed 50% fall in stroke and ischemic heart disease between 1972 and 1994.[95]
Soon more drugs became available to treat hypertension. In 1975, the Lasker Special Public Health Award was awarded to the team that developed chlorothiazide.[95] The British physician James W. Black developed beta blockers in the early 1960s;[98] these were initially used for angina, but turned out to lower blood pressure. Black received the 1976 Lasker Award and in 1988 the Nobel Prize in Physiology or Medicine for his discovery.[95] The next class of antihypertensives to be discovered was that of the calcium channel blockers. The first member was verapamil, a derivative of papaverine that was initially thought to be a beta blocker and used for angina, but then turned out to have a different mode of action and was shown to lower blood pressure.[95] The renin-angiotensin system was known to play an important role in blood pressure regulation, and angiotensin converting enzyme (ACE) inhibitors were developed through rational drug design. In 1977 captopril, an orally active agent, was described;[99] this led to the development of a number of other ACE inhibitors[95]. More recently angiotensin receptor blockers and renin inhibitors have also been introduced as antihypertensive agents.
The National Heart, Lung, and Blood Institute (NHLBI) estimated in 2002 that hypertension cost the United States $47.2 billion.[100]
High blood pressure is the most common chronic medical problem prompting visits to primary health care providers, yet it is estimated that only 34% of the 50 million American adults with hypertension have their blood pressure controlled to a level of <140/90 mm Hg.[101] Thus, about two thirds of Americans with hypertension are at increased risk for heart disease. The medical, economic, and human costs of untreated and inadequately controlled high blood pressure are enormous. Adequate management of hypertension can be hampered by inadequacies in the diagnosis, treatment, and/or control of high blood pressure.[102] Health care providers face many obstacles to achieving blood pressure control from their patients, including resistance to taking multiple medications to reach blood pressure goals. Patients also face the challenges of adhering to medicine schedules and making lifestyle changes. Nonetheless, the achievement of blood pressure goals is possible, and most importantly, lowering blood pressure significantly reduces the risk of death due to heart disease, the development of other debilitating conditions, and the cost associated with advanced medical care.,[103][104]
The World Health Organization attributes hypertension, or high blood pressure, as the leading cause of cardiovascular mortality. The World Hypertension League (WHL), an umbrella organization of 85 national hypertension societies and leagues, recognized that more than 50% of the hypertensive population worldwide are unaware of their condition.[105] To address this problem, the WHL initiated a global awareness campaign on hypertension in 2005 and dedicated May 17 of each year as World Hypertension Day (WHD). Over the past three years, more national societies have been engaging in WHD and have been innovative in their activities to get the message to the public. In 2007, there was record participation from 47 member countries of the WHL. During the week of WHD, all these countries – in partnership with their local governments, professional societies, nongovernmental organizations and private industries – promoted hypertension awareness among the public through several media and public rallies. Using mass media such as Internet and television, the message reached more than 250 million people. As the momentum picks up year after year, the WHL is confident that almost all the estimated 1.5 billion people affected by elevated blood pressure can be reached.[106]