Hypertension

From Self-sufficiency
Revision as of 21:27, 19 September 2010 by JCramp1 (Talk) (Inserted reference)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to: navigation, search
Hypertension
Classification and external resources
File:Grade 1 hypertension.jpg
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 is a chronic medical condition in which the systemic arterial blood pressure is elevated. It is the opposite of hypotension. It is classified as either primary (essential) or secondary. About 90–95% of cases are termed "primary hypertension", which refers to high blood pressure for which no medical cause can be found.[1] The remaining 5–10% of cases (Secondary hypertension) are caused by other conditions that affect the kidneys, arteries, heart, or endocrine system.[2]

Persistent hypertension is one of the risk factors for stroke, myocardial infarction, heart failure and arterial aneurysm, and is a leading cause of chronic kidney failure.[3] Moderate elevation of arterial blood pressure leads to shortened life expectancy. Dietary and lifestyle changes can improve blood pressure control and decrease the risk of associated health complications, although drug treatment may prove necessary in patients for whom lifestyle changes prove ineffective or insufficient.[4]

Classification

File:Cardiac cycle pressure only.png
The variation in pressure in the left ventricle (blue line) and the aorta (red line) over two cardiac cycles ("heart beats"), showing the definitions of systolic and diastolic pressure
Classification 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 1 140–159 18.7–21.2 90–99 12.0–13.2
Stage 2 ≥160 ≥21.3 ≥100 ≥13.3
Isolated systolic
hypertension
≥140 ≥18.7 <90 <12.0
Source: American Heart Association (2003).[5]

Blood pressure is usually classified based on the systolic and diastolic blood pressures. Systolic blood pressure is the blood pressure in vessels during a heart beat. Diastolic blood pressure is the pressure between heartbeats. A systolic or the diastolic blood pressure measurement higher than the accepted normal values for the age of the individual is classified as prehypertension or hypertension.

Hypertension[6] has several sub-classifications including, 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. These classifications are made after averaging a patient's resting blood pressure readings taken on two or more office visits. Individuals older than 50 years are classified as having hypertension if their blood pressure is consistently at least 140 mmHg systolic or 90 mmHg diastolic. Patients with blood pressures higher than 130/80 mmHg with concomitant presence of diabetes mellitus or kidney disease require further treatment.[5]

Hypertension is also classified as resistant if medications do not reduce blood pressure to normal levels.[5]

Exercise hypertension is an excessively high elevation in blood pressure during exercise.[7][8][9] The range considered normal for systolic values during exercise is between 200 and 230 mm Hg.[10] Exercise hypertension may indicate that an individual is at risk for developing hypertension at rest.[9][10]

Signs and symptoms

Mild to moderate essential hypertension is usually asymptomatic.[11]

Accelerated hypertension

Accelerated hypertension is associated with headache, drowsiness, confusion, vision disorders, nausea, and vomiting symptoms which are collectively referred to as hypertensive encephalopathy.[citation needed] Hypertensive encephalopathy is caused by severe small blood vessel congestion and brain swelling, which is reversible if blood pressure is lowered.[12]

Children

Some signs and symptoms are especially important in newborns and infants such as failure to thrive, seizures, irritability, lack of energy, and difficulty breathing.[13] In children, hypertension can cause headache, fatigue, blurred vision, nosebleeds, and facial paralysis.[13]

Secondary hypertension

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, accumlated 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.[14] Signs and symptoms associated with growth hormone excess include coarsening of facial features, protrusion of the lower jaw, enlargement of the tongue,[15] excessive hair growth, darkening of the skin color, and excessive sweating.[16]: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.[17] and also cause of mental pressure.

Pregnancy

Hypertension in pregnant women is known as 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.[18]

Causes

Essential hypertension

Essential hypertension is the most prevalent hypertension type, affecting 90–95% of hypertensive patients.[1] Although no direct cause has identified itself, there are many factors such as sedentary lifestyle,[19] stress, visceral obesity, potassium deficiency (hypokalemia),[19] obesity[20] (more than 85% of cases occur in those with a body mass index greater than 25),[21] salt (sodium) sensitivity,[22] alcohol intake,[23] and vitamin D deficiency that increase the risk of developing hypertension.[24][25] Risk also increases with aging,[26] some inherited genetic mutations,[27] and having a family history of hypertension.[28] An elevation of renin, a hormone secreted by the kidney, is another risk factor,[29] as is sympathetic nervous system overactivity.[30] Insulin resistance which is a component of syndrome X, or the metabolic syndrome is also thought to contribute to hypertension.[29][31] Recent studies have implicated low birth weight as a risk factor for adult essential hypertension.[32]

Secondary hypertension

Secondary hypertension by definition results from an identifiable cause. This type is important to recognize since it's treated differently than 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 and well recognized secondary causes such as Cushing's syndrome,[33] which is a condition where the adrenal glands overproduce the hormone cortisol.[33] In addition, hypertension is 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.

Pathophysiology

File:Arterial pressure diagram.png
A diagram explaining factors affecting arterial pressure

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.[36]

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 long standing elevated blood pressures.

Diagnosis

Hypertension is generally diagnosed on the basis of a persistently high blood pressure. Usually this requires three separate sphygmomanometer (see figure) measurements at least one week apart. Initial assessment of the hypertensive patient should include a complete history and physical examination. Exceptionally, if the elevation is extreme, or if symptoms of organ damage are present then the diagnosis may be given and treatment started immediately.

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.[28] Laboratory tests can also be performed to identify possible causes of secondary hypertension, and determine if hypertension has caused damage to the heart, eyes, and kidneys. Additional tests for Diabetes and high cholesterol levels are also usually performed because they are additional risk factors for the development of heart disease require treatment.[1] Tests typically performed are classified as follows:

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[37] others[38][39][40][41][42][43]

Creatinine (renal function) testing is done to determine if kidney disease is present, which can be either the cause or result of hypertension. In addition, it 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 of the heart being under strain from high blood pressure. It may also show if there is thickening of the heart muscle (left ventricular hypertrophy) or has experienced a prior minor heart distubance 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.

Prevention

The degree to which hypertension can be prevented depends on a number of features including current blood pressure level, sodium/potassium balance, detection and omission of environmental toxins, changes in end/target organs (retina, kidney, heart, among others), risk factors for cardiovascular diseases and the age at diagnosis of prehypertension or at risk for hypertension. A prolonged assessment in which repeated measurements of blood pressure are taken provides the most accurate assessment of blood pressure levels. Following this, lifestyle changes are recommended to lower blood pressure, before the initiation of prescription drug therapy. The process of managing prehypertension according the guidelines of the British Hypertension Society suggest the following lifestyle changes:

Treatment

Lifestyle modifications

The first line of treatment for hypertension is the same as the recommended preventative lifestyle changes such as the dietary changes, physical exercise, and weight loss, which have all been shown to significantly reduce blood pressure in people with hypertension.[53] 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.[4] 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.[54][55][56]

Regarding dietary changes, a low sodium diet is beneficial; A Cochrane review published in 2008 concluded that a long term (more than 4 weeks) low sodium diet in Caucasians has a useful effect to reduce blood pressure, both in people with hypertension and in people with normal blood pressure.[57] 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,[58] 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".

Medications

Several classes of medications, collectively referred to as antihypertensive drugs, are currently available for treating hypertension. Agents within a particular class generally share a similar pharmacologic mechanism of action, and in many cases have an affinity for similar cellular receptors. An exception to this rule is the diuretics, which are grouped together for the sake of simplicity but actually exert their effects by a number of different mechanisms.

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.[59] The aim of treatment should be 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).[60] Comorbidity also plays a role in determining target blood pressure, with lower BP targets applying to patients with end-organ damage or proteinuria.[4]

Often multiple drugs are combined to achieve the goal blood pressure. Commonly used prescription drugs include:[61]

Some examples of common combined prescription drug treatments include:

  • A fixed combination of an ACE inhibitor and a calcium channel blocker. One example of this is the combination of perindopril and amlodipine, the efficacy of which has been demonstrated in individuals with glucose intolerance or metabolic syndrome.[62]
  • A fixed combination of an ACE inhibitor and a calcium channel blocker.
  • A fixed combination of a diuretic and an ARB.

Resistant

Guidelines for treating resistant hypertension have been published in the UK[61] and US.[63]

Complications

File:Main complications of persistent high blood pressure.svg
Diagram illustrating the main complications of persistent high blood pressure.

Hypertension is the most important risk factor for death in industrialized countries.[64] It increases hardening of the arteries[65] thus predisposes individuals to heart disease,[66] peripheral vascular disease,[67] and strokes.[68] Types of heart disease that may occur include: myocardial infarction,[68] heart failure,[69] and left ventricular hypertrophy[70] Other complications include:

Epidemiology

In the year 2000 it is estimated that nearly one billion people or ~26% of the adult population have hypertension worldwide.[73] It was common in both developed (333 million ) and undeveloped (639 million) countries.[73] 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.[74]

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.[75] The prevalence of hypertension in the United States is increasing and reached 29% in 2004.[76][77] It is more common in blacks 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] The most common cause of secondary hypertension is primary aldosteronism.[39] The incidence of exercise hypertension is reported to range from 1–10%.[10]

Pediatrics

The prevalence of high blood pressure in the young is increasing.[78] 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.[79]

History

File:William Harvey ( 1578-1657) Venenbild.jpg
Image of veins from Harvey's Exercitatio Anatomica de Motu Cordis et Sanguinis in Animalibus

Some cite the writings of Sushruta in the 6th century BC as being the first mention of symptoms like those of hypertension.[80] Others propose even earlier descriptions dating as far as 2600 years before Christ. Main treatment for what was called the "hard pulse disease" consisted in reducing the quantity of blood in a subject by the sectioning of veins or the application of leeches.[81] Well known individuals such as The Yellow Emperor of China, Cornelius Celsus, Galen, and Hipocrates advocated such treatments.[81]

Our modern understanding of hypertension began with the work of physician William Harvey (1578–1657), who was the first to describe correctly the systemic circulation of blood being pumped around the body by the heart in his book "De motu cordis". The basis for measuring blood pressure were established by Stephen Hales in 1733.[81] Initial descriptions of hypertension as a disease came among others from Thomas Young in 1808 and specially Richard Bright in 1836.[81] The first ever elevated blood pressure in a patient without kidney disease was reported by Frederick Mahomed (1849–1884).[82] It was not until 1904 that sodium restriction was advocated while a rice diet was popularized around 1940.[81]

Studies in the 1920s demonstrated the public health impact of untreated high blood pressure; treatment options were limited at the time, and deaths from malignant hypertension and its complications were common. A prominent victim of severe hypertension leading to cerebral hemorrhage was Franklin D. Roosevelt (1882–1945). The Framingham Heart Study added to the epidemiological understanding of hypertension and its relationship with coronary artery disease. 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.[83] Before pharmacological treatment for hypertension became possible, three treatment modalities were used, all with numerous side-effects: strict sodium restriction, sympathectomy (surgical ablation of parts of the sympathetic nervous system), and pyrogen therapy (injection of substances that caused a fever, indirectly reducing blood pressure).[81][83]

The first chemical for hypertension, sodium thiocyanate, was used in 1900 but had many side effects and was unpopular.[81] 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 randomized controlled trial sponsored by the Veterans Administration using these drugs had to be stopped early because those not receiving treatment were developing more complications and it was deemed unethical to withhold treatment from them. These studies prompted public health campaigns to increase public awareness of hypertension and the advice to get blood pressure measured and treated. These measures appear to have contributed at least in part of the observed 50% fall in stroke and ischemic heart disease beween 1972 and 1994.[83]

A major breakthrough was achieved with the discovery of the first well-tolerated orally available agents. The first was chlorothiazide, the first thiazide and developed from the antibiotic sulfanilamide, which became available in 1958;[81][84] it increased salt excretion while preventing fluid accumulation. In 1975, the Lasker Special Public Health Award was awarded to the team that developed chlorothiazide.[83] The British physician James W. Black developed beta blockers in the early 1960s;[85] 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.[83] 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.[83] ACE inhibitors were developed through rational drug design; the renin-angiotensin system was known to play an important role in blood pressure regulation, and snake venom from Bothrops jararaca could lower blood pressure through inhibition of ACE. In 1977 captopril, an orally active agent, was described;[86] this led to the development of a number of other ACE inhibitors.[83]

Society and culture

Economics

The National Heart, Lung, and Blood Institute (NHLBI) estimated in 2002 that hypertension cost the United States $47.2 billion.[87]

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[citation needed]. 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.[88] 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.,[89][90]

Awareness

File:HTNstudyupd.png
Graph showing, prevalence of awareness, treatment and control of hypertension compared between the four studies of NHANES[76]

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.[91] 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.[92]

References

Cite error: Invalid <references> tag; parameter "group" is allowed only.

Use <references />, or <references group="..." />

Further reading

External links

af:Hipertensie ar:فرط ضغط الدم az:Arterial hipertenziya zh-min-nan:Ko-hoeh-ap bar:Bluadhochdruck bs:Hipertenzija bg:Артериална хипертония ca:Hipertensió arterial ceb:Alta presyon cs:Hypertenze de:Arterielle Hypertonie dv:ލޭމައްޗަށްދިއުން et:Hüpertensioon es:Hipertensión arterial eo:Alta sangopremo eu:Hipertentsio fa:زیادی فشار خون fr:Hypertension artérielle ko:고혈압 hi:उच्च रक्तचाप hr:Hipertenzija id:Tekanan darah tinggi is:Háþrýstingur it:Ipertensione ku:Hîpertansiyon lv:Hipertensīvā sirds slimība lt:Hipertenzija hu:Magas vérnyomás ml:രക്താതിമര്‍ദ്ദം ms:Darah tinggi my:သွေးတိုးရောဂါ nl:Hypertensie ja:高血圧 no:Hypertensjon pl:Nadciśnienie tętnicze pt:Hipertensão arterial qu:Llasaq yawar ru:Артериальная гипертензия sq:Hipertensioni simple:Hypertension sr:Хипертензија fi:Verenpainetauti sv:Högt blodtryck tl:Altapresyon ta:உயர் இரத்த அழுத்தம் te:అధిక రక్తపోటు th:โรคความดันโลหิตสูง tr:Yüksek tansiyon uk:Артеріальна гіпертензія ur:فرط تناؤ

zh:高血壓
  1. 1.0 1.1 1.2 1.3 1.4 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  2. Secondary hypertension, Mayo Foundation for Medical Education and Research (2008)[1], Retrieved May 10, 2010
  3. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  4. 4.0 4.1 4.2 Nelson, Mark. "Drug treatment of elevated blood pressure". Australian Prescriber (33): 108–112. Retrieved August 11, 2010. 
  5. 5.0 5.1 5.2 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  6. "High blood pressure - NHS". National Health Service (NHS). ____. Retrieved same as submission date.  Check date values in: |access-date=, |date= (help)
  7. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  8. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  9. 9.0 9.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  10. 10.0 10.1 10.2 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  11. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  12. Papadakis, Maxine A.; McPhee, Stephen J. (2008). Current Medical Diagnosis and Treatment 2009 (Current Medical Diagnosis and Treatment). McGraw-Hill Professional. ISBN 0-07-159124-9. 
  13. 13.0 13.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  14. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  15. Khandwala, Hasnain M (February 13, 2009). "Acromegaly". eMedicine Endocrinology. Medscape. Retrieved 2009-06-16. 
  16. James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology (10th ed.). Saunders. ISBN 0721629210. 
  17. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  18. Gibson, Paul (July 30, 2009). "Hypertension and Pregnancy". eMedicine Obstetrics and Gynecology. Medscape. Retrieved 2009-06-16. 
  19. 19.0 19.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  20. Wofford MR, Hall JE (2004). "Pathophysiology and treatment of obesity hypertension". Current Pharmaceutical Design. 10 (29): 3621–37. doi:10.2174/1381612043382855. PMID 15579059. 
  21. Haslam DW, James WP (2005). "Obesity". Lancet. 366 (9492): 1197–209. doi:10.1016/S0140-6736(05)67483-1. PMID 16198769. 
  22. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  23. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  24. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  25. Lee JH, O'Keefe JH, Bell D, Hensrud DD, Holick MF (2008). "Vitamin D deficiency an important, common, and easily treatable cardiovascular risk factor?". J. Am. Coll. Cardiol. 52 (24): 1949–56. doi:10.1016/j.jacc.2008.08.050. PMID 19055985. 
  26. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  27. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  28. 28.0 28.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  29. 29.0 29.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  30. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  31. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  32. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  33. 33.0 33.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  34. Pimenta E, Oparil S (2009). "Role of aliskiren in cardio-renal protection and use in hypertensives with multiple risk factors". Vascular Health and Risk Management. 5 (1): 453–63. PMC 2686262Freely accessible. PMID 19475781. 
  35. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  36. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  37. Loscalzo, Joseph; Fauci, Anthony S.; Braunwald, Eugene; Dennis L. Kasper; Hauser, Stephen L; Longo, Dan L. (2008). Harrison's principles of internal medicine. McGraw-Hill Medical. ISBN 0-07-147691-1. 
  38. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  39. 39.0 39.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  40. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  41. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  42. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  43. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  44. Elley CR, Arroll B (2002). "Review: aerobic exercise reduces systolic and diastolic blood pressure in adults". ACP J. Club. 137 (3): 109. PMID 12418849. 
  45. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  46. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  47. Addison WLT (1928 March). "The use of sodium chloride, potassium chloride, sodium bromide, and potassium bromide in cases of arterial hypertension which are amenable to potassium chloride". Can Med Assoc J. 18 (3): 281–5. PMC 1710082Freely accessible. PMID 20316740.  Check date values in: |date= (help)
  48. Benson, Herbert (1975). The Relaxation Response. New York: Morrow. ISBN 0688029558. 
  49. "Biofeedback". Mayo Clinic. 2006. 
  50. Device-Guided Paced Breathing Lowers Blood Pressure. . InterCure. 2006-05-16. http://www.emaxhealth.com/106/5912.html. Retrieved 2009-07-03. 
  51. Elliott WJ, Izzo JL (2006). "Device-guided breathing to lower blood pressure: case report and clinical overview". MedGenMed. 8 (3): 23. PMC 1781326Freely accessible. PMID 17406163. 
  52. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  53. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  54. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  55. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  56. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  57. He FJ, MacGregor GA. Effect of longer-term modest salt reduction on blood pressure. Cochrane Database of Systematic Reviews 2004, Issue 1. Art. No.: CD004937. DOI: 10.1002/14651858.CD004937.
  58. "Your Guide To Lowering Your Blood Pressure With DASH" (PDF). Retrieved 2009-06-08. 
  59. Law M, Wald N, Morris J (2003). "Lowering blood pressure to prevent myocardial infarction and stroke: a new preventive strategy" (PDF). Health Technol Assess. 7 (31): 1–94. PMID 14604498. 
  60. Shaw, Gina (2009-03-07). "Prehypertension: Early-stage High Blood Pressure". WebMD. Retrieved 2009-07-03. 
  61. 61.0 61.1 "CG34 Hypertension - quick reference guide" (PDF). National Institute for Health and Clinical Excellence. 28 June 2006. Retrieved 2009-03-04. 
  62. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  63. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  64. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  65. Riccioni G (2009). "The effect of antihypertensive drugs on carotid intima media thickness: an up-to-date review". Current Medicinal Chemistry. 16 (8): 988–96. doi:10.2174/092986709787581923. PMID 19275607. 
  66. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  67. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  68. 68.0 68.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  69. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  70. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  71. Rodríguez NA, Zurutuza A (2008). "[Ophthalmological manifestations of arterial hypertension]". Anales Del Sistema Sanitario De Navarra (in Spanish; Castilian). 31 Suppl 3: 13–22. PMID 19169291. Retrieved 2009-06-21. 
  72. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  73. 73.0 73.1 Kearney PM, Whelton M, Reynolds K, Muntner P, Whelton PK, He J (2005). "Global burden of hypertension: analysis of worldwide data". Lancet. 365 (9455): 217–23. doi:10.1016/S0140-6736(05)17741-1. PMID 15652604. 
  74. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  75. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  76. 76.0 76.1 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  77. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  78. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  79. GREGORY B. LUMA, M.D., and ROSEANN T. SPIOTTA, M.D., Jamaica Hospital Medical Center (2006). "Hypertension in Children and Adolescents". Hypertension in Children and Adolescents. American Academy of Family Physician. Retrieved 2007-07-24. 
  80. Dwivedi, Girish & Dwivedi, Shridhar (2007). History of Medicine: Sushruta – the Clinician – Teacher par Excellence. National Informatics Centre (Government of India).
  81. 81.0 81.1 81.2 81.3 81.4 81.5 81.6 81.7 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  82. edited by J.D. Swales. (1995). Manual of hypertension. Oxford: Blackwell Science. pp. xiii. ISBN 0-86542-861-1. 
  83. 83.0 83.1 83.2 83.3 83.4 83.5 83.6 Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  84. Novello FC, Sprague JM (1957). "Benzothiadiazine dioxides as novel diuretics". J Am Chem Soc. 79: 2028. doi:10.1021/ja01565a079. 
  85. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  86. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  87. "What is Hypertension? - WrongDiagnosis.com". 
  88. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  89. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  90. Coca A (2008). "Economic benefits of treating high-risk hypertension with angiotensin II receptor antagonists (blockers)". Clinical Drug Investigation. 28 (4): 211–20. doi:10.2165/00044011-200828040-00002. PMID 18345711. 
  91. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.
  92. Lua error in package.lua at line 80: module 'Module:Citation/CS1/Suggestions' not found.