Hypertension: Difference between revisions
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::* Family history of [[hypertension]] | ::* Family history of [[hypertension]] | ||
*[[Secondary hypertension]] | *[[Secondary hypertension]] | ||
::*[[BP]]lability, suddenly rising [[BP]] with pallor and [[dizziness]] ([[pheochromocytoma]]) | ::*[[BP]] lability, suddenly rising [[BP]] with pallor and [[dizziness]] ([[pheochromocytoma]]) | ||
::* [[Snoring]], [[hypersomnolence]] ([[obstructive sleep apnea]]) | ::* [[Snoring]], [[hypersomnolence]] ([[obstructive sleep apnea]]) | ||
::*[[Prostatism]] ([[chronic kidney disease]] due to [[post-renal]] [[urinary tract obstruction]]) | ::*[[Prostatism]] ([[chronic kidney disease]] due to [[post-renal]] [[urinary tract obstruction]]) |
Revision as of 11:03, 13 December 2020
Hypertension Main page |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Usama Talib, BSc, MD [2]
Overview
Historical Perspective
- [Disease name] was first discovered by [scientist name], a [nationality + occupation], in [year] during/following [event].
- In [year], [gene] mutations were first identified in the pathogenesis of [disease name].
- In [year], the first [discovery] was developed by [scientist] to treat/diagnose [disease name].
Classification
Hypertension may be classified according to the underlying disorder into two groups:
- Gradually rising in blood pressure
- History of environmental exposure (weight gain, high-sodium diet, decreased physical activity, job change leading increased travel, excessive consumption of alcohol
- Family history of hypertension
- BP lability, suddenly rising BP with pallor and dizziness (pheochromocytoma)
- Snoring, hypersomnolence (obstructive sleep apnea)
- Prostatism (chronic kidney disease due to post-renal urinary tract obstruction)
- Muscle cramps, weakness (hypokalemia from primary aldosteronism or secondary aldosteronism due to renovascular disease)
- Weight loss, palpitations, heat intolerance (hyperthyroidism)
- Edema, fatigue, frequent urination (kidney disease or failure)
- History of coarctation repair (residual hypertension associated with coarctation)
- Central obesity, facial rounding, easy bruisability (Cushing syndrome)
- Medication or substance use(alcohol, NSAIDS, cocaine, amphetamines
- Absence of family history of hypertension
- Resistant hypertension is defined as a higher level of BP above the goal in spite of concurrent use of three antihypertensive drugs including a long-acting calcium channel blocker, angiotensin-converting enzyme inhibitor or angiotensin receptor blocker, and a diuretic.
Hypertension Guidline | ACC/AHA | ESC/ESH |
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Definition of hypertension (mmHg) | ≥130/80 | ≥140/90 |
Normal blood pressure range (mmHg) |
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Hypertension stage (mmHg) |
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Age specific blood pressure targets(9mmHg) |
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Blood pressure category | Systolic blood pressure | Diastolic blood pressure |
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Normal | <120/80 mmHg | <80 mmHg |
Elevated | 120-129 mmHg | <80 mmHg |
Stage 1 hypertension | 130–139 mm Hg | 80–89 mm Hg |
Stage 2 hypertension | ≥140 mm Hg | ≥90 mm Hg |
Pathophysiology
- The pathogenesis of [disease name] is characterized by [feature1], [feature2], and [feature3].
- The [gene name] gene/Mutation in [gene name] has been associated with the development of [disease name], involving the [molecular pathway] pathway.
- On gross pathology, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
- On microscopic histopathological analysis, [feature1], [feature2], and [feature3] are characteristic findings of [disease name].
Causes
Common causes of hypertension include:
- Genetic susceptibility
- Hypertension is a Polygenic disorder
- Findings of 25 rare mutations,120 single-nucleotide polymorphisms in hypertensive patients
- Monogenic forms of hypertension: glucocorticoid-remediable aldosteronism, Liddle syndrome, Gordon’s syndrome
- Association between high blood pressure with age and increased defects in the gene
Environmental exposure
- Direct relationship between body mass index and BP
- Strong relationship between waist-to hip ratio, distribution of central fat and BP
- Relation between Obesity at a young age with further hypertension
- Inverse relation between physical fitness and physical activity with BP
- Modest exercise activity reduces the risk of BP
Pharmacological causes of hypertension |
Management: |
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Differentiating [disease name] from other Diseases
- [Disease name] must be differentiated from other diseases that cause [clinical feature 1], [clinical feature 2], and [clinical feature 3], such as:
- [Differential dx1]
- [Differential dx2]
- [Differential dx3]
Epidemiology and Demographics
- The prevalence of [disease name] is approximately [number or range] per 100,000 individuals worldwide.
- In [year], the incidence of [disease name] was estimated to be [number or range] cases per 100,000 individuals in [location].
Age
- Patients of all age groups may develop [disease name].
- [Disease name] is more commonly observed among patients aged [age range] years old.
- [Disease name] is more commonly observed among [elderly patients/young patients/children].
Gender
- [Disease name] affects men and women equally.
- [Gender 1] are more commonly affected with [disease name] than [gender 2].
- The [gender 1] to [Gender 2] ratio is approximately [number > 1] to 1.
Race
- There is no racial predilection for [disease name].
- [Disease name] usually affects individuals of the [race 1] race.
- [Race 2] individuals are less likely to develop [disease name].
Risk Factors
- Common risk factors in the development of hypertension are Diabetes mellitus Family history of hypertension, Dyslipidemia, Increased age, Obesity, Low socioeconomic state, Physical inactivity/low fitness, Male sex, Unhealthy diet, Obstructive sleep apnea, Psychological stress.
Modifiable risk factors | Fixed risk factors |
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Current smoker, secondhand smoking | Chronic kidney disease |
Diabetes mellitus | Family history |
Dyslipidemia/hypercholesterolemia | Increased age |
Obesity | Low socioeconomic/educational status |
Physical inactivity/low fitness | Male sex |
Unhealthy diet |
Natural History, Complications and Prognosis
- The majority of patients with [disease name] remain asymptomatic for [duration/years].
- Early clinical features include [manifestation 1], [manifestation 2], and [manifestation 3].
- If left untreated, [#%] of patients with [disease name] may progress to develop [manifestation 1], [manifestation 2], and [manifestation 3].
- Common complications of [disease name] include [complication 1], [complication 2], and [complication 3].
- Prognosis is generally [excellent/good/poor], and the [1/5/10year mortality/survival rate] of patients with [disease name] is approximately [#%].
New onset or uncontrolled hypertension in adult | |||||||||||||||||||||||||||||||||||||||||||||||||
* Drug resistance hypertension
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Yes | No | ||||||||||||||||||||||||||||||||||||||||||||||||
Screening for secondary hypertension | No need for screening | ||||||||||||||||||||||||||||||||||||||||||||||||
Diagnosis
Diagnostic Criteria
- The diagnosis of [disease name] is made when at least [number] of the following [number] diagnostic criteria are met:
- [criterion 1]
- [criterion 2]
- [criterion 3]
- [criterion 4]
Blood pressure measurement | Definition |
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Systolic blood pressure (SBP) | First Korotkoff sound |
Diastolic blood pressure(DBP) | Fifth Korotkoff sound |
Pulse pressure | SBP minus DBP |
Mean arterial pressure | DBP plus one third pulse pressure |
Mid- blood pressure | (SBP+DBP) divided by 2 |
Key steps for accurate blood pressure measurement | Educations |
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Properly prepare the patient | |
Using proper technique | cuff size 80 % of arm |
Taking proper measurement |
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Documentation of reading blood pressure | [[ Systolic blood pressure] is the onset of the first Korotkoff sound and [[diastolic blood pressure] is the disappearance of all Korotkoff sounds |
Average the reading | using ≥2 readings obtained on ≥2 occasions for determination the level of blood pressure |
Providing blood pressure reading to patient | Providing patients the SBP/DBP readings both verbally and in writing |
Arm circumference | cuff size |
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22-26 cm | Small adult |
27-34 cm | Adult |
35-44 cm | Large adult |
45-52 cm | Adult thigh |
Office BP≥130/80 mm Hg, but < 160/100 mmHg after 3 months of life style modification, suspected white coat hypertension | |||||||||||||||||||
Daytime ABPM or HBPM, BP<130/80 mmHg | |||||||||||||||||||
Yes
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Office BP: 120-129/<80 mmHg after 3 months of lifestyle modification, suspected masked hypertension | |||||||||||||||||||
Daytime ABPM or HBPM, BP≥130/80 mm Hg | |||||||||||||||||||
Yes
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2017 ACC/AHA Guideline |
Screening for Primary adlostronism: |
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History and Symptoms
- [Disease name] is usually asymptomatic.
- Symptoms of [disease name] may include the following:
- [symptom 1]
- [symptom 2]
- [symptom 3]
- [symptom 4]
- [symptom 5]
- [symptom 6]
Physical Examination
- Patients with [disease name] usually appear [general appearance].
- Physical examination may be remarkable for:
- [finding 1]
- [finding 2]
- [finding 3]
- [finding 4]
- [finding 5]
- [finding 6]
Conditions | Physical examination |
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Renal parenchymal disease | |
Renovascular disease |
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Primary aldosteronism | |
Obstructive sleep apnea |
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Drug or alcohol induced | |
Pheochromocytoma/paraganglioma | |
Cushing syndrome | |
Hypothyroidism | |
Hyperthyroidism | |
Coarctation of aorta |
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Congenital adrenal hyperplasia |
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Acromegaly |
Laboratory Findings
- Basic laboratory test should be taken in patients with the diagnosis of hypertension include:
- Fasting blood sugar
- Complete blood count
- Lipid profile
- Serum creatinine with eGFR
- Serum sodium, potassium, calcium
- Thyroid-stimulating hormone
- Urinalysis
- Optional laboratory test in hypertensive patients include:
- Uric acid
- Urinary albumin to creatinine ratio
Electrocardiogram
There are no ECG findings associated with [disease name].
OR
An ECG may be helpful in the diagnosis of [disease name]. Findings on an ECG suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
X-ray
There are no x-ray findings associated with [disease name].
OR
An x-ray may be helpful in the diagnosis of [disease name]. Findings on an x-ray suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
There are no x-ray findings associated with [disease name]. However, an x-ray may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
Echocardiography or Ultrasound
There are no echocardiography/ultrasound findings associated with [disease name].
OR
Echocardiography/ultrasound may be helpful in the diagnosis of [disease name]. Findings on an echocardiography/ultrasound suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
There are no echocardiography/ultrasound findings associated with [disease name]. However, an echocardiography/ultrasound may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
CT scan
There are no CT scan findings associated with [disease name].
OR
[Location] CT scan may be helpful in the diagnosis of [disease name]. Findings on CT scan suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
There are no CT scan findings associated with [disease name]. However, a CT scan may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
MRI
There are no MRI findings associated with [disease name].
OR
[Location] MRI may be helpful in the diagnosis of [disease name]. Findings on MRI suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
There are no MRI findings associated with [disease name]. However, a MRI may be helpful in the diagnosis of complications of [disease name], which include [complication 1], [complication 2], and [complication 3].
Other Imaging Findings
There are no other imaging findings associated with [disease name].
OR
[Imaging modality] may be helpful in the diagnosis of [disease name]. Findings on an [imaging modality] suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
Other Diagnostic Studies
There are no other diagnostic studies associated with [disease name].
OR
[Diagnostic study] may be helpful in the diagnosis of [disease name]. Findings suggestive of/diagnostic of [disease name] include [finding 1], [finding 2], and [finding 3].
OR
Other diagnostic studies for [disease name] include [diagnostic study 1], which demonstrates [finding 1], [finding 2], and [finding 3], and [diagnostic study 2], which demonstrates [finding 1], [finding 2], and [finding 3].
Treatment
Medical Therapy
- There is no treatment for [disease name]; the mainstay of therapy is supportive care.
- The mainstay of therapy for [disease name] is [medical therapy 1] and [medical therapy 2].
- [Medical therapy 1] acts by [mechanism of action 1].
- Response to [medical therapy 1] can be monitored with [test/physical finding/imaging] every [frequency/duration].
Treatment strategy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
Nomal BP (BP<120/80 mmHg) | Elevated BP(BP120-129/<80mmHg | Stage1 hypertension(BP 130-139/80-89mmHg | Stage 2 hypertension (BP≥ 140/90 | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Life style modifications | Nonpharmocological therapy(class1) | 10 years CVD risk≥ 10% | Non pharmacological therapy and BPlowering medication | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Reevaulation in 1 year (class 2a) | Reevaulation in 3-6 months(class 1) | Nonpharmocological therapy(class1) | Non pharmacological therapy and BPlowering medication | ||||||||||||||||||||||||||||||||||||||||||||||||||||
Reevaulation in 3-6 months(class 1) | Reevaulation in 1 months(class 1) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
BPgoal reached | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
NO, Evaluation and optimization the adherence to medical therapy | Yes,Reevaulation in 3-6 months(class 1) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||
Intensification of medical therapy | |||||||||||||||||||||||||||||||||||||||||||||||||||||||
First line of treatment | Drug_ Dosage(mg/day)_ Frequency | Comments | ||||||||||||||||||||||||||||||
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Thiazide or thiazidetype diuretics |
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ACE inhibitors |
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ARB |
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CCB—dihydropyridines |
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CCB—nondihydropyridines |
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Second line of treatment | Drug_ Dosage(mg/day)_ Frequency | Comments | ||||||||||||||||||||||||||||||
Diuretics—loop |
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Diuretics—potassium sparing |
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Diuretics—aldosterone antagonists |
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Betablocker-cardioselective |
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Betablocker-cardioselective and vasodilatory |
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Beta blockers—noncardioselective |
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Not recommended, especially in IHD or heart failure | ||||||||||||||||||||||||||||||
Beta blockers—intrinsic sympathomimetic activity |
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Not recommended , especially in IHD or heart failure | ||||||||||||||||||||||||||||||
Beta blockers—combined alpha-beta receptor |
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Carvedilol is preferred in heart failure reduced EF | ||||||||||||||||||||||||||||||
Direct renin inhibitor |
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Alpha-1 blockers |
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Central alpha2-agonist and other centrally acting drugs |
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Direct vasodilators |
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Class I, Level of evidence:A |
In patients with atherosclerotic renal artery stenosis, medical therapy is recommended |
Class IIb, Level of evidence:C |
Revascularization (percutaneous renal artery angioplasty and/ or stent placement) indicates in patients with refractory hypertension, worsening
renal function, intractable heart failure, nonatherosclerotic disease (fibromuscular dysplasia) |
Class IIb, Level of evidence:B |
The effectiveness of continuous positive airway pressure (CPAP) to decrease blood pressure in patients with obstructive sleep apnea and hypertension is not verified |
Surgery
- Surgery is the mainstay of therapy for [disease name].
- [Surgical procedure] in conjunction with [chemotherapy/radiation] is the most common approach to the treatment of [disease name].
- [Surgical procedure] can only be performed for patients with [disease stage] [disease name].
Prevention
- There are no primary preventive measures available for [disease name].
- Effective measures for the primary prevention of [disease name] include [measure1], [measure2], and [measure3].
- Once diagnosed and successfully treated, patients with [disease name] are followed-up every [duration]. Follow-up testing includes [test 1], [test 2], and [test 3].
Recommendations for masked hypertension and white coated hypertension : (Class IIa, Level of Evidence B) |
❑ Screening white coated hypertension in patients with systolic blood pressure 130-160 mmHg and diastolic blood pressure 80=-110 mmHg by using ABPM or HBPM before diagnosis of hypertension |
(Class IIa, Level of Evidence C) |
❑ Periodic monitoring blood pressure with ABPM or HBPM for detection of transient or sustained hypertension in white coated hypertension |
(Class IIa, Level of Evidence C) |
❑ Finding white coated hypertension by HBPM and ABPM in high office blood pressure inspite of receiving treatment,is recommended |
(Class IIa, Level of Evidence B) |
❑ Finding mask hypertension by HBPM or ABPM in office blood pressure 120-129 /75-79 mmHg |
(Class IIb, Level of Evidence C) |
❑ Finding white coated hypertension by HBPM or ABPM if office blood pressure 10 mmHg higher than normal in spite of receiving multiple medications |
References
Overview
Hypertension is generally defined as an elevated systolic blood pressure (SBP) ≥ 140 mmHg and/or diastolic blood pressure (DBP) ≥ 90 mmHg. Hypertension can be chronic or acute. While 95% of the cases of chronic hypertension are primary, 5% of chronic hypertension is secondary to other underlying causes. Hypertensive crisis is the acute elevation of blood pressure and it can be classified into hypertensive emergency or hypertensive urgency when end organ damage is present or absent respectively.
Causes
When a full evaluation yields no clear etiology for the elevated blood pressure:
- Primary hypertension, also called essential hypertension.
Secondary hypertension can be caused by:
- Apnea
- Hyperaldosteronism
- Renal failure
- Coarctation of aorta
- Cushing's syndrome
- Drugs
- Diet
- Pheochromocytoma
- Obesity
- Hyperparathyroidism
For detailed causes of secondary hypertension, click here.
Classification
For more details about each specific type of hypertension, click on the links in blue in the algorithm below.
In order to distinguish primary hypertension from secondary hypertension, click here.
Hypertension | |||||||||||||||||||||||||||||||
Chronic hypertension | Hypertensive crisis Acute elevation of blood pressure - Systolic blood pressure >180 mm Hg OR - Diastolic blood pressure >120 mm Hg | ||||||||||||||||||||||||||||||
Primary hypertension (also known as essential hypertension) (95% of the cases) | Secondary hypertension (5% of the cases) | Hypertensive emergency Evidence of end organ damage | Hypertensive urgency No evidence of end organ damage | ||||||||||||||||||||||||||||
Screening
The age to begin screening for hypertension varies between 13-20 years of age, according to different authorities. Generally, hypertension is defined as SBP > 140 mmHg and/or DBP > 90 mmHg. In specific populations, however, routine follow-up target BP may be different; and initiation of treatment may be considered at even lower BP values than those considered for the normal population.