Presented by Annie Ingram, MSN, NP-C
Transcript of Presented by Annie Ingram, MSN, NP-C
Hypertension is the chronic elevation in blood pressure that, long term, causes end-organ damage, and increases morbidity and mortality. It occurs due to the abnormal functioning of the arterial pressure related to the central nervous system, renin-angiotensin-aldosterone system, endothelial dysfunction, genetics, and environmental factors.
Hypertension in the most common
primary diagnosis in America,
estimating 35 million office visits per
year
The National Health and Nutrition
Examination Survey estimates that 50
million or more Americans have
hypertension
Hypertension affects half of people age
60-69, and ¾ of people aged 70 and
greater
Worldwide hypertension is estimated to
be 1 billion people, with approximately
7.1 million deaths per year related to
hypertension
The Framingham heart study found that those with normal BP at age 55 have a 90% risk of developing hypertension in their lifetime
The World Health Organization reports that hypertension causes 62% of cerebrovascular disease and 49% of ischemic heart disease
It is estimated that 30% of adults are unaware that they have hypertension, 40% with hypertension are not on medications, and 2/3 of individuals with hypertension are not controlled to BP <140/90
For people age 40-70, for every
20mmHg increase in systolic BP or 10mmHg increase in diastolic BP, there is a doubled risk of Cardiovascular disease
The higher the BP, the greater the risk of stroke, heart attack, heart failure, and kidney disease
Estimations state that for people with stage 1 hypertension, sustaining a 12mmHg reduction in SBP over 10 years will prevent 1 death in 11 people
Antihypertensive therapy is associated with reductions in MI of approximately 20-25%, stroke 35-40%, and heart failure approximately 50%
Recent data suggests that the majority of people with hypertension with require two or more antihypertensive medications to achieve goal
The pathophysiology of hypertension
involves cardiac output, peripheral
vascular resistance, the renin-
angiotensin-aldosterone system, and
the autonomic nervous system
To maintain a normal blood pressure, a balance of cardiac output and peripheral vascular resistance must be maintained. Most patients with primary hypertension have a normal cardiac output, but a raised peripheral resistance. Peripheral vascular resistance is determined by small arterioles, the walls of which contain smooth muscle cells. Contraction of these cells is thought to be related to a rise in intracellular calcium concentration. This may explain the vasodilatory effects of medications that block the calcium channels. Prolonged smooth muscle constriction causes thickening of the arteriolar vessel, leading to a rise in peripheral vascular resistance.
The renin-angiotensin system is probably the
most important endocrine system that
affects blood pressure control. Renin is
secreted from the juxtaglomerular apparatus
of the kidney in response to glomerular
underperfusion or a reduced salt intake. It is
also released in response to stimulation from
the sympathetic nervous system.
Renin is responsible for converting renin substrate (angiotensinogen) to angiotensin I, a physiologically inactive substance which is rapidly converted to angiotensin II by angiotensin converting enzyme. Angiotensin II is a potent vasoconstrictor, thus a rise in blood pressure is seen. In addition it stimulates the release of aldosterone from the adrenal gland, which results in a further rise in blood pressure related to sodium and water retention.
Sympathetic nervous system stimulation can cause both arteriolar constriction and arteriolar dilatation. Thus the autonomic nervous system has an important role in maintaining a normal blood pressure. It is also important in the mediation of short-term changes in blood pressure in response to stress and physical exercise.
Most likely, hypertension is related
to an interaction between the
autonomic nervous system and the
renin-angiotensin system, together
with other factors such as sodium,
circulating volume, and genetics.
Normal - < 120/80 mm Hg
Pre-hypertension - 120-139/80-89 mm Hg
Hypertension Stage I - 140-159/90-99 mm Hg
Hypertension Stage II - >or= 160/100 mm Hg
The diagnosis of hypertension should be
made from at least 2 blood pressure
readings one to two weeks apart
Patients should not smoke or consume
caffeine for at least two hours before
blood pressure measurement. The blood
pressure should be measured in both
arms, and the higher reading should be
used
Ambulatory blood pressure monitoring
is an important tool if “white coat”
hypertension is suspected, which
occurs in about 15% of the population.
Normal ambulatory blood pressure for
awake periods is <135/85, asleep
periods <120/70, and average over 24
hours of <130/80.
past known blood pressure readings
family history
past or current symptoms or diagnosis of heart disease, CKD, asthma, COPD, diabetes, dislipidemia, or sleep apnea
smoking history
physical activity or inactivity
excessive alcohol, fat, or sodium intake
all medications currently prescribed or over-the-counter
Risk factors for hypertension include:
family history
race (most common in blacks)
stress
obesity
a high diet in saturated fats or sodium
tobacco use
sedentary lifestyle
aging
Secondary hypertension may result from: renal vascular disease primary hyperaldestoronism Cushing’s syndrome thyroid, pituitary, or parathyroid
dysfunction coarctation of the aorta pregnancy neurologic disorders use of hormonal contraceptives, cocaine,
or some medications
Clozapine
Corticosteroids
Haemopoietic agents (darbepoetin, epoetin)
Immunomodifiers (cyclosporin, tacrolimus)
Leflunomide
Monoamine oxidase inhibitors: reversible
Non-steroidal anti-inflammatory drugs
Oral contraceptives
Oral decongestants (e.g. pseudoephedrine)
Sibutramine
Stimulants (dexamphetamine sulfate, methylphenidate hydrochloride)
Venlafaxine (dose-related)
Rebound hypertension may occur following abrupt withdrawal of
the following:
• bromocriptine
• clonidine
American mistletoe
Angel’s trumpet
Butcher’s broom
Caffeine-containing products (e.g. guarana, black tea, cola
nut, green tea, mate)
Ephedra (ma huang)
Gentian
Ginger preparations
Ginseng preparations
Licorice
Melatonin
Peyote
Phenylalanine
Sage
St John’s wort
Appropriate BP measurement
An optic fundi exam
A BMI calculation
Pulse rate, rhythm, and character
Jugular venous pulse and pressure
Ascultation for carotid, abdominal, and
femoral bruits
Palpation of the thyroid gland
Evidence of cardiac enlargement (displaced
apex, extra heart sounds)
Crackles or wheezing in the lungs
Exam of the abdomen for enlarged kidneys,
masses, or pulsations
Palpation of lower extremity pulses
Assessment for pedal edema
A neurologic assessment
ECG
Urinalysis
Blood glucose
GFR
Serum potassium, hemaglobin, and
calcium
Lipid panel
Urine albumin and creatinine
The goal of antihypertensive
treatment is to reduce cardiovascular
and renal morbidity and mortality.
Therefore the goal BP should be
<140/90 for healthy adults, or <130/80
for those with diabetes or renal
disease.
Weight reduction in those
overweight
Adopting a DASH diet
Lowering dietary sodium intake
Increasing physical activity
Smoking cessation
Moderating alcohol consumption
The DASH (Dietary Approaches to Stop
Hypertension) involves reducing dietary
sodium and eating a variety of foods rich in
nutrients that help lower blood pressure,
such as potassium, calcium and magnesium.
It centers around eating whole grains, fruits,
vegetables, and low-fat dairy items.
A 1600mg sodium DASH diet has been shown
to be similar in its antihypertensive effects
to single drug therapy.
Regular physical activity has a
strong cardioprotective effect.
Regular aerobic exercise can lower
SBP by an average of 4mmHg and
DBP by 2.5mmHg.
The recommended amount of
activity is at least 30 minutes of
moderate-intensity physical activity
3-5 days per week.
For persons who are overweight,
every 1% reduction in body weight
lowers systolic BP by an average of
1mmHg. Weight loss of 10kg can
reduce SBP by 6-10mmHg.
Moderate to heavy alcohol intake can
increase blood pressure, therefore in
these patients, limiting alcohol
consumption can substantially lower
blood pressure.
Alcohol intake should be limited to a
maximun of 2 drinks per day for men,
and 1 drink per day for women, with at
least 2 alcohol free days per week.
Initial drug choice should be based
on the patient’s age, presence of
associated comorbid conditions or
end-organ damage, interactions with
other medications, cost, and
compliance.
Most clinical trials have found Thiazide-type diuretics to be the basis of antihypertensive therapy
In trials such a the Antihypertensive and Lipid Lowering Treatment to Prevent Heart Attack Trial, diuretics were shown to be number one in preventing the cardiovascular complications of hypertension
Diuretics are also more affordable than many other antihypertensive agents
Thiazide-type diuretics should be used as initial therapy for most newly diagnosed hypertensive patients
Other first-line treatment options are an
ACE Inhibitor, ARB, or dihydropyridine
Calcium Channel Blocker
Thiazide diuretics inhibit the sodium and chloride transporter in the distal convoluted tubule of the kidney, thus increasing the excretion of sodium and water, as well as increasing potassium loss. This diuresis decreases blood volume and blood pressure.
Side effects include:
Hyperglycemia
Hypokalemia
Increased uric acid level
Hypercalcemia
Impotence
Photosensitivity
They should be used cautiously in patients at risk for developing diabetes.
ACE inhibitors block the conversion
of angiotensin I to angiotensin II,
thus lowering peripheral arteriolar
resistance and lowering blood
pressure.
Side effects include:
Hypotension
Cough
Hyperkalemia
Headache
Dizziness
Fatigue
Nausea
Renal impairment
ACE inhibitors are contraindicated in pregnancy
and bilateral renal artery stenosis.
ARBs are receptor antagonists that block angiotensin II receptors on blood vessels and other tissues such as the heart. These receptors stimulate vascular smooth muscle contraction.
Because ARBs do not inhibit ACE, they do not cause an increase in bradykinin, which produces some of the side effects of ACE inhibitors (cough and angioedema).
Side effects include:
Hyperkalemia
Hypotension
Dizziness
Headache
Drowsiness
Diarrhea
Abnormal taste sensation (metallic or salty taste)
Rash
ARBs are contraindicated in pregnancy and bilateral renal artery stenosis.
Calcium channel blockers work by blocking calcium channels in cardiac muscle and blood vessels. This decreases intracellular calcium leading to a reduction in muscle contraction.
In the heart, a decrease in calcium available for each beat results in a decrease in cardiac contractility, which in turn decreases cardiac output.
In blood vessels, a decrease in calcium results in less contraction of the vascular smooth muscle, causing vasodilatation and therefore decrease in peripheral vascular resistance.
There are two types of Calcium Channel Blockers:
Dihydropyridine, such as amlodipine, nifedipine, and felodipine
Non-dihydropyridine, such as verapamil and diltiazem.
Dihydropyridine CCBs reduce peripheral vascular resistance. Side effects include dizziness, tachycardia,
bradycardia, headache, flushing, edema, and constipation.
Non-dihydropyridine CCBs reduce myocardial oxygen demand and reverse coronary vasospasm. Side effects include excessive bradycardia,
impaired electrical conduction (e.g., atrioventricular nodal block), and depressed contractility.
Beta-adrenergic blocking agents, or
beta blockers, work by blocking the
neurotransmitters norepinephrine and
epinephrine (part of the sympathetic
nervous system) from binding to
receptors in different parts of the
body. This causes smooth muscle cells
to relax.
There are three types of beta
receptors:
Beta1, located mainly in the heart
and kidneys
Beta2, located in the lungs, GI tract,
liver, uterus, vascular smooth
muscle, and skeletal muscle
Beta3, located in fat cells
First generation beta blockers, such as propranolol and sotalol, are non-selective, therefore they will block the receptors of beta1 and beta2 cells.
Second generation beta blockers, such as metoprolol, are selective and will only block the receptors of beta1 cells. This reduces heart rate, force of contraction, and cardiac output.
Beta blockers also affect the production of renin, which in turn relaxes smooth muscle cells and lowers blood pressure.
Side effects of beta blockers include: Bradycardia
Cold extremities
Fatigue
Insomnia
Dizziness
Wheezing
Digestive problems
Rash
Erectile dysfunction
They should be used cautiously in patients with asthma.
Thiazide-type diretics have been shown to slow the progression of osteoporosis.
Beta Blockerss are also useful for the treatment of atrial tachyarrhythmias, migraine, thyrotoxicosis, essential tremor, and perioperative hypertension.
Calcium Channel Blockers can be useful in Raynaud’s syndrome and certain arrhythmias.
Thiazide diuretics should be used cautiously in patients with a history of gout or hyponatremia.
BBs should be avoided in patients with reactive airway disease or 2nd or 3rd degree heart block.
ACEIs and ARBs should not be given to women who are or may become pregnant. ACEIs should not be used in patients with a history of angioedema.
Thiazide diuretics have been associated with increased risk of new-onset diabetes, and should be used with caution in patients with glucose intolerance.
Start with the lowest recommended dose of the selected agent.
If the drug is not well tolerated, switch to a drug of a different class.
If target blood pressure is not reached, increase the first agent, or add a second agent.
Addition of a second agent should be considered when adaquate doses of the first agent have not produced adaquate results. It is better to add a second agent before maxing out a first, to decrease the likelihood of potential side effects that can be seen with higher doses.
If a patient is taking a midrange dose and is still >5-10mmHg above goal, adding a second agent is more litely to be effective than increasing the dose.
If blood pressure is still above target, increase one agent at a time. Trial each dose regimen for at leaset 6 weeks, because most drugs take at least 3-4 weeks to achieve maximum benefit.
Once a combination regimen is tolerated and doses are established, the patient could be switched to a combined preparation.
If blood pressure remains elevated
despite optimal doses of at least two
agents after a reasonable time, consider
the following potential reasons: Non-compliance to therapy- compliance decreases
as number of times per day dose increases (79%
once daily, 69% BID, 65% TID, 51% QID)
Use of medications that may increase blood
pressure (NSAIDS, stimulants, sympathomimetics,
alcohol, contraceptives, estrogen, corticosteroids,
licorice, caffeine pills, cold medicines, ephedra,
ginseng, St. John’s wort)
secondary hypertension, such as CKD/obstructive uropathy, renovascular hypertension, aortic coarctation, cushing’s syndrome, thyroid disease
undiagnosed sleep apnea
undisclosed alcohol, tobacco, or drug use
undisclosed or unrecognized high sodium diets
“white coat” hypertension- for which 24 hour ambulatory blood pressure monitoring may be helpful
Most people will require at lease two
medications to control their hypertension
Guidelines recommend a combination
therapy as initial therapy in high-risk
hypertensive individuals, when initial BP
is >20/10 above goal
Avoid: ACE Inhibitors plus potassium-
sparing diuretics, Beta-blockers plus
Verapamil, and ACE Inhibitors plus ARBs
ACEIs and CCBs: Lotrel (amlodipine-
benazepril), Lexxel (trandolapril-
verapamil)
ACEIs and diuretics: Lotensin HCT
(Benazepril-HCTZ), Zestoretic (Lisinopril-
HCTZ), Vaseretic (Enalapril-HCTZ)
ARBs and diuretics: Atacand HCT
(Candesartan-HCTZ), Hyzaar (Losartan-
HCTZ), Benicar HCT (Olmesartan-HCTZ),
Diovan HCT (Valsartan-HCTZ)
BBs and diuretics: Tenoretic (Atenolol-
chlorthalidone), Lopressor HCT (Metoprolol-
HCTZ)
Diuretic and diuretic: Aldactazide
(Aldactone-HCTZ), Maxzide (Triamterene-
HCTZ)
Follow-up should include monthly blood pressure checks until goal is reached. More frequent visits may be indicated for patients with stage II hypertension, or those with comorbid conditions.
After blood pressure is shown to be at goal, visits can generally be moved to every 3 to 6 months
Serum creatinine and potassium should be monitored 1-2 times per year
Tobacco avoidance should be strongly encouraged
Low dose aspirin therapy can be considered when a patient is at goal, but not sooner due to risk of hemorrhagic stroke with uncontrolled HTN
Patient motivation improves blood pressure control and should be encouraged at each visit. Home blood pressure monitoring can help patients take ownership of their hypertension, and so become motivated to adhere to treatment.
The cost of medications can also affect compliance. Wal-mart has a $4 drug list, that can be helpful for those without insurance.
Amiloride-HCTZ 5mg-50mg
Atenolol-Chlorthalidone 100mg
Atenolol 25, 50, 100mg tab
Benazepril 5, 10, 20, 40mg
Bisoprolol-HCTZ 2.5mg-6.25mg tab
Bisoprolol-HCTZ 5mg-6.25mg
Bisoprolol-HCTZ 10mg-6.25mg tab
Captopril 12.5, 25, 50, 100mg
Carvedilol 3.125, 6.25, 12.5, 25mg tab
Clonidine 0.1, 0.2mg tab
Diltiazem 30, 60, 90, 120mg tab
Doxazosin 1, 2, 4, 8mg tab
Enalapril-HCTZ 5mg-12.5mg
Enalapril 2.5, 5, 10, 20mg tab
Furosemide 20, 40, 80mg tab
Hydralazine 10, 25mg tab
Hydrochlorothiazide(HCTZ)12.5mg cap
Hydrochlorothiazide (HCTZ) 25, 50mg tab
Indapamide 1.25, 2.5mg tab
Isosorbide Mononitrate 30, 60mg ER tab
Lisinopril-HCTZ 10mg-12.5mg
Lisinopril-HCTZ 20mg-12.5mg
Lisinopril-HCTZ 20mg-25mg
Lisinopril 2.5, 5, 10, 20mg tab
Methyldopa 250mg tab
Metoprolol Tartrate 25, 50, 100mg tab
Nadolol 20, 40mg tab
Prazosin HCL 1mg cap
Propranolol 10, 20, 40, 80mg
Sotalol HCL 80mg tab
Spironolactone 25mg tab
Terazosin 1, 2, 5, 10mg cap
Triamterene-HCTZ 75mg-50mg tab
Triamterene-HCTZ 37.5mg-25mg tab
Verapamil 80, 120mg tab
Withdrawl of antihypertensives may be
considered in patients who have
achieved target blood pressure at low
doses and agree to continue lifestyle
modifications, undergo regular blood
pressure monitoring, and reinstitute
antihypertensives if necessary.
Ischemic heart disease The most common form of target organ
damage associated with hypertension is Ischemic heart disease.
In patients with hypertension and stable angina, beta-blockers or long acting calcium-channel blockers are indicated.
In patients with ACS, treatment should be beta blockers and ace inhibitors, as well as nitrates.
For patients post-MI, beta blockers, ACEIs, and aldosterone antagonists have shown to be the most benificial. Aspirin and lipid therapy should also be initiated.
Heart failure
For paitents with systolic heart failure, or left ventricular dysfunction, ACEIs and BBs are recommended.
For those who are symptomatic or at end-stage heart disease, ACEIS, BBs, ARBs, aldosterone blockers, and loop diuretics are indicated.
Diabetic Hypertension
Usually a combination of two or more antihypertensives will be needed to achieve a blood pressure of <130/80.
Thiazide diuretics, BBs, ACEIs, ARBs, and CCBs have been shown to reduce Cardiovascular disease and stroke in diabetic patients.
ACEIs and ARBs have been shown to slow the progression of diabetic nephropathy and reduce albuminuria.
Chronic Kidney Disease
In patients with CKD, the goal of therapy is to slow deterioration of renal function, and prevent cardiovascular disease.
Target blood pressure in these patients is <130/80.
ACEIs and ARBs have shown to slow the progression of renal disease. A rise of as much as 35% above baseline in serum creatinine is found to be acceptable and should not cause discontinuation of therapy unless hyperkalemia develops.
With advanced renal disease, loop diuretics will also be necessary in combination with other antihypertensives.
Cerebrovascular disease
In an acute stroke, blood pressure is recommended to be maintained around 160/100 until the condition has stabilized.
A combination of thiazide-type diuretics and ACEIs have been shown to lower recurrent stroke rates.
Aggressive antihypertensive therapy appears to be safe to reinitiate 1-2 weeks after the acute event, when the patient has been deemed clinically stable.
Pregnancy
Methyldopa, Beta Blockers, and
vasodialators are considered to be the
safest medications.
ACEIs and ARBs should not be used due to
the possibility of fetal defects.
Methydopa and labetalol are the most
widely used medications to treat pregnant
women.
Hypertensive Emergency Hypertensive Urgency is defined as SBP > or
=180 and/or DBP >or=120 without evidence of target organ dysfunction. These patients require immidiate intervention and may need to be hospitalized.
Hypertensive Emergency is defined as SBP >or= 180 and/or DBP >or=120 with evidence of target organ dysfunction, such as coronary ischemia, disordered cerebral function, cerebrovascular events, pulmonary edema, and renal failure. These patients require hospitalization and immediate treatment.
References Campbell, N. Hemmelgarn, B. (2012). New recommendations for the use of ambulatory
blood pressure monitoring in the diagnosis of hypertension. Canadian Medical
Association Journal, 184(6), 633-634.
Corrao, G., Nicotra, F., Parodi, A, Zambon, A. (2011). Cardiovascular protection by
initial and subsequent combination of antihypertensive drugs in daily life practice.
Hypertension, 58(4), 566-572.
Mukherjee, D. (2012). Atherogenic vascular stiffness and hypertension: Cause or effect?
The Journal of the American Medical Association, 308(9), 919-920.
Park, C., Youn, H., Chae, S. (2012). Evaluation of the dose-relationship of Amlodipine
and Losartan combination in patients with essential hypertension. American Journal
Cardiovascular Drugs, 12(1), 35-47.
References Sever, P., Messereli, F. (2011). Hypertension management 2011: Optimal medical
therapy. European Heart Journal, 32(20), 2499-2506.
http://www.heartfoundation.org.au/SiteCollectionDocuments/HypertensionGuidelines2008to2010
Update.pdf Retrieved December 11, 2012
http://www.icsi.org/hypertension_4/hypertension_diagnosis_and_treatment_4.html Retrieved
December 11, 2012
http://www.nhlbi.nih.gov/guidelines/hypertension/jnc7full.pdf Retrieved December 11, 2012
3. Which of the following is a potential secondary drug-induced cause of hypertension?
C) Phenylpropanolamine
4. Which of the following patients is at very high risk for cardiovascular disease and should immediately receive a medication to lower blood pressure?
C) A 68-year-old man with heart failure and a baseline blood pressure of 150/88 mm Hg
5. Which of the following would be most appropriate for a patient with hypertension who has had a myocardial infarction?
C) Metoprolol
6. Which of the following is the most appropriate blood pressure goal for a 65-year-old African-American with hypertension and no other medical problems?
A) <140/90 mm Hg
7. In order to minimize the risk of hypokalemia from diuretics, the most appropriate strategy would include:
A) limiting the dose of hydrochlorothiazide to 12.5 to 25 mg
8. In a patient with heart failure, the best combination of medications would be:
C) Lisinopril and Coreg
9. Which of the following is an appropriate agent and starting dose for a patient with uncomplicated hypertension?
A) Atenolol 25 mg once daily
10. Which drug is most likely to cause vasodilation-type side effects (headache, flushing) because it blocks the movement of calcium across smooth muscle cells?
E) Verapamil
11. When patients with renal insufficiency develop severe cough from ACE inhibitors, what would be the best alternative to provide renal protection?
C) Losartan
12. Which of the following is true concerning clonidine?
A) It has been used for smoking cessation and narcotic withdrawal.
14. What potential side effects would you mention to a patient recently started on nifedipine?
D) Leg edema
15. A 39-year-old woman with hypertension is taking HCTZ, enalapril (Vasotec), and diltiazem (Cardizem). She desires to become pregnant. The most important step would be to
D) discontinue enalapril.
17. Which one of the following nondrug measures is likely to be most effective to lower blood pressure chronically?
C) Lose 10-15 pounds