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Antihypertensive Medications

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StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2020 Jan-.

Antihypertensive Medications

Authors
Hassan Khalil1; Roman Zeltser2.

Affiliations
1
The George Washington University
2
Hofstra Northwell School of Medicine

Last Update: May 23, 2020.

Indications

Hypertension (HTN) is considered one of the leading causes of increased cardiovascular disease.

The 2017 American College of Cardiology (ACC) and American Heart Association (AHA) definition of
HTN stages is:

 Normal blood pressure (BP): systolic BP is less than 120, and diastolic BP is less than 80.

 Elevated BP: systolic BP 120 to 130 and diastolic BP is less than 80.

 Stage 1 HTN: systolic BP 130 to 139 or diastolic BP 80 to 89.

 Stage 2 HTN: systolic BP at least 140 or diastolic at least 90.

 Hypertensive crises: systolic BP over 180 and/or diastolic BP over 120.

In the 2019 ACC/AHA Guideline on the Primary Prevention of Cardiovascular Disease: all patients with
elevated blood pressure are recommended to have lifestyle modifications as initial treatment, including
weight loss, healthy heart diet, increased physical activity, low sodium diet, and limitation of alcohol
consumption.

In patients with stage 1 HTN recommendations are to start antihypertensive medications if the patient has
a 10-year ASCVD risk of 10% or higher with a target of BP less than 130/80 to prevent patients from
cardiovascular events. The recommendation is for patients with stage 1 HTN and 10-year ASCVD risk
less than 10% to have lifestyle modification measures.

Recommendations are for all patients with stage 2 HTN to start antihypertensive medications to lower BP
to a target lower than 130/80 even if the 10-year ASCVD risk is less than 10%.

In patients with chronic kidney disease, the target BP is 130/80

Patients with type 2 diabetes mellitus (T2DM) it is recommended to start on antihypertensive medications
if BP is more than 130/80 with a goal of BP lower than 130/80.
Antihypertensive medication treatment usually starts as monotherapy after failure of conservative
management with lifestyle modification. The use of combination therapy is common when patients fail the
monotherapy approach.

Lowering blood pressure does reduce cardiovascular risks, maintaining systolic blood pressure less than
130 mm Hg has shown to prevent complications in patients with heart failure, diabetes, coronary artery
disease, stroke, and other cardiovascular diseases.[1] The response to initial monotherapy is affected by
age and race.

There are multiple classes of antihypertensive medications used for the treatment of HTN; the most
recommended classes used as first-line for treatment are:

Thiazide-type diuretics

Calcium channel blockers

Angiotensin-converting enzyme (ACE) inhibitors and angiotensin II receptor blockers (ARBs)

Thiazide diuretics

Thiazide and thiazide-like diuretics are usually the first-line of treatment for hypertension; in JNC8
guidelines the thiazide diuretics can be used as the first-line treatment for HTN (either alone or in
combination with other antihypertensives) in all age groups regardless of race unless patient has
evidence of chronic kidney disease where angiotensin-converting enzyme inhibitor or angiotensin II
receptor blocker is indicated.[2]

The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial ALLHAT study
recommended thiazide diuretics as the first line of treatment for hypertension unless there are
contraindications.

Treatment with hydrochlorothiazide as a single agent with a dose of 12.5 mg or 25 mg daily showed no
evidence of decreasing morbidity or mortality.[3]

Thiazide-type diuretics (chlorthalidone and indapamide) have demonstrated to be superior to prevent

cardiovascular disease at a lower cost. Recommendations are to start them as first-line treatment for
hypertension. Multiple studies have shown that thiazide-like diuretics (chlorthalidone and indapamide) are
more potent than hydrochlorothiazide in hypertension treatment. They are better at decreasing the risk of
cardiovascular disease comparing to hydrochlorothiazide.[4][5][6]

Chlorthalidone is the drug of choice to start as monotherapy for hypertension. Studies show it to be the
best diuretic to control blood pressure and to prevent mortality and morbidity.[7][8] It is more effective
than hydrochlorothiazide in lowering blood pressure when the researchers monitored 24-hour ambulatory
blood pressures.[5] Hydrochlorothiazide has a shorter effect during the day in a study that compared the
office blood pressure reading with the 24 hours ambulatory blood pressure readings.[9] Switching to
chlorthalidone from hydrochlorothiazide decreases systolic blood pressure by 7 to 8 mm Hg.[10]

The Antihypertensive and Lipid-Lowering Treatment to Prevent Heart Attack Trial (ALLHAT) showed that
chlorthalidone at 12.5 to 25 mg/day caused less cardiovascular complications than amlodipine and
lisinopril

Chlorthalidone is the first choice for older patients with osteoporosis, as it showed less incidence of pelvic
fractures when compared to amlodipine and lisinopril.[11] Chlorthalidone, when compared with doxazosin
mesylate, was better in preventing cardiovascular disease, when compared with lisinopril was found to be
better in preventing cardiovascular disease including strokes and heart failure incidence, and when
compared with amlodipine was better in preventing heart failure.[12]

Calcium channel blockers CCBs

Same as thiazide-type diuretics CCBs are recommended in JNC8 guidelines to be used as a first-line
treatment alone or in combination with other antihypertensives in all patients with HTN regardless of age
and race with the exception of patients with chronic kidney disease where ACE inhibitors or ARBs are the
recommended first-line treatment.[2]

CCBs are shown to decrease all cardiovascular events other than heart failure similar to thiazide
diuretics, and they can be used as the best alternative to thiazides when patients do not tolerate
thiazides.[7]

CCBs divide into two groups: dihydropyridines and non-dihydropyridines

Dihydropyridines are more potent as vasodilators and used more for HTN treatment. They have less
effect on heart contractility and conduction. For this, they are used more for the management of HTN.
Nifedipine and amlodipine are the most used medications in this group.

Non-dihydropyridines are less potent as vasodilators and have a better effect on cardiac contractility and
conduction. They are used more as antiarrhythmic medications and less for HTN treatment.

For African descent patients, initial treatment for hypertension (without evidence of heart failure or chronic
kidney disease) should include CCB or a thiazide diuretic.[7]

Long-acting nifedipine has greater antihypertensive action when compared to amlodipine.[10]

Dihydropyridines should not be a primary treatment for congestive heart failure (CHF) but are a safe
additional treatment in these patients for better blood pressure control or angina pectoris.

Non-dihydropyridines are relatively contraindicated in patients with CHF with reduced ejection fraction,
second and third-degree heart blocks, and in patients with sick sinus syndrome.

When compared to valsartan in a study, amlodipine was found to have better control of 24-hour
ambulatory blood pressure. In the ASCOT trial, amlodipine was found to be better than atenolol in
lowering the risk of cardiovascular disease and is associated with less risk of diabetes
development.[13] When compared to thiazide diuretics, amlodipine was equally effective in lowering
cardiovascular disease risk regardless of patient's weight, while thiazides are less effective in normal
body mass index (BMI) patients than in patients with obesity.[14]

ACE inhibitors and ARBs

ACE inhibitors and ARBs are the antihypertensive of choice for patients with heart failure and chronic
kidney disease. They are indicated as first-line treatment for patients with chronic kidney disease with
evidence of proteinuria. JNC8 guidelines list these two classes of antihypertensive medications as first-
line treatment for HTN for non-black patients, along with thiazides and CCBs.[2]

Independent of their antihypertensive effect, they are proven to have cardio-protective effect in patients
who carry a high risk of cardiovascular disease
Both classes have similar efficacy and share the same indications for treatment, they are both
recommended as first-line treatment for patients with left ventricular dysfunction, and ST-elevation MI or
non-ST elevation MI with the presence of diabetes, systolic dysfunction or anterior infarct.

Thiazide is better than ACE inhibitors in decreasing blood pressure and preventing stroke, CCBs are
better than ACE inhibitors in lowering blood pressure, and in preventing from stroke and heart failure.[7]

Ramipril has shown to decrease mortality, the incidence of stroke, and MIs when used in patients with
symptomatic heart failure or asymptomatic patients with low ejection fraction. The research found
perindopril to decrease cardiovascular events when used in a patient with stable coronary artery disease
and normal systolic dysfunction. When compared with Atenolol, Losartan was found to be better in
decreasing morbidity and mortality and better in lowering blood pressure.

Comparing ramipril with telmisartan, they were equivalent in effect in diabetic or heart failure patients, with
telmisartan correlating with less angioedema.[15]

Beta-blockers

Beta-blockers are not indicated as primary treatment for hypertension unless there is a specific indication
of heart failure and myocardial infarction.[16]

Beta-blockers are associated with decreased cardiovascular morbidity and mortality when used in
younger patients, but less protective in patients older than 65 and were noted to be associated with
increased risk of strokes.[16][17][16][18]

Combination therapy

When a patient fails a monotherapy for HTN, a combination should merit consideration. A combination
of two antihypertensive medications should be a therapeutic option for patients with stage 2
hypertension.[7] One study showed a reduction in blood pressure when drugs from two different classes
are combined is about five times greater than when the dose of one drug dose doubles.[19]

A combination of ARB-diuretic or ACE inhibitor-CBB is superior to the beta-blocker-diuretic

combination.[20] The beta-blocker and diuretic combination is associated with a higher incidence of
diabetes. Clinicians should use combinations that contain beta-blockers when beta-blockers are indicated
as in patients with heart failure, tachycardia, or post-MI patients. Combination of thiazide with a
potassium-sparing diuretic is as effective as CCB monotherapy in HTN management and showed less
incidence of hypokalemia when compared to hydrochlorothiazide monotherapy [20]

Combination of CCB and diuretics are less available as ARBs or ACE inhibitors based combinations are
preferred when a combination is required, these types of combinations (ACE inhibitors or ARBs based
combinations) should be used in patients with CKD.[20][21]

The combination of benazepril-amlodipine is superior to benazepril-hydrochlorothiazide combination in

decreasing the incidence of cardiovascular events in patients with high risk, and it decreases the
progression of nephropathy.[22][23]

The ACE inhibitor-ARB combination is not recommended; it showed a higher incidence of side effects
with no added benefits.[15][24]

When the combination of 2 medications does not achieve the treatment goal, a third agent should be
added, which is usually done by adding a third agent of the first line group of medications (thiazide-like
diuretics, CCB, ACE inhibitors, and ARBs).
When the patient fails the three-drug regimen, the clinician should consider treatment for resistant HTN,
adding a fourth antihypertensive agent can be from any of the other classes.[20]

Loop diuretics are more effective than thiazides in patients with a low estimated glomerular filtration
rate of less than 30 mL/min. They have approval for the treatment of peripheral edema associated with
congestive heart failure and other noncardiac causes of edema as in liver and kidney diseases.[25] Loop
diuretics are not first-line agents for HTN treatment.[26]

Potassium Sparing Diuretics: "Mineralocorticoid receptor antagonists" are not usually used as first-
line treatment. Spironolactone and eplerenone are considered good in hypertension treatment when
added to other antihypertensive medications in resistant HTN, this group of medication is effective when
added to triple hypertension medications regimen but should be used cautiously when added to ACE
inhibitors or ARBs due to higher incidence of hyperkalemia.[27][28][29] They are effective in the treatment
of heart failure as they are proven to decrease mortality rates, and they help to decrease hypokalemia
rates. Spironolactone is superior to doxazosin and bisoprolol in lowering blood pressure when added to
first-line antihypertensive agents in treating resistant hypertension.[30]

Hydralazine can be added for treatment of resistant hypertension, either alone or in combination with
nitrates, in case of heart failure. Hydralazine is associated with increased sympathetic tone and increases
sodium avidity, adding beta-blocker, and loop diuretics help to decrease these effects.[10]

Clonidine: is a central alpha-2 agonist, it is not a first-line therapy, but can be used as an additional agent
when the patient fails combination therapy, the transdermal form is preferred.[10]

Minoxidil is usually an option when the patient fails treatment with hydralazine, it usually provides good
blood pressure control, but it is associated with fluid retention, for which adding a loop diuretic is helpful. It
increases the sympathetic tone that may require adding a beta-blocker.[10]

Alpha-blockers should not be used in the treatment of hypertension as a first-line agent because they
are not as effective in the prevention of cardiovascular disease when compared with other first-line
agents.[7]

Mechanism of Action

Thiazide and Thiazide like diuretics: mechanism of action for thiazide-type diuretics is not fully
understood. Thiazides inhibit the transport of sodium in the distal tubule; this occurs by blocking the Na/Cl
channels.[31] Thiazides can have a small effect on the proximal tube by impairing sodium transport, but
the main action is on the distal tubule. Thiazides cause initial volume depletion associated with decreased
cardiac output which recovers within 6 to 8 weeks of starting the treatment in a reverse autoregulation
mechanism while the blood pressure remains controlled, thiazide diuretics can acutely activate the renin-
angiotensin system and cause systemic vascular resistance which prevents a good response to the
diuretic treatment, this increase in renin-angiotensin activity may resolve with chronic thiazide treatment,
addition of ACE inhibitor or ARB can enhance the blood pressure control. Also, the thiazide-type diuretics
have a modest vasodilation effect, although the mechanism is still unclear.[32]

Calcium channel blockers: The mechanism of action of CCBs is related to inhibition of Ca2+ entry to
the cells; this occurs by binding to the L-type voltage-gated calcium channels located in the heart
muscle.[33] This effect can cause peripheral vasodilation, which is seen mainly in dihydropyridines, or
negative inotropic effect on the heart muscle in non-dihydropyridines, which inhibits the sinoatrial and
atrioventricular nodes leading to slow cardiac contractility and conduction.[33]
 ACE inhibitors decrease the blood pressure by inhibiting the angiotensin-converting enzyme, this
causes a decline in the production of angiotensin II, and increases the bradykinin level, by inhibiting its
degeneration, which leads to vasodilation.[34]

ARBs work by blocking the binding of angiotensin II to the angiotensin 1 AT1 receptors, which inhibit the
angiotensin II effect. In contrast to ACE inhibitors, ARBs do not affect the kinin levels.

Beta-blockers work by inhibiting the catecholamines from binding to the Beta 1,2 and 3 receptors. Beta-1
receptors are found primarily in the heart muscle, beta-2 receptors are located in the bronchial and
peripheral vascular smooth muscles, and beta-3 receptors appear in adipose tissue of the heart. Cardio-
selective beta-blockers (e.g., metoprolol succinate, metoprolol tartrate, atenolol, betaxolol, and
acebutolol) inhibit only beta-1 receptors and cause fewer bronchospasms. By inhibiting the
catecholamines binding to the beta receptors, the beta-blockers have a negative inotropic effect, which
results in vasodilation of coronary and peripheral arteries and decreases the heart rate, which helps to
reduce the oxygen consumption.[35]

Loop diuretics work by increasing the sodium exertion at the level of the medullary and cortical aspects
of the thick ascending limb. This action causes a decrease in volume, which leads to decreased blood
pressure.[25]

Potassium Sparing Diuretics: Act on the principle cells which are in the late distal tubule and the
collecting duct, they inhibit the sodium reabsorption at this level in association with decreased exertion of
potassium and hydrogen ions. Spironolactone and eplerenone are considered mineralocorticoid receptor
antagonists, and they inhibit the mineralocorticoid receptor.

Hydralazine is an arteriolar vasodilator; it inhibits Ca2+ release in the smooth muscles of the vessels by
decreasing its cytoplasmic concentration.[36]

Clonidine: stimulates alpha-2 receptors located in the rostral ventrolateral medulla, which reduces the
sympathetic outflow from the central nervous system and decreases plasma norepinephrine levels
leading to decreased cardiac output.

Minoxidil is an arteriolar vasodilator; it opens the adenosine triphosphate-sensitive potassium channels

located in the smooth muscles of the vessels.

Alpha-blockers act by inhibiting alpha-1 receptors, which decrease vascular smooth muscle
contractions, leading to vasodilation.[37]

Administration

Thiazide type diuretics are given only as oral forms, Hydrochlorothiazide is available in 12.5 and 25 mg
tablets, but the daily dose can be up to 50 mg daily.[31] Chlorthalidone is available in 25 and 50 mg
tablets, but the daily dose can be up to 100 mg daily.[31]

Dihydropyridine calcium channel blockers are administered orally. Amlodipine's maximum dose is 10 mg
daily.[38] Nifedipine extended-release maximum dose is 120 mg daily.[39] Non-dihydropyridine CCBs are
available in oral and intravenous forms; diltiazem intravenous IV form is useful for heart rate control in
cardiac arrhythmias.[40] The maximum oral dose of diltiazem is 480 mg daily.[40] Verapamil is available
in oral and IV forms as well. The IV form is used for tachyarrhythmias, especially atrial fibrillation. Oral
verapamil dose can by up to a maximum of 480 mg daily.[41]

All ACE inhibitors are given orally; enalapril is the only exception as it has an IV form.[34] On the other
hand, all ARBs are only oral dose forms.[42]
 Beta-blockers are available in oral and IV forms.[35] Loop diuretics are available as oral or IV
forms, while potassium-sparing diuretics are used mainly in oral forms.[25]

Hydralazine administration can be oral or intravenous.[36] The maximum hydralazine oral dose is 300 mg
daily.[36]

Clonidine transdermal form is the preferred method of administration as the oral forms can increase the
risk of rebound hypertension.[10] Transdermal maximum clonidine dose is 0.3 mg weekly, while oral
immediate-release form maximum dose is 0.3 mg three times daily.[43]

Minoxidil is given orally for hypertension treatment. Alpha-blockers are available only orally for
hypertension treatment.[44]

Adverse Effects

Thiazides Side effects

Thiazide and thiazide-like diuretics are associated with multiple side effects. Most of these side effects
are directly related to the dose of the diuretic, hypokalemia, and hyponatremia are the most common
metabolic effects, followed by hyperuricemia, hypomagnesemia, hyperlipidemia, and increased glucose
levels.[45][31]

Chlorthalidone was found in a study to have an increased risk of hospitalization due to severe
hypokalemia in the elderly. Other non-dose related side effects are sexual dysfunction and sleep
disturbance.

CCB Side effects

The treatment with dihydropyridine CCBs is often associated with peripheral edema. Long-acting
nifedipine is associated with a higher incidence of edema when compared to amlodipine; the edema is
related to the dose of the CCB. It is not related to sodium or fluid retention nor to developing heart
failure.[10] Since CCBs induced edema is not a result of volume increase, it does not improve with
diuretics therapy, on the other hand, the combination of CCBs with ACE inhibitors, or with ARBs to a
lesser effect, showed decreased risk of developing peripheral edema.[46] Dihydropyridines can cause
lightheadedness, flushing, headaches, and gingival hyperplasia.[33]

Non-dihydropyridines are associated with bradycardia and can cause constipation in 25% of patients.

CCBs inhibit platelet aggregation and are associated with increased risk of gastrointestinal bleed; caution
is necessary when prescribing these agents to older patients and patients with a high risk of GI bleed.

ACE Is and ARBs Side effects

The most common side effects related to ACE inhibitors are cough, hypotension, fatigue, and azotemia,
Reversible renal impairment is a common side effect, especially if the patient develops volume depletion
due to diarrhea or vomiting.

Cough can occur in up to 20% of patients on ACE inhibitors. It takes up to 14 to 28 days after
discontinuation for the cough to resolve, the incidence of cough is less common with ARB treatment,
comparing losartan with hydrochlorothiazide showed a similar incidence of cough in both medications.
ARBs are safe to use in asthma patients; candesartan did not show a correlation with an increase in the
incidence of cough in patients with asthma when was compared with CCBs. Ramipril demonstrated a
higher rate of cough incidence comparing to telmisartan.[15]
ACE inhibitor treatment is commonly associated with mild hyperkalemia. Even in patients with normal
renal function, the risk of hyperkalemia increases in patients with renal failure, diabetes, or
CHF.[47] Ramipril and telmisartan are similar in rates of developing hyperkalemia, acute kidney injury,
and syncope. but telmisartan is associated with more incidence of symptomatic hypotension.[15]

Angioedema is a rare side effect of ACE inhibitors; it appears in 0.3 % of patients on ramipril, ARBs are
less associated with angioedema comparing to ACE inhibitors.[15]

In Black patients, ARBs correlated with less incidence of both cough and angioedema.[7]

Beta-blockers —Common side effects of beta-blockers are bradycardia, constipation, depression,

fatigue, and sexual dysfunction. Additionally, they are associated with bronchospasm and worsening
symptoms of peripheral vascular disease. They can cause a flare-up of Raynaud syndrome.[35]

Loop diuretics: are associated with electrolyte imbalance, mainly hypokalemia, hyponatremia,
hypomagnesemia, and hypochloremia.[25] Other metabolic adverse reactions are dehydration,
hyperuricemia, and hyperlipidemia. Ototoxicity and deafness may occur with loop diuretics treatment.[26]

Side effects of the Mineralocorticoid receptor antagonists: Hyperkalemia is the major side effect of
this group of medications. They can cause metabolic acidosis as a result of decreased exertion of
hydrogen ions. Erectile dysfunction and gynecomastia in men and irregular menstrual periods in women
can occur as well.[10]

Hydralazine: can cause headaches, flushing, palpitations, dizziness, hypotension symptoms, and
dizziness as a result of the sympathetic system stimulation.[36] It is associated with drug-induced lupus
erythematosus, hemolytic anemia, and other immune phenomena.[36]

Clonidine common side effects are drowsiness, headache, dizziness, irritability, nausea and vomiting,
constipation, upper abdominal pain, and bradycardia, but other serious side effects can occur as
angioedema, atrioventricular block, and severe hypotension.[43]

Minoxidil is associated with hirsutism.[48]

Alpha-blockers are associated with tachycardia and orthostatic hypotension as a result of venous
dilation.[37]

Contraindications

Thiazide type diuretics are contraindicated if the patient is anuric, and in patients with sulfonamide
allergies.[31]

CCBs are contraindicated in patients with hypersensitivity to the drug.[33] Non-dihydropyridines

contraindications are patients with heart failure with reduced ejection fraction, patients who have sick
sinus syndrome, and patients with second or third-degree AV blockade.[33] Dihydropyridine should be
avoided in cardiogenic shock patients, severe aortic stenosis, and unstable angina; special caution is
necessary when dihydropyridine is useful in hepatic impaired patients.[39][38]

ACE inhibitors are contraindicated in patients who have a history of previous hypersensitivity to ACE
inhibitors, history of ACE inhibitor-related angioedema, other types of angioedema, pregnancy, or the use
of aliskiren.[49] Relative contraindications are patients with volume depletion, abnormal renal function,
and patients with aortic valve stenosis.[49] ARBs are contraindicated in pregnancy.[42] A combination of
ACE inhibitors and ARBs is relatively contraindicated, and other relative contraindications for ARBs
treatment are patients with volume depletion, patients on other medications that cause hyperkalemia, or
patients with abnormal renal function.[42]

Beta-blockers are contraindicated in asthma patients, especially the nonselective beta-blockers. Relative
contraindications are hypotension and bradycardia. They should be avoided in patients with cocaine-
induced coronary artery spasm.[35]

Loop diuretics are contraindicated in patients with hypersensitivity to sulfonamides, anuric patients, and
patients with hepatic coma.[25]

Potassium-sparing diuretics are contraindicated in patients with chronic kidney disease, hyperkalemia,
and caution is necessary when combining them with ACE inhibitors, ARBs, and aliskiren.[50] They are
contraindicated in patients with hypersensitivity to this class.

Clonidine is contraindicated in patients with hypersensitivity to alpha-2 agonists and should be avoided in
patients with depression and recent myocardial infarctions.[43]

Hydralazine is contraindicated if the patient has a history of hydralazine allergy, and in patients with
coronary artery disease, as hydralazine can stimulate the sympathetic system, and in patients with
rheumatic mitral valve disease, as pulmonary artery pressure can increase due to hydralazine
treatment.[51][36]

Minoxidil is contraindicated in pregnant and breastfeeding females, and patients with hypersensitivity to
minoxidil.[48]

Contraindications to alpha-blockers include patients with a history of orthostatic hypotension and patients
on phosphodiesterase inhibitors.[44]

Monitoring

Thiazides and loop diuretics can cause hypokalemia, while potassium-sparing diuretics cause
hyperkalemia.[25][31] Electrolytes should be monitored in patients on diuretics, and uric acid is
recommended to be monitored in patients on thiazides and loop diuretics too.[25][50] Monitoring for
ototoxicity and deafness should be considered in patients on loop diuretics.[25]

Hyperkalemia is common in ACE inhibitors and ARBs treatment, and special caution is required when
they are combined with potassium-sparing diuretics.[49][42] Potassium levels should be closely
monitored in patients with chronic kidney disease when ACE inhibitors, ARBs, or potassium-sparing
diuretics are used.[42] ACE inhibitors and ARBs can cause acute kidney injury, and renal function
requires monitoring.[49][42]

Monitoring for hypotension and edema is necessary for patients on dihydropyridine CCBs. Non-
dihydropyridine CCBs and beta-blockers are known to cause bradycardia, and heart rate requires
monitoring, especially if these two medications are combined. QTc interval needs monitoring in patients
on sotalol.[33][35]

Monitoring for tachyarrhythmias and orthostatic hypotension is a recommendation in patients on alpha-

blockers.[37][44]

Complete blood count and ANA levels are advisable for monitoring when the patient is on hydralazine
treatment.[36] Special caution is necessary if patients develop arthralgia, fever, or other systemic
symptoms.[52]
Toxicity

Thiazides and loop diuretics toxicity can cause electrolyte abnormalities ( mainly hypokalemia and
hyponatremia) and metabolic acidosis (hypochloremic). Severe dehydration can occur. No antidotes are
available for these types of diuretics, and treatment is mainly volume and electrolytes replacement.[25]

Potassium-sparing diuretics toxicity presents as severe hyperkalemia; the main treatment is to stop all
medications that cause elevated potassium levels, IV hydration, IV calcium gluconate, IV insulin with
glucose, sodium bicarbonate and potassium binding resins.[50]

Non-dihydropyridine CCB toxicity occurs due to the decreased ionotropy effect on the cardiac muscle
leading to bradycardia and hypotension. A complete heart block and idioventricular rhythm can
occur.[33] Dihydropyridine CCBs cause peripheral vasodilation and severe hypotension but have less
effect on the heart rate.[33] IV hydration is recommended for hypotension, IV atropine, and external
pacemaker for bradycardia, calcium chloride or calcium gluconate intravenously can help in hypotension
if IV hydration does not improve blood pressure. IV vasopressors can be an option if blood pressure does
not improve.[33]

ACE inhibitors and ARBs toxicity can cause severe hypotension, hyperkalemia, and hyponatremia. No
antidotes are available, IV hydration and management for hyperkalemia are recommended.[34]

Similar to CCBs, beta-blockers cause hypotension and bradycardia and may lead to second or third-
degree AV blocks. IV glucagon is the initial antidote, IV hydration, and external pacemaker may be
required if no response.[35]

Hydralazine toxicity can cause severe hypotension, tachycardia, and skin flushing; in severe cases,
patients may develop cardiac shock or myocardial ischemia. No antidote is available, IV hydration and IV
vasopressors are the intervention for severe cases. Beta-blockers can be used for severe
tachycardia.[36]

Clonidine toxicity can present as lethargy, hypotension, bradycardia, and miosis. In severe cases,
respiratory depression may develop. Treatment is supportive care with hydration and vasopressors,
dopamine and norepinephrine are a common choice in this scenario. IV atropine is an option for severe
bradycardia, and the use of an external pacemaker is reserved for cases resistant to atropine
treatment.[53]

Minoxidil toxicity can cause tachycardia and hypotension. Treatment is supportive with IV hydration and
vasopressors.[48]

Alpha-blockers toxicity can cause severe hypotension, and IV hydration and vasopressors are the primary
treatment option.[54]

Enhancing Healthcare Team Outcomes

Antihypertensives are a broad group of medications, and health care workers are recommended to have
special caution in monitoring adherence and possible adverse reactions of these medications. Treatment
of HTN is essential in preventing cardiovascular disease, and choosing the precise class of medication is
essential to achieve the appropriate control with fewer side effects.An interprofessional team of clinicians,
nurses, and pharmacists is required to monitor patients on these medications. The clinician starts the
antihypertensive regimen; this should be followed by special attention from the pharmacies to check on
the drug-drug interactions, patient adherence to treatment, and to perform medication reconciliation. The
nurse plays a vital role in monitoring the patient's adherence and determining barriers to good response
to the treatment, including monitoring diet and activity levels, and evaluation of the home environment.
Home visiting nurses will be able to monitor blood pressure and heart rate response to the treatment and
to identify early adverse reactions. Both pharmacists and nurses should inform the clinician of any
possible concerns of adherence, adverse reactions, or home environmental changes. This
comprehensive interprofessional team effort helps to achieve the maximal benefits of the regimen and the
best care delivery to the patient and family. [Level V]

Questions

To access free multiple choice questions on this topic, click here.

References
1.
Ettehad D, Emdin CA, Kiran A, Anderson SG, Callender T, Emberson J, Chalmers J, Rodgers
A, Rahimi K. Blood pressure lowering for prevention of cardiovascular disease and death: a
systematic review and meta-analysis. Lancet. 2016 Mar 05;387(10022):957-967. [PubMed:
26724178]
2.
Armstrong C., Joint National Committee. JNC8 guidelines for the management of
hypertension in adults. Am Fam Physician. 2014 Oct 01;90(7):503-4. [PubMed: 25369633]
3.
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