Benazepril


Continuing Education Activity

Benazepril is a drug used in the management of hypertension. It is in the ACE inhibitor class of medications. This activity outlines the indications, action, and contraindications for benazepril as a valuable agent in managing hypertension (and other disorders when applicable). This activity will highlight the mechanism of action, adverse event profile, and other key factors (e.g., off-label uses, dosing, pharmacodynamics, pharmacokinetics, monitoring, relevant interactions) pertinent for interprofessional healthcare team members in the management of patients with hypertension and related conditions.

Objectives:

  • Outline the indications for initiating therapy with benazepril.
  • Describe the mechanism of action of benazepril.
  • Identify the potential side effects of benazepril therapy.
  • Summarize interprofessional team strategies for improving coordination and communication to improve patient-centered outcomes in patients receiving treatment with benazepril.

Indications

Benazepril hydrochloride is FDA approved for the treatment of hypertension, either alone or in combination with other antihypertensive agents. Benazepril can be combined with thiazide diuretics.[1] 

Mechanism of Action

Reduction of Blood Pressure

Angiotensin-converting enzyme (ACE) plays a critical role in the renin-angiotensin-aldosterone system. This pathway is a process that eventually results in vasoconstriction, increased sympathetic activity, and Na+ retention, which in turn increased water retention and blood pressure. One step in this pathway is the cleavage of angiotensin I to angiotensin II, performed by the ACE enzyme. Therefore, ACE inhibitors block the renin-angiotensin pathway by halting this step, leading to decreased systemic arterial blood pressure and increased Na+ excretion in the urine.[2] ACE inhibitors also play a role in bradykinin metabolism. Bradykinin, a natural vasodilator, is degraded by ACE enzymes into inactive metabolites. However, with the ACE enzyme inhibited, this vasodilator’s effect is preserved, reducing blood pressure.[2]

Attenuation of Adverse Cardiac Remodeling in Heart Failure

In patients with heart failure, the renin-angiotensin-aldosterone system (RAAS) becomes active due to the low cardiac output leading to reduced renal artery perfusion. It activates the RAAS pathway to increase intravascular volume to augment blood pressure, which increases the cardiac output via the Frank-Starling mechanism. However, this attempt at maintaining homeostasis ultimately results in increased preload of the heart, contributing to adverse cardiac remodeling. This cascade can quickly become detrimental and leads to eccentric hypertrophy. ACE inhibitors reduce adverse cardiac remodeling in patients with heart failure.[2]

Patients who adhere to a low-potassium diet, monitor blood pressure and renal function regularly, and adhere to a strict regimen of consistent dosage times with benazepril should expect a lower blood pressure and reduced adverse cardiac remodeling.

Administration

Benazepril should be taken once or twice a day at consistent times, and patients can take it with or without food.[3] There are differences in efficacy in the morning versus afternoon dosages, with morning administration resulting in a more sustained effect (efficacy lasting approximately 19 hours). A total dose of more than 80 mg per day is not studied. Dosage adjustment should be performed to measure peak (2 to 6 hours after dosing) and trough responses. If a single daily dose administration regimen does not give enough trough response, an increase in dosage or divided administration should be considered. If blood pressure is not controlled with benazepril alone, a diuretic can be added. When patients are treated with diuretics, the recommended starting dose of benazepril is 5 mg to avoid excessive hypotension.[4]

Adults

The recommended starting dosage is 10 mg once a day, with a maintenance dosage ranging from 20 to 40 mg per day. Benazepril should be taken once or twice a day at consistent times.[3]

Children

The recommended starting dosage is 0.2 mg/kg once daily, and the maintenance dosage is 0.1 to 0.6 mg/kg once daily. Benazepril should be taken once a day at consistent times.[3]

Renal Impairment

In patients with renal impairment, the recommended starting dose is 5 mg/day in one dosage. The dose is increased in a stepwise manner to achieve the desired blood pressure.[3]

Adverse Effects

Warnings

Head and Neck Angioedema

In the clinical trials, 0.5% of patients experienced angioedema while on benazepril. Angioedema involves the face, tongue, glottis, or larynx, and it can progress to airway obstruction. Benazepril should be discontinued if the patient develops angioedema.[5]

Intestinal Angioedema

Patients presenting with abdominal pain require monitoring for intestinal angioedema. In some patients, abdominal pain can present along with nausea and vomiting. An abdominal CT scan or ultrasound is necessary to diagnose or rule out intestinal angioedema.[5]

Hepatic Failure

ACE inhibitors can rarely cause hepatic failure. This process begins with cholestatic jaundice and progresses to fulminant hepatic necrosis with possible death. Patients on ACE inhibitors who develop jaundice and/or hepatic enzyme elevation should discontinue ACE inhibitors and be monitored closely for signs of hepatic failure.[6]

Neutropenia/Agranulocytosis

In patients with renal impairment and systemic lupus erythematosus (SLE), ACE inhibitors can induce agranulocytosis and bone marrow suppression. If a patient is known to have a collagen-vascular disease associated with reduced renal function, then white blood cell counts should be monitored closely.[7]]

Other Adverse Drug Reactions

Cough

The mechanism of action that causes a dry cough in patients taking ACE inhibitors is related to the reduced bradykinin degradation. Bradykinin (BK) is a known mediator present in the upper respiratory tract, which can cause cough. The incidence of ACE inhibitor-related cough is 5% to 35%.[2][8][9]  

Hypotension

Benazepril has been rarely associated with hypotension in uncomplicated patients with hypertension. Significant hypotension is most likely to occur in patients who have been volume and salt depleted due to diuretic therapy, salt restriction, dialysis, diarrhea, or vomiting. Volume and salt depletion should be corrected before initiating therapy with benazepril. Treatment with benazepril should be restored once the blood pressure and volume are restored.[1][2]

Renal Insufficiency

In patients with volume depletion, hypotension leading to decreased renal perfusion can occur, leading to permanent renal impairment. The prescriber should take action to ensure euvolemia and reduce the dosage of the ACE inhibitor. Furthermore, if a patient has bilateral renal artery stenosis, initiation of an ACE inhibitor therapy can precipitate renal failure due to the reduction of glomerular hydrostatic pressure.[1]

Hyperkalemia

Because ACE inhibitors reduce the serum aldosterone concentration, they can increase serum potassium concentration. Patients with renal insufficiency, diabetes, or patients taking diuretic therapy are at high risk of developing hyperkalemia. [2]

Consider reducing doses of other prescriptions of diuretics, lithium, and potassium, or carefully monitoring for adverse drug reactions. Frequent monitoring of serum lithium levels is recommended when the patient is also given lithium. If a diuretic is used concomitantly, the risk of lithium toxicity may be increased.[3]

Contraindications

Benazepril should not be used when there is a history of hypersensitivity to benazepril or any other ACE inhibitor.[1] 

Benazepril is contraindicated in patients with prior history of angioedema or a history of angioedema caused by ACE inhibitors.[1]

Benazepril is contraindicated in pregnancy, and failure to cease an ACE inhibitor can result in fetal teratogenicity and death. Use of benazepril in the second and third trimesters is associated with fetal and neonatal injury, including hypotension, neonatal skull hypoplasia, anuria, reversible or irreversible renal failure, and death. Infants who have histories of in utero exposure to benazepril should be closely monitored for hypotension, oliguria, and hyperkalemia.[1]]

Do not use benazepril when the patients used valsartan or sacubitril within the last 36 hours.[3] 

Do not use benazepril when patients with diabetes are treated with aliskiren.[3]

Monitoring

To determine proper maintenance dosages, the patient’s blood pressure requires daily monitoring. Benazepril efficacy diminishes after 12 to 19 hours, so blood pressure monitoring should be planned accordingly.[3]The renal function is monitored by regular checkups of serum creatinine, BUN, and potassium. In patients with renal dysfunction, evaluation of baseline kidney function should take place before treatment and afterward at two-week intervals for three months after initiation of treatment.[10][11]

Toxicity

There are no reports of renal failure in patients taking benazepril, and the frequency of neutropenia and proteinuria are insignificant (rates of adverse drug reactions in patients treated with benazepril compared to placebo were statistically insignificant in clinical trials). Compared to other ACE inhibitors, benazepril demonstrated a reduced rate of inducing systematic hypotension and the same rate of inducing adverse drug reactions such as coughing, hyperkalemia, and serum creatinine elevation.[12]

Enhancing Healthcare Team Outcomes

Prescribers starting patients on benazepril for any of its indicated uses should coordinate their efforts with other interprofessional healthcare team members, including clinicians, mid-level practitioners, pharmacists, and nursing staff. Pharmacists should check for appropriate dosing, potential drug interactions, and contraindications. Nurses should help with regular blood pressure checkups and ensure proper administration of the drug, reporting any abnormalities to the team. An interprofessional team approach is always necessary when administering any medication, and benazepril is no exception; this will increase the chances of therapeutic success and minimize adverse drug reactions. [Level 5]


Article Details

Article Author

Sujata Dahal

Article Editor:

Mohit Gupta

Updated:

6/11/2021 9:44:41 AM

PubMed Link:

Benazepril

References

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