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ACE Inhibitor Drugs (PM 19)

Duration: 53:49

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mauro@*.com

Dec 01 2025, 1:07 pm

Thank You 🙏

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mauro@*.com

Dec 01 2025, 1:07 pm

Thank You 🙏

Join Dr. Mobeen Syed for a detailed exploration of ACE inhibitors (ACEIs), one of the most widely used classes of cardiovascular drugs. This lecture explains why there are so many ACEIs, how they differ in dosage, half-life, absorption, and clearance, and how these differences shape clinical decision-making. From short-acting captopril for hypertensive emergencies to long-acting agents like ramipril and perindopril proven in outcome trials, you will learn how to select the right drug for the right patient. Special attention is given to considerations in renal and hepatic impairment, patient compliance, and IV versus oral use. By the end of this session, you’ll be able to confidently differentiate ACE inhibitors not just by name, but by their real-world pharmacology and clinical pearls.

Objectives:
By the end of this session, learners will be able to:

Explain the rationale for the development of multiple ACE inhibitors and describe their key pharmacological differences (activation, duration, clearance).

Differentiate ACE inhibitors based on duration of action (short, intermediate, long), route of administration (oral vs IV), and prodrug vs active drug status.

Identify clinical considerations in selecting an ACE inhibitor, including:

Hypertensive emergency use (e.g., captopril, enalaprilat IV).

Chronic therapy and patient compliance (once-daily vs multiple-daily dosing).

Impact of renal or hepatic impairment on drug choice (e.g., fosinopril in CKD).

Apply clinical pearls from major outcome studies (e.g., ramipril in HOPE, perindopril in EUROPA) to therapeutic decision-making.

Recognize common adverse effects shared by the ACEI class (cough, angioedema, hyperkalemia) and understand subtle differences in risk.

Objectives:
By the end of this session, learners will be able to:

Explain the rationale for the development of multiple ACE inhibitors and describe their key pharmacological differences (activation, duration, clearance).

Differentiate ACE inhibitors based on duration of action (short, intermediate, long), route of administration (oral vs IV), and prodrug vs active drug status.

Identify clinical considerations in selecting an ACE inhibitor, including:

Hypertensive emergency use (e.g., captopril, enalaprilat IV).

Chronic therapy and patient compliance (once-daily vs multiple-daily dosing).

Impact of renal or hepatic impairment on drug choice (e.g., fosinopril in CKD).

Apply clinical pearls from major outcome studies (e.g., ramipril in HOPE, perindopril in EUROPA) to therapeutic decision-making.

Recognize common adverse effects shared by the ACEI class (cough, angioedema, hyperkalemia) and understand subtle differences in risk.

Following answers are created by ChatGPT. Occasionally the answer may be harmful, incorrect, false, misleading, incomplete, or limited in knowledge of world. Please contact your doctor for all healthcare decisions. Also, double check the answer provided by the AI below.

Faculty

In addition to the presenter, following authors may have helped with the content writing, review, or approval:

CME, CE, CEU and Other Credit Types:

ACCME Accreditation Statement
The DrBeen Corp is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians.

AMA Credit Designation Statement
The DrBeen Corp designates this enduring material for a maximum of 1 AMA PRA Category 1 Credits™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.


Disclosure Information

In accordance with the disclosure policies of DrBeen Corp and the ACCME (Accreditation Council for Continuing Medical Education), we are committed to upholding principles of balance, independence, objectivity, and scientific rigor in all of our Continuing Medical Education (CME) and Continuing Education (CE) activities. These policies include the careful management and mitigation of any relevant financial relationships with organizations that are not eligible.
All members of the Activity Planning Committee and presenters have disclosed their relevant financial relationships. The DrBeen Corp CE Committee has thoroughly reviewed these disclosures and determined that these relationships are not deemed inappropriate in the context of their respective presentations. Additionally, they are found to be consistent with the educational objectives and the integrity of the activity.

Faculty Disclosures
Author declares no conflict of interest.

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