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Related Concept Videos

Heart Failure Drugs: Inotropic Agents01:26

Heart Failure Drugs: Inotropic Agents

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Positive inotropic agents are commonly used as the first line of treatment for heart failure. One such agent is digoxin, derived from the genus Digitalis, which has been known for centuries but effectively utilized since 1785. However, these cardiac glycosides can have potentially toxic effects due to their mechanism of action, which involves inhibiting Na+/K+-ATPase and increasing contractility. Digoxin is absorbed orally and distributed in various tissues, including the CNS. It has a long...
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Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

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The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
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Heart Failure Drugs: β-Blockers01:22

Heart Failure Drugs: β-Blockers

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β-adrenergic antagonists, commonly known as β-blockers, block the effects of sympathetic neurotransmitters such as noradrenaline (NA) and adrenaline (ADR). They have several beneficial effects in heart failure treatment. They reduce heart rate, the force of contraction, and cardiac muscle relaxation. They also slow the atrial-ventricular conduction rate and raise the threshold for arrhythmias. The concentration of β-blockers determines their effects on bronchodilation,...
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Antiarrhythmic Drugs: Class I Agents as Sodium Channel Blockers01:22

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Class I antiarrhythmic drugs are used to treat various types of arrhythmias or irregular heart rhythms. These drugs block the sodium (Na+) channels in the cardiac cells, thereby affecting the movement of electrical impulses across the heart. Class I antiarrhythmic drugs are divided into three subgroups: Class IA, Class IB, and Class IC, each with distinct mechanisms of action and effects on the heart.
Class 1A Antiarrhythmic Drugs: These drugs work by moderately blocking sodium channels,...
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Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

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Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
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Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

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Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
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A Doxorubicin-induced Cardiomyopathy Model in Adult Zebrafish
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Multiple cardiotoxicities during osimertinib therapy.

Hasan Kobat1, Michael Davidson2, Islam Elkonaissi3

  • 1Department of Pharmacy, School of Life Sciences, Pharmacy and Chemistry, Kingston University London, Kingston Upon Thames, UK.

Journal of Oncology Pharmacy Practice : Official Publication of the International Society of Oncology Pharmacy Practitioners
|March 21, 2023
PubMed
Summary
This summary is machine-generated.

Osimertinib, a treatment for EGFR-mutated lung cancer, can cause cardiac toxicity including QTc prolongation, atrial fibrillation, and heart failure. Early cardiac risk assessment and monitoring are crucial for patient safety.

Keywords:
Lung canceranti-cancer treatmentcardiotoxicitycase reportdrug safety

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Area of Science:

  • Oncology
  • Cardiology
  • Pharmacology

Background:

  • Osimertinib is a tyrosine-kinase inhibitor for metastatic non-small cell lung cancer with EGFR mutations.
  • Patients on osimertinib face an increased risk of cardiac toxicity.
  • This case highlights multiple cardiotoxicities observed during osimertinib therapy.

Purpose of the Study:

  • To report a case of a patient experiencing multiple cardiotoxicities during osimertinib treatment.
  • To emphasize the importance of cardiac monitoring in patients receiving osimertinib.
  • To discuss strategies for mitigating cardiac risks associated with osimertinib therapy.

Main Methods:

  • A 72-year-old male patient with lung adenocarcinoma received osimertinib.
  • The patient developed QTc prolongation, atrial fibrillation, and heart failure during treatment.
  • Cardiac assessments included electrocardiography and echocardiography.

Main Results:

  • The patient experienced QTc prolongation at 15 months of osimertinib therapy.
  • Subsequently, he developed rate-controlled atrial fibrillation and severely impaired left ventricular systolic function (LVEF: 30%).
  • Management involved discontinuing rosuvastatin, initiating antiarrhythmics and heart failure medications, while continuing osimertinib.

Conclusions:

  • Osimertinib therapy requires careful cardiac monitoring.
  • Baseline cardiac risk stratification and assessment of concomitant medications are recommended.
  • Regular electrocardiography and echocardiography surveillance may reduce the risk of cardiac toxicity.