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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...
887
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

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Heart failure and kidney perfusion are interconnected in a complex way. Reduced renal perfusion and venous congestion are two significant factors that contribute to renal dysfunction in heart failure. The kidneys, primarily responsible for fluid balance in the body, are adversely affected due to compromised cardiac output and increased venous pressure. In response to reduced renal perfusion, the kidneys activate neurohumoral mechanisms to restore balance. However, these mechanisms can be...
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Pathophysiology of Heart Failure01:17

Pathophysiology of Heart Failure

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Heart failure (HF) is a progressive syndrome involving ventricles that leads to inadequate cardiac output. It can be classified based on location and output or ejection fraction. Ejection fraction (EF) is an essential measurement in the diagnosis and surveillance of HF. Reduced EF corresponds to systolic heart failure (HFrEF). However, HF with preserved ejection fraction (HFpEF) is becoming increasingly prevalent. Also known as diastolic HF, this form of HF is related to aging. The...
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Heart Failure I: Introduction01:27

Heart Failure I: Introduction

179
Heart failure refers to a clinical syndrome caused by structural or functional cardiac disorders that prevent the heart from pumping an adequate amount of blood to meet the body's metabolic needs. This condition often arises from myocardial infarction or ischemia, leading to decreased cardiac output, reduced tissue perfusion, impaired gas exchange, fluid volume imbalance, and decreased functional ability.Heart failure can result from disruptions in the mechanisms that regulate cardiac output...
179
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

133
Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
133
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

635
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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Voltage-Dependent Potassium Current Recording on H9c2 Cardiomyocytes via the Whole-Cell Patch-Clamp Technique
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Hyperkalaemia in Heart Failure.

Umar Ismail1, Kiran Sidhu1, Shelley Zieroth1

  • 1Section of Cardiology, Max Rady College of Medicine, University of Manitoba Winnipeg, Manitoba, Canada.

Cardiac Failure Review
|June 7, 2021
PubMed
Summary
This summary is machine-generated.

New potassium binders, patiromer and sodium zirconium cyclosilicate, offer hope for managing hyperkalemia in heart failure patients. These therapies may enable better use of crucial heart failure medications.

Keywords:
Chronic kidney diseaseheart failurehyperkalaemiapatiromersodium zirconium cyclosilicate

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Area of Science:

  • Cardiology
  • Nephrology
  • Pharmacology

Background:

  • Hyperkalemia is common in heart failure (HF), often exacerbated by RAAS inhibitors and angiotensin-neprilysin inhibitors.
  • Comorbidities like diabetes and chronic kidney disease increase hyperkalemia risk in HF patients.
  • Limited effective therapies previously hindered optimal HF treatment due to hyperkalemia concerns.

Purpose of the Study:

  • To review novel potassium-binding resins for managing hyperkalemia in heart failure.
  • To assess the potential of these agents in facilitating guideline-directed medical therapy.

Main Methods:

  • Review of clinical data on patiromer sorbitex calcium and sodium zirconium cyclosilicate.
  • Analysis of their efficacy and tolerability in hyperkalemia management.
  • Evaluation of their role in optimizing RAAS inhibition in HF patients.

Main Results:

  • Patiromer and sodium zirconium cyclosilicate demonstrate promise in managing recurrent hyperkalemia.
  • These novel resins show potential for improving tolerability of key HF therapies.
  • Their use may allow for achievement of target doses of RAAS inhibitors.

Conclusions:

  • Novel potassium binders offer a new therapeutic option for hyperkalemia in HF.
  • These agents can help overcome treatment limitations imposed by hyperkalemia.
  • Optimized medical therapy for HF patients with hyperkalemia may be achievable.