Management Considerations for Acute Coronary Syndromes in Chronic Kidney Disease

Matthew I Tomey1, Janice Y Chyou2

  • 1Mount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, 1190 Fifth Avenue, Box 1030, New York, NY, 10029, USA. matthew.tomey@mountsinai.org.

PubMed

Insights

Patients with chronic kidney disease (CKD) face worse outcomes from acute coronary syndromes (ACS) due to management gaps. Optimizing ACS care in CKD requires addressing underuse of therapies and preventing acute kidney injury.

Area of Science:

  • Cardiology
  • Nephrology
  • Clinical Medicine

Background:

  • Patients with chronic kidney disease (CKD) have a higher propensity for adverse outcomes following acute coronary syndromes (ACS).
  • Underrepresentation in clinical trials and underuse of evidence-based treatments exacerbate the biological risks associated with CKD in ACS patients.
  • Current management strategies for ACS in CKD patients require critical appraisal and optimization.

Purpose of the Study:

  • To critically appraise contemporary evidence regarding the management of ACS in patients with CKD.
  • To offer practical approaches for clinicians to optimize ACS management in this high-risk population.
  • To address the challenges posed by CKD in the context of ACS care.

Main Methods:

  • Narrative review of current evidence.
  • Analysis of updated multisociety chest pain guidelines.
  • Evaluation of evolving tools for predicting and preventing acute kidney injury.
  • Assessment of advancements in percutaneous coronary intervention (PCI) and pharmacotherapy.

Main Results:

  • Updated guidelines highlight diverse ACS presentations, crucial for CKD patient recognition.
  • Improved tools enhance the safety and accessibility of PCI for high-risk CKD patients.
  • Advances in radial access, PCI quality, intravascular imaging, and pharmacotherapy are refining risk-benefit assessments for ACS in CKD.
  • Key opportunities include reducing underuse of therapies, preventing acute kidney injury, and dedicated research for CKD-specific ACS management.

Conclusions:

  • Optimizing ACS management in CKD necessitates addressing underuse of evidence-based therapies and enhancing treatment safety.
  • Preventing acute kidney injury is crucial for improving outcomes in CKD patients undergoing ACS interventions.
  • Further research specifically investigating ACS management in the context of CKD is essential.
Abstract

Related Concept Videos

Factors Affecting Renal Clearance: Renal Impairment01:17

Factors Affecting Renal Clearance: Renal Impairment

Renal dysfunction significantly impairs the renal clearance of drugs, leading to potential complications in drug therapy. Renal failure, which can be caused by various factors, poses a significant challenge in the elimination of drugs from the body.
One condition associated with renal failure is uremia. Uremia is characterized by impaired glomerular filtration and fluid accumulation in the body. This condition hinders the renal clearance of drugs, resulting in drug accumulation and potential...
91
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

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...
429
Renal Failure: Dose Adjustments01:11

Renal Failure: Dose Adjustments

In patients with renal impairment, drugs undergo significant changes in their pharmacokinetics, which require dosage adjustments to ensure safe and effective therapy.
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
88
Heart Failure Drugs: Diuretics01:22

Heart Failure Drugs: Diuretics

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...
375
Factors Affecting Renal Clearance: Drug's Physicochemical Properties and Plasma Levels01:31

Factors Affecting Renal Clearance: Drug's Physicochemical Properties and Plasma Levels

Renal clearance of a drug is influenced by various factors, including its physicochemical properties and plasma levels. These factors play a significant role in determining how efficiently the kidneys eliminate a drug.
One important factor is the drug's molecular size. The kidneys readily excrete smaller molecules below 300 Daltons (Da). On the other hand, molecules weighing between 300 and 500 Da are excreted through both urine and bile. Larger molecules above 500 Da tend to be excreted...
223
Antihypertensive Drugs: Direct Renin Inhibitors01:25

Antihypertensive Drugs: Direct Renin Inhibitors

The renin-angiotensin-aldosterone system (RAAS) is an intricate physiological pathway involving numerous enzymes and hormones, including renin, angiotensin-converting enzyme (ACE), angiotensin I and II, and aldosterone. Imbalances within this system increase the production of angiotensin II and aldosterone. Increased angiotensin II levels promote vasoconstriction and blood pressure elevation. Concurrently, higher aldosterone levels stimulate sodium and water reabsorption in the kidneys,...
625