Coronary artery disease and percutaneous coronary intervention in patients with severe chronic kidney disease

Doosup Shin1, Keyvan Karimi Galougahi1, Mandeep Singh2

  • 1Department of Cardiology, St Francis Hospital and Heart Center, Roslyn, New York, USA.

Insights

Coronary artery disease (CAD) in chronic kidney disease (CKD) patients poses risks. Zero-contrast percutaneous coronary intervention (PCI) offers a safer alternative for these high-risk individuals, improving outcomes.

Area of Science:

  • Cardiology
  • Nephrology
  • Interventional Cardiology

Background:

  • Coronary artery disease (CAD) is a major cause of death in chronic kidney disease (CKD) patients.
  • CKD patients often have atypical CAD symptoms and face procedural risks like contrast-induced nephropathy.
  • The fear of renal injury can lead to delayed necessary interventions, termed 'renalism'.

Purpose of the Study:

  • To review the challenges of diagnosing and managing CAD in CKD patients.
  • To explore the limitations of traditional diagnostic and interventional methods.
  • To introduce emerging contrast-sparing techniques for CAD management in CKD.

Main Methods:

  • Review of current literature on CAD in CKD.
  • Discussion of clinical presentations and diagnostic limitations.
  • Overview of ultra-low contrast angiography (ULCA) and zero-contrast percutaneous coronary intervention (PCI).

Main Results:

  • ULCA and zero-contrast PCI demonstrate safety and feasibility, even in complex cases.
  • These techniques minimize or eliminate contrast exposure, reducing renal risks.
  • Emerging contrast-sparing methods show promise for high-risk CKD patients.

Conclusions:

  • Zero-contrast PCI is a potentially essential strategy for revascularization in high-risk CKD patients.
  • These techniques enhance procedural safety while maintaining therapeutic effectiveness.
  • Advancements in contrast-sparing interventions are crucial for improving CAD management in CKD.

Related Concept Videos

Hormonal Regulation01:33

Hormonal Regulation

The renin-aldosterone system is an endocrine system which guides the renal absorption of water and electrolytes, thus managing blood pressure and osmoregulation. Activation of the system begins in the kidneys with a small cluster of cells adjacent to the afferent and efferent blood vessels of the renal corpuscle. As the nephrons are filtering blood, juxtaglomerular cells monitor blood pressure. If they detect a decrease in pressure, they release the hormone renin into the bloodstream.
32.9K
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...
381
Dialysis01:27

Dialysis

Renal failure occurs when the kidneys lose their ability to filter waste products from the blood effectively. It can be classified into two types: acute renal failure (ARF) and chronic renal failure (CRF).
Acute kidney injury develops suddenly and can be caused by pre-renal causes (e.g., hypovolemia, shock), intrinsic renal causes (e.g., acute tubular necrosis), or post-renal causes (e.g., urinary obstruction). In contrast, chronic renal failure progresses gradually over time and is often...
261
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...
62
Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers01:26

Treatment for Pulmonary Arterial Hypertension: Receptor Tyrosine Kinase Inhibitors and Calcium Channel Blockers

Receptor tyrosine kinase inhibitors (TKIs) and calcium channel blockers (CCBs) are two critical categories of drugs employed in the treatment of pulmonary artery hypertension (PAH). PAH is a disease that causes high blood pressure in the pulmonary arteries, resulting in chest pain, fatigue, and shortness of breath.
TKIs, such as imatinib (Gleevec), are particularly effective in tackling the growth and mitogenic factors that become upregulated in PAH patients. These factors contribute to the...
135
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...
338