Chronic kidney disease (CKD) is an independent risk factor for the development of coronary artery disease, and for more severe coronary heart disease (CHD).
CKD is also associated with adverse outcomes in those with existing cardiovascular disease.
This includes increased mortality after an acute coronary syndrome, after percutaneous coronary intervention (PCI) with or without stenting, and after coronary artery bypass. In addition, patients with CKD are more likely to present with atypical symptoms, which may delay diagnosis and adversely affect outcomes.
Managing Heart Failure in Patients on Dialysismagdyelmasry3
•
Heart failure and end-stage kidney disease (ESKD) commonly coexist; 1 comorbidity worsens the prognosis of the other.
•
Although patients with ESKD compose an extremely high-risk population, they have been excluded from landmark clinical trials in heart failure, and there is, thus, a paucity of data regarding the management of heart failure in patients on dialysis.
•
Trial-level evidence is warranted in the future to endorse the efficacy and safety of therapeutic interventions in patients with heart failure and on dialysis. Collaborations between cardiologists and nephrologists are needed to devise an optimal treatment strategy for these patients.
Chronic coronary syndrome (CCS) is a term that defines coronary artery disease as a chronic progressive course. It has been introduced to replace the previous term ‘stable coronary artery disease’.
Managing Heart Failure in Patients on Dialysismagdyelmasry3
•
Heart failure and end-stage kidney disease (ESKD) commonly coexist; 1 comorbidity worsens the prognosis of the other.
•
Although patients with ESKD compose an extremely high-risk population, they have been excluded from landmark clinical trials in heart failure, and there is, thus, a paucity of data regarding the management of heart failure in patients on dialysis.
•
Trial-level evidence is warranted in the future to endorse the efficacy and safety of therapeutic interventions in patients with heart failure and on dialysis. Collaborations between cardiologists and nephrologists are needed to devise an optimal treatment strategy for these patients.
Chronic coronary syndrome (CCS) is a term that defines coronary artery disease as a chronic progressive course. It has been introduced to replace the previous term ‘stable coronary artery disease’.
Coronary heart disease is best addressed by a comprehensive approach aimed at halting atherosclerotic disease and reducing the risk of thrombosis. Unfortunately, our success in optimal risk factor modification in patients with stable CHD remains poor: only 41% of patients achieved all basic goals in the recent ISCHEMIA trial, with success rates likely even lower outside the rigorous clinical trial context. A greater focus on achieving prevention goals in patients with CHD will have a substantial impact on patient outcome and rates of hospitalization and more resources and incentives should be allocated for improved secondary prevention.
The ISCHEMIA trial suggests that even selected, high-risk patients with extensive ischemic burden do not benefit from revascularization barring unacceptable angina despite OMT. As ISCHEMIA excluded patients with unacceptable angina, advanced heart failure, and those with unprotected left main disease, our evaluation may be geared to identify such patients for consideration of revascularization alongside an initial strategy of OMT.
Atherosclerosis is a systemic disease of the arterial circulation, with focal areas of more severe manifestation. From an imaging standpoint, the paradigm of ischemia testing may have come to an end. Recent evidence from COURAGE, PROMISE, SCOT-HEART, and ISCHEMIA has demonstrated that functional testing for inducible myocardial ischemia is inferior to anatomic assessment for risk stratifying and managing patients with suspected or known CHD. Consistent with a large body of evidence, risk from CHD is mediated by the extent of atherosclerotic disease burden and not by the extent of inducible ischemia. Given that 55% of patients had nonobstructive CHD by CT in PROMISE, which was associated with 77% of cardiovascular deaths and myocardial infarctions at follow-up, there is immense opportunity to impact the disease at an earlier stage in a very large population of patients with occult CHD.
Long term outcomes in patients with h fr-ef treated with cabg vs pciRamachandra Barik
RESULTS A total of 12 113 patients (mean [SD] age, 64.8 (11.0) years for the PCI group and 65.6[9.7] years for the CABG group; 5084 (72.5%) male for the PCI group and 4229 (82.9%) malefor the PCI group) were propensity score matched on 30 baseline characteristics: 2397 patients undergoing PCI and 2397 patients undergoing CABG. The median follow-up was 5.2
years (interquartile range, 5.0-5.3). Patients who received PCI had significantly higher rates of
mortality (hazard ratio [HR], 1.6; 95% CI, 1.3-1.7), death from cardiovascular disease (HR 1.4,95% CI, 1.1-1.6), MACE (HR, 2.0; 95% CI, 1.9-2.2), subsequent revascularization (HR, 3.7; 95%
CI, 3.2-4.3), and hospitalization for MI (HR, 3.2; 95% CI, 2.6-3.8) and heart failure (HR, 1.5;95% CI, 1.3-1.6) compared with matched patients who underwent CABG.
Updated Hypertension Management – ESH 2023.pdfDr. Nayan Ray
Hypertension is the most prevalent CV disorder in the world and according to the WHO, it affects 1.28 billion adults aged 30–79 years worldwide, two-thirds living in low-income and middle-income countries.
In 2019, the global age-standardized average prevalence of hypertension in adults aged 30–79 years was reported to be 34% in men and 32% in women.
At younger ages (<50 years), hypertension is more prevalent in men, whereas a steeper increase of SBP in women from their third decade (and more so following menopause) makes the prevalence of hypertension greater in women in older age categories (>65 years).
Rule of Halves
Half the people with high blood pressure are not known (“rule 1”),
Half of those known are not treated (“rule 2”) and
Half of those treated are not controlled (“rule 3”)'
Definition:
Hypertension is defined based on repeated office SBP values ≥ 140 mmHg and/or DBP ≥ 90 mmHg.
Renal function is greatly important in risk stratification, pharmacologic therapy, and the prognosis of patients with heart failure (HF).
The deterioration of heart function can result in the worsening renal function (WRF) and vice versa.
Besides the heart function itself, the Pharmacologic Treatment of HF is closely related to renal function as regards initiation, titration, and discontinuation, making the situation more complex.
More Related Content
Similar to Coronary Revascularization in Chronic Kidney Disease Patient.pptx
Coronary heart disease is best addressed by a comprehensive approach aimed at halting atherosclerotic disease and reducing the risk of thrombosis. Unfortunately, our success in optimal risk factor modification in patients with stable CHD remains poor: only 41% of patients achieved all basic goals in the recent ISCHEMIA trial, with success rates likely even lower outside the rigorous clinical trial context. A greater focus on achieving prevention goals in patients with CHD will have a substantial impact on patient outcome and rates of hospitalization and more resources and incentives should be allocated for improved secondary prevention.
The ISCHEMIA trial suggests that even selected, high-risk patients with extensive ischemic burden do not benefit from revascularization barring unacceptable angina despite OMT. As ISCHEMIA excluded patients with unacceptable angina, advanced heart failure, and those with unprotected left main disease, our evaluation may be geared to identify such patients for consideration of revascularization alongside an initial strategy of OMT.
Atherosclerosis is a systemic disease of the arterial circulation, with focal areas of more severe manifestation. From an imaging standpoint, the paradigm of ischemia testing may have come to an end. Recent evidence from COURAGE, PROMISE, SCOT-HEART, and ISCHEMIA has demonstrated that functional testing for inducible myocardial ischemia is inferior to anatomic assessment for risk stratifying and managing patients with suspected or known CHD. Consistent with a large body of evidence, risk from CHD is mediated by the extent of atherosclerotic disease burden and not by the extent of inducible ischemia. Given that 55% of patients had nonobstructive CHD by CT in PROMISE, which was associated with 77% of cardiovascular deaths and myocardial infarctions at follow-up, there is immense opportunity to impact the disease at an earlier stage in a very large population of patients with occult CHD.
Long term outcomes in patients with h fr-ef treated with cabg vs pciRamachandra Barik
RESULTS A total of 12 113 patients (mean [SD] age, 64.8 (11.0) years for the PCI group and 65.6[9.7] years for the CABG group; 5084 (72.5%) male for the PCI group and 4229 (82.9%) malefor the PCI group) were propensity score matched on 30 baseline characteristics: 2397 patients undergoing PCI and 2397 patients undergoing CABG. The median follow-up was 5.2
years (interquartile range, 5.0-5.3). Patients who received PCI had significantly higher rates of
mortality (hazard ratio [HR], 1.6; 95% CI, 1.3-1.7), death from cardiovascular disease (HR 1.4,95% CI, 1.1-1.6), MACE (HR, 2.0; 95% CI, 1.9-2.2), subsequent revascularization (HR, 3.7; 95%
CI, 3.2-4.3), and hospitalization for MI (HR, 3.2; 95% CI, 2.6-3.8) and heart failure (HR, 1.5;95% CI, 1.3-1.6) compared with matched patients who underwent CABG.
Updated Hypertension Management – ESH 2023.pdfDr. Nayan Ray
Hypertension is the most prevalent CV disorder in the world and according to the WHO, it affects 1.28 billion adults aged 30–79 years worldwide, two-thirds living in low-income and middle-income countries.
In 2019, the global age-standardized average prevalence of hypertension in adults aged 30–79 years was reported to be 34% in men and 32% in women.
At younger ages (<50 years), hypertension is more prevalent in men, whereas a steeper increase of SBP in women from their third decade (and more so following menopause) makes the prevalence of hypertension greater in women in older age categories (>65 years).
Rule of Halves
Half the people with high blood pressure are not known (“rule 1”),
Half of those known are not treated (“rule 2”) and
Half of those treated are not controlled (“rule 3”)'
Definition:
Hypertension is defined based on repeated office SBP values ≥ 140 mmHg and/or DBP ≥ 90 mmHg.
Renal function is greatly important in risk stratification, pharmacologic therapy, and the prognosis of patients with heart failure (HF).
The deterioration of heart function can result in the worsening renal function (WRF) and vice versa.
Besides the heart function itself, the Pharmacologic Treatment of HF is closely related to renal function as regards initiation, titration, and discontinuation, making the situation more complex.
Cardiac arrest is the cessation of functional cardiac contraction and is the final common pathway in death from any pathology.
In the clinical context, cardiac arrest refers to the sudden loss of cardiac output that prompts an emergency response.
Pathogenesis, prognosis and management of in-hospital and out-of-hospital cardiac arrest are subtly different; however, the basic principles of cardiopulmonary resuscitation (CPR) are to maintain forward flow of oxygenated blood, correct the causative factor and restore spontaneous circulation.
CVD Risk Managemnt- Focus on HTN & Dys.pdfDr. Nayan Ray
Cardiovascular disease is a major cause of disability and premature death throughout the world and contributes substantially to the escalating costs of health care.
The underlying pathology is atherosclerosis, which develops over many years and is usually advanced by the time symptoms occur, generally in middle age.
Acute coronary and cerebrovascular events frequently occur suddenly and are often fatal before medical care can be given.
Modification of risk factors has been shown to reduce mortality and morbidity in people with diagnosed or undiagnosed cardiovascular disease.
In patients with coronary artery disease (CAD), percutaneous coronary interventions (PCI) are the cornerstone of treatment for those presenting with an acute coronary syndrome (ACS); PCI has also been largely adopted in patients with chronic coronary syndromes (CCS).
Adjunctive pharmacotherapy, in particular antithrombotic therapy, has a pivotal role in optimising outcomes in patients undergoing PCI23. In fact, patients undergoing PCI may develop both acute and long-term ischaemic events.
Therefore, antithrombotic drugs, in particular antiplatelet agents, are key to the treatment and prevention of both local and systemic thrombotic complications.
Having more than two year experiences, presently anticoagulant is an essential component of management of COVID 19
Its role is recommended in moderate to severe to critically ill patients with different opinion in the dosage
Giving anticoagulants in asymptomatic or mild cases is still need to be validated though there are suggestions in favor.
There is recommendation for post discharge patients who had clinically suspected/established thromboembolism events
Dyslipidemia in Chronic Kidney Diseases.pdfDr. Nayan Ray
Dyslipidaemia in Chronic Kidney Disease: An Approach to Pathogenesis and Treatment
Slides Include:
1. Stages of CKD
2. Developments of atherogenesis
3. Lipoprotein in CKD
4. Drug Therapies
5.Summary KDIGO Guideline
Management of HTN according to gender. This slides will answer some questions such as
1. Why there is BP variability difference between male and female?
2. What's the regulatory mechanism of HTN in gender?
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
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Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
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Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
2. NYN/DMA/BPL
Introduction
• Chronic kidney disease (CKD) is an independent risk factor for the
development of coronary artery disease, and for more severe coronary
heart disease (CHD).
• CKD is also associated with adverse outcomes in those with existing
cardiovascular disease.
• This includes increased mortality after an acute coronary syndrome,
after percutaneous coronary intervention (PCI) with or without stenting,
and after coronary artery bypass. In addition, patients with CKD are
more likely to present with atypical symptoms, which may delay
diagnosis and adversely affect outcomes.
https://www.uptodate.com/contents/chronic-kidney-disease-and-coronary-heart-disease#H4
3. NYN/DMA/BPL
ETIOLOGY.
• As glomerular filtration
rate (GFR) declines below
w60 to 75 ml/min/1.73 m2,
the probability of
developing CAD increases
linearly and patients with
CKD stages G3a to G4 (15-
60 ml/min/1.73 m2) have
approximately double and
triple the CVD mortality
risk, respectively, relative
to patients without CKD.
Sarnak et al.
CKD and Coronary Artery Disease: A KDIGO Conference Report
J A C C VO L . 7 4 , N O . 1 4 , 2 0 1 9
4. NYN/DMA/BPL
Prevalence
• The prevalence of CHD in 2016 was 42 and 34 percent among patients
on hemodialysis and peritoneal dialysis, respectively. When stratified by
age, younger patients (22 to 44 years old) had a lower prevalence of
CHD than older patients (>45 years old; 15 to 20 versus 33 to 53 percent,
respectively).
• The prevalence of acute myocardial infarction was 14 and 12 percent
among hemodialysis and peritoneal dialysis patients, respectively.
• In 2016, the adjusted mortality rate was 166 per 1000 patient-years for
hemodialysis patients and 154 per 1000 patient-years for peritoneal
dialysis patients. Cardiac disease accounted for 37 percent of deaths, of
which 11 percent were attributed to acute myocardial infarction and
CHD and 78 percent to arrhythmia and cardiac arrest. The two-year
mortality rate was 34 percent for patients with CHD compared with 18
percent in those without CHD.
6. Data Source: Special analyses, Medicare 5% sample. Abbreviations: AF, atrial fibrillation; AMI, acute myocardial infarction; CAD, coronary artery disease; CKD,
chronic kidney disease; CVA/TIA, cerebrovascular accident/transient ischemic attack; CVD, cardiovascular disease; HF, heart failure; PAD, peripheral arterial
disease; SCA/VA, sudden cardiac arrest and ventricular arrhythmias; VHD, valvular heart disease; VTE/PE, venous thromboembolism and pulmonary embolism
Prevalence of common cardiovascular diseases in patients with or
without CKD, 2016
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
7. Prevalence of (a) cardiovascular comorbidities & (b) annual incidence of cardiovascular
procedures, by CKD status, age, race, & sex, 2016
(a) Cardiovascular comorbidities
# Patients
% Patients
Overall 66-69 70-74 75-84 85+ White Blk/Af Am Other Male Female
Any CVD
Without CKD 1,086,232 32.4 19.8 27.3 39.2 52.1 33.4 28.7 23.8 36.3 29.5
Any CKD 175,840 64.5 50.0 56.9 66.9 76.5 65.3 62.1 57.3 68.1 61.0
Coronary artery disease (CAD)
Without CKD 1,086,232 15.6 10.0 13.9 19.4 22.1 16.2 12.3 11.9 21.2 11.5
Any CKD 175,840 37.9 29.3 34.4 40.2 42.8 38.8 33.2 33.3 45.0 31.1
Acute myocardial infarction (AMI)
Without CKD 1,086,232 2.3 1.6 2.1 2.7 3.4 2.4 1.9 1.6 3.1 1.7
Any CKD 175,840 9.3 8.1 8.5 9.5 10.4 9.5 8.2 7.6 11.0 7.6
Heart failure (HF)
Without CKD 1,086,232 6.1 3.1 4.3 7.2 13.3 6.2 7.1 4.2 6.5 5.9
Any CKD 175,840 25.9 18.3 20.1 25.7 36.1 25.9 28.4 21.5 25.9 25.9
Valvular heart disease (VHD)
Without CKD 1,086,232 5.1 2.6 3.9 6.6 9.3 5.4 3.4 3.5 5.0 5.2
Any CKD 175,840 12.8 7.5 9.3 13.6 18.1 13.4 10.1 10.2 12.8 12.9
Cerebrovascular accident/transient ischemic attack (CVA/TIA)
Without CKD 1,086,232 6.7 3.7 5.5 8.6 11.0 6.8 7.2 4.9 6.9 6.6
Any CKD 175,840 16.1 11.4 13.8 17.5 18.9 15.9 18.6 14.7 16.4 15.8
Peripheral artery disease (PAD)
Without CKD 1,086,232 9.7 4.8 7.1 11.6 20.1 9.8 10.6 7.1 10.0 9.4
Any CKD 175,840 25.2 17.4 20.9 26.0 32.8 25.3 26.3 22.2 26.6 24.0
Atrial fibrillation (AF)
Without CKD 1,086,232 9.8 4.4 7.0 12.5 19.8 10.5 4.8 5.3 11.2 8.7
Any CKD 175,840 23.8 13.5 17.3 25.3 33.7 25.5 15.0 15.6 26.1 21.6
Cardiac arrest and ventricular arrhythmias (SCA/VA)
Without CKD 1,086,232 1.4 1.0 1.4 1.8 1.8 1.5 1.1 0.9 2.0 1.0
Any CKD 175,840 4.1 3.4 3.9 4.4 4.3 4.1 4.5 3.0 5.5 2.8
Venous thromboembolism and pulmonary embolism (VTE/PE)
Without CKD 1,086,232 1.2 0.8 1.0 1.3 1.8 1.2 1.3 0.6 1.2 1.1
Any CKD 175,840 3.7 3.3 3.4 3.8 4.2 3.7 5.1 2.2 3.7 3.8
2018 Annual Data Report
Volume 1 CKD, Chapter 4
Data Source: Special analyses, Medicare 5%
sample. Patients aged 66 and older, alive,
without end-stage renal disease, and residing
in the United States on 12/31/2016with fee-
for-service coverage for the entire calendar
year. Abbreviations: AF, atrial fibrillation; AMI,
acute myocardial infarction; Blk/Af Am, Black
African American; CABG, coronary artery
bypass grafting; CAD, coronary artery disease;
CAS/CEA, carotid artery stenting and carotid
endarterectomy; CKD, chronic kidney disease;
CVA/TIA, cerebrovascular accident/transient
ischemic attack; CVD, cardiovascular disease;
HF, heart failure; ICD/CRT-D, implantable
cardioverter defibrillators/cardiac
resynchronization therapy with defibrillator
devices; PAD, peripheral arterial disease; PCI,
percutaneous coronary interventions; SCA/VA,
sudden cardiac arrest and ventricular
arrhythmias; VHD, valvular heart disease;
VTE/PE, venous thromboembolism and
pulmonary embolism. (a) The denominators for
overall prevalence of all cardiovascular
comorbidities were Medicare enrollees aged
66+ by CKD status. (b) The denominators for
overall prevalence of PCI and CABG were
Medicare enrollees aged 66+ with CAD by CKD
status. The denominators for overall prevalence
of ICD/CRT-D were Medicare enrollees aged
66+ with HF by CKD status. The denominators
for overall prevalence of CAS/CEA were
Medicare enrollees aged 66+ with CAD,
CVA/TIA, or PAD by CKD status
8. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease, and residing in the United States on 12/31/2016 with fee-for-service coverage for the entire calendar year. Abbreviations: AF, atrial fibrillation; AMI, acute
myocardial infarction; Blk/Af Am, Black African American; CABG, coronary artery bypass grafting; CAD, coronary artery disease; CAS/CEA, carotid artery stenting and carotid endarterectomy; CKD, chronic kidney disease; CVA/TIA, cerebrovascular accident/transient ischemic
attack; CVD, cardiovascular disease; HF, heart failure; ICD/CRT-D, implantable cardioverter defibrillators/cardiac resynchronization therapy with defibrillator devices; PAD, peripheral arterial disease; PCI, percutaneous coronary interventions; SCA/VA, sudden cardiac arrest and
ventricular arrhythmias; VHD, valvular heart disease; VTE/PE, venous thromboembolism and pulmonary embolism. (a) The denominators for overall prevalence of all cardiovascular comorbidities were Medicare enrollees aged 66+ by CKD status. (b) The denominators for
overall prevalence of PCI and CABG were Medicare enrollees aged 66+ with CAD by CKD status. The denominators for overall prevalence of ICD/CRT-D were Medicare enrollees aged 66+ with HF by CKD status. The denominators for overall prevalence of CAS/CEA were
Medicare enrollees aged 66+ with CAD, CVA/TIA, or PAD by CKD status.
Prevalence of (a) cardiovascular comorbidities & (b) annual incidence of cardiovascular
procedures, by CKD status, age, race, & sex, 2016 (continued)
NYN/DMA/BPL
(b) Cardiovascular procedures
# Patients
% Patients
Overall 66-69 70-74 75-84 85+ White
Blk/Af
Am
Other Male Female
Revascularization – percutaneous coronary interventions (PCI)
Without CKD 169,959 2.1 3.0 2.5 1.9 1.3 2.1 1.5 2.2 2.2 2.0
Any CKD 66,659 3.1 4.1 3.5 3.4 2.0 3.1 2.9 3.3 3.2 2.9
Revascularization – coronary artery bypass graft (CABG)
Without CKD 169,959 1.1 1.8 1.5 1.0 0.2 1.1 0.6 1.3 1.3 0.7
Any CKD 66,659 1.5 2.7 2.4 1.6 0.3 1.6 1.0 1.0 2.0 0.9
Implantable cardioverter defibrillators & cardiac resynchronization therapy with defibrillator (ICD/CRT-D)
Without CKD 66,426 0.6 0.6 0.8 0.6 0.3 0.6 0.4 0.6 0.8 0.4
Any CKD 45,552 1.0 1.5 1.4 1.1 0.6 1.0 1.4 1.0 1.4 0.7
Carotid artery stenting and carotid artery endarterectomy (CAS/CEA)
Without CKD 268,808 0.5 0.6 0.7 0.6 0.2 0.6 0.3 0.4 0.6 0.4
Any CKD 93,656 0.7 0.8 0.8 0.8 0.4 0.7 0.4 0.6 0.8 0.6
2018 Annual Data Report
Volume 1 CKD, Chapter 4
9. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(a) Coronary artery disease (CAD)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
10. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(b) Acute myocardial infarction (AMI)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
11. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(c) Heart failure (HF)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
12. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(d) Valvular heart disease (VHD)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
13. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(e) Cerebrovascular accident/transient ischemic attack (CVA/TIA)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
14. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(f) Peripheral arterial disease (PAD)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
15. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(g) Atrial fibrillation (AF)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
16. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(h) Sudden cardiac arrest and ventricular arrhythmias (SCA/VA)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
17. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal
disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire calendar year.
Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
(i) Venous thromboembolism and pulmonary embolism (VTE/PE)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
18. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease, and residing in the
United States on 12/31/2016 with fee-for-service coverage for the entire calendar year. Abbreviation: CKD, chronic kidney disease.
Heart failure in patients with or without CKD, 2016
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
19. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease, and
residing in the United States on 12/31/2014 with fee-for-service coverage for the entire calendar year. Survival was adjusted for
age, sex, race, diabetic status, and hypertension status. Abbreviation: CKD, chronic kidney disease.
Adjusted survival of patients by CKD and heart failure status, 2015-2016
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
20. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage
renal disease, and residing in the United States on 12/31/2014, with fee-for-service coverage for the entire
calendar year. Abbreviations: AF, atrial fibrillation; AMI, acute myocardial infarction; CAD, coronary artery
disease; CKD, chronic kidney disease; CVA/TIA, cerebrovascular accident/transient ischemic attack; HF, heart
failure; PAD, peripheral arterial disease; SCA/VA, sudden cardiac arrest and ventricular arrhythmias; VHD,
valvular heart disease; VTE/PE, venous thromboembolism and pulmonary embolism.
Two-year survival of patients with a prevalent cardiovascular disease, by CKD status,
adjusted for age and sex, 2015-2016
NYN/DMA/BPL
CKD status
Cardiovascular
disease
No CKD
(%)
CKD
(%)
Stages 1 to 2
(%)
Stage 3
(%)
Stages 4 to 5
(%)
CAD 87.4 76.6 81.1 77.6 67.4
AMI 81.7 68.5 74.5 69.0 58.6
HF 75.6 64.6 70.2 65.8 55.7
VHD 86.3 72.1 78.2 72.8 61.1
CVA/TIA 83.3 73.2 76.8 74.6 64.1
PAD 81.3 72.3 76.4 73.6 61.7
AF 82.9 70.0 75.6 71.0 59.6
SCA/VA 86.0 68.8 75.4 68.7 57.9
VTE/PE 81.4 69.6 75.4 71.2 59.3
2018 Annual Data Report
Volume 1 CKD, Chapter 4
21. RISK FACTORS
• Traditional risk factors
• Diabetes (54 percent),
• Low serum high-density lipoprotein (HDL) cholesterol (33
percent),
• Hypertension (96 percent),
• Left ventricular hypertrophy by electrocardiographic criteria (22
percent),
• low physical activity (80 percent), and
• Increased age.
NYN/DMA/BPL
Risk factors and epidemiology of coronary heart disease in end-stage kidney disease
22. Risk factors unique to chronic kidney disease
•Chronic kidney disease alone
•Uremia and renal replacement therapy
•Disorders of mineral metabolism
NYN/DMA/BPL
23. Putative mechanisms of CAD in CKD.
NYN/DMA/BPL
Clinical and Experimental Nephrology (2019) 23:725–732
https://doi.org/10.1007/s10157-019-01718-5
24. CAC in CKD
• Vascular calcification is commonly observed in CKD, because, in addition to
several classical risk factors, patients with CKD also have certain unconventional
risk factors of vascular calcification
• Among the various risk factors, mineral bone disorder is believed to be the most
crucial factor for patients with CKD.
• The underlying mechanisms include the role of elevated serum phosphate levels,
parathyroid hormone levels, and fibroblast growth factor 23 levels as well as
decreased active vitamin D and klotho.
• Although these factors exert a considerable influence on the progression of
vascular calcification in CKD, phosphate is the most important factor
• The supposed mechanisms of vascular calcification involve the transformation of
vascular smooth muscle cells into osteoblast-like cells by the uptake of
phosphorus into cells through sodium-dependent phosphorus co-transporters
and decrease of inhibitors against vascular calcification
NYN/DMA/BPL
Clinical and Experimental Nephrology (2019) 23:725–732
https://doi.org/10.1007/s10157-019-01718-5
25. • Even in the general population, serum phosphate levels are significantly associated
with CAC prevalence [36]. Serum phosphate levels are also significantly associated
with not only increased CAD, but also increased the other CVD events.
• Furthermore, the results of a meta-analysis have demonstrated that the presence of
vascular calcification is significantly associated with higher CVD events and mortality
NYN/DMA/BPL
Clinical and Experimental Nephrology (2019) 23:725–732
https://doi.org/10.1007/s10157-019-01718-5
26. Treatment of CAD in CKD
• In general, aggressive treatment for CAD involves percutaneous
coronary intervention (PCI) and coronary artery bypass grafting
(CABG).
• It is very challenging to decide which treatment is better for patients
with CKD, and the strategy is controversial.
• PCI is a treatment for a local vascular lesion, and CABG is a treatment
for the total vessel.
NYN/DMA/BPL
Clinical and Experimental Nephrology (2019) 23:725–732
https://doi.org/10.1007/s10157-019-01718-5
28. Indications for revascularization
• Stable CAD
• Persistent angina despite OMT
• Possible survival benefit (LM disease, 3v CAD, 2v CAD involving
proximal LAD)
• NSTE-ACS
• Early invasive strategy if refractory angina, hemodynamic instability
without comorbidities such as CKD
• Early invasive strategy not recommended if kidney failure, because
risks likely outweigh benefits (Class IIIC recommendation)
• Invasive strategy reasonable in patients with CKD stages G2 to G3b
(Class IIA recommendation)
• Early invasive strategy for STEMI
NYN/DMA/BPL
29. PCI
• Percutaneous coronary intervention (PCI) in patients with significant
renal dysfunction is challenging because of the lesion characteristics
and the risk of contrast-induced acute kidney injury (CI-AKI).
• Indication:
(1) An emergency case,
(2) Early-to-moderate stage CKD,
(3) High risk involved in surgical approach, (4)
(4) Short expected life span, and
(5) Contraindication for CABG (single-vessel disease or two-vessel
disease except for left anterior descending and/or left main
trunk).
NYN/DMA/BPL
Clinical and Experimental Nephrology (2019) 23:725–732
https://doi.org/10.1007/s10157-019-01718-5
30. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease,
and residing in the United States on the index date, which was the date of the first procedure claim, with fee-for-service
coverage for the entire year prior to this date. Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a cardiovascular procedure, by CKD
status, adjusted for age and sex, 2014-2016
(a) Percutaneous coronary interventions (PCI)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
31. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease,
and residing in the United States on the index date, which was the date of the first procedure claim, with fee-for-service
coverage for the entire year prior to this date. Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a cardiovascular procedure, by CKD status,
adjusted for age and sex, 2014-2016
(b) Coronary artery bypass grafting (CABG)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
33. NYN/DMA/BPL
Study type: Retrospective Analysis
Data Source & Time : 2006–2012 National In patient Sample Database
Population Size: 579,747 for NSTE-ACS and 293,950 admissions
for STEMI
Results: Performance of PCI increased over time among patients
presenting with NSTE-ACS and STEMI in the presence of advanced CKD
and independently predicted lower in-hospital mortality.
37. • Objective. To assess the safety and short-term outcomes of IVUS-
guided zero-contrast PCI in chronic kidney disease (CKD) patients
with complex demographics or lesion morphology
• Results. A total of 15 patients (27 vessels), all men (mean age, 70.0 ±
11.0 years), underwent zero-contrast PCI. )e mean estimated
glomerular filtration rate (eGFR) and serum creatinine were 30.8 ±
7.3 mL/min/1.73m2 and 2.6 ± 1.3 mg/dL, respectively. )e mean BMC2
risk for dialysis was 2.1 ± 1.1%, mean SYNTAX score was 20.3 ± 10.3,
and mean left ventricular ejection fraction (LVEF) was 42.4 ± 11.6%.
Four patients (26.6%) underwent left main coronary artery (LMCA)
PCI including one LMCA bifurcation. One patient underwent chronic
total occlusion PCI. Technical and procedural success were 100%
without any periprocedural complications. No major adverse
cardiovascular events (MACE) were reported, and no patient required
dialysis within three months of follow-up.
NYN/DMA/BPL
38. Methods
Study Design and Population:
This was a prospective single-center observational study. Clinical and
procedural data were obtained from all consecutive patients who
underwent zero-contrast PCI at our tertiary care center between
November 2019 and May 2020. Percutaneous coronary intervention
was planned in patients with significant stenosis (angiographic
diameter stenosis ≥70% in non- LMCA and ≥50% in LMCA, IVUS
measured minimal luminal area of <6mm2 in LMCA lesions, or flow
fraction reserve [FFR] ≤ 0.8) and indication for revascularization.
Patients underwent “zero-contrast PCI” if they had met any of the
following criteria: (1) eGFR < 30 mL/min/1.73m2; (2) eGFR < 45
mL/min/1.73m2 (Stage 3b, 4, and 5 CKD) among patients aged >75
years or with left ventricular ejection fraction (LVEF) < 35%.
NYN/DMA/BPL
39. Procedures
• A detailed history was collected along with baseline clinical
characteristics and laboratory investigations.
• Baseline echocardiography and electrocardiographic changes were
recorded before the procedure to facilitate the detection of changes
during the procedure. Standard techniques and catheters were used
during the PCI procedure.
• All procedures were carried out by a single operator with an
experience of 200 LMCA PCI and 150 chronic total occlusion (CTO)
PCI per year.
• Procedures were performed via femoral access and 7F guide
catheters in all cases, except for one, where a 6F catheter and radial
access was used. Stenting strategy (particularly in bifurcation lesions),
lesion preparation, the number of stents, and postdilatation were left
to the operator’s discretion.
NYN/DMA/BPL
40. NYN/DMA/BPL
• In general, rotational atherectomy was used when IVUS detected calcium arc
>180° and calcium length ≥5 mm.
• Post-dilatation was performed mostly using noncompliant (NC) balloons.
Informed consent was obtained from all patients before the procedure.
• Blood transfusion was planned if postprocedure hemoglobin had reduced to 8
gm%. Boston scientific iLAB ultrasound imaging system with OptiCross 6
coronary imaging catheter (40 MHz) was used for IVUS runs. The study was
approved by the institutional review board.
47. Conclusion
IVUS-guided zero-contrast PCI was found to be feasible and safe in CAD
patients with moderate-to-severe CKD when done by experts. )is
technique can be used safely in patients who are at high risk for CI-AKI,
in centers where there is expertise for the performance of complex PCI
with intravascular imaging guidance.
NYN/DMA/BPL
48. NYN/DMA/BPL
OBJECTIVES: This study investigated the comparative effectiveness of
percutaneous coronary intervention (PCI) versus coronary artery bypass graft
(CABG) surgery in patients with LMCAD and low or intermediate anatomical
complexity according to baseline renal function from the multicenter
randomized EXCEL (Evaluation of XIENCE Versus Coronary Artery Bypass Surgery
for Effectiveness of Left Main Revascularization) trial.
49. • METHODS CKD was defined as an estimated glomerular filtration rate
<60 ml/min/1.73 m2 using the CKD Epidemiology Collaboration
equation. Acute renal failure (ARF) was defined as a serum creatinine
increase $5.0 mg/dl from baseline or a new requirement for dialysis.
The primary composite endpoint was the composite of death,
myocardial infarction (MI), or stroke at 3-year follow-up.
NYN/DMA/BPL
50. NYN/DMA/BPL
The left y-axis refers to the histogram of the number of patients with estimated glomerular
filtration rate (eGFR) per 5 ml/min/1.73 m2 increments. The right y-axis refers to the cumulative
frequency distribution curve of eGFR values. The median (25%, 75%) eGFR was 79.2 (64.0, 91.3)
ml/min/1.73 m2, and the mean SD eGFR was 77.2 +- 19.1 ml/min/1.73 m2 (range 6.5 to 139.2
ml/min/1.73 m2).
CKD-EPI ¼ Chronic Kidney Disease Epidemiology Collaboration.
52. Gennaro Giustino et al. J Am Coll Cardiol 2018; 72:754-765.
3-Year Outcomes for PCI Versus CABG in Patients With or Without CKD
53. CONCLUSIONS
• Patients with CKD undergoing revascularization for LMCAD in the
EXCEL trial had increased rates of ARF and reduced event-free
survival. ARF occurred less frequently after PCI compared with CABG.
There were no significant differences between PCI and CABG in terms
of death, stroke, or MI at 3 years in patients with and without CKD.
NYN/DMA/BPL
(EXCEL Clinical Trial [EXCEL]; NCT01205776) (J Am
Coll Cardiol 2018;72:754–65)
56. Conclusions
• PCI for patients with CKD and multi-vessel disease (multi-vessel CAD)
had advantages over CABG with regard to short-term all-cause death
and cerebrovascular accidents, but disadvantages regarding the risk
of myocardial death, MI, and RR; there was no significant difference
in the risk of long-term all-cause death and MACCE. Large
randomized controlled trials are needed to confirm our findings.
NYN/DMA/BPL
58. NYN/DMA/BPL
Population Criteria: Cohort of 4,687 adults who
underwent cardiac catheterization, had a serum
creatinine value measured within 30 days, and had
more than one vessel with ≥50% stenosis.
59. • Compared with medical management, CABG was associated with a reduced
risk of death for patients of any nondialysis CKD severity (HR range 0.43–
0.59).
• There were no significant mortality differences between CABG and PCI,
except a decreased death risk in CABG-treated severe CKD patients (HR
range 0.54–0.55).
• Compared with medical management and PCI, CABG was associated
• with a lower risk of death, MI, or revascularization in non-dialysis CKD
patients (HR range
• 0.41–0.64).
• There were similar associations between eGFR decrease and mortality
increase across all multi-vessel CAD patient treatment groups.
• When accounting for treatment propensity, surgical revascularization was
associated with improved outcomes in patients of all CKD severities
NYN/DMA/BPL
60. PCI vs. CABG for multivessel disease in
patients with CKD
• Data from mainly nonrandomized studies
Non dialysis CKD patients
• Short term: higher risk of death, stroke, AKI with CABG vs. PCI
• Long term: similar risk of death but higher MI and repeat
• revascularization with PCI when compared with CABG
Dialysis patients
• Short term: higher risk of death and stroke with CABG vs. PCI
• Long term: higher risk of death, MI, and repeat revascularization
• with PCI when compared with CABG
NYN/DMA/BPL
61. Prevention of AKI in PCI vs. CABG
• No benefit of bicarbonate and/or NAC on reduction of AKI over
normal saline
• Risk of dialysis-dependent AKI low with ultra-low volume contrast
strategies and hydration
• Risk of AKI considerably higher with CABG than PCI
• Preservation of residual kidney function by prevention of AKI critical
for PD and perhaps for HD patients
• Recommended strategies to reduce risk include stopping offending
drugs (e.g., NSAID, diuretics), hydration, titrating BP to maintain
perfusion during surgery, low contrast volumes and/or zero contrast
PCI
• Rates of CI-AKI are low in high-risk patients—should rarely be a
reason to withhold needed PCI in CKD patients
NYN/DMA/BPL
62. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease,
and residing in the United States on the index date, which was the date of the first procedure claim, with fee-for-service
coverage for the entire year prior to this date. Abbreviation: CKD, chronic kidney disease.
Probability of survival of patients with a cardiovascular procedure, by CKD status,
adjusted for age and sex, 2014-2016
(d) Carotid artery stenting and carotid endarterectomy (CAS/CEA)
NYN/DMA/BPL
2018 Annual Data Report
Volume 1 CKD, Chapter 4
63. Data Source: Special analyses, Medicare 5% sample. Patients aged 66 and older, alive, without end-stage renal disease, and residing
in the United States on the index date, which was the date of the first procedure claim, with fee-for-service coverage for the entire
year prior to this date. Abbreviations: CABG, coronary artery bypass grafting; CAS/CEA, carotid artery stenting and carotid
endarterectomy; CKD, chronic kidney disease; ICD/CRT-D, implantable cardioverter defibrillators/cardiac resynchronization therapy
with defibrillator devices; PCI, percutaneous coronary interventions.
Two-year survival of patients with a cardiovascular procedure, by CKD
status, adjusted for age and sex, 2014-2016
NYN/DMA/BPL
CKD status
Cardiovascular
procedure
No CKD
(%)
CKD
(%)
Stages 1 to 2
(%)
Stage 3
(%)
Stages 4 to 5
(%)
PCI 83.2 73.0 76.3 74.1 64.3
CABG 89.3 81.8 85.3 82.2 71.8
ICD/CRT-D 79.2 60.3 68.3 60.3 55.1
CAS/CEA 86.4 78.2 78.5 79.0 70.1
2018 Annual Data Report
Volume 1 CKD, Chapter 4
64. Conclusion
• Coronary revascularization decisions for patients with CKD present a
dilemma for clinicians because of high baseline risks of mortality
and future cardiovascular events.
• This population differs from the general population regarding
characteristics of coronary plaque composition and behavior,
• However, this high-risk population has been excluded from all
randomized trials evaluating outcomes of revascularization.
NYN/DMA/BPL
J Am Soc Nephrol. 2016 Dec; 27(12): 3521–3529.
65. • Compared with percutaneous strategies, surgical revascularization
seems to have long–term survival benefit on the basis of
observational data but associates with substantially higher short–
term mortality rates.
• Percutaneous revascularization with drug-eluting and bare metal
stents associates with a high risk of in-stent restenosis and need for
future revascularization, perhaps contributing to the higher long–
term mortality hazard.
• Off–pump coronary bypass surgery and the newest generation of
drug–eluting stent platforms offer no definitive benefits.
NYN/DMA/BPL
References:
1.Sarnak MJ, Levey AS, Schoolwerth AC, et al. Kidney disease as a risk factor for development of cardiovascular disease: a statement from the American Heart Association Councils on Kidney in Cardiovascular Disease, High Blood Pressure Research, Clinical Cardiology, and Epidemiology and Prevention. Circulation 2003; 108:2154.
2.US Renal Data System. USRDS 2009 Annual Data report: Atlas of end-stage renal disease in the United States. Am J Kidney Dis 2010; 55(Suppl 1):S1.
3,Chen J, Muntner P, Hamm LL, et al. The metabolic syndrome and chronic kidney disease in U.S. adults. Ann Intern Med 2004; 140:167.
3.Kaysen GA, Eiserich JP. The role of oxidative stress-altered lipoprotein structure and function and microinflammation on cardiovascular risk in patients with minor renal dysfunction. J Am Soc Nephrol 2004; 15:538.
4.Ix JH, Shlipak MG, Liu HH, et al. Association between renal insufficiency and inducible ischemia in patients with coronary artery disease: the heart and soul study. J Am Soc Nephrol 2003; 14:3233.
5.Muntner P, He J, Hamm L, et al. Renal insufficiency and subsequent death resulting from cardiovascular disease in the United States. J Am Soc Nephrol 2002; 13:745.
Drey N, Roderick P, Mullee M, Rogerson M. A population-based study of the incidence and outcomes of diagnosed chronic kidney disease. Am J Kidney Dis 2003; 42:677.
6.Shlipak MG, Stehman-Breen C, Vittinghoff E, et al. Creatinine levels and cardiovascular events in women with heart disease: do small changes matter? Am J Kidney Dis 2004; 43:37.
7.Shlipak MG, Heidenreich PA, Noguchi H, et al. Association of renal insufficiency with treatment and outcomes after myocardial infarction in elderly patients. Ann Intern Med 2002; 137:555.
8.Wright RS, Reeder GS, Herzog CA, et al. Acute myocardial infarction and renal dysfunction: a high-risk combination. Ann Intern Med 2002; 137:563.
Al Suwaidi J, Reddan DN, Williams K, et al. Prognostic implications of abnormalities in renal function in patients with acute coronary syndromes. Circulation 2002; 106:974.
Gibson CM, Pinto DS, Murphy SA, et al. Association of creatinine and creatinine clearance on presentation in acute myocardial infarction with subsequent mortality. J Am Coll Cardiol 2003; 42:1535.
McCullough PA, Nowak RM, Foreback C, et al. Emergency evaluation of chest pain in patients with advanced kidney disease. Arch Intern Med 2002; 162:2464.
Freeman RV, Mehta RH, Al Badr W, et al. Influence of concurrent renal dysfunction on outcomes of patients with acute coronary syndromes and implications of the use of glycoprotein IIb/IIIa inhibitors. J Am Coll Cardiol 2003; 41:718.
Best PJ, Lennon R, Ting HH, et al. The impact of renal insufficiency on clinical outcomes in patients undergoing percutaneous coronary interventions. J Am Coll Cardiol 2002; 39:1113.
Reinecke H, Trey T, Matzkies F, et al. Grade of chronic renal failure, and acute and long-term outcome after percutaneous coronary interventions. Kidney Int 2003; 63:696.
Sosnov J, Lessard D, Goldberg RJ, et al. Differential symptoms of acute myocardial infarction in patients with kidney disease: a community-wide perspective. Am J Kidney Dis 2006; 47:378.
Herzog CA, Littrell K, Arko C, et al. Clinical characteristics of dialysis patients with acute myocardial infarction in the United States: a collaborative project of the United States Renal Data System and the National Registry of Myocardial Infarction. Circulation 2007; 116:1465.
Zero-Contrast Percutaneous Coronary Intervention
Protocol. Coronary angiogram (CAG) was performed using
ultra-low-volume contrast (total contrast volume in ml was
less than the eGFR in mL/min/1.73m2). After angiography,
guide catheter engagement was confirmed by passing the
guidewire and identifying the wire course along the vessel in
comparison with angiogram alongside the same fluoroscopic
projection. Additional wires (hydrophobic or hydrophilic)
were placed in the side branches to silhouette the main vessel
and major side branches. With the guidance of IVUS across
the main vessel and side branches (in left main cases), the
lesion length, proximal and distal reference vessel diameters,
calcium arc and length and landing zones were identified.
Fluoroscopically, proximal and distal landing zones were
identified by the length from the nearest side branch. “Cine
store” was done during IVUS run to identify the landing
zones. In the case of aorto-ostial lesions, “floating wire
technique” was used. After the initial IVUS run, lesion
preparation was done using a semicompliant balloon,
scoring/cutting balloon, or rotational atherectomy,
according to the lesion morphology. Repeat IVUS was done
to assess the adequacy of lesion preparation and extent of
dissection (if any) and confirm the measurements. Fluoroscopic
projection was not changed during stent deployment.
After stenting, IVUS run was done to detect
significant edge dissection, stent underexpansion, malapposition,
minimal stent areas (MSA), and ostial coverage.
Postdilatation was done if needed. A serial echocardiogram
was done to rule out pericardial effusion.