Cardiac Pacemakers: Function,
Troubleshooting, and Management
Part 1 of a 2-Part Series
Siva K. Mulpuru, MD, Malini Madhavan, MBBS, Christopher J. McLeod, MBCHB, PHD, Yong-Mei Cha, MD,
Paul A. Friedman, MD
The sinoatrial (SA) node is the dominant pacemaker of the
heart which initiates the process of impulse generation in the
cardiac tissue, thereby defining the rate and rhythm of cardiac
contraction. The automaticity of the conduction cells in the
SA node is due to ion channels which are inter-linked by
molecular, histological and electrophysiological mechanisms
causing spontaneous diastolic depolarization and generation of
an impulse. The SA nodal action potentials are then transmitted
to the ventricles by electrical coupling of the myocytes in
different areas of the heart. Regulatory pathways overseeing
cardiac impulse generation and conduction provide effective
and safe pacing, and help maintain the rate according to the
physiological demands of the individual’s body. Failure of
physiological pacing due to any pathology in the SA or atrioventricular
node necessitates implantation of a permanent
pacemaker. Implantable pacemakers, despite technological
advances, are not without practical limitations including a
defined battery life leading to lead and/or generator replacement
at periodic intervals, vascular complications, occasional
component failure, electronic interference from external/
internal sources, e.g. myopotentials, electromechanical interference,
etc., inadequate or incomplete physiological rate response
to autonomic influences (devices have certain algorithms
to address these issues) and most importantly the risk of
infection. A biological pacemaker is therefore emerging as a
promising technique to counter these challenges.
The sinoatrial (SA) node is the dominant pacemaker of the
heart which initiates the process of impulse generation in the
cardiac tissue, thereby defining the rate and rhythm of cardiac
contraction. The automaticity of the conduction cells in the
SA node is due to ion channels which are inter-linked by
molecular, histological and electrophysiological mechanisms
causing spontaneous diastolic depolarization and generation of
an impulse. The SA nodal action potentials are then transmitted
to the ventricles by electrical coupling of the myocytes in
different areas of the heart. Regulatory pathways overseeing
cardiac impulse generation and conduction provide effective
and safe pacing, and help maintain the rate according to the
physiological demands of the individual’s body. Failure of
physiological pacing due to any pathology in the SA or atrioventricular
node necessitates implantation of a permanent
pacemaker. Implantable pacemakers, despite technological
advances, are not without practical limitations including a
defined battery life leading to lead and/or generator replacement
at periodic intervals, vascular complications, occasional
component failure, electronic interference from external/
internal sources, e.g. myopotentials, electromechanical interference,
etc., inadequate or incomplete physiological rate response
to autonomic influences (devices have certain algorithms
to address these issues) and most importantly the risk of
infection. A biological pacemaker is therefore emerging as a
promising technique to counter these challenges.
Cardiac Pacemakers: Function,
Troubleshooting, and Management
Part 1 of a 2-Part Series
Siva K. Mulpuru, MD, Malini Madhavan, MBBS, Christopher J. McLeod, MBCHB, PHD, Yong-Mei Cha, MD,
Paul A. Friedman, MD
Cardiac Pacemakers: Function,
Troubleshooting, and Management
Part 1 of a 2-Part Series
Siva K. Mulpuru, MD, Malini Madhavan, MBBS, Christopher J. McLeod, MBCHB, PHD, Yong-Mei Cha, MD,
Paul A. Friedman, MD
Critical Care Summit Egypt 2015 Common Arrhythmias in the ICUDr.Mahmoud Abbas
Lecture presented by Dr Khaled Farouk at Egyptian Critical Care Summit 2015, the leading ICU event and medical exhibition in Egypt. www.criticalcareegypt.com
Admixture lesions in congenital cyanotic heart diseaseRamachandra Barik
Admixture lesions in congenital cyanotic heart disease
Jaganmohan A Tharakan
Department of Cardiology, Sree Chitra Tirunal Institute for Medical Sciences and Technology, Trivandrum, India
Fragmented QRS Complex is associated with the Left Ventricular Remodeling in ...submissionclinmedima
A total of 140 patients with AMI were enrolled. Accoridng to the presence of fQRS in presenting electrocardiogram. The patients were divided into fQRS group and NonfQRS group. Real-time three-dimensional echocardiograph parameters measured in-hospital and 6-month follow-up period were collected.
FragmentedQRSComplexisassociatedwiththeLeftVentricular Remodeling in Patients...semualkaira
A total of 140 patients with AMI were enrolled. Accoridng to the presence of
fQRS in presenting electrocardiogram. The patients were divided into fQRS group and NonfQRS group. Real-time three-dimensional echocardiograph parameters measured in-hospital
and 6-month follow-up period were collected. The difference between two groups and the
influencing factors of left ventricular remodeling were analyzed.
Invasive coronary physiology to select patients for coronary revascularisation has become established in contemporary guidelines for the management of stable coronary artery disease. Compared to revascularisation based on angiography alone, the use of coronary physiology has been shown to improve clinical outcomes and cost efficiency. However, recent data from randomised controlled trials have cast doubt upon
the value of ischaemia testing to select patients for revascularisation. Importantly, 20-40% of patients have
persistence or recurrence of angina after angiographically successful percutaneous coronary intervention
(PCI). This state-of-the-art review is focused on the transitioning role of invasive coronary physiology from
its use as a dichotomous test for ischaemia with fixed cut-points, towards its utility for real-time guidance of PCI to optimise physiological results. We summarise the contemporary evidence base for ischaemia testing
in stable coronary artery disease, examine emerging indices which allow advanced physiological guidance
of PCI, and discuss the rationale and evidence base for post-PCI physiological assessments to assess the success of revascularisation.
RECENT ADVANCES IN THE MANAGEMENT OF REFRACTORY HEART FAILUREApollo Hospitals
Heart failure is a pathophysiological state in which structural or functional cardiac disorder impairs the ability of the heart to function as a pump to support the physiological circulation. The medical therapy remains the
mainstay of treatment in these patients. The medical therapy can improve the quality of life and the longevity in
these patients, but this becomes insufficient in refractory heart failure. The heart failure is considered refractory when patients continued to be symptomatic despite optimal dose of medications, characterized by advanced structural heart disease. These patients will need frequent hospitalizations and the overall prognosis is very poor.
The Clinical Pharmacist in Cardiac Rehabilitation Phase I at Sarawak General ...guestaf1e4
A Health Related Quality of Life Study in Patients with Acute Coronary Syndromes: The Cost-Effectiveness of Clinical Pharmacy Service in the Phase I, and Short Course Phase II Cardiac Rehabilitation Program
Authors of proposal: 1, 2 Professor Dr. Sim Kui Hian, 4 Professor Dr. Mohd. Izham Mohd Ibrahim, 1, 2 Dr. Alan Fong Yean Yip, 3 Yanti Nasyuhana Sani, 3 Tiong Lee Len, 3 Bibi Faridha Mohd Salleh, 4 Dr Mohd. Azmi Ahmad Hassali, 4 Prof. Dr Yahaya Hassan, 3 Lawrence Anchah, 5 Karen Tang Siew Lang, 1 Hii Ai Ching,1 Sii Lik Ngoh
1 Dept of Cardiology, Sarawak General Hospital.
2 Clinical Research Centre, Sarawak General Hospital.
3 Dept of Pharmacy, Sarawak General Hospital.
4 School Pharmaceutical Sciences, Universiti Sains Malaysia.
5 Dept of Physiotherapy, Sarawak General Hospital.
NIH Reference No.: (4) dlm.KKM/NIHSEC/08/0804/P07-161, dated 3rd September 2007
Completed 20th Dec 2009
Researcher: Lawrence Anak Ancah, B. Pharm, M. Clinical Pharm, Candidate for Ph.D Cinical Pharmacy in Cardiovascular & HRQoL
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.
Wellens syndrome. Wellens syndrome (also referred to as LAD coronary T-wave syndrome) refers to an ECG pattern specific for critical stenosis of the proximal left anterior descending artery. The anomalies described occur in patients with recent anginal chest pain, and do not have chest pain when the ECG is recorded.
Congenital defects can put a strain on the heart, causing it to work harder. To stop your heart from getting weaker with this extra work, your doctor may try to treat you with medications. They are aimed at easing the burden on the heart muscle. You need to control your blood pressure if you have any type of heart problem.
Changing your lifestyle can help control and manage high blood pressure. Your health care provider may recommend that you make lifestyle changes including:
Eating a heart-healthy diet with less salt
Getting regular physical activity
Maintaining a healthy weight or losing weight
Limiting alcohol
Not smoking
Getting 7 to 9 hours of sleep daily
CRISPR technologies have progressed by leaps and bounds over the past decade, not only having a transformative effect on
biomedical research but also yielding new therapies that are poised to enter the clinic. In this review, I give an overview of (i)
the various CRISPR DNA-editing technologies, including standard nuclease gene editing, base editing, prime editing, and epigenome editing, (ii) their impact on cardiovascular basic science research, including animal models, human pluripotent stem
cell models, and functional screens, and (iii) emerging therapeutic applications for patients with cardiovascular diseases, focusing on the examples of Hypercholesterolemia, transthyretin amyloidosis, and Duchenne muscular dystrophy.
A post-splenectomy patient suffers from frequent infections due to capsulated bacteria like Streptococcus
pneumoniae, Hemophilus influenzae, and Neisseria meningitidis despite vaccination because of a lack of
memory B lymphocytes. Pacemaker implantation after splenectomy is less common. Our patient underwent
splenectomy for splenic rupture after a road traffic accident. He developed a complete heart block after
seven years, during which a dual-chamber pacemaker was implanted. However, he was operated on seven
times to treat the complication related to that pacemaker over a period of one year because of various
reasons, which have been shared in this case report. The clinical translation of this interesting observation
is that, though the pacemaker implantation procedure is a well-established procedure, the procedural
outcome is influenced by patient factors like the absence of a spleen, procedural factors like septic measures,
and device factors like the reuse of an already-used pacemaker or leads.
Transcatheter closure of patent ductus arteriosus (PDA) is feasible in low-birth-weight infants. A female baby was born prematurely with a birth weight of 924 g. She had a PDA measuring 3.7 mm. She was dependent on positive pressure ventilation for congestive heart failure in addition to the heart failure medications. She could not be discharged from the hospital even after 79 days of birth, and even though her weight reached 1.9 kg in the neonatal intensive care unit. We attempted to plug the PDA using an Amplatzer Piccolo Occluder, but the device failed to anchor. Then, the PDA was plugged using a 4-6 Amplatzer Duct Occluder using a 6-Fr sheath which was challenging.
Accidental misplacement of the limb lead electrodes is a common cause of ECG abnormality and may simulate pathology such as ectopic atrial rhythm, chamber enlargement or myocardial ischaemia and infarction
A Case of Device Closure of an Eccentric Atrial Septal Defect Using a Large D...Ramachandra Barik
Device closure of an eccentric atrial septal defect can be challenging and needs technical modifications to avoid unnecessary complications. Here, we present a case of a 45-year-old woman who underwent device closure of an eccentric defect with a large device. The patient developed pericardial effusion and left-sided pleural effusion due to injury to the junction of right atrium and superior vena cava because of the malalignment of the delivery sheath and left atrial disc before the device was pulled across the eccentric defect despite releasing the left atrial disc in the left atrium in place of the left pulmonary vein. These two serious complications were managed conservatively with close monitoring of the case during and after the procedure.
Trio of Rheumatic Mitral Stenosis, Right Posterior Septal Accessory Pathway a...Ramachandra Barik
A 57-year-old male presented with recurrent palpitations. He was diagnosed with rheumatic mitral stenosis, right posterior septal accessory pathway and atrial flutter. An electrophysiological study after percutaneous balloon mitral valvotomy showed that the palpitations were due to atrial flutter with right bundle branch aberrancy. The right posterior septal pathway was a bystander because it had a higher refractory period than the atrioventricular node.
Percutaneous balloon dilatation, first described by
Andreas Gruentzig in 1979, was initially performed
without the use of guidewires.1 The prototype
balloon catheter was developed as a double lumen
catheter (one lumen for pressure monitoring or
distal perfusion, the other lumen for balloon inflation/deflation) with a short fixed and atraumatic
guidewire at the tip. Indeed, initially the technique
involved advancing a rather rigid balloon catheter
freely without much torque control into a coronary
artery. Bends, tortuosities, angulations, bifurcations,
and eccentric lesions could hardly, if at all, be negotiated, resulting in a rather frustrating low procedural success rate whenever the initial limited
indications (proximal, short, concentric, noncalcified) were negated.2 Luck was almost as
important as expertise, not only for the operator,
but also for the patient. It is to the merit of
Simpson who, in 1982, introduced the novelty of
advancing the balloon catheter over a removable
guidewire, which had first been advanced in the
target vessel.3 This major technical improvement
resulted overnight in a notable increase in the procedural success rate. Guidewires have since evolved
into very sophisticated devices.
Optical coherence tomography-guided algorithm for percutaneous coronary intervention. Vessel diameter should be assessed using the external elastic lamina (EEL)-EEL diameter at the reference segments, and rounded down to select interventional devices (balloons, stents). If the EEL cannot be identified, luminal measures are used and rounded up to 0.5 mm larger for selection of the devices. Optical coherence tomography (OCT)-guided optimisation strategies post stent implantation per EEL-based diameter measurement and per lumen-based diameter measurement are shown. For instance, if the distal EEL-EEL diameter measures 3.2 mm×3.1 mm (i.e., the mean EEL-based diameter is 3.15 mm), this number is rounded down to the next available stent size and post-dilation balloon to be used at the distal segment. Thus, a 3.0 mm stent and non-compliant balloon diameter is selected. If the proximal EEL cannot be visualised, the mean lumen diameter should be used for device sizing. For instance, if the mean proximal lumen diameter measures 3.4 mm, this number is rounded up to the next available balloon diameter (within up to 0.5 mm larger) for post-dilation. MLA: minimal lumen area; MSA: minimal stent area;NC: non-compliant
Brugada syndrome (BrS) is an inherited cardiac disorder,
characterised by a typical ECG pattern and an increased
risk of arrhythmias and sudden cardiac death (SCD).
BrS is a challenging entity, in regard to diagnosis as
well as arrhythmia risk prediction and management.
Nowadays, asymptomatic patients represent the majority
of newly diagnosed patients with BrS, and its incidence
is expected to rise due to (genetic) family screening.
Progress in our understanding of the genetic and
molecular pathophysiology is limited by the absence
of a true gold standard, with consensus on its clinical
definition changing over time. Nevertheless, novel
insights continue to arise from detailed and in-depth
studies, including the complex genetic and molecular
basis. This includes the increasingly recognised
relevance of an underlying structural substrate. Risk
stratification in patients with BrS remains challenging,
particularly in those who are asymptomatic, but recent
studies have demonstrated the potential usefulness
of risk scores to identify patients at high risk of
arrhythmia and SCD. Development and validation of
a model that incorporates clinical and genetic factors,
comorbidities, age and gender, and environmental
aspects may facilitate improved prediction of disease
expressivity and arrhythmia/SCD risk, and potentially
guide patient management and therapy. This review
provides an update of the diagnosis, pathophysiology
and management of BrS, and discusses its future
perspectives.
The Human Developmental Cell Atlas (HDCA) initiative, which is part of the Human Cell Atlas, aims to create a comprehensive reference map of cells during development. This will be critical to understanding normal organogenesis, the effect of mutations, environmental factors and infectious agents on human development, congenital and childhood disorders, and the cellular basis of ageing, cancer and regenerative medicine. Here we outline the HDCA initiative and the challenges of mapping and modelling human development using state-of-the-art technologies to create a reference atlas across gestation. Similar to the Human Genome Project, the HDCA will integrate the output from a growing community of scientists who are mapping human development into a unified atlas. We describe the early milestones that have been achieved and the use of human stem-cell-derived cultures, organoids and animal models to inform the HDCA, especially for prenatal tissues that are hard to acquire. Finally, we provide a roadmap towards a complete atlas of human development.
The treatment of patients with advanced acute heart failure is still challenging.
Intra-aortic balloon pump (IABP) has widely been used in the management of
patients with cardiogenic shock. However, according to international guidelines, its
routinary use in patients with cardiogenic shock is not recommended. This recommendation is derived from the results of the IABP-SHOCK II trial, which demonstrated
that IABP does not reduce all-cause mortality in patients with acute myocardial infarction and cardiogenic shock. The present position paper, released by the Italian
Association of Hospital Cardiologists, reviews the available data derived from clinical
studies. It also provides practical recommendations for the optimal use of IABP in
the treatment of cardiogenic shock and advanced acute heart failure.
Left ventricular false tendons (LVFTs) are fibromuscular
structures, connecting the left ventricular
free wall or papillary muscle and the ventricular
septum.
There is some discussion about safety issues during
intense exercise in athletes with LVFTs, as these
bands have been associated with ventricular arrhythmias
and abnormal cardiac remodelling. However,
presence of LVFTs appears to be much more common
than previously noted as imaging techniques
have improved and the association between LVFTs
and abnormal remodelling could very well be explained
by better visibility in a dilated left ventricular
lumen.
Although LVFTsmay result in electrocardiographic abnormalities
and could form a substrate for ventricular
arrhythmias, it should be considered as a normal
anatomic variant. Persons with LVFTs do not appear
to have increased risk for ventricular arrhythmias or
sudden cardiac death.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
The prostate is an exocrine gland of the male mammalian reproductive system
It is a walnut-sized gland that forms part of the male reproductive system and is located in front of the rectum and just below the urinary bladder
Function is to store and secrete a clear, slightly alkaline fluid that constitutes 10-30% of the volume of the seminal fluid that along with the spermatozoa, constitutes semen
A healthy human prostate measures (4cm-vertical, by 3cm-horizontal, 2cm ant-post ).
It surrounds the urethra just below the urinary bladder. It has anterior, median, posterior and two lateral lobes
It’s work is regulated by androgens which are responsible for male sex characteristics
Generalised disease of the prostate due to hormonal derangement which leads to non malignant enlargement of the gland (increase in the number of epithelial cells and stromal tissue)to cause compression of the urethra leading to symptoms (LUTS
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
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
Anti ulcer drugs and their Advance pharmacology ||
Anti-ulcer drugs are medications used to prevent and treat ulcers in the stomach and upper part of the small intestine (duodenal ulcers). These ulcers are often caused by an imbalance between stomach acid and the mucosal lining, which protects the stomach lining.
||Scope: Overview of various classes of anti-ulcer drugs, their mechanisms of action, indications, side effects, and clinical considerations.
Couples presenting to the infertility clinic- Do they really have infertility...Sujoy Dasgupta
Dr Sujoy Dasgupta presented the study on "Couples presenting to the infertility clinic- Do they really have infertility? – The unexplored stories of non-consummation" in the 13th Congress of the Asia Pacific Initiative on Reproduction (ASPIRE 2024) at Manila on 24 May, 2024.
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Factory Supply Best Quality Pmk Oil CAS 28578–16–7 PMK Powder in Stockrebeccabio
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Ve...kevinkariuki227
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
The hemodynamic and autonomic determinants of elevated blood pressure in obes...
Cardiac pacemakers part-II
1. STATE-OF-THE-ART REVIEW
Advances and Future Directions
in Cardiac Pacemakers
Part 2 of a 2-Part Series
Malini Madhavan, MBBS, Siva K. Mulpuru, MD, Christopher J. McLeod, MBCHB, PHD, Yong-Mei Cha, MD,
Paul A. Friedman, MD
JACC JOURNAL CME
This article has been selected as the month’s JACC Journal CME activity,
available online at http://www.acc.org/jacc-journals-cme by selecting the
CME tab on the top navigation bar.
Accreditation and Designation Statement
The American College of Cardiology Foundation (ACCF) is accredited by
the Accreditation Council for Continuing Medical Education (ACCME) to
provide continuing medical education for physicians.
The ACCF designates this Journal-based CME activity for a maximum
of 1 AMA PRA Category 1 Credit(s). Physicians should only claim
credit commensurate with the extent of their participation in the activity.
Method of Participation and Receipt of CME Certificate
To obtain credit for JACC CME, you must:
1. Be an ACC member or JACC subscriber.
2. Carefully read the CME-designated article available online and in this
issue of the journal.
3. Answer the post-test questions. At least 2 out of the 3 questions
provided must be answered correctly to obtain CME credit.
4. Complete a brief evaluation.
5. Claim your CME credit and receive your certificate electronically by
following the instructions given at the conclusion of the activity.
CME Objective for This Article: After reading this article, the reader should
be able to: 1) identify the predictors of response to cardiac resynchroni-
zation therapy that guide patient selection; 2) identify causes of failure to
respond to cardiac resynchronization therapy and choose corresponding
treatment; 3) compare patient outcomes with available remote moni-
toring technologies; and 4) select appropriate patients for single
component leadless pacemakers.
CME Editor Disclosure: JACC CME Editor Ragavendra R. Baliga, MD, FACC,
has reported that he has no financial relationships or interests to disclose.
Author Disclosures: Dr. Friedman receives research support from St.
Jude Medical; and is a consultant and advisory board member for
Medtronic and Boston Scientific. All other authors have reported that
they have no relationships relevant to the contents of this paper to
disclose.
Medium of Participation: Print (article only); online (article and quiz).
CME Term of Approval
Issue Date: January 17, 2017
Expiration Date: January 16, 2018
From the Department of Cardiovascular Diseases, Mayo Clinic, Rochester, Minnesota. Dr. Friedman receives research support
from St. Jude Medical; and is a consultant and advisory board member for Medtronic and Boston Scientific. All other authors have
reported that they have no relationships relevant to the contents of this paper to disclose.
Manuscript received July 22, 2016; revised manuscript received October 17, 2016, accepted October 26, 2016.
Listen to this manuscript’s
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J O U R N A L O F T H E A M E R I C A N C O L L E G E O F C A R D I O L O G Y V O L . 6 9 , N O . 2 , 2 0 1 7
ª 2 0 1 7 B Y T H E A M E R I C A N C O L L E G E O F C A R D I O L O G Y F O U N D A T I O N
P U B L I S H E D B Y E L S E V I E R
I S S N 0 7 3 5 - 1 0 9 7 / $ 3 6 . 0 0
h t t p : / / d x . d o i . o r g / 1 0 . 1 0 1 6 / j . j a c c . 2 0 1 6 . 1 0 . 0 6 4
3. criteria indicative of ventricular dyssynchrony.
A summary of the results of selected large, random-
ized, clinical trials of CRT stratified by key patient
characteristics is presented in Figure 4A (5). The
guidelines for implantation of a CRT device from the
American Heart Association (6) are summarized in
Figure 4B, and are discussed later.
Electrocardiographic criteria. A wide QRS complex is a
marker of electrical dyssynchrony and, in the pres-
ence of an LBBB pattern, is the most powerful pre-
dictor of CRT response. All of the randomized
controlled trials (RCTs) that have shown improve-
ment in HF symptoms and survival using patients
enrolled in CRT with a minimal QRS duration of 120
to 150 ms (3,4,7). The wider the QRS complex, the
greater the likelihood of response. There is interplay
between the type of bundle branch block and the QRS
duration, likely because a sufficiently wide right
bundle branch block (RBBB) (>150 ms) re-
flects delay in both bundles, so that delay of
the LV lateral wall activation is present, and
CRT is thus effective. However, the presence
of bifascicular block (RBBB with left anterior
fascicular block) was not predictive of CRT
response in the MADIT-CRT (Multicenter
Automatic Defibrillator Implantation Trial
With Cardiac Resynchronization Therapy)
(8). Current guidelines require the presence
of LBBB if the QRS complex is relatively
narrow (120 to 149 ms) for a Class I
indication for CRT (6). CRT is not indicated
when the QRS complex is <120 ms, as it may
potentially cause harm (6,9). Women are
more likely to benefit from CRT than men,
particularly when the QRS duration is <150
ms (10). When patients with depressed ventricular
CENTRAL ILLUSTRATION Future Directions in Cardiac Pacing: The Need for Advances in Cardiac Pacing and
Emerging Techniques
Improve cardiac resynchronization
and cardiac efficiency
Goal: Increase the number
of pacing sites:
Cardiac resynchronization therapy
with multipoint/multisite pacing
allows simultaneous pacing of
multiple sites at the same time
Goal: Recruit His-Purkinje
conduction
His-bundle pacing recruits the
His-Purkinje system to mimic
normal cardiac activation
Reduce hardware to reduce lead
failure, valve injury, device infection
Goal: Eliminate pacemaker
leads
Introduction of single-component
leadless pacemakers
Goal: Eliminate leads from
left ventricle endocardial
pacing
Introduction of multicomponent
leadless pacemaker for left
ventricular endocardial pacing
Eliminate batteries
and other hardware
Goal: Eliminate need for
battery replacement
In development: Batteryless
pacemakers that harvest the
mechanical energy of cardiac
contraction to power the pacemaker
Goal: Eliminate need for
hardware
In development: Biological
pacemakers that are gene-
or cell-based
CARDIAC PACEMAKERS: RECENT ADVANCES AND FUTURE DIRECTIONS
Madhavan, M. et al. J Am Coll Cardiol. 2017;69(2):211–35.
Several strategies have been developed and are emerging to enhance device therapy. Pump efficiency is addressed with multisite left ventricle pacing and, potentially,
His-Purkinje recruitment. Hardware reduction and simplification include leadless pacemakers (single component and multicomponent), and future advances may
eliminate the need for batteries, which deplete over time.
A B B R E V I A T I O N S
A N D A C R O N Y M S
CRT = cardiac
resynchronization therapy
EF = ejection fraction
HF = heart failure
LBBB = left bundle branch
block
LV = left ventricle/ventricular
RBBB = right bundle branch
block
RI = remote interrogation
RM = remote monitoring
RV = right ventricle/ventricular
TTM = transtelephonic
monitoring
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213
4. function and a pacemaker manifest an LBBB that is
caused by frequent RV pacing, upgrading to a CRT
system often improves ventricular function.
An intrinsic LBBB or a mechanical dyssynchrony
induced by a high percentage of RV apical pacing are
the main substrates for resynchronization. In a meta-
analysis of RCTs, the benefit of CRT was limited to
those patients with LBBB (11). Patients with RBBB and
a nonspecific intraventricular conduction delay with
a QRS complex >150 ms may still be considered for
CRT, although the strength of the indication is
smaller and the likelihood of nonresponse is greater
(6). Certain subgroups of patients with non-LBBB QRS
morphologies, such as those with echocardiographic
dyssynchrony, may have better outcomes after CRT
(12).
Severity of HF. Initial RCTs predominantly enrolled
patients with EF #35% and NYHA functional class III
or ambulatory class IV (no hospital admissions within
1 month) HF (7). Subsequent trials included patients
with EF #30% to 40% and asymptomatic or mild HF
(NYHA functional classes I and II) (4,13). However, the
majority of trial participants had symptomatic HF
(NYHA functional class II to IV); hence, the evidence
supporting CRT for these patients is much stronger
(6). Clinical scenarios that warrant special consider-
ation are discussed later.
Atrial fibrillation. Experience in randomized trials of
CRT in patients with atrial fibrillation (AF) and with
symptomatic HF, QRS complex $120 ms, and no other
indication for pacing is limited. The MUSTIC (Multi-
site Stimulation in Cardiomyopathies) trial reported
improvement in functional status in patients with
both sinus rhythm and AF (14). A meta-analysis of
observational studies reported a greater mortality risk
and a higher rate of CRT nonresponse in AF compared
with sinus rhythm (15). Current guidelines recom-
mend CRT implantation in patients with AF, HF,
FIGURE 1 CRT for the Treatment of Heart Failure
Left bundle branch block causes delayed electrical and mechanical activation of the LV, which in turn results in atrioventricular, interven-
tricular, and intraventricular dyssynchrony, consequently reducing LV pump function. This results in adverse LV remodeling over time. CRT,
by pacing the right and left ventricles near-simultaneously, aims to correct mechanical dyssynchrony, improve LV function, and over time,
cause reverse remodeling. CRT ¼ cardiac resynchronization therapy; LV ¼ left ventricle/ventricular.
FIGURE 2 Response to CRT
Status
What defines a responder vs. “non-responder”?
Time
Non-responderNegative
responders
“Non
progressor”
Responder
Super-
Responder
CRT
Implantation
Response to CRT is determined by a host of parameters, including patient
symptoms, objective measurements of functional capacity, and cardiac
function. Those who demonstrate improvement in these parameters are
termed responders, with super-responders referring to a subgroup with near
normalization of LV function. Patients who demonstrate stabilization of LV
function without experiencing the progressive decline that is expected with
heart failure are termed nonprogressors. A small proportion of patients may
experience a rapid decline in LV function following CRT (negative
responders). Reproduced with permission from Steffel et al. (74).
Abbreviations as in Figure 1.
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5. LVEF #35%, and QRS complex $120 ms (6). However,
it is critical to control the ventricular response in AF
to provide >99% BiV pacing (6).
CRT in patients who require pacing for bradycardia. RV
apical pacing induces electrical and mechanical dys-
synchrony, and has been associated with an increased
risk of HF, particularly when pacing is frequent
(>40%) and LV systolic function is depressed (16). In
patients with atrioventricular (AV) block who require
pacing, EF #50%, and NYHA functional class I to III
HF, BiV pacing (with a defibrillator, if indicated) re-
duces the combined endpoint of mortality, intrave-
nous therapy for HF, or reduction in LV end-systolic
volume compared with RV-only pacing (17). BiV pac-
ing can reasonably be considered in patients who are
anticipated to require a high percentage of ventricu-
lar pacing and have EF #50% with mild HF symptoms
(17).
Measurement of mechanical dyssynchrony for
patient selection. Only patients with a QRS
complex $120 ms were enrolled in initial CRT studies.
Because many patients with EF <35% and symptom-
atic HF have a narrow QRS complex, to identify po-
tential resynchronization candidates, several studies
used echocardiography to identify mechanical dys-
synchrony by assessing the time difference between
activation of the LV septum and lateral wall with
M-mode, tissue Doppler, speckle tracking, or other
modalities (18). Three multicenter trials failed to
show substantial improvement in CRT response with
dyssynchrony assessment by these means, and 1
found increased mortality in patients with a QRS
complex <130 ms and echocardiographic dyssyn-
chrony (3,19,20). Whether these study findings reflect
limitations of the specific echocardiographic assess-
ments used or whether the strategy of using a me-
chanical measurement to select an electrical therapy
is doomed to failure is unclear. At present, there is no
role for routine echocardiographic assessment of
dyssynchrony in patient selection for CRT.
Lead position. Positioning of the LV lead at the site
of latest activation to maximize resynchronization
seems intuitive. The effect of the location of the LV
lead for assessing CRT response has been extensively
studied. Broadly, 3 metrics have been used to char-
acterize the LV lead position to determine its effect
on CRT response: anatomic LV lead position, LV local
electrogram timing, and mechanical delay or scar
assessment at the LV lead site.
Anatomic LV lead position. The ideal site for LV pacing
is the subject of debate. However, it is clear that the
closer the LV and RV electrodes are placed, the lower
the potential for resynchronization. As a general rule
of thumb, maximizing the distance between the RV
and LV electrodes in the horizontal plane in the lateral
view (or left anterior oblique [LAO] view) is associated
with a better CRT response (21). Apical positions are
unattractive, in part because they necessarily result in
FIGURE 3 Techniques to Optimize CRT and Future Directions
Heart
Failure
Optimizing
CRT
response
Future
directions
Role of CRT in
• Mild heart failure
• Narrow QRS complex
• Frequent RV pacing
without heart failure
Role of
• Echocardiographic / MRI
guided lead placement
• Endocardial LV pacing
• Leadless CRT
• His bundle pacing
Role of
• Multisite and multipoint pacing
• Routine AV node ablation in AF
• Ejection fraction (≤35%)
• Left bundle branch block
• QRS duration ≥150 ms
• Symptomatic heart failure
• Frequent ventricular pacing
• Appropriate lead position
• Posterior and lateral LV
• LV base (avoid apex)
• Site of latest electrical
activation (QLV)
• Optimize LV capture, paced
QRS morphology using ECG
• True BiV pacing >95%
• In select cases,
echocardiographic optimization
• Rate control in atrial fibrillation
(AV node ablation)
• Treat frequent PVC
Patient selection
for CRT
CRT
implantation
Post implantation
maximal LV
synchronization
& BiV pacing
CRT
response
Optimizing response to CRT implantation requires careful attention to patient selection and lead implantation. Following implantation, close
follow-up to ensure optimal LV lead capture, and BiV pacing are essential. AF ¼ atrial fibrillation; AV ¼ atrioventricular; BiV ¼ biventricular;
MRI ¼ magnetic resonance imaging; PVC ¼ premature ventricular contraction; RV ¼ right ventricle/ventricular; other abbreviations as in
Figure 1.
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6. less separation between the RV and LV leads, and in
part due to potentially nonphysiological ventricular
activation. This is supported by a randomized clinical
trial showing worse outcomes with apical pacing sites
(22). Posterior and lateral positions are generally
preferred (23). However, compelling differences in
outcomes with different lead positions in large studies
have been inconsistently found, perhaps due to the
FIGURE 4 Effect of CRT in Randomized Clinical Trials and Indications for CRT for Patients in Sinus Rhythm
QRS
duration (ms)
NYHA
functional class
Level of
recommendation
QRS
morphology
LBBB
LVEF ≤35%, QRS Duration ≥120 ms and Sinus Rhythm
Non-LBBB
Significant (>40%)
ventricular pacing
≥150
≥150
≥150
≥150
Any QRS
Class I
Class IIa
II, III,
ambulatory IV
2
1.6
1.2
0.8
0.4
0
QRS <150ms QRS ≥150ms
REVERSE MADIT-CRT
n=
303
n=
307
n=
645
n=
627
n=
324
n=
314
n=
290
n=
505
n=
1175
n=
1036
NYHA Functional Class 1/2
RR(95%CI)
Class 2/3 Class 3/4
RAFT COMPANION CARE-HF
II, III,
ambulatory IV
III, ambulatory IV
III, ambulatory IV
II
I, II
I, II, III,
ambulatory IV
I
+ LVEF ≤30%
+ ischemic heart
disease
Class IIa
Class IIb
Class IIb
Class IIb
Class IIa
Class III (no CRT)
120-149
120-149
120-149
A
B
(A) Effect of CRT on composite clinical outcomes in large randomized clinical trials. The effect of CRT on composite clinical outcomes in
selected large randomized trials is stratified by patient characteristics, including NYHA functional class and QRS duration. Patients with
severely prolonged QRS duration (>150 ms) were more likely to have improved outcomes compared with those with QRS duration <150 ms.
The New York Heart Association (NYHA) functional class was less predictive of clinical improvement. Adapted from Sipahi et al. (5). (B)
Indications for CRT for patients in sinus rhythm: guidelines from the American Heart Association/American College of Cardiology. Severity of
heart failure symptoms, ejection fraction, cardiac rhythm, QRS morphology, and QRS duration are considered when selecting patients for CRT.
CARE-HF ¼ Cardiac Resynchronization-Heart Failure; CI ¼ confidence interval; COMPANION ¼ Comparison of Medical Therapy, Pacing, and
Defibrillation in Heart Failure; LBBB ¼ left bundle branch block; LVEF ¼ left ventricular ejection fraction; MADIT-CRT ¼ Multicenter
Automatic Defibrillator Implantation Trial–Cardiac Resynchronization Therapy; NYHA ¼ New York Heart Association; RAFT ¼
Resynchronization-Defibrillation for Ambulatory Heart Failure Trial; REVERSE ¼ Resynchronization Reverses Remodeling in Systolic Left
Ventricular Dysfunction; RR ¼ relative risk.
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7. presence of a large target region in patients with LBBB
or due to patient-specific variations in the ideal site of
pacing.
LV local electrogram timing. The site of latest electrical
activation can be identified using the timing of the
local LV electrogram recorded during lead implanta-
tion. As an LV lead is moved within a coronary sinus
tributary, the greater the time interval between the
start of the surface QRS complex and the local elec-
trogram (the QLV interval), the larger the local delay.
Longer QLV intervals result in a more favorable acute
hemodynamic response to CRT, long-term reverse LV
remodeling, and improved quality of life (24). A QLV
interval >50% of the QRS width was associated with
fewer HF hospitalizations and death in 1 small study
(25). Larger studies are examining the feasibility
of testing multiple coronary vein tributaries.
Although data regarding the feasibility of consistent
lead implantation at the site of latest activation
and the long-term clinical outcome using the
QLV interval are lacking, this approach appears
promising.
Mechanical delay or scar assessment to identify the LV
lead site. In contrast to the inability of imaging-based
indexes of delayed activation to select patients for
CRT (see earlier discussion), these techniques appear
promising when used to select attractive LV pacing
sites. Optimal LV pacing sites are those with the latest
mechanical activation, and undesirable sites are
those with scarring, which may limit the amount of
LV myocardium captured by the pacing pulse. Use of
echocardiographic speckle tracking and tissue
Doppler imaging improved CRT response in small
studies (26,27). With speckle tracking, the ultrasound
backscatter “fingerprint” is used to track the motion
of specific myocardial segments. The randomized
controlled TARGET (Targeted Left Ventricular Lead
Placement to Guide Cardiac Resynchronization
Therapy) study found a reduction in death and HF
hospitalization in patients with LV lead placement at
the site of latest activation identified using speckle
tracking (28). The STARTER (Speckle Tracking
Assisted Resynchronization Therapy for Electrode
Region) RCT reported that patients with QRS width
120 to 149 ms and non-LBBB morphology, a group at
high risk of nonresponse, were most likely to benefit
from echocardiography-guided lead placement (27).
Cardiac magnetic resonance imaging may be useful as
well; BiV pacing from sites of late gadolinium
enhancement (e.g., scar) increases mortality (29). The
concept of avoiding scar for lead placement was
further supported by the TARGET trial, in which
echocardiogram speckle tracking was used to avoid
lead implantation at sites of scarring (28).
Computational models. Computational models of
electromechanical cardiac function have shown
promise in improving patient selection, lead locali-
zation, and device optimization for optimal CRT, and
are the subject of ongoing research (30).
Multisite pacing. Because dyssynchrony is the un-
derlying substrate for CRT, it has been proposed that
pacing from more than 1 LV site may improve
resynchronization and outcomes. Multisite pacing
using 2 or more LV leads and multipoint pacing using
1 LV multipolar lead have shown promise in
improving CRT response. The use of 2 epicardial cor-
onary venous leads compared with 1 improves acute
hemodynamic response, EF, LV end-systolic volume,
and symptoms of HF in small, randomized trials (31).
The implantation of 2 LV leads has been shown to be
feasible and safe in the short term, but has a
high long-term failure rate due to the inability to
chronically capture using a Y adaptor to pace
simultaneously from 2 leads, and due to rapid battery
depletion (31,32). Studies of the effectiveness of
multilead, multisite pacing have had mixed results
(33).
Multipoint pacing through a single quadripolar
lead has emerged as a feasible and safe option for
providing CRT. Quadripolar leads offer the advantage
of multiple programmable pacing vectors, hence
minimizing the chance of lead abandonment due
to a high pacing threshold or phrenic nerve capture.
In a national database of quadripolar lead implanta-
tion, the risk of lead deactivation and replacement
was lower with quadripolar than with bipolar leads
(34). In addition, emerging evidence from small co-
horts shows hemodynamic advantages to multipoint
pacing using a quadripolar lead, with acute
improvement in LV systolic function (35). The ability
to choose a pacing vector with the best hemodynamic
response and the ability to capture a large region of
LV myocardium by pacing from widely spaced elec-
trodes are potential explanations for the observed
improvement. In a nationwide study of over 18,000
recipients of a quadripolar lead, mortality was noted
to be lower compared with patients receiving CRT
with a bipolar lead (34). Ongoing RCTs are comparing
the efficacy of quadripolar versus bipolar leads.
Endocardial LV pacing. Although all CRT has been
delivered via epicardial electrodes, epicardial LV
pacing introduces multiple mechanisms of nonre-
sponse, including unsuitable coronary venous anat-
omy, lead dislodgement, phrenic nerve capture, and
nonphysiological epicardial-to-endocardial activa-
tion. Endocardial LV pacing may allow for pacing
from any noninfarcted LV site; it results in a narrower
QRS complex and improved acute hemodynamic
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8. FIGURE 5 Radiographic Lead Position of Coronary Venous Lead and Paced QRS Morphology: Electroanatomic Correlation
Lead I
Inferior Leads
30°
30°
RV apex
III II
I
aVF
aVLaVR
LV posterior wall
RV apex
LV free wall
LV anterior wall
1 RV
2 LV
VI
VI
1
2
B
A
(A) Anatomy of the coronary veins in the LAO and RAO views. Tributaries of the CS are best assessed using angiography in the LAO and RAO
views during lead placement. The LAO view helps distinguish between lead placement in the lateral wall (preferred) and the septum. The RAO
view helps assess whether the lead is anterior versus posterior and basal (preferred) versus apical. (B) Correlation between paced QRS
morphology and CS lead position. The QRS morphology during coronary venous pacing can be used to confirm capture and assess satisfactory
lead positioning and the contribution of LV activation to the overall biventricular paced morphology. Electrocardiographic vectors in the
limb leads and the precordial leads as they correlate with coronary venous tributaries are presented here. Pacing from the lateral LV wall
results in a predominantly negative vector in leads I and aVL. The inferior limb leads II, III, and aVF distinguish anterior from posterior LV
pacing, with a predominantly positive vector resulting from pacing anteriorly and a negative vector resulting from posterior pacing. Pre-
cordial lead V1 is placed anteriorly and rightward on the chest. Hence, pacing the LV, the posteriorly placed ventricle, results in a pre-
dominantly positive vector (i.e., right bundle branch morphology). The exception is pacing the anterior interventricular vein, which will
produce a negative vector in V1 (i.e., left bundle branch morphology). (C to F) Twelve-lead ECG and chest x-ray in the posteroanterior and
lateral views showing correlation between lead position and paced QRS morphology in the (C) anterior interventricular vein, (D) anterolateral
vein, (E) posterolateral vein, and (F) middle cardiac vein. Arrows in C to F point to the tip of the coronary sinus lead. CS ¼ coronary sinus;
LAO ¼ left anterior oblique; RAO ¼ right anterior oblique.
Continued on the next page
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9. FIGURE 5 Continued
Continued on the next page
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10. function compared with epicardial pacing (36).
Endocardial pacing may be preferred due to greater
flexibility in selecting the site of lead implantation,
absence of phrenic nerve stimulation, and more
physiological LV activation. Endocardial LV pacing
using conventional pacing leads placed transapically,
or through the interatrial or interventricular septum,
has been described in small case series (37,38).
Despite the attractive resynchronization potential,
this technique is marred by a prohibitive risk of sys-
temic thromboembolism and mitral valve regurgita-
tion. Leadless LV electrodes under development have
shown promise in reducing these complications (as
discussed later).
FIGURE 5 Continued
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11. POST-IMPLANTATION MANAGEMENT. CRT nonre-
sponse, the absence of improvement in LV systolic
function and HF symptoms, is present in 30% of re-
cipients (39). Early recognition of nonresponse and its
causes permits interventions to improve outcomes.
A multidisciplinary approach to CRT optimization has
been shown to identify a cause in 74% of
nonresponders, leading to changes in device settings
or therapy (40). Common causes for nonresponse
include suboptimal lead position, lack of baseline
dyssynchrony, LV lead malfunction, inadequate de-
vice settings, loss of BiV pacing, and arrhythmias (40).
Successful CRT requires ongoing assessment of
the efficacy of BiV pacing following implantation.
FIGURE 6 Optimization of the VV Interval Using Electrocardiography
(A) Simultaneous pacing of the LV and RV (LV offset 0 ms) results in a negative vector in lead V1 and an R-wave in lead I due to activation of the majority of the LV by
pacing from the RV. Serial electrocardiograms are obtained with increasing pre-excitation of the LV lead in (B) (LV offset 20 ms) and (C) (LV offset 40 ms). When the
LV is paced prior to the RV, the QRS morphology reflects progressively greater contribution from LV pacing with resultant positive vector in V1 and negative vector in
lead I. Abbreviations as in Figures 1 and 3.
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12. Follow-up visits assess: 1) HF symptoms; 2) LV lead
capture threshold; 3) percentage BiV pacing; 4) device
settings; and 5) presence of arrhythmias. When
appropriate, further investigation may include an
electrocardiogram (ECG), echocardiogram, oxygen
consumption treadmill test, 6-min walk, and Holter
monitor. CRT response is improved by ensuring: 1)
effective LV capture; 2) a high percentage of BiV
pacing; and, uncommonly, 3) optimization of AV and
VV intervals; or 4) LV lead repositioning.
Assessing LV capture: importance of the 12-lead
ECG. Poor LV lead performance due to dislodgement,
FIGURE 7 Anodal Stimulation in a BiV Device
Anodal stimulation may occur when LV pacing is configured with the LV electrode as cathode and the RV ring or coil (in a defibrillator) as
anode. (A) Capture typically occurs at the LV electrode only (cathodal-only capture) producing LV paced morphology. (B) If capture occurs at
the anode alone, the QRS morphology resembles RV pacing and leads to loss of resynchronization. Anodal stimulation is more likely to occur at
high pacing output. (C) Capture at both the cathode and anode may rarely occur, resulting in a narrow QRS complex with maintenance of
cardiac resynchronization. (D) Electrocardiogram during pacing from the LV tip electrode (cathode) to the RV coil (anode) with reducing
pacing output. (Left) Pacing at output of 5 V produces a QRS complex resembling RV pacing consistent with anodal only stimulation. (Right)
As the pacing output is reduced to 4 V, there is a change in QRS to LV pacing morphology. This represents loss of anodal stimulation with
capture at the cathode as the pacing output is reduced. Abbreviations as in Figures 1 and 3.
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13. high capture thresholds, phrenic nerve capture, or
structural lead dysfunction may affect CRT. A 12-lead
ECG facilitates assessment of LV lead performance
and its contribution to overall ventricular activation.
The QRS morphology during LV and BiV pacing is
determined by lead position, capture latency, and the
presence of anodal capture. Figure 5 shows the cor-
relation between radiographic lead position and
12-lead QRS morphology during BiV pacing. Capture
of the LV free wall is associated with a dominant
R-wave in V1 and a QS complex in lead I, which
indicate a wave front propagating away from the
LV toward the RV. The absence of these features
can indicate: 1) loss of LV capture; 2) LV lead
dislodgement; 3) LV capture latency or conduction
delay, resulting in the majority of the LV being acti-
vated by an RV lead-initiated wave front; 4) fusion
between CRT and intrinsic complexes; or 5) anodal
capture.
The LV lead capture threshold is tested indepen-
dently (RV lead output programmed off) with a real-
time ECG to record the paced QRS morphology and to
identify loss of capture. Conceptually, if an LV lead is
placed in a zone of slow electrical conduction, during
synchronous BiV pacing, very little LV myocardium is
stimulated by the wave front initiated by the LV elec-
trode, and little resynchronization is present. Pre-
exciting the tissue at the LV electrode (by pacing
the LV ahead of the RV, also known as LV offset) to give
the slowly propagating wave front a “head start”
results in its greater contribution to LV activation
(Online Video 1). Serial ECGs performed with varying
VV intervals can be used to identify the LV offset in-
terval that produces a dominant R-wave in V1 and QS
complex in lead I (Figure 6). In an observational study,
increasing R-wave amplitudes in V1 and a change in
axis from left to right with CRT was associated with
favorable LV remodeling (41). Although there are no
systematic studies of the value of ECG optimization,
this is a widely available, inexpensive, and simple tool
that the authors frequently use.
Anodal stimulation is an often under-recognized
cause for a lack of CRT response (42). During pacing,
electrons exit the cathode and return via the anode,
with capture desired at the cathode. CRT devices
allow multiple programmable pacing configurations.
If pacing occurs between an LV electrode (cathode) and
RV ring electrode (anode), and myocardial stimulation
occurs only at the RV anode, effective CRT is not
delivered (Figure 7). Anodal-only capture is corrected
by adjusting the pacing output or configuration.
Percentage BiV pacing: ensuring continuous
CRT. The percentage of QRS complexes that are
resynchronized (i.e., the CRT “dose”) correlates with
HF outcome and mortality. Hayes et al. (43) reported
optimal improvement in survival with >98.4% BiV
pacing; a goal of >95% is commonly used. In a large
national registry, 40% and 11% of patients had <98%
FIGURE 8 His Bundle Pacing
(A) Right anterior oblique and (B) left anterior oblique views of the heart showing placement of the lead on the proximal conduction system.
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14. and <90% BiV pacing, respectively (44). Among
patients with <98% pacing, atrial arrhythmias, pre-
mature ventricular contractions (PVCs), and inap-
propriately programmed AV intervals account for
30%, 17%, and 35% of pacing loss, respectively (44).
Device interrogation provides the percentage of BiV
pacing, as well as clues to the reason for its loss. CRT
devices have the capability to provide “trigger” pac-
ing from the LV lead in response to a sensed event on
the RV lead. This leads to fusion or pseudofusion
between the intrinsic beat and LV pacing.
Triggered LV pacing does not afford the same hemo-
dynamic benefits of “true” BiV pacing, and hence
should be minimized. Although some device manu-
facturers provide data regarding frequency of trig-
gered LV pacing, Holter monitoring may be required
to detect fused QRS morphologies in others.
Frequent PVCs interfere with CRT and may inde-
pendently worsen HF due to dyssynchrony. Treat-
ment with beta-blockers or membrane-active
antiarrhythmic drugs, and in select patients, catheter
ablation of PVCs may improve CRT response (45).
Intrinsically conducted AF results in fusion and
pseudofusion between LV pacing and native con-
duction, leading to loss of BiV pacing. Ablation of the
AV node restores BiV pacing and improves CRT
response (46). Routine AV node ablation in CRT re-
cipients with permanent AF is controversial, as the
benefits of response are weighed against the risks
associated with pacemaker dependency. Hence, in
patients with permanent AF, an initial strategy of
pharmacological rate control with rapid escalation to
AV node ablation if >99% BiV pacing is not achieved
is reasonable. The role of antiarrhythmic drug
FIGURE 9 ECG Demonstrating Effects of His Bundle Pacing
(Left) Atrial pacing is seen with native RBBB configuration. When high output pacing (VVI mode) is performed (middle), the QRS normalizes in duration representing
recruitment of the right and left ventricular conduction system. (Right) When the output is reduced, RBBB morphology is reproducible with loss of the recruitment of
the left-sided conduction system. ECG ¼ electrocardiogram; RBBB ¼ right bundle branch block.
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15. therapy and catheter ablation to restore sinus rhythm
in paroxysmal AF in improving CRT response needs
further investigation.
Optimizing device programming: programming
AV and VV intervals. A number of studies have
optimized device AV and VV intervals to determine
whether CRT response may be improved. ECG-based,
echocardiographic, and intracardiac electrogram-
based AV and VV interval optimization have all
been tested. Although in selected cases such a strategy
is used, trials of routine optimization using echocar-
diography and device-based AA and VV interval opti-
mization have been universally disappointing.
Optimization is not routinely performed.
FIGURE 10 Evolution of Techniques for Monitoring of Pacemakers: Transtelephonic, Inductive, and Remote Wandless Monitoring
Although transtelephonic and inductive monitoring provide intermittent monitoring, radiofrequency wandless monitoring can provide device- and patient-related
information more continuously. Modified from Slotwiner et al. (75). PM ¼ pacemaker; RF ¼ radiofrequency.
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16. PARA-HISIAN PACING. As noted earlier, chronic RV
apical pacing is associated with an increased risk of
death, HF hospitalization, and persistent AF. BiV
pacing is superior to RV pacing in patients with
reduced EF (16). However, procedural complexity,
complications, increased lead burden, CRT nonre-
sponse, and long-term costs of device replacement
have led to interest in selective pacing of the prox-
imal conduction system to mimic the natural activa-
tion of the ventricles (Figure 8). His-bundle capture
enables rapid activation of the ventricles by engaging
the highly branching Purkinje network. On the ECG,
selective capture of the His bundle results in a QRS
complex similar to normal conduction (Figure 9).
There is an isoelectric interval from the pacing stim-
ulus to the QRS complex that is often equal to the HV
interval. The restoration of a narrow QRS complex by
His pacing represents an intact His-Purkinje system
or the capability of overcoming impaired conduction
within the His-Purkinje system by pacing current
(Figure 6). Para-Hisian pacing can be achieved using a
small-caliber pacing lead (Select Secure Model
3830, Medtronic, Minneapolis, Minnesota) delivered
through specially designed sheaths (C 315 HIS) to map
the AV septal region (Figure 8). Unipolar pacing aids
selective capture of myocardial tissue at the lead tip,
and is successful in 84% of patients (47,48). In pa-
tients with a wide complex, unstable escape rhythms,
and diffuse infra-Hisian disease, it may not be
feasible to map and place a pacing lead that results in
a narrow QRS complex. Select Secure leads placed in
the ventricle have a cumulative survival probability
of 97.2% at 78 months, although data on long-term
performance is lacking. Reliable selection of patients
who are likely to have recruitment of the left-sided
conduction system is challenging. His bundle pacing
in patients with AV block results in higher rates of
His-Purkinje system recruitment when the block is at
the AV nodal level (93% to 98%) compared with when
it is at the infranodal level (52% to 76%) (47). With
His-bundle pacing, sensed R waves are often smaller
than with pacing at other sites due to the paucity of
ventricular myocardium near the membranous
septum. The pacing thresholds are often higher when
compared with traditional sites, resulting in shorter
battery life. There are limited data regarding extrac-
tion of leads placed on the membranous septum.
Technical aspects of His-bundle pacing are discussed
elsewhere (49). Although promising as a superior
alternative to RV apical pacing, larger studies
involving longer follow-up are required before wide-
spread adoption.
FIGURE 11 RM Use Is Associated With Better Patient Survival
1.00
0.95
0.90
0.85
0.80
0.75
0.70
0.65
0.60
0 1
No. at Risk
Cox survival
2
%RM
High
Low
RM none (0)
High
Low
RM
67,920
59,786
141,765
High %RM vs RM none; HR: 2.10 (2.04-2.16) P<0.001
Low %RM vs RM none; HR: 1.58 (1.54-1.62) P<0.001
High %RM vs low %RM; HR: 1.32 (1.27-1.36) P<0.001
66,096
57,221
129,137
60,519
52,473
115,230
29,812
30,715
62,720
7,726
10,236
18,032
533
1,042
1,735
Years From Implant
ProportionSurviving
3 4 5
In 269,471 patients with pacemakers and implantable cardioverter-defibrillators remotely monitored with the Merlin network, survival
improved with greater use of RM. RM was not used in 53% of this cohort (RM None). Among those using RM at least once, high and low RM
use was defined using a cutpoint of 75%. Patient survival was noted to improve in a graded fashion as the percentage of RM use increased.
Adapted with permission from Varma et al. (55). HR ¼ hazard ratio; RM ¼ remote monitoring.
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17. REMOTE MONITORING OF PACEMAKERS
AND DIAGNOSTICS
Worldwide, 7 million people live with a cardiovascu-
lar implantable electronic device to treat bradycar-
dias, tachyarrhythmias, or HF and require effective
monitoring for long-term care. RM and remote inter-
rogation (RI) refer to acquisition of system or patient
information from a cardiovascular implantable elec-
tronic device and transmitting it to a clinic distant
from the patient to enhance care. When properly
implemented, they can substantially reduce clinic
burden and care delay, and can improve patient
outcomes. Specifically, RI is routine and scheduled,
requires coordination between the patient and clinic,
and mirrors an office checkup; RM is automatic data
transmission that typically requires no action by the
patient that is triggered by clinical and device func-
tion alerts.
RM TECHNOLOGY. Transtelephonic monitoring.
Transtelephonic monitoring (TTM) has been in use
since approximately 1970, and requires a patient to
make contact with skin electrodes (such as bracelets)
that record a single-lead ECG and transmit it through
an analog phone to the clinic (Figure 10). By observing
the ECG and pacemaker magnet behavior, device
status and battery function can be deduced. Due to
the complexity for patients and clinic, and the
marked superiority of RI and RM, new pacemakers
do not use TTM, although many patients with
legacy devices continue to use it.
Inductive transmission. RI typically uses inductive
transmission. A patient holds a transmitter’s induc-
tive wand over the pacemaker to perform a full
interrogation. The transmitter, in turn, connects via a
landline or cellular connection to a server, which
delivers a full device interrogation to the clinic that is
often identical to the report created by an in-office
visit. This includes: 1) battery status; 2) lead integ-
rity; 3) lead sensing and pacing (threshold) function;
4) activity sensor statistics; 5) pacing frequency; and
6) stored arrhythmic events.
Radiofrequency RM. A wandless transmitter with
radiofrequency capabilities automatically connects to
the implanted pacemaker, with no action required on
the patient’s part, as long as he or she is within range.
Typically, the transmitter is placed on or near a
nightstand to enable daily communication in the
event of alerts (e.g., device or rhythm abnormalities).
Episodically, full transmissions that include all of the
information available with RI are performed. Patients
also can manually force a transmission by pushing a
button on the transmitter.
In contrast to RI and TTM, RM checks patient and
device status on a daily basis (as opposed to every
3 months), is fully automatic, and can verify trans-
missions and generate alerts when they are absent.
Evidence suggests that this form of monitoring de-
tects abnormalities sooner and may improve survival;
new pacemakers either include this capability or will
do so in the near future (50).
FIGURE 13 Single-Component Leadless Pacemakers
The MICRA (Medtronic, Minneapolis, Minnesota) and Nanostim (St. Jude Medical, St.
Paul, Minnesota) leadless pacemakers are compared. Reprinted with permission from
Miller et al. (61) and Link et al. (76).
FIGURE 12 Mechanisms of Complications in Pacemaker With Extravascular Pockets
and Transvenous Leads
Limitations of traditional transvenous pacemakers include increased risk of infection,
thromboembolism, and lead failure, among others. PFO ¼ patent foramen ovale.
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18. MONITORING OF DEVICE AND LEAD FUNCTION. RM
effectively detects system malfunction with less
delay than clinic visits with TTM (51). In a random-
ized study comparing RM versus in-person clinic
visits augmented by TTM, the remote arm had a
shorter mean time to first diagnosis of clinically
actionable events (5.7 months vs. 7.7 months). Events
included significant pacing threshold increases or
loss of capture, changes in lead impedance, and
generator battery depletion to replacement indicators
(51). Furthermore, a randomized trial of long-term
RM versus in-clinic follow-up of pacemaker re-
cipients showed that the RM group had a similar rate
of death and hospitalization for device-related or
cardiovascular adverse events, demonstrating its
safety (52).
DETECTION OF SUPRAVENTRICULAR ARRHYTHMIA
AND STROKE PREVENTION. Detection of asymp-
tomatic AF using RM permits timely therapy,
including the introduction of anticoagulation therapy
to prevent stroke in at-risk individuals (53). Remotely
monitored patients are also less likely to be hospi-
talized for atrial arrhythmias (52). In patients without
clinical AF, subclinical atrial arrhythmias lasting
6 min or longer are associated with a significantly
increased risk of ischemic stroke or embolism (54).
Ongoing trials will determine the effect of therapy for
these brief, asymptomatic events. Unrelated to
stroke, atrial tachyarrhythmia detection permits
medical therapy and rate control interventions,
potentially accounting for the reduction in inappro-
priate shocks with RM and improving HF.
FIGURE 14 Leadless Pacemaker Implantation
(Left panels) (Top) Anatomic specimen in the RAO view, corresponding to the cine image below. The angled vertical line separates the
RA from the RV. (Bottom) A delivery catheter has entered the RA, crossed the tricuspid valve, and positioned the leadless pacemaker at the
RV apical septum. Contrast medium injection highlights the pacemaker’s position and RV trabeculations. (Right panels) (Top) Anatomic
specimen in the LAO view, with a circle around the LV and RV indicating the crescent-shaped RV. The top right specimen is cut to show the
internal RV. (Bottom) Corresponding cine image showing the septal pacemaker position. RA ¼ right atrium; other abbreviations as in
Figures 3 and 5.
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19. DETECTION OF VENTRICULAR TACHYARRHYTHMIA.
The benefit of detection of ventricular arrhythmia by
RM has been demonstrated in multiple implantable
cardioverter-defibrillator (ICD) studies and registries;
its role in patients with pacemakers is less clear.
A meta-analysis comparing RM to in-clinic visits
demonstrated a nonsignificant trend toward reduced
cardiovascular mortality, a similar overall shock rate,
a significantly reduced inappropriate shock rate, and
shorter time to the detection of atrial and ventricular
arrhythmias with RM (50).
RM AND SURVIVAL. RM permits analytics on large
patient numbers. In the ALTITUDE registry and Merlin
network, the use of RM was associated with a lower
mortality in recipients of pacemakers, ICDs, and CRT
(Figure 11) (55,56). The improved survival may have
resulted from early recognition and management of
arrhythmia and HF. However, a meta-analysis of RM
trials found no difference in survival compared with
in-office visits (indicating safety), with a potential
survival benefit limited to systems using daily trans-
mission verification (radiofrequency systems) (50).
HF MONITORING. Current ICDs and CRT devices can
monitor for HF using thoracic impedance as a surro-
gate for pulmonary congestion. This is sometimes
used in combination with other parameters, such as
heart rate variability, patient activity level, rapid
ventricular rate during AF, and low CRT pacing, to
detect possible worsening of HF. Although these
programs can provide early warning of worsening HF,
their use has not been shown to improve HF clinical
outcomes and survival (57,58).
LEADLESS PACING
Cardiac pacemakers are extremely effective for
treating symptomatic bradycardia. However, the
same system paradigm has been in use for the past
FIGURE 15 Leadless Pacemaker Fixation Mechanism and Radiographic Appearance
Proximal
Retrieval Feature
Anode
Cathode
Atraumatic
Nitinol Tines
Left
Ventricle
Right
Ventricle
Inferior Vena
Cava
INFERIOR
VENA CAVA
ANTERIOR VIEW
OF HEART
RIGHT
VENTRICULAR
APEX
Coiled
spring
ENDOCARDIUM
Anode
Delivery
catheter
RIGHT
VENTRICLE
RIGHT
ATRIUM
RIGHT
VENTRICLE
LEFT
VENTRICLE
Docking
interface
Nanostim
leadless cardiac
pacemaker
Cathode
(Left) Nanostim active fixation leadless pacemaker. (Right) Micra passive fixation transcatheter pacing system. Top panels adapted from Reddy et al. (62) and
Reynolds et al. (63).
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20. 50 years, namely, an implanted extravascular pulse
generator connected to a lead that traverses the
vasculature to make contact with the endocardium.
Although reliable and effective, complications are
almost universally caused by the lead, which is a
polyurethane- or silicone-encapsulated conductor
that is subject to repetitive mechanical motion with
each cardiac cycle and with shoulder girdle motion,
exposing its constituent materials to mechanical
stress and fracture (Figure 12) (59). Because pulse
generator pockets are extravascular, they may
serve as a nidus for bacterial growth by providing a
surface for bacterial biofilm elaboration; the lead then
serves as a conduit for bacterial entry to the blood
pool. Moreover, leads are inherently thrombogenic,
eliciting fibrotic reactions that make removal techni-
cally challenging, with a risk of venous perforation,
valve disruption, hemothorax, and death. Lead
thrombogenicity also introduces a risk of stroke in the
setting of venosystemic shunts. Last, by crossing the
tricuspid valve, a lead can impinge on leaflet motion,
promote clinically significant tricuspid regurgitation,
and impair the response to cardiac resynchronization
(60). Given the effectiveness of pacemakers and the
host of potential lead-related complications, a lead-
less pacemaker was developed.
Leadless pacemakers have been developed using
2 distinct strategies: single-component and multi-
component systems (61). With single-component
systems, the entire pacemaker (battery, electronics,
stimulating electrodes, and sensors) is compressed
into a small capsule that is delivered into the heart
using a deflectable sheath. Advantages of this strategy
include greater energy efficiency, system simplicity,
and ease of implantation. Limitations, however,
include retrieval of intracardiac systems years later
after battery depletion, and uncertain thrombus and
infection risk. With a multicomponent system, a small
“seed” is placed within a cardiac chamber to act
as an energy transducer. A second, extrathoracic
FIGURE 16 Complications With Transcatheter Leadless Pacemakers Versus Historical Transvenous Control Subjects
100%
80%
60%
40%
20%
0%
0
2667
725
Control
Transcatheter
Number at Risk
2396
659
2313
505
2267
497
2187
303
2120
298
1965
289
1793
71
1729
68
1702
64
1669
62
1633
62
1537
62
30 60 90 120 150
Days From Implant
MajorComplicationRate(%)
0
10%
Historical Control
Transcatheter Pacemaker
HR: 0.49 (95% CI: 0.33-0.75)
P-value: 0.001
8%
6%
4%
2%
0%
90 183 270 365
183 210 240 270 300 330 365
In this Micra TPS (Medtronic, Minneapolis, Minnesota) study post hoc analysis, the 725 study patients were compared with 2,667 patients who
received transvenous pacemakers in previous studies as a historical control cohort. Leadless study patients were older and had more
comorbidities than control subjects. At 6-month follow-up, patients with leadless pacemakers had significantly fewer major complications
than control patients (HR: 0.49; p < 0.001), with study patients experiencing fewer hospitalizations, system revisions, and dislodgments.
Reprinted with permission from Reynolds et al. (63). Abbreviations as in Figure 4.
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21. component beams energy (ultrasound or radio waves)
to the seed, and the seed then converts the energy to a
pacing pulse.
SINGLE-COMPONENT LEADLESS PACING. In single-
component leadless pacemakers, the pulse generator
and sensing and pacing electrodes are all entirely self-
contained in a capsule designed for intraventricular
placement, eliminating the need for pockets and
leads. There are currently 2 devices that have been
widely tested in humans: the Nanostim leadless car-
diac pacemaker (LCP) (St. Jude Medical, St. Paul,
Minnesota), and the MICRA transcatheter pacing sys-
tem (TPS) (Medtronic), both of which can deliver
single-chamber rate-responsive ventricular paci-
ng (Figure 13) (62,63). The systems are placed via an
18- (LCP) or 24-F (TPS) sheath inserted in a femoral
vein, and are delivered to the RV apical septum
(Figure 14). The systems differ with regard to fixation
mechanism. The LCP uses an active fixation helix, with
rotation of the entire device via a delivery catheter
handle control knob at the time of implantation,
whereas the TPS has integrated electrically inert
nitinol tines that are used solely for fixation (Figure 15).
In the initial trial experience for both systems, suc-
cessful implantation occurred in over 95% of cases,
with major complications in 4% to 6.5% of cases,
perforation or effusion in 1.5% to 1.6% of cases, and
adequate pacing measures at 6 months in 90% to
98.3%. (62,63). The TPS is physically smaller than the
LCP (0.8 cm3
vs. 1.0 cm3
), but has a larger diameter
(24-F vs. 18-F introducer sheath) and a smaller battery,
with shorter anticipated longevity at nominal settings
(9.6 years vs. 14.7 years) (61). The TPS uses autocapture
technology to algorithmically use the lower energy
pacing pulses to extend longevity, and uses radio-
frequency telemetry, which may permit daily alerts
and passive follow-up for true RM. The LCP uses
conductive telemetry, which saves battery charge, but
requires placement of patches on the skin for
FIGURE 17 Multicomponent Leadless Pacing System
The battery/transmitter unit detects the pacing stimulus from the coimplant, and an ultrasound pulse is sent to the receiver electrode, which
converts the ultrasound energy to a pacing pulse. ICD ¼ implantable cardioverter-defibrillator; other abbreviations as in Figures 1 and 3.
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22. pacemaker communication. Direct comparisons be-
tween systems have not been performed.
Ideal management of leadless pacemakers after
battery depletion is not known. Little data exists
regarding removal of chronically implanted systems.
Both available pacemakers have a posterior docking
button designed to facilitate late device retrieval
(Online Videos 2A, 2B, and 2C, Online Figure 1). In the
TPS experience, 7 of 9 attempts at percutaneous
retrieval were successful, including all attempts
within 6 months of implantation (64). Specifically
designed removal tools have been developed for the
LCP. Fourteen of 15 removal attempts were successful
in a recent report; 4 of 4 acute removals (<6 weeks) and
10 of 11 chronic removals (implant duration 88 to 1,188
days) (65). The 1 failed removal was because of inac-
cessibility of the proximal hub due to its position under
the tricuspid valve. Given that leadless pacemakers
are one-fiftieth the volume of the typical RV,
device deactivation and insertion of a replacement
may be a viable strategy for battery depletion for those
patients who outlive their pacemaker’s battery.
Both leadless pacemaker systems have been
compared with cohorts of transvenous pacemaker
recipients, although direct, prospective randomized
comparisons are lacking (Figure 16 describes the
MICRA study) (63,66). In these analyses, the leadless
pacemaker was associated with fewer short- and
intermediate-term complications. This was driven
largely by reductions in or the absence of lead com-
plications, infections, and pocket complications.
Across all leadless devices, infections appear rare,
perhaps due to the lack of an extravascular pocket
with direct connection to the bloodstream (63,66).
The major limitation of current-generation leadless
pacemakers is their ability to only perform single-
chamber ventricular pacing. Thus, for most patients
with sinus node dysfunction, or sinus rhythm and AV
block, dual-chamber transvenous devices are
preferred. Similarly, patients in need of cardiac
resynchronization are not candidates for single-
component leadless pacemakers. Patients with infe-
rior vena cava filters and mechanical tricuspid
valves are not candidates. Although chronic device
embolization has not been reported, it remains a po-
tential concern. The accuracy of rate-responsive fea-
tures, given that sensors are intracardiac, is not well
understood. And last, as noted earlier, optimal man-
agement at the time of battery depletion is not
known. Nonetheless, given the lack of a surgical
wound, absence of post-implant arm restrictions, and
reduced rate of complications, leadless pacemakers
represent a paradigm shift that will likely be clinically
transformative. Dual-chamber systems are currently
under active development; design challenges include
device–device communication and fixation in the
thin-walled right atrium.
MULTICOMPONENT LEADLESS PACING. The WiSE-
CRT system (EBR Systems, Sunnyvale, California)
uses a multicomponent strategy to provide leadless
cardiac resynchronization. A tiny (9.1 mm  2.7 mm,
0.05 cm3
) receiver electrode composed of polyester-
covered titanium is implanted endocardially in the
LV. A subcutaneous pulse generator is placed in the
left lateral thorax and generates ultrasound pulses,
which are converted to electrical pacing stimuli by
the endocardial seed (Figure 17). All patients in the
WiSE-CRT study had a traditional pacemaker or
defibrillator; the subcutaneous WiSE-CRT pulse
generator detected the RV pacing pulse from the
standard system, which triggered endocardial LV
pacing. In the initial trial, patients with failed coro-
nary sinus lead placement, nonresponse to CRT, or
need for an upgrade to CRT were enrolled. Data from
small studies demonstrated significant QRS narrow-
ing, absolute EF improvements of 5%, and im-
provements in composite clinical scores at 6 months
(67). The initial WiSE-CRT study was stopped for
safety reasons: 3 patients (18%) developed pericar-
dial effusions associated with seed delivery (68).
Following delivery system redesign, early data from
14 patients demonstrated no implant-related adverse
events (69). Leadless endocardial LV pacing holds
promise in that it may be more physiological, afford
greater opportunities for LV pacing site selection,
lead to a greater CRT response with lower risk of
proarrhythmia, eliminate phrenic nerve stimulation,
and mitigate against the risks of mitral regurgitation
and lead-related thrombus. However, the technology
is early in its development, and there are many un-
knowns. Challenges may include identification of
acoustic windows in a subset of patients, energy
inefficiency and early battery depletion, theoretical
hazards of chronic sonification of cardiac tissues,
and uncertain susceptibility to environmental inter-
ference. Other mechanisms for 2-stage leadless
pacing are under early exploration. Pre-clinical ex-
periments have been performed using magnetic in-
duction rather than ultrasound to drive an
endocardial seed (70). Other multicomponent lead-
less systems including the integration of a subcu-
taneous ICD with a leadless pacemaker are under
development, allowing for antibradycardia pacing
and antitachycardia pacing in conjunction with a
subcutaneous ICD (61).
BATTERYLESS PACING. Battery depletion and
pulse generator exchanges represent sources of
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23. complications for transvenous systems and uncer-
tainty in leadless systems. Cardiac and pulmonary
motion provide an inexhaustible source of energy
during the life of a patient. Piezoelectric nanowires
have been deployed on flexible devices to generate
voltages as large as 1 to 2 V and currents up to 100 nA,
sufficient to power the microelectronics of a pace-
maker (71). Motion harvesting pacemakers remain in
the realm of research, although devices have been
built and tested in animal models.
Biological pacemakers modify nonpacemaker
myocytes to provide automaticity using gene therapy
technologies, or add pacemaker syncytia to the heart
through adult or embryonic stem cell therapies
(72,73). Biological pacemakers are in the early stages
of development, and current challenges include dif-
ficulty ensuring long-term engraftment and potential
for proarrhythmia.
CONCLUSIONS
Pacemakers have evolved from simple devices that
prevent catastrophic bradycardia to complex, highly
programmable systems. Cardiac resynchronization is
established for the treatment of HF, but patient se-
lection, optimization of response, management of
nonresponders, and multisite LV pacing remain areas
of active investigation. His-bundle pacing and lead-
less pacing offer fundamental shifts in approach and
potentially improved clinical outcomes. On the hori-
zon may be batteryless pacemakers that transform
mechanical motion into usable electrical energy.
REPRINT REQUESTS AND CORRESPONDENCE: Dr.
Paul A. Friedman, Department of Cardiovascular
Medicine, Mayo Clinic, 200 First Street SW, Rochester,
Minnesota 55902. E-mail: pfriedman@mayo.edu.
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KEY WORDS His bundle pacing, leadless
pacing, remote monitoring,
resynchronization
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