This document provides an overview of paediatric cardiology, including common cardiovascular presentations such as collapse, cyanosis, syncope, palpitations, and chest pain in children. It discusses the normal heart rate and ECG patterns in children of different ages. Specific conditions covered include supraventricular tachycardia, ventricular tachycardia, long QT syndrome, atrial flutter/fibrillation, pre-excitation syndromes, and various forms of congenital heart disease. Guidelines are provided for evaluation and emergency management of these conditions, including use of prostaglandins, hyperoxia testing, and treatment of arrhythmias and heart failure. Kawasaki disease is reviewed as a cause of acquired heart disease in children
This document provides an overview of various cardiac arrhythmia syndromes including Brugada syndrome, long QT syndrome, short QT syndrome, arrhythmogenic right ventricular dysplasia, Wolff-Parkinson-White syndrome, and hypertrophic cardiomyopathy. It discusses the clinical features, ECG findings, diagnostic criteria, and disposition for each condition. Key advice includes carefully examining leads V1-V3 for abnormalities, being aware of rare conditions like short QT syndrome, and consulting cardiology when these complex syndromes are suspected.
Cardiology 1.4. Palpitations - by Dr. Farjad IkramFarjad Ikram
Introduction to one of the more common symptoms of cardiac, psychiatric and metabolic disease. Palpitation is the uncomfortable awareness of heart beat and can often be the only symptom of underlying fatal arrhythmias.
Template design credits - http://www.slidescarnival.com
This document discusses various types of arrhythmias that can occur in children. It begins by describing the normal electrical conduction system of the heart and then discusses different types of tachyarrhythmias and bradyarrhythmias. Common pediatric tachyarrhythmias mentioned include supraventricular tachycardia, atrial flutter, atrial fibrillation, ventricular tachycardia, and ventricular fibrillation. Long QT syndrome is also summarized. Treatment options for unstable and stable rhythms are provided.
1. The heart's electrical conduction system coordinates the contraction of the heart muscles. Abnormalities in this system can cause arrhythmias or irregular heart rhythms.
2. Pediatric arrhythmias are classified as tachyarrhythmias (fast rhythms) or bradyarrhythmias (slow rhythms) and can originate from the atria, junction, or ventricles.
3. Common tachyarrhythmias include supraventricular tachycardia, which has several subtypes like AV nodal re-entrant tachycardia. Bradyarrhythmias include sinus bradycardia and various types of heart block.
This document discusses various types of arrhythmias that can occur in children, including tachyarrhythmias and bradyarrhythmias. It provides details on the electrical conduction system of the heart and then describes different supraventricular and ventricular arrhythmias, their typical ECG presentations, causes, symptoms, and treatment approaches. Specific arrhythmias covered include sinus tachycardia, premature atrial contractions, supraventricular tachycardia, ventricular tachycardia, ventricular fibrillation, atrial flutter, atrial fibrillation, sinus bradycardia, heart blocks, and congenital complete atrioventricular block.
Cardiology 1.1. Chest pain - by Dr. Farjad IkramFarjad Ikram
Introduction to one of the most common symptoms that can represent a wide range of diseases, from benign to life-threatening, covering number of systems including gastrointestinal, cardiovascular, pulmonary, musculoskeletal and psychiatric. Includes a brief explanation of anti-anginal therapy.
Template design credits - http://www.slidescarnival.com
This document summarizes information about palpitations, including their causes, general approach to evaluation, and associated conditions. It notes that palpitations can be caused by cardiac, metabolic, respiratory, or psychiatric issues. The evaluation involves determining stability, performing an ECG, and taking a history on duration, rate, and rhythm. Associated symptoms like chest pain or dyspnea should be assessed. Conditions like WPW syndrome, Brugada syndrome, and long QT syndrome can predispose patients to arrhythmias and should be considered.
Approach to a Child with Congenital Heart DiseseCSN Vittal
This document discusses congenital heart diseases (CHD), specifically ventricular septal defects (VSD). It begins by outlining the approach to diagnosing and classifying CHD. It then describes the different types of VSDs based on their anatomical location, including perimembranous, muscular, inlet, and supracristal defects. The clinical manifestations, physical exam findings, ECG patterns, chest x-ray appearances, and echocardiogram features of VSDs are discussed in detail.
This document provides an overview of various cardiac arrhythmia syndromes including Brugada syndrome, long QT syndrome, short QT syndrome, arrhythmogenic right ventricular dysplasia, Wolff-Parkinson-White syndrome, and hypertrophic cardiomyopathy. It discusses the clinical features, ECG findings, diagnostic criteria, and disposition for each condition. Key advice includes carefully examining leads V1-V3 for abnormalities, being aware of rare conditions like short QT syndrome, and consulting cardiology when these complex syndromes are suspected.
Cardiology 1.4. Palpitations - by Dr. Farjad IkramFarjad Ikram
Introduction to one of the more common symptoms of cardiac, psychiatric and metabolic disease. Palpitation is the uncomfortable awareness of heart beat and can often be the only symptom of underlying fatal arrhythmias.
Template design credits - http://www.slidescarnival.com
This document discusses various types of arrhythmias that can occur in children. It begins by describing the normal electrical conduction system of the heart and then discusses different types of tachyarrhythmias and bradyarrhythmias. Common pediatric tachyarrhythmias mentioned include supraventricular tachycardia, atrial flutter, atrial fibrillation, ventricular tachycardia, and ventricular fibrillation. Long QT syndrome is also summarized. Treatment options for unstable and stable rhythms are provided.
1. The heart's electrical conduction system coordinates the contraction of the heart muscles. Abnormalities in this system can cause arrhythmias or irregular heart rhythms.
2. Pediatric arrhythmias are classified as tachyarrhythmias (fast rhythms) or bradyarrhythmias (slow rhythms) and can originate from the atria, junction, or ventricles.
3. Common tachyarrhythmias include supraventricular tachycardia, which has several subtypes like AV nodal re-entrant tachycardia. Bradyarrhythmias include sinus bradycardia and various types of heart block.
This document discusses various types of arrhythmias that can occur in children, including tachyarrhythmias and bradyarrhythmias. It provides details on the electrical conduction system of the heart and then describes different supraventricular and ventricular arrhythmias, their typical ECG presentations, causes, symptoms, and treatment approaches. Specific arrhythmias covered include sinus tachycardia, premature atrial contractions, supraventricular tachycardia, ventricular tachycardia, ventricular fibrillation, atrial flutter, atrial fibrillation, sinus bradycardia, heart blocks, and congenital complete atrioventricular block.
Cardiology 1.1. Chest pain - by Dr. Farjad IkramFarjad Ikram
Introduction to one of the most common symptoms that can represent a wide range of diseases, from benign to life-threatening, covering number of systems including gastrointestinal, cardiovascular, pulmonary, musculoskeletal and psychiatric. Includes a brief explanation of anti-anginal therapy.
Template design credits - http://www.slidescarnival.com
This document summarizes information about palpitations, including their causes, general approach to evaluation, and associated conditions. It notes that palpitations can be caused by cardiac, metabolic, respiratory, or psychiatric issues. The evaluation involves determining stability, performing an ECG, and taking a history on duration, rate, and rhythm. Associated symptoms like chest pain or dyspnea should be assessed. Conditions like WPW syndrome, Brugada syndrome, and long QT syndrome can predispose patients to arrhythmias and should be considered.
Approach to a Child with Congenital Heart DiseseCSN Vittal
This document discusses congenital heart diseases (CHD), specifically ventricular septal defects (VSD). It begins by outlining the approach to diagnosing and classifying CHD. It then describes the different types of VSDs based on their anatomical location, including perimembranous, muscular, inlet, and supracristal defects. The clinical manifestations, physical exam findings, ECG patterns, chest x-ray appearances, and echocardiogram features of VSDs are discussed in detail.
This document provides an overview of arrhythmia, including:
- Arrhythmia is any disturbance in the rate, regularity, site of origin, or conduction of the cardiac electrical impulse. It can arise from problems in the sinus node, atrial cells, AV junction, or ventricular cells.
- Arrhythmias are classified based on a combination of rate, site of origin, and morphology as either bradyarrhythmias or tachyarrhythmias.
- Common types of narrow complex tachycardias include sinus tachycardia, atrial fibrillation/flutter, AV nodal reentrant tachycardia, and AV reentrant tachycardias associated with
Cynotic congenital heart disease UG Class Dr Jyothi.pptxhamsinin16
Cyanotic congenital heart disease can cause reduced or increased pulmonary blood flow. Conditions with reduced flow include tetralogy of Fallot and pulmonary atresia. Clinical features include cyanosis, murmurs, and cyanotic spells treated with oxygen, morphine, and drugs to increase systemic vascular resistance. Conditions with increased pulmonary blood flow include transposition of the great arteries and total anomalous pulmonary venous return. Long-term management may involve staged surgical repairs throughout childhood and adulthood. Eisenmenger syndrome can develop from untreated ventricular septal defects, patent ductus arteriosus, or atrial septal defects.
The following powerpoint presentation is about the current AF guidelines, prepared by Dr Jawad Siraj, who is a final year resident as Cardiology Unit, PGMI, LRH, Peshawar
This document discusses various pediatric dysrhythmias, their typical presentations, and treatment approaches. It describes that sinus arrhythmia, wandering atrial pacemaker, and isolated premature contractions are usually normal variants that do not require treatment. Supraventricular tachycardia is the most common arrhythmia requiring treatment and can often be terminated with vagal maneuvers, adenosine, or cardioversion. First degree atrioventricular block is commonly seen in neonates but generally does not cause bradycardia. Third degree atrioventricular block may require a pacemaker, especially if associated with slower heart rates or symptoms. Ventricular arrhythmias like tachycardia or fibrillation indicate serious underlying
This document summarizes the diagnosis and management of common cardiac emergencies in children. It presents several case studies and uses them to discuss key considerations like differentiating various causes of cyanosis, shock, or arrhythmias in infants and children. For each case, it analyzes presenting signs and test results to identify the underlying condition. It then outlines the initial emergency management principles, focusing on stabilization, organ support, and addressing specific issues like restoring blood flow or minimizing pulmonary pressures. The document emphasizes the importance of early diagnosis and intervention for high mortality cardiac conditions in children.
Wolff-Parkinson-White syndrome is a congenital heart condition caused by an abnormal accessory electrical pathway between the atria and ventricles. This pathway can lead to arrhythmias like atrial fibrillation or tachycardia that cause symptoms like palpitations, fainting, and blackouts. While sometimes the pathways disappear on their own, treatment options include catheter ablation to destroy the pathways or medications to prevent arrhythmias. The condition is diagnosed through ECG and affects about 1 in 100,000 people, most often diagnosed in childhood or adolescence.
A teaching session I gave in 2012 to Cardiology / Acute Medicine trainees when I was working as a Staff Specialist / Professor of Cardiology in Darwin, Australia.
Atrial fibrillation with emphasis on managementRaghavAgrawal94
Comprehensive slides on the history, risk factors, pathophysiology, clinical features, diagnosis, management, complications and trials of Atrial Fibrillation(AF/AFib) for the use of Internal medicine residents or physicians
This case report describes a 14-year-old male who presented with episodes of palpitations, tachycardia, dyspnea and chest heaviness. His heart rate was found to be 190 bpm during episodes. He was diagnosed with reentrant supraventricular tachycardia. An ECG showed reentrant supraventricular tachycardia. He was treated with vasocardin and a beta blocker. He was discharged after a 24-hour ECG holter showed no further episodes while on medication.
Takotsubo cardiomyopathy, also known as "broken heart syndrome," is a temporary heart condition that mimics a heart attack. It's typically triggered by intense emotional or physical stress, causing a sudden weakening of the heart muscle. Symptoms can include chest pain, shortness of breath, and irregular heartbeats. The condition usually resolves on its own within days to weeks, and treatment focuses on managing symptoms and addressing the underlying stressors.
This document provides an overview of pediatric arrhythmias, including how to assess unstable vs stable rhythms, how to interpret normal vs abnormal ECG findings, and treatment recommendations for common arrhythmias like supraventricular tachycardia, atrial flutter, ventricular tachycardia, and heart block. Key recommendations include using vagal maneuvers, adenosine, synchronized cardioversion, or pacing as first-line treatments depending on the specific arrhythmia and patient stability. Ongoing management may involve antiarrhythmic medications, ablation procedures, or implantable defibrillators as needed to control symptoms and prevent complications.
This document discusses the diagnosis and management of cardiac arrhythmias. It begins with an introduction stating that cardiac arrhythmias lead to sudden cardiac death for 250,000 people annually in the United States. The document then covers the history of understanding arrhythmias, the major types of arrhythmias and heart blocks, how to analyze arrhythmias, evaluate patients presenting with arrhythmias, investigate arrhythmias, and manage common arrhythmias like atrial fibrillation, supraventricular tachycardia, and ventricular tachycardia. Treatment options discussed include medical management, surgical correction, ablation, pacemakers, and defibrillators.
This document discusses pediatric cardiology emergencies, dividing them into newborn emergencies and infant/childhood emergencies. Newborn emergencies include cyanosis caused by obstructive lesions like pulmonary atresia or abnormal circulations like transposition of the great arteries, treated with prostaglandins. Low cardiac output in newborns can be caused by left-sided obstructive lesions, muscle diseases, or heart rate problems and is treated with inotropes and afterload reduction. Infant/childhood emergencies include hypercyanotic spells in conditions like tetralogy of Fallot, congestive heart failure with different causes at different ages, and arrhythmias including supraventricular tachy
This document discusses acyanotic congenital heart disease. It classifies acyanotic defects into left-to-right shunts including ventricular septal defects (VSD), atrial septal defects (ASD), and patent ductus arteriosus (PDA). It also discusses obstructive lesions such as aortic stenosis and pulmonary stenosis. The document provides details on the prevalence, clinical presentation, diagnosis and management of VSD and PDA. VSD is the most common congenital heart defect, presenting with heart murmur and signs of heart failure. PDA presents with murmur and respiratory distress. Both are diagnosed by echocardiogram and managed medically or surgically.
This document provides guidance on evaluating palpitations in children. It describes how to take a history regarding the sensations, triggers, and associated symptoms. A physical exam and ECG can help identify potential cardiac causes like arrhythmias. While most palpitations have non-serious causes like anxiety, further workup may be needed if risk factors are present like a family history of sudden cardiac death. Conditions like supraventricular tachycardia and long QT syndrome can potentially cause palpitations.
This document provides an overview of Ebstein's anomaly, a congenital heart defect characterized by abnormal attachment of the tricuspid valve leaflets to the myocardium. It discusses the history and typical features of the condition, including displaced valve leaflets, enlargement of the right ventricle and atrium, and arrhythmias. The document outlines evaluation with echocardiogram, ECG and chest x-ray, and indicates interventions like tricuspid valve repair are recommended for those with cyanosis, heart failure or decreased functional capacity. While neonatal Ebstein's carries a poor prognosis, satisfactory valve repair can result in good medium and long-term outcomes.
Approach to cyanotic congenital heart diseaseikramdr01
This document provides guidance on diagnosing cyanotic congenital heart disease through a practical clinical approach. It emphasizes the importance of suspecting heart disease in any child who does not clearly fit the initial diagnosis or has significant desaturation. Key signs to look for include cyanosis, differential pulse oximetry readings, and clues from chest X-ray and ECG. The approach involves classifying heart defects based on hemodynamics like pulmonary blood flow and systemic saturation. For neonates, focus is on duct-dependent lesions presenting with cyanosis or shock. Beyond the neonatal period, diagnosis involves assessing cyanosis and pulmonary congestion to identify lesions like left-to-right shunts, tetralogy of Fallot physiology,
This document provides guidelines for managing supraventricular tachycardia (SVT) in adult patients. SVT is defined as a tachycardia with atrial and/or ventricular rates over 100 bpm involving tissue above the His bundle. Common types of SVT include atrioventricular nodal reentrant tachycardia (AVNRT), atrioventricular reentrant tachycardia (AVRT), atrial tachycardia (AT), multifocal atrial tachycardia (MAT), sinus node reentry tachycardia, and junctional tachycardia. The document reviews the clinical presentation, differential diagnosis, evaluation and treatment of these arrhythmias. It
This document provides guidance on diagnosing cyanotic congenital heart disease through a practical clinical approach. It emphasizes the importance of suspecting heart disease in any child who does not clearly fit the initial diagnosis, and in any child with significant desaturation. Key clues from history, examination, chest X-ray and ECG are discussed. The approach is age-oriented, focusing on duct-dependent lesions in neonates and classifying lesions based on cyanosis and pulmonary blood flow in infants. A functional classification of hemodynamic effects is prioritized over anatomical diagnosis. Early diagnosis of duct-dependent lesions or signs of low cardiac output is critical to prevent deterioration.
How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
Odoo 17 CRM allows us to track why we lose sales opportunities with "Lost Reasons." This helps analyze our sales process and identify areas for improvement. Here's how to configure lost reasons in Odoo 17 CRM
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
This document provides an overview of arrhythmia, including:
- Arrhythmia is any disturbance in the rate, regularity, site of origin, or conduction of the cardiac electrical impulse. It can arise from problems in the sinus node, atrial cells, AV junction, or ventricular cells.
- Arrhythmias are classified based on a combination of rate, site of origin, and morphology as either bradyarrhythmias or tachyarrhythmias.
- Common types of narrow complex tachycardias include sinus tachycardia, atrial fibrillation/flutter, AV nodal reentrant tachycardia, and AV reentrant tachycardias associated with
Cynotic congenital heart disease UG Class Dr Jyothi.pptxhamsinin16
Cyanotic congenital heart disease can cause reduced or increased pulmonary blood flow. Conditions with reduced flow include tetralogy of Fallot and pulmonary atresia. Clinical features include cyanosis, murmurs, and cyanotic spells treated with oxygen, morphine, and drugs to increase systemic vascular resistance. Conditions with increased pulmonary blood flow include transposition of the great arteries and total anomalous pulmonary venous return. Long-term management may involve staged surgical repairs throughout childhood and adulthood. Eisenmenger syndrome can develop from untreated ventricular septal defects, patent ductus arteriosus, or atrial septal defects.
The following powerpoint presentation is about the current AF guidelines, prepared by Dr Jawad Siraj, who is a final year resident as Cardiology Unit, PGMI, LRH, Peshawar
This document discusses various pediatric dysrhythmias, their typical presentations, and treatment approaches. It describes that sinus arrhythmia, wandering atrial pacemaker, and isolated premature contractions are usually normal variants that do not require treatment. Supraventricular tachycardia is the most common arrhythmia requiring treatment and can often be terminated with vagal maneuvers, adenosine, or cardioversion. First degree atrioventricular block is commonly seen in neonates but generally does not cause bradycardia. Third degree atrioventricular block may require a pacemaker, especially if associated with slower heart rates or symptoms. Ventricular arrhythmias like tachycardia or fibrillation indicate serious underlying
This document summarizes the diagnosis and management of common cardiac emergencies in children. It presents several case studies and uses them to discuss key considerations like differentiating various causes of cyanosis, shock, or arrhythmias in infants and children. For each case, it analyzes presenting signs and test results to identify the underlying condition. It then outlines the initial emergency management principles, focusing on stabilization, organ support, and addressing specific issues like restoring blood flow or minimizing pulmonary pressures. The document emphasizes the importance of early diagnosis and intervention for high mortality cardiac conditions in children.
Wolff-Parkinson-White syndrome is a congenital heart condition caused by an abnormal accessory electrical pathway between the atria and ventricles. This pathway can lead to arrhythmias like atrial fibrillation or tachycardia that cause symptoms like palpitations, fainting, and blackouts. While sometimes the pathways disappear on their own, treatment options include catheter ablation to destroy the pathways or medications to prevent arrhythmias. The condition is diagnosed through ECG and affects about 1 in 100,000 people, most often diagnosed in childhood or adolescence.
A teaching session I gave in 2012 to Cardiology / Acute Medicine trainees when I was working as a Staff Specialist / Professor of Cardiology in Darwin, Australia.
Atrial fibrillation with emphasis on managementRaghavAgrawal94
Comprehensive slides on the history, risk factors, pathophysiology, clinical features, diagnosis, management, complications and trials of Atrial Fibrillation(AF/AFib) for the use of Internal medicine residents or physicians
This case report describes a 14-year-old male who presented with episodes of palpitations, tachycardia, dyspnea and chest heaviness. His heart rate was found to be 190 bpm during episodes. He was diagnosed with reentrant supraventricular tachycardia. An ECG showed reentrant supraventricular tachycardia. He was treated with vasocardin and a beta blocker. He was discharged after a 24-hour ECG holter showed no further episodes while on medication.
Takotsubo cardiomyopathy, also known as "broken heart syndrome," is a temporary heart condition that mimics a heart attack. It's typically triggered by intense emotional or physical stress, causing a sudden weakening of the heart muscle. Symptoms can include chest pain, shortness of breath, and irregular heartbeats. The condition usually resolves on its own within days to weeks, and treatment focuses on managing symptoms and addressing the underlying stressors.
This document provides an overview of pediatric arrhythmias, including how to assess unstable vs stable rhythms, how to interpret normal vs abnormal ECG findings, and treatment recommendations for common arrhythmias like supraventricular tachycardia, atrial flutter, ventricular tachycardia, and heart block. Key recommendations include using vagal maneuvers, adenosine, synchronized cardioversion, or pacing as first-line treatments depending on the specific arrhythmia and patient stability. Ongoing management may involve antiarrhythmic medications, ablation procedures, or implantable defibrillators as needed to control symptoms and prevent complications.
This document discusses the diagnosis and management of cardiac arrhythmias. It begins with an introduction stating that cardiac arrhythmias lead to sudden cardiac death for 250,000 people annually in the United States. The document then covers the history of understanding arrhythmias, the major types of arrhythmias and heart blocks, how to analyze arrhythmias, evaluate patients presenting with arrhythmias, investigate arrhythmias, and manage common arrhythmias like atrial fibrillation, supraventricular tachycardia, and ventricular tachycardia. Treatment options discussed include medical management, surgical correction, ablation, pacemakers, and defibrillators.
This document discusses pediatric cardiology emergencies, dividing them into newborn emergencies and infant/childhood emergencies. Newborn emergencies include cyanosis caused by obstructive lesions like pulmonary atresia or abnormal circulations like transposition of the great arteries, treated with prostaglandins. Low cardiac output in newborns can be caused by left-sided obstructive lesions, muscle diseases, or heart rate problems and is treated with inotropes and afterload reduction. Infant/childhood emergencies include hypercyanotic spells in conditions like tetralogy of Fallot, congestive heart failure with different causes at different ages, and arrhythmias including supraventricular tachy
This document discusses acyanotic congenital heart disease. It classifies acyanotic defects into left-to-right shunts including ventricular septal defects (VSD), atrial septal defects (ASD), and patent ductus arteriosus (PDA). It also discusses obstructive lesions such as aortic stenosis and pulmonary stenosis. The document provides details on the prevalence, clinical presentation, diagnosis and management of VSD and PDA. VSD is the most common congenital heart defect, presenting with heart murmur and signs of heart failure. PDA presents with murmur and respiratory distress. Both are diagnosed by echocardiogram and managed medically or surgically.
This document provides guidance on evaluating palpitations in children. It describes how to take a history regarding the sensations, triggers, and associated symptoms. A physical exam and ECG can help identify potential cardiac causes like arrhythmias. While most palpitations have non-serious causes like anxiety, further workup may be needed if risk factors are present like a family history of sudden cardiac death. Conditions like supraventricular tachycardia and long QT syndrome can potentially cause palpitations.
This document provides an overview of Ebstein's anomaly, a congenital heart defect characterized by abnormal attachment of the tricuspid valve leaflets to the myocardium. It discusses the history and typical features of the condition, including displaced valve leaflets, enlargement of the right ventricle and atrium, and arrhythmias. The document outlines evaluation with echocardiogram, ECG and chest x-ray, and indicates interventions like tricuspid valve repair are recommended for those with cyanosis, heart failure or decreased functional capacity. While neonatal Ebstein's carries a poor prognosis, satisfactory valve repair can result in good medium and long-term outcomes.
Approach to cyanotic congenital heart diseaseikramdr01
This document provides guidance on diagnosing cyanotic congenital heart disease through a practical clinical approach. It emphasizes the importance of suspecting heart disease in any child who does not clearly fit the initial diagnosis or has significant desaturation. Key signs to look for include cyanosis, differential pulse oximetry readings, and clues from chest X-ray and ECG. The approach involves classifying heart defects based on hemodynamics like pulmonary blood flow and systemic saturation. For neonates, focus is on duct-dependent lesions presenting with cyanosis or shock. Beyond the neonatal period, diagnosis involves assessing cyanosis and pulmonary congestion to identify lesions like left-to-right shunts, tetralogy of Fallot physiology,
This document provides guidelines for managing supraventricular tachycardia (SVT) in adult patients. SVT is defined as a tachycardia with atrial and/or ventricular rates over 100 bpm involving tissue above the His bundle. Common types of SVT include atrioventricular nodal reentrant tachycardia (AVNRT), atrioventricular reentrant tachycardia (AVRT), atrial tachycardia (AT), multifocal atrial tachycardia (MAT), sinus node reentry tachycardia, and junctional tachycardia. The document reviews the clinical presentation, differential diagnosis, evaluation and treatment of these arrhythmias. It
This document provides guidance on diagnosing cyanotic congenital heart disease through a practical clinical approach. It emphasizes the importance of suspecting heart disease in any child who does not clearly fit the initial diagnosis, and in any child with significant desaturation. Key clues from history, examination, chest X-ray and ECG are discussed. The approach is age-oriented, focusing on duct-dependent lesions in neonates and classifying lesions based on cyanosis and pulmonary blood flow in infants. A functional classification of hemodynamic effects is prioritized over anatomical diagnosis. Early diagnosis of duct-dependent lesions or signs of low cardiac output is critical to prevent deterioration.
How to Manage Your Lost Opportunities in Odoo 17 CRMCeline George
Odoo 17 CRM allows us to track why we lose sales opportunities with "Lost Reasons." This helps analyze our sales process and identify areas for improvement. Here's how to configure lost reasons in Odoo 17 CRM
it describes the bony anatomy including the femoral head , acetabulum, labrum . also discusses the capsule , ligaments . muscle that act on the hip joint and the range of motion are outlined. factors affecting hip joint stability and weight transmission through the joint are summarized.
Walmart Business+ and Spark Good for Nonprofits.pdfTechSoup
"Learn about all the ways Walmart supports nonprofit organizations.
You will hear from Liz Willett, the Head of Nonprofits, and hear about what Walmart is doing to help nonprofits, including Walmart Business and Spark Good. Walmart Business+ is a new offer for nonprofits that offers discounts and also streamlines nonprofits order and expense tracking, saving time and money.
The webinar may also give some examples on how nonprofits can best leverage Walmart Business+.
The event will cover the following::
Walmart Business + (https://business.walmart.com/plus) is a new shopping experience for nonprofits, schools, and local business customers that connects an exclusive online shopping experience to stores. Benefits include free delivery and shipping, a 'Spend Analytics” feature, special discounts, deals and tax-exempt shopping.
Special TechSoup offer for a free 180 days membership, and up to $150 in discounts on eligible orders.
Spark Good (walmart.com/sparkgood) is a charitable platform that enables nonprofits to receive donations directly from customers and associates.
Answers about how you can do more with Walmart!"
Main Java[All of the Base Concepts}.docxadhitya5119
This is part 1 of my Java Learning Journey. This Contains Custom methods, classes, constructors, packages, multithreading , try- catch block, finally block and more.
Exploiting Artificial Intelligence for Empowering Researchers and Faculty, In...Dr. Vinod Kumar Kanvaria
Exploiting Artificial Intelligence for Empowering Researchers and Faculty,
International FDP on Fundamentals of Research in Social Sciences
at Integral University, Lucknow, 06.06.2024
By Dr. Vinod Kumar Kanvaria
This presentation was provided by Steph Pollock of The American Psychological Association’s Journals Program, and Damita Snow, of The American Society of Civil Engineers (ASCE), for the initial session of NISO's 2024 Training Series "DEIA in the Scholarly Landscape." Session One: 'Setting Expectations: a DEIA Primer,' was held June 6, 2024.
Strategies for Effective Upskilling is a presentation by Chinwendu Peace in a Your Skill Boost Masterclass organisation by the Excellence Foundation for South Sudan on 08th and 09th June 2024 from 1 PM to 3 PM on each day.
The simplified electron and muon model, Oscillating Spacetime: The Foundation...RitikBhardwaj56
Discover the Simplified Electron and Muon Model: A New Wave-Based Approach to Understanding Particles delves into a groundbreaking theory that presents electrons and muons as rotating soliton waves within oscillating spacetime. Geared towards students, researchers, and science buffs, this book breaks down complex ideas into simple explanations. It covers topics such as electron waves, temporal dynamics, and the implications of this model on particle physics. With clear illustrations and easy-to-follow explanations, readers will gain a new outlook on the universe's fundamental nature.
LAND USE LAND COVER AND NDVI OF MIRZAPUR DISTRICT, UPRAHUL
This Dissertation explores the particular circumstances of Mirzapur, a region located in the
core of India. Mirzapur, with its varied terrains and abundant biodiversity, offers an optimal
environment for investigating the changes in vegetation cover dynamics. Our study utilizes
advanced technologies such as GIS (Geographic Information Systems) and Remote sensing to
analyze the transformations that have taken place over the course of a decade.
The complex relationship between human activities and the environment has been the focus
of extensive research and worry. As the global community grapples with swift urbanization,
population expansion, and economic progress, the effects on natural ecosystems are becoming
more evident. A crucial element of this impact is the alteration of vegetation cover, which plays a
significant role in maintaining the ecological equilibrium of our planet.Land serves as the foundation for all human activities and provides the necessary materials for
these activities. As the most crucial natural resource, its utilization by humans results in different
'Land uses,' which are determined by both human activities and the physical characteristics of the
land.
The utilization of land is impacted by human needs and environmental factors. In countries
like India, rapid population growth and the emphasis on extensive resource exploitation can lead
to significant land degradation, adversely affecting the region's land cover.
Therefore, human intervention has significantly influenced land use patterns over many
centuries, evolving its structure over time and space. In the present era, these changes have
accelerated due to factors such as agriculture and urbanization. Information regarding land use and
cover is essential for various planning and management tasks related to the Earth's surface,
providing crucial environmental data for scientific, resource management, policy purposes, and
diverse human activities.
Accurate understanding of land use and cover is imperative for the development planning
of any area. Consequently, a wide range of professionals, including earth system scientists, land
and water managers, and urban planners, are interested in obtaining data on land use and cover
changes, conversion trends, and other related patterns. The spatial dimensions of land use and
cover support policymakers and scientists in making well-informed decisions, as alterations in
these patterns indicate shifts in economic and social conditions. Monitoring such changes with the
help of Advanced technologies like Remote Sensing and Geographic Information Systems is
crucial for coordinated efforts across different administrative levels. Advanced technologies like
Remote Sensing and Geographic Information Systems
9
Changes in vegetation cover refer to variations in the distribution, composition, and overall
structure of plant communities across different temporal and spatial scales. These changes can
occur natural.
6. ECGs in children
• Heart rate >100 beats/min
• Rightward QRS axis > +90°
• T wave inversions in V1-3 (“juvenile T-wave pattern”)
• Dominant R wave in V1
• RSR’ pattern in V1
• Marked sinus arrhythmia
• Short PR interval (< 120ms) and QRS duration
(<80ms)
• Slightly peaked P waves
• Q waves in the inferior and left precordial leads.
7. The normal ECG
• QRS variable with age - Newborn 50-80ms, at 16
years 75-115ms
• cQTC under 6/12: 490ms, 440ms otherwise
• Notched t waves; may be normal in V2&3
• Transient Wenckebach during sleep
8. The normal ECG
• Parameters vary through age
• Right ventricular dominance owing to high
pulmonary pressures, normalise at ~6/12
• T waves; usually upright in most leads for first 7/7,
then downwards in most leads until adolescence.
•Upright t waves in childhood may reflect RVH.
10. Chest pain
Common but usually benign presentation
4436 presentations age < 19 yrs over 3 1/2 year period
in a tertiary PED in USA
•0.6% deemed cardiac
•37% arrhythmia
•29% pericardial
•17% myocarditis
•13% AMI
•4% PE
American Journal of Emergency Medicine Volume 29, Issue 6 , Pages 632-638, July 2011)
11. Non cardiac chest pain
• 56% musculoskeletal
• 12% asthma/ wheeze
• 8% infection
• 6% GI – gastritis and GORD
• 4% sickle cell disease
12. Texidor’s twinge
• Precordial catch syndrome:
• acute, non-radiating left sided chest pain in an
adolescent
• occurs suddenly, exacerbated during inspiration and
resolves in a few minutes
14. Syncope
• 15-20% all children will have an episode
Neurally mediated
Vasovagal
Reflex anoxic seizures
Orthostatic
Cardiac
Structural
Cardiomyopathy
Arrythmias
Non CVS
Psychogenic
Factitious
Neurological non syncope e.g. Seizure
15. Syncope Red Flags
• History of cardiac disease
• Family history of SCD
• Recurrent episodes
• Exertional
• Prolonged LoC
• Associated chest pain / palpitations
• Medications that can alter cardiac conduction
18. Cardiac arrhythmias in children
• Likely to be the result rather than the cause of
acute illness
• Often preceded by hypoxia, acidosis and / or
hypotension
• Primary cardiac arrhythmias are uncommon
21. Bradycardia - causes
• Bradyarrythmias rare in structurally normal
hearts
• Usually pre-terminal following hypoxia and
ischaemia
• Vagal stimulation
• Raised ICP
• Poisoning with digoxin/ beta-blockers
• Congenital CHB seen in infants of mothers
with anti ro and la antibodies
27. Supraventricular Tachycardia
• Most common primary cardiac arrhythmia in
children
• Paroxysmal, regular, narrow QRS complexes
• Caused by re-entry mechanism through an accessory
pathway or AV conduction system
• HR > 220 bpm in infants or > 180 bpm in children
33. Long QT - congenital
Normal QTc < 400ms, > 460 ms abnormal
Easiest to reproducibly measure in II & V5
Channelopathy
Genetic mutations identifies in 90% familial cases
Subtypes 1-14
Risk of torsades and VF
May present with syncope (VT), risk greatest with QT > 500ms
Ask about family history of syncope, sudden death and epilepsy
European registry 1993; 8% 5 yr mortality
Treatment with BB
36. Atrial Flutter and Fibrillation
• Rare
• Underlying CHD, status post-open heart surgery
• Cardioversion in decompensated
• In haemodynamically stable children,
amiodarone or elective cardioversion
37. Pre-excitation syndromes
• Commonest WPW
• Ventricular Pre-excitation in SR,
short PR and delta wave
• Commonest arrhythmia is
orthodromic AV re-entry
tachycardia
• Antidromic less common
39. The collapsed infant
• Wide differential
• Always cover for sepsis
Congenital heart disease
• May present as lethargy, poor feeding, "not right",
cyanosis to complete cardiovascular collapse
40. Congenital heart disease
Foetal PVR>SVR; blood
bypasses lungs through
ductus arteriosus and
foramen ovale
DA usually closes 24-36hrs
post birth – may be much
longer
FO closes when left atrium
volume increases
41. Congenital heart disease
• Failure of normal development or
• Persistence of foetal circulation
• 7-9% live births
• Acyanotic or Cyanotic heart disease
42. Acyanotic Heart Disease
VSD (25%)
ASD
PDA
PV stenosis
CoA
AS
Hypoplastic left heart
HOCM
Dextrocardia
Cyanotic Heart Disease
Tetralogy
Transposition
Tricuspid atresia
TAPVD
46. Innocent murmurs
• Common in children
• Never diastolic
• Soft, Short, midsystolic,
low intensity
• Localised
• Often vibratory or
musical
• Increase with output,
(fever)
• No thrill/ heave or
radiation
• Asymptomatic
• May resolve in few
months
• Commonest at lower left
sternal edge
• Venous hum
47. Evaluation
• Pre-natal (USS)
• Family history
• Birth history (birth state, trauma, risk infection)
• Is this cardiac? (murmur + cyanosis + absent pulses)
Pre- and post ductal oxygen saturations
ABG
4 limb BP (>10mmHg difference suggests coarctation)
ECG
CXR
Echo
48. ED management
• ABC – sats 75-85%
• Correct metabolic acidosis and shock with fluid and
bicarb
• 2 lines/ UVC if possible
• Antibiotics anyway!
• Gentle handling
• Keep warm
• Prostoglandin – ductal patency
• Inotropes
• Ventilate – in air if possible, PEEP 4-6cmH2O
49. Prostaglandin
• PGE2 infusion (dinoprostone)
• In duct dependent lesion
• Hyperoxia test suggestive, femoral pulses
diminished, metabolic acidosis persistent after
volume and inotropes
• Ensure antibiotics given!
• Beware of apnoea. May cause hypotension,
jitteriness and jerks
• No absolute contraindications
53. • 18 month old girl
6 days of high fever
Miserable
Swollen hands and feet with pain and redness
Immediate action?
Investigations?
Working diagnosis?
Further management?
55. Kawasaki Disease
• Commonest cause of acquired heart disease in
children in the UK
• Febrile, exanthematous, multi-system vasculitis in
children <5y
• Coronary arteritis with aneurysm formation in 20-
30% in untreated patients
56. Diagnosing Kawasaki disease
• Fever of 5 days plus any 4 physical exam findings:
Rash
Cervical lymphadenopathy (at least 1.5 cm in
diameter)
Bilateral conjunctival injection
Oral mucosal changes
Peripheral extremity changes
57. Kawasaki disease
• Admission as in-patient
• ECG, ECHO
• IV immunoglobulins
• Aspirin high dose
• Paediatric/Cardiology F/U (repeat ECHO at 6
weeks)