This document discusses the role of mechanical ventilation in congenital heart disease. It begins by defining mechanical ventilation and its history. It then covers the goals, ideal design, and components of mechanical ventilation. Several sections discuss how mechanical ventilators work, including different modes, parameters, and the effect on the cardiovascular system. The document concludes by covering indications for mechanical ventilation in congenital heart disease and initial ventilator settings.
High frequency oscillatory ventilation (HFOV) is a type of mechanical ventilation that uses a constant distending pressure (mean airway pressure [MAP]) with pressure variations oscillating around the MAP at very high rates (up to 900 cycles per minute). This creates small tidal volumes, often less than the dead space.
Cardiac catheterization is useful for assessing left-to-right shunts through three main techniques: oximetry runs to detect oxygen saturation step-ups, indicator dye dilution to detect early recirculation of dye injected into the proximal chamber, and angiocardiography to directly visualize the anatomic site of the shunt. While oximetry is best to localize the shunt, dye dilution can detect smaller shunts and angiography confirms anatomy. Together these techniques allow diagnosis and quantification of left-to-right intracardiac shunts.
1. Aortic regurgitation occurs when blood leaks backwards from the aorta into the left ventricle during diastole due to failure of the aortic valve leaflets to coapt properly.
2. It can be acute, caused by things like infective endocarditis or aortic dissection, or chronic, caused by conditions like bicuspid aortic valve or hypertension.
3. Chronic AR is often well-tolerated for years as the left ventricle dilates and hypertrophies to accommodate the increased volume, but acute AR can rapidly lead to heart failure and shock if not emergently treated.
The document discusses pulmonary arterial hypertension (PAH), defining it as a sustained elevation of pulmonary arterial pressure. It describes the types of PAH and the histological findings seen. There is an imbalance of vasoactive mediators like prostacyclin and thromboxane A2 as well as endothelin-1, nitric oxide, serotonin, and vascular endothelial growth factor in PAH patients. Clinical signs include breathlessness and physical exam findings of right heart strain. Diagnostic testing involves echocardiogram, chest imaging, pulmonary function tests, and right heart catheterization.
This document discusses temporary pacemakers. It explains that temporary pacemakers are indicated for bradyarrhythmias, conduction blocks, and permanent pacemaker malfunctions. It describes the principles of pacing, including electrical concepts, pacing types, wiring systems, modes of pacing, and parameters like output and sensitivity. It illustrates normal pacemaker behavior and various abnormalities including failure to capture, failure to sense, oversensing, competition, and Wenckebach behavior. It discusses evaluating underlying rhythm, assessing pacemaker strips, and troubleshooting issues like changing settings, electrodes, batteries, or reversing polarity.
Critical Congenital Heart Disease (CCHD) refers to several heart defects present at birth that require intervention. Some key points:
- CCHD includes defects where blood flow depends on an open ductus arteriosus after birth, such as Tetralogy of Fallot.
- Clinical presentation varies but may include cyanosis, heart murmur, respiratory distress. Diagnosis involves tests like echocardiogram, EKG, chest x-ray.
- Management depends on the specific defect but may include prostaglandin E1 to keep the ductus arteriosus open, then surgery to repair the anatomical issues. Early detection through newborn pulse oximetry screening can help identify cases
The document discusses several newer modes of mechanical ventilation including volume assured pressure support (VAPS), volume support (VS), pressure regulated volume control (PRVC), and adaptive support ventilation (ASV). VAPS switches between pressure control and volume control modes within a breath to ensure a minimum tidal volume. VS adjusts pressure support levels between breaths to maintain a target tidal volume. PRVC aims to deliver a set tidal volume with the lowest possible airway pressure by modifying flow and time. ASV automatically adapts support levels to provide a minimum minute ventilation with the least work of breathing.
This document discusses anesthesia considerations for children with congenital heart disease (CHD). It begins by classifying common CHD types as left-to-right shunts which increase pulmonary blood flow or right-to-left shunts which decrease it. The goal of anesthesia management is then to manipulate systemic and pulmonary vascular resistances to optimize blood flow based on the individual defect. Thorough preoperative evaluation and understanding of the child's specific anatomy and hemodynamics are essential to tailoring the anesthetic plan.
High frequency oscillatory ventilation (HFOV) is a type of mechanical ventilation that uses a constant distending pressure (mean airway pressure [MAP]) with pressure variations oscillating around the MAP at very high rates (up to 900 cycles per minute). This creates small tidal volumes, often less than the dead space.
Cardiac catheterization is useful for assessing left-to-right shunts through three main techniques: oximetry runs to detect oxygen saturation step-ups, indicator dye dilution to detect early recirculation of dye injected into the proximal chamber, and angiocardiography to directly visualize the anatomic site of the shunt. While oximetry is best to localize the shunt, dye dilution can detect smaller shunts and angiography confirms anatomy. Together these techniques allow diagnosis and quantification of left-to-right intracardiac shunts.
1. Aortic regurgitation occurs when blood leaks backwards from the aorta into the left ventricle during diastole due to failure of the aortic valve leaflets to coapt properly.
2. It can be acute, caused by things like infective endocarditis or aortic dissection, or chronic, caused by conditions like bicuspid aortic valve or hypertension.
3. Chronic AR is often well-tolerated for years as the left ventricle dilates and hypertrophies to accommodate the increased volume, but acute AR can rapidly lead to heart failure and shock if not emergently treated.
The document discusses pulmonary arterial hypertension (PAH), defining it as a sustained elevation of pulmonary arterial pressure. It describes the types of PAH and the histological findings seen. There is an imbalance of vasoactive mediators like prostacyclin and thromboxane A2 as well as endothelin-1, nitric oxide, serotonin, and vascular endothelial growth factor in PAH patients. Clinical signs include breathlessness and physical exam findings of right heart strain. Diagnostic testing involves echocardiogram, chest imaging, pulmonary function tests, and right heart catheterization.
This document discusses temporary pacemakers. It explains that temporary pacemakers are indicated for bradyarrhythmias, conduction blocks, and permanent pacemaker malfunctions. It describes the principles of pacing, including electrical concepts, pacing types, wiring systems, modes of pacing, and parameters like output and sensitivity. It illustrates normal pacemaker behavior and various abnormalities including failure to capture, failure to sense, oversensing, competition, and Wenckebach behavior. It discusses evaluating underlying rhythm, assessing pacemaker strips, and troubleshooting issues like changing settings, electrodes, batteries, or reversing polarity.
Critical Congenital Heart Disease (CCHD) refers to several heart defects present at birth that require intervention. Some key points:
- CCHD includes defects where blood flow depends on an open ductus arteriosus after birth, such as Tetralogy of Fallot.
- Clinical presentation varies but may include cyanosis, heart murmur, respiratory distress. Diagnosis involves tests like echocardiogram, EKG, chest x-ray.
- Management depends on the specific defect but may include prostaglandin E1 to keep the ductus arteriosus open, then surgery to repair the anatomical issues. Early detection through newborn pulse oximetry screening can help identify cases
The document discusses several newer modes of mechanical ventilation including volume assured pressure support (VAPS), volume support (VS), pressure regulated volume control (PRVC), and adaptive support ventilation (ASV). VAPS switches between pressure control and volume control modes within a breath to ensure a minimum tidal volume. VS adjusts pressure support levels between breaths to maintain a target tidal volume. PRVC aims to deliver a set tidal volume with the lowest possible airway pressure by modifying flow and time. ASV automatically adapts support levels to provide a minimum minute ventilation with the least work of breathing.
This document discusses anesthesia considerations for children with congenital heart disease (CHD). It begins by classifying common CHD types as left-to-right shunts which increase pulmonary blood flow or right-to-left shunts which decrease it. The goal of anesthesia management is then to manipulate systemic and pulmonary vascular resistances to optimize blood flow based on the individual defect. Thorough preoperative evaluation and understanding of the child's specific anatomy and hemodynamics are essential to tailoring the anesthetic plan.
Anaesthesia for cardiopulmonary bypass surgery [autosaved]Nida fatima
This document discusses cardiopulmonary bypass (CPB), which involves diverting blood away from the heart and through an external circuit that oxygenates the blood and returns it to the body. CPB allows surgery to be performed on an unbeating heart while still providing circulation. The key components of a CPB machine and roles of the perfusionist in managing it are described. Steps in CPB like priming, hypothermia, myocardial preservation via cardioplegia, and monitoring techniques are summarized.
The document discusses the history and development of pulmonary artery catheters. It describes how Dr. Swan and Dr. Ganz invented the balloon-tipped catheter and how it allows direct measurement of pressures in the heart and lungs. The document outlines the proper insertion technique and provides normal values for pressures measured in different areas of the heart and lungs. It also discusses indications, contraindications, and complications of pulmonary artery catheter use.
The term inotropic state is most commonly used in reference to various drugs that affect the strength of contraction of heart muscle (myocardial contractility). However, it can also refer to pathological conditions. For example, enlarged heart muscle (ventricular hypertrophy) can increase inotropic state, whereas dead heart muscle (myocardial infarction) can decrease it.
- Pulmonary artery hypertension (PAH) is defined as a mean pulmonary artery pressure of ≥25 mmHg at rest. It is characterized by pre-capillary pulmonary hypertension with a pulmonary wedge pressure <15 mmHg and a pulmonary vascular resistance >3 Wood units.
- The pathophysiology involves sustained vasoconstriction, vascular remodeling, in situ thrombosis, and increased arterial stiffness. Genetic factors like BMPR2 mutations also contribute to PAH development.
- Clinical features range from mild breathlessness to signs of right heart failure. Diagnostic tests include echocardiography, CT scans, V/Q scans, right heart catheterization and lab tests.
- Treatment involves oxygen therapy, diure
This document discusses diastolic dysfunction, its diagnosis using echocardiography, and anesthetic considerations. It defines diastolic dysfunction as the inability of the ventricle to fill at low atrial pressures. The key aspects of diastolic function evaluation by echocardiography include trans-mitral flow patterns, pulmonary venous flow, tissue Doppler imaging, and mitral annular velocities. Anesthetic goals are to maintain preload and afterload while avoiding drugs that may worsen diastolic function. Specific drugs like milrinone and levosimendan can have beneficial effects on diastolic function in patients with heart failure. Careful preoperative evaluation and postoperative monitoring are important for patients with diast
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,
Wolff–Parkinson–White syndrome (WPW) is one of several disorders of the conduction system of the heart that are commonly referred to as pre-excitation syndromes. WPW is caused by the presence of an abnormal accessory electrical conduction pathway between the atria and the ventricles. Electrical signals travelling down this abnormal pathway (known as the bundle of Kent) may stimulate the ventricles to contract prematurely, resulting in a unique type of supraventricular tachycardia referred to as an atrioventricular reciprocating tachycardia.The incidence of WPW is between 0.1% and 0.3% in the general population.Sudden cardiac death in people with WPW is rare (incidence of less than 0.6%), and is usually caused by the propagation of an atrial tachydysrhythmia (rapid and abnormal heart rate) to the ventricles by the abnormal accessory pathway.
This document provides an overview of the classification, pathophysiology, preoperative evaluation, and anesthetic management considerations for patients undergoing surgery with congenital heart defects such as atrial septal defects (ASD) and ventricular septal defects (VSD). It discusses the pathophysiology of left-to-right and right-to-left shunting, preoperative assessment including history, examination, investigations, and risk factors. It also outlines goals and techniques for anesthesia including bubble avoidance, optimizing oxygen delivery and ventilation, and avoiding hypovolemia and increases in left-to-right shunting. Specific considerations for inhalational and intravenous induction agents, central neuraxial blockade, pregnancy, and Eisenmenger
1. Mitral stenosis is most commonly caused by rheumatic fever and results in thickening and calcification of the mitral valve, reducing the valve orifice area and obstructing blood flow from the left atrium to ventricle.
2. The pathophysiology involves elevated left atrial pressure, pulmonary hypertension, and reduced cardiac output. Symptoms range from easy fatigability to pulmonary edema.
3. Physical exam findings include an opening snap, rumbling diastolic murmur, and signs of right heart failure in severe cases. Severity is graded based on orifice area, pulmonary artery pressure, and NYHA functional
1. High frequency ventilation (HFV) uses small tidal volumes and high respiratory rates to ventilate patients with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). HFV aims to recruit and protect the injured lung better than conventional mechanical ventilation (CMV).
2. Two main types of HFV are high frequency oscillatory ventilation (HFOV) and high frequency jet ventilation (HFJV). HFOV uses a piston to displace gas at 180-900 breaths per minute, while HFJV uses gas jets at 240-480 bpm.
3. Early intervention with HFV may improve outcomes compared to using it as a rescue therapy after prolonged CMV fails. Matching the
The document discusses acute right ventricular (RV) failure, including:
1) The RV's main job is to maintain low right atrial pressure to optimize venous return to the heart. RV dysfunction can lead to reduced cardiac output.
2) Treatment for RV failure differs from left ventricular failure - RV failure may require fluid administration while left sided failure uses diuretics.
3) RV infarction is associated with worse outcomes than left ventricular infarction such as higher mortality, and requires a tailored treatment approach including fluid administration in some cases rather than diuretics. Early revascularization can help recovery.
This document summarizes dobutamine stress echocardiography (DSE). Key points include:
- DSE uses the drug dobutamine to simulate exercise and increase heart rate, contractility, and myocardial oxygen demand to detect ischemia.
- It is useful for evaluating ischemia, viability, and valvular dysfunction in patients unable to exercise.
- The document reviews the DSE protocol, interpretation of wall motion abnormalities, indications, side effects, and applications for assessing ischemic heart disease, viability, valvular stenosis like mitral and aortic stenosis, and pulmonary hypertension.
Congenital cyanotic heart disease approachVarsha Shah
This document discusses cyanotic congenital heart disease (CCHD). It notes that the incidence of moderate to severe CHD is 6-8 per 1,000 live births. The top five diagnoses presenting in the first week of life include transposition of the great arteries, hypoplastic left ventricle, tetralogy of Fallot, coarctation of the aorta, and ventricular septal defect. Clinical findings, ECG patterns, and prognosis after surgery are reviewed for various CCHDs, including tetralogy of Fallot, transposition of the great arteries, tricuspid atresia, Ebstein's anomaly, and hypoplastic left heart syndrome. Medical management including prostagland
This document discusses Eisenmenger syndrome, a condition where pulmonary hypertension develops due to increased blood flow through defects between the systemic and pulmonary circulations. It provides details on causes, clinical features, pathology findings, and treatments. Key points include:
- Eisenmenger syndrome is caused by defects like VSDs, ASDs, and PDA that allow high blood flow to the lungs and cause pulmonary hypertension over time.
- Common causes of death include hemoptysis from pulmonary artery ruptures, heart failure, and complications from attempted defect repair surgery.
- Pathological findings show thickened pulmonary arteries that resemble the fetal pattern and contribute to high pulmonary vascular resistance.
- Medical treatments are generally ineffective once int
Anaesthetic management of pheochromocytomaSiti Azila
Pheochromocytoma is a rare tumor of the adrenal medulla that secretes excessive catecholamines. Preoperative management focuses on controlling blood pressure and heart rate through alpha and beta blockers. During surgery, hemodynamic fluctuations must be closely monitored and treated to prevent hypertensive crises from catecholamine release. Postoperatively, blood pressure, pain, and residual tumor effects are monitored and treated as needed. Thorough preoperative preparation and meticulous intraoperative management are required due to the risks posed by catecholamine secretion.
I'm afraid I don't have enough information to answer these questions. The document provided is an overview of techniques for detecting intracardiac shunts and quantifying cardiac output and shunt flow. It does not include a specific patient case. Could you please provide more details about a patient for me to reference in answering your questions?
The majority of pediatric airway emergencies occur in children under 1 year old and are primarily caused by upper airway obstruction from infectious diseases like viral croup. The pediatric airway has unique anatomical features like a higher larynx and narrower subglottic airway that make it more prone to obstruction. Initial management focuses on airway stabilization through suction, positioning, oxygen therapy, and supportive care. Further treatment depends on the specific condition but may include nebulization, intubation, tracheostomy, or endoscopic evaluation and intervention. Outcomes are generally good with resolution of acute issues and management of any underlying structural abnormalities.
Pulmonary arterial hypertension in congenital heart disease Ramachandra Barik
Pulmonary hypertension (PH) is an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, leg swelling and other symptoms. Pulmonary hypertension can be a severe disease with a markedly decreased exercise tolerance and heart failure. It was first identified by Ernst von Romberg in 1891. According to the most recent classification, it can be one of five different types: arterial, venous, hypoxic, thromboembolic or miscellaneous.
Mechanical ventilation uses endotracheal intubation and a ventilator to replace spontaneous respiration and ventilation.
The ventilator provides the function of the respiratory muscles, endotracheal tube establishes a patent and unobstructed airway and the exogenous oxygen source gives a patient a therapeutic concentration of the gas.
This document discusses mechanical ventilation, including its definition, goals, indications, equipment, types, modes, parameters, alarms, weaning guidelines, complications, and nursing care. The main goals of mechanical ventilation are to maintain adequate oxygenation and carbon dioxide elimination. It is indicated when a patient's spontaneous breathing is inadequate. Common types include invasive ventilation via endotracheal tubes or tracheostomies, and non-invasive ventilation like CPAP and BiPAP. Modes include volume-cycled, pressure-cycled, and high frequency ventilation. Nursing care focuses on maintaining a patent airway and monitoring the patient's condition.
Anaesthesia for cardiopulmonary bypass surgery [autosaved]Nida fatima
This document discusses cardiopulmonary bypass (CPB), which involves diverting blood away from the heart and through an external circuit that oxygenates the blood and returns it to the body. CPB allows surgery to be performed on an unbeating heart while still providing circulation. The key components of a CPB machine and roles of the perfusionist in managing it are described. Steps in CPB like priming, hypothermia, myocardial preservation via cardioplegia, and monitoring techniques are summarized.
The document discusses the history and development of pulmonary artery catheters. It describes how Dr. Swan and Dr. Ganz invented the balloon-tipped catheter and how it allows direct measurement of pressures in the heart and lungs. The document outlines the proper insertion technique and provides normal values for pressures measured in different areas of the heart and lungs. It also discusses indications, contraindications, and complications of pulmonary artery catheter use.
The term inotropic state is most commonly used in reference to various drugs that affect the strength of contraction of heart muscle (myocardial contractility). However, it can also refer to pathological conditions. For example, enlarged heart muscle (ventricular hypertrophy) can increase inotropic state, whereas dead heart muscle (myocardial infarction) can decrease it.
- Pulmonary artery hypertension (PAH) is defined as a mean pulmonary artery pressure of ≥25 mmHg at rest. It is characterized by pre-capillary pulmonary hypertension with a pulmonary wedge pressure <15 mmHg and a pulmonary vascular resistance >3 Wood units.
- The pathophysiology involves sustained vasoconstriction, vascular remodeling, in situ thrombosis, and increased arterial stiffness. Genetic factors like BMPR2 mutations also contribute to PAH development.
- Clinical features range from mild breathlessness to signs of right heart failure. Diagnostic tests include echocardiography, CT scans, V/Q scans, right heart catheterization and lab tests.
- Treatment involves oxygen therapy, diure
This document discusses diastolic dysfunction, its diagnosis using echocardiography, and anesthetic considerations. It defines diastolic dysfunction as the inability of the ventricle to fill at low atrial pressures. The key aspects of diastolic function evaluation by echocardiography include trans-mitral flow patterns, pulmonary venous flow, tissue Doppler imaging, and mitral annular velocities. Anesthetic goals are to maintain preload and afterload while avoiding drugs that may worsen diastolic function. Specific drugs like milrinone and levosimendan can have beneficial effects on diastolic function in patients with heart failure. Careful preoperative evaluation and postoperative monitoring are important for patients with diast
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,
Wolff–Parkinson–White syndrome (WPW) is one of several disorders of the conduction system of the heart that are commonly referred to as pre-excitation syndromes. WPW is caused by the presence of an abnormal accessory electrical conduction pathway between the atria and the ventricles. Electrical signals travelling down this abnormal pathway (known as the bundle of Kent) may stimulate the ventricles to contract prematurely, resulting in a unique type of supraventricular tachycardia referred to as an atrioventricular reciprocating tachycardia.The incidence of WPW is between 0.1% and 0.3% in the general population.Sudden cardiac death in people with WPW is rare (incidence of less than 0.6%), and is usually caused by the propagation of an atrial tachydysrhythmia (rapid and abnormal heart rate) to the ventricles by the abnormal accessory pathway.
This document provides an overview of the classification, pathophysiology, preoperative evaluation, and anesthetic management considerations for patients undergoing surgery with congenital heart defects such as atrial septal defects (ASD) and ventricular septal defects (VSD). It discusses the pathophysiology of left-to-right and right-to-left shunting, preoperative assessment including history, examination, investigations, and risk factors. It also outlines goals and techniques for anesthesia including bubble avoidance, optimizing oxygen delivery and ventilation, and avoiding hypovolemia and increases in left-to-right shunting. Specific considerations for inhalational and intravenous induction agents, central neuraxial blockade, pregnancy, and Eisenmenger
1. Mitral stenosis is most commonly caused by rheumatic fever and results in thickening and calcification of the mitral valve, reducing the valve orifice area and obstructing blood flow from the left atrium to ventricle.
2. The pathophysiology involves elevated left atrial pressure, pulmonary hypertension, and reduced cardiac output. Symptoms range from easy fatigability to pulmonary edema.
3. Physical exam findings include an opening snap, rumbling diastolic murmur, and signs of right heart failure in severe cases. Severity is graded based on orifice area, pulmonary artery pressure, and NYHA functional
1. High frequency ventilation (HFV) uses small tidal volumes and high respiratory rates to ventilate patients with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS). HFV aims to recruit and protect the injured lung better than conventional mechanical ventilation (CMV).
2. Two main types of HFV are high frequency oscillatory ventilation (HFOV) and high frequency jet ventilation (HFJV). HFOV uses a piston to displace gas at 180-900 breaths per minute, while HFJV uses gas jets at 240-480 bpm.
3. Early intervention with HFV may improve outcomes compared to using it as a rescue therapy after prolonged CMV fails. Matching the
The document discusses acute right ventricular (RV) failure, including:
1) The RV's main job is to maintain low right atrial pressure to optimize venous return to the heart. RV dysfunction can lead to reduced cardiac output.
2) Treatment for RV failure differs from left ventricular failure - RV failure may require fluid administration while left sided failure uses diuretics.
3) RV infarction is associated with worse outcomes than left ventricular infarction such as higher mortality, and requires a tailored treatment approach including fluid administration in some cases rather than diuretics. Early revascularization can help recovery.
This document summarizes dobutamine stress echocardiography (DSE). Key points include:
- DSE uses the drug dobutamine to simulate exercise and increase heart rate, contractility, and myocardial oxygen demand to detect ischemia.
- It is useful for evaluating ischemia, viability, and valvular dysfunction in patients unable to exercise.
- The document reviews the DSE protocol, interpretation of wall motion abnormalities, indications, side effects, and applications for assessing ischemic heart disease, viability, valvular stenosis like mitral and aortic stenosis, and pulmonary hypertension.
Congenital cyanotic heart disease approachVarsha Shah
This document discusses cyanotic congenital heart disease (CCHD). It notes that the incidence of moderate to severe CHD is 6-8 per 1,000 live births. The top five diagnoses presenting in the first week of life include transposition of the great arteries, hypoplastic left ventricle, tetralogy of Fallot, coarctation of the aorta, and ventricular septal defect. Clinical findings, ECG patterns, and prognosis after surgery are reviewed for various CCHDs, including tetralogy of Fallot, transposition of the great arteries, tricuspid atresia, Ebstein's anomaly, and hypoplastic left heart syndrome. Medical management including prostagland
This document discusses Eisenmenger syndrome, a condition where pulmonary hypertension develops due to increased blood flow through defects between the systemic and pulmonary circulations. It provides details on causes, clinical features, pathology findings, and treatments. Key points include:
- Eisenmenger syndrome is caused by defects like VSDs, ASDs, and PDA that allow high blood flow to the lungs and cause pulmonary hypertension over time.
- Common causes of death include hemoptysis from pulmonary artery ruptures, heart failure, and complications from attempted defect repair surgery.
- Pathological findings show thickened pulmonary arteries that resemble the fetal pattern and contribute to high pulmonary vascular resistance.
- Medical treatments are generally ineffective once int
Anaesthetic management of pheochromocytomaSiti Azila
Pheochromocytoma is a rare tumor of the adrenal medulla that secretes excessive catecholamines. Preoperative management focuses on controlling blood pressure and heart rate through alpha and beta blockers. During surgery, hemodynamic fluctuations must be closely monitored and treated to prevent hypertensive crises from catecholamine release. Postoperatively, blood pressure, pain, and residual tumor effects are monitored and treated as needed. Thorough preoperative preparation and meticulous intraoperative management are required due to the risks posed by catecholamine secretion.
I'm afraid I don't have enough information to answer these questions. The document provided is an overview of techniques for detecting intracardiac shunts and quantifying cardiac output and shunt flow. It does not include a specific patient case. Could you please provide more details about a patient for me to reference in answering your questions?
The majority of pediatric airway emergencies occur in children under 1 year old and are primarily caused by upper airway obstruction from infectious diseases like viral croup. The pediatric airway has unique anatomical features like a higher larynx and narrower subglottic airway that make it more prone to obstruction. Initial management focuses on airway stabilization through suction, positioning, oxygen therapy, and supportive care. Further treatment depends on the specific condition but may include nebulization, intubation, tracheostomy, or endoscopic evaluation and intervention. Outcomes are generally good with resolution of acute issues and management of any underlying structural abnormalities.
Pulmonary arterial hypertension in congenital heart disease Ramachandra Barik
Pulmonary hypertension (PH) is an increase of blood pressure in the pulmonary artery, pulmonary vein, or pulmonary capillaries, together known as the lung vasculature, leading to shortness of breath, dizziness, fainting, leg swelling and other symptoms. Pulmonary hypertension can be a severe disease with a markedly decreased exercise tolerance and heart failure. It was first identified by Ernst von Romberg in 1891. According to the most recent classification, it can be one of five different types: arterial, venous, hypoxic, thromboembolic or miscellaneous.
Mechanical ventilation uses endotracheal intubation and a ventilator to replace spontaneous respiration and ventilation.
The ventilator provides the function of the respiratory muscles, endotracheal tube establishes a patent and unobstructed airway and the exogenous oxygen source gives a patient a therapeutic concentration of the gas.
This document discusses mechanical ventilation, including its definition, goals, indications, equipment, types, modes, parameters, alarms, weaning guidelines, complications, and nursing care. The main goals of mechanical ventilation are to maintain adequate oxygenation and carbon dioxide elimination. It is indicated when a patient's spontaneous breathing is inadequate. Common types include invasive ventilation via endotracheal tubes or tracheostomies, and non-invasive ventilation like CPAP and BiPAP. Modes include volume-cycled, pressure-cycled, and high frequency ventilation. Nursing care focuses on maintaining a patent airway and monitoring the patient's condition.
This document discusses mechanical ventilation, including its purposes, types, modes, settings, complications, weaning process, and nursing care of patients on ventilators. The main types are negative pressure ventilators like iron lungs and positive pressure ventilators. Common modes include assist-control, SIMV, PSV and APRV. Key settings include tidal volume, rate, sensitivity and PEEP. Weaning involves gradually reducing support in stages. Nursing care focuses on airway management, ventilation, safety, communication and weaning progress.
Mechanical ventilation provides positive pressure ventilation to support patients who are unable to breathe adequately on their own. The document discusses various modes of mechanical ventilation including controlled mandatory ventilation, volume control ventilation, pressure control ventilation, assisted-control ventilation, synchronized intermittent mandatory ventilation, and pressure support ventilation. It explains the basic parameters used in mechanical ventilation like tidal volume, respiratory rate, PEEP, and I:E ratio. It also discusses principles of weaning a patient from mechanical ventilation and assessing readiness for weaning.
This document provides information on mechanical ventilation including its history, types of ventilators, modes of ventilation, parameters monitored, indications for use, and weaning processes. It begins with a brief overview of mechanical ventilation and then covers topics such as positive and negative pressure ventilators, volume versus pressure modes, and common modes like assist-control, SIMV, PCV and PSV. Key parameters monitored during mechanical ventilation are also outlined. The document concludes with descriptions of different weaning methods like T-piece trials, CPAP, SIMV and PSV weaning.
Mechanical ventilation and physiotherapy managementMuskan Rastogi
Mechanical ventilation involves using a machine to breathe for patients who cannot breathe effectively on their own. It works by delivering pressurized air into the lungs via a tube in the airway. Physiotherapists help optimize ventilation, clear secretions, prevent complications, and facilitate weaning patients off the ventilator using techniques like suctioning, drainage positions, percussion, and vibrations. The ventilator settings control aspects of breathing like tidal volume, oxygen levels, and respiratory rate. Modes include mandatory breaths or assisting patients' own breaths. Weaning gradually reduces support as the patient recovers lung function and the ability to breathe independently.
introduction to mechanical ventilator.pptxTirusew1
The document provides information about mechanical ventilators including:
- Mechanical ventilators deliver gas to the lungs through positive or negative pressure to support patient breathing.
- The main components of a ventilator include gas mixers, pneumatic systems, pressure regulators, sensors, air generating systems, and filters.
- Common settings that can be adjusted include respiratory rate, tidal volume, PEEP, flow rate, and fraction of inspired oxygen.
- Main ventilation modes discussed are control ventilation, assist-control ventilation, pressure support ventilation, PRVC, SIMV, CPAP, and BiPAP. Each mode has a different way of supporting patient breathing and are used in different clinical situations
Invasive and Non Invasive ventilation .pptxowaisiqbal763
This document discusses invasive and non-invasive mechanical ventilation. It begins by defining key terms like ventilation, ventilator, and the different types of mechanical ventilation. It then covers the indications for mechanical ventilation including acute respiratory failure, prophylactic support, and hyperventilation therapy. The document discusses various ventilator modes like controlled mandatory ventilation, assist-control, intermittent mandatory ventilation, and more. It also covers settings, problems that can arise, and non-invasive ventilation options like CPAP, BiPAP, and pressure support ventilation.
This document discusses different modes of mechanical ventilation. It begins by defining key terms like trigger, cycle, and limit. It then describes the four phases of a mechanical breath - trigger, limit, cycle, and expiration. The main modes discussed are volume-controlled ventilation, pressure-controlled ventilation, and pressure support ventilation. Volume-controlled ventilation delivers a set tidal volume, pressure-controlled ventilation delivers a set pressure level, and pressure support ventilation provides pressure assistance for patient-triggered breaths. Other modes like synchronized intermittent mandatory ventilation are also summarized briefly.
Mechanical ventilation in neonates by dr naved akhterDr Naved Akhter
Mechanical ventilation is used to support gas exchange and clinical status in neonates. The goals are to maintain sufficient oxygenation and ventilation until the underlying disease resolves, while protecting the lungs from damage. Modes of ventilation include mandatory, SIMV, assist/control, and pressure support. Parameters like tidal volume, PIP, PEEP, and FiO2 are adjusted based on blood gas levels to optimize oxygenation and ventilation. Ventilator graphics and pulmonary monitoring are used to assess patient-ventilator interaction and guide management.
Mechanical ventilators- Applications and Usageshashi sinha
The Medical Ventilators are also known as Mechanical Ventilators, Artificial Ventilators etc. We will henceforth refer all these as Ventilators.
When a patient breathes on its own it is known as Spontaneous Breathing and when the patient is unable to breathe on its own we use a device called Ventilator which helps the patient breathe artificially. This is called Mechanical Ventilation and is a method to mechanically assist the patient to breathe and in extreme cases replace the entire breathing process. Spontaneous breathing is done by a process called Respiratory System.
This document discusses mechanical ventilation and care of children requiring long-term ventilation. It covers the physiology of ventilation, indications for mechanical ventilation, types of ventilators including transport, ICU, neonatal and PAP ventilators. It describes various ventilation modes like PC, VC, PRVC, SIMV and their applications. Factors in weaning from ventilation are discussed along with complications and troubleshooting. Non-invasive ventilation options like CPAP, BiPAP and protocols for safe weaning are also summarized.
This document discusses different modes of mechanical ventilation. It begins by introducing mechanical ventilation and its purpose of providing respiratory support. It then describes the basic components of a ventilator and ventilator circuit. The document outlines several modes of mechanical ventilation including controlled mechanical ventilation, assist-control ventilation, intermittent mandatory ventilation, and synchronized intermittent mandatory ventilation. It provides details on the characteristics, advantages, and disadvantages of each mode.
The document provides an overview of mechanical ventilation including its basic principles, types, indications, purposes, modes, settings, advantages, complications, weaning process, and nursing care of patients on ventilators. Mechanical ventilation delivers mechanically generated breaths to oxygenate the blood and remove carbon dioxide. It can be invasive or non-invasive. Modes include controlled mandatory ventilation, synchronized intermittent mandatory ventilation, pressure support ventilation, continuous positive airway pressure, and bi-level positive airway pressure. Nurses monitor patients closely, assess readiness for weaning, and provide comfort during the process.
This document discusses various modes of mechanical ventilation. It begins by describing the basic components and functions of a ventilator. The document then explains the key parameters that ventilators can control including tidal volume, frequency, pressure, and time settings. Several common ventilation modes are described including controlled mandatory ventilation (CMV), assist-control ventilation, intermittent mandatory ventilation (IMV), and synchronized intermittent mandatory ventilation (SIMV). Each mode is defined by how the ventilator delivers breaths in terms of being time-triggered or patient-triggered and how breaths are cycled. The advantages and disadvantages of different modes are also briefly discussed.
This document discusses various modes of mechanical ventilation including volume-controlled, pressure-controlled, assist-control, synchronized intermittent mandatory ventilation (SIMV), and pressure support ventilation. It defines key terms like tidal volume, respiratory rate, trigger variables, limit variables, and cycle variables. Each mode is described in terms of how breaths are triggered, the variables controlled, and whether breaths are mandatory or spontaneous.
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3. History:
• The earliest breathing machine was
the Drinker respirator. It was
invented in 1928 and was known as
an ‘iron lung’ for people whose
breathing muscles had
been paralyzed by polio. They used
negative pressure to help patients
breathe while lying inside the iron
lung’s airtight chamber.
•In 1949, American engineer John
Haven Emerson developed an
positive pressure anesthetic
ventilator.
4. Goals of Mechanical Ventilation:
1. Achieve and maintain adequate
pulmonary gas exchange
2. Minimize the risk of lung injury
3. Reduce patient work of breathing
4. Optimize patient comfort
5. To normalize blood gases and provide
comfortable breathing
5. Ideal Ventilator Design
1. Achieves all the important goals of mechanical
ventilation
2. Provides a variety of modes that can ventilate
even the most challenging pulmonary diseases
3. Has monitoring capabilities to adequately assess
ventilator and patient performance
4. Has safety features and alarms that offer lung
protective strategies
7. How mechanical Ventilator works:
A) Breath:
A breath is one cycle of positive flow (inspiration) and negative flow
(expiration)
Inspiratory time is defined as the period from the start of positive flow to the
start of negative flow.
Expiratory time is defined as the period from the start of expiratory flow to
the start of inspiratory flow.
Mechanical
Time (sec)
Spontaneous
Paw(cmH2O)
Inspiration
Expiration
Expiration
Inspiration
8. How mechanical Ventilator works:
A) Breath: A breath is assisted if the ventilator does work on the patient.
an assisted breath is identified as a breath for which airway pressure
(displayed on the ventilator) rises above baseline during inspiration.
An unassisted breath is one for which the ventilator simply provides the
inspiratory flow demanded by the patient and pressure stays constant
throughout the breath.
Assisted Controlled
9. How mechanical Ventilator works:
B) Control: A ventilator assists breathing using either –
1) Volume control (VC) means that
1) both volume and flow are preset prior to inspiration.
2) The ventilator will continue to "force" that set volume into the lungs
regardless of the pressures being generated, i.e Vt is guaranteed.
2) Pressure control (PC) means that the pressure of each breath remains
constant. In other words, when the ventilator reaches a preset pressure
limit inspiration is terminated. The amount of volume delivered is entirely
dependent on the lung compliance of the patient. The main benefit of
pressure controlled ventilation is -
a. airway pressures are controlled.
b. mechanically ventilated much more comfortable and better tolerated.
c. It also decreases the risk of barotrauma to the alveoli and bronchi.
3) Time control (TC) means that none of the main variables (pressure,
volume, or flow) are preset. In this case only the inspiratory and expiratory
times are preset.
10. How mechanical Ventilator works:
Trigger: The start of inspiration is called the trigger
1. Time triggering: The machine is set to give a
breath every 8 seconds, or 10 seconds, or
whatever rate you program into the machine.
2. Pressure triggering: When a pt initiates a
breath, the ventilator circuit detects a drop in
intrathoracic pressure & delivers a breath to
the patient.
3. Flow triggering: during pt induced inspiration,
ventilators detect changes in flow & delivers a
breath to the pt.
11. How mechanical Ventilator works:
• Cycle: The end of inspiration is called the cycle event.
The cycling of a mechanical ventilator breath occurs after a set value is reached.
Four variables are used to determine when to cycle to exhalation:
1. Pressure Cycling
1. When a certain pressure threshold is reached, inspiration is cycled into
exhalation.
2. Pressure cycling can be viewed as a safety feature to avoid elevated and
sustained inspiratory pressure.
2. Time Cycling
1. MV breath switches from inspiration to expiration after a set time threshold is
reached. This can be accomplished by setting the respiratory rate, inspiratory
time, or inspiratory-expiratory ratio.
3. Volume Cycling
1. The ventilator cycles to expiration once a set tidal volume has been delivered.
4. Flow Cycling
1. For a given tidal volume when the patients inspiratory flow is decreased to a
predetermined level (25% of peak inspiratory flow) the breath would cycle
into exhalation.
13. Modes of Ventilation:
the manner or method a breath is delivered by the ventilator
1. Continuous Mandatory Ventilation (CMV)
Previously known as controlled mechanical
ventilation
2. Assist/Control Ventilation (A/C)
3. Synchronized Intermittent Mandatory Ventilation
(SIMV)
4. Spontaneous Modes
1. Pressure Support Ventilation (PSV)
2. Continuous Positive Airway Pressure (CPAP)
14. CMV
•When the termination of a breath is
under the control of the mechanical
ventilator, it is referred to as a
mandatory breath.
•Indication:
•seizure,
•chest injury
• if pt “fights” the vent
•complete rest for pt. for 24 hr.,
•In this mode pt. is properly
medicated with a combination of
sedatives, respiratory depressants
and neuromuscular blockers.
Mechanical
Time
(sec)
Paw(cmH2O)
Time
Triggered
Breath
15. Volume control
Tadal volume ml
RR b/m
PEEP cmH2O
PIP depends on pt
Fio2 %
Ti / I: E 0.1 – 5 Sec with
I:E 1:2
Trigger Flow > 0
Pressure - 20 to 0
Pause time 0 – 30% or
0-1.5 sec
Inspiratory
Rise time
Adult : 0 to 0.4
Infant: 0 to 0.2
OTHER NAME: IPPV /CMV, VCV-
A/C, Volume A/C,
VC-CMV, VC-AC
Pressure control
Tidal volume ml
RR b/m
PEEP cmH2O
PIP cmH2O above
PEEP
Fio2 %
Ti / I: E 0.1 – 5 Sec with
I:E 1:2
Trigger Flow > 0
Pressure - 20 to 0
Inspiratory
Rise time
Adult : 0 to 0.4
Infant: 0 to 0.2
OTHER
NAME:
P-CMV, PCV-A/C,
Pressure A/C
16. Assist/Control Ventilation (A/C)
•Assist-control refers to a mode of ventilation when a patient receives a
combination of ventilator-initiated and patient-initiated mandatory breaths.
•If a patient on an AC of 14 with a total breathing rate of 16 breaths per minute, is
triggering two additional breaths per minute, but, all 16 breaths are being delivered
by the ventilator.
•Advantages of AC mode:
•Increased patient comfort
•Easy corrections for respiratory acidosis/alkalosis.
•Low work breathing for the patient.
•Disadvantages of AC mode:
•barotrauma is a concern in stiff lungs.
•If exhalation time is inadequate auto-PEEP develops. diminished venous
return hypotension.
•hyperventilation
17. SIMV
Breaths are given at a set minimal rate, however if the patient chooses to
breath over the set rate no additional support is given
Like AC, SIMV can deliver set tidal volumes (volume control) or a set pressure
and time (pressure control)
“synchronized window” refers to the time just prior to time triggering in which the vent. is
responsive to the pt.’s effort (0.5 sec is typical)
Advantages include maintaining resp. muscle strength, reduces V/Q mismatch, decreases
mean airway press., helps wean pt
SIMV is usually associated with greater work of breathing than AC ventilation and
therefore is less frequently used as the initial ventilator mode
18. SPONTANEOUS
•A spontaneous breath is a breath for which the patient
both triggers and cycles the breath.
•A spontaneous breath may be
•assisted or
•unassisted.
•Rate and tidal volume during spontaneous breathing
are determined by patient. Role of ventilator during
spontaneous vent. is to provide the
•flow adequate to fulfill a patient’s insp. demand
•provide adjunctive modes such as PEEP or PS to
complement the spontaneous effort
Time (sec)Inspiration
Expiration
19. CPAP:
•PEEP is applied on expiration.
•PEEP causing alveoli to remain open and not fully
deflate.
•This mechanism for maintaining inflated alveoli helps
increase partial pressure of oxygen in arterial blood,
and an increase in PEEP increases the PaO2
SPONTANEOUS
20. Pressure support:
The patient initiates every breath and the ventilator delivers breath
with the preset pressure value.
In Pressure Support
•Patient regulates their own respiratory rate and their tidal
volume.
•the set inspiratory pressure support level is kept constant
•a decelerating flow.
•Pressure support improves oxygenation, ventilation and
decreases work of breathing.
•Cycling: when the inspiratory flow rate decreases, inspiration
ends and expiration starts
PSV is entirely dependent on the patient’s effort; if the patient
becomes apneic, the ventilator will not provide any mechanical
breath.
SPONTANEOUS
21. Parameters of MV:
Tidal volume (Vt) : (Tidal Volume - the amount of air delivered with
each breath.)
8-10 ml/kg
Respiratory Rate - number of breaths per minute
Ti / I : E 0.1 – 5 Sec with
I:E 1:2
Pressures
PIP (maximum amount of pressured delivered during each
breath ) - 16-20cmH2O
PEEP 3-5 cmH2O
Pressure support 5-10
FiO2 – fraction of inspired oxygen
Trigger:
Flow > 0
Pressure - 2 to 0
Mode
Flow pattern
22. Effect of MV on cardiovascular system
• The cardiovascular and respiratory systems act as a
functional unit.
• Mechanical ventilation – modifies pulmonary volumes,
• Tidal volume by influencing autonomic nervous system
reactivity can provoke tachy- or brady-cardia
• Decreases cardiac filling volumes (pre-load)
• alters pulmonary vascular resistances.
• intrathoracic pressures are enlarged, which cause
• decrease in right atrium filling and
• an increase in right ventricle afterload.
23. Effect of MV in cardiovascular system: contd.
• If coronary flow is impaired, myocardial contractility is
reduced.
• In cardiac failure – MV is especially beneficial because :
– it corrects hypoxia and respiratory acidosis,
– decreases the work of breathing, and
– improves stroke volume.
• Mechanical ventilation in congenital heart diseases is indicated
either –
– as lifesaving support or
– as physiopathological treatment to modify the ratio
between pulmonary and systemic flow
24. Indication of MV
1. Respiratory failure:
• Hypoxia (PaO2 < 50)
• Hypercapnia (PaCO2 > 50)
• Respiratory distress (RR increased), use of accessory muscles
2. Shock
3. Chest trauma
4. Neuromuscular dysfunction
5. stroke & General anaesthesia
6. Electrolyte imbalance
7. Acute severe airflow obstruction
8. Acute lung injury/ARDS
9. Inability to protect airway
10. Congenital heart disease
25. Indication of MV
Cardiac indication:
1. CHF
• Sepsis Syndrome
• cardiomyopathy,
• infectious myocarditis
2. Tachyarrhythmias
3. Cardiogenic Shock : In the immediate postoperative
period in complex congenital heart disease –
1. patients should be on controlled mechanical
ventilation until hemodynamic functions improve.
2. Adequate PEEP should be applied to prevent and
relieve atelectasis.
26. Indication of MV: congenital heart disease
CHD causing CHF or cardiogenic shock thus requiring MV are:
•Defects with increased pulmonary blood flow (if excessive pulmonary blood
flow is present, the aim of respiratory support is to increase pulmonary
vascular resistance by using high levels of airway pressure and even by
delivering FiO2<21%. )
1. Very large ASD, VSD, PDA volume overload
2. Truncus arteriosus: CHF in older children due to post repair truncal
insuffciency or conduit stenosis.
3. TAPVC – comes with heart failure
•Left Heart Outflow Tract Obstruction
1. Aortic stenosis (AS) : severe aortic insuffciency and ultimately left
heart failure is seen in
1. Critical AS in the neonatal period &
2. older children following repair of AS suffer from restenosis
2. Coarctation of the aorta (CoA) : may present as late as 8 weeks of
age with signs of cardiogenic shock.
3. Hypoplastic left-sided heart syndrome (HLHS): commonly presents
within the fIrst 7 days of life.
27. Indication of MV: congenital heart disease
•Defects with decreased pulmonary blood flow (there is low
pulmonary flow, the lowest possible intrathoracic pressures
should be used, especially in cases of pulmonary hypertension,
which will also require high FiO2.) Immediate intervention is
indicated in any cyanotic infant whose ABG shows :
•pH <7.28 or
•PaCO2 >50 mmHg
•PaO2 <50 mmHg on a
•FiO2 >0.5
1. Tetralogy of fallot (TOF) : for management of recurrent severe
tet spells
2. Critical pulmonary stenosis (PS) and pulmonary atresia with
intact ventricular septum
3. Transposition of great arteries (TGA) associated VSD may
present with CHF
28. Indication of MV: congenital heart disease
•Arrhythmias.
•Dilated and hypertrophic cardiomyopathies are a common
etiology of pediatric heart failure.
•hypotension due to low cardiac output and in the most
severe cases, fulminant pulmonary edema
•ET intubation indicated to:
1. Decrease work of breathing (to decrease the
metabolic demands of both the respiratory muscles
and heart, thus decreasing stress on the already
failing cardiopulmonary system)
2. PIP: higher mean airway pressure will decrease
intrapulmonary shunting created by the fluid filled
alveolus.
3. PEEP: higher, it may limit venous return to the heart
29.
30.
31. ET intubation:
• ET tube size:
– Gestational age /10, if cuffed 0.5 size less
• Depth of insertion:
– internal tube diameter (in mm)×3.
– in children >2 years of age: Depth of insertion (cm)=(age in
years/2)+12; [eg. 10yr/2+12=17cm
• Confirm placement:
– Capnography
– Lung sound
– Vapour in ET tube
– No gastric distension
– Stat improving
• cuffed ET Tube cuff pressure should be below 20 cm H2O.
• Uncuffed TTs should be sized to allow a leak ∼20 cm H2O
32. Initial ventilator setting:
Initial
ventilator
setting
Premature
neonate
Neonate Infant
/small child
< 12 kg
Large child
> 12 kg or,
Adolescent
Mode Pressure
control
Pressure
control
Volume
control+PS
Volume
control
Rate 40-50 20-25 Infant/Small
Child 16-20
12-16
PEEP 3-5 3-5 3-5 3-5
Ti 0.3 – 0.4 0.5 – 0.6 0.6-0.7 0.7-0.9
PIP 16-20 16-20 16-20 18-25
Vt 5-8 ml / kg 5-8 ml / kg 5-8 ml / kg 5-8 ml / kg
Fio2 0.6 and titrate or 100% and wean down
33. Complication of mechanical ventilation
1. Increased airway pressures and lung volumes
1. Barotrauma/volutrauma(stretch injury):-
pneumothorax, pneumopericardium,
pneumoperitoneum, subcutaneous emphysema.
2. Decreased cardiac filling and poor perfusion.
3. Other organ dysfunction-renal, hepatic, and CNS.
Pulmonary parenchymal damage.
4. Adverse effects on gas exchange.
5. Increased extravascular lung water.
2. Endotracheal/tracheostomy tube
1. Tracheal mucosal swelling,
2. ulceration or damage.
3. sinusitis/middle ear infection.
4. Laryngeal edema, subglottic stenosis.
5. Granuloma formation leading to airway obstruction.
35. Weaning
1. Is the cause of respiratory failure gone or
getting better ? –
2. Is the patient well oxygenated and ventilated ?
3. Can the heart tolerate the increased work of
breathing?
36. Extubation : indication
•“Awake ” patient
•control of airway reflexes,
•minimal secretions
•Minimal oxygen requirement
•Minimal rate -SIMV rate of < 10,
•Minimize pressure support (5- 10)
•Adequate muscle tone
•Minimal/no inotropic support,
•normal electrolytes and no fluid overload
37. Extubation - Procedure
1. Keep NPO 4hrs before planned extubation
2. Suction endotracheal tube and deflate cuff if using a cuffed tube.
3. Suction the oral cavity and nostrils.
4. Following instrument should be ready –
1. laryngoscope and correct size ETTube.
2. Nebulisation with beta stimulant/adrenaline
3. Intravenous steroids dexamethasone 0.6mg/kg iv(maximum dose of 12mg)
4. Ideally, ventilator to be on standby at least 24hrs post extubation.
5. Intravenous frusemide
6. Do blood gas 20mins after extubation;
7. Post extubation CXR not needed routinely but only if clinically indicated by desaturation
or increased work of breathing.
• Anticipate extubation failure in all patients and parents should be made aware earlier on so
that there is no disappointment.