This document discusses Uhl's anomaly and arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). It presents a case study of a 50-year-old man with palpitations and ventricular ectopic beats. Key differences between Uhl's anomaly and ARVD/C are described. Uhl's anomaly is a rare congenital disorder characterized by a thin-walled right ventricle, while ARVD/C is an inherited cardiomyopathy characterized by structural abnormalities and fatty infiltration of the right ventricle myocardium. Diagnostic criteria for ARVD/C include family history, electrocardiogram abnormalities, arrhythmias on monitoring, and structural changes seen on imaging like echocard
Pedatrics morbidity and mortality nov 2021 aaronkemboiarn
The document summarizes pediatric admissions and mortality data from Longisa County Referral Hospital for November 2021. It reports that the pediatric ward admitted 88 children, with 1 mortality and 3 referrals. The top admission diagnoses were pneumonia, anemia, and gastroenteritis. The neonatal unit admitted 81 babies, with 15 mortalities and 2 referrals. The leading admission diagnoses were birth asphyxia, prematurity/low birth weight, and neonatal sepsis. It then presents a case of severe birth asphyxia in a baby who did not survive.
Sickle cell disease is a genetic blood disorder characterized by abnormal, rigid red blood cells that can cause painful crises and organ damage. The document discusses the clinical features, pathophysiology, epidemiology, predictors of complications, and considerations for preoperative preparation and anesthesia management in patients with sickle cell disease undergoing surgery. Managing risks like dehydration, hypoxia, acidosis and low temperature is important to prevent sickle cell crises in the perioperative period.
Maternal collapse by dr alka mukherjee &; dr apurva mukherjeealka mukherjee
Not all maternal deaths are preceded by an identifiable collapse, and not all maternal collapses result in death. Maternal collapse occurs any time during pregnancy, up to 42 days following delivery and is an acute event involving cardiorespiratory systems and/or brain, resulting in impaired consciousness or death.1
Maternal deaths are generally quantified as a maternal mortality ratio (MMR), expressed as the number of maternal deaths per 100,000 women giving birth. It includes deaths that occur due to complications of the pregnancy (direct deaths), and those resulting from worsening of other disease processes due to the pregnancy (indirect deaths). Deaths that occur from causes completely unrelated to pregnancy or birth are termed When faced with an acute maternal collapse, it is helpful to think of potential causes as falling into five categories, or the 5 Hs for simplicity:4
Head including eclampsia, stroke, epilepsy, vasovagal
Heart including myocardial infarction, arrhythmia, cardiomyopathy, thoracic aortic dissection
Hypoxia including pulmonary embolus, pulmonary oedema, anaphylaxis, asthma
Haemorrhage including abruption, uterine atony, genital tract trauma, uterine rupture, uterine inversion, ruptured aortic aneurysm
wHole body and Hazards amniotic fluid embolus, hypoglycaemia, trauma, anaesthetic complications, drug reactions (illicit or prescribed), sepsis
The likelihood of any one of these being causative will obviously depend somewhat on the timing of the collapse – early or late pregnancy, intrapartum, immediately postpartum, remotely postpartum.
Maternal cardiac arrest represents a small subset of women affected by maternal collapse. The incidence is approximately 1 in 30,000 ongoing pregnancies, with a high likelihood of death for both the mother and the fetus. The vast majority of us will never need to attend a maternal cardiac arrest, and doing so is uniquely stressful. For these reasons, it is important to have a framework in mind of how to deal with a maternal cardiac arrest, and to have practised the response to this situation.
incidental deaths, and are not included in calculation of the MMR.
• Several other risk factors for maternal death are recognised. These include:
• Maternal age 35 and older
• Obesity
• Lower socioeconomic status
• Pre-existing mental health issues, substance use and domestic violence, all of which may be exacerbated by pregnancy and the puerperium
• Medical co-morbidities, particularly asthma, autoimmune diseases, inflammatory and atopic disorders, haematological disorders, essential hypertension, infections and musculoskeletal disorders
One of the important developments in improving identification of a pregnant or postnatal patient at risk of collapse during hospital admission has been the development of maternity-specific Early Warning Charts.
This document provides an overview of the approach to managing cerebrovascular accidents (CVAs), also known as strokes. It begins with definitions, epidemiology, and risk factors. It then discusses the clinical presentation and neurological deficits associated with different blood vessels. Common complications are also reviewed. The approach to initial management focuses on resuscitation, history and examination, investigations, and acute treatment including medications, monitoring, and prevention of secondary complications. Long-term management involves rehabilitation, lifestyle modifications, and managing risk factors to prevent further strokes. Prognosis varies depending on the stroke subtype but overall many patients experience disability or death.
1. Sickle cell disease is a group of inherited blood disorders caused by a mutation in the beta-globin gene resulting in abnormal hemoglobin S. This document discusses sickle cell anemia, its inheritance, pathophysiology, clinical manifestations, complications, and management.
2. Key symptoms include painful vaso-occlusive crises, acute chest syndrome, strokes, and susceptibility to infections. Management involves prevention, pain management, antibiotics, hydroxyurea, and blood transfusions.
3. Understanding the inheritance patterns and genetic counseling is important as sickle cell disease has a major health impact and often requires lifelong multidisciplinary care.
This case discusses a 7-year-old male who presented with a 6-day fever and convulsions. His symptoms did not improve with initial treatment. Extensive testing did not identify an infectious cause. He was diagnosed with autoimmune encephalitis based on his clinical presentation and improvement with immunotherapies. The document discusses how autoimmune causes now surpass viral infections as the most common cause of encephalitis in developing countries. It emphasizes the importance of considering and treating non-infectious autoimmune etiologies to achieve better neurological outcomes.
This document discusses Uhl's anomaly and arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C). It presents a case study of a 50-year-old man with palpitations and ventricular ectopic beats. Key differences between Uhl's anomaly and ARVD/C are described. Uhl's anomaly is a rare congenital disorder characterized by a thin-walled right ventricle, while ARVD/C is an inherited cardiomyopathy characterized by structural abnormalities and fatty infiltration of the right ventricle myocardium. Diagnostic criteria for ARVD/C include family history, electrocardiogram abnormalities, arrhythmias on monitoring, and structural changes seen on imaging like echocard
Pedatrics morbidity and mortality nov 2021 aaronkemboiarn
The document summarizes pediatric admissions and mortality data from Longisa County Referral Hospital for November 2021. It reports that the pediatric ward admitted 88 children, with 1 mortality and 3 referrals. The top admission diagnoses were pneumonia, anemia, and gastroenteritis. The neonatal unit admitted 81 babies, with 15 mortalities and 2 referrals. The leading admission diagnoses were birth asphyxia, prematurity/low birth weight, and neonatal sepsis. It then presents a case of severe birth asphyxia in a baby who did not survive.
Sickle cell disease is a genetic blood disorder characterized by abnormal, rigid red blood cells that can cause painful crises and organ damage. The document discusses the clinical features, pathophysiology, epidemiology, predictors of complications, and considerations for preoperative preparation and anesthesia management in patients with sickle cell disease undergoing surgery. Managing risks like dehydration, hypoxia, acidosis and low temperature is important to prevent sickle cell crises in the perioperative period.
Maternal collapse by dr alka mukherjee &; dr apurva mukherjeealka mukherjee
Not all maternal deaths are preceded by an identifiable collapse, and not all maternal collapses result in death. Maternal collapse occurs any time during pregnancy, up to 42 days following delivery and is an acute event involving cardiorespiratory systems and/or brain, resulting in impaired consciousness or death.1
Maternal deaths are generally quantified as a maternal mortality ratio (MMR), expressed as the number of maternal deaths per 100,000 women giving birth. It includes deaths that occur due to complications of the pregnancy (direct deaths), and those resulting from worsening of other disease processes due to the pregnancy (indirect deaths). Deaths that occur from causes completely unrelated to pregnancy or birth are termed When faced with an acute maternal collapse, it is helpful to think of potential causes as falling into five categories, or the 5 Hs for simplicity:4
Head including eclampsia, stroke, epilepsy, vasovagal
Heart including myocardial infarction, arrhythmia, cardiomyopathy, thoracic aortic dissection
Hypoxia including pulmonary embolus, pulmonary oedema, anaphylaxis, asthma
Haemorrhage including abruption, uterine atony, genital tract trauma, uterine rupture, uterine inversion, ruptured aortic aneurysm
wHole body and Hazards amniotic fluid embolus, hypoglycaemia, trauma, anaesthetic complications, drug reactions (illicit or prescribed), sepsis
The likelihood of any one of these being causative will obviously depend somewhat on the timing of the collapse – early or late pregnancy, intrapartum, immediately postpartum, remotely postpartum.
Maternal cardiac arrest represents a small subset of women affected by maternal collapse. The incidence is approximately 1 in 30,000 ongoing pregnancies, with a high likelihood of death for both the mother and the fetus. The vast majority of us will never need to attend a maternal cardiac arrest, and doing so is uniquely stressful. For these reasons, it is important to have a framework in mind of how to deal with a maternal cardiac arrest, and to have practised the response to this situation.
incidental deaths, and are not included in calculation of the MMR.
• Several other risk factors for maternal death are recognised. These include:
• Maternal age 35 and older
• Obesity
• Lower socioeconomic status
• Pre-existing mental health issues, substance use and domestic violence, all of which may be exacerbated by pregnancy and the puerperium
• Medical co-morbidities, particularly asthma, autoimmune diseases, inflammatory and atopic disorders, haematological disorders, essential hypertension, infections and musculoskeletal disorders
One of the important developments in improving identification of a pregnant or postnatal patient at risk of collapse during hospital admission has been the development of maternity-specific Early Warning Charts.
This document provides an overview of the approach to managing cerebrovascular accidents (CVAs), also known as strokes. It begins with definitions, epidemiology, and risk factors. It then discusses the clinical presentation and neurological deficits associated with different blood vessels. Common complications are also reviewed. The approach to initial management focuses on resuscitation, history and examination, investigations, and acute treatment including medications, monitoring, and prevention of secondary complications. Long-term management involves rehabilitation, lifestyle modifications, and managing risk factors to prevent further strokes. Prognosis varies depending on the stroke subtype but overall many patients experience disability or death.
1. Sickle cell disease is a group of inherited blood disorders caused by a mutation in the beta-globin gene resulting in abnormal hemoglobin S. This document discusses sickle cell anemia, its inheritance, pathophysiology, clinical manifestations, complications, and management.
2. Key symptoms include painful vaso-occlusive crises, acute chest syndrome, strokes, and susceptibility to infections. Management involves prevention, pain management, antibiotics, hydroxyurea, and blood transfusions.
3. Understanding the inheritance patterns and genetic counseling is important as sickle cell disease has a major health impact and often requires lifelong multidisciplinary care.
This case discusses a 7-year-old male who presented with a 6-day fever and convulsions. His symptoms did not improve with initial treatment. Extensive testing did not identify an infectious cause. He was diagnosed with autoimmune encephalitis based on his clinical presentation and improvement with immunotherapies. The document discusses how autoimmune causes now surpass viral infections as the most common cause of encephalitis in developing countries. It emphasizes the importance of considering and treating non-infectious autoimmune etiologies to achieve better neurological outcomes.
Acute Flaccid Paralysis (AFP) is defined as sudden onset of weakness or paralysis in a previously normal limb over 15 days in patients under 15 years old. Guillain-Barré Syndrome (GBS) is the most common cause of AFP and is an acute acquired inflammatory demyelinating polyneuropathy. It has an annual incidence of 0.6 to 2.4 cases per 100,000 people and usually occurs 2-4 weeks after a respiratory or GI infection. GBS is diagnosed through CSF analysis showing elevated proteins and electrophysiological studies showing demyelination. Treatment involves monitoring, IVIG or plasma exchange to shorten recovery time, and PICU care if respiratory involvement is present.
An Overview of acute flaccid pralysis in Children.pdfzainjoiya3
Acute Flaccid Paralysis (AFP) is defined as sudden onset of weakness or paralysis in a previously normal limb over 15 days in a patient under 15 years old. Guillain-Barré Syndrome is the most common cause of AFP in healthy children and is an acute immune-mediated polyneuropathy often following a respiratory or gastrointestinal infection. It presents with ascending limb weakness, loss of reflexes, and in severe cases involves cranial nerves and respiratory muscles. Accurate differential diagnosis from other causes of AFP like polio, transverse myelitis, or traumatic neuritis is important for surveillance and treatment.
1. The patient presented with headache and right-sided hemiplegia, consistent with an acute stroke.
2. Strokes in sickle cell disease are most commonly ischemic and occur bimodally, peaking in younger children and those over 30 years old. Hemorrhagic strokes are rarer and peak during the second decade.
3. Diagnostic workup includes blood tests and neuroimaging to determine if the stroke is ischemic or hemorrhagic, as management differs between the two.
This document provides an overview of sickle cell disease, including:
- It is a genetic blood disorder caused by a mutation resulting in abnormal rigid red blood cells.
- Clinical features include anemia, pain crises, infections, stroke risk and organ damage over time.
- Diagnosis involves blood tests and genetic screening.
- Management focuses on hydration, pain control, antibiotics for infection, blood transfusions for crises, and lifelong folic acid supplementation.
Drs. Lena, Avery, and Davis’s CMC Abdominal Imaging Mastery Project: August C...Sean M. Fox
Dr. Kelsey Lena is an Emergency Medicine Resident and Drs. Michael Avery and Joshua Davis are Surgery Residents at Carolinas Medical Center in Charlotte, NC. They are interested in medical education. With the guidance of Drs. Kyle Cunningham and Michael Gibbs, they aim to help augment our understanding of emergent abdominal imaging. Follow along with the EMGuideWire.com team as they post these monthly educational, self-guided radiology slides. This month’s topics include:
• Splenic Rupture
• Obstructive jaundice
• Ovarian Torsion
This case presentation describes a 58-year-old female patient who presented with fever, myalgia, severe headaches, and generalized weakness. Investigations revealed anemia, elevated inflammatory markers, and a positive transesophageal echocardiogram showing mitral valve vegetation. The patient was diagnosed with infective endocarditis of the mitral valve and underwent mitral valve replacement surgery. The document then provides details on the definition, diagnosis, and treatment of infective endocarditis, including descriptions of the Duke criteria for diagnosis and appropriate antibiotic therapy based on the infecting organism.
Antiphospholipid syndrome (APS) is an acquired autoimmune condition characterized by arterial or venous thrombosis and/or pregnancy morbidity in the presence of antiphospholipid antibodies. The document discusses the history, incidence, definition, classification, clinical manifestations, diagnostic criteria, treatment and management of APS. APS can affect multiple organ systems and present with a wide variety of clinical symptoms. Prompt diagnosis and treatment with anticoagulation and immunosuppression is important to prevent morbidity and mortality.
PUBERTY MENORRHAGIA & BLEEDING DISORDERS Made Easy Dr Sharda Jain Lifecare Centre
This document discusses evaluation and treatment of puberty menorrhagia and bleeding disorders. It begins with classifications of abnormal uterine bleeding and an overview of common causes of puberty menorrhagia such as dysfunctional uterine bleeding and bleeding disorders. Evaluation involves a detailed history, physical exam, ultrasound, and lab tests to rule out other causes before screening for bleeding disorders. Common bleeding disorders seen in puberty menorrhagia are von Willebrand disease, platelet function defects, and coagulation factor deficiencies. Treatment depends on the underlying cause but may include combined oral contraceptives, antifibrinolytic agents, plasma concentrates, and managing anemia.
Atrial fibrillation is characterized by disorganized electrical activity in the atria leading to irregular heartbeat. Risk factors include increasing age, hypertension, diabetes, obesity, sleep apnea, smoking, and family history. Symptoms include irregular pulse and murmurs. Diagnosis is made through ECG and echocardiogram. Treatment involves rate or rhythm control with medications, catheter ablation, anticoagulation to prevent stroke, and treating any underlying causes. Guidelines from AHA and ESC provide recommendations on management strategies.
Intra dialytic hypotension ,,, prof Alaa SabryFarragBahbah
This document describes a case of intradialytic hypotension in a 65-year-old man on hemodialysis. During one of his dialysis treatments, he developed hypotension with symptoms of feeling poorly and diaphoresis. His dry weight was increased in response, but he experienced another episode of hypotension several days later. The document then discusses intradialytic hypotension in general, including definitions, mechanisms, complications, and approaches to assessing volume status in hemodialysis patients.
Hypertensive emergencies require immediate blood pressure reduction to prevent end organ damage. They are characterized by severely elevated blood pressure and signs of acute target organ injury. The goal is to lower mean arterial pressure by 20-25% within minutes to hours using intravenous antihypertensive drugs like sodium nitroprusside. Hypertensive urgencies also involve severely high blood pressure but without acute organ injury, allowing for oral drugs to safely lower blood pressure within 24 hours. Rapid blood pressure reduction is avoided to prevent hypotension in both conditions.
This document summarizes the importance of preoperative investigations and assessments. It outlines key tests that should be performed for major surgeries, such as complete blood count, serum creatinine, ECG, coagulation screening, and chest x-rays. Additional tests like blood glucose, liver function tests, and arterial blood gases are recommended for patients with certain medical conditions. The results of preoperative investigations help optimize patient health prior to surgery and identify risks. A thorough preoperative evaluation is essential to reduce preventable complications.
Pre-operative assessment, evaluation and preparation of a patient of Diabetes...Saptaparni Hazra
This document provides guidance on preoperative evaluation and preparation of patients with diabetes mellitus undergoing surgery. Key points include determining the type and control of the patient's diabetes, assessing for complications, identifying high-risk patients, and optimizing diabetes management in the perioperative period. Intraoperative glucose should be managed between 140-180 mg/dL to minimize risk, and subcutaneous or intravenous insulin may be used depending on the surgical scenario and hemodynamic stability of the patient. Thorough preoperative evaluation and careful perioperative glucose management are essential in patients with diabetes.
This document discusses acute kidney injury (AKI), formerly known as acute renal failure (ARF). It covers the definition and classification of AKI, common causes of AKI such as infections and toxins, risk factors, diagnosis through creatinine levels and urine output monitoring, management approaches including fluid management and renal replacement therapy, and outcomes after AKI such as risk of chronic kidney disease. Case examples are provided to illustrate approaches to diagnosing and managing AKI in different clinical scenarios.
Approach to Sepsis & Septic Shock in Emergency Medicine.AngelGovekar
Sepsis and septic shock result from a dysregulated host response to infection. Sepsis criteria include suspected or proven infection and an increase in the SOFA score of 2 or more, while septic shock requires sepsis with vasopressor need to maintain blood pressure and elevated lactate. Treatment involves early recognition, source control with antibiotics, initial fluid boluses of 1-2L for hypotension or elevated lactate, vasopressors if needed, and lactate clearance-guided resuscitation.
This document discusses the management of patients with coronary vascular disorders. It covers topics such as coronary atherosclerosis, risk factors for coronary artery disease, clinical manifestations of coronary artery disease including angina pectoris and myocardial infarction, diagnostic testing, and treatment options including medications, percutaneous coronary intervention, and coronary artery bypass grafts. Nursing care focuses on relieving symptoms, preventing further damage, maintaining perfusion, reducing anxiety, and monitoring for complications through assessment, patient education, and collaboration.
Hyperviscosity syndrome (HVS) occurs when increased levels of proteins, cells, or other components in the blood cause it to become abnormally viscous or thick. This leads to reduced blood flow and organ damage. HVS is diagnosed based on clinical signs and symptoms along with laboratory tests showing elevated blood viscosity. Treatment involves reducing the cause of viscosity, typically through plasmapheresis to remove excess proteins in multiple myeloma or Waldenstrom macroglobulinemia. Prompt treatment is needed to prevent organ damage and vision loss from HVS.
This document provides an analysis of a 65-year-old male with chronic hepatitis C and cirrhosis who presented for follow up of anemia. He has a history of multiple failed hepatitis C treatments and complications of cirrhosis including ascites, encephalopathy, and esophageal varices. His current medications and management plan are outlined, focusing on preventing further liver damage and complications through lifestyle changes, medication adherence, screening for hepatocellular carcinoma, and treatment of ascites and encephalopathy. Economic and ethical considerations related to his condition are also discussed.
Sickle cell disease is a genetic blood disorder caused by a mutation in the beta-globin gene. This mutation causes red blood cells to become sickle shaped and leads to anemia, pain crises, and organ damage. The disease is inherited in an autosomal recessive pattern and is most common in those with ancestry from sub-Saharan Africa, India, Saudi Arabia, and Mediterranean countries. Management involves staying hydrated, treating infections, managing pain, and potentially receiving blood transfusions or hydroxyurea therapy to reduce complications. Lifelong monitoring of health and adherence to prophylactic treatments and immunizations is important for sickle cell patients.
Hypertension Emergencies and their managementpptxUzomaBende
This Presentation talks about Hyprtension, the mode of presentation of hypertensive crisis and the effective management of hypertensive crisis to prevent case fatalities.
Acute Flaccid Paralysis (AFP) is defined as sudden onset of weakness or paralysis in a previously normal limb over 15 days in patients under 15 years old. Guillain-Barré Syndrome (GBS) is the most common cause of AFP and is an acute acquired inflammatory demyelinating polyneuropathy. It has an annual incidence of 0.6 to 2.4 cases per 100,000 people and usually occurs 2-4 weeks after a respiratory or GI infection. GBS is diagnosed through CSF analysis showing elevated proteins and electrophysiological studies showing demyelination. Treatment involves monitoring, IVIG or plasma exchange to shorten recovery time, and PICU care if respiratory involvement is present.
An Overview of acute flaccid pralysis in Children.pdfzainjoiya3
Acute Flaccid Paralysis (AFP) is defined as sudden onset of weakness or paralysis in a previously normal limb over 15 days in a patient under 15 years old. Guillain-Barré Syndrome is the most common cause of AFP in healthy children and is an acute immune-mediated polyneuropathy often following a respiratory or gastrointestinal infection. It presents with ascending limb weakness, loss of reflexes, and in severe cases involves cranial nerves and respiratory muscles. Accurate differential diagnosis from other causes of AFP like polio, transverse myelitis, or traumatic neuritis is important for surveillance and treatment.
1. The patient presented with headache and right-sided hemiplegia, consistent with an acute stroke.
2. Strokes in sickle cell disease are most commonly ischemic and occur bimodally, peaking in younger children and those over 30 years old. Hemorrhagic strokes are rarer and peak during the second decade.
3. Diagnostic workup includes blood tests and neuroimaging to determine if the stroke is ischemic or hemorrhagic, as management differs between the two.
This document provides an overview of sickle cell disease, including:
- It is a genetic blood disorder caused by a mutation resulting in abnormal rigid red blood cells.
- Clinical features include anemia, pain crises, infections, stroke risk and organ damage over time.
- Diagnosis involves blood tests and genetic screening.
- Management focuses on hydration, pain control, antibiotics for infection, blood transfusions for crises, and lifelong folic acid supplementation.
Drs. Lena, Avery, and Davis’s CMC Abdominal Imaging Mastery Project: August C...Sean M. Fox
Dr. Kelsey Lena is an Emergency Medicine Resident and Drs. Michael Avery and Joshua Davis are Surgery Residents at Carolinas Medical Center in Charlotte, NC. They are interested in medical education. With the guidance of Drs. Kyle Cunningham and Michael Gibbs, they aim to help augment our understanding of emergent abdominal imaging. Follow along with the EMGuideWire.com team as they post these monthly educational, self-guided radiology slides. This month’s topics include:
• Splenic Rupture
• Obstructive jaundice
• Ovarian Torsion
This case presentation describes a 58-year-old female patient who presented with fever, myalgia, severe headaches, and generalized weakness. Investigations revealed anemia, elevated inflammatory markers, and a positive transesophageal echocardiogram showing mitral valve vegetation. The patient was diagnosed with infective endocarditis of the mitral valve and underwent mitral valve replacement surgery. The document then provides details on the definition, diagnosis, and treatment of infective endocarditis, including descriptions of the Duke criteria for diagnosis and appropriate antibiotic therapy based on the infecting organism.
Antiphospholipid syndrome (APS) is an acquired autoimmune condition characterized by arterial or venous thrombosis and/or pregnancy morbidity in the presence of antiphospholipid antibodies. The document discusses the history, incidence, definition, classification, clinical manifestations, diagnostic criteria, treatment and management of APS. APS can affect multiple organ systems and present with a wide variety of clinical symptoms. Prompt diagnosis and treatment with anticoagulation and immunosuppression is important to prevent morbidity and mortality.
PUBERTY MENORRHAGIA & BLEEDING DISORDERS Made Easy Dr Sharda Jain Lifecare Centre
This document discusses evaluation and treatment of puberty menorrhagia and bleeding disorders. It begins with classifications of abnormal uterine bleeding and an overview of common causes of puberty menorrhagia such as dysfunctional uterine bleeding and bleeding disorders. Evaluation involves a detailed history, physical exam, ultrasound, and lab tests to rule out other causes before screening for bleeding disorders. Common bleeding disorders seen in puberty menorrhagia are von Willebrand disease, platelet function defects, and coagulation factor deficiencies. Treatment depends on the underlying cause but may include combined oral contraceptives, antifibrinolytic agents, plasma concentrates, and managing anemia.
Atrial fibrillation is characterized by disorganized electrical activity in the atria leading to irregular heartbeat. Risk factors include increasing age, hypertension, diabetes, obesity, sleep apnea, smoking, and family history. Symptoms include irregular pulse and murmurs. Diagnosis is made through ECG and echocardiogram. Treatment involves rate or rhythm control with medications, catheter ablation, anticoagulation to prevent stroke, and treating any underlying causes. Guidelines from AHA and ESC provide recommendations on management strategies.
Intra dialytic hypotension ,,, prof Alaa SabryFarragBahbah
This document describes a case of intradialytic hypotension in a 65-year-old man on hemodialysis. During one of his dialysis treatments, he developed hypotension with symptoms of feeling poorly and diaphoresis. His dry weight was increased in response, but he experienced another episode of hypotension several days later. The document then discusses intradialytic hypotension in general, including definitions, mechanisms, complications, and approaches to assessing volume status in hemodialysis patients.
Hypertensive emergencies require immediate blood pressure reduction to prevent end organ damage. They are characterized by severely elevated blood pressure and signs of acute target organ injury. The goal is to lower mean arterial pressure by 20-25% within minutes to hours using intravenous antihypertensive drugs like sodium nitroprusside. Hypertensive urgencies also involve severely high blood pressure but without acute organ injury, allowing for oral drugs to safely lower blood pressure within 24 hours. Rapid blood pressure reduction is avoided to prevent hypotension in both conditions.
This document summarizes the importance of preoperative investigations and assessments. It outlines key tests that should be performed for major surgeries, such as complete blood count, serum creatinine, ECG, coagulation screening, and chest x-rays. Additional tests like blood glucose, liver function tests, and arterial blood gases are recommended for patients with certain medical conditions. The results of preoperative investigations help optimize patient health prior to surgery and identify risks. A thorough preoperative evaluation is essential to reduce preventable complications.
Pre-operative assessment, evaluation and preparation of a patient of Diabetes...Saptaparni Hazra
This document provides guidance on preoperative evaluation and preparation of patients with diabetes mellitus undergoing surgery. Key points include determining the type and control of the patient's diabetes, assessing for complications, identifying high-risk patients, and optimizing diabetes management in the perioperative period. Intraoperative glucose should be managed between 140-180 mg/dL to minimize risk, and subcutaneous or intravenous insulin may be used depending on the surgical scenario and hemodynamic stability of the patient. Thorough preoperative evaluation and careful perioperative glucose management are essential in patients with diabetes.
This document discusses acute kidney injury (AKI), formerly known as acute renal failure (ARF). It covers the definition and classification of AKI, common causes of AKI such as infections and toxins, risk factors, diagnosis through creatinine levels and urine output monitoring, management approaches including fluid management and renal replacement therapy, and outcomes after AKI such as risk of chronic kidney disease. Case examples are provided to illustrate approaches to diagnosing and managing AKI in different clinical scenarios.
Approach to Sepsis & Septic Shock in Emergency Medicine.AngelGovekar
Sepsis and septic shock result from a dysregulated host response to infection. Sepsis criteria include suspected or proven infection and an increase in the SOFA score of 2 or more, while septic shock requires sepsis with vasopressor need to maintain blood pressure and elevated lactate. Treatment involves early recognition, source control with antibiotics, initial fluid boluses of 1-2L for hypotension or elevated lactate, vasopressors if needed, and lactate clearance-guided resuscitation.
This document discusses the management of patients with coronary vascular disorders. It covers topics such as coronary atherosclerosis, risk factors for coronary artery disease, clinical manifestations of coronary artery disease including angina pectoris and myocardial infarction, diagnostic testing, and treatment options including medications, percutaneous coronary intervention, and coronary artery bypass grafts. Nursing care focuses on relieving symptoms, preventing further damage, maintaining perfusion, reducing anxiety, and monitoring for complications through assessment, patient education, and collaboration.
Hyperviscosity syndrome (HVS) occurs when increased levels of proteins, cells, or other components in the blood cause it to become abnormally viscous or thick. This leads to reduced blood flow and organ damage. HVS is diagnosed based on clinical signs and symptoms along with laboratory tests showing elevated blood viscosity. Treatment involves reducing the cause of viscosity, typically through plasmapheresis to remove excess proteins in multiple myeloma or Waldenstrom macroglobulinemia. Prompt treatment is needed to prevent organ damage and vision loss from HVS.
This document provides an analysis of a 65-year-old male with chronic hepatitis C and cirrhosis who presented for follow up of anemia. He has a history of multiple failed hepatitis C treatments and complications of cirrhosis including ascites, encephalopathy, and esophageal varices. His current medications and management plan are outlined, focusing on preventing further liver damage and complications through lifestyle changes, medication adherence, screening for hepatocellular carcinoma, and treatment of ascites and encephalopathy. Economic and ethical considerations related to his condition are also discussed.
Sickle cell disease is a genetic blood disorder caused by a mutation in the beta-globin gene. This mutation causes red blood cells to become sickle shaped and leads to anemia, pain crises, and organ damage. The disease is inherited in an autosomal recessive pattern and is most common in those with ancestry from sub-Saharan Africa, India, Saudi Arabia, and Mediterranean countries. Management involves staying hydrated, treating infections, managing pain, and potentially receiving blood transfusions or hydroxyurea therapy to reduce complications. Lifelong monitoring of health and adherence to prophylactic treatments and immunizations is important for sickle cell patients.
Hypertension Emergencies and their managementpptxUzomaBende
This Presentation talks about Hyprtension, the mode of presentation of hypertensive crisis and the effective management of hypertensive crisis to prevent case fatalities.
Similar to Recognition and transfer of the Critically ill patient ELUMELU DAWACS 2024 UPDATE .pdf (20)
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Our backs are like superheroes, holding us up and helping us move around. But sometimes, even superheroes can get hurt. That’s where slip discs come in.
8 Surprising Reasons To Meditate 40 Minutes A Day That Can Change Your Life.pptxHolistified Wellness
We’re talking about Vedic Meditation, a form of meditation that has been around for at least 5,000 years. Back then, the people who lived in the Indus Valley, now known as India and Pakistan, practised meditation as a fundamental part of daily life. This knowledge that has given us yoga and Ayurveda, was known as Veda, hence the name Vedic. And though there are some written records, the practice has been passed down verbally from generation to generation.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
Osteoporosis - Definition , Evaluation and Management .pdfJim Jacob Roy
Osteoporosis is an increasing cause of morbidity among the elderly.
In this document , a brief outline of osteoporosis is given , including the risk factors of osteoporosis fractures , the indications for testing bone mineral density and the management of osteoporosis
Recognition and transfer of the Critically ill patient ELUMELU DAWACS 2024 UPDATE .pdf
1. WEST AFRICAN COLLEGE OF SURGEONS
COLLEGE OUEST AFRICAN DES CHIRURGIENS
Diploma in Anaesthesia Update Course
March 2024
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
2. RECOGNITION AND TRANSFER OF THE CRITICALLY ILL PATIENT
DR A V ELUMELU
DA(WACS); FWACS
National Hospital Abuja.
Samtah General Hospital KSA
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
3. COURSE OUTLINE
• DEFINITION
• BASELINE CLINICAL EVALUATION
• CLINICAL FEATURES: SYSTEMIC
• SCORING SYSTEMS
• INITIAL MANAGEMENT
• PATIENT TRANSPORTION
• MODES
• HAZARDS
• CHECKLIST
• SUMMARY
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
4. CRITICAL ILLNESS
• Critical illness is a general state which may arise
from various medical conditions, surgical
pathologies or injury with the potential for
threatened or actual impairment of vital organ
function.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
5. CRITICAL ILLNESS
• Critical illness is any disease process which causes
physiological instability, potentially leading to
disability or death within minutes or hours.
• The medical condition in which a patient, because
of major surgery or severe illness, requires
immediate intensive medical support of vital organ
functions in order to survive.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
6. CRITICAL ILLNESS: DEFINITION
• A state of ill health with vital organ dysfunction, a high risk
of imminent death if care is not provided and the potential
for reversibility (R K Kayambankadzanja et al BMJ Open, 12,
9.)
• No defined consensus of an exact definition of a critically ill
patient.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
7. THE CRITICALLY ILL PATIENT
• We must remember that the critically ill state is defined
more by the patients condition or physio-pathological state
rather than the patients actual diagnosis.
• Though some medical diagnoses are critical illness states in
themselves
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
8. BASELINE CLINICAL EVALUATION OF PATIENTS
• To recognize critical illness or critical changes, one must have
a baseline knowledge of expected physiological parameters
or the actual clinical findings of patients for age, gender and
ethnicity.
• Careful clinical evaluation: History and physical examination
• Baseline vital signs at first visit must be checked and recorded
and thereafter recorded at regular intervals.
• Documentation is key
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
9. BASELINE CLINICAL EVALUATION OF
PATIENTS
• Level of consciousness,
demeanor.
• Motor activity
• Airway and Respiration
• Pulse
• Blood Pressure
• Temperature
• Urine output
• Multi-parameter monitoring
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
10. POINT OF CARE TESTING
• Blood glucose estimation
• Arterial Blood Gas analysis
• Hemocue, Estimation of Hemoglobin
• Portable ultrasonography
• Electrocardiography/Bedside Echocardiography
• Radiological tests: X rays , CT
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
11. ARTERIAL BLOOD GAS MACHINE AND
I-STAT
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
13. In the critically ill patient there is a marked deviation from the expected normal or from the baseline features.
There is an actual or impending compromise of the systems: airway, respiratory, neurological, cardiovascular or other systems.
Biochemical changes may be profound and equally life threatening.
Irrespective of the underlying diagnosis, there are clinical features that alert one to the critical state of the patient.
HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT
• In the critically ill patient there is a marked deviation from
the expected normal or from the baseline features.
• There is an actual or impending compromise of the
systems: airway, respiratory, neurological, cardiovascular
or other systems.
• Biochemical changes may be profound and equally life
threatening.
• Irrespective of the underlying diagnosis, there are clinical
features that alert one to the critical state of the patient.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
14. HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT:
Neurological Signs
▪Confusion, Failure to obey commands, agitation, mania
▪Reduced GCS <10/15. Sudden drop in GCS >2 points
▪Absent cough or Gag reflexes
▪Seizures - prolonged or repeated
▪Facial weakness, hemiparesis, hypotonia
▪Change in the size and light reflexes of the pupils
▪Delayed recovery from anaesthesia for the postoperative
patient
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
15. THE CRITICALLY ILL PATIENT: Neurological
❖AVPU: Alert, Response to Verbal, Pain stimulus or
Unresponsive
❖Glasgow Coma Scale: Eye opening-4, Best Verbal-5,
Best Motor -6. (15/15)
❖GCS: Best score is 15, lowest score is 3
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
16. .
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
17. HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT:
Respiratory Signs
▪Any form of airway obstruction
▪Respiratory distress: Stridor/wheezing, Intercostal
recession, Abdominal seesawing, use of accessory muscles.
▪Inability to speak in complete sentences
▪RR <8 or >35cpm
▪Respiratory failure (type I or 2), respiratory arrest
▪Low SpO2, below 92% in room air
▪Pulmonary oedema, pneumothorax, thoracic trauma
▪ABG: PaCO2 >60mmHg (>8kPa), low PaO2, Respiratory Acidosis
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
18. HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT:
Cardiovascular signs
▪Cardiac Arrest
▪Life threatening Cardiac Arrhythmias (SVT, VF, VT, AF,
bradycardia)
▪Pulse <50/>140 bpm
▪SBP <60/>200mmHg
▪Tissue Hypoxia: Metabolic acidosis, Raised serum Lactate,
Poor peripheral perfusion, mottling of the skin.
▪Muffled heart sounds
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
19. HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT:
Cardiovascular signs
▪Poor response to volume resuscitation
▪Oliguria <0.5ml/kg/hr
▪Delayed capillary refill. Greater than 5 seconds
▪ECG changes: ST elevation, T wave abnormalities, heart
block with clinical deterioration
▪Haemorrhage from any source
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
20. HOW TO RECOGNIZE THE CRITICALLY ILL PATIENT:
Biochemical/Laboratory findings
• ABG Changes: severe acidosis/alkalosis
• Hyperglycaemia, Hypoglycaemia
• Electrolyte disorders: Hyper or Hyponatremia, Hypo or
hyperkalaemia, Hypocalcaemia
• Severe anemia
• Altered clotting profile
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
21. THE CRITICALLY ILL PATIENT:
• Any patient may present as critically ill.
• All age ranges: neonatal to geriatric
• In hospital or out of hospital
• Acute onset, acute deterioration or a slow decline in
constitution.
• Patient may have multiple pathologies /co-morbidities
• May be on medications, multiple meds or may have
missed doses
• May be part of a mass wave of patients – mass casualty
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
22. THE CRITICALLY ILL PATIENT: In Hospital
The critically ill patient may be identified from different
locations:
➢in the emergency department having presented from
home
➢or referred from another healthcare facility,
➢ may be identified on the ward,
➢ in the operating theatre,
➢ Labour ward or
➢ other patient care areas within the hospital.
➢At the scene of disaster : patient retrieval team
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
23. THE CRITICALLY ILL PATIENT
➢The critically ill patient is vulnerable, unstable and
complex.
➢Single or multiple organs may be failing or at risk of
failure.
➢Significant morbidity and high risk of mortality
➢A systematic approach is needed to recognize
clinical deterioration and escalate care
➢Sadly these may be missed
➢Team based care approach is needed
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
24. THE CRITICALLY ILL PATIENT
The proper management of a critically ill patient
requires:
✓Early identification of the critically ill patient
✓Identification of the immediate life threatening
problems
✓Prompt intervention to save the life of the patient.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
25. SOME CRITICAL CLINICAL CONDITIONS
▪Neurological- Coma, Seizures, SOLs, CVA, neuromuscular disorders
▪Cardiovascular – Arrhythmias, MI, Failure, Arrest
▪Airway and Respiratory –Actual or potential Airway compromise,
Respiratory Embarrassment or failure
▪Metabolic disorders – Diabetic comas, hormone disorders,
electrolyte imbalances
▪Poisonings and Envenomation – Accidental/Intentional: Self,
Homicide, Iatrogenic. Snake bites
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
26. SOME CRITICAL CLINICAL CONDITIONS
▪Trauma: RTA, Assault, Falls, Drowning, Burns, Electrocution
▪Sepsis and Inflammatory disorders
▪Hypersensitivity reactions, Allergies
▪Acute abdomen
▪Abdominal or pelvic disorders
▪Disorders of pregnancy
▪Haemorrhage from any cause
▪Extensive, Highly invasive or prolonged surgery
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
27. THE CRITICALLY ILL PATIENT: Initial Management
IN THE CRITICALLY ILL PATIENT:
➢ The pace of assessment and therapy is quicker
➢ Simultaneous evaluation and therapy are carried out to
arrest the situation
➢ Expeditious transportation may be needed to the
Operating Theatre, ICU, Radiology suite or another
hospital for investigations, interventions and definitive
care.
➢ Escalate and call for help or assistance as early as
possible.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
28. THE CRITICALLY ILL PATIENT: Initial Management
1. SAFETY: Scene safety, Basic PPE
2. FIRST GLANCE: Initial Impression, Demeanor of pt/caregivers. Pt
responsiveness
3. INITIAL ASSESMENT (Primary Survey):
A- Airway. B- Breathing, C-Circulation, D-Disability, E- Exposure
Maintain patients dignity
4. IMMEDIATE MANAGEMENT:
Also following the A B C format
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
29. THE CRITICALLY ILL PATIENT: Safety
and PPE
the new normal!
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
30. A: Airway
▪ Look, feel and listen.
▪ Head tilt, Chin lift, jaw thrust. Suction the airway.
▪ Oropharyngeal airway, nasopharyngeal airway
▪ Left lateral positioning if the situation and clinical
condition permits
▪ Pulse Oximetry
▪ Attach all monitors
▪ Call for the Crash cart if needed
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
31. A: Airway
Commence Oxygen:
✓ by nasal prongs (4 – 6 LPM; 24 – 44%)
✓simple face mask (6 – 10 LPM; 35-50%) or a
✓Non-rebreather face mask with a reservoir bag ( 10-
15LPM; 60-80%)
✓Venturi mask: FIO2 can be more precisely titrated
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
35. AIRWAY
• Where the airway is compromised:
• Secure the airway: Supraglottic device
• Definitive control of the airway by tracheal intubation.
• The critically ill patient is not as robust as the ASA I patient
coming for elective surgery!
• All precautions must be taken to prevent profound
hypotension, bradycardia or cardiac arrest after
intubation.
• Volume loading, judicious use of sedative medication or
muscle relaxant and always prepare for difficult intubation
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
36. B:
BREATHING
• Assessment of the Airway and Breathing go hand in
hand/overlap.
• Check if the respiratory effort is adequate.
• Check for chest expansion. Auscultate and percuss the lung
fields
• If respiratory effort is inadequate or ineffective, ventilations
may be commenced using a Bag-valve-mask device.
• Non invasive Ventilation using a BIPAP machine may be used
–conscious patient.
• Intubation and IPPV as the situation may demand.
• Appropriate sedation must be given for IPPV
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
37. B: BREATHING
Bag – Valve-mask device (Ambubag)
BIPAP Ventilation
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
38. B: BREATHING
High flow nasal oxygenation/Tracheal
Intubation
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
39. C - CIRCULATION
• Check for pulse: rate, pattern, volume. Pallor, cyanosis, capillary refill.
• If no palpable carotid pulse in an unresponsive patient, call a code,
Cardiac arrest team to respond. Commence CPR .
• Blood pressure, ECG
• Secure good large bore vascular access.
• Blood samples: VBG/ABG, CBC, LFT, RFT, serum electrolytes, Troponin
• Commence IV fluids: crystalloids, colloid or blood products
• Inotropic support may be commenced as needed. MAP > 65mmHg
• Control bleeding. Call the appropriate specialty. Team work!
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
40. D - DISABILITY
• Check the neurological status: AVPU, GCS, Pupils
• Check glucose
• Examine muscle tone and reflexes
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
41. E - EXPOSURE
• The patient should be exposed and thoroughly examined
for any other clinical features or injuries, including an
inspection of the back and the perineum.
• Patients dignity must be maintained
• Appropriate covering thereafter to prevent hypothermia
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
42. MANAGEMENT..
➢ Secondary Survey: REEVALUATE patient, again using the
ABCDE format. Focused history.
➢ SAMPLE HISTORY:
• Signs and Symptoms
• Allergies. Age
• Medication
• Past Medical History
• Last meal
• Events leading to presentation
43. NEXT STEPS..
• Specific investigations and therapies should be
commenced depending on the likely pathology
• For instance: radiological interventions
• Emperical antimicrobials commenced after culture samples
• Decision is made as to the appropriate place for the
patient: ICU, OT, Interventional radiology, CATH lab, higher
center
• There will be a constant and continuing assessment and
definitive management of the patient
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
44. THE CRITICALLY ILL PATIENT: THE SICK IN-PATIENT
• 50% of in-hospital cardiac arrests are said to occur in the
wards.
• Slow deterioration of the in patient is not easily picked up
and the signs may be subtle.
• Why? High patient to nurse ratio, Inexperience, voice not
listened to, not knowing what to do.
• Conversely, alarm may be raised but more experienced
senior staff may not react in a timely fashion.
• Early Warning schemes have been introduced in some
systems and countries to help
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
45. CARDIAC ARREST (Reversible Causes)
▪ Hypovolaemia Toxins
▪ Hypoxia Tamponad(cardiac)
▪ Hydrogen ion (acidosis) TensionPneumothorax
▪ Hypo/Hyperkalaemia Thrombosis(coronary)
▪ Hypothermia Thrombosis(pulmonary)
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
46. EARLY WARNING SCORES (EWS)
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
48. THE CRITICALLY ILL IN-PATIENT
• Acute event or a subtle deterioration
• Early warning Scores were developed to pick important changes
• There should be a clear chain of reporting when deterioration of
the patient is noted and documented.
• For In patients, there is the advantage of a clear diagnosis and
treatment plan as well as documentation to help out.
• ABCDE approach is still to be undertaken, with activation of the
available team and decision made to escalate care as needed.
• Rapid response teams, Cardiac Arrest teams, Medical Emergency
teams have all been developed in different health care systems
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
49. THE CRITICALLY ILL PAEDIATRIC PATIENT
• We may be called upon to assist with the care of a critically ill
paediatric patient, usually for intubation and ventilatory support.
• Hypoxia is the commonest cause of Cardiac arrest in children.
• The patient may range in size from the underweight poorly
nourished 2 year old to the overweight school age child.
• Congenital abnormalities and inborn errors of metabolism occur. Be
mindful of the likely clinical situations that occur in this age group.
• A careful stepwise approach using the ABCDE format and teamwork
is also necessary here.
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
50. TRANSFER OF THE CRITICALLY
ILL PATIENT
• .
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
51. PATIENT TRANSFERS:
• Patients are transported from one location to another for:
• Investigations to make a proper diagnosis,
• For Therapeutic purposes or for Definitive intervention
• To a specific ward/ICU/hospital for continued management
• To a higher medical facility for specific care or if there is
clinical deterioration.
• Elective and planned OR Emergent
• Stable patient or an unstable critically ill patient
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
52. PATIENT TRANSFER
• Intra-hospital
• Inter-hospital
• In between regions/countries- Medical evacuation
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
53. BEFORE THE PATIENT TRANSFER
• Determine the reason for the transfer
• Inform and confirm from the receiving department
or facility.
• Inform and explain situation to the patient or
caregivers
• Informed Consent, if applicable
• Logistics, payment, insurance should be worked out
by the relevant authorities/personnel
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
54. MODES OF TRANSPORTATION
oHospital Trolley
oHospital bed
oAmbulance (50miles/80km/2hr)
oRotary wing Aircraft (50-150miles/80-240km)
oFixed Wing Aircraft (>150miles/240km)
oWatercraft
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
55. PATIENT PREPARATION: Patient trolley/bed
▪The patient trolley should have side rails and be tiltable
head up
▪There should be a head rail, a foot rail and wheels with
foot operated brakes
▪There should be ports for IV poles to be attached
▪It should have straps to secure the patient in firmly.
▪Proper coverage for the patient with hospital bedsheets,
blanket or reflective space blanket as needed
▪The pathway for the trolley should be as smooth as
possible
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
58. MODES OF TRANSPORTATION:
By Helicopter or by Water Ambulance
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
59. MODES OF TRANSPORTATION:
In more resource challenged
locations
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
60. REQUIREMENTS FOR TRANSPORTING
THE CRITICALLY ILL PATIENT
➢Experienced Staff – properly trained
➢Appropriate equipment for Transfer
➢Full assessment and Investigation of the Patient
➢Extensive Monitoring
➢Careful Stabilization of Patient
➢Reassessment
➢Continuing Care during Transport
➢Direct handover
➢Documentation and Audit
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
61. STAFFING
➢ For a Critically ill patient, a doctor competent in
resuscitation, Airway care, ventilation and organ support
should accompany the patient.
➢ Ideally an Intensivist/ Anaesthetist/Emergency Physician
not less than an SR in rank
➢ This is not always the situation.
➢ Accompanied by a competent Nurse and/or a Paramedical
Staff or Technician.
➢ Good rapport within the staff
➢ Insurance Cover for disability or death during transfer
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
62. VEHICLE
❑The Transport Vehicle should be road/air/seaworthy –
adequate fuel.
❑Vehicles papers should be up to date.
❑It should have good trolley Access and Fixing systems –
Trolley, Patient & Equipment
❑Good Lighting
❑Temperature Controls
❑Adequate space for the medical Attendants and Equipment
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
63. EQUIPMENT
➢ Robust, Lightweight, Battery powered. Well secured.
➢ Sufficient oxygen for the duration of transfer + reserve for
1-2 hrs.
➢ Portable ventilator with disconnection alarms
➢ Portable multi-parameter monitor with illuminated display
(displaying HR, SPO2, RR, ECG, Capnography)
➢ Syringe drivers, Infusion pumps
➢ Suction machine
➢ Defibrillator
➢ Warming Blanket
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
64. ROBUST AND PORTABLE EQUIPMENT
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
66. PATIENT PREPARATION
▪Ensure the airway is secure. Intubate if necessary. Secure ETT with
ties
▪Breathing –Check ventilator (Back up Bag-valve device)
▪IV Access -2 lines, Central access if possible, all well secured
▪Meds- Sedation, Analgesics, Neuromuscular Blockade, emergency
meds.
▪All should be drawn up and labelled.
▪Chest tubes – secured properly below the level of the thorax. Clamps
available
▪Urethral catheters – strapped to the inner thigh with tape
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
67. CHECKLIST
➢Ensure the patient is resuscitated and stable
➢All lines and tubings should not be tangled and should
be firmly secured
➢Referring Hospital notified and ready to accept
patient
➢Documents: Referral note, Med records, X-rays,
Transport checklist and records
➢Relatives informed and Consent forms duly signed
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
68. CHECKLIST
➢Adequate Oxygen. Have back up oxygen cylinders
➢Equipment –Functional with extra batteries for back
up
➢Cash, ATM/Phone cards, a Charged phone and a list
of numbers to call.
➢Clear return arrangements
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
69. HAZARDS OF PATIENT TRANSPORT: To the patient
PHYSIOLOGICAL:
Acceleration and deceleration forces have effects on the patient:
❖Cardiovascular Instability, Cardiac arrest
❖Raised Intracranial pressure
❖Change in respiratory rate, Hypoxaemia, Hypo/Hypercapnia
PHYSICAL:
❖Entanglement and Displacement of IV lines, Airway devices,
drains and Catheters
❖Expansion of air filled spaces at high altitudes: Inflate ETT cuff
with saline
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
70. HAZARDS OF TRANSPORTATION
MECHANICAL:
❖Equipment Failure
❖Exhaustion of oxygen
❖Battery failure for medical devices
❖Cramped, noisy, Vibrating space
❖Vehicular accidents (injury/death)
❖ OTHER: Motion sickness,
❖ Misunderstanding/disputes with personnel
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
71. HAZARDS: ACCIDENTS
Five dead as medical transport plane crashes in
Nevada US
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
72. DURING TRANSPORT
• Constant vigilance of clinical condition/vital signs
• Medications and fluids should be continued as prescribed
(Never let the IV get blocked with blood clot or to get
tissued)
• Pace of transport should be timely but not high risk driving
• The patient should be assessed constantly
• Vasopressors and other emergency medication should be
available. CPR may even need to be carried out.
• Proper documentation is also mandatory
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
73. ARRIVAL
• Upon arrival, information should be handed over
to the receiving facility with clear
communication.
• The patient should again be assessed. He may
need further intervention.
• Proper documentation is also mandatory
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
74. DOCUMENTATION
• A very important medical and legal requirement. Medical
records/report
• A report documenting the patients condition prior to transfer,
during the transfer and upon arrival. Interventions and
medications given during transfer must be documented,
• All handed over to the receiving team/facility. A copy kept
with the transfer team/referring facility
• Pre return checklist (Personnel, equipment, Patient
information)
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
75. SUMMARY
• The critically ill patient, of any age, is at constant risk of death or
serious disability with grave consequences for the patient, family,
the health care system and the greater community
• Proper recognition, assessment and timely interventions may
possibly reverse the clinical state with a good outcome.
• Proper recognition for the need, the plan and flawless execution of
patient transport is invaluable
• A systematic team based approach yields the best outcomes
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
76. READ
• Early warning scores (EWS)
• SOFA/qSOFA
• APACHE scores
• AAGBI guidelines on Interhospital
transfer
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
77. RELEVANT
TRAININGS/CERTIFICATIONS
• AHA Basic Life Support (BLS)
• AHA Advanced Cardiac Life Support (ACLS)
• Paediatric Advanced Life Support (PALS)
• Advanced Trauma Life Support (ATLS)
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
78. REFERENCES
• Critical Illness. Newton L E, Heimburger D C. Handbook of Clinical
neurology 2014
• Towards definitions of critical illness and critical care using concept
analysis. Kayambankadzanja, Schell C O, Warnberg M G et al BMJ
Open, vol 12,issue 9.
• ABCDE Assessment oxfordmedicaleducation.com
• Case files Critical Care. Second edition. Toy, Liu, Suarez
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024
79. THE CRITICALLY ILL PATIENT
DR AFFIONG V ELUMELU. WACS DIPLOMA IN ANAESTHESIA
UPDATE; MARCH 2024