This document provides information on dengue, including its case definition, epidemiology, pathophysiology, clinical features, investigations, management, complications, and treatment. A probable dengue case is defined as an acute febrile illness with two or more symptoms like headache and retro-orbital pain. A confirmed case requires virus isolation or serology testing. Dengue is endemic in over 100 countries and is transmitted by the Aedes aegypti mosquito. It has four serotypes and causes a spectrum of disease from mild fever to severe dengue hemorrhagic fever and dengue shock syndrome. Management involves fluid management and supportive care. There is currently no approved vaccine for dengue.
1. Neutropenic fever and tumor lysis syndrome are hematologic oncologic emergencies that require prompt assessment and treatment to prevent complications and death.
2. Patients at high risk for complications from neutropenic fever should receive inpatient empiric antibiotics targeting pseudomonas such as an antipseudomonal beta-lactam with vancomycin.
3. For persistent fevers, the treatment regimen should be modified based on cultures and the patient should be reassessed for new infections, including invasive fungal infections if fevers persist for more than 4 days. Catheter-related bloodstream infections also require prompt management.
This document discusses sepsis management in the emergency department. It outlines the scope of the problem, defining terms like SIRS, sepsis, severe sepsis, septic shock and MODS. It discusses appropriate antibiotic usage and early goal directed therapy. Sepsis affects millions of ED visits annually and causes hundreds of thousands of deaths. Early identification and treatment, including antibiotics within 3 hours and goal directed resuscitation improving oxygen delivery, can significantly reduce mortality.
The document defines acute liver failure in children and discusses its causes, presentation, management, and complications. Acute liver failure is characterized by liver dysfunction within 8 weeks without preexisting liver disease and includes coagulopathy and hepatic encephalopathy. Common causes include viral hepatitis, acetaminophen toxicity, and idiosyncratic drug reactions. Management involves supportive care to maintain organ function, treatment of specific causes, and potentially liver transplantation for severe cases.
ACUTE PANCREATITIS- EPIGASTRIC PAIN
#surgicaleducator #epigastricabdominalpain #acutepancreatitis #usmle #babysurgeon #surgicaltutor
Dear Viewers,
Greetings from Surgical Educator
Today I have uploaded a video on Acute Pancreatitis- a didactic lecture. I have already uploaded 2 more videos on the same topic, one in case based learning of abdominal pain and another one in image based questions for Hepato-biliary- pancreatic pathologies.
It is one of the common surgical problems you see in surgical wards.
I have discussed the various causes for Epigastric pain, etiology, pathology, clinical features, investigations, scoring systems, complications and treatment of Acute Pancreatitis.
I have also included a mind map and a treatment algorithm for Acute Pancreatitis.
I hope the video will be very useful and you will enjoy it.
You can watch all my surgical teaching videos in the following link:
youtube.com/c/surgicaleducator
Thank you for watching the video.
This document provides information on malaria, including its epidemiology, clinical features, diagnosis, and complications. It discusses that malaria is a major public health problem, with half of the world's population at risk. Clinical features include fever, chills, and headaches. Malaria can be uncomplicated or complicated/severe, with the latter presenting dangers like cerebral malaria, anemia, and respiratory distress. Diagnosis involves microscopy of blood smears or rapid diagnostic tests detecting malaria antigens.
The document provides information on common hospital-acquired infections including fever, sepsis, urinary tract infections, soft tissue infections like cellulitis, pneumonia, and Clostridium difficile infection. It discusses definitions, risk factors, clinical presentations, diagnostic testing, and treatment recommendations for each condition based on clinical severity and patient risk factors.
The document summarizes the case of an 8-year-old girl admitted to the hospital with tea-colored urine. She was diagnosed with acute glomerulonephritis based on lab tests showing hematuria, proteinuria, and low complement levels. Her symptoms improved over her hospital stay with IV fluids and medications. She was discharged after 6 days with medications and advised to follow up in 2 weeks and longer term to monitor resolution of her symptoms.
Dengue Hemorrhagic Fever is caused by dengue viruses of the Flavivirus family. There are four serotypes of the virus. The virus is transmitted to humans through the bites of infected female Aedes mosquitoes. Diagnosis involves identifying thrombocytopenia, hemoconcentration, and other clinical manifestations. Treatment depends on the clinical classification and involves supportive care, fluid management, and close monitoring, especially during the critical leakage phase when plasma is leaking from blood vessels.
The document summarizes neonatal sepsis, including its definition, epidemiology, causes, symptoms, diagnosis, and treatment. It discusses the pathophysiology of neonatal immune deficiency that predisposes infants to sepsis. Early and late onset sepsis are described, along with common pathogens for each. Risk factors like prematurity, maternal infections, and invasive procedures are outlined. The clinical presentation of sepsis is generally non-specific. Evaluation includes blood tests and cultures. Treatment involves initial broad-spectrum antibiotics tailored based on results and infant risk factors. Prevention strategies like vaccines and hand washing are mentioned.
This document discusses several diseases that present with hematuria or proteinuria in children. It describes a case of acute post-streptococcal glomerulonephritis in a 10-year-old boy presenting with edema and Coca-Cola colored urine. It then provides details on the etiology, clinical presentation, diagnosis, complications and treatment of this condition. It also summarizes several other conditions like IgA nephropathy, Alport syndrome, hemolytic uremic syndrome, polycystic kidney disease, nephrotic syndrome, undescended testes, testicular torsion, and epididymitis.
The document discusses dengue and dengue hemorrhagic fever (DHF) in adults. It provides epidemiological data showing over 2.5 billion people in 100 countries are at risk of dengue infection. It reviews clinical manifestations and laboratory findings in adults with dengue fever (DF) and DHF. Key points include thrombocytopenia being common, with over 25% of DHF patients having platelet counts less than 20,000/mm3. Bleeding is a risk, especially for those with severe thrombocytopenia, liver dysfunction, or shock. Proper fluid management and monitoring are important for treating DHF to avoid complications.
Children with congenital heart disease or rheumatic heart disease are at highest risk for developing bacterial endocarditis. It commonly presents with fever, heart murmur, and embolic phenomena. Diagnosis is made using modified Duke criteria, which considers major and minor clinical criteria as well as positive blood cultures. Treatment involves prolonged intravenous antibiotics targeting the causative organism. Surgery may be needed for complications like heart failure or abscesses. Prevention focuses on antibiotic prophylaxis for high-risk patients during certain medical procedures.
- Systemic Lupus Erythematosus (SLE) is an incurable, multisystemic autoimmune disease that predominantly affects women and has variable rates of median age of onset depending on ethnicity.
- SLE can affect many different body systems and has a variety of potential symptoms and complications, including renal, neurological, and hematological manifestations.
- Treatment involves managing symptoms with medications like hydroxychloroquine, corticosteroids, immunosuppressants, and emerging therapies targeting B cells and cytokines.
Legionnaires' disease is a form of atypical pneumonia caused by Legionella bacteria, mainly L. pneumophila. It is contracted through inhalation of contaminated aerosolized water droplets. Risk factors include smoking, immunosuppression, and age over 50. Symptoms include fever, cough, shortness of breath, and confusion. Diagnosis involves urine antigen testing, culture, or PCR. Treatment guidelines recommend macrolides or fluoroquinolones. Prevention focuses on maintaining cooling towers and water systems to avoid bacterial growth.
This document provides information on nephrotic syndrome, specifically defining it as a clinical syndrome characterized by heavy proteinuria, hypoproteinemia, edema, and hypercholesterolemia. It describes the epidemiology, classification, pathophysiology, clinical manifestations, investigations, diagnosis, management, and prognosis of nephrotic syndrome. The key points are that minimal change disease is the most common type, presenting with edema, ascites, weight gain, and respiratory distress in children aged 1-10 years. Investigations show proteinuria, hypoalbuminemia, and normal renal function. Management involves steroid therapy, addressing complications, and educating parents on infection prevention and immunization.
1. Sickle cell disease is an inherited blood disorder that affects hemoglobin and causes red blood cells to take on a sickle, or crescent, shape.
2. The prevalence of sickle cell disease varies by ethnicity, with the highest rates seen in African Americans at about 1 in 375 individuals.
3. Complications of sickle cell disease include anemia, infections, acute pain episodes, stroke, and damage to organs like the lungs, kidneys, spleen, and liver over time if not properly managed.
Diagnosis and examination of swollen lymph nodes ppt.pptxriazsohail448
油
The document discusses the diagnosis and evaluation of lymphadenopathy. It notes that lymphadenopathy can be localized, involving a single area, or generalized, involving two or more noncontiguous areas. For unexplained lymphadenopathy, localized cases may warrant biopsy if symptoms persist for 3-4 weeks, while generalized cases almost always indicate a systemic disease and biopsy is recommended. Risk factors for lymphoma are also outlined. Proper biopsy is important for diagnosis before treatment decisions. A case study example of a patient with cervical and supraclavicular lymphadenopathy and symptoms is then presented and worked through.
Acute pancreatitis is an inflammatory condition of the pancreas caused by the early activation of digestive enzymes within the pancreas. It can range from mild to severe, and in severe cases, it can lead to organ failure. The most common causes are gallstones, alcohol use, and viral infections. Symptoms include severe abdominal pain, nausea, vomiting, and fever. Laboratory tests show elevated levels of pancreatic enzymes in the blood. Severity is assessed using the Ranson score or APACHE II score. Treatment involves intravenous fluids, bowel rest, pain medications, and treating the underlying cause. Complications can include pancreatic pseudocysts, abscesses, and necrosis.
This patient, a 4-year-old boy, presented with prolonged fever, rash, fatigue, bone pain, conjunctivitis, and severe anemia. Laboratory tests showed high inflammatory markers, hypoalbuminemia, and hyperferritinemia. Imaging found hepatosplenomegaly and pericarditis with effusion. Infectious etiologies were ruled out. The presentation and lab results were consistent with a diagnosis of systemic juvenile idiopathic arthritis, also known as Still's disease. The patient was started on prednisone to treat this autoimmune condition characterized by intermittent fever, rash, and arthritis.
Parkinson Plus Syndrome - Multiple System Atrophy: Case Report.
Poster used in CMC MAC 2021.
ABSTRACT
A 61yr/Male, K/C/O T2DM & Parkinsons disease(PD) on T.Metformin and T.Syndopa for 3 years, presented to us with complaints of unsteadiness of gait, dysarthria, bilateral upper limb tremor. These symptoms started gradually and has been there for last 3 years and it is progressive. Initially, it started as inability to write and difficulty in mixing food due to tremulousness of both hands which worsens with activity. Then it progressed to slurred speech and then to gait unsteadiness. Patient also has urinary incontinence for last 2 years. Patients symptoms are more in severity for last 6 months. On examination, patient was having orthostatic hypotension, cogwheel rigidity on bilateral wrist movement and pendular knee jerks. All cerebellar signs were present bilaterally including finger nose test abnormality, past pointing, dysdiadochokinesia, heel shin test abnormality, gross truncal ataxia, wide based gait, impaired tandem walking, gaze evoked nystagmus, scanning speech.
Presence of cerebellar signs, autonomic disturbances, poor response to syndopa, rapid progression, lack of resting tremor at presentation, symmetrical involvement, early speech and gait involvement - are usually NOT seen in PD. So, evaluated further. MRI Brain T2 showed classical cruciform hyperintensity in pons (Hot cross bun sign) & diffuse cerebellar atrophy. Hence the diagnosis MULTIPLE SYSTEM ATROPHY (MSA-C) - Shy Drager Syndrome. This shows the importance of identifying atypical features in PD.
More Related Content
Similar to Leptospirosis Protocol for NABH accredition (20)
This document provides information on malaria, including its epidemiology, clinical features, diagnosis, and complications. It discusses that malaria is a major public health problem, with half of the world's population at risk. Clinical features include fever, chills, and headaches. Malaria can be uncomplicated or complicated/severe, with the latter presenting dangers like cerebral malaria, anemia, and respiratory distress. Diagnosis involves microscopy of blood smears or rapid diagnostic tests detecting malaria antigens.
The document provides information on common hospital-acquired infections including fever, sepsis, urinary tract infections, soft tissue infections like cellulitis, pneumonia, and Clostridium difficile infection. It discusses definitions, risk factors, clinical presentations, diagnostic testing, and treatment recommendations for each condition based on clinical severity and patient risk factors.
The document summarizes the case of an 8-year-old girl admitted to the hospital with tea-colored urine. She was diagnosed with acute glomerulonephritis based on lab tests showing hematuria, proteinuria, and low complement levels. Her symptoms improved over her hospital stay with IV fluids and medications. She was discharged after 6 days with medications and advised to follow up in 2 weeks and longer term to monitor resolution of her symptoms.
Dengue Hemorrhagic Fever is caused by dengue viruses of the Flavivirus family. There are four serotypes of the virus. The virus is transmitted to humans through the bites of infected female Aedes mosquitoes. Diagnosis involves identifying thrombocytopenia, hemoconcentration, and other clinical manifestations. Treatment depends on the clinical classification and involves supportive care, fluid management, and close monitoring, especially during the critical leakage phase when plasma is leaking from blood vessels.
The document summarizes neonatal sepsis, including its definition, epidemiology, causes, symptoms, diagnosis, and treatment. It discusses the pathophysiology of neonatal immune deficiency that predisposes infants to sepsis. Early and late onset sepsis are described, along with common pathogens for each. Risk factors like prematurity, maternal infections, and invasive procedures are outlined. The clinical presentation of sepsis is generally non-specific. Evaluation includes blood tests and cultures. Treatment involves initial broad-spectrum antibiotics tailored based on results and infant risk factors. Prevention strategies like vaccines and hand washing are mentioned.
This document discusses several diseases that present with hematuria or proteinuria in children. It describes a case of acute post-streptococcal glomerulonephritis in a 10-year-old boy presenting with edema and Coca-Cola colored urine. It then provides details on the etiology, clinical presentation, diagnosis, complications and treatment of this condition. It also summarizes several other conditions like IgA nephropathy, Alport syndrome, hemolytic uremic syndrome, polycystic kidney disease, nephrotic syndrome, undescended testes, testicular torsion, and epididymitis.
The document discusses dengue and dengue hemorrhagic fever (DHF) in adults. It provides epidemiological data showing over 2.5 billion people in 100 countries are at risk of dengue infection. It reviews clinical manifestations and laboratory findings in adults with dengue fever (DF) and DHF. Key points include thrombocytopenia being common, with over 25% of DHF patients having platelet counts less than 20,000/mm3. Bleeding is a risk, especially for those with severe thrombocytopenia, liver dysfunction, or shock. Proper fluid management and monitoring are important for treating DHF to avoid complications.
Children with congenital heart disease or rheumatic heart disease are at highest risk for developing bacterial endocarditis. It commonly presents with fever, heart murmur, and embolic phenomena. Diagnosis is made using modified Duke criteria, which considers major and minor clinical criteria as well as positive blood cultures. Treatment involves prolonged intravenous antibiotics targeting the causative organism. Surgery may be needed for complications like heart failure or abscesses. Prevention focuses on antibiotic prophylaxis for high-risk patients during certain medical procedures.
- Systemic Lupus Erythematosus (SLE) is an incurable, multisystemic autoimmune disease that predominantly affects women and has variable rates of median age of onset depending on ethnicity.
- SLE can affect many different body systems and has a variety of potential symptoms and complications, including renal, neurological, and hematological manifestations.
- Treatment involves managing symptoms with medications like hydroxychloroquine, corticosteroids, immunosuppressants, and emerging therapies targeting B cells and cytokines.
Legionnaires' disease is a form of atypical pneumonia caused by Legionella bacteria, mainly L. pneumophila. It is contracted through inhalation of contaminated aerosolized water droplets. Risk factors include smoking, immunosuppression, and age over 50. Symptoms include fever, cough, shortness of breath, and confusion. Diagnosis involves urine antigen testing, culture, or PCR. Treatment guidelines recommend macrolides or fluoroquinolones. Prevention focuses on maintaining cooling towers and water systems to avoid bacterial growth.
This document provides information on nephrotic syndrome, specifically defining it as a clinical syndrome characterized by heavy proteinuria, hypoproteinemia, edema, and hypercholesterolemia. It describes the epidemiology, classification, pathophysiology, clinical manifestations, investigations, diagnosis, management, and prognosis of nephrotic syndrome. The key points are that minimal change disease is the most common type, presenting with edema, ascites, weight gain, and respiratory distress in children aged 1-10 years. Investigations show proteinuria, hypoalbuminemia, and normal renal function. Management involves steroid therapy, addressing complications, and educating parents on infection prevention and immunization.
1. Sickle cell disease is an inherited blood disorder that affects hemoglobin and causes red blood cells to take on a sickle, or crescent, shape.
2. The prevalence of sickle cell disease varies by ethnicity, with the highest rates seen in African Americans at about 1 in 375 individuals.
3. Complications of sickle cell disease include anemia, infections, acute pain episodes, stroke, and damage to organs like the lungs, kidneys, spleen, and liver over time if not properly managed.
Diagnosis and examination of swollen lymph nodes ppt.pptxriazsohail448
油
The document discusses the diagnosis and evaluation of lymphadenopathy. It notes that lymphadenopathy can be localized, involving a single area, or generalized, involving two or more noncontiguous areas. For unexplained lymphadenopathy, localized cases may warrant biopsy if symptoms persist for 3-4 weeks, while generalized cases almost always indicate a systemic disease and biopsy is recommended. Risk factors for lymphoma are also outlined. Proper biopsy is important for diagnosis before treatment decisions. A case study example of a patient with cervical and supraclavicular lymphadenopathy and symptoms is then presented and worked through.
Acute pancreatitis is an inflammatory condition of the pancreas caused by the early activation of digestive enzymes within the pancreas. It can range from mild to severe, and in severe cases, it can lead to organ failure. The most common causes are gallstones, alcohol use, and viral infections. Symptoms include severe abdominal pain, nausea, vomiting, and fever. Laboratory tests show elevated levels of pancreatic enzymes in the blood. Severity is assessed using the Ranson score or APACHE II score. Treatment involves intravenous fluids, bowel rest, pain medications, and treating the underlying cause. Complications can include pancreatic pseudocysts, abscesses, and necrosis.
This patient, a 4-year-old boy, presented with prolonged fever, rash, fatigue, bone pain, conjunctivitis, and severe anemia. Laboratory tests showed high inflammatory markers, hypoalbuminemia, and hyperferritinemia. Imaging found hepatosplenomegaly and pericarditis with effusion. Infectious etiologies were ruled out. The presentation and lab results were consistent with a diagnosis of systemic juvenile idiopathic arthritis, also known as Still's disease. The patient was started on prednisone to treat this autoimmune condition characterized by intermittent fever, rash, and arthritis.
Parkinson Plus Syndrome - Multiple System Atrophy: Case Report.
Poster used in CMC MAC 2021.
ABSTRACT
A 61yr/Male, K/C/O T2DM & Parkinsons disease(PD) on T.Metformin and T.Syndopa for 3 years, presented to us with complaints of unsteadiness of gait, dysarthria, bilateral upper limb tremor. These symptoms started gradually and has been there for last 3 years and it is progressive. Initially, it started as inability to write and difficulty in mixing food due to tremulousness of both hands which worsens with activity. Then it progressed to slurred speech and then to gait unsteadiness. Patient also has urinary incontinence for last 2 years. Patients symptoms are more in severity for last 6 months. On examination, patient was having orthostatic hypotension, cogwheel rigidity on bilateral wrist movement and pendular knee jerks. All cerebellar signs were present bilaterally including finger nose test abnormality, past pointing, dysdiadochokinesia, heel shin test abnormality, gross truncal ataxia, wide based gait, impaired tandem walking, gaze evoked nystagmus, scanning speech.
Presence of cerebellar signs, autonomic disturbances, poor response to syndopa, rapid progression, lack of resting tremor at presentation, symmetrical involvement, early speech and gait involvement - are usually NOT seen in PD. So, evaluated further. MRI Brain T2 showed classical cruciform hyperintensity in pons (Hot cross bun sign) & diffuse cerebellar atrophy. Hence the diagnosis MULTIPLE SYSTEM ATROPHY (MSA-C) - Shy Drager Syndrome. This shows the importance of identifying atypical features in PD.
Allergy Induced Acute Coronary Syndrome - Kounis Syndrome: Case Report.
Poster used in CMC MAC 2021.
OBJECTIVE: To discuss a rare occurrence of allergic reaction to NSAID causing Myocardial Infarction.
BACKGROUND: A 21-year-old obese female with no other comorbidities was referred to us with history of chest pain, generalized urticarial rashes and itch suddenly following Inj.IM Diclofenac, which was given for heel pain relief. She was hemodynamically stable, but tachypneic, orthopneic and was having bilateral basal crepitations. ECG revealed significant ST depression & T inversion in II,III,aVF and V2-V6 and ST elevation in aVR. CXR showed pulmonary edema. Diagnosed as ACS following anaphylaxis and loading dose was given along with IM adrenaline, antihistamines, and steroids. Echo revealed global hypokinesia of LV. Cardiac enzymes were elevated. Meanwhile, she had a prompt relief of chestpain, but dyspnea worsened and warranted NIV support. Repeat ECG revealed regression of ST changes correlating with chest pain relief. After 2 days of NIV, patients dyspnea improved and weaned from NIV. CAG revealed normal epicardial coronaries. Serial cardiac enzyme levels showed falling trend and ECG was completely normal with no significant ST-T changes. Pre-discharge, repeat echo showed persistence of global hypokinesia. 2weeks later, repeat echo showed dramatic improvement with normal LV systolic function suggesting recovery from myocardial stunning.
RESULTS: This qualifies for the diagnosis of MINOCA (Myocardial Infarction with No Obstructive Coronary Arteries). In the setting of allergic trigger, vasospasm or coronary hypersensitivity is the underlying mechanism- described as KOUNIS SYNDROME.
CONCLUSION: ECG changes and chest discomforts that occur in allergic reactions are not always secondary to distributive/anaphylactic shock. Sometimes heart could be the primarily affected organ by the allergic reaction as in this case. Although <200cases reported globally until 2017, its suspected to be frequently overlooked, hence likely to be more prevalent.
Case Report: Brugada Syndrome - A Cardiac Channelopathy.
Poster used for presentation in CMC MAC 2021.
OBJECTIVE: To discuss an interesting case of Brugada syndrome presenting as seizures.
BACKGROUND: A 25-year-old well-informed male presented to us with complaints of seizure on day 3 of an acute febrile illness. He was conscious, oriented, GCS15/15 and system examinations were unremarkable. He had a similar history of seizure during fever 1 year back and was started on anti-epileptics since then and was treated with empirical antibiotics and CSF analysis, MRI brain with seizure protocol and EEG were completely normal during that episode. As described by patient, both episodes were very similar and was like darkening of visual field followed by LOC and bystanders witnessed few jerks involving both sides of body followed by regaining consciousness. This raised suspicion for syncope and ECG revealed RBBB-rSR pattern and saddleback STE in V1-V3(type2-brugada pattern-not diagnostic on its own). But on probing, patient revealed SCD in his father at age 42.
RESULTS: Echo revealed structurally normal heart. Expert opinion sought and flecainide challenge test revealed the classical type1 brugada pattern (diagnostic) with coved STE and T inversion in V1-V3 clinching the diagnosis of BRUGADA SYNDROME. Genetic testing for channelopathy was unremarkable. Type 1 Brugada pattern (on provocative testing) along with syncopal event and family history strongly warranted AICD insertion and patient opted for subcutaneous ICD. 6 months later, ICD interrogation revealed occurrence of 1 episode of NSVT, which fell below the ICD intervention threshold.
CONCLUSION: Brugada syndrome is a rare cardiac channelopathy with high risk of SCD in the absence of intervention. Events during fever and family history are very classical. It has male preponderance and more seen in Southeast Asia. All cases of suspected syncopal attacks warrant a thorough search for ECG markers of SCD.
Case Presentation PPT - For TAPICON 2021
Case Report: Allergy Induced Myocardial Infarction - Kounis Syndrome / Coronary Hypersensitivity Disorder / Vasospastic Angina.
Abstract
A young female with no coronary risk factors presented to us with history of chest pain, generalized urticarial rashes and itch suddenly following Inj.IM Diclofenac, which was given for heel pain relief. She was hemodynamically stable, but tachypneic, orthopneic with bilateral basal crepitations.
ECG showed significant ST depression & T inversion in II,III,aVF and V2-V6 and ST elevation in aVR. CXR showed pulmonary edema. Echo revealed global hypokinesia of LV. Cardiac enzymes were elevated. Treated for acute coronary syndrome (ACS) and her pain got relieved. CAG showed normal epicardial coronaries. Repeat ECG showed regression of ST changes correlating with chest pain relief and enzymes were also falling.
Pre-discharge, ECG normalised but echo showed persistence of global hypokinesia. Two weeks later, repeat echo showed dramatic improvement with normal LV systolic function suggesting recovery from myocardial stunning.
This qualifies for the diagnosis of MINOCA (Myocardial Infarction with No Obstructive Coronary Arteries). In the setting of allergic trigger, vasospasm or coronary hypersensitivity is the underlying mechanism - described as KOUNIS SYNDROME.
ECG changes and chest discomforts that occur in allergic reactions are NOT ALWAYS SECONDARY to distributive/anaphylactic shock. Sometimes heart could be the primarily affected organ by the allergic reaction. It is frequently overlooked and its timely recognition and appropriate intervention will improve the outcome.
- 37/M presented with acute onset paraparesis and paresthesia of both lower limbs that progressed over 1 week and has been static for 3 months
- He has a history of HIV/AIDS on ART and treated disseminated TB 1 year ago
- Exam shows flaccid paraparesis, sensory loss from L1, absent reflexes from C5-S1, and bladder involvement but no bowel involvement
- Differential includes infectious myeloradiculopathy (TB, HIV, CMV) or acute CIDP
- Investigations and management are planned including MRI, LP, immunological workup and immunosuppression
This document discusses a colloid cyst found in the third ventricle of the brain. Key details include:
- Colloid cysts are non-neoplastic epithelial cysts typically located in the anterior roof of the third ventricle.
- Patients usually present in the third to fifth decade of life with symptoms of increased intracranial pressure like headache or visual disturbances.
- On CT, a colloid cyst appears as a hyperdense, round lesion in the characteristic location of the third ventricle roof.
- Surgical excision is the curative treatment, with the aim of relieving hydrocephalus and removing the cyst. The transcortical transventricular approach has a high epilepsy
This document discusses the etiopathogenesis of abnormal uterine bleeding (AUB). AUB has various potential causes that are classified as organic (systemic, local/pelvic, iatrogenic) or dysfunctional (anovulatory, ovulatory). Dysfunctional uterine bleeding is further divided into anovulatory (80% of cases) and ovulatory (20% of cases). Anovulatory bleeding is caused by hormonal imbalances that prevent ovulation, while ovulatory bleeding results from issues with the luteal phase like insufficient progesterone support or prolonged luteal function. The pathophysiology involves an imbalance of prostaglandins produced by the endometrium in response to estrogen and progesterone levels.
This document discusses tuberculosis of the small intestine, focusing on the ileocecal region as the most common site of infection. It describes the clinical presentation, investigations, and management of intestinal TB. Key points include: intestinal TB most often presents with abdominal pain, weight loss, and fever; diagnosis involves imaging, ascitic fluid analysis, and biopsy; treatment is usually antibiotic therapy but surgery may be needed for complications like obstruction or perforation.
Local Anesthetic Use in the Vulnerable PatientsReza Aminnejad
油
Local anesthetics are a cornerstone of pain management, but their use requires special consideration in vulnerable groups such as pediatric, elderly, diabetic, or obese patients. In this presentation, well explore how factors like age and physiology influence local anesthetics' selection, dosing, and safety. By understanding these differences, we can optimize patient care and minimize risks.
Cardiac Arrhythmia definition, classification, normal sinus rhythm, characteristics , types and management with medical ,surgical & nursing, health education and nursing diagnosis for paramedical students.
Title: Regulation of Tubular Reabsorption A Comprehensive Overview
Description:
This lecture provides a detailed and structured explanation of the mechanisms regulating tubular reabsorption in the kidneys. It explores how different physiological and hormonal factors influence glomerular filtration and reabsorption rates, ensuring fluid and electrolyte balance in the body.
Who Should Read This?
This presentation is designed for:
鏝 Medical Students (MBBS, BDS, Nursing, Allied Health Sciences) preparing for physiology exams.
鏝 Medical Educators & Professors looking for structured teaching material.
鏝 Healthcare Professionals (doctors, nephrologists, and physiologists) seeking a refresher on renal physiology.
鏝 Postgraduate Students & Researchers in the field of medical sciences and physiology.
What Youll Learn:
Local Regulation of Tubular Reabsorption
鏝 Glomerulo-Tubular Balance its mechanism and clinical significance
鏝 Net reabsorptive forces affecting peritubular capillaries
鏝 Role of peritubular hydrostatic and colloid osmotic pressures
Hormonal Regulation of Tubular Reabsorption
鏝 Effects of Aldosterone, Angiotensin II, ADH, and Natriuretic Peptides
鏝 Clinical conditions like Addisons disease & Conn Syndrome
鏝 Mechanisms of pressure natriuresis and diuresis
Nervous System Regulation
鏝 Sympathetic Nervous System activation and its effects on sodium reabsorption
Clinical Correlations & Case Discussions
鏝 How renal regulation is altered in hypertension, hypotension, and proteinuria
鏝 Comparison of Glomerulo-Tubular Balance vs. Tubulo-Glomerular Feedback
This presentation provides detailed diagrams, flowcharts, and calculations to enhance understanding and retention. Whether you are studying, teaching, or practicing medicine, this lecture will serve as a valuable resource for mastering renal physiology.
Keywords for Easy Search:
#Physiology #RenalPhysiology #TubularReabsorption #GlomeruloTubularBalance #HormonalRegulation #MedicalEducation #Nephrology
Solubilization in Pharmaceutical Sciences: Concepts, Mechanisms & Enhancement...KHUSHAL CHAVAN
油
This presentation provides an in-depth understanding of solubilization and its critical role in pharmaceutical formulations. It covers:
Definition & Mechanisms of Solubilization
Role of surfactants, micelles, and bile salts in drug solubility
Factors affecting solubilization (pH, polarity, particle size, temperature, etc.)
Methods to enhance drug solubility (Buffers, Co-solvents, Surfactants, Complexation, Solid Dispersions)
Advanced approaches (Polymorphism, Salt Formation, Co-crystallization, Prodrugs)
This resource is valuable for pharmaceutical scientists, formulation experts, regulatory professionals, and students interested in improving drug solubility and bioavailability.
legal Rights of individual, children and women.pptxRishika Rawat
油
A legal right is a claim or entitlement that is recognized and protected by the law. It can also refer to the power or privilege that the law grants to a person. Human rights include the right to life and liberty, freedom from slavery and torture, freedom of opinion and expression, the right to work and education
Dr. Vincenzo Giordano began his medical career 2011 at Aberdeen Royal Infirmary in the Department of Cardiothoracic Surgery. Here, he performed complex adult cardiothoracic surgical procedures, significantly enhancing his proficiency in patient critical care, as evidenced by his FCCS certification.
This presentation provides a detailed exploration of the morphological and microscopic features of pneumonia, covering its histopathology, classification, and clinical significance. Designed for medical students, pathologists, and healthcare professionals, this lecture differentiates bacterial vs. viral pneumonia, explains lobar, bronchopneumonia, and interstitial pneumonia, and discusses diagnostic imaging patterns.
Key Topics Covered:
Normal lung histology vs. pneumonia-affected lung
Morphological changes in lobar, bronchopneumonia, and interstitial pneumonia
Microscopic features: Fibroblastic plugs, alveolar septal thickening, inflammatory cell infiltration
Stages of lobar pneumonia: Congestion, Red hepatization, Gray hepatization, Resolution
Common causative pathogens (Streptococcus pneumoniae, Klebsiella pneumoniae, Mycoplasma, etc.)
Clinical case study with diagnostic approach and differentials
Who Should Watch?
This is an essential resource for medical students, pathology trainees, and respiratory health professionals looking to enhance their understanding of pneumonias morphological aspects.
Acute & Chronic Inflammation, Chemical mediators in Inflammation and Wound he...Ganapathi Vankudoth
油
A complete information of Inflammation, it includes types of Inflammation, purpose of Inflammation, pathogenesis of acute inflammation, chemical mediators in inflammation, types of chronic inflammation, wound healing and Inflammation in skin repair, phases of wound healing, factors influencing wound healing and types of wound healing.
Dr. Anik Roy Chowdhury
MBBS, BCS(Health), DA, MD (Resident)
Department of Anesthesiology, ICU & Pain Medicine
Shaheed Suhrawardy Medical College Hospital (ShSMCH)
HUMAN SEXUALITY AND SEXUAL RESPONCE CYCLEdaminipatel37
油
Leptospirosis Protocol for NABH accredition
1. LEPTOSPIROSIS - DIAGNOSIS & MANAGEMENT GUIDELINES
MODIFIED FAINES CRITERIA (2012)
PRESUMPTIVE DIAGNOSIS: PART A or PART (A+B) = 26 or more
PART (A+B+C) = 25 or more
POSSIBLE DIAGNOSIS: Scores between 20 and 25
CASE DEFINITION (ICMR & WHO-SEAR)
Suspected case Acute febrile illness with:
Myalgia (especially calf tenderness)
Conjunctival su
ff
usion
Headache
Prostration
History of exposure to possible leptospira-contaminated environment
Probable case Suspected case with:
Rapid diagnostic test positivity (IgM ELISA or MSAT)
Con
fi
rmed case Suspected or Probable case with:
Isolation of leptospira in culture or
PCR positivity or
MAT (single titre of 1:400 or above / fourfold rise in serial titres)
CLINICAL
(PART-A)
EPIDEMIOLOGICAL
(PART-B)
LABORATORY
(PART-C)
Headache 2 Rainfall 5 Isolation by
culture**
DIAGNOSIS
CERTAIN
Fever 2 Contact with
contaminated
environment
4 Positive PCR 25
Temperature
> 39* C
2 Animal contact 1 ELISA IgM
Positive*
15
Conjunctival
su
ff
usion
4 MSAT Positive* 15
Meningism 4 MAT*
(Single high
titre or Rising
titre - 4x rise)
15
Myalgia 4
Conjunctival
su
ff
usion +
Meningism +
Myalgia
10 *any one of the
tests only should
be considered
for scoring
Jaundice 1
Albuminuria /
Azotemia
2
Hemoptysis /
Dyspnea
2
**Ideal time for culture
Blood - Within 10 days
Urine - 10 to 30 days
CSF - Within 5 to 10 days
2. Leptospirosis - Suspected / Probable / Con
fi
rmed
90% of cases are
Mild Leptospirosis
(Fever, myalgia,
conjunctival suffusion,
headache BUT NO
JAUNDICE)
Around 10% cases are
Moderate / Severe Leptospirosis
(Fever, myalgia, conjunctival suffusion, headache + JAUNDICE +/-
Multi-organ involvement
Based on clinical
spectrum
OP Treatment
Doxycycline 100mg PO
BD x 7 days or
Amoxicillin 500mg PO
TDS x 7 days or
Ampicillin 500mg
PO TDS x 7days or
Azithromycin 500mg PO
OD x 3 days
Other supportive Rx*
*advise adequate
hydration, bed rest,
antipyretics etc.
RED FLAG SIGNS
(tachypnea, tachycardia
disproportionate to fever,
shock, altered sensorium,
oliguria, bleeding
manifestations etc.)
IP Treatment (Antibiotic Rx +/- Organ speci
fi
c Rx)
Antibiotic therapy:
Penicillin 1.5 million units IV QID x 7 days or
Ceftriaxone 1g IV BD x 7 days or
Doxycycline 200mg IV stat, then 100mg IV BD x 7days
(Doxycycline contraindicated in pregnancy)
Organ speci
fi
c therapy:
RENAL: renal involvement is common.
Mild - only proteinuria and no RFT derangement: No intervention
Severe - AKI: Fluid management +/- diuretics, electrolyte correction,
avoid nephrotoxic drugs, avoid hypotension and hypovolemia +/- RRT (if
indicated by standard RRT guidelines)
HEPATIC: acute liver failure is rare.
Avoid precipitating factors of hepatic encephalopathy - drugs
(hepatotoxic drugs, sedatives etc.), hypovolemia, hypokalemia,
alkalosis, constipation, UGI bleeding.
Jaundice, Hepatomegaly: No intervention
Hepatic encephalopathy: lactulose, rifaximin etc.
LUNG: Most dangerous complication
ARDS / Pulmonary hemorrhage: Continuous O2 therapy, Mechanical
ventilation (if indicated)
HEART:
Myocarditis / Arrhythmia: treatment of speci
fi
c arrhythmia
Shock: treat hypovolemia with
fl
uid replacement. If not responding, add
dopamine or dobutamine.
HEMATOLOGICAL:
Thrombocytopenia: Platelet transfusion (if indicated)
Coagulopathy: Vit.K 5-10mg IV x 3 days +/- Fresh Frozen Plasma
DIC: FFP +/- blood transfusion
NEUROLOGICAL:
Aseptic meningitis: Symptomatic and supportive management.
Hypokalemic paralysis: IV Potassium supplementation
MUSCULOSKELETAL:
Myalgia / Myositis / Rhabdomyolysis : Monitor CPK levels, adequate
hydration, monitor urine output and serum electrolytes.
Arthralgia: No intervention +/- analgesic-antipyretics
All Absent
Any one or more is
present
Always rule out other tropical diseases.
Mixed infections are common.
Important differential diagnosis include:
-Malaria
-Scrub typhus
-Dengue
-Hepatitis
-Enteric fever etc.
3. Leptospirosis
Zoonotic
Pathogenic spirochete Leptospira interrogans
Rodents and Cattle excrete these organisms in their urine, which contaminates soil and
waterbodies
Mode of transmission: contact of abraded skin or mucous membrane with contaminated
environment
Incubation period: Average 5-14 days with a range 2- 30 days
Risk factors:
o Heavy rainfall and water logging
o Natural disasters like floods
o Seasonal at the onset of monsoon
o Farmers
o Agricultural field workers
o Fishermen
o Sewer workers
o Livestock handlers
o Mason
o Residence in endemic area
Presentation spectrum:
o Anicteric Leptospirosis: (90%) Mild form presents like Acute undifferentiated fever
o Icteric Leptospirosis: (5-10%) Moderate-Severe form
o Weils Disease (0-5%) Severe form
When to suspect Leptospirosis?
o Acute febrile illness + Risk factors + one or more of the following:
Headache
Myalgia
Prostration
Calf muscle tenderness
Conjunctival suffusion
Oliguria / Frothy urine
Jaundice
Haemorrhagic manifestations
Meningeal irritation
Nausea, Vomiting, Abdominal pain, Diarrhoea
Lab investigations to support diagnosis: (Blood, CSF, Urine sample)
o MAT titre of 100/200/400 or above based on endemicity (preferred)
o IgM based immune assays
o Seroconversion or Four-fold rise in MAT titre between acute and convalescent sera
o Direct isolation of organism
o PCR test
4. Lab investigations to assess severity:
o CBC, ESR
o RFT, LFT
o S. Electrolytes
o Urine Routine examination
o CPK
o CXR, ABG
Management:
o IVF and correction of electrolytes
o Mild cases:
Tab. Doxycycline 100mg PO BD X 7 days (preferred) or
Tab. Azithromycin 500mg PO OD X 3 days
o Moderate / Severe cases:
Inj. Penicillin 1.5 million units IV or IM Q6H X 7 days or
Inj. Ceftriaxone 2g IV OD X 7 days
o Chemoprophylaxis:
Tab. Doxycycline 200mg PO once a week or
Tab. Azithromycin 250mg PO once/ twice a week
5. DIAGNOSTIC:
A + B = /> 26
OR
A + B + C = /> 25
POSSIBLE:
A + B = Between 20 to 25
CRITERIA