This document provides reference ranges and interpretations for various common lab values. It discusses lab abnormalities that may indicate conditions like diabetes, liver and kidney dysfunction, malnutrition, and more. Key labs it outlines include glucose, BUN, creatinine, albumin, electrolytes, liver enzymes, lipids, and others. It also covers labs relevant to conditions like alcoholism, refeeding syndrome, and heart-related diseases.
PA is a type of vitamin B12 deficiency that results from an impaired update of vitamin B12 due to lack of Intrinsic factor. It is an autoimmune disease, diagnosed by using family history, physical examination and laboratory diagnosis.
Symptoms associated with a lemon tint of skin, painful tongue, diarrhoea, peripheral neuropathy and myelopathy, splenomegaly, shortness of breath yellowish eyes, dementia, muscle pain and weakness.
Megaloblastic Anaemia is an example of macrocytic anaemia. The impaired DNA synthesis due to lack of vitamin B 12 and folic acid.This presentation to learn about aetiology, causes, clinical features, lab diagnosis and treatment of Megaloblastic Anaemia
This document summarizes the case of a 65-year-old female patient who presented with shortness of breath, loss of appetite, weight loss, back pain, and abdominal pain over the past 6 months. Clinical examination and initial tests revealed anemia and low platelet count. Further testing showed abnormal bone marrow pathology and enlarged lymph nodes. This raised suspicion for lymphoma or secondary deposits in lymph nodes and bone marrow. An ultrasound-guided lymph node biopsy was planned to determine a final diagnosis of either lymphoma or another cause of the abnormalities.
Acute anemia can be caused by hemorrhage or hemolysis, resulting in a precipitous drop in red blood cells. Common causes seen in the emergency department include traumatic injury, gastrointestinal bleeding, or ruptured aneurysm. Physical exam may reveal signs of blood loss or organ damage. Treatment involves fluid resuscitation, blood transfusions tailored to the cause of anemia, and treating any underlying condition causing bleeding. Goals are to restore hemodynamics and replace lost red blood cells.
The document discusses alcohol-related liver disease (ALD). It notes that heavy drinking can lead to alcoholic fatty liver, alcoholic hepatitis, and cirrhosis. Symptoms range from asymptomatic fatty liver to jaundice, abdominal pain, and fever in later stages. Liver function tests are used to diagnose and monitor ALD. Complications include ascites, bleeding, and hepatic encephalopathy. Prognosis depends on the Child-Pugh score, with 5-year survival rates ranging from 100% in stage A to 35% in stage C disease.
This patient presents with concerning symptoms including weakness, fatigue, shortness of breath, new headache and left-sided weakness, easy bruising, bleeding gums, and fever. Her physical exam reveals a fever and petechiae. Her symptoms and exam are suggestive of thrombotic thrombocytopenic purpura (TTP), which is characterized by thrombocytopenia, microangiopathic hemolytic anemia, fever, renal insufficiency, and neurologic symptoms. A smear would likely show schistocytes, indicating microangiopathic hemolytic anemia. Immediate treatment is needed for this life-threatening condition.
This document provides reference ranges and interpretations for numerous blood tests that can be used to assess red blood cells, white blood cells, platelets, electrolytes, kidney and liver function, blood glucose, arterial blood gases, and coagulation. Key tests discussed include complete blood count (CBC), hemoglobin, hematocrit, white blood cell differential, platelet count, electrolytes like sodium, potassium, chloride, serum creatinine and BUN for kidney function, liver enzymes, glucose, HbA1c, pH, PCO2, PO2, and bicarbonate from arterial blood gases. Normal ranges and potential causes for abnormal high or low results are outlined for each test parameter.
This document discusses a case of alcoholic liver disease being investigated by Dr. N. Gautam. It provides background information on liver anatomy, alcohol metabolism, and the pathophysiology and clinical presentations of alcoholic liver disease. It describes the typical laboratory investigations performed for ALD including liver enzymes, bilirubin, proteins, and coagulation factors. The document then presents findings from a 45-year-old chronic alcoholic male patient presenting with abdominal pain, jaundice and altered sensorium, with laboratory results consistent with severe alcoholic hepatitis.
PA is a type of vitamin B12 deficiency that results from an impaired update of vitamin B12 due to lack of Intrinsic factor. It is an autoimmune disease, diagnosed by using family history, physical examination and laboratory diagnosis.
Symptoms associated with a lemon tint of skin, painful tongue, diarrhoea, peripheral neuropathy and myelopathy, splenomegaly, shortness of breath yellowish eyes, dementia, muscle pain and weakness.
Megaloblastic Anaemia is an example of macrocytic anaemia. The impaired DNA synthesis due to lack of vitamin B 12 and folic acid.This presentation to learn about aetiology, causes, clinical features, lab diagnosis and treatment of Megaloblastic Anaemia
This document summarizes the case of a 65-year-old female patient who presented with shortness of breath, loss of appetite, weight loss, back pain, and abdominal pain over the past 6 months. Clinical examination and initial tests revealed anemia and low platelet count. Further testing showed abnormal bone marrow pathology and enlarged lymph nodes. This raised suspicion for lymphoma or secondary deposits in lymph nodes and bone marrow. An ultrasound-guided lymph node biopsy was planned to determine a final diagnosis of either lymphoma or another cause of the abnormalities.
Acute anemia can be caused by hemorrhage or hemolysis, resulting in a precipitous drop in red blood cells. Common causes seen in the emergency department include traumatic injury, gastrointestinal bleeding, or ruptured aneurysm. Physical exam may reveal signs of blood loss or organ damage. Treatment involves fluid resuscitation, blood transfusions tailored to the cause of anemia, and treating any underlying condition causing bleeding. Goals are to restore hemodynamics and replace lost red blood cells.
The document discusses alcohol-related liver disease (ALD). It notes that heavy drinking can lead to alcoholic fatty liver, alcoholic hepatitis, and cirrhosis. Symptoms range from asymptomatic fatty liver to jaundice, abdominal pain, and fever in later stages. Liver function tests are used to diagnose and monitor ALD. Complications include ascites, bleeding, and hepatic encephalopathy. Prognosis depends on the Child-Pugh score, with 5-year survival rates ranging from 100% in stage A to 35% in stage C disease.
This patient presents with concerning symptoms including weakness, fatigue, shortness of breath, new headache and left-sided weakness, easy bruising, bleeding gums, and fever. Her physical exam reveals a fever and petechiae. Her symptoms and exam are suggestive of thrombotic thrombocytopenic purpura (TTP), which is characterized by thrombocytopenia, microangiopathic hemolytic anemia, fever, renal insufficiency, and neurologic symptoms. A smear would likely show schistocytes, indicating microangiopathic hemolytic anemia. Immediate treatment is needed for this life-threatening condition.
This document provides reference ranges and interpretations for numerous blood tests that can be used to assess red blood cells, white blood cells, platelets, electrolytes, kidney and liver function, blood glucose, arterial blood gases, and coagulation. Key tests discussed include complete blood count (CBC), hemoglobin, hematocrit, white blood cell differential, platelet count, electrolytes like sodium, potassium, chloride, serum creatinine and BUN for kidney function, liver enzymes, glucose, HbA1c, pH, PCO2, PO2, and bicarbonate from arterial blood gases. Normal ranges and potential causes for abnormal high or low results are outlined for each test parameter.
This document discusses a case of alcoholic liver disease being investigated by Dr. N. Gautam. It provides background information on liver anatomy, alcohol metabolism, and the pathophysiology and clinical presentations of alcoholic liver disease. It describes the typical laboratory investigations performed for ALD including liver enzymes, bilirubin, proteins, and coagulation factors. The document then presents findings from a 45-year-old chronic alcoholic male patient presenting with abdominal pain, jaundice and altered sensorium, with laboratory results consistent with severe alcoholic hepatitis.
This document defines anemia and discusses its causes, signs, and treatment options. Anemia is a low red blood cell or hemoglobin level that can be caused by blood loss, insufficient red blood cell production, or red blood cell destruction. Common causes include iron deficiency, vitamin B12 or folate deficiency, and genetic disorders. Signs of anemia range from fatigue to pale skin and shortness of breath. Treatment depends on the underlying cause but may involve oral iron, B12, folate supplements or B12 injections as well as blood transfusions in severe cases.
This document discusses hypercalcemia, which is defined as a serum calcium level above 10.5 mg/dl. It outlines the various causes of hypercalcemia including primary hyperparathyroidism, certain cancers, granulomatous diseases, and certain medications. The clinical presentation of hypercalcemia can include symptoms affecting the stones, bones, abdominal organs, psyche, and other nonspecific symptoms. Diagnosis involves blood tests to measure calcium and PTH levels along with imaging tests. Treatment focuses on rehydration, bisphosphonates, glucocorticoids, calcitonin, surgery, and dialysis depending on the severity and underlying cause of the hypercalcemia.
Iron Deficiency Anemia. B12 & Folat Deficiency AnemiaEneutron
This document discusses different types of anemia including iron-deficiency anemia, vitamin B12 deficiency anemia, and folate deficiency anemia. It defines anemia as a condition where red blood cells are not providing adequate oxygen to tissues. Symptoms are described such as tiredness, breathlessness, and pale skin. Laboratory tests outlined include low hemoglobin and iron levels. Causes of iron-deficiency anemia include blood loss and poor diet. Vitamin B12 deficiency can cause neurological symptoms and megaloblastic changes in bone marrow. Treatment involves oral or injectable iron, vitamin B12 injections, and folic acid supplements.
The document discusses various red blood cell disorders and anemias. It covers the etiology, pathogenesis, clinical features, laboratory evaluation, and management of different types of anemias including aplastic anemia, iron deficiency anemia, megaloblastic anemia, anemia of chronic disease, and hemolytic anemias like sickle cell disease. It provides details on the causes, symptoms, diagnostic criteria and treatment approaches for these conditions.
This document summarizes anemia, including its definition, classification, causes, signs and symptoms, diagnostic evaluation, and treatment. Anemia is defined as a deficiency in red blood cells, hemoglobin, or hematocrit. It is classified based on size, color, and cause of the red blood cells. Common causes include blood loss, decreased red blood cell production, and increased red blood cell breakdown. Signs and symptoms vary based on severity but can include fatigue, paleness, shortness of breath, and heart palpitations. Diagnostic testing includes complete blood count and iron studies. Treatment involves treating the underlying cause, oral or intravenous iron supplementation, blood transfusions, and medications.
This document discusses megaloblastic anemias, which are caused by a deficiency in vitamin B12 or folic acid. These deficiencies impair DNA synthesis during erythropoiesis, leading to large, abnormally developed red blood cells. Key findings include macrocytic anemia, hypersegmented neutrophils, and megaloblasts visible in bone marrow samples showing nuclear-cytoplasmic asynchrony. Pernicious anemia, an autoimmune disorder causing vitamin B12 deficiency, is described. Treatment involves vitamin B12 or folate supplementation.
This case study describes a 70-year-old male patient admitted to the hospital with abdominal distention, weakness, decreased appetite, and weight loss. His medical history revealed he was an alcoholic and smoker. Diagnostic tests showed signs of liver damage. Alcoholic liver cirrhosis occurs in stages from fatty liver to inflammation and scarring of the liver. Risk factors include quantity of alcohol consumed, genetics, and malnutrition. Treatment requires stopping alcohol consumption and may include vitamins, diet, and transplantation for severe cases.
Hypercalcemia is commonly caused by primary hyperparathyroidism or malignancy. It can be life-threatening in severe cases. Diagnosis involves measuring serum calcium, PTH, and assessing for underlying causes. Treatment depends on the underlying condition but may involve surgery for hyperparathyroidism or addressing the malignancy. Complications can impact the kidneys, GI tract, cardiovascular system, muscles and bones.
Hypocalcemia has various presentations and can lead to significant morbidity if left untreated. The most common cause is hypoalbuminemia from conditions like cirrhosis or malnutrition that lower serum calcium levels. Other potential causes include vitamin D deficiency, parathyroid issues, medications, and critical illnesses like sepsis. Treatment involves identifying and addressing the underlying cause, as well as replacing calcium, often intravenously, to resolve symptoms and normalize calcium levels. Calcium levels must be closely monitored during treatment until stabilized.
Approach to patient with hypo/hyper calcaemiaNassr ALBarhi
This document discusses calcium homeostasis and disorders of calcium metabolism. It begins by describing the functions of calcium in the body and where calcium is stored. It then discusses calcium regulation by parathyroid hormone, vitamin D, and calcitonin. Causes, signs and symptoms, and treatment approaches for hypercalcemia and hypocalcemia are reviewed. The key points are that calcium levels are tightly controlled by hormones to maintain levels between 2.25-2.62 mmol/L and that disorders can result from excess or deficiencies of these regulating hormones.
1) Megaloblastic anemia is caused by vitamin B12 or folic acid deficiency and results in large, oval red blood cells (macrocytes).
2) Causes of vitamin B12 and folic acid deficiency include lack of intake, increased demands, absorption issues, and autoimmune conditions affecting vitamin B12 absorption.
3) Symptoms include anemia symptoms and neurological symptoms. Laboratory tests show macrocytic anemia with low red blood cell and platelet counts and presence of polysegmented neutrophils.
This document provides information on the definition, presentation, evaluation, investigation and treatment of anemia. It defines anemia as a hemoglobin level below certain thresholds based on sex. Anemia is often identified through screening tests but can sometimes present with symptoms of advanced anemia. Evaluation involves taking a medical history and performing a physical exam and blood tests. Based on test results, anemias are classified and specific treatment is given depending on the underlying cause, such as iron supplementation for iron deficiency anemia or blood transfusions for acute blood loss.
This document defines anemia and discusses its etiology, pathophysiology, classification, diagnostic tests, and treatment, specifically focusing on iron deficiency anemia. It states that anemia is a decrease in red blood cells or hemoglobin, and is the most common hematologic disorder. The main causes of anemia are blood loss, deficient red blood cell production, and increased red blood cell destruction. Iron deficiency anemia, one of the most prevalent nutritional deficiencies worldwide, occurs due to an imbalance between iron needs and supply.
Alcohol consumption can lead to various liver diseases known as alcoholic liver disease (ALD). Chronic heavy drinking is responsible for 50% of chronic liver disease cases in India. Symptoms of ALD may not appear until the disease is advanced and include fatigue, abdominal swelling and pain, and jaundice. Alcohol is metabolized in the liver, producing reactive oxygen species that can cause oxidative stress, fatty liver, inflammation, fibrosis and eventually cirrhosis over many years. Diagnosis involves assessing drinking history, symptoms, lab tests and biopsy. Treatment focuses on abstaining from alcohol. Corticosteroids and antioxidants may help in some cases. Liver transplantation is an option for end-stage ALD but is not usually recommended for
This document provides an overview of evaluating and diagnosing liver disease. It discusses classifying liver diseases as hepatocellular, cholestatic, or mixed based on etiology and evaluating disease severity and stage. Common symptoms, diagnostic tests, clinical findings, and classifications such as Child-Pugh staging for cirrhosis are outlined.
Chronic renal failure refers to the irreversible deterioration of renal function over years. It initially presents as biochemical abnormalities and eventually leads to uraemic symptoms as the excretory, metabolic and endocrine functions of the kidneys fail. Common causes include diabetes, hypertension, and glomerulonephritis. Management involves identifying and treating the underlying disease, slowing progression, managing complications, and renal replacement therapy for end-stage disease.
I add more Information to the previous Slideshare of (Anemia)
I hope it will be more useful
What is Anemia in Pregnancy
how it affect the pregnancy
What are the types and risk factors
how to manage it
The liver plays a vital role in many metabolic functions, but can fail due to disease, toxicity, or other stress factors. Early liver failure involves inflammation and scarring of the liver tissue, while advanced failure occurs when compensatory mechanisms are overwhelmed and toxic substances build up. Acute liver failure has many potential causes including viral hepatitis, toxic drugs, and shock. Medical tests like bloodwork and imaging can help identify the underlying cause and extent of damage. Key nursing priorities include monitoring for complications like fluid imbalance and hepatic encephalopathy. Treatment focuses on supportive care, dietary modifications, and addressing any underlying triggers.
Eating disorders have the highest mortality rate of any psychiatric illness. Cardiac complications are the most common cause of death, followed by suicide. Overall death rates from eating disorders approach 20%. Eating disorder not otherwise specified (EDNOS) may have an even higher mortality and complication rate than anorexia nervosa or bulimia nervosa. Laboratory tests can show metabolic abnormalities, anemia, thyroid dysfunction, low sex hormones, and abnormal lipid and bone mineral density levels.
This document defines anemia and discusses its causes, signs, and treatment options. Anemia is a low red blood cell or hemoglobin level that can be caused by blood loss, insufficient red blood cell production, or red blood cell destruction. Common causes include iron deficiency, vitamin B12 or folate deficiency, and genetic disorders. Signs of anemia range from fatigue to pale skin and shortness of breath. Treatment depends on the underlying cause but may involve oral iron, B12, folate supplements or B12 injections as well as blood transfusions in severe cases.
This document discusses hypercalcemia, which is defined as a serum calcium level above 10.5 mg/dl. It outlines the various causes of hypercalcemia including primary hyperparathyroidism, certain cancers, granulomatous diseases, and certain medications. The clinical presentation of hypercalcemia can include symptoms affecting the stones, bones, abdominal organs, psyche, and other nonspecific symptoms. Diagnosis involves blood tests to measure calcium and PTH levels along with imaging tests. Treatment focuses on rehydration, bisphosphonates, glucocorticoids, calcitonin, surgery, and dialysis depending on the severity and underlying cause of the hypercalcemia.
Iron Deficiency Anemia. B12 & Folat Deficiency AnemiaEneutron
This document discusses different types of anemia including iron-deficiency anemia, vitamin B12 deficiency anemia, and folate deficiency anemia. It defines anemia as a condition where red blood cells are not providing adequate oxygen to tissues. Symptoms are described such as tiredness, breathlessness, and pale skin. Laboratory tests outlined include low hemoglobin and iron levels. Causes of iron-deficiency anemia include blood loss and poor diet. Vitamin B12 deficiency can cause neurological symptoms and megaloblastic changes in bone marrow. Treatment involves oral or injectable iron, vitamin B12 injections, and folic acid supplements.
The document discusses various red blood cell disorders and anemias. It covers the etiology, pathogenesis, clinical features, laboratory evaluation, and management of different types of anemias including aplastic anemia, iron deficiency anemia, megaloblastic anemia, anemia of chronic disease, and hemolytic anemias like sickle cell disease. It provides details on the causes, symptoms, diagnostic criteria and treatment approaches for these conditions.
This document summarizes anemia, including its definition, classification, causes, signs and symptoms, diagnostic evaluation, and treatment. Anemia is defined as a deficiency in red blood cells, hemoglobin, or hematocrit. It is classified based on size, color, and cause of the red blood cells. Common causes include blood loss, decreased red blood cell production, and increased red blood cell breakdown. Signs and symptoms vary based on severity but can include fatigue, paleness, shortness of breath, and heart palpitations. Diagnostic testing includes complete blood count and iron studies. Treatment involves treating the underlying cause, oral or intravenous iron supplementation, blood transfusions, and medications.
This document discusses megaloblastic anemias, which are caused by a deficiency in vitamin B12 or folic acid. These deficiencies impair DNA synthesis during erythropoiesis, leading to large, abnormally developed red blood cells. Key findings include macrocytic anemia, hypersegmented neutrophils, and megaloblasts visible in bone marrow samples showing nuclear-cytoplasmic asynchrony. Pernicious anemia, an autoimmune disorder causing vitamin B12 deficiency, is described. Treatment involves vitamin B12 or folate supplementation.
This case study describes a 70-year-old male patient admitted to the hospital with abdominal distention, weakness, decreased appetite, and weight loss. His medical history revealed he was an alcoholic and smoker. Diagnostic tests showed signs of liver damage. Alcoholic liver cirrhosis occurs in stages from fatty liver to inflammation and scarring of the liver. Risk factors include quantity of alcohol consumed, genetics, and malnutrition. Treatment requires stopping alcohol consumption and may include vitamins, diet, and transplantation for severe cases.
Hypercalcemia is commonly caused by primary hyperparathyroidism or malignancy. It can be life-threatening in severe cases. Diagnosis involves measuring serum calcium, PTH, and assessing for underlying causes. Treatment depends on the underlying condition but may involve surgery for hyperparathyroidism or addressing the malignancy. Complications can impact the kidneys, GI tract, cardiovascular system, muscles and bones.
Hypocalcemia has various presentations and can lead to significant morbidity if left untreated. The most common cause is hypoalbuminemia from conditions like cirrhosis or malnutrition that lower serum calcium levels. Other potential causes include vitamin D deficiency, parathyroid issues, medications, and critical illnesses like sepsis. Treatment involves identifying and addressing the underlying cause, as well as replacing calcium, often intravenously, to resolve symptoms and normalize calcium levels. Calcium levels must be closely monitored during treatment until stabilized.
Approach to patient with hypo/hyper calcaemiaNassr ALBarhi
This document discusses calcium homeostasis and disorders of calcium metabolism. It begins by describing the functions of calcium in the body and where calcium is stored. It then discusses calcium regulation by parathyroid hormone, vitamin D, and calcitonin. Causes, signs and symptoms, and treatment approaches for hypercalcemia and hypocalcemia are reviewed. The key points are that calcium levels are tightly controlled by hormones to maintain levels between 2.25-2.62 mmol/L and that disorders can result from excess or deficiencies of these regulating hormones.
1) Megaloblastic anemia is caused by vitamin B12 or folic acid deficiency and results in large, oval red blood cells (macrocytes).
2) Causes of vitamin B12 and folic acid deficiency include lack of intake, increased demands, absorption issues, and autoimmune conditions affecting vitamin B12 absorption.
3) Symptoms include anemia symptoms and neurological symptoms. Laboratory tests show macrocytic anemia with low red blood cell and platelet counts and presence of polysegmented neutrophils.
This document provides information on the definition, presentation, evaluation, investigation and treatment of anemia. It defines anemia as a hemoglobin level below certain thresholds based on sex. Anemia is often identified through screening tests but can sometimes present with symptoms of advanced anemia. Evaluation involves taking a medical history and performing a physical exam and blood tests. Based on test results, anemias are classified and specific treatment is given depending on the underlying cause, such as iron supplementation for iron deficiency anemia or blood transfusions for acute blood loss.
This document defines anemia and discusses its etiology, pathophysiology, classification, diagnostic tests, and treatment, specifically focusing on iron deficiency anemia. It states that anemia is a decrease in red blood cells or hemoglobin, and is the most common hematologic disorder. The main causes of anemia are blood loss, deficient red blood cell production, and increased red blood cell destruction. Iron deficiency anemia, one of the most prevalent nutritional deficiencies worldwide, occurs due to an imbalance between iron needs and supply.
Alcohol consumption can lead to various liver diseases known as alcoholic liver disease (ALD). Chronic heavy drinking is responsible for 50% of chronic liver disease cases in India. Symptoms of ALD may not appear until the disease is advanced and include fatigue, abdominal swelling and pain, and jaundice. Alcohol is metabolized in the liver, producing reactive oxygen species that can cause oxidative stress, fatty liver, inflammation, fibrosis and eventually cirrhosis over many years. Diagnosis involves assessing drinking history, symptoms, lab tests and biopsy. Treatment focuses on abstaining from alcohol. Corticosteroids and antioxidants may help in some cases. Liver transplantation is an option for end-stage ALD but is not usually recommended for
This document provides an overview of evaluating and diagnosing liver disease. It discusses classifying liver diseases as hepatocellular, cholestatic, or mixed based on etiology and evaluating disease severity and stage. Common symptoms, diagnostic tests, clinical findings, and classifications such as Child-Pugh staging for cirrhosis are outlined.
Chronic renal failure refers to the irreversible deterioration of renal function over years. It initially presents as biochemical abnormalities and eventually leads to uraemic symptoms as the excretory, metabolic and endocrine functions of the kidneys fail. Common causes include diabetes, hypertension, and glomerulonephritis. Management involves identifying and treating the underlying disease, slowing progression, managing complications, and renal replacement therapy for end-stage disease.
I add more Information to the previous Slideshare of (Anemia)
I hope it will be more useful
What is Anemia in Pregnancy
how it affect the pregnancy
What are the types and risk factors
how to manage it
The liver plays a vital role in many metabolic functions, but can fail due to disease, toxicity, or other stress factors. Early liver failure involves inflammation and scarring of the liver tissue, while advanced failure occurs when compensatory mechanisms are overwhelmed and toxic substances build up. Acute liver failure has many potential causes including viral hepatitis, toxic drugs, and shock. Medical tests like bloodwork and imaging can help identify the underlying cause and extent of damage. Key nursing priorities include monitoring for complications like fluid imbalance and hepatic encephalopathy. Treatment focuses on supportive care, dietary modifications, and addressing any underlying triggers.
Eating disorders have the highest mortality rate of any psychiatric illness. Cardiac complications are the most common cause of death, followed by suicide. Overall death rates from eating disorders approach 20%. Eating disorder not otherwise specified (EDNOS) may have an even higher mortality and complication rate than anorexia nervosa or bulimia nervosa. Laboratory tests can show metabolic abnormalities, anemia, thyroid dysfunction, low sex hormones, and abnormal lipid and bone mineral density levels.
This document summarizes cirrhosis of the liver. It defines cirrhosis as irreversible liver damage characterized by abnormal liver structure and function. The main causes listed are chronic alcohol abuse, hepatitis B and C, non-alcoholic steatohepatitis (NASH), and genetic disorders. Complications include hepatic failure, portal hypertension, ascites, variceal bleeding, and hepatocellular carcinoma. Tests used to diagnose and monitor cirrhosis are also outlined. Management focuses on treating the underlying cause, nutrition, screening for complications, and liver transplantation in severe cases.
This document discusses calcium homeostasis and hypercalcemia. It notes that calcium is critical for many physiological functions and is mainly stored in bones. Hypercalcemia can be caused by primary hyperparathyroidism, vitamin D excess, certain malignancies, and other conditions. The diagnostic approach involves distinguishing between hyperparathyroidism and hypercalcemia of malignancy based on lab tests. Treatment focuses on rehydration, increasing calciuresis, and decreasing bone resorption or intestinal calcium absorption using medications like calcitonin, bisphosphonates, glucocorticoids, or dialysis depending on the severity of hypercalcemia.
This document provides an overview of how to interpret common laboratory tests used at LECOM@SHU. It describes what each test measures, normal ranges, how each test is collected, and potential causes for abnormal results. The tests covered include BMP/CMP profiles, complete blood counts, coagulation studies, and urinalysis. Guidance is provided on interpreting individual components like electrolytes, kidney and liver enzymes, hematocrit, and signs of infection or other issues on urinalysis.
CN is a 41-year-old female on hemodialysis for stage 5 chronic kidney disease. Her current diet provides too much phosphorus and calcium compared to recommendations. She takes several medications to manage complications of kidney disease, including hyperparathyroidism. Her lab values show abnormalities consistent with kidney failure. Her diet needs modification to meet nutrient guidelines for dialysis patients and support medication treatment of her conditions.
The document discusses chronic kidney disease (CKD), defining it as kidney damage or decreased kidney function for more than 3 months. It stages CKD based on glomerular filtration rate (GFR) and describes risk factors, complications, diagnostic tests, and treatment approaches based on CKD stage. The primary goals of treatment are slowing progression and managing complications through modifying risk factors, medical therapy, and preparing for renal replacement therapy if needed.
This document discusses diabetic kidney disease and nephropathy. Diabetic nephropathy is the leading cause of renal failure, with 50% of dialysis patients having diabetes. Risk factors include poor blood glucose control, long diabetes duration, hypertension, and family history. Symptoms include protein in urine, high blood pressure, and declining renal function. Screening for microalbuminuria is important. Strict glycemic control and keeping blood pressure below 130/80 can prevent or slow progression. Treatment involves diet, medication, fluid management, and potentially renal replacement therapies like hemodialysis if kidney function declines severely.
roles of veterinary laborotary diagnostic with special reference to biochemistryRashmi Swain
Clinical biochemistry refers to analyzing blood plasma and other body fluids to diagnose and monitor disease. A basic panel of tests includes total protein, albumin, globulin, urea, creatinine, ALT, and alkaline phosphatase. These provide information on conditions like dehydration, inflammation, liver and kidney disease. Additional tests can be added depending on symptoms, to recognize patterns characteristic of different diseases.
The document discusses general hematology and various blood disorders. It covers red blood cell disorders like anemia, bone marrow failure syndromes, and red blood cell membrane defects. It also discusses bleeding disorders, platelet disorders, coagulation defects, and leukemia. Key points about various conditions like iron deficiency anemia, thalassemia, sickle cell disease, immune hemolytic anemia, and vitamin deficiencies are summarized. Screening tests for evaluation of hemostatic abnormalities are also mentioned.
This document provides guidelines for the management of hypokalemia according to NICE guidelines. It defines hypokalemia as a serum potassium level below 3.5 mmol/L. The major causes are decreased intake, increased losses through the kidneys or GI tract, and shifts in distribution. Treatment involves identifying and correcting the underlying cause, monitoring for magnesium deficiency, and replacing potassium orally or intravenously depending on the severity. Close monitoring of serum potassium levels, ECG, renal function, and for side effects is important when replacing potassium.
Chronic and excessive alcohol consumption can lead to a spectrum of alcoholic liver disease (ALD) ranging from fatty liver to cirrhosis. The risk and severity increases with the amount of alcohol consumed daily over many years. Diagnosis involves documenting a history of heavy drinking and liver-related abnormalities. Treatment focuses on abstinence to prevent progression of disease. Corticosteroids may help severe alcoholic hepatitis while liver transplantation is an option for end-stage cirrhosis. Long-term management involves screening for complications and lifestyle changes to support abstinence and liver health.
This document discusses chronic kidney disease (CKD), including its causes, symptoms, complications, diagnostic tests, management, and treatment options. It notes that CKD refers to irreversible deterioration of renal function over years and is asymptomatic until the glomerular filtration rate falls below 30 mL/min/1.73 m2. Common symptoms when it falls below 15-20 mL/min/1.73 m2 include tiredness, breathlessness, pruritus, and in advanced cases, Kussmaul breathing and coma. The aims of management are to monitor renal function, prevent further damage, limit complications, treat risk factors, and prepare for renal replacement therapy. Treatment involves controlling blood pressure and proteinuria, managing
Nonalcoholic fatty liver disease (NAFLD) is the most common liver disorder worldwide, affecting up to 25% of the general population. It is strongly associated with obesity, type 2 diabetes, and metabolic syndrome. The pathogenesis involves insulin resistance leading to fatty infiltration of the liver followed by oxidative stress causing inflammation and fibrosis. Clinical features are often asymptomatic, though elevated liver enzymes and hepatomegaly may be seen. Diagnosis relies on excluding other causes of liver disease and imaging or biopsy. Potential therapies focus on lifestyle changes like diet, exercise and weight loss as well as treatments targeting underlying conditions and antioxidants.
This document discusses jaundice, its causes, and approach to postoperative jaundice. It defines jaundice as yellow discoloration from hyperbilirubinemia. Causes of postoperative jaundice include hemolysis, hepatic dysfunction unrelated to surgery, and obstructive causes. The workup involves liver function tests to determine if the jaundice is prehepatic, hepatocellular, or obstructive. Management depends on the identified cause, but generally involves supportive care, discontinuing hepatotoxic drugs, treating sepsis aggressively, and considering surgery for biliary obstruction.
CASE PRESENTATION ONCIRRHOSIS OF LIVER WITH PORTAL HYPERTENSION, HEPATIC EN...Akhil Joseph
A DETAIL CASE PRESENTATION ON CIRRHOSIS OF LIVER WITH PORTAL HYPERTENSION, HEPATIC ENCEPHALOPATHY AND GRADE II OESOPHAGEAL VARICES WITH CONGESTIVE GASTROPATHY. LIVER CIRRHOSIS AND ALL ITS COMPLICATION IN A PATIENT.
This document discusses alcoholic liver disease (ALD). It begins by defining ALD and its stages - fatty liver, alcoholic hepatitis, and cirrhosis. It then discusses risk factors like gender, genetics, and drinking patterns. Symptoms for each stage are provided. The pathophysiology of steatosis, hepatitis, and cirrhosis are explained. Diagnostic tests including blood tests, imaging, and biopsy are outlined. Management of ALD focuses on abstinence, nutrition, medications to prevent complications, and potentially transplantation for late-stage disease.
This document discusses alcoholic liver disease (ALD), including its causes, risk factors, symptoms, diagnosis, and treatment options. It notes that ALD encompasses conditions like fatty liver, alcoholic hepatitis, and cirrhosis that result from excessive alcohol consumption over time. Heavy drinking, especially in men who consume 60-80 grams per day for over 20 years or women who drink over 20 grams per day, significantly increases risk. Symptoms may not appear initially but can include abdominal pain, nausea, fatigue, and jaundice as the disease progresses. Treatment focuses on abstinence from alcohol as well as nutrition supplementation and medications to manage complications like ascites and hepatic encephalopathy.
1. How to interpret different lab values
(These values are based on Mountain Home Lab values)
Glucose normal 74-106 mg/dL
High: DM, Stress chronic hepatic function, pancreatitis, chronic malnutrition or
re-feeding syndrome
Low: medications, enzyme deficiencies, tumors, insulin overdose, alcohol abuse,
starvation
BUN: normal 7-18mg/dL
High: Rapid protein catabolism/tissue necrosis(Burns, cancer) or impairment of
kidney function, dehydration, MI, excessive pro intake, Rhabdomyolysis
Low: malnutrition, Malabsorption, liver disease, over- hydration (excessive IV
fluids)
Creatinine: normal: 0.6-1.3
High: CHF, impaired renal function, shock, diabetic acidosis, muscle damage,
starvation, high meat intake.
Low: severe loss of muscle mass, liver disease, over-hydration
GFR: Non-black : 60 mL/min (adult) each hospital usually leaves this open for
interpretation.
GFR black: <70mL/min
High: burns over-hydration
Low: CHF, renal disease
Albumin: normal 3.4-5.0g/dL
High: dehydration, high minerals in blood
Low: acute/ chronic infections, liver dysfunction, heart failure, edema, diarrhea,
over-hydration, cancer, ESRD, burns, malnutrition, alcoholism
Prealbumin (PAB): Normal Value: 16-35 mg/dL
Better marker for nutrition, influenced by inflammation status.
Half life 2-3 days
High: renal failure
Low: hepatic disease, stress, infection, malnutrition, low pro intake
AST: normal men: 12-78 U/L
Women: 12-78U/L
High: liver disease, MI, pancreatitis, alcoholism, cancer, burns
Low: taking vitamin C, uncontrolled DM
ALT: normal men: 15-37U/L
Women: 15-37U/L
High: liver disease, cirrhosis, alcoholism, pancreatitis
2. Low: malnutrition, urinary infection
Bilirubin: Normal Values: Total: 0.2-1 mg/dL
Direct: < 0.3mg/dL
High: hepatitis, jaundice, drug intoxication, prolonged fasting, cirrhosis,
obstruction of common bile duct, or hepatic ducts due to stones
Ammonia (NH3): Normal value: 7-27 umol/dL (adult)
High: liver disease, hepatic encephalopathy, severe heart disease
Lipase: Normal Value: 26-63 U/L (adults)
High: pancreatitis, renal insufficiency, gallstones
Low: protein malnutrition, viral hepatitis
Amylase: Normal Value: 30-110 U/L (adults)
High: pancreatitis, alcohol poisoning, renal insufficiency, acute cholecystitis
Low: hepatitis, cirrhosis, severe burns
Electrolytes and minerals:
Calcium: 8.5-10.1 mg/dL
High: Chronic renal disease, high Ca and Vit D intake
Low: elevated phosphorus, diarrhea, low Mg, starvation, Malabsorption, low
albumin, Vit D deficiency, over-hydration, steatorrhea
Sodium: 136-145 mEq/L (adults)
High: dehydration, coma
Low: over-hydration, edema, vomiting, diarrhea, starvation
Potassium: Normal Value: 3.5-5.1 mEq/L
High: renal failure, tissue damage
Low: malabsorption, malnutrition, diarrhea, vomiting, hepatic disease, c acidosis,
re-feeding syndrome
Chloride: Normal Value: 98-107 mEq/L
High: dehydration, anemia, diarrhea, renal insufficiency
Low: Emesis, gastric suction, over-hydration, fever
Phosphorus: Normal Value: 2.5-4.9 mg/dl
High: ESRD, hypocalcemia,
Low: alcoholism, re-feeding syndrome
Magnesium: Normal Values: 1.8-2.4mEq/L
3. High: renal failure, dehydration
Low: chronic diarrhea, alcoholism, pancreatitis, renal disease, cirrhosis, re-
feeding syndrome, over-hydration
Labs for heart related disease
Creatine phosphokinase (CPK): Normal Value:
High: Hepatic or uremic coma, striated muscle disease, muscular dystrophy, MI,
CVA, trama, alcoholic liver disease, encephalitis. Enzyme found in the heart muscle,
skeletal muscle and brain. Damage cell releases enzymes and levels increase.
(other name for CPK) Creatine Kinase: Normal Value 24-170 U/L (adult)
High: muscle breakdown, Rhabdomyolysis
Lactate Dehydrogenase (LDH): Normal Value 105-230 U/L
High: Acute MI, Heart failure, alcoholic liver disease, hepatitis, cancer, leukemia,
renal failure, anemia, muscular dystrophy. Enzymes found in many tissues, but does rise
24-72 hours after MI. Levels return to normal in about 4 days.
Troponin:
High: Cardiac contractile proteins, released as myocardial tissue dies. These
levels are detected with great sensitivity and are detectable 20 minutes following injury.
Last 4-10 hrs after MI onset, chronic renal failure
Apoliprotein Apo a or Apo B:
Low levels of Apo A = increase risk of CAD
C-Reactive Protein (CRP): Normal Value: 0.8 mg/dl mod risk: 1-3mg ↑ > 3mg
Increases in: trauma, infection, inflammation, surgery, neoplastic disease. When
increased risk for CHD & other cardio disease
Cholesterol: desirable range 51-200mg borderline: 200-239 high risk > 240 Child: 70-
175
High: CHD, DM, obesity, high fat diet, alcohol intake, CRF, Acute MI
Low: malnutrition, low lipids in blood, malapsorption, Hepatic disease, low fat
diet, sepsis, anemia
Total Chol. < 150 = malnutrition
HDL: Low <40mg/dL High: >60 mg/dL
High: vigorus exercise, insulin therapy, moderate alcohol intake
Low: starvation, obesity, liver disease, DM, smoking, AIDS
LDL: Optimal: < 100mg/dL, above optimal: 100-129 mg/dL, borderline: 130-159
mg/dL, high: 160-189mg/dL, very high: > 190mg/dL
High: hyperlipidemia, high fat diet, hepatic disease, acute trauma, DM
4. Low AIDS
Triglycerides: Desirable <150 mg/dl
High: >200 mg/dl assoc with vascular disease
>500 mg/dl pancreatic risk
>1000 mg/dl substantial pancreatic risk
Blood related lab values
WBC (leukocytes):
Leukocytosis: (high WBC) >11,300/mm3 (4.4-11.3x10^3)
Acute infection, leukemia, trauma, toxins, drugs, cancer
Leukopenia: (low WBC) <4400/mm3
Viral infection, overwhelming bacterial infections, medications, HIV, AIDS
Ferritin: Normal Value: Men: 20-250 ng/ml
Women: 10-120 ng/ml
Indicator of Iron status for iron deficiency anemia
Classification of Anemia
Normocytic (normal)
Microcytic (small)
-Impaired heme synthesis
-Resulting from inability to absorb, transport, store, use iron or impaired
ability/deficiency of protein, iron, Vit A, Vit C, copper.
Pernicious Anemia
Marcrocytic (large)
-Results from decrease ability to synthesize new cells and DNA
-Due to deficiency in B12, folate, thiamin, pyridoxine
Megaloblastic Anemia
-There is a folic acid or vitamin B12 deficiency that causes immature,
large RBC in an abnormal shape
Another issue that can occur in a hospital setting that labs will help to identify, is when
patients receive high volumes of fluids, labs to look for changes in with a sudden
decrease: Na, Creat, BUN, alb, Ca, Cl, Mg
Sudden increase: GFR, K, Phos
Other things to look for would be a severely positive I&O, weight gain and edema.
5. Issues to look for with alcoholism
In some cases, such as alcoholism, when AST and ALT are elevated it can be prudent to
check the lipase, amylase and lipid panel to check for possible underlying pancreas
issues.
Labs associated with alcoholics
High: AST, ALT, Bili, Ammonia
Low: Glucose, BUN, Creat, Alb, amylase, lipase, Mg, Phos
Refeeding syndrome
Alcoholics are very susceptible to this syndrome. When they drink their calories and stop
eating the balance in their body goes.
When a patient has had poor nutrition intake for quite some time a syndrome can occur;
this syndrome is called re-feeding syndrome (RFS). The most common lab value
associated with RFS is hypophosphatemia. You will usually see this occur within 4 days
of starting to feed a patient.
In starvation fat and protein stores are catabolised to produce energy. This results in
an intracellular loss of phosphate. Malnourished patients’ intracellular phosphate stores can
be depleted despite normal serum phosphate concentrations. This is seen when people who
have severe malnutrition are given large amounts of carbohydrates in a short period of
time, and their secretion of insulin increases; this stimulates cellular uptake of phosphate,
which can lead to profound hypophosphataemia, together with cellular uptake of potassium
and magnesium. When you see the decrease of phosphorus in the blood, you usually see
an increase of phosphate in the urine. You will also see hypokalemia, hypomagnesemia,
hyperglycemia.
Major effects of a low phosphate resulting in -
1) Muscle - myopathy, rhabdomyolysis
2) Haematology - haemolysis, tissue hypoxia, reduced white cell and platelet
function
3) Neurology - malaise, confusion, coma
4) Skeleton - rickets, osteomalacia
People at risk for RFS:
1) elderly, who may have dementia and a poor PO intake
2) People with chronic malnutrition issues such as gastric bypass or lap-band
procedure, rapid weight loss, severe exacerbations of crohns disease and
more.
3) Chronic alcoholics
4) Patients unfed for 7-10 days with evidence of stress/depletion
5) Anorexia Nervosa
6) Oncology patients on chemotherapy
6. 7) Chronic antacid users
8) Chronic diuretic users
9) Classic Marasmus
10) Hyperglycemia eg DM
Re-feeding syndrome can be a very serious issue and can lead to death it can also lead to
other significant risks including confusion, coma and convulsions and cardiac failure.
7. 7) Chronic antacid users
8) Chronic diuretic users
9) Classic Marasmus
10) Hyperglycemia eg DM
Re-feeding syndrome can be a very serious issue and can lead to death it can also lead to
other significant risks including confusion, coma and convulsions and cardiac failure.