CHI335 - Blood Circulation PDF

Summary

This document provides information about blood, circulation, and related conditions, such as types of anemia and haematopoiesis. It also includes learning outcomes, and introductions. This document is suitable for undergraduate students studying these topics.

Full Transcript

CHI335 Diagnosis I Learning Outcomes  Describe haematopoiesis, identify the components of blood, and their functions  Describe the components of plasma and their functions  Compare and contrast the various types of anaemia and their management  Discuss the various condition...

CHI335 Diagnosis I Learning Outcomes  Describe haematopoiesis, identify the components of blood, and their functions  Describe the components of plasma and their functions  Compare and contrast the various types of anaemia and their management  Discuss the various conditions caused by changes to white blood cell and platelet function, including leukaemia, thrombocytopenia, etc. Learning Outcomes  Outline the factors that are believed to contribute to polycythaemia  Explain the steps of Haemostasis and its disorders  Explains some common forms of coagulopathies, such as haemophilia  Differentiate between the presentation of haemophilia and von Willebrand disease  Describe and explain disorders with circulation Introduction  Blood represents life when…  Takes oxygen and nutrients to tissues  Takes Carbon dioxide and wastes away from tissues  Transport hormones  Regulates heat  Circulation  Process of transporting blood to and from the body tissues Blood  4 to 6 litres of blood in the human body  A connective tissue since it has a nonliving matrix and living cells  Plasma is the nonliving fluid component of blood  Cellular Components of Blood are the cells and cell fragments  Erythrocytes (red blood cells, RBCs)  Leukocytes (white blood cells, WBCs)  Thrombocytes (platelets) Haematopoiesis  Formation of blood cells from stem cells  During foetal development  RBCs are made in the yolk sac, the liver, and the spleen  After birth  Most blood cells are produced in red bone marrow by stem cells called haemocytoblasts Haematopoiesis Haematopoiesis  Erythropoietin  Regulates erythropoiesis, production of RBCs  Produced by the kidneys when oxygen concentrations in the blood get low (late compensation)  Vitamin B12 and folic acid for DNA replication & cell division  Iron is necessary to make haemoglobin  Iron-deficiency anaemia Blood Sample & Blood Smear Centrifuged sample of blood  The percentage of RBCs in relationship to the total blood volume is called the haematocrit  Normal haematocrit is about 37 to 43 percent in females and 43 to 49 percent in males  On top of the RBCs is the plasma  Between is a thin layer that is whitish in colour and is referred to as the “buffy coat”  White blood cells and platelets Plasma  Liquid portion of blood  Nutrients  Amino acids, glucose, nucleotides, and lipids that have all been absorbed from the digestive tract  Lipids must be combined with protein molecules to be transported by plasma (lipoproteins)  Different types of lipoproteins are chylomicrons, very low- density lipoproteins (VLDL), low-density lipoproteins (LDL), and high-density lipoproteins (HDL) Plasma  Gases  Dissolved in plasma  Oxygen, carbon dioxide, and nitrogen  Electrolytes  Dissolved in the plasma  Sodium, potassium, calcium, magnesium, chloride, bicarbonate, phosphate, and sulphate  Non-protein nitrogenous substances  Urea and uric acid Plasma Proteins Cellular Components of Blood RBCs  Small cells that have a biconcave shape  Mature RBCs do not have a nucleus  Contain a pigment called haemoglobin whose function is to bind to oxygen and transport it  Haemoglobin that carries oxygen is called oxyhaemoglobin and is bright red in colour  Carbaminohemoglobin refers to haemoglobin that carries carbon dioxide  Carboxyhaemoglobin is a stable complex of carbon monoxide and haemoglobin RBCs  A normal RBC count is about 4 – 6 million erythrocytes per cubic millimetre of blood Normal haemoglobin  Adult haemoglobin (HbA) molecule Source: Adapted from Martini & Nath (2009), Figure 19.3. RBCs  The average life span of an erythrocyte is approximately 120 days  Old RBCs are filtered out by macrophages in the liver and spleen  Haem is recycled to be used again in new RBCs  Globin is metabolised into biliverdin which is then converted to bilirubin in the liver  Bilirubin is used to make bile, a substance that emulsifies or breaks apart fat molecules Anaemia  Indicates a reduced oxygen-carrying capacity  Is a constellation of signs and symptoms but not a diagnosis  Anaemia is confirmed by measuring the level of haemoglobin  Normal Hb level in men is 14 to 18 gr/dl – must know  Normal Hb level in women is 12 to 16 gr/dl – must know  Presentation  Next slide… Anaemia – Presentation Anaemia – Aetiology  Altered production of red cells or haemoglobin  Loss of blood  Increased erythrocyte destruction  A combination of these Anaemia – Aetiology RBC morphology & Anaemia  Prefix  Examples  Micro- = small  Normochromic: normal in  Normo- = normal colour  Macro- = big  Hypochromic: light in colour  Hypo- = low  Normocytic: normal size cell  Microcytic: small cell  Suffix  Macrocytic: big cell  Chromic = colour  Cytic = cell Anaemia  Classified by RBCs’ size  Microcytic anaemia  e.g. iron-deficiency anaemia and thalassaemia  Macrocytic anaemia  e.g. pernicious anaemia and folate-deficiency anaemia  Normocytic anaemia  e.g. aplastic, haemolytic and anaemia of chronic disease Anaemia by RBCs’ size Iron-deficiency anaemia (IDA)  Often secondary to dietary deficiencies  Occasionally, due to malabsorption disorders  Individuals susceptible to iron-deficiency anaemia  People living in chronic poverty  Pregnant women  Females with Menorrhagia  People with ulcers or conditions associated with chronic blood loss  Haemorrhage can lead to a depletion in body iron stores (e.g. chronic blood loss, associated with bleeding lesions within the GIT), resulting in iron-deficiency anaemia Vit B12 & folate-deficiency anaemia  A deficiency in vit B12 or folate will cause anaemia  Vitamin B12 and folic acid are required for DNA synthesis and cell division  Because of enough B12 stores in the liver, this disorder has a slow, insidious onset that can take 2 years for symptoms to manifest  Folate deficiencies are mainly associated with malnutrition/poor diet, increased demand, and alcoholism Pernicious anaemia  Is an AI disease: Auto-antibody against Intrinsic Factor (IF) required for absorption of vit B12 from the diet Aplastic anaemia  An anaemia due to bone marrow destruction  e.g. Chemotherapy and radiation therapy, some cancers and toxins Sickle cell anaemia  A genetic disorder which leads to a malformation of erythrocytes into the characteristic sickle shape Sickle cells cannot transit capillary beds and Creates multiple blood flow obstructions leading to Significantly  O2 supply and Multiple micro-infarcted centres in the tissues Sickle cell anaemia  These affected cells are rigid, fragile and prone to breakage Source: © University of Alabama at Birmingham, Department of Pathology. Polycythaemia  An overproduction of red cells leading to  Abnormal high RBCs and haemoglobin  Increase in blood viscosity  Therefore, a greater risk of thrombosis & thromboembolism  Secondary polycythaemia  Is a physiological response to hypoxia, which causes secretion of erythropoietin →  production of erythrocytes   likelihood of developing secondary polycythaemia  Chronic obstructive pulmonary disorder (COPD)  Congestive heart failure  Living at high altitudes Primary Polycythaemia Aka polycythaemia vera or rubra vera  A rare condition marked by  production of erythrocyte, white cell and platelet + splenomegaly  The greatest concern is  blood viscosity  Blood flow becomes sluggish   thrombus formation  Occlusion of blood vessels of virtually all sizes  Marked tissue and organ ischaemia and infarction  Reasons for death in primary polycythaemia  CVA (more common)  MI WBCs  Categorised into two groups based on whether they have granules in their cytoplasm  Granulocytes  Neutrophils, eosinophils, and basophils  Agranulocytes  Monocytes and lymphocytes  All leukocytes contain a nucleus WBCs  Neutrophils (60%)  They have phagocytic capabilities  Destruction of bacteria  Their number increase in the early stage of acute inflammation  Eosinophils (3%)  Fight parasitic infections  Their number also increased acute or active allergies  Basophils (

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