In Chapter 11, we delve into the intricate system of blood, also known as hematology. This field encompasses not just the study of blood’s composition but also the disorders that afflict its cellular components. Key to understanding hematology are essential vocabulary terms and concepts. For instance, erythrocytes (RBCs) refer to red blood cells responsible for oxygen transport, while leukocytes (WBCs) denote white blood cells, which play crucial roles in the immune system. Additionally, we will explore various blood groups and the process of hemostasis—the body’s way of stopping bleeding. This chapter will also highlight methods for assessing blood disorders and briefly touch upon relevant pharmacology. Understanding the blood system is significant not only for medical professionals but for anyone interested in the body’s function and maintaining health.
Blood Volume and Composition:
The average adult possesses approximately 10 pints (5 liters) of blood.
Blood consists of 45% formed elements, primarily erythrocytes, which are crucial for oxygen transport.
Components include plasma (55%), which is a yellowish fluid containing proteins such as albumin, globulin (antibodies), and fibrinogen (involved in clotting).
Hematocrit and Hemoglobin:
Hematocrit (HCT) is the percentage of blood volume occupied by red blood cells; it is measured alongside hemoglobin, indicating the blood’s oxygen-carrying capacity.
Blood serves a myriad of functions critical to sustaining life. These include:
Homeostasis Maintenance: Regulating body fluids and electrolytes.
Body Temperature Regulation: Distributing warm blood to internal organs.
Nutrient & Waste Transport: Facilitating the transfer and detoxification of various substances.
Hormonal Transport: Conveying hormones from glands to target organs.
Gaseous Transport: Carrying oxygen and carbon dioxide to and from the lungs.
Immune Defense: Utilizing chemicals and cells in the blood to protect against pathogens.
Clot Formation: Essential for wound healing.
pH and Osmosis Regulation: Maintaining a stable internal environment within a narrow pH range (7.35-7.45).
Structure: Erythrocytes are biconcave discs that enhance gas exchange.
Production: Erythropoiesis, the formation of RBCs, occurs in red bone marrow and involves the release of reticulocytes, which mature into erythrocytes within five days.
Function: Chiefly engaged in oxygen (via oxyhemoglobin) and carbon dioxide transport. They also convey nitric oxide, aiding in vascular health.
Erythrocytes have a lifespan of approximately 120 days.
As they age, they break down in the spleen and liver, where macrophages recycle their components.
Granulocytes: Contain granules rich in enzymes.
Neutrophils: 50-70% of WBCs, responsible for phagocytosis of pathogens.
Eosinophils: 2-4%, involved in allergic reactions and combating parasites.
Basophils: <1%, release histamine to promote blood flow.
Agranulocytes: Lack granules.
Monocytes: 3-8%, mature into macrophages, performing phagocytosis.
Lymphocytes: 25-30%, pivotal for immune response via B and T cells.
ABO System:
Four types: A, B, AB (universal recipient), and O (universal donor).
Antigens A and B determine compatibility and blood type.
Rh Factor:
Presence or absence of the Rh antigen defines blood as positive or negative.
Complications arise in Rh-negative individuals carrying an Rh-positive fetus, leading to hemolytic disease of the newborn.
Need for accurate blood typing before transfusions due to potential mismatches causing severe reactions.
Continuous monitoring during transfusions is critical.
Vascular Spasm: Immediate constriction of the injured vessel.
Platelet Plug Formation: Aggregation of platelets at the injury site.
Blood Coagulation: Formation of a stable clot through various coagulation factors, primarily involving thrombin.
Anemia: Various forms, including:
Iron Deficiency Anemia: Resulting from blood loss or dietary deficiency.
Pernicious Anemia: Caused by vitamin B12 deficiency.
Sickle Cell Anemia: Genetic disorder affecting RBC shape.
Aplastic Anemia: Failure of bone marrow to produce adequate cells.
Leukocytosis: Increased WBC count due to infections or allergies.
Leukopenia: Decreased WBC count, impairing immune response.
Leukemia: Malignancies of blood-forming tissues leading to increased immature leukocytes.
Complete Blood Count (CBC): Evaluates various blood components and identifies abnormalities.
Bone Marrow Biopsy: Determines the underlying causes of blood disorders.
Transfusion: Replenishing blood components as needed.
Bone Marrow Transplant: Transferring healthy marrow to treat severe blood disorders.
Gene Therapy: Exploring treatment for genetic blood diseases.
Chapter 11 provides a comprehensive overview of the blood system and hematology. By understanding the structure and functions of blood components, the mechanisms of diseases, and relevant diagnostic and therapeutic approaches, we come to appreciate the complexity and essential nature of blood in human physiology. The importance of accurate blood typing and the significance of disorders highlight the need for continued research and advancements in the field to enhance patient outcomes and health management. Effective management of blood disorders holds the potential to improve the quality of life for countless individuals worldwide.