A condition in which the body does not have enough healthy red blood cells
Polycythemia
An increase in the absolute red blood cell (RBC) mass in the body
General effects of anemia
Reduction in oxygen-carrying capacity, Tissue hypoxia, Compensatory mechanisms to restore tissue oxygenation
Aplastic anemia
A rare but serious blood condition that occurs when your bone marrow cannot make enough new blood cells for your body to work normally
Etiology and pathogenesis of aplastic anemia
Stem cell disorder, Caused by injury to bone marrow stem cells
Anemia of chronic renal failure
Anemia is a common complication of chronic kidney disease (CKD). CKD means your kidneys are damaged and can't filter blood the way they should. This damage can cause wastes and fluid to build up in your body.
Etiology and pathogenesis of anemia of chronic renal failure
Failure of the renal endocrine function, Failure of the renal excretory function, Leads to hemolysis, bone marrow cell depression, and blood loss
Hemolysis
The medical term used to describe the destruction of red blood cells
Vitamin B12–deficiency anemia
Also known as cobalamin deficiency, is a condition that develops when your body can't make enough healthy red blood cells because it doesn't have enough vitamin B12
Etiology and pathogenesis of vitamin B12 or folate deficiency anemia
Caused by a disruption in DNA synthesis of the blast cells in the bone marrow
Pernicious anemia
A decrease in red blood cells that occurs when the intestines cannot properly absorb vitamin B12
Leukemia
Abnormal immature white blood cells (called blasts) multiply uncontrollably, filling up the bone marrow, and preventing production of other cells important for survival, namely red blood cells and platelets. This leads to infections, anemia and abnormal bleeding.
Iron deficiency anemia
Etiology and pathogenesis: Nutritional deficiency
Thalassemia
An inherited (i.e., passed from parents to children through genes) blood disorder caused when the body doesn't make enough of a protein called hemoglobin
Etiology and pathogenesis of thalassemia
Associated with mutant genes that suppress the rate of synthesis of globin chains. α-thalassemia, β-thalassemia
Sickle cell anemia (SCD)
Hemoglobin S is an abnormal form of hemoglobin that causes the red cells to become rigid, and sickle shaped.
Etiology and pathogenesis of sickle cell anemia
Defect of hemoglobin synthesis, Sickle hemoglobin S
Hemolytic disease of the newborn
Etiology and pathogenesis: Fetal red cells cross the placenta, stimulate maternal antibodies, Fetal-maternal ABO incompatibility, Fetal-maternal Rh incompatibility
Acute blood loss
Etiology and pathogenesis: Due to trauma or secondary to a disease process, Rapidly decreases overall blood volume and impairs oxygen delivery
Other extrinsic abnormalities causing anemia
Mechanical heart valves or cardiopulmonary bypass machines, may cause hemolysis
Drugs and chemicals, physical agents or infectious diseases may result in anemia
Venom has been associated with hemolytic anemia
Hypersplenism (an overactive spleen) can cause anemia, leukopenia....severe enough to require splenectomy
Leukopenia
Low white blood cell count
Platelets/thrombocytes
A component of blood whose function (along with the coagulation factors) is to react to bleeding from blood vessel injury by clumping, thereby initiating a blood clot
Blood clotting/coagulation
An important process that prevents excessive bleeding when a blood vessel is injured
Vascular purpura
Purpura—patches of petechiae, or pinpoint hemorrhages, on the skin—are present. Primary cause: abnormality of the vessels or the tissues that support them
Thrombocytopenia
Common cause of generalized bleeding, Caused by decreased platelet production, decreased platelet survival, splenic sequestration, or platelet dilution
Thrombocytosis
Platelet count greater than 400,000/mm3, Transitory: after stress or physical exercise, Secondary or reactive: response to hemorrhage, inflammatory diseases, malignancy infection, hemolysis, or splenectomy
Qualitative platelet disorders
Defect in platelet function, Normal number of platelets, Rarely inherited, commonly acquired, Associated with drugs, especially aspirin; with renal failure; or with a coexisting hematologic disease, such as leukemia
Hemophilia
Common severe inherited coagulation disorder, X-linked recessive disorder, Transmitted by an asymptomatic carrier female to an affected son, Hemophilia A, Hemophilia B
Vitamin K deficiency bleeding in infancy
Seen in the newborn, typically 48 to 72 hours after birth, through 6 months of age, More common in breast-fed babies (who do not receive vitamin K supplement) than in formula-fed babies, Rare in Western countries because of routine administration of vitamin K to newborns
Acquired vitamin K deficiency
May result in bleeding as a result of a coagulation defect, May occur with malnutrition, malabsorption (including biliary disease), chronic hepatic disease, antibiotic therapy, and oral anticoagulation therapy with warfarin
Blood pressure
The pressure exerted by the blood on the vessel wall, Blood pressure is the product of cardiac output and peripheral resistance
Peripheral resistance
The resistance to the flow of blood caused by the friction between the blood and the lumen of the vessel, The viscosity of the blood also contributes to the peripheral resistance, Constriction of blood vessels and arterial stiffness increase peripheral resistance
Cardiac output
Depends on venous return and force of contraction of the left ventricle
Systolic pressure
The maximum pressure in the arteries during contraction of the ventricle
Diastolic pressure
The minimum pressure in the arteries during the end of ventricular relaxation
During each cardiac cycle the blood pressure varies from a maximum to a minimum