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Chapters 13
PN111L
| Term | Definition |
|---|---|
| Primary Functions of Blood | Transport of oxygen, carbon dioxide, nutrients, hormones, and wastes; regulate body temperature, pH, and fluid balance; protect against blood loss and pathogens |
| Composition of Blood | RBCs, WBCs, and platelets. |
| Blood pH | Normal blood pH is 7.35–7.45 |
| What causes acidosis. | Low blood ph |
| Plasma Proteins | Albumins, Globulins, Fibrinogen& Prothrombin |
| What do albumins do | maintain osmotic balance |
| what do globulins do | antibodies |
| What do fibrinogen& Prothrombin do | clotting |
| RBC Function | Transport O2 and CO2; maintain acid-base balance |
| RBC Count | 4.2–6.2 million/mm³ of blood |
| What test looks at the RBC | CBC |
| Hemoglobin (Hb) | Carries oxygen (as oxyhemoglobin) and carbon dioxide (as carbaminohemoglobin). |
| What are the blood types | A(+,-); B (+,-); AB(+,-); O(+,-) |
| who is the universal donor | O- |
| Who is the universal recipient | AB+ |
| What does it mean to be Rh- | no Rh factor present in the RBC no anti-Rh antibodies present naturally in plasma, incompatibility may cause erythroblastosis fetalis. |
| What does it mean to be Rh+ | Rh factors are present in the RBC |
| Polycythemia | Excessive RBC production leading to thick blood, hypertension; treated by blood removal or chemo. |
| Types of Anemia | Hemorrhagic, aplastic, iron-deficiency, pernicious (B12 deficiency), hemolytic, sickle cell. |
| WBC Count | Normal: 5000–10,000/mm³. |
| Low WBC | Leukopenia |
| High WBC | Leukocytosis |
| WBC Types | Neutrophils (phagocytosis), Eosinophils (parasites/allergy), Basophils (histamine, heparin), Lymphocytes (immunity), Monocytes (macrophages). |
| Platelets | 150,000–400,000/mm³; help form platelet plug and clot |
| Clotting Mechanism in order | Prothrombin → Thrombin → Fibrinogen → Fibrin to form clot. |
| Clotting Disorders and define them | Thrombus (stationary clot), Embolus (moving clot), Hemophilia (lack factor VIII), Thrombocytopenia (low platelets). |
| Vitamin K Role | Required to synthesize clotting factors; infants may need supplementation |
| Blood Volume | Average 4–6 L, about 7–9% of total body weight. |
| Serum | Plasma minus clotting factors; contains antibodies. |
| Define Blood Formation | Red bone marrow produces all blood cells except some lymphocytes and monocytes, which are formed in lymphoid tissue. |
| Aspiration Biopsy Cytology | Examines bone marrow to diagnose blood diseases |
| Normocytes | Normal-sized RBCs (8–9 μm). |
| Microcytic vs. Macrocytic RBCs | Microcytic: small; Macrocytic: large |
| Normochromic vs. Hypochromic RBCs | Normochromic: normal Hb; Hypochromic: low Hb. |
| Sickle Cell Anemia | RBCs sickle under low oxygen, causing blockages and pain crises. Most common in African Americans |
| Thalassemia | Inherited anemia with microcytic, short-lived RBCs; severe cases need transfusion or stem cell transplant. Most common in Mediterranean decent |
| Leukemia Types Explain then | CLL (slow B-cell cancer), ALL (childhood rapid onset), CML (granulocyte cancer, treatable with Gleevec), AML (rapid, poor prognosis). |
| Multiple Myeloma | Cancer of plasma cells; causes bone fractures and recurrent infections |
| Infectious Mononucleosis | Viral infection causing leukocytosis, sore throat, and fatigue; spreads via saliva |
| Prothrombin Time Test | Measures clotting time to adjust anticoagulant drug dosage; standardized by INR system |
| Coumadin & Heparin | Coumadin inhibits prothrombin synthesis; Heparin inhibits conversion of prothrombin to thrombin |
| Tissue Plasminogen Activator (TPA) | Drug used to dissolve existing clots. |
| Thrombocytopenia Signs | Bleeding under skin (purpura); risk of catastrophic bleeding if platelets < 20,000/mm³. |