Week 9- Hematologic and Hepatic/Biliary Disease Flashcards
PART 1: HEMATOLOGIC DISEASE
PART 1: HEMATOLOGIC DISEASE
Blood consists of what (4) things?
- Plasma
- Erythrocytes
- Leukocytes
- Platelets
Act as inflammatory/immune responses.
Leukocytes
Together with coagulation factors in plasma, control the clotting of the blood.
Platelets
Carries antibodies and nutrients to tissues and removes waste from tissues.
Plasma
Carry O2 to tissues and removes CO2 from them.
Erythrocytes
S/Sx of Hematologic Disorder with minimal exertion. (5)
- Dyspnea
- Chest pain
- Palpitations
- Severe weakness
- Fatigue
Neurological S/Sx of Hematologic Disorder. (5)
- HA
- Drowsiness
- Dizziness
- Syncope
- Polyneuropathy
Other S/Sx of Hematologic Disorder. (3)
- Skin/fingernail changes
- Blood in stool
- Easy bruising
List some hematologic disorders. (8)
- Anemia
- Polycythemia
- Sickle Cell Anemia
- Leukocytosis
- Leukopenia
- Thrombocytosis
- Thrombocytopenia
- Hemophilia
Anemia:
- What is it?
- Results in abnormality in quality/quantity of __________.
- What are the most common causes? (3)
- What is an important PT consideration with someone who has Anemia?
- Reduction of RBC/hemoglobin resulting in decreased O2 carrying capacity of blood.
- erythrocytes
- EXCESSIVE BLOOD LOSS, increased destruction of erythrocytes, decreased production of erythrocytes
- Diminished exercise tolerance expected in patients with anemia and exercise should be approved by MD.
Polycythemia:
- What is it?
- What is an important PT consideration for someone with polycythemia?
- Increase in number of RBCs and concentration of hemoglobin resulting in increased whole blood viscosity and increased blood volume.
- Results in thickening of blood and increased risk for clotting leading to stroke.
Sickle Cell Anemia:
- What is it?
- Inherited autosomal _______ disorder that is more common in _________________.
- Characterized by presence of abnormal form of _________.
- Altered shape of cell to ______/_______ shape.
- Series of crises or acute manifestations of symptoms characterized by the condition.
- Hereditary form of anemia in which a mutated form of hemoglobin distorts the red blood cells into a crescent shape at low oxygen levels.
- recessive disorder more common in AA
- hemoglobin
- sickled/curved
Sickle Cell Anemia S/Sx:
- ______ caused by blockage of sickled RBCs.
- May be in _______, ______, or _______ of the body.
- Joint pain most often occurs in ________ or ______.
- How long can painful episodes last?
- May cause ______-______ syndrome. What is this?
- Most common factors that may cause a crisis?
- pain
- organ, bone, or joint
- shoulder or hip
- hours or up to 5-6 days
- Hand-Foot Syndrome (painful swelling in dorsum of hands and feet)
- extreme temperatures, strenuous physical activity
Leukocytosis:
- What is leukocytosis?
- What is it a sign of?
- What is a normal WBC count? What is considered leukocytosis?
- High level of WBC in the blood.
- Sign of inflammatory response.
- 5000-10000, >10000 leukocytes/mm
Leukopenia:
- What is leukopenia?
- Can occur due to _____/_______, overwhelming infections, dietary deficiencies, and autoimmune diseases.
- What is a normal WBC count? What is considered leukopenia?
- What are 2 important PT considerations related to leukopenia?
- Reduction in number of WBC in the blood.
- chemo/radiation
- 5000-10000, <5000 leukocytes/mm
- WASH HANDS, pt with known leukopenia presenting with constitutional S/Sx requires immediate referral
Thrombocytosis:
- What is thrombocytosis?
- Is it usually permanent or temporary?
- What is an important PT consideration with thrombocytosis?
- Increase in platelet count.
- usually temporary
- Associated with tendency to clot, secondary to high platelet count and increased blood viscocity.
Thrombocytopenia:
- What is thrombocytopenia?
- Results from decreased platelet ________ or increased _________.
- What are 2 important PT considerations related to thrombocytopenia?
- What are the main causes? (3)
- Decrease in platelet count
- decreasing platelet production or increased platelet destruction
- PT needs to be alert to severe bruising, external hematomas, joint swelling, and multiple petechiae. Strenuous exercise or exercise involving straining/bearing down could cause hemorrhage (AVOID VALSALVA).
- Chemotherapy, radiation, and medications (NSAIDs, coumadin/warfarin)
Thrombocytopenia S/Sx. (5)
- Bleeding after minor trauma
- Spontaneous bleeding (petechiae, purpura spots, epistaxis)
- Excessive menstruation
- Gingival bleeding
- Melena
Hemophilia:
-What is hemophilia?
-What causes it?
-Bleed ______ but not ______ than those without the condition.
What is the most common site of bleeding?
-What is the 2nd most common site of bleeding?
- Hereditary blood clotting disorder.
- Caused by abnormality of functional plasma-clotting proteins.
- longer but not faster
- Bleeding into the joint (knee, elbow, ankle, hip, shoulder)
- Bleeding into muscles 2nd most common site (flexor muscle groups)
Hemophilia S/Sx. (11)
Hemarthrosis
- Stiffening into position of comfort
- Decreased ROM
- Pain
- Swelling
- Tenderness
- Heat
Muscle Hemorrhage (FLEXORS)
- Gradually intensifying pain.
- Protective spasm of the muscle.
- Limitation of movement at the surrounding joints.
- Muscle assumes the position of comfort.
- Loss of sensation.
Hematologic Disease Screening:
- Previous Hx of _________/_______ therapy.
- Chronic or long-term use of _______ or other _______.
- __________ bleeding.
- Recent major ________/__________.
- chemo/radiation therapy
- aspirin or other NSAIDs
- spontaneous bleeding
- major surgery/transplantation