CV2 Clotting disorder and anemia Flashcards

1
Q

What is anemia and what are the common signs & symptoms?

A

Anemia is a reduction in the oxygen-carrying capacity of red blood cells, which can result from reduced RBC numbers, hemoglobin content, or defective RBC structure.
Common signs & symptoms:

Fatigue

Pallor

Cold peripheries

Dizziness

Shortness of breath

Heart palpitations

Gastrointestinal effects

Neurological effects

Epithelial changes (e.g., hair/nail brittleness)

Jaundice

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2
Q

What are the causes, risk factors, pathophysiology, and treatment options of iron deficiency anemia?

A

Causes: Inadequate dietary intake, poor absorption, excessive loss (e.g., menstruation, blood loss).
Risk Factors: Growth periods (infancy, adolescence), pregnancy, heavy menstruation, blood loss, poor diet, intestinal conditions.
Pathophysiology: Insufficient iron results in reduced hemoglobin production and impaired RBC oxygen-carrying capacity.
Treatment: Iron supplementation (ferrous sulfate or gluconate), dietary changes, treating underlying conditions (e.g., gastrointestinal issues).

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3
Q

What causes macrocytic anemias?

A

Macrocytic anemias are caused by vitamin B12 or folate deficiencies, which impair DNA synthesis in developing RBCs, leading to large, immature RBCs.
Common causes:

Inadequate dietary intake

Poor absorption (e.g., pernicious anemia for B12)

Increased renal loss (e.g., dialysis)

Increased demand (e.g., pregnancy)

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4
Q

How can you distinguish between different types of anemia?

A

Anemia types can be distinguished by:

Size: Microcytic (small), normocytic (normal), macrocytic (large)

Hemoglobin content: Hypochromic (low), normochromic (normal)

Cause: Blood loss, RBC destruction, defective RBC/hemoglobin production, chronic disease, etc.
Common types: Iron deficiency, thalassemia, aplastic, hemolytic, macrocytic, sickle cell, and anemia of chronic disease.

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5
Q

What is the pathophysiology of thrombocytopenia and hemophilia?

A

Thrombocytopenia: Abnormally low platelet count (<150 x 10^9/L), leading to reduced clotting ability and increased bleeding risk. Can result from decreased platelet production or increased destruction.
Signs & Symptoms: Bruising, petechiae, mucosal bleeding.

Hemophilia: A genetic disorder (X-linked) causing deficiencies in clotting factors VIII (Hemophilia A) or IX (Hemophilia B), leading to impaired coagulation and prolonged bleeding.
Signs & Symptoms: Prolonged bleeding, easy bruising, joint bleeding.

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6
Q

What is the pathophysiology of disseminated intravascular coagulation (DIC), including causative factors and signs & symptoms?

A

Pathophysiology: DIC is characterized by widespread clot formation (thrombosis) followed by excessive clot breakdown (fibrinolysis), leading to both clotting and bleeding issues.
Causative Factors: Severe endothelial damage (e.g., sepsis, trauma, pregnancy complications).
Signs & Symptoms: Petechiae, purpura, bleeding from wounds, mucosal bleeding, internal organ damage, respiratory distress, shock.

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7
Q

What is the pathophysiology of deep vein thrombosis (DVT), including risk factors and signs & symptoms?

A

Pathophysiology: DVT occurs when a thrombus forms in the deep veins, usually of the lower limbs. This can result from endothelial injury, blood stasis, or hypercoagulability.
Risk Factors: Surgery, immobility, obesity, smoking, dehydration, pregnancy, coagulopathies.
Signs & Symptoms: Swelling, pain, redness, warmth in the affected limb, sometimes asymptomatic.

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8
Q

How does pulmonary embolism relate to deep vein thrombosis (DVT)?

A

Pulmonary embolism occurs when a thrombus (embolus) from a DVT dislodges and travels to the lungs, blocking a pulmonary artery.
Pathophysiology: The embolus causes obstruction of pulmonary blood flow, leading to tissue hypoxia, vasoconstriction, and potential cardiac and respiratory failure.
Signs & Symptoms: Sudden shortness of breath, chest pain, cough, coughing up blood, shock, increased heart rate.

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