HEMA Flashcards

1
Q

suspect ___ if there’s an increase in plasma

A

Ca

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2
Q

Signs & Symptoms: Fatigue, pallor, weakness, shortness of breath, dizziness, brittle nails, and pica (craving non-food substances). Low HCT and HgB

Management: Iron supplementation, dietary intake of iron-rich foods (red meat, leafy greens, fortified cereals), and vitamin C to enhance iron absorption.

Diagnostic Tests: Complete Blood Count (CBC) with low hemoglobin and hematocrit, low serum ferritin, and low transferrin saturation.

Prevention: Balanced diet rich in iron, avoiding excessive intake of inhibitors such as tea and coffee.

A

IDA

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3
Q

Signs & Symptoms: Fatigue, glossitis (swollen tongue), irritability, diarrhea, and neural tube defects in pregnant women.
Disruptive vit B9 and B12

Management: Folic acid supplementation, consuming folate-rich foods (leafy greens, citrus fruits, legumes, fortified grains).

Diagnostic Tests: CBC showing macrocytic anemia, serum folate levels.

Prevention: Adequate folic acid intake, especially in pregnancy.

A

Folic Acid Deficiency Anemia (FADA)

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4
Q

Signs & Symptoms: Fatigue, beefy red tongue, numbness and tingling in extremities, memory loss, and impaired coordination.

Management: Vitamin B12 IM injections or oral supplementation, dietary intake of animal-based products, possible blood transfusion

Diagnostic Tests: CBC showing macrocytic anemia, serum B12 levels, Schilling test (24 hour urine specimen.

Prevention: B12-rich diet (eggs, meat, dairy), routine screening in at-risk populations.

A

Pernicious Anemia (Vitamin B12 Deficiency)

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5
Q

Signs & Symptoms: DIfferent RBC shape, Pain crises, delayed growth, frequent infections, stroke risk, joint swelling, dyspnea

Management: Hydration, pain management, hydroxyurea therapy, blood transfusions in severe cases, check capillary refill

Diagnostic Tests: Hemoglobin electrophoresis, sickle cell test, peripheral blood smear.

Prevention: Genetic counseling, early screening, infection prevention measures.

DO NOT BRING THE CHILD TO HIGH ALTITUDE PLACES

A

Sickle Cell Anemia

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6
Q

A rare blood disorder where the bone marrow produces excessive RBCs WBC, Platelet, leading to increased blood viscosity.

Signs & Symptoms: Headaches, dizziness, itching (especially after bathing), high blood pressure, blood clot risk.

Prone to: Thromboembolism, organ infiltration, Ruddy (reddish) complexion, hepatomegaly and cerebral hypoxia

Management: Phlebotomy (blood removal), low-dose aspirin, hydroxyurea, and adequate hydration.

Diagnostic Tests: CBC with increased RBC, JAK2 gene mutation testing.

Prevention: No known prevention, but lifestyle modifications can help reduce complications.

A

POLYCYTHEMIA VERA (Bone marrow hyperplasia)

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7
Q

Caused by viral infection

Signs & Symptoms: Easy bruising, petechiae, prolonged bleeding from cuts.

POSITION: Modified Trendelenburg

Management: Platelet transfusions, corticosteroids, treatment of underlying cause, Immunoglobulin

Diagnostic Tests: CBC with low platelet count, bone marrow biopsy if necessary.

Prevention: Avoidance of medications that lower platelet count (e.g., NSAIDs, alcohol restriction).

A

Immune Thrombocytopenic Purpura (ITP)

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8
Q

Autosomal Dominant

Signs & Symptoms: Prolonged bleeding time, Spontaneous bruising, bleeding gums, heavy menstruation, epistaxis,

Management: FACTOR 8 replacement, Desmopression

Diagnostic Tests: CBC with low platelets, platelet antibody testing.

Prevention: No definitive prevention, genetic counseling recommended

A

Von Willebrand’s Disease

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9
Q

Signs & Symptoms: Fatigue, pallor, slow growth, SOB, bone deformities in severe cases, spleno/hepatomegaly

Management: Blood transfusions, iron chelation therapy, folic acid supplementation.

Diagnostic Tests: Hemoglobin electrophoresis, genetic testing.

Prevention: Genetic screening, prenatal testing.

DOC: DEFEROXAMINE

A

Thalassemia

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10
Q

Mother = Carrier
Deficiency of factor 8 and 9
Common in male but transmitted in Female
Diagnosed after circumcision

Signs & Symptoms: Prolonged bleeding, hemarthrosis (joint bleeding), easy bruising.

Management: Factor VIII or IX replacement therapy, desmopressin in mild cases, No contact sports,

Diagnostic Tests: Coagulation studies (pPTT, aPTT), factor assays.

Prevention: Genetic counseling, avoiding trauma.

A

Hemophilia

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11
Q

Lack of factor 9

A

Christmas Disease

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