
Hematology
NCLEX Clinical Study Booklet · 11 cards
Iron Deficiency Anemia.
AnemiaWhat is Iron Deficiency Anemia?
- Insufficient iron → decreased hemoglobin.
- The most common anemia.
What are the Causes / Risk Factors?
- Chronic blood loss (GI, menstrual)
- Inadequate intake
- Malabsorption
- Pregnancy
What are the Symptoms?
- Fatigue, weakness, pallor
- Tachycardia, dyspnea on exertion
- Brittle, spoon-shaped nails (koilonychia)
- Pica
- Glossitis
How is it Diagnosed?
- ↓Hgb/Hct
- ↓ferritin, ↓serum iron
- Microcytic, hypochromic RBCs
What is the Treatment?
- Oral iron (with vitamin C, empty stomach)
- Iron-rich foods (red meat, leafy greens)
- IV iron if needed
- Expect dark stools; use a straw for liquid iron
NCLEX TipTake oral iron with vitamin C on an empty stomach for absorption. Expect dark stools; use a straw for liquid iron.
Pernicious / B12 Anemia.
AnemiaWhat is Pernicious / B12 Anemia?
- Vitamin B12 deficiency (often lack of intrinsic factor).
- Megaloblastic anemia with neuro symptoms.
What are the Causes / Risk Factors?
- Lack of intrinsic factor (autoimmune, gastrectomy)
- Poor intake (vegan diet)
- Malabsorption (Crohn's)
What are the Symptoms?
- Fatigue, pallor
- Glossitis (beefy red tongue)
- NEURO: paresthesias, ataxia, poor balance
- Cognitive changes
How is it Diagnosed?
- ↓B12
- Macrocytic RBCs
- Schilling test (historical)
What is the Treatment?
- Lifelong IM B12 injections (if intrinsic factor lacking)
- B12-rich foods / supplements
- Safety (neuro deficits)
NCLEX TipPernicious anemia from lack of intrinsic factor needs lifelong IM B12 — oral won't be absorbed. Watch neuro symptoms.
Aplastic Anemia.
AnemiaWhat is Aplastic Anemia?
- Bone marrow failure → pancytopenia (↓RBCs, WBCs, platelets).
- All cell lines are low.
What are the Causes / Risk Factors?
- Idiopathic (autoimmune)
- Radiation / chemo, toxins
- Certain drugs
- Viral infections
What are the Symptoms?
- Fatigue, pallor (anemia)
- Infections (↓WBC)
- Bleeding, bruising, petechiae (↓platelets)
How is it Diagnosed?
- Pancytopenia on CBC
- Bone marrow biopsy (hypocellular)
What is the Treatment?
- Remove cause; transfusions
- Immunosuppressants
- Bone marrow transplant
- Neutropenic AND bleeding precautions
NCLEX TipAplastic anemia = pancytopenia. Institute neutropenic precautions (infection) AND bleeding precautions (low platelets).
Sickle Cell Anemia.
AnemiaWhat is Sickle Cell Anemia?
- Inherited RBC disorder — cells sickle under stress.
- Sickled cells cause vaso-occlusive crises.
What are the Causes / Risk Factors?
- Autosomal recessive (HgbS)
- Crises triggered by hypoxia, dehydration, infection, stress, cold, high altitude
What are the Symptoms?
- Severe pain (vaso-occlusive crisis)
- Swelling of hands/feet
- Fatigue, jaundice
- Splenomegaly
- Delayed growth, frequent infections
How is it Diagnosed?
- Hemoglobin electrophoresis
- Sickled RBCs on smear
- ↓Hgb
What is the Treatment?
- Crisis: HYDRATION (IV fluids), OXYGEN, pain control (opioids), rest, warmth
- Hydroxyurea (reduces crises)
- Avoid triggers (dehydration, hypoxia, cold)
- Folic acid; vaccines/prophylaxis
NCLEX TipSickle cell crisis care = Hydration, Oxygen, Pain control, and rest. Avoid triggers: dehydration, hypoxia, cold, infection.
Leukemia.
CancerWhat is Leukemia?
- Cancer of blood-forming tissue — overproduction of abnormal WBCs.
- Crowds out normal cells.
What are the Causes / Risk Factors?
- Genetic factors
- Radiation / chemical exposure
- Prior chemotherapy
- Down syndrome
What are the Symptoms?
- Fatigue, pallor (anemia)
- Frequent infections, fever
- Bleeding, bruising, petechiae (↓platelets)
- Bone pain, lymphadenopathy
- Weight loss
How is it Diagnosed?
- CBC (abnormal WBCs)
- Bone marrow biopsy (definitive)
What is the Treatment?
- Chemotherapy, radiation
- Bone marrow / stem cell transplant
- NEUTROPENIC precautions (infection = #1 cause of death)
- Bleeding precautions; transfusions
NCLEX TipInfection is the leading cause of death in leukemia — strict neutropenic precautions. Also watch bleeding from low platelets.
Lymphoma.
CancerWhat is Lymphoma?
- Cancer of the lymphatic system.
- Hodgkin's (Reed-Sternberg cells) vs Non-Hodgkin's.
What are the Causes / Risk Factors?
- Epstein-Barr virus (Hodgkin's)
- Immunosuppression
- Autoimmune disease
What are the Symptoms?
- Painless lymph node enlargement (neck)
- Fever, night sweats, weight loss (B symptoms)
- Fatigue, pruritus
- Pain with alcohol (Hodgkin's)
How is it Diagnosed?
- Lymph node biopsy (Reed-Sternberg = Hodgkin's)
- CT / PET staging
- CBC
What is the Treatment?
- Chemotherapy, radiation
- Immunotherapy
- Neutropenic precautions during treatment
- Manage side effects; support
NCLEX TipPainless lymph node swelling + fever, night sweats, weight loss (B symptoms). Reed-Sternberg cells confirm Hodgkin's.
Thrombocytopenia / ITP.
BleedingWhat is Thrombocytopenia / ITP?
- Low platelet count → bleeding risk.
- ITP = immune destruction of platelets.
What are the Causes / Risk Factors?
- Immune (ITP)
- Chemo, radiation
- Heparin (HIT)
- Leukemia, DIC, splenomegaly
What are the Symptoms?
- Petechiae, purpura, ecchymoses
- Bleeding gums, epistaxis
- Prolonged bleeding
- Heavy menses
- Internal bleeding risk (platelets <20k)
How is it Diagnosed?
- ↓platelet count
- CBC; bone marrow if needed
What is the Treatment?
- Corticosteroids, IVIG (ITP)
- Platelet transfusion (severe)
- BLEEDING precautions (soft toothbrush, electric razor, no IM injections)
- Avoid aspirin / NSAIDs
NCLEX TipBleeding precautions: soft toothbrush, electric razor, no IM injections, avoid aspirin/NSAIDs. Watch for internal bleeding.
Hemophilia.
BleedingWhat is Hemophilia?
- Inherited clotting factor deficiency (A = factor VIII, B = factor IX).
- X-linked; primarily affects males.
What are the Causes / Risk Factors?
- X-linked recessive inheritance
- Factor VIII (A) or IX (B) deficiency
What are the Symptoms?
- Prolonged bleeding
- Hemarthrosis (joint bleeding → damage)
- Easy bruising
- Bleeding after minor injury / surgery
How is it Diagnosed?
- Prolonged PTT
- ↓clotting factor levels
- Genetic testing
What is the Treatment?
- Replace the deficient factor (VIII or IX)
- RICE for joint bleeds; avoid aspirin/NSAIDs
- No contact sports; safety
- Dental / injury precautions
NCLEX TipHemophilia: replace the missing clotting factor. Avoid aspirin/NSAIDs and IM injections; protect joints from bleeds.
DIC.
EmergencyWhat is DIC?
- Disseminated Intravascular Coagulation — widespread clotting THEN bleeding.
- Clotting factors and platelets are consumed.
What are the Causes / Risk Factors?
- Sepsis (common)
- Obstetric complications
- Trauma, burns
- Malignancy, shock
What are the Symptoms?
- Simultaneous clotting AND bleeding
- Bleeding from multiple sites (IV, gums, oozing)
- Petechiae, purpura
- Organ ischemia (microclots)
- Shock
How is it Diagnosed?
- ↓platelets, ↓fibrinogen
- ↑PT/PTT, ↑D-dimer
- Schistocytes on smear
What is the Treatment?
- Treat the underlying cause (priority)
- Replace platelets / factors (FFP, cryoprecipitate)
- Heparin (controversial, early)
- Monitor bleeding, perfusion, organ function
NCLEX TipDIC = clotting and bleeding at the same time. The priority is treating the underlying cause (often sepsis).
Blood Transfusion.
TransfusionBefore & During
- Verify order, consent, and type & crossmatch
- TWO nurses verify patient & blood at the bedside
- Use 0.9% NS only; 18–20 g IV; blood filter tubing
- Stay with the patient the first 15 min; baseline vitals
Transfusion Reactions
- Hemolytic (ABO mismatch): fever, chills, flank/back pain, hypotension — STOP
- Febrile: fever, chills
- Allergic: hives/itching; anaphylaxis: wheezing, hypotension
- TACO (overload): dyspnea, crackles, HTN
If a Reaction Occurs
- STOP the transfusion immediately
- Keep the line open with 0.9% NS (new tubing)
- Notify provider & blood bank; recheck IDs
- Send the blood bag & a sample; treat symptoms
NCLEX TipAny transfusion reaction → STOP the blood first, then run normal saline through new tubing and notify the provider/blood bank.
Polycythemia Vera.
ChronicWhat is Polycythemia Vera?
- Overproduction of RBCs → thick, viscous blood.
- High clot risk.
What are the Causes / Risk Factors?
- Bone marrow disorder (JAK2 mutation)
- Chronic hypoxia (secondary)
What are the Symptoms?
- Ruddy (reddish) complexion
- Headache, dizziness
- Hypertension
- Pruritus (after a warm bath)
- Thrombosis risk (clots)
- Splenomegaly
How is it Diagnosed?
- ↑RBC, Hgb, Hct
- ↑blood viscosity
- JAK2 testing
What is the Treatment?
- Therapeutic phlebotomy (remove blood)
- ↑fluids; avoid dehydration
- Anticoagulants / aspirin (clot prevention)
- Monitor for thrombosis / bleeding
NCLEX TipPolycythemia vera = too many RBCs → clot risk. Phlebotomy removes blood; push fluids and prevent clots.
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