Heme Flashcards

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1
Q

Acute hemorrhage

A

Class 1: up to 15% blood loss
-minimal changes in vitals

Class 2: 15-30% blood loss
- tachycardia, tachypnea, dec pulse pressure

Severe hemmorrhage
-big drop in BP, tachycardia, weak pulse, elevated RR. Dec urine output, mental status changes

Normal for reticulocytosis after blood loss

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2
Q

Neutropenia

A

Most common causes: benign ethnic neutropenia and drug-induced neutropenia. Medication induced.
If febrile and you suspect bacterial infection - need urgent eval

Dx: CDC w/ diff and blood smear

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3
Q

Vit B12 Deficiency

A

S&S: Gradual onset symmetric peripheral neuropathy in feet/arms. Numbness, ataxia (positive Romberg), loss of vibration, and position sense, impaired memory, and dementia (severe cases)

Dx: Peripheral smear shows macro-ovalocytes, some megaloblasts, and multisegmented neutrophils (>5 or 6 lobes). The mean corpuscular volume (MCV) is >100 fL.

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4
Q

Hodgkin’s Lymphoma

A

Cancer of beta lymphocytes (B cells)

S&S: Night sweats, fevers, and pain with ingestion of alcoholic drinks. Generalized pruritus with painless enlarged lymph nodes (neck). Anorexia and weight loss.

Dx: Identified by the presence of Reed–Sternberg cells.

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5
Q

Non-hodgkin’s Lymphoma

A

Cancer of B-cells

S&S: night sweats, fever, weight loss, generalized lymphadenopathy (painless).

The prognosis is poor.

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6
Q

Multiple Myeloma

A

Cancer of plasma cells

S&S: fatigue, weakness, and bone pain that is usually located in the back or chest.

Dx: Causes proteinuria with Bence–Jones proteins, hypercalcemia, and normocytic anemia.

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7
Q

Thrombocytopenia

A

Defined as a platelet count of <150,000/μL.

Symptoms usually do not show until the platelet count is <100,000/μL.
Look for easy bruising (ecchymosis, petechiae), bleeding gums, spontaneous nosebleeds, and hematuria.

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8
Q

Hemophilia A

A

X-linked recessive dz, factor VIII deficiency

S&S: easy bruising, excessive bruising, bleeding into joints (hemarthrosis), bleeding for several hours to days (circumcision, dental extractions), severe bleeding with trauma, heavy menses, and hematuria.

Dx: activated partial thromboplastin time (aPTT) is prolonged, and the prothrombin time (PT), fibrinogen, and platelets are normal.

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9
Q

Normal lab values

A

Hemoglobin
Males: 14.0 to 18.0 g/dL
Females: 12.0 to 16.0 g/dL

Hematocrit
The proportion of red blood cells (RBCs) in 1 mL of plasma
Males: 42% to 52%
Females: 37% to 47%

Mean Corpuscular Volume (MCV)
Normal: 80 to 100 fL (femtoliter)

MCHC
Normal: 31.0 to 37.0 g/dL

MCH
Normal: 25.0 to 35.0 pg/cell

TIBC

Normal: 250 to 410 mcg/dL

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10
Q

Secondary Polycythemia

A

Common w/ chronic smokers, COPD, and people living at high altitudes

Hematocrit in adults of more than 48% in women and more than 52% in men
Hemoglobin in adults of more than 16.5% in women and more than 18.5% in men

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11
Q

Iron-Deficiency Anemia

A

Cause: usually blood loss, heavy periods, low diet intake

S&S: asymptomatic if mild.
Moderate-to-severe cases may have pallor of the skin, conjunctivae, and nail beds. Complaints of daily fatigue and exertional dyspnea. May have glossitis (sore and shiny red tongue) and angular cheilitis (irritated skin or fissures at the corners of the mouth). Cravings for nonfood items such as ice or dirt (pica).
Severe anemia will cause spoon-shaped nails (koilonychia), systolic murmurs, tachycardia, or heart failure.

Dx:
MCV (size) and MCHC (color) can still be in the normal range, and the RBCs will be normocytic and normochromic.
Decreased hemoglobin and hematocrit

Tx:
Correct cause if possible
Ferrous sulfate (take with vit C for absorption)
Increase fluid/fiber
H&H will normalize in 2 months
SE: constipation, black-colored stools
˙

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12
Q

Thalassemia Minor

A

Genetic disorder, bone marrow produces abnormal hemoglobin

S&S: asymptomatic

Dx: hemoglobin electrophoresis
In beta-thalassemia, abnormal (elevated hemoglobin A2 [HbA2] and Hb F, or fetal hemoglobin)
In alpha thalassemia, abnormal (Hb Barts, absence of Hb A)

MCV <80 fL (microcytic)
MCHC ↓ (hypochromic)

TX: none needed

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13
Q

Anemia of Chronic Disease

A

Autoimmune diseases (e.g., rheumatoid arthritis [RA], lupus) or chronic inflammatory disorders impair bone marrow function and cause normocytic anemia (MCV 80–100 fL).

The erythrocyte sedimentation rate (ESR or sed rate) or C-reactive protein (CRP) are elevated.

Treatment of underlying autoimmune disease will reduce systemic inflammation and may help the bone marrow recover.

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14
Q

Anemia of Chronic Kidney Disease

A

Occurs due to the decrease in renal EPO production secondary to the CKD

Obtain CBC, serum ferritin, serum transferrin saturation, vitamin B12, folate, and reticulocyte count.

Tx: The anemia should be treated using conventional methods. If not improving, then erythropoiesis-stimulating agents should be used.

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15
Q

Vitamin B12–Deficiency Anemia

A

Cause: malabsorption, pernicious anemia

Chronic can cause nerve damage and brain damage when severe

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16
Q

Pernicious Anemia

A

Cassation of intrinsic factor (needed to absorb vit B12)

S&S: Gradual onset
Tingling/numbness of hands and feet
Neuropathy starts in peripheral nerves and migrates centrally
Difficulty walking (gross motor)
Difficulty in performing fine motor skills (han
Decreased reflexes in affected extremity, decreased vibration sense, abnormal Romberg

Dx: Always check both serum B12 and serum folate levels in macrocytic anemias
Antibody tests: Antiparietal and anti-intrinsic factor (IF) antibody
Homocysteine level: Elevated
24h urine MMA elevated

TX:
Initially, give B12 injections
Alternative is very high oral doses of B12

17
Q

Aplastic Anemia

A

destruction of the pluripotent stem cells inside the bone marrow and has multiple causes (e.g., radiation, adverse effects of a drug, viral infection).
Bone marrow production slows or stops

S&S: fatigue and weakness. Skin and mucosa are a pale color. Tachycardia and systolic flow murmur. Thrombocytopenia results in large bruises from trauma and bleeding

Dx: pancytopenia (leukopenia, anemia, thrombocytopenia).
Gold standard is the bone marrow biopsy.

Tx:
Refer to hematologist

18
Q

Hemochromatosis

A

intestinal absorption of iron increases, leading to total-body iron overload

S&S: chronic fatigue, skin hyperpigmentation (bronze), swelling of the second and third metacarpal phalangeal joints (fingers), and generalized joint stiffness

Tx:
therapeutic phlebotomy

19
Q

Folic Acid–Deficiency Anemia

A

damage to the DNA of RBCs, which causes macrocytosis

Cause: Inadequate dietary intake (elderly, infants, alcoholics, overcooking vegetables, low citrus intake)

S&S: same as anemia, no neurological complaints

Dx: Decreased hemoglobin and hematocrit, increased MCV

Tx: Correct primary cause. Improve diet.
folic acid PO

20
Q
A