Heme Flashcards
Acute hemorrhage
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
Neutropenia
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
Vit B12 Deficiency
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.
Hodgkin’s Lymphoma
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.
Non-hodgkin’s Lymphoma
Cancer of B-cells
S&S: night sweats, fever, weight loss, generalized lymphadenopathy (painless).
The prognosis is poor.
Multiple Myeloma
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.
Thrombocytopenia
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.
Hemophilia 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.
Normal lab values
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
Secondary Polycythemia
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
Iron-Deficiency Anemia
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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Thalassemia Minor
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
Anemia of Chronic Disease
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.
Anemia of Chronic Kidney Disease
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.
Vitamin B12–Deficiency Anemia
Cause: malabsorption, pernicious anemia
Chronic can cause nerve damage and brain damage when severe