Medical Laboratory Scientist flashcards
Medical Laboratory Scientist · Build recall with a focused review session.
31 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Anion gap formula
- Anion gap equals sodium minus the sum of chloride and bicarbonate. A value above the reference range suggests unmeasured anions such as lactate, ketones, or toxins.
- Osmolal gap
- Measured osmolality minus calculated osmolality. A gap greater than 10 suggests unmeasured osmoles such as methanol, ethylene glycol, or isopropanol.
- Friedewald LDL calculation
- LDL cholesterol equals total cholesterol minus HDL cholesterol minus triglycerides divided by five. It is invalid when triglycerides exceed 400 mg/dL.
- Corrected sodium in hyperglycemia
- Add 1.6 mEq/L to measured sodium for every 100 mg/dL glucose above 100. Hyperglycemia dilutes sodium and can mask true hyponatremia.
- INR formula
- The international normalized ratio equals the patient prothrombin time divided by the mean normal prothrombin time, raised to the ISI power. It standardizes warfarin monitoring.
- Mixing study interpretation
- Correction of a prolonged aPTT after mixing with normal plasma suggests factor deficiency. Failure to correct suggests an inhibitor such as a lupus anticoagulant or factor antibody.
- DIC laboratory pattern
- Disseminated intravascular coagulation shows prolonged PT and aPTT, low fibrinogen, elevated D-dimer, thrombocytopenia, and schistocytes. An ISTH score of five or more supports overt DIC.
- Direct oral anticoagulant effects
- Apixaban and rivaroxaban variably prolong PT, while dabigatran prolongs aPTT. Specific calibrated anti-Xa or dilute thrombin time assays are preferred for quantification.
- MCV calculation
- Mean corpuscular volume equals hematocrit divided by red cell count in millions per microliter, multiplied by ten. It classifies anemia as microcytic, normocytic, or macrocytic.
- Reticulocyte index
- The corrected reticulocyte percentage multiplied by the patient hematocrit divided by normal hematocrit, then divided by a maturation factor. It assesses marrow response.
- Iron deficiency iron studies
- Iron deficiency shows low ferritin, low serum iron, high TIBC, and low transferrin saturation. Anemia of chronic disease shows low iron and TIBC with normal or high ferritin.
- CML genetic hallmark
- Chronic myeloid leukemia carries the Philadelphia chromosome, t(9;22), producing BCR-ABL1. Peripheral blood shows a left shift with basophilia and thrombocytosis.
- Hereditary spherocytosis findings
- Hereditary spherocytosis shows spherocytes, elevated MCHC, increased RDW, negative direct antiglobulin test, and splenomegaly. Eosin-5-maleimide binding is a sensitive screening test.
- ANA testing limitations
- Antinuclear antibody testing is sensitive but not specific for systemic lupus erythematosus. Confirm with anti-dsDNA or anti-Sm, which are more specific, and correlate clinically.
- SLE-specific autoantibodies
- Anti-double-stranded DNA and anti-Smith antibodies are highly specific for systemic lupus erythematosus. Anti-histone antibodies suggest drug-induced lupus.
- Complement consumption pattern
- Low C3 and C4 with low CH50 suggests complement consumption, as in active lupus or infection. Isolated low CH50 suggests terminal complement pathway deficiency.
- Type I hypersensitivity
- IgE-mediated mast cell degranulation causes immediate reactions such as anaphylaxis. Serum tryptase is elevated during anaphylaxis and specific IgE testing identifies allergens.
- ABO reverse grouping
- Reverse grouping uses A1 and B reagent red cells to detect patient anti-A and anti-B. Discrepancies with forward typing must be resolved before transfusion.
- DAT positive interpretation
- A positive direct antiglobulin test with IgG and C3 suggests immune hemolysis. An eluate may identify the antibody coating red cells in autoimmune or delayed hemolytic reactions.
- Blood component storage
- Red cells are stored at 1-6°C for 35-42 days, platelets at 20-24°C with agitation for 5-7 days, and fresh frozen plasma at -18°C or colder for 12 months.
- Emergency release blood
- Group O red cells, O-negative for females of childbearing age, and AB or group-specific plasma may be issued before compatibility testing is complete.
- Westgard rejection rules
- The 1-3s, 2-2s, R-4s, 4-1s, and 10x rules indicate rejection. The 1-2s rule is a warning that prompts inspection of the Levey-Jennings chart.
- CLIA test complexity
- CLIA categorizes tests as waived, moderate, or high complexity. Non-waived testing requires a qualified laboratory director, documented personnel, and proficiency testing.
- Gram stain principle
- Gram-positive organisms retain crystal violet due to thick peptidoglycan and stain purple. Gram-negative organisms have thin peptidoglycan and stain pink after safranin counterstain.
- Staphylococcus aureus identification
- Staphylococcus aureus is catalase positive, coagulase positive, and ferments mannitol. Methicillin resistance is detected by cefoxitin disk or mecA PCR.
- Blood culture collection
- Collect two sets of aerobic and anaerobic bottles from separate sites before antibiotics. Incubate for five days and perform Gram stain and subculture on positive bottles.
- Real-time PCR Ct value
- The cycle threshold is the PCR cycle at which fluorescence exceeds background. Lower Ct values generally indicate higher target nucleic acid concentration.
- Nucleic acid purity ratios
- A260/A280 near 1.8 indicates pure DNA, while near 2.0 indicates pure RNA. A260/A230 assesses contamination by salts and organic solvents.
- CLSI order of draw
- Blood culture, light blue citrate, serum red or gold, green heparin, lavender EDTA, pink EDTA, then gray fluoride oxalate. Order prevents additive cross-contamination.
- Tourniquet time limit
- Leave the tourniquet on for no more than one minute. Prolonged application causes hemoconcentration and falsely elevates potassium, proteins, and cell counts.
- Acute hemolytic reaction
- Suspect acute hemolytic transfusion reaction with fever, chills, flank pain, and hemoglobinuria. Stop the transfusion, maintain IV access, and return the unit to blood bank.