Antibody Screening Methods

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Questions and Answers

What is the primary purpose of antibody screening?

  • To detect unexpected antibodies (correct)
  • To diagnose blood-related disorders
  • To determine the strength of antibodies
  • To identify the type of antibodies present

What is the temperature used in the 37°C incubation phase of antibody screening?

  • 40°C
  • 37°C (correct)
  • Room temperature
  • 0°C

What is the purpose of the antiglobulin phase in antibody screening?

  • To enhance the sensitivity of the test (correct)
  • To detect IgG antibodies
  • To identify the type of antibodies
  • To detect IgM antibodies

What is the grading scale used to interpret the agglutination reactions in antibody screening?

<p>Both A and B (C)</p> Signup and view all the answers

What is the result of a positive direct Coombs' test?

<p>Agglutination or clumping of red blood cells (B)</p> Signup and view all the answers

What is the main difference between the tube method and the gel method of antibody screening?

<p>The medium used for antigen-antibody reaction (C)</p> Signup and view all the answers

What is a factor that can affect agglutination in antibody screening?

<p>All of the above (D)</p> Signup and view all the answers

What is the purpose of antibody screening in blood banking?

<p>To detect unexpected antibodies in the donor's blood (D)</p> Signup and view all the answers

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Study Notes

Antibody Screening

  • Purpose: to detect unexpected antibodies in a patient's blood

Categories of Unexpected Antibodies

  • Not mentioned in the text

How is Antibody Screening Performed?

  • Method of antibody screening: Tube Method
  • The tube method involves:
    • Immediate Spin Phase
    • 37°C Incubation Phase
    • Antiglobulin Phase

Tube Method

  • Immediate Spin Phase: initial centrifugation of the sample
  • 37°C Incubation Phase: incubation of the sample at 37°C to enhance antibody detection
  • Antiglobulin Phase: addition of antiglobulin to detect IgG antibodies

Grading of Agglutination Reactions

  • Turgeon method:
    • 0: no aggregates
    • mf: few isolated aggregates, mostly free-floating cells, supernatant appears red
    • Weak (+/-): tiny aggregates, many free RBCs, turbid and reddish supernatant
    • 1+: a few small aggregates just visible macroscopically, many free erythrocytes, turbid and reddish supernatant
    • 2+: medium-sized aggregates, some free erythrocytes, clear supernatant
    • 3+: several large aggregates, some free erythrocytes, clear supernatant
    • 4+: all the erythrocytes are combined into one solid aggregate, clear supernatant
  • Harmening method:
    • 0: no agglutination or hemolysis
    • W+: tiny agglutinates, turbid background
    • 1+: small agglutinates, turbid background
    • 2+: medium-sized agglutinates, clear background
    • 3+: several large agglutinates, clear background
    • 4+: one solid agglutinate

Direct Coomb's Test

  • Procedure:
    • Steps 1-6 not mentioned in the text
  • Interpretation:
    • Positive: agglutination/clumping of red blood cells
    • Negative: no clumping or agglutination

Factors Affecting Agglutination

  • 7 factors mentioned, not specified in the text

Gel Method

  • Procedure:
    • Steps 1-9 not mentioned in the text

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