Three (3) true positives (antigen is present and patient's sera reacted) and three (3) true negatives (antigen is not present and patient's sera did not react): Question 3 options: Is a tool that can be used to increase the probability that any alloantibodies identified is/are correct Is an AABB requirement in order to prove each alloantibody specificity Proves that the antibody procedure was performed correctly Gives a P value of 95%

Three (3) true positives (antigen is present and patient's sera reacted) and three (3) true negatives (antigen is not present and patient's sera did not react): Question 3 options: Is a tool that can be used to increase the probability that any alloantibodies identified is/are correct Is an AABB requirement in order to prove each alloantibody specificity Proves that the antibody procedure was performed correctly Gives a P value of 95%

Principles Of Pharmacology Med Assist

6th Edition

ISBN:9781337512442

Author:RICE

Publisher:RICE

Chapter10: Medication Administration Essentials

Section: Chapter Questions

Problem 1RQ

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Due to a clerical error, several blood samples at a blood bank were not labeled. The three list below were conducted on each sample to identify each blood type. Test 1 = Unknown sample mixed with “anti-A” serum (contains type A antibodies) Test 2 = Unknown sample mixed with “anti-B” serum (contains type B antibodies) Test 3 = Unknown sample mixed with “anti-Rh” serum (contains type Rh antibodies) (A) When unknown sample A was tested, agglutination (clumping) of red blood cells occurred in test 1, 2 and 3. The blood type of sample A is… (B) When unknown sample B was tested, no agglutination (clumping) of red blood cells occurred in any tests. The blood type of sample B is… (C) When unknown sample C was tested, agglutination (clumping) of red blood cells occurred in test 2 and 3, but not 1. The blood type of sample C is…
Which of the following media is capable of detecting all clinically significant antibodies while avoiding all clinically insignificant antibodies? Question 1 options: Gel technology Tube technique with PEG No single media is capable of doing this Solid phase
Please answer all of these if you know the answer :((( thank you so much!
The technician decided to antigen type the patient to confirm predictions from the antibody panel. Antigen type results are given below. Given these results, which of the following statements is BEST supported? Rh Kell Duffy Kidd anti-D anti-C anti-E anti-c anti-e anti-K anti-Fya anti-Fyb anti-Jka anti-Jkb 3+ 0 3+ 3+ 0 0 0 3+ 2+ 2+ Question 7 options: A) K and Fya antibodies are likely because patient would not readily produce antibodies against their own cells. B) An anti-e antibody must be present due to the lack of antigen on the patient cells. C) Jka and Jkb antibodies are likely because an autoantibody is present. D) Rh antibodies are likely because the patient is Rh negative.
A technologist failed to notice that the centrifuge had not properly centrifuged the test tubes prepared for antibody identification. The time of centrifugation was 15 seconds instead of 30 seconds. What would be the potential error in the interpretation of this test? can please any one provide me ans?
Patient Testing Solution (Mr. Smith) Reaction Phenotype (Blood Type) Possible Genotypes for blood type (Clumping? Antibody-A Antibody-B | Antibody-Rh clumping no clumping clumping A+ AA or AO 1. a) Using a Punnett square determines one possibility of what the patient's (Mr. Smith) parent's blood types could be. For the Punnett square, ignore the Rh+ and Rh-. b) Could the parents be a possible donor? Explain why or why not? You may consider Rh+ and Rh- here. c)Which donor would you recommend, if any? Explain your choice using concepts and vocabulary from the course. You may use words, drawings or diagrams to clarify your choice. (Approximately 1 paragraph in length). 20 tv MacBook Pro & %23 $ % 2 3 4 7 E R Y P D F K C V 36 MOSISO comm nd
When a patient exhibits a four-fold or greater rise in antibody titer against a specific microbial antigen between acute-phase and convalescent-phase serum samples, this is considered to be a "seroconversion". Which of the following would be a correct interpretation of a seroconversion? None of the other four answers are a correct interpretation of a seroconversion These findings cannot be interpreted because antibodies aren't specific enough for antigens There is no evidence of current active infection because that would require that the antibody titer is decreasing rather than increasing These results show that the microbe itself has been detected in the patient's sample(s) The results show evidence of current or recent infection by the specific microbe because there has been an active immunologic response to its antigen
In (b), why would it be more efficient to use labeled anti-human IgG rather than label the patient’s antibodies?
Give Detailed Solution with explanation needed (:don't give Handwritten answer))
What p-value is associated with t-1.03 and n3D26 for a 1-sided t-test? O p=0.15 0.10 > p > 0.05 0.40>p>0.30 20>p>0.15
Using the table answer the question

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	Is a tool that can be used to increase the probability that any alloantibodies identified is/are correct
	Is an AABB requirement in order to prove each alloantibody specificity
	Proves that the antibody procedure was performed correctly
	Gives a P value of 95%