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IS MODULE 12, 13, 14

Total questions: 101

Worksheet time: 1hrs 16mins

Name
Class
Date
1.

AKA lateral flow assays

a)

Particle Agglutination

b)

ICT

c)

Neutralization Assays

d)

Western Blot

2.

In lateral flow assays, presence of bands on Control and Test lines is interpreted as?

a)

Nonreactive

b)

Reactive

c)

Invalid

d)

Neither of the above

3.

In lateral flow assays, presence of bands on Control line only is interpreted as?

a)

Nonreactive

b)

Reactive

c)

Invalid

d)

Neither of the above

4.

In lateral flow assays, no control band formation but presence of band on test line is interpreted as?

a)

Nonreactive

b)

Reactive

c)

Invalid

d)

Neither of the above

5.

All are advantages of ICT except?

a)

Most can be stored in room temperature

b)

No special materials/instruments needed

c)

HBV 1 and 2 can be differentiated

d)

Good choice in field testing

6.

All are disadvantages of ICT except?

a)

Not recommended for donor screening

b)

Not suitable for large numbers of sera

c)

QC monitoring impossible

d)

Not specific but is less expensive

7.

For HIV ICT, if the result is nonreactive, what is the next thing that the medical technologist should do?

a)

Repeat the test.

b)

Repeat in duplicate.

c)

Refer to NRL-SLH/SACCL for confirmatory testing.

d)

Report

8.

For HIV ICT, if the result is reactive, what is the next thing that the medical technologist should do?

a)

Repeat the test.

b)

Repeat in duplicate. Report and recommend for confirmatory

testing.

c)

Repeat in duplicate. Refer to NRL-SLH/SACCL for confirmatory testing.

d)

Report

9.

For HBV ICT, if the result is reactive, what is the next thing that the medical technologist should do?

a)

Repeat the test.

b)

Repeat in duplicate. Report and recommend for confirmatory

testing.

c)

Repeat in duplicate. Refer to NRL-SLH/SACCL for confirmatory testing.

d)

Report

10.

This is based on the principle that sensitized particles are agglutinated by the presence of antibodies in human serum or plasma.

a)

Particle Agglutination

b)

ICT

c)

Neutralization Assays

d)

Western Blot

11.

This test method can be used as a screening test or a confirmatory test depending on the target analyte.

a)

Particle Agglutination

b)

ICT

c)

Neutralization Assays

d)

Western Blot

12.

Particle agglutination test can be used as a confirmatory test for:

a)

HIV

b)

HBV

c)

HCV

d)

Syphilis

13.

Advantages of particle agglutination includes all of the following except?

a)

Highly specific

b)

Simple, easy to perform

c)

No machine needed

d)

No washing procedure

e)

Economical and macroscopic in nature

14.

Disadvantages of particle agglutination includes all of the following except?

a)

QC monitoring impossible

b)

Prone to biological False Positives

c)

Test is subjective

d)

Weak agglutination

e)

Affected by Postzone reaction

15.

For HIV particle agglutination test, reactive result:

a)

Repeat test in duplicate. If still INCONCLUSIVE, refer to NRL-SLH/SACCL for confirmatory testing

b)

Perform Absorption test.

c)

Repeat in duplicate. If still reactive, refer to NRL-SLH/SACCL for confirmatory testing

d)

Report.

16.

For HBV particle agglutination test, reactive result:

a)

Repeat test in duplicate. If still INCONCLUSIVE, refer to NRL-SLH/SACCL for confirmatory testing

b)

Perform Absorption test.

c)

Repeat in duplicate. If still reactive, refer to NRL-SLH/SACCL for confirmatory testing

d)

Report.

17.

For HBV particle agglutination test, nonreactive result:

a)

Repeat test in duplicate. If still INCONCLUSIVE, refer to NRL-SLH/SACCL for confirmatory testing

b)

Perform Absorption test.

c)

Repeat in duplicate. If still reactive, refer to NRL-SLH/SACCL for confirmatory testing

d)

Report.

18.

On this method, the enzyme converts a substrate to a reaction product that fluoresces when excited by light of a particular wavelength.

a)

Chemiluminescent EIA

b)

Indirect ELISA

c)

Sandwich ELISA

d)

Competitive ELISA

e)

Enzyme-Linked Fluorescent Assays (ELFA)

19.

This method combines the principle of Sandwich ELISA (1st well) and Competitive ELISA

a)

Particle Agglutination

b)

ICT

c)

Neutralization Assays

d)

Western Blot

20.

In neutralization assay, decrease in absorbance/OD observed on the 2nd well compared to the 1st well with same sample is reported as:

a)

Negative

b)

Positive

c)

Invalid

d)

Inconclusive

21.

It is a blood test that detects antibodies to the hepatitis C virus (HCV).

a)

Particle Agglutination

b)

Western Blot

c)

Neutralization Assays

d)

RIBA

22.

What is the causative agent of Lyme disease?

a)

Borrelia burgdorferi

b)

Epstein Barr Virus

c)

Treponema pallidum

d)

Ricketsial specie

23.

It is a multisystem illness involving the skin, the nervous system, the heart, and the joints.

a)

Lyme Disease

b)

Kissing Disease

c)

Infectious mononucleosis

d)

Scarlet fever

24.

What specie of Borrelia is found in North America?

a)

B. afzelii

b)

B. garinii

c)

B. sensu stricto

d)

B. burgdorferi sensu stricto

25.

Which of the following is not a characteristic of B. burgdorferi?

a)

Loosely coiled spirochete

b)

5 to 25 mm long and 0.2 to 0.5 mm in diameter

c)

Has lipoprotein antigens, labeled OSP-A to OSP-F

d)

5-7 endoflagella or periplasmic flagella.

26.

What is main reservoir of B. burgdorferi?

a)

Man

b)

Chimpanzee

c)

white-footed mouse

d)

Ixodes species

27.

What is the vector of Lyme disease?

a)

Man

b)

Chimpanzee

c)

white-footed mouse

d)

Ixodes species

28.

This is considered the hallmark of early infection with B. burgdorferi.

a)

Erythrema Migrans

b)

Neurological involvement

c)

Cardiac involvement

d)

Facial palsy

29.

This test is recommended as the primary test for the evaluation of antibody response in Lyme disease.

a)

Western Blot

b)

Enzyme Immunoassay

c)

Immunofluorescence Assay

d)

PCR

30.

It is used as a supplemental test for Lyme disease.

a)

Western Blot

b)

Enzyme Immunoassay

c)

Immunofluorescence Assay

d)

PCR

31.

Stage 2 of Lyme Disease infection:

a)

Skin, nervous system, heart, or joints may be affected

b)

Peripheral neuropathy and encephalomyelitis.

c)

Patient may be asymptomatic or have nonspecific flulike symptoms such as malaise, headache, fever, arthralgias, and fatigue.

d)

Presence of small red papule where the bite occurred, which rapidly expands to form a large ring-like erythema and often a central area that exhibits partial clearing.

32.

Stage 3 (late stage) of Lyme Disease infection:

a)

Skin, nervous system, heart, or joints may be affected

b)

Peripheral neuropathy and encephalomyelitis.

c)

Patient may be asymptomatic or have nonspecific flulike symptoms such as malaise, headache, fever, arthralgias, and fatigue.

d)

Presence of small red papule where the bite occurred, which rapidly expands to form a large ring-like erythema and often a central area that exhibits partial clearing.

33.

Treatment for Borreliasis on a child over age years of age.

a)

Amoxicillin

b)

Cefuroxime axetil

c)

Doxycyclin

d)

Ceftriaxone

34.

All of the following drugs can be used as IV therapy in patients with Lyme Infection except?

a)

Ceftriaxone

b)

Cefotaxime

c)

Penicillin G

d)

Amoxicillin

35.

The Epstein Barr Virus infects what specific immune cells?

a)

CD4 T cells

b)

CD8 T cells

c)

B cells

d)

Neutrophils

36.

Which of the following is considered as the antigen that is detected during early infection with Epstein Barr Virus?

a)

VCA

b)

EA-D

c)

EBNA

d)

MA

37.

Which of the following is considered as antigen that appears during latent phase of infection with Epstein Barr Virus?

a)

VCA

b)

EA-D

c)

EBNA

d)

MA

38.

Which of the following is considered as antigen that appears during late phase of infection with Epstein Barr Virus?

a)

VCA

b)

EA-D

c)

EBNA

d)

MA

39.

Which of the following is not a clinical manifestation of S. pyogenes infection?

a)

impetigo

b)

pharyngitis

c)

scarlet fever

d)

carbuncles

40.

Which of the following is a sequelae of S. pyogenes infection?

a)

impetigo

b)

pharyngitis

c)

scarlet fever

d)

Acute rheumatic Fever

41.

This method of S. pyogenes detection is based on the principle of neutralization testing wherein result is based on the titer.

a)

Anti-DNAse B

b)

ASO Titration Test

c)

ASO (Anti-streptolysin O) test

d)

Anti-streptococcal Hyaluronidase test

42.

This method of S. pyogenes detection is enzyme-inhibition variation of mucin clot test wherein patient serum containing the antibody will inhibit hyaluronidase from hydrolyzing the substrate.

a)

Anti-DNAse B

b)

ASO Titration Test

c)

ASO (Anti-streptolysin O) test

d)

Anti-streptococcal Hyaluronidase test

43.

This method of S. pyogenes detection is based on the principle of neutralization testing wherein it detects antibodies capable of preventing DNAse(streptodornase) from depolymerizing.

a)

Anti-DNAse B

b)

ASO Titration Test

c)

ASO (Anti-streptolysin O) test

d)

Anti-streptococcal Hyaluronidase test

44.

What is the normal value of anti-streptococcal hyaluronidase test?

a)

<256

b)

<200 Todd Units

c)

>256

d)

>200 Todd Units

45.

What is the normal value of ASO Titration test?

a)

<256

b)

<200 Todd Units

c)

>256

d)

>200 Todd Units

46.

This test detects antibodies to Salmonella.

a)

Widal Test

b)

Weil-felix test

c)

Optimal Assay

d)

Malquick Standby test

47.

This test detects detects Plasmodium falciparum’s Histidine Rich Protein (HRP-2).

a)

Widal Test

b)

Weil-felix test

c)

Optimal Assay

d)

Malaquick Standby test

48.

This test is the the gold standard for the diagnosis of malaria.

a)

Thick and thin smear

b)

Weil-felix test

c)

Optimal Assay

d)

Malaquick Standby test

49.

This test is capable of detecting live malarial parasite and can distinguish species of malaria.

a)

Thick and thin smear

b)

Weil-felix test

c)

Optimal Assay

d)

Malaquick Standby test

50.

What is the causative agent of Primary atypical Pneumonia?

a)

Streptococcus pneumoniae

b)

Mycoplasma pneumoniae

c)

Legionnaires pneumoniae

d)

Chlamydia pneumoniae

51.

It the agent of spotted fever and typhus.

a)

Rickettsia

b)

Mycoplasma

c)

Chlamydia

d)

Streptococci

52.

A 27-nm RNA virus, incubation period is 2-6 weeks and the mode of transmission is via fecal-oral route

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

53.

A 42-nm DNA virus, incubation period is 4 weeks-6 months and the mode of transmission is via Parenteral inoculation, or equivalent and direct contact

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

54.

A 32-nm pesti-virus–like RNA virus and mode of transmission is similar with HBV

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

55.

A 27-34 nm non- enveloped RNA virus with a similar ,ode of transmission to HAV and its incubation period is 2-9 weeks

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

e)

Hepatitis E

56.

A 36-nm, incomplete RNA virus with HBsAg coats that requires HBV presence for survival

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

e)

Hepatitis E

57.

Hepatitis B antibodies are detectable serologically at about ____ after infection

a)

30-60 days

b)

20-50 days

c)

15-30 days

d)

45-70 days

58.

How many percent of HBV neonatal infection are attributed to acute Hepatitis B?

a)

90%-95%

b)

80%-85%

c)

70%-85%

d)

95%-100%

59.

Chronic HBV infection usually leads to all of the following except?

a)

Fulminant hepatic failure

b)

Cirrhosis

c)

Hepatocellular Carcinoma

d)

Death

60.

Acute HBV infection usually leads to?

a)

Fulminant hepatic failure

b)

Cirrhosis

c)

Hepatocellular Carcinoma

d)

Death

61.

Which of the following is not a characteristic of acute hepatitis infection ?

a)

Abdominal pain

b)

Nausea and vomiting

c)

Extreme fatigue

d)

Dark urine

e)

Scarring of the liver

62.

Hepatitis B marker that is indicative of current infection.

a)

HBsAg

b)

HBeAg

c)

HBcAg

d)

Anti-HBs

63.

Hepatitis B marker of infectivity.

a)

HBsAg

b)

HBeAg

c)

HBcAg

d)

Anti-HBs

64.

Hepatitis B marker is not included in the Hepa B profile because it is found on the nuclei of hepatocytes.

a)

HBsAg

b)

HBeAg

c)

HBcAg

d)

Anti-HBs

65.

Hepatitis B marker for immunity to further infection

a)

HBsAg

b)

HBeAg

c)

HBcAg

d)

Anti-HBs

66.

This is increase in level among Hepa B carriers.

a)

HBsAg

b)

Anti-HBe

c)

Anti-HBc

d)

Anti-HBs

67.

If this is present, it indicates a good prognostic sign and sign of recovery.

a)

HBsAg

b)

Anti-HBe

c)

Anti-HBc

d)

Anti-HBs

68.

Positive HBsAg and HBeAg, Positive Anti-HBc IgM, increase ALT

a)

Early acute infection

b)

Acute infection

c)

Core window period

d)

Chronic active HBV infection

e)

Chronic Inactive HBV carrier

69.

Positive HBsAg and HBeAg, Two-fold increase in ALT

a)

Early acute infection

b)

Acute infection

c)

Core window period

d)

Chronic active HBV infection

e)

Chronic Inactive HBV carrier

70.

Positive HBsAg and HBeAg, Positive Anti-HBC IgG, increase in ALT

a)

Early acute infection

b)

Acute infection

c)

Core window period

d)

Chronic active HBV infection

e)

Chronic Inactive HBV carrier

71.

Positive HBsAg, Positive Anti-HBC IgG, normal in ALT

a)

Early acute infection

b)

Acute infection

c)

Core window period

d)

Chronic active HBV infection

e)

Chronic Inactive HBV carrier

72.

Positive Anti-HBc IgG, normal ALT, Positive anti-HBs

a)

Convalescence

b)

Immunization with Hepatitis B vaccine

c)

Core window period

d)

Past HBV infection with immunity

e)

Chronic Inactive HBV carrier

73.

normal ALT, Positive anti-HBs

a)

Convalescence

b)

Immunization with Hepatitis B vaccine

c)

Core window period

d)

Past HBV infection with immunity

e)

Chronic Inactive HBV carrier

74.

Positive Anti-HBc-IgM and Positive or negative Anti-HBe, normal ALT

a)

Convalescence

b)

Immunization with Hepatitis B vaccine

c)

Core window period

d)

Past HBV infection with immunity

e)

Chronic Inactive HBV carrier

75.

Screening test for HCV

a)

Rapid Anti-HCV

b)

HCV PCR

c)

Liver biopsy

d)

HCV viral load

76.

Monitoring test for HCV

a)

Rapid Anti-HCV

b)

HCV PCR

c)

Liver biopsy

d)

HCV viral load

77.

All are confirmatory tests for HCV except?

a)

Genotyping

b)

HCV PCR

c)

Liver biopsy

d)

HCV viral load

78.

Aka serum hepatitis

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

e)

Hepatitis E

79.

Most common cause of post transfusion Hepatitis

a)

Hepatitis A

b)

Hepatitis B

c)

Hepatitis C

d)

Hepatitis D

e)

Hepatitis E

80.

Agent of yaw

a)

T. pallidum subspecie pertenue

b)

T. pallidum subspecie endemicum

c)

T. pallidum subspecie carateum

d)

T. pallidum subspecie pallidum

81.

Agent of pinta

a)

T. pallidum subspecie pertenue

b)

T. pallidum subspecie endemicum

c)

T. pallidum subspecie carateum

d)

T. pallidum subspecie pallidum

82.

Agent of nonvenereal endemic syphilis

a)

T. pallidum subspecie pertenue

b)

T. pallidum subspecie endemicum

c)

T. pallidum subspecie carateum

d)

T. pallidum subspecie pallidum

83.

Who was known to have carried the syphilis infection to Europe?

a)

Christopher Columbus

b)

John Tyndall

c)

Charles Darwin

d)

Ferdinand Magellan

84.

Pathogenesis of syphilis infection includes all of the following except?

a)

Skin or mucus membrane penetration

b)

Replication

c)

Entry to lymphatic and circulatory

d)

Widespread

dissemination

e)

Exit from the host

85.

Presence of gummatous

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

86.

Patient is asymptomatic, begins to 2 years of infection up to 4 years.

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

87.

Symptoms that appear on this stage includes generalized lymphadenopathy, or enlargement of the lymph nodes; malaise; fever; pharyngitis; and a rash on the skin and mucous membranes.

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

88.

Rashes appear on the palms of the hands and the soles of the feet.

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

89.

Characterized by chancre that develops between 10 and 90 days after infection, with about 21 days being the average.

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

90.

This may occur due to primary, secondary, and early latent periods of maternal infection.

a)

Primary Syphilis

b)

Secondary Syphilis

c)

Latent Syphilis

d)

Tertiary Syphilis

e)

Congenital Syphilis

91.

On this laboratory method, observation of motility is the key to identification of the syphilis.

a)

FTA-ABS

b)

Direct demonstration technique by Dark Field Microscopy

c)

Direct Fluorescent-Antibody Staining for T. pallidum

d)

Levaditi’s Silver Impregnation Method

92.

The main disadvantage of non-treponemal test?

a)

Time consuming

b)

Expensive

c)

Not easily adapted to automation

d)

Prone to false positives

93.

This method is the recommended for detection of syphilis on CSF.

a)

RPR

b)

VDRL

c)

Fluorescent Treponemal Antibody Absorption Test

d)

Treponema Pallidum Immobilization Test

94.

What is the component of RPR that makes the reaction visible hence results are read macroscopically?

a)

Charcoal

b)

ethylenediaminetetraacetic acid

c)

choline chloride

d)

thimerosal

95.

On this method, serum-antigen mixture is placed in a rotator for 8 minutes for 100 rpm

a)

RPR

b)

VDRL

c)

Fluorescent Treponemal Antibody Absorption Test

d)

Treponema Pallidum Immobilization Test

96.

On this method, serum-antigen mixture is rotated for 4 minutes on a rotator at 180 rpm

a)

RPR

b)

VDRL

c)

Fluorescent Treponemal Antibody Absorption Test

d)

Treponema Pallidum Immobilization Test

97.

What is the needle gauge used on qualitative VDRL testing?

a)

18

b)

19

c)

23

d)

25

98.

Result of RPR is considered reactive if there is a presence of:

a)

medium to large clumps

b)

small clumps

c)

no clumps or slight roughness compared to antigen control

d)

None of the above

99.

This method is commonly used as confirmatory method for syphilis infection detection.

a)

RPR

b)

VDRL

c)

Fluorescent Treponemal Antibody Absorption Test

d)

Treponema Pallidum Immobilization Test

100.

Treponema Pallidum Immobilization Test has a positive result if there is a presence of:

a)

>50% Immobilized

b)

<20% Immobilized

c)

20-50% immobilized

d)

<50% Immobilized

101.

This method uses glutaraldehyde-stabilized turkey RBCs during testing.

a)

Hemagglutination Treponemal Test for Syphilis (HATTS)

b)

TP-PA (Treponema pallidum Particle Agglutination)

c)

Microhemagglutinin-Treponema pallidum (MHA-TP)

d)

Treponema Pallidum Hemagglutination (TPHA)