TB (3 questions) Flashcards

1
Q

Cause of TB

A

Mycobacterium tuberculosis, an acid-fast bacilli that typically infects the lungs and respiratory track. It also infect brain, the kidneys, or the spine.

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2
Q

How does TB spread?

A

person to person via droplet nuclei containing tubercle bacilli through the air.

AIRBORNE precautions are needed in hospital setting

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3
Q

Who is at higher risk for exposure or infection with TB?

A
  • Close contacts of people with infectious TB disease;
  • people born in areas of the world where TB is common (foreign-born);
  • low-income groups with poor access to health care;
  • people who inject illegal drugs;
  • infants, children, and adolescents exposed to adults in high-risk categories;
  • & high-risk racial or ethnic minority populations, as locally defined.
  • Also, people who live or work in certain settings such as nursing homes, correctional facilities, homeless shelters, and drug treatment centers and other people who may be exposed to TB on the job, such as health care workers.
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4
Q

Risk of developing TB disease if infected w/latent TB, if no risk factors

A

10% over a lifetime. 50% of those people will develop the infection within the 1st 2 years after exposure.

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5
Q

What groups are at higher risk for developing TB disease once infected?

A
  • **people with HIV infection (strongest known risk factor for development of TB dz)
  • people who were recently infected with M. tuberculosis,
  • people with certain medical conditions (DM, silicosis, severe KD, organ transplant, immunosuppressive therapy, etc)
  • people who inject illegal drugs (IVDU),
  • and people with a history of inadequately treated TB.
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6
Q

For people infected w/ both TB and HIV, what is the risk of developing TB disease?

A

~ 7% - 10% each year

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7
Q

For people infected w/ both TB and diabetes, what is the risk of developing TB disease?

A

30% over lifetime

(~3x as high as those w/no risk factors)

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8
Q

How can we test for TB infection?

A
  • TST/Manatoux Skin Test (PPD)
  • nterferon-gamma release assays (IGRA) such as the QFT-G
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9
Q

How is TST test done?

A
  • injecting tuberculin intradermally.
  • After 48 - 72 hours, pt’s arm is examined for a rxn (an induration—firmness/swelling, NOT REDNESS).
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10
Q

Reasons for a false positive TST?

A
  • infection w/ non-tuberculosis mycobacteria (NTM);
  • Vaccination w BCG;
  • administration of incorrect antigen,
  • incorrect measuring/interpretation of TST rxn
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11
Q

Reasons for a false negative TST?

A
  • Anergy // Recent TB infection (w/i. past 8-10 wks)
  • Very young age (< 6 months)
  • Recent live-virus measles or smallpox vaccination
  • Incorrect method of giving the TST
  • Incorrect measuring or interpretation of TST reaction
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12
Q

What is one strategy used to tell the difference between boosted reactions and those caused by recent infection?

A

Two step testing

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13
Q

TST: induration of > 5mm positive for what populations?

A
  • living w/HIV
  • recent contacts of persons w/infectious TB
  • previously had TB disease
  • organ transplants or other immunosuppressed pts (including prolonged course PO or IV corticosteroids or TNF-alpha antagonists)
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14
Q

TST: induration of > 10mm positive for what populations?

A
  • moved to U.S. w/in 5 years from areas of world where TB common (e.g, Asia, Africa, Eastern Europe, Russia, Latin America)
  • inject illegal drugs
  • Mycobacteriology lab workers
  • Live or work in high risk congregate settings
  • medical conditions that put at risk for TB (silicosis, DM, severe KD, certain cancers, certain intestinal conditions)
  • kids <4yo
  • infants, kids, adolescents exposed to adults in high-risk categories
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15
Q

TST: induration of > 15mm positive for what populations?

A

people w/no known risk factors for TB

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16
Q

What is QFT-G?

A

FDA approved interferon-gamma release assay BLOOD tets for TB infection

17
Q

How is QFT-collected & processed?

A
  • The patient’s blood samples must be delivered to a qualified laboratory wi 12 hours of collecting the samples.
  • Blood samples are mixed & incubated w/ antigens found in M. TB strains and with control substances.
  • Results of QFT-G depend upon amt of IFN-γ released in response to the antigens and the control substances.
18
Q

Advantages of QFT-G

A
  • requires only one patient visit
  • results w/i 24 hours
  • Unlike the TST, the QFT-G does not cause the booster phenomenon so *results are not affected by BCG vaccination
  • Less chance of having an incorrect reading of results as compared to the TST.
  • The QFT-G can be used in all circumstances in which the TST is currently used.
19
Q

Disadvantages of QFT-G

A
  • blood samples must be processed within 12 hrs at a qualified laboratory
  • limited data on the use of it in certain populations (kids <17, HIV/AIDs, and other medical conditions)
  • Limited data on using QFT-G on persons who have been recently exposed to TB (contacts) and other populations at high risk for LTBI.
20
Q

What are the five components for conducting a complete medical evaluation for diagnosing TB dz?

A
  1. Medical history
  2. Physical examination.
  3. TST or a QFT-G
  4. Chest x-ray.
  5. Bacteriologic examination.
21
Q

Medical Hx / What are the Sx of TB?

A
  1. coughing lasting for 3 + weeks, pain in chest when breathing or coughing, and coughing up sputum or blood.
  2. General symptoms of TB disease (pulmonary or extrapulmonary) include weight loss, fatigue, malaise, fever, and night sweats.
22
Q

How does a CXR help in the evaluation of TB?

A
  • helps r/o possibility of pulmonary TB disease in a person who has a +TST or QFTG.
  • CXR also help determine if there are lung abnormalities in people who have symptoms of TB disease.
    *
23
Q

Disadvantages of CXR in evaluation of TB

A
  • CXR results CANNOT confirm that a person has TB disease.
  • CXR for people living with HIV and pulmonary TB may appear unsual or even normal.
24
Q

How is the bacteriologic examination done for TB?

A
  1. sputum specimen smeared onto a slide, stained, and examined under a microscope for the presence of acid-fast bacilli.
    1. When acid-fast bacilli are seen in a smear, they are counted, and the smear is classified according to this #
    2. Patients with positive smears are considered infectious.
  2. Next, based on clinical and laboratory decision, nucleic acid amplification (NAA) tests can be used on the sputum specimen to help identify the microorganisms
  3. **A positive culture for M. tuberculosis confirms the diagnosis of TB disease
  4. Finally, the cultured specimen is also tested for drug susceptibility. The results of drug susceptibility tests can help clinicians choose the appropriate drugs for each
25
Q

Characteristics of latent TB: skin or blood test

A

positive for TB infection

26
Q

Characteristics of latent TB: CXR and sputum culture

A

CXR normal, sputum negative

27
Q

Characteristics of latent TB: activity bacteria in body

A

Has TB bacteria in his/her body that are alive, but inactive

28
Q

Characteristics of latent TB: feels sick or not?

A

Does not feel sick

29
Q

Characteristics of latent TB: contagious

A

Cannot spread TB bacteria to others

30
Q

Characteristics of latent TB: Tx

A
  • Needs treatment for latent TB infection to prevent TB disease;
  • however, if exposed and infected by a person with multidrug-resistant TB (MDR TB) or extensively drug-resistant TB (XDR TB), preventive treatment may not be an option
31
Q

Tx of TB: criteria to be non-infectious

A
  • Patients who have been receiving adequate treatment for 2 weeks
  • whose symptoms have improved (coughing less and no longer have a fever), and
  • who have three consecutive negative sputum smears from sputum collected in 8-24 hour intervals (one being a morning specimen)
32
Q

What new shorter TB regimen is now available?

A
  • Isoniazide and Rifapentine 1/week for 3 months (12 dose therapy) under DOT.
    *
33
Q

What is the advantage of the 12 dose TB regimen?

A
  • The 12-dose regimen may ensure better completion rates as it simplifies and shortens treatment from 270 daily doses over nine months, to 12 once-weekly doses over three months by directly observed therapy (DOT).
34
Q

Who is eligible for the 12 dose TB regimen?

A
  • otherwise healthy people, 12 years of age and older, who were recently in contact with someone who has TB disease.
  • including young children, pregnant women or women who expect to become pregnant during treatment, and HIV-infected people taking antiretroviral therapy.
35
Q

Resistant TB: primary vs secondary

A

Primary: resistant strain is transmitted

Secondary: resistance d/t inappropriate or non-adhered to regimen

36
Q

What is monoresistant TB?

A

tubercule bacilli are resistant to any one TB treatment drug

37
Q

What is polyresistant TB?

A

resistant to at least two TB drugs (but not both isoniazid and rifampin).

38
Q

What is multidrug-resistant TB?

A

tubercle bacilli are resistant to at least isoniazid and rifampin, the two best first-line TB tx

39
Q

What is extensively resistant TB?

A

tubercle bacilli are resistant to isoniazid and rifampin, plus resistant to any fluoroquinolone and at least one of three injectable second-line drugs