Infectious Flashcards

1
Q

TB microbiology

A

a. Caused by Mycobacterium tuberculosis
b. Mycobacteria are acid-fast bacilli(AFB)_ considered slow growing but hardy organisms
c. Inhibited by the cellular arm of the immune system( high risk in HIV pt )

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2
Q

Transmission of TB

A

a. Transmission occurs via inhalation of aerosolized droplets containing the active
organism
b. Only those people with active TB are contagious (e.g., by coughing, sneezing)
c. People with primary TB are not contagious

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3
Q

Primary TB

A

• Bacilli are inhaled and deposited into the lung, then ingested by alveolar macrophages
• Surviving organisms multiply and disseminate via lymphatics and the blood-stream. Granulomas form and “wall off’ the mycobacteria. The granulomas in oxygen-rich areas, such as the lungs, allow these organisms to remain viable (they are aerobes). After the resolution of the primary infection, the organism remains dormant within the granuloma
• An insult to the immune system may activate the TB at any time
• Only 5% to 10% of individuals with primary TB will develop active disease in their lifetime

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4
Q

Secondary TB ( reactivation )

A

• Occurs when the host’s immunity is weakened (e.g., HIV infection, malignanc immunosuppressants, substance abuse, poor nutrition)
• Usually manifests in the most oxygenated portions of the lungs–the apical/ posterior segments
• Produces clinical manifestations of TB

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5
Q

Extrapulmonary TB

A

• Individuals with impaired immunity may not be able to contain the bacteria at either the primary or the secondary stage of the infection
• This may result in active disease throughout the body
• It is common in patients with HIV because their cellular immunity is impaired

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6
Q

RF of TB

A

a. HIV-positive patients
b. Recent immigrants (within the past 5 years)
c. Prisoners
d. Healthcare workers
e. Close contacts of someone with TB f. Alcoholics
g. Diabetics
h. Glucocorticoid/immunosuppressant use
I. Hematologic malignancy
j. Injection drug users

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7
Q

Clinical features of primary TB

A
  1. Primary TB
    a. Usually asymptomat.
    b. Pleural effusion may develop
    c. If the immune response is incomplete, the pulmonary and constitutional symptoms of TB may develop. This is known as progressive primary TB
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8
Q

Clinical features of Secondary (active) TB

A

a. Constitutional symptoms fever, night sweats, weight loss, and malaise are common
b. Cough progresses from dry cough to purulent sputum. Hemoptysis suggests
advanced TB
c. Apical rales may be present on examination

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9
Q

Clinical features of Extrapulmonary TB

A

a. May involve any organ.
b. Miliary TB refers to hematogenous dissemination of the tubercle bacilli
• May be due to a reactivation of dormant, disseminated foci or a new infection
• Also common in patients with HIV
• May present with organomegaly, reticulonodular infiltrates on CXR, and choroi-dal tubercles in the eye

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10
Q

Radiographic Findings in
Primary TB

A

Ghon complex–calcified primary focus with an associated lymph node
Ranke complex–when Ghon complex undergoes fibrosis and calcification

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11
Q

Diagnosis of TB is challenging in HIV patients because:

A

• PPD skin test result is negative.
• Patients have “atypical”
CXR findings.
• Sputum smears are more likely to be negative.
• Granuloma formation may not be present in the late

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12
Q

Diagnosis

A

CXR
Sputum ( acid fast bacilli)
Definitive diagnosis takes 4-8 w
PCR ** can detect specific DNA more rapidly**
PPD
It’s a screening test for who may have been exposed to TVB
Just for patients with risk factors
Takes 2-3 days
If patients has never had a PPD test before repeat it in 1-2 w if the first test is (-)
If PPD is positive CXR is needed to rule out active disease

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13
Q

CXR finding of TB

A

Upper lobe infiltrates with cavitations

.Chon complex and Ranke complex: evidence of healed primary TB

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14
Q

Why INH should always be started with vitamin B6 (pyridoxine)?

A

to prevent symptoms of B 6 deficiency which include :
stomatitis, glossitis, cheilosis convulsions, hyperirritability, peripheral neuropathy, and sideroblastic anemia.

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15
Q

Rx of TB

A

isoniazid (INH), rifampin, pyrazines and ethambutol or streptomycin.
For 2 months followed by a 4-month phase of INH and rifampin.
2. Prophylactic treatment for latent :
9 months of INH after active TB has been excluded (negative CXR, sputum both).

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16
Q

Imp notes for Rx TB

A

• For a positive TB exposure and a positive PPD test (but no active disease), treatment is INH only.
• If the patient has active
TB, multiagent therapy is indicated.

All TB medications can cause hepatotoxicity. Discontinue treatment only if liver transaminases rise to 3-5 times the upper limit of normal