Lecture 5: Fever of Unknown Origin & TB Flashcards

1
Q

What is the definition of fever

  • in the AM
  • in the PM

in combination w/ ________

A

Definition of Fever

> 37.2 in AM
37.7 in PM

in combination w/incr in hypothalmic set point

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2
Q

What is the nornmal range for body temp

A

normal body temp range = 35.6 - 38.2

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3
Q

Comparing Temps

  1. elderly: higher or lower than avg body temp
  2. rectal temps: higher or lower than oral and core temps
  3. What is the effect ovulation has on temp?
  4. lowest temp at what time? what time for highest?
  5. 2 things that cause incr in oral temp
A

Comparing Temps

  1. elderly = lower than avd body temp
  2. rectal temps = higher than oral or core
  3. ovulation incr temp
  4. lowest temp = 6am, highest = 4-6pm
  5. incr oral temp w/smoking + chewing
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4
Q
  1. exposure
  2. aging
  3. sepsis
  4. CHF
  5. drug OD
  6. Hypoglycemia
  7. Renal or Hepatic Failure

are all causes of what?

A
  1. exposure
  2. aging
  3. sepsis
  4. CHF
  5. drug OD
  6. Hypoglycemia
  7. Renal or Hepatic Failure

all causes of HYPOthermia

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5
Q
  1. hypothalmic lesion
  2. Thyrotoxicosis
  3. Anticholinergic blockade
  4. Exercise

are all causes of what?

A
  1. hypothalmic lesion
  2. Thyrotoxicosis
  3. Anticholinergic blockade
  4. Exercise

all causes of HYPERthermia

others (obvious): heat stroke, malig hyperthermia

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6
Q

What are 2 major benefits of fever

A
  1. decr viral replication to fight infxn

2. suppress microbial growth

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7
Q
  1. incr immunoglobulin synthesis
  2. activation of T cells
  3. incr cytokine production
  4. incr NK cell activity
  5. incr phagocytic activity

are examples of ______

A
  1. incr immunoglobulin synthesis
  2. activation of T cells
  3. incr cytokine production
  4. incr NK cell activity
  5. incr phagocytic activity

are examples of the benefits of fever

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8
Q

What is the definition of FUO (Fever of Unknown Origin)
- 4 components

MEMORIZE AND KNOW THIS!!

A

definition of FUO (Fever of Unknown Origin)

  1. Fever > 38.3C
  2. illness lasting 3 wks
  3. NOT immunocompromised
  4. failure to reach dx w/ labs, XR
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9
Q

What is the MC etiology of FUO

A

MC etiology of FUO = Infections

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10
Q

Etiology of FUO: Infections

  • are most caused by microbes in the environment or by normal flora in our body
A

Etiology of FUO: Infections

-Infections mostly caused by normal flora in our body

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11
Q

Etiology of FUO

-what are the 4 other major classifications for the cause of FUPO>

A

Etiology of FUO

  1. Neoplasia
  2. Misc
  3. Connective Tissue D/o
  4. Undiagnosed
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12
Q

FUO workup

- what 3 tests are generalized/less invasive and a good place to start when working up FUO

A

FUO workup

  1. CBC w/diff
  2. CMP
  3. UA & culture
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13
Q

what is more common as the cause of FUO

  • uncommon dzs -OR-
  • uncommon manifestations of common dzs
A

Cause of FUO

  • Uncommon manifestations of COMMON DZs MORE COMMON than uncommon dz
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14
Q

FUO

- once the site of infection determined what should be done next

A

FUO

  • site of infection determined –> start empiric therapy
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15
Q

Etiology of FUO

-what is a common infectious cause of FUO

A

common infectious cause of FUO = TB!!!!

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16
Q

Tuberculosis

  1. what is the name of the species that causes this infection
  2. what is the hallmark of this dz
  3. how is this dz spread
A

Tuberculosis

  1. cause = mycobacterium tuberculosis
  2. hallmark = CASEATING granulomas
  3. spread is by respiratory droplets
17
Q

TB

  1. what 2 groups = incr risk of exposure to TB
  2. what 2 groups = incr risk of TB infxn
  3. what types of pts = incr risk of active TB once infected
    (gen and 1 spp example)
A

TB

  1. Incr risk of exposure to TB
    - close contacts of pts w/active TB + healthcare workers
  2. Incr risk of TB infxn
    - immigrants from high prev area, homeless
  3. Incr risk of active TB once infected
    - immunodeficient pts –> HIV+
18
Q

What cells in the body are responsible for the pathophysiology and granuloma formation seen in TB

A

alveolar macrophages

19
Q

What are the 3 outcomes of a TB infection

A

Outcomes of TB infection

  1. Primary TB
  2. Latent/Chronic TB
  3. Reactivation/2ndary TB
20
Q

3 Outcomes of TB infection

  1. what is the ONLY outcome where pts are NOT contagious
  2. which outcome is a/w apical cavitary lesions
  3. which outcome is characterized/controlled by granuloma formation and a (+) PPD
  4. which outcome is the result of the initial infection
A

3 Outcomes of TB infection

  1. ONLY outcome where pts are NOT contagious = LATENT/Chronic TB
  2. which outcome is a/w apical cavitary lesions
    - Reactivation/2ndary TB
  3. which outcome is characterized/controlled by granuloma formation and a (+) PPD
    - Latent/Chronic TB
  4. which outcome is the result of the initial infection
    - Primary TB
21
Q

3 Outcomes of TB infection: Reactivation/2ndary TB

  • what causes the reactivation of Latent TB
A

3 Outcomes of TB infection: Reactivation/2ndary TB

  • cause of reactivation of latent TB = waning of immune defense
22
Q

why is the formation of caseating granulomas (central necrosis, acidic, Low O2) imp in TB

A

creates a hostile enviro for MTB

23
Q

Pt presents w/ constitutional Sxs, chronic productive cough and pleuritic chest pain. On lung exam you note rales, consolidation and dullness in the middle R lobe.

Dx? (be specific)

A

Dx = Primary TB (middle/lower lobe consolidation)

24
Q

Extrapulmonary TB

  1. name of d/o that affects the vertebra
  2. name of the term for affecting the LNs
A

Extrapulmonary TB

  1. name of d/o that affects the vertebra = Pott’s Dz
  2. name of the term for affecting the LNs = scrofula
25
If a pt has HIV and TB what do they have an incr risk of
HIV + TB = incr risk of reactivation TB
26
Name of the test to screen for TB
PPD
27
PPD: Screening for TB 1. how long wait to see result? 2. what is a positive result? 3. what rxn size is considered (+) for HIV+, immunosuppressed, or close contact w/active TB pt 4. what rxn size is considered (+) for pts w/no RFs for TB
PPD: Screening for TB 1. wait 48-72hrs 2. (+) result = transverse induration 3. > 5 mm = (+) for HIV+, immunosuppressed, or close contact w/active TB pt 4. > 15 mm = (+) for pts w/no RFs for TB
28
What are the names of the 3 diagnostic studies used in suspected cases of ACTIVE TB
3 diagnostic studies used in suspected cases of Active TB 1. Acid fast smear (bacilli) + sputum culture x 3 days 2. CXR (PA + Lateral) 3. Interferon Gamma Release Assay (Quantiferon)
29
what is the gold std for dx TB
AFB (Acid Fast Bacilli) cultures
30
What is the main indication of CXR for TB
to r/o active TB
31
Patterns of TB seen on CXR 1. what type of TB is a/w middle/lower lobe consolidation? 2. what type of TB is a/w apical cavitary lesions? 3. what type of TB is a/w diffuse, small nodular lesions?
Patterns of TB seen on CXR 1. middle/lower lobe consolidation = Primary TB 2. apical cavitary lesions = reactivation TB 3. Diffuse, small nodular lesions = Miliary TB
32
What is seen on CXR that indicates primary TB has healed
Granuloma on CXR indicates primary TB has healed
33
Active TB Tx 1. Names of drugs given? 2. how long these 4 drugs given? 3. how long is the TOTAL active TB tx? 4. what 2 drugs given after the initial phase (continuation phase)
Active TB Tx 1. Drugs = RIPE or RIPS - Rifampin, INH (+ Vit B6), Pyrazinamide, Ethambutol (or Streptomycin) 2. given for 2 months 3. total duration of active TB tx = 6 mos 4. Continuation phase drugs = RI - Rifampin + INH (+ Vit B6)
34
PPx of TB - when should ppx be started
PPx of TB indicated when exposure to TB and (-) CXR
35
Latent TB and PPx TB Tx 1. what 2 things given in both situations 2. how does the length of Tx differ if pt is HIV+ 3. what is the minimum ppx duration needed
Latent TB and PPx TB Tx 1. INH + Vit B6 2. HIV+ --> longer tx 3. need ppx for at least 2 wks