Immunocompromise Flashcards

1
Q

what does being immunocompromised mean

A

state of health where actuarial risk of infection is increased

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2
Q

what are 3 person centered aspects that affect the immune system

A
  1. macrobiome
  2. microbiome
  3. Host
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3
Q

5 primary defences that affect the microbiome

A
  1. flow
  2. gravity and motility
  3. skin and mucosal integrity
  4. pH and chemical factors
  5. normal flora
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4
Q

what happens if alter flow

A

predisposes to infection - usually from own microbiome

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5
Q

3 examples of low flow

A
  1. endobroncial tumor
  2. men with BPH get bladder infections
  3. women with lymphedema for breast cancer get cellulitis
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6
Q

what are diffs. between bacteria in mouth vs. gut

A

mouth - gram-pos. and araerobes

gut - gram negs

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7
Q

2 adv of gravity

A
  1. no butt to mouth transfer

2. shower and clean effectively

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8
Q

problems assoc. with bedrest

A
  1. pneumonia is often due to fecal organisms

2. skin wounds infected with fecal organisms

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9
Q

2 examples of altered pH

A
  1. intubated patients treated with gastric acid supressants - more pneumonia
  2. patients with dry mouth at risk for more cavities and caires
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10
Q

3 functions of skin

A
  1. barrier
  2. has immune cells within it
  3. has mucosae that secrete mucus and works with cilia to move stuff out
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11
Q

examples of altered skin/mucosa

A
  1. bed sores
  2. surg. site infections
  3. burn wounds
  4. IV drug use
  5. febrile neutropenia
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12
Q

what is mech. of bed sores

A

pressure on “dependent’ areas causes ischemia and get necrosis - flora get in

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13
Q

what is burn mortality related to (2)

A
  1. age

2. body surgface burned

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14
Q

what happens in IV drug use

A
  • poke bacteria into system from skin (staph)

- local abscess, endocariditis, celulitis

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15
Q

2 most common causes of altered normal flora

A
  1. antibiotics

2. poor infection control

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16
Q

what is C. diff

A

anaerobic gram pos. bacteria that resisits all but a few antibiotics

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17
Q

ho do people get C. diff

A

2% already have it or in hospital - shows up once normal flora reduced with antibiotics

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18
Q

c.diff Sx

A
  • diarrhea, colitis,
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19
Q

what is mucosal candidiasis

A

normal to have yeast, but held in control normally,

  • alteration leads to an overgrowth
  • vagina, penis, throat (thrush - usually with HIV)
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20
Q

what is candidemia

A

blood infection of candida

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21
Q

2 risk factors for candidemia

A
  1. broad spectrum antibiotics

2. indwelling IV cath.

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22
Q

what is problem with prosthetic devices

A

get infected with staph causing a biofilm on device

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23
Q

what is problem with PICC lines

A

pulls infection in from skin and often goes to heart

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24
Q

what is diff. about infection for intra vs. extravascular devices

A

intra can remain at risk through contact with blood, whereas extra tend to only get infected during insertion

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25
Q

2 types of complement deficiency

A
  1. congenital - rare

2. aquired - acute (serious insult) or chroni (autoimmune)

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26
Q

what is most common and important complement deficiney

A

late complement (c5-9)

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27
Q

what is late complement deficency

A
  • increased risk of meningococcal infection (nesseria)
  • later onset of meningococcus (17 vs. 5)
  • 50% are recurrent
  • 1/10 mortality
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28
Q

how to help late complement def.

A

vaccines for meningococcal

29
Q

what are 2 possible problems with neutrophils

A
  1. neutropenia - not enough

2. defect - don’t work right

30
Q

possible ways of neutropenia

A
  1. inherited
  2. drug induced
  3. chemo
  4. autoimmune
31
Q

4 possible neutrophil dysfunctions

A
  1. adhesion defects
  2. chemotactic defects
  3. opsinic
  4. intracellular killing
32
Q

complication diffs. between neutropenia and defects

A

penia - sepsis

defects - local infections

33
Q

what can complicate neutropenia

A

lack of primary defence systems

34
Q

primary defences that are down in chemo-induced neutropenia - febrile neutro

A
  1. feel sick and in bed -
  2. venous cath - skin organisms
  3. mucotitis - GI barriers disrupted
  4. previous/prophylaxis antibiotics - fungi later on
35
Q

things in timeline in febrile neutropenia

A
  1. mucosistis - 1 week
  2. fever - 1 week
  3. venous cath infection - 3 weeks
  4. lung infections - after venous cath
36
Q

what is main clue to lung infection

A

fever- rest is subtle

37
Q

2 consequences of neutrophil recovery

A
  1. asymptomatic pulm. infiltrates

2. hepatosplenic candidiasis

38
Q

why do neutrophil things happen

A

actually fixing after an infection was already there

39
Q

3 things that make hospitalization a state of immunocompromise

A
  1. antibiotics
  2. procedures
  3. contact with other sicko and lack of hand washing
40
Q

what does adaptive immune system protect against

A

exogenous (macrobiome)

- viruses, bacteria, fungi, parasites

41
Q

3 things Ig protect against

A
  1. resp tract from pneumococcal
  2. Gi from giardia, campylobacter
  3. skin from strep
42
Q

what are types of Ig deficiencies (2)

A
  1. hypogammaimmunoglobunemia - all Ig low - more common

2. dysgamma…. - some Ig low

43
Q

3 aquired causes of Ig def.

A
  1. nephrotic synd. - loss
  2. malabsorbtions - GI
  3. CLL
44
Q

what is infection risk for cirrosis

A

spontaneous bacterial peritonitis - portal hypertension leads to backup as opposed to without, where don’t get leak out

45
Q

what happens in CLL

A
  • cell mediated immunocompromise

- sinus, resp, infection - incapulated organisms

46
Q

what is immune function of spleen

A

clears encapsulated bacteria

47
Q

what is risk for asplenia

A

overwhelming post-splenectomy infeciton (OPSI)

48
Q

group at risk in OPSI

A

children

49
Q

infection in OPSI

A

pneumoniae and meningo - vaccinate to prevent

50
Q

4 main comorbids with HIV

A
  1. virus
  2. bact
  3. fungi
  4. protozoa
51
Q

viruses with HIV

A
  • reactivation with previous virus

- severe or community aquires -hepC, flu

52
Q

bact. with HIV

A

mycobacteria -TB

53
Q

fungi with HIV

A
  • mucosal condidiasis

2. other

54
Q

protozoa with HIV

A
  • toxoplasma

- intestinal protozoa

55
Q

3 sources of stem cell transplants (HSCT)

A
  1. autologous -self
  2. allogenic - matched donor
  3. syngenic - identical twin donor
56
Q

what must be done before HSCT

A

conditioning - chemo and/or radiation

57
Q

consequences of conditioning (4)

A
  1. transient neutropenia
  2. qualitative defects in phago
  3. major defects on humoral and cellular immunity
  4. mucusitis - causes gut leakage
58
Q

what happens if donor lymphocytes not HLA matched

A

graft-vs. host disease

59
Q

what happens in GVHD

A
  1. conditioning causes leakage of gut bacteria
  2. microbe activate effector cells
  3. dendritic cells with Ag go to lymph
  4. proliferation of donor Tcekk
  5. inflammation and attack other organs
60
Q

what is given to deal with mucusitis in GVHD

A
  1. venous cath. for IV meds
  2. TPN
  3. supportive blood products
61
Q

what happens d30-100 post graft

A

herpes viruses very important

62
Q

what happens d100+

A
  • generally out of the woods
  • if cell mediated def. - viruses
  • if humoral mediated def. - encapsulated bact
63
Q

what are polyoma viruses

A

DNA viruses with latency aquired in childhood

64
Q

what is BK virus

A

normally held in check but with HSCT can get renal graft failure (BK neuropathy)

65
Q

3 HSCT prevention strategies

A
  1. prophylaxis
  2. pre-emptive treatment
  3. minimize exposure
66
Q

what is CMV

A

cytoalomegalovirus - 8-90% of adults have -causes serious illness and hard to treat

67
Q

when do HSCT get CMV

A

if the recipient has no CMV-ABs but the donor has CMV

68
Q

what is frequent complication of lung transplant

A

pneumonia - hosts own flora

69
Q

what is cause of lymphoproliferative disorder

A

infection with EB virus (immortalizes B-cells)