May4 M1-Fever in Immune Compromised Hosts Flashcards

1
Q

febrile neutropenia def

A
  1. fever >38.3 once or >38 twice with 1 hr interval

2. ANC < 500

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2
Q

organisms to consider in febneut

A
  • gram- enteric rods (gut mucositis)
  • gram+ cocci like CoNS and MSSA, MRSA. Also, pseudomonas (central line infection)
  • candida (central line and gut), aspergillus (lungs)
  • Strep pneumo, resp viruses, C.diff (usual org causing fever)
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3
Q

main cause of febneut in cancer chemo pts

A
  • unexplained fever (39%)
  • clinically defined infection (17%)
  • microbiologically defined infections (44%)
  • # 1 bacteremia with gram+ cocci*
  • # 2 bacteremia with gram - bacilli*
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4
Q

cause of the unexplained fever in febneut patients

A

LPS and exotoxin shedding from gram- organisms inthe gut (can cross to blood bc barrier problem) but no invasion

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5
Q

(imp?) causes of fever in a NEWLY diagnosed cancer patient (no chemo yet)

A
  • tumour or cancer fever

- community stuff (S pneumo, resp viruses)

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6
Q

febneut patient with no symptoms: how to approach

A
  1. think of bacteria from denuded gut
  2. think of community things (pneumonia, respiratory viruses)
  3. persistent fever even on broad spectrum Abx, think fungal (candida, aspergillus)
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7
Q

febneut approach in symptomatic patient:

A
  • redness or painful IV = central line sepsis

- diarrhea: think C.diff

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8
Q

(imp) most common cause of bacteremia in cancer chemo patient

A

CoNS (staph epidermidis)

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9
Q

febneut approach in patient with symptoms of mucositis and shock

A

-gut bacteria
-pneumonia, resp viruses
-fungi
-CoNS
(all the previously said) and
STREP VIRIDANS (add this one if see these symptoms)

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10
Q

(imp?) organisms that must always be covered at least (as empiric Abx for the febneut)

A
  • gut bacteria (including anaerobes)
  • pseudomonas
  • staph aureus
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11
Q

(imp?) organisms that must always be covered if there is presence of mucositis or shock (as empiric Abx for the febneut)

A
  • gut bacteria (including anaerobes)
  • pseudomonas
  • staph aureus
  • strep viridans
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12
Q

(imp?) organisms that we must worry about when choosing empiric Abx for febneut if we know or are worried about resistance

A
  • MRSA
  • VRE
  • ESBL (extended spectrum beta lactamases, are gram- bacteria)
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13
Q

(EXAM) broad spectrum Abx required to cover gram- of gut, staph aureus and pseudomonas

A

-broad spectrum beta-lactams (meaning beta-lactam + bli, like Pip/Tazo)
-aminoglycosides IV
-vanco IV
(if oral therapy at home = ciproflaxin + clindamycin)

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14
Q

when give empiric antifungal tx in febneut

A
  • NOT in beginning unless clinical evidence for FUNGAL infection
  • only if fever persists >4 days in cancer pt for febneut
  • *never stop Abx**
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15
Q

how to investigate for fungal infection in febneut when suspect it

A
  • check where candida caused disease: 1. liver and spleen imaging 2. retinal exam 3. chest CT
  • invasive pulmonary aspergillosis will be seen on chest CT
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16
Q

(imp?) best anti-fungal against aspergillosis in febneut pts

A

voriconazole

17
Q

when to give empiric anti-viral tx in febneut

A

NOT in the beginning and usually never UNLESS

  • characteristic rash of VZV, shingles or herpes
  • severe resp illness (influenza)
18
Q

3 phases of BMT

A
  • phase 1: pre-engraftment (neutropenia, barrier breakdown, mucositis and CVC access)
  • phase 2: post-engraftment (impaired cellular and humoral immunity. these cells recover in that order: NK, CD8 T. still restricted T cell repertoire
  • phase 3: late phase (impaired cellular and humoral immunity. these cells recovering: B, CD4 T. repertoire diversifies.
19
Q

(important) infections in phase 1 of BMT (bacteria, viruses, fungi)

A
  • gram- rods (bacilli)
  • gram+ organisms
  • HSV
  • resp and enteric viruses
  • aspergillus
  • candida
20
Q

(important) infections in phase 2 of BMT (bacteria, viruses, fungi)

A

-reactivation of latent viruses and organisms (CMV, EBV, HSV, VZV, TB)
-aspergillosis
(chronic viruses back. gut healing so less gram-)

21
Q

(important) infections in phase 3 of BMT (bacteria, viruses, fungi)

A
  • encapsulated bacteria (prob now bc immune system never back 100%)
  • VZV
  • aspergillus
  • pneumocystis
  • opportunistic pathogens
22
Q

(important) what organisms to cover in febneut

A

-gut organisms (including anaerobes)
-pseudomonas aeruginosa
-staph aureus
-respiratory
organisms
(beta-lactam+bli comination AND aminoglycoside)

23
Q

(important) when to use big things like vanco in febneut

A

ONLY if:

  • shock
  • mucositis
  • line sepsis
  • known MRSA
  • known bacteremia with g+ cocci
24
Q

infections in people with humoral immunity dysfunction

A
  • Strep pneumo
  • H. influenza
  • mycoplasma spp
  • moraxella
  • recurrent sinopulmonary infections with community organisms*
25
Q

function of humoral immunity against infections

A
  • secretory Abs in mouth and resp tract

- not functioning = sinusitis, recurrent ear infection, pneumonias

26
Q

cellular immunity dysfunction: infections you get

A
  • IC organisms: salmonella, listeria, mycobacterium spp

- fungi (inc. pneumocystis), viruses, parasites (inc. toxoplasma)

27
Q

cellular immunity dysfunction can happen how

A
  • SCID (no lymphoid tissue, no tonsils)
  • HIV
  • large amount systemic CSs
28
Q

complement immunity dysfunction = get what recurrent infection

A

Neisseria meningitidis

prob in MAC

29
Q

infections in neutropenic pts (not due to chemo)

A

community organisms

  • S. pneumo
  • S. aureus
  • Mycoplasma spp
  • resp viruses
  • N meningitidis
  • UTIs
30
Q

infection in Jobe’s syndrome

A

staph aureus (skin disease boils and all that)

31
Q

infections in CGD (chronic granulomatous disease, macrophages can’t do oxidative burst after phagocytosis)

A

catalase + organisms

  • S aureus
  • Aspergillus
32
Q

infections in asplenic or splenic dysfct people

A

encapsulated organisms (S pneumo, H influenza, N meningitidis) and also salmonella spp if have sickle cell

33
Q

management of fever in babies <3 months

A

medical emergency (especially if under 6 months of age)

34
Q

organisms babies can get infected with because of maternal stool and vaginal organisms and maternal organisms

A
  • enteric gram- rods
  • GBS
  • listeria
  • S aureus (MSSA, MRSA)
  • GAS
  • HSV (sepsis, encephalitis)
35
Q

organisms premature babies can be infected

A

candida albicans and all the previous (-enteric gram- rods

  • GBS
  • listeria
  • S aureus (MSSA, MRSA)
  • GAS
  • HSV (sepsis, encephalitis))
36
Q

approach to febrile neonates <1 months

A
  • presume serious bacterial infection
  • full septic workup (blood, urine cultures), LP culture
  • empiric Abx covering gram-, listeria, GBS
  • CXR, nasopharyngeal viral studies, stool culture
  • meningitis doses of ampicillin and cefotaxime if suspected
37
Q

acyclovir to febrile neonates: yes or no

A
  • not in current practice

- but delaying it increases mortality…

38
Q

tx of febrile neonates <1 month

A
  • ampicillin IV
  • gentamicin IV
  • cefotaxime IV for meningitis (3rd gen cephalosporin)
39
Q

tx of febrile neonates between 1-3 months of age

A

-option 1: ampicillin IV
+ gentamicin IV
-option 2: -ampicillin IV + cefotaxime IV for meningitis (3rd gen cephalosporin)