infectious diarrhea and CDI Flashcards

1
Q

definition of acute infectious diarrhea

A

passage of loose or watery stool >=3 times in a 24h period that lasts for <14 days

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2
Q

sources of infectious diarrhea

A
  • international trvel
  • food or water borne
  • exposure to infeced animal or feces
  • recent antimicrobial use
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3
Q

how is acute infectious diarrhea trasnmitted

A

likely fecal to oral route

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4
Q

what diagnositic testing is doen for acute infectious diarrhea

A
  • lab test not routinely done
  • rec in pt with diarrhea with fever, bloody or mucoid stools, severe ab cramping or tenderness, signs of sepsis
  • test of salmonella, shigella,cD…

stool culture and PCR done

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5
Q

when is ab tx recommended for acute infectious diarrhea?

A
  • pt has severe disease (fever, bloody or mucoid stools, severe ab cramping or tenderness)
  • pt appears septic
  • pt is immunocomprimised host
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6
Q

what is the empiric therapy for AID?

A
  • Ceftriaxone 2g IV q24h
    or
  • ciprofloxacin 500mg PO BD
    for 3-5 days
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7
Q

what is Clostridioides difficile(C.diff)

A
  • gram pos, anaerobic, sport forming, otxin producing bacillus
  • colonize intestinal tract
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8
Q

how iare c diff infections caused

A

facilitated by disruption of norma; intestinal flora

often due to ab therapy

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9
Q

what are the clinical manifestations of CDI

A
  • diarrhea without colitis: >= 3 ep of unformed stools in 24h
  • colitis: fver, ab pain, nausea, anorexia
  • severe colitis: sepsis, sig leukocytosis, renal impairment
  • fulminant colitis (severe + complicated): eg. toxic megacolon, colonic perforation, intestinal paralysis
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10
Q

risk factors of cdi

A

pharmacotherapy

  • number and days of systemic concomitant ab use
  • high risk ab (eg. clindamycin, FQ)
  • PPI

past healthcare exposure

  • prior hospitalisation
  • duration of hospitalisation
  • long term care residnecy

host immunity
- lack of ab response to65 yo

C c diff toxin

  • severity of underlying illness
  • comorb

increasing age
- >65 yo

CDI experience
- prior CDI infection

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11
Q

risk factors of cdi

A

antibiotic

  • highest risk during ab tx and 1 month post
  • high risk ab: clindamycin, 3/4th gen cephalosporin, FQ
  • exposure dep: number, dose and duration of ab

ppi

  • reduction of gastric acid may allow ingested c diff to survive
  • discont. unnec ppi
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12
Q

diagnosis of cdi

A
  • unexplained and new onset diarrhea
    AND
    positive stool test result for toxigenic c diff or its toxins
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13
Q

what are the 3 major tests done to diagnose cdi?

A
  • glutamate dehydrogenase GDH EIA: detect c diff common antigen
  • toxin A and B EIA: detect toxins a and b
  • nucleic acid amplication tests (NAAT): detects c diff toxigenic genes, may detect colonisation and not true cdi
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14
Q

how is CDI transmitted

A
  • likely fecal to oral route

- healthcare setting: exposure to contaminated envr or hands of healthcare personnel, transiently contam with spores

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15
Q

how is cdi controlled

A
  • isolatio measurs for infected pt
  • appropriate PPE when caring for infected pt
  • practice good hand hygeien before and after contact with pt
  • infection control strategies implemented ine every suspected case, not only confirmed

envr management
- sporicidal disinfectant to cleanse reusable equipment

antimicrobial stewardship
- minimise freq and duration of high risk ab therapy

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16
Q

tx for initial episode, non severe CDI

A
  • vancomycin (VAN) 125mg PO q6h for 10 days
  • fidazomicin (FDX) 200mg PO q12h for 10 days (not not registered in sg)

alt tx
- metronidazole 400mg PO q8h for 10 days

17
Q

tx for initial episode, severe CDI

A
  • VAN 125mg PO q6h for 10 days
  • fidazomicin (FDX) 200mg PO q12h for 10 days
  • metronidazole NOT REC
18
Q

tx for initial episode, fulminant CDI

A
  • VAN 500mg PO q6h by mouth or NG tube
  • metronidazole 500mg IV q8h

if ileus:

  • combi of VAN and metronidazole rec
  • consider adding PR VAN 500mg in 100ml NS PR q6h (rectal instillation via enema)
19
Q

what are some advantage of fidaxoamicin vs other CDI tx

A
  • display narrow sepc of activity
  • bactericifal (VAN is bacteriostatic)
  • lower MIC agaisnt c diff
  • prolonged post ab effect, require less frequent dosing
  • higher rate of sx cure with FDX
  • FDX assc with lower CDI recurrence rate
20
Q

diadvantage of FDX

A
  • expensive
  • limited data to support use in complicated cdi
  • not registered in sg
21
Q

tx of recurrent episodes of cdi

first recurrence

A

if metronidazole was used for initial
- VAN 125mg PO q6h for 10 days

if vAN of FDX used
- prolonged tapered or pulsed VAN regimen:
VAN125mg PO q6h x 10-14 days ==>
Van 125mg PO q12h x 7 days==>
VAN 125mg q24h x 7 days ==>
VAN 125mg PO every 2-3 days for 2-8 weeks

if VAN was used for initial
- FDX 200mg PO q12h for 10 days

22
Q

tx of recurrent episodes of cdi

2nd/3rd recurrence

A
  • tapered for pulsed VAN regimen
  • VAN 125mg PO q6h x 10 days followed by rifaximin 400mg PO q8h x 20 days
  • FDX 200mg PO q12h for 10 days

if failed appropriate ab therapy (for >= 2 recurrences)
- fecal microbiota transplantation: restore gut microbiata diversity via instillation of healthy donor stools into GIT of pt with recurrent cdi

23
Q

how do we monitor therapy of cdi

A

assess for resolution of sx

  • improvement in diarrhea freq and consistency (within few days of initiating tx with near complete resolution within 10 days)
  • resolution of leukocytosis
  • not rec to repeat stool testing to assess cure (significant proportion woudl test psoitive despite improvement)