Clostridioides difficile: Difference between revisions

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Clostridioides difficile
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(Added risk factors and citations)
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== Microbiology ==
+
== Background ==
  +
=== Microbiology ===
 
 
* Spore-forming, anaerobic, Gram-positive bacillus
 
* Spore-forming, anaerobic, Gram-positive bacillus
   
== Clinical Presentation ==
+
=== Risk factors ===
  +
* Antibiotic exposure, typically broad-spectrum antibiotics especially those with anaerobic coverage[[CiteRef::brown2013me]]
  +
** Clindamycin
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** Fluoroquinolones (especially with NAP1 strain)
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** Cephalosporins
  +
** Monobactams
  +
** Carbapenems
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* PPI use
   
  +
  +
== Clinical Presentation ==
 
* Profuse watery diarrhea
 
* Profuse watery diarrhea
   
 
=== Severity ===
 
=== Severity ===
 
 
{| class="wikitable"
 
{| class="wikitable"
  +
! Severity !! Definition[[CiteRef::loo2018as]]
! Severity
 
! Definition
 
 
|-
 
|-
 
| Mild || WBC ≤15 AND creatinine ≤1.5 x baseline
| Mild
 
| WBC ≤15 AND creatinine ≤1.5 x baseline
 
 
|-
 
|-
| Severe, uncomplicated
+
| Severe, uncomplicated || WBC >15 OR creatinine >1.5 x baseline OR hypoalbuminemia
| WBC >15 OR creatinine >1.5 x baseline OR hypoalbuminemia
 
 
|-
 
|-
| Severe, complicated
+
| Severe, complicated || Hypotension OR shock OR ileus OR megacolon
| Hypotension OR shock OR ileus OR megacolon
 
 
|}
 
|}
   
 
=== Children ===
 
=== Children ===
 
 
* Asymptomatic carriage is common in infants (37% at 1 month, decreasing to adult levels of 3-5% by 3 years) [[CiteRef::pediatrics2012cl]]
 
* Asymptomatic carriage is common in infants (37% at 1 month, decreasing to adult levels of 3-5% by 3 years) [[CiteRef::pediatrics2012cl]]
 
** Thought to be related to a lack of the binding target of ''C. difficile'' toxin
 
** Thought to be related to a lack of the binding target of ''C. difficile'' toxin
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== Management ==
 
== Management ==
 
 
{| class="wikitable"
 
{| class="wikitable"
 
! Severity
 
! Severity
! First-line
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! First-line[[CiteRef::loo2018as]]
 
! Alternatives
 
! Alternatives
 
|-
 
|-
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== Further Reading ==
 
== Further Reading ==
 
 
* [https://www.ammi.ca/Content/AMMI%20Canada%20treatment%20practice%20guidelines%20for%20Clostridium%20difficile%20infection%2Epdf AMMI treatment practice guidelines for Clostridium difficile infection 2018]
 
* [https://www.ammi.ca/Content/AMMI%20Canada%20treatment%20practice%20guidelines%20for%20Clostridium%20difficile%20infection%2Epdf AMMI treatment practice guidelines for Clostridium difficile infection 2018]
 
* Clostridioides difficile: diagnosis and treatments. ''BMJ''. 2019;366:l4609. doi: [https://doi.org/10.1136/bmj.l46091 10.1136/bmj.l46091]
 
* Clostridioides difficile: diagnosis and treatments. ''BMJ''. 2019;366:l4609. doi: [https://doi.org/10.1136/bmj.l46091 10.1136/bmj.l46091]

Revision as of 10:08, 31 October 2019

Background

Microbiology

  • Spore-forming, anaerobic, Gram-positive bacillus

Risk factors

  • Antibiotic exposure, typically broad-spectrum antibiotics especially those with anaerobic coverage1
    • Clindamycin
    • Fluoroquinolones (especially with NAP1 strain)
    • Cephalosporins
    • Monobactams
    • Carbapenems
  • PPI use


Clinical Presentation

  • Profuse watery diarrhea

Severity

Severity Definition2
Mild WBC ≤15 AND creatinine ≤1.5 x baseline
Severe, uncomplicated WBC >15 OR creatinine >1.5 x baseline OR hypoalbuminemia
Severe, complicated Hypotension OR shock OR ileus OR megacolon

Children

  • Asymptomatic carriage is common in infants (37% at 1 month, decreasing to adult levels of 3-5% by 3 years) 3
    • Thought to be related to a lack of the binding target of C. difficile toxin
  • Clinical disease is rare before 12 to 24 months of age

Management

Severity First-line2 Alternatives
Initial episode
Mild to moderate Vancomycin 125 mg po QID for 10-14 days Fidaxomicin 200 mg po BID for 10 days
Metronidazole 500 mg po TID for 10-14 days
Severe, uncomplicated Vancomycin 125 mg po QID for 10-14 days
Fidaxomicin 200 mg po BID for 10 days
Severe, complicated Vancomycin 125-500 mg po QID for 10-14 days plus metronidazole 500 mg IV q8h Fidaxomicin 200 mg po BID for 10 days plus metronidazole 500 mg IV q8h
Consider rectal vancomycin if ileus
Recurrent episode
First recurrence, mild to moderate Vancomycin 125 mg po QID for 14 days Fidaxomicin 200 mg po BID for 10 days
First recurrence, severe, uncomplicated Vancomycin 125 mg po QID for 14 days
Fidaxomicin 200 mg po BID for 10 days
Second or subsequent recurrence Vancomycin as prolonged tapered or pulsed regimen Consider fecal microbiota tranplantation after vancomycin
  • For rectal vancomycin, add 500 mg to 100 mL normal saline and give as retention enema every 6 hours
  • A sample vancomycin taper: 125 mg po QID for 14 days, then 125 mg po TID for 7 days, then 125 mg po BID for 7 days, then 125 mg po daily for 7 days, then 125 mg po q2-3d for 2 to 8 weeks

Further Reading

References

  1. ^  Kevin A. Brown, Nagham Khanafer, Nick Daneman, David N. Fisman. Meta-Analysis of Antibiotics and the Risk of Community-Associated Clostridium difficile Infection. Antimicrobial Agents and Chemotherapy. 2013;57(5):2326-2332. doi:10.1128/aac.02176-12.
  2. a b  Vivian G Loo, Ian Davis, John Embil, Gerald A Evans, Susy Hota, Christine Lee, Todd C Lee, Yves Longtin, Thomas Louie, Paul Moayyedi, Susan Poutanen, Andrew E Simor, Theodore Steiner, Nisha Thampi, Louis Valiquette. Association of Medical Microbiology and Infectious Disease Canada treatment practice guidelines for Clostridium difficile infection. Official Journal of the Association of Medical Microbiology and Infectious Disease Canada. 2018;3(2):71-92. doi:10.3138/jammi.2018.02.13.
  3. ^   Clostridium difficile Infection in Infants and Children. Pediatrics. 2012;131(1):196-200. doi:10.1542/peds.2012-2992.