Pseudomonas aeruginosa: Difference between revisions

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Pseudomonas aeruginosa
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===Microbiology===
 
===Microbiology===
   
*Oxidase [[Oxidase::positive]], non-fermenting [[Stain::Gram-negative]] [[Cellular shape::bacillus]]
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*Oxidase [[Oxidase::positive]], non-fermenting [[Stain::Gram-negative]] [[Shape::bacillus]]
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  +
=== Definitions of Drug Resistance ===
  +
  +
* '''Multidrug resistant (MDR)''' is defined as non-susceptibility to at least 1 antibiotic in at least 3 antibiotic classes (penicillins, cephalosporins, fluoroquinolones, aminoglycosides, and carbapanems)
  +
** Results from decreased OprD, AmpC hyperproduction, upregulation of efflux pumps, and PBP target mutations
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** Carbapenemase production is uncommon but increasing
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* '''Extensively drug-resistant (XDR)''' is resistant to more than one antimicrobial agent in all the antimicrobial categories, except in two or less
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* '''Pan-drug-resistant (PDR)''' is resistant to all antimicrobial agents in all antimicrobial categories
   
 
===Mechanisms of Resistance===
 
===Mechanisms of Resistance===
   
*Broad intrinsic and acquired antibiotic resistance
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*Broad intrinsic and acquired antibiotic resistance[[CiteRef::livermore2002mu]]
 
*Membrane impermeability
 
*Membrane impermeability
**Decreased or absent OprD porin: resistance to carbapenems ([[imipenem]] and [[meropenem]])
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**Decreased or absent OprD porin: resistance to [[carbapenems]] ([[imipenem]] and [[meropenem]]) that may spare other β-lactams
 
**Membrane changes: resistance to polymixins ([[colistin]])
 
**Membrane changes: resistance to polymixins ([[colistin]])
 
**Reduced aminoglycoside transport: resistance to [[aminoglycosides]]
 
**Reduced aminoglycoside transport: resistance to [[aminoglycosides]]
 
*Efflux pumps
 
*Efflux pumps
**MexAB-OprM: resistance to fluoroquinolones and all β-lactams except [[imipenem]]
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**MexAB-OprM: resistance to [[fluoroquinolones]] and all [[β-lactams]] except [[imipenem]]
**MexCD-OprJ: resistance to fluoroquinolones and most β-lactams ([[cefoperazone]], [[cefpirome]], [[cefepime]], [[meropenem]]) but not [[imipenem]]
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**MexCD-OprJ: resistance to [[fluoroquinolones]] and most [[β-lactams]] ([[cefoperazone]], [[cefpirome]], [[cefepime]], [[meropenem]]) but not [[imipenem]]
**MexEF-OprN: resistance to fluoroquinolones and all β-lactams
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**MexEF-OprN: resistance to [[fluoroquinolones]] and all [[β-lactams]]
**MexXY-OprM: resistance to fluoroquinolones, most β-lactams (but not [[imipenem]]), and [[aminoglycosides]]
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**MexXY-OprM: resistance to [[fluoroquinolones]], [[tetracyclines]] including [[tigecycline]], most [[β-lactams]] (but not [[imipenem]] or [[ceftazidime]]), and [[aminoglycosides]]
 
*β-lactamases
 
*β-lactamases
**Derepressed AmpC β-lactamase: resistance to penicillins and cephalosporins (except [[ceftolozane]])
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**Derepressed AmpC β-lactamase: resistance to [[penicillins]] and [[cephalosporins]] (except [[ceftolozane]])
**Acquired carbapenemases such as NDM-1: resistance to essentially all β-lactam antibiotics
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**Acquired [[carbapenemases]] such as NDM-1: resistance to essentially all [[β-lactams]]
 
*Aminoglycoside-modifying enzymes: resistance to [[aminoglycosides]]
 
*Aminoglycoside-modifying enzymes: resistance to [[aminoglycosides]]
 
*Target site mutations
 
*Target site mutations
**Topoisomerase II (gyrA) or IV (parC) point mutations: resistance to fluoroquinolones
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**Topoisomerase II (gyrA) or IV (parC) point mutations: resistance to [[fluoroquinolones]]
   
 
===Epidemiology===
 
===Epidemiology===
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*Refer to [[antipseudomonal antibiotics]] for specific treatment options
 
*Refer to [[antipseudomonal antibiotics]] for specific treatment options
  +
*Preferred: [[piperacillin-tazobactam]], [[ceftazidime]], [[cefepime]], [[aztreonam]]
  +
**If repeat testing confirms resistant to carbapenems but susceptibility to other β-lactams (which is most commonly caused by decreased OprD), use an extended infusion of a β-lactam
  +
*Alternatives: [[meropenem]] or [[imipenem]]
 
*Double coverage (ß-lactam + non-ß-lactam) in cases of severe infection in order to ensure activity against the infection
 
*Double coverage (ß-lactam + non-ß-lactam) in cases of severe infection in order to ensure activity against the infection
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  +
=== Multidrug-Resistant Isolates ===
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* MDR-PA is defined as non-susceptibility to at least 1 antibiotic in at least 3 antibiotic classes (penicillins, cephalosporins, fluoroquinolones, aminoglycosides, and carbapanems)
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** Results from decreased OprD, AmpC hyperproduction, upregulation of efflux pumps, and PBP target mutations
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** Carbapenemase production is uncommon but increasing
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* Difficult-to-treat [[Pseudomonas aeruginosa]] is defined as non-susceptibility to all of: [[piperacillin-tazobactam]], [[ceftazidime]], [[cefepime]], [[aztreonam]], [[meropenem]], [[imipenem-cilastatin]], [[ciprofloxacin]], and [[levofloxacin]]
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* Consider any of the following options:
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** [[Amikacin]] 20 mg/kg IV once, followed by dosing per levels (see [[Aminoglycosides#Dosing|Aminoglycosides]])
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** [[Cefiderocol]] 2 g IV 18h infused over 3 hours
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** [[Ceftazidime-avibactam]] 2.5 g IV q8h infused over 3 hours
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** [[Ceftolozane-tazobactam]] 3 g IV q8h infused over 3 hours
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** [[Colistin]]
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** [[Gentamicin]] 7 mg/kg IV once followed by dosing per levels (see [[Aminoglycosides#Dosing|Aminoglycosides]])
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** [[Imipenem-relebactam]] 1.25 g IV q6h infused over 30 minutes
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** [[Plazomicin]] 15 mg/kg IV once followed by dosing per levels (see [[Aminoglycosides#Dosing|Aminoglycosides]])
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** [[Polymixin B]]
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** [[Tobramycin]] 7 mg/kg IV once followed by dosing per levels (see [[Aminoglycosides#Dosing|Aminoglycosides]])
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*Preference for [[ceftolozane-tazobactam]], [[ceftazidime-avibactam]], and [[imipenem-relebactam]], as well as [[cefiderocol]] if UTI
   
 
{{DISPLAYTITLE:''Pseudomonas aeruginosa''}}
 
{{DISPLAYTITLE:''Pseudomonas aeruginosa''}}

Latest revision as of 11:35, 11 July 2023

Background

Microbiology

  • Oxidase positive, non-fermenting Gram-negative bacillus

Definitions of Drug Resistance

  • Multidrug resistant (MDR) is defined as non-susceptibility to at least 1 antibiotic in at least 3 antibiotic classes (penicillins, cephalosporins, fluoroquinolones, aminoglycosides, and carbapanems)
    • Results from decreased OprD, AmpC hyperproduction, upregulation of efflux pumps, and PBP target mutations
    • Carbapenemase production is uncommon but increasing
  • Extensively drug-resistant (XDR) is resistant to more than one antimicrobial agent in all the antimicrobial categories, except in two or less
  • Pan-drug-resistant (PDR) is resistant to all antimicrobial agents in all antimicrobial categories

Mechanisms of Resistance

Epidemiology

  • Loves moist and wet environments
  • Causes healthcare-associated infections
    • UTI, SSI, bacteremia, HAP, VAP
    • Especially common in cystic fibrosis

Treatment

  • Refer to antipseudomonal antibiotics for specific treatment options
  • Preferred: piperacillin-tazobactam, ceftazidime, cefepime, aztreonam
    • If repeat testing confirms resistant to carbapenems but susceptibility to other β-lactams (which is most commonly caused by decreased OprD), use an extended infusion of a β-lactam
  • Alternatives: meropenem or imipenem
  • Double coverage (ß-lactam + non-ß-lactam) in cases of severe infection in order to ensure activity against the infection

Multidrug-Resistant Isolates

References

  1. ^  D. M. Livermore. Multiple Mechanisms of Antimicrobial Resistance in Pseudomonas aeruginosa: Our Worst Nightmare?. Clinical Infectious Diseases. 2002;34(5):634-640. doi:10.1086/338782.