The genus Pseudomonas >140 species,> saprophytic & >25 species are associated with humans. Most known to cause disease in humans are associated with opportunistic infections.
⬆️ MR : ⬇️ host defenses, resistance to ABX & production of extracellular enzymes & toxins.
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Often found in water in sinks & can contaminate respiratory equipment, which can serve as an environmental reservoir, especially in ICUs. Is the most serious pathogen causing ventilator-associated pneumonia & remains the most important pathogen in patients with CF.
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The green pigment produced by Pseudomonas aeruginosa is easily seen on Mueller-Hinton agar plate used for disk antimicrobial susceptibility testing.
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Resistance mechanism
-AmpC beta-lactamase
-Extended-spectrum beta-lactamase
-Downregulation of the outer membrane protein OprD, a carbapenem-specific porin
-Multidrug efflux pumps
-Ability of the organism to form a biofilm
-Possible transfer of a 16S rRNA methylase gene.
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Virulence Factors of Pseudomonas aeruginosa:
The three major types of virulence factors in P. aeruginosa include; factors involved in attachment and motility, factors involved in colonization, & factors involved in chronic infection.
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Pathogenesis of Pseudomonas aeruginosa:👇👇👇
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Rx of P. aeruginosa Infec:
A large SR & MA found that the most effective measures for preventing the development of an MDR inf in the ICU was combination of standard care (hand hygiene & contact precautions), antimicrobial stewardship, environmental cleaning, & source control.
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Common antibiotics that are used as first-line therapy include carbapenems, cephalosporins, aminoglycosides, and fluoroquinolones.
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Oral antibiotics:
Fluoroquinolones are the only antibiotic class available as an oral formulation that is reliably active. Ciprofloxacin: dosed 750 mg orally x 12 hours & levofloxacin 750 mg x daily. For PA alone infection, levofloxacin has no advantage over ciprofloxacin.
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Multidrug-Resistant PA Infections:
A significant clinical challenge and can substantially complicate the approach to selection of optimal antibiotic therapy.
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Combination antibiotic therapy is not routinely recommended for infections caused by DR-PA if in vitro susceptibility to a first-line antibiotic (i.e., ceftolozane-tazobactam, ceftazidime-avibactam, or imipenem-cilastatin-relebactam) has been confirmed.
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Nebulized antibiotics for the treatment of respiratory infections caused by DR-P aeruginosa is not recommended.
Most ID guidelines are based- either expert opinions or evidence-based medicine. Historically, duration of ABX Rx were based on arbitrary extension of days(magic numbers like 7, 10 & 14 days) rather than on reliable evidence with the main aim to ⬇️ failures & avoid underRx.
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There is growing evidence to support for shorter courses. It is important for prescribers to be up to date with best practices. Duration of therapy plays a pivotal role in antimicrobial stewardship programme within the global effort to optimize antibiotic use &⬇️resistance.
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4-chloro-N-(2-furyl-methyl)-5-sulfamoyl-anthranilic acid, member of the sulfa’s. Potent natriuretic drug, inhibits Na+-K+-2Cl− cotransporter in the ascending limb of the loop of Henle.
Direct Vd effects results in its therapeutic effectiveness in the Rx of acute pulm edema.
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Vasodilation leads to reduced responsiveness to vasoconstrictors, such as angiotensin II and noradrenaline, and decreased production of endogenous natriuretic hormones with vasoconstricting properties.
Mast cell–derived mediators tend to affect layers superficial to subcutaneous tissue, including the dermal-epidermal junction. These mediators cause urticaria & pruritus.
In bradykinin-mediated angioedema, the dermis is usually spared, so urticaria & pruritus are absent.