Tissue penetration of antimicrobials: Difference between revisions

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== Summary ==
==Summary==
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{| class="wikitable"
!Class
!Class
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*† if inflammation present
*† if inflammation present


== Prostate ==
==Prostate==


* Poorly penetrated by most antibiotics
*Poorly penetrated by most antibiotics
* Penetration is higher with a high concentration gradient, high lipid solubility, low degree of ionization, high dissociation constant, low protein binding, and small molecular size
*Penetration is higher with a high concentration gradient, high lipid solubility, low degree of ionization, high dissociation constant, low protein binding, and small molecular size
* [[Fluoroquinolones]] are the mainstay of therapy, though there is increasing resistance
*[[Fluoroquinolones]] are the mainstay of therapy, though there is increasing resistance
* [[TMP-SMX]] often used, but unclear if the [[sulfamethoxazole]] component actually reaches the prostate
*[[TMP-SMX]] often used, though conflicting data about its penetration into the prostate
* [[Minocycline]], [[doxycycline]], and [[macrolides]] achieve high levels in the prostate but are rarely indicated for the causative organisms
*[[Minocycline]], [[doxycycline]], and [[macrolides]] achieve high levels in the prostate but are rarely indicated for the causative organisms
* Third-generation [[cephalosporins]] and [[carbapenems]] can be used
*Third-generation [[cephalosporins]] and [[carbapenems]] can be used
* [[Piperacillin]], [[aztreonam]], [[imipenem]], and some [[aminoglycosides]] are likely useful
*[[Piperacillin]], [[aztreonam]], [[imipenem]], and some [[aminoglycosides]] are likely useful


[[Category:Antimicrobials]]
[[Category:Antimicrobials]]

Revision as of 18:44, 16 September 2020

Summary

Class Antimicrobial Blood CNS Urine Prostate Necrotic
Antibiotics: Ξ²-Lactams
Penicillins Ξ²-lactamase inhibitors –
ampicillin + –
piperacillin-tazobactam +†
Cephalosporins first-generation cephalosporins – –
second-generation cephalosporins –
third-generation cephalosporins +†
cefepime +
ceftazidime + +
Cephamycins cephamycins –
cefoxitin –
Carbapenems imipenem +
Antibiotics: Non-Ξ²-Lactams
Aminoglycosides –
Chloramphenicol chloramphenicol +
Fluoroquinolones –? + +
Fosfomycin fosfomycin +
Lincosamides clindamycin – +
Macrolides macrolides – +
Nitrofurans nitrofurantoin – – + – –
Nitroimidazoles metronidazole +
Rifamycins rifampin +
Sulfonamides trimethoprim-sulfamethoxazole +
Tetracyclines tetracyclines – +
doxycycline + +
Antifungals
Azoles fluconazole +
Class Antimicrobial Blood CNS Urine Prostate Necrotic
  • † if inflammation present

Prostate

  • Poorly penetrated by most antibiotics
  • Penetration is higher with a high concentration gradient, high lipid solubility, low degree of ionization, high dissociation constant, low protein binding, and small molecular size
  • Fluoroquinolones are the mainstay of therapy, though there is increasing resistance
  • TMP-SMX often used, though conflicting data about its penetration into the prostate
  • Minocycline, doxycycline, and macrolides achieve high levels in the prostate but are rarely indicated for the causative organisms
  • Third-generation cephalosporins and carbapenems can be used
  • Piperacillin, aztreonam, imipenem, and some aminoglycosides are likely useful

References

  1. ^  Cornelia B. Landersdorfer, JΓΌrgen B. Bulitta, Martina Kinzig, Ulrike Holzgrabe, Fritz SΓΆrgel. Penetration of Antibacterials into Bone. Clinical Pharmacokinetics. 2009;48(2):89-124. doi:10.2165/00003088-200948020-00002.
  2. ^  L. Brockhaus, D. Goldblum, L. Eggenschwiler, S. Zimmerli, C. Marzolini. Revisiting systemic treatment of bacterial endophthalmitis: a review of intravitreal penetration of systemic antibiotics. Clinical Microbiology and Infection. 2019;25(11):1364-1369. doi:10.1016/j.cmi.2019.01.017.