Aminoglycosides: Difference between revisions

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==Background==
<br />


*Derived from [[Streptomyces]] (mycins &amp; kacins) or [[Micromonospora]] (micins)
== Background ==

*Derived from [[Streptomyces species]] (mycins &amp; kacins) or [[Micromonospora species]] (micins)


===Mechanism of Action===
===Mechanism of Action===
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*Good coverage of Gram-negative aerobes
*Good coverage of Gram-negative aerobes
**Except Stenotrophomonas and Burkholderia
**Except [[Stenotrophomonas]] and [[Burkholderia]]
*Streptomycin also covers mycobacterium
*[[Streptomycin]] also covers mycobacterium
*Some protozoal coverage
*Some protozoal coverage
*Can cover Gram-positives if cell wall is disrupted (e.g. by beta-lactam)
*Can cover Gram-positives if cell wall is disrupted (e.g. by beta-lactam)
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*Altered 50S ribosomal subunit
*Altered 50S ribosomal subunit
*Decreased uptake and accumulation (Pseudomonas)
*Decreased uptake and accumulation ([[Pseudomonas]])
*Decreased membrane permeability
*Decreased membrane permeability
*Efflux (E. coli)
*Efflux pump ([[Escherichia coli]])
*Aminoglycoside-modifying enzymes (Enterococcus)
*Aminoglycoside-modifying enzymes ([[Enterococcus]])


===Pharmacokinetics and Pharmacodynamics===
===Pharmacokinetics and Pharmacodynamics===
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===Initial Dose===
===Initial Dose===


If actual body weight more than 20% higher than ideal body weight, need to calculate adjusted body weight (ABW)
*If actual body weight more than 20% higher than [https://www.mdcalc.com/ideal-body-weight-adjusted-body-weight ideal body weight], need to calculate [https://www.mdcalc.com/ideal-body-weight-adjusted-body-weight adjusted body weight] (ABW)


$$ABW = IBW + 0.4 \times (actual BW - IBW)$$
$$ABW = IBW + 0.4 \times (actual BW - IBW)$$
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===Traditional Dosing===
===Traditional Dosing===


*Q8H dosing
*Used for Enterococcus IE, meningitis, septic shock, ascites, AKI/CKD, prefnancy, surgical prophylaxis, burns, osteomyelitis
*Used for [[Enterococcus]] IE, [[meningitis]], [[septic shock]], [[ascites]], [[AKI]]/[[CKD]], [[pregnancy]], surgical prophylaxis, [[Burn infection|burns]], [[osteomyelitis]]
*1.7mg/kg (5-7.5mg/kg amikacin)
*1.7 mg/kg (5-7.5 mg/kg [[amikacin]]) IV q8h


===Extended Interval Dosing===
===Extended Interval Dosing===


*Q24H dosing, which is safer but less well-studied
*7mg/kg (15mg/kg amikacin)
*7 mg/kg (15 mg/kg [[amikacin]]) IV, frequency depends on [[CrCl]]
*Use Hartford nomogram with a random level (but remember to halve the amikacin level first)
*CrCl ≥60 q24h
**[[CrCl]] ≥60 q24h
**[https://www.mdcalc.com/creatinine-clearance-cockcroft-gault-equation CrCl] 40-59 q36h
*CrCl 40-59 q36h
**[https://www.mdcalc.com/creatinine-clearance-cockcroft-gault-equation CrCl] 20-39 q48h
*CrCl 20-39 q48h
*CrCl ≤19 don't use
**[https://www.mdcalc.com/creatinine-clearance-cockcroft-gault-equation CrCl] ≤19 don't use
*Use [[Hartford nomogram]] with a random level (but remember to halve the [[amikacin]] level first)


===Dialysis Dosing===
===Dialysis Dosing===
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===Synergy===
===Synergy===


*1mg/kg divided q8-12h, peak target 3-5, trough &lt;2
*1 mg/kg divided q8-12h, peak target 3-5, trough &lt;2


=== Monitoring ===
===Monitoring===


====Peak====
====Peak====


*30min after third dose
*30 minutes after third dose
*Response is based on peak:MIC ratio, target is 8-10 times
*Response is based on peak:MIC ratio, target is 8-10 times
*If below target, increase dose
*If below target, increase dose
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====Trough====
====Trough====


*Prior to 4th dose, or a random level at 24-48h in renal failure
*Prior to 4th dose, or a random level at 24 to 48h in renal failure
*Side effects are predicted by trough levels
*Side effects are predicted by trough levels
*Tobra &lt;0.5 (extended) or &lt;2 (traditional)
*[[Tobramycin]] &lt;0.5 (extended) or &lt;2 (traditional)
*Amikacin &lt;1 (extended) or &lt;?? (traditional)
*[[Amikacin]] &lt;1 (extended) or &lt;?? (traditional)
*If above target, increase interval
*If above target, increase interval


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[[File:Hartford_nomogram.png]]
[[File:Hartford_nomogram.png]]


*Dosing interval is whichever is the line just above the random level
* Double the concentration for [[amikacin]]
*Double the concentration for [[amikacin]]


== Safety ==
==Safety==


===Adverse Drug Reactions===
===Adverse Drug Reactions===

Latest revision as of 18:46, 11 January 2024

Background

Mechanism of Action

  • Requires electron transport chain (ETC) to cross over the membrane
    • Anaerobes are therefore inherently resistant
  • Reversibly binds 30S ribosomal subunit, which stops proofreading and causes accumulation of bad proteins

Spectrum of Activity

  • Good coverage of Gram-negative aerobes
  • Streptomycin also covers mycobacterium
  • Some protozoal coverage
  • Can cover Gram-positives if cell wall is disrupted (e.g. by beta-lactam)

Mechanisms of Resistance

Pharmacokinetics and Pharmacodynamics

  • Poor membrane penetration, therefore doesn't cross over into lungs and CSF
  • Half-life 2-3 hours (longer in CKD)
  • Excreted 99% unchanged in urine
  • Displays concentration-depedent killing with a prolonged post-antibiotic effect (2-13 hours)

Dosing

Initial Dose

$$ABW = IBW + 0.4 \times (actual BW - IBW)$$

Traditional Dosing

Extended Interval Dosing

  • Q24H dosing, which is safer but less well-studied
  • 7 mg/kg (15 mg/kg amikacin) IV, frequency depends on CrCl
  • Use Hartford nomogram with a random level (but remember to halve the amikacin level first)

Dialysis Dosing

  • Pre-HD levels with post-HD doses, though this may change

Synergy

  • 1 mg/kg divided q8-12h, peak target 3-5, trough <2

Monitoring

Peak

  • 30 minutes after third dose
  • Response is based on peak:MIC ratio, target is 8-10 times
  • If below target, increase dose

Trough

  • Prior to 4th dose, or a random level at 24 to 48h in renal failure
  • Side effects are predicted by trough levels
  • Tobramycin <0.5 (extended) or <2 (traditional)
  • Amikacin <1 (extended) or <?? (traditional)
  • If above target, increase interval

Hartford Nomogram

Hartford nomogram.png

  • Dosing interval is whichever is the line just above the random level
  • Double the concentration for amikacin

Safety

Adverse Drug Reactions

  • Nephrotoxicity (0-50%), usually non-oliguric AKI with decreased Ca/Mg resorption, often reversible
    • Decreased protein synthesis
    • Decreased cellular respiration
    • Increased apoptosis
    • Necrosis in proximal tubules
  • Ototoxicity (0-60%), irreversible
    • Cumulative effect
    • Distribute into the perilymph of the ear, and cause free radical formation causing apoptosis of hair cells
    • Needs hearing tests, because it can be subclinical
      • Monitor audiometry weekly
  • Vestibulotoxicity (0-20%), irreversible
  • Rarely, neuromuscular blockade

Monitoring

  • Trough levels
  • Creatinine
  • Weekly audiometry