Acyclovir: Difference between revisions

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== Background ==
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*Acyclic guanosine analog that competes with deoxyguanosine triphosphate to inhibit viral DNA polymerase
 
*Acyclic guanosine analog that competes with deoxyguanosine triphosphate to inhibit viral DNA polymerase
 
*Resistance mediated by mutation in or decrease of thymidine kinase
 
*Resistance mediated by mutation in or decrease of thymidine kinase
 
*Good penetration into CNS and vitreous if administered intravenously, though not orally[[CiteRef::huynh2008vi]]
 
*Good penetration into CNS and vitreous if administered intravenously, though not orally[[CiteRef::huynh2008vi]]
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== Dosing ==
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* Usual dose:
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** 5-10 mg/kg ideal body weight IV q8h
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** 200-400 mg PO 5 times daily
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** 800 mg PO 5 times daily (high dose)
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* [[Herpes encephalitis]]: 10 mg/kg ideal body weight IV q8h
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=== Renal Adjustment ===
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* Oral
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** CrCl 30-49: usual dose
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** CrCl 10-29: usual dose
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** CrCl <10: usual dose q12h
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** Intermittent dialysis: 50% of usual dose q24h, given after dialysis on dialysis days
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** Continuous dialysis: usual dose
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* Intravenous
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** CrCl 30-49: usual dose q12h
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** CrCl 10-29: usual dose q24h
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** CrCl <10: 50% of dose q24h
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** Intermittent dialysis: 50% of usual dose q24h, given after dialysis on dialysis days
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** Continuous dialysis: usual dose
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== Safety ==
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*Adverse drug reactions include:
 
*Adverse drug reactions include:
 
**[[Adverse drug reaction::Acute kidney injury]] from crystal deposition, so maintain hydration
 
**[[Adverse drug reaction::Acute kidney injury]] from crystal deposition, so maintain hydration

Latest revision as of 20:25, 2 May 2021

Background

  • Acyclic guanosine analog that competes with deoxyguanosine triphosphate to inhibit viral DNA polymerase
  • Resistance mediated by mutation in or decrease of thymidine kinase
  • Good penetration into CNS and vitreous if administered intravenously, though not orally1

Dosing

  • Usual dose:
    • 5-10 mg/kg ideal body weight IV q8h
    • 200-400 mg PO 5 times daily
    • 800 mg PO 5 times daily (high dose)
  • Herpes encephalitis: 10 mg/kg ideal body weight IV q8h

Renal Adjustment

  • Oral
    • CrCl 30-49: usual dose
    • CrCl 10-29: usual dose
    • CrCl <10: usual dose q12h
    • Intermittent dialysis: 50% of usual dose q24h, given after dialysis on dialysis days
    • Continuous dialysis: usual dose
  • Intravenous
    • CrCl 30-49: usual dose q12h
    • CrCl 10-29: usual dose q24h
    • CrCl <10: 50% of dose q24h
    • Intermittent dialysis: 50% of usual dose q24h, given after dialysis on dialysis days
    • Continuous dialysis: usual dose

Safety

  • Adverse drug reactions include:

References

  1. ^  Tony H. Huynh, Mark W. Johnson, Grant M. Comer, Douglas N. Fish. Vitreous Penetration of Orally Administered Valacyclovir. American Journal of Ophthalmology. 2008;145(4):682-686. doi:10.1016/j.ajo.2007.11.016.