Ganciclovir: Difference between revisions

From IDWiki
No edit summary
()
Line 1: Line 1:
== Background ==
+
==Background==
   
 
*Guanosine nucleoside analogue similar to acyclovir
 
*Guanosine nucleoside analogue similar to acyclovir
 
*Indications: {{#ask: [[Is treated by::ganciclovir]] | default=none}}
 
*Indications: {{#ask: [[Is treated by::ganciclovir]] | default=none}}
   
=== Mechanism of Action ===
+
===Mechanism of Action===
   
 
*Analog of deoxyguanosine, competes with deoxyguanosine to inhibit viral DNA polymerase
 
*Analog of deoxyguanosine, competes with deoxyguanosine to inhibit viral DNA polymerase
   
=== Mechanisms of Resistance ===
+
===Mechanisms of Resistance===
   
 
*Resistance in [[CMV]]
 
*Resistance in [[CMV]]
Line 14: Line 14:
 
**Can also develop through mutations in the target UL54 DNA polymerase
 
**Can also develop through mutations in the target UL54 DNA polymerase
   
=== Spectrum of Activity ===
+
===Spectrum of Activity===
   
* Active against [[HSV-1]], [[HSV-2]], [[VZV]], [[CMV]], [[HHV-6]], and [[HHV-8]]
+
*Active against [[HSV-1]], [[HSV-2]], [[VZV]], [[CMV]], [[HHV-6]], and [[HHV-8]]
   
=== Pharmacokinetics and Pharmacodynamics ===
+
===Pharmacokinetics and Pharmacodynamics===
   
 
*Oral bioavailability 6-8%
 
*Oral bioavailability 6-8%
  +
*CNS penetration 24-67% of serum levels
   
== Safety ==
+
== Dosing ==
   
  +
=== Pediatric Dosing ===
* Major toxicity is cytopenias
 
  +
  +
* Ganciclovir 5-6 mg/kg IV q12h
  +
  +
==Safety==
  +
 
*Major toxicity is cytopenias
  +
**Usually develops in first one to two weeks of treatment
  +
**Contraindicated when neutrophils <0.5 cells/mL or platelets <25 cells/mL
  +
  +
=== Drug-Drug Interactions ===
  +
  +
* [[Zidovudine]], [[didanosine]], [[probenecid]], and [[imipenem-cilastatin]] (increases risk of seizures)
   
 
[[Category:Antivirals]]
 
[[Category:Antivirals]]

Revision as of 21:17, 11 September 2020

Background

Mechanism of Action

  • Analog of deoxyguanosine, competes with deoxyguanosine to inhibit viral DNA polymerase

Mechanisms of Resistance

  • Resistance in CMV
    • Most often conferred by mutations of UL97 kinase, which is required in order to phosphorylate ganciclovir into its active form
    • Can also develop through mutations in the target UL54 DNA polymerase

Spectrum of Activity

Pharmacokinetics and Pharmacodynamics

  • Oral bioavailability 6-8%
  • CNS penetration 24-67% of serum levels

Dosing

Pediatric Dosing

  • Ganciclovir 5-6 mg/kg IV q12h

Safety

  • Major toxicity is cytopenias
    • Usually develops in first one to two weeks of treatment
    • Contraindicated when neutrophils <0.5 cells/mL or platelets <25 cells/mL

Drug-Drug Interactions