Voriconazole: Difference between revisions
From IDWiki
No edit summary |
(→) |
||
Line 4: | Line 4: | ||
*Indications include {{#ask: [[Is treated by::voriconazole]]}} |
*Indications include {{#ask: [[Is treated by::voriconazole]]}} |
||
=== |
===Mechanism of Action=== |
||
* |
*Like all azoles, inhibits Erg11/Cyp51p lanosterol 14-α-demethylase in the ergosterol synthesis pathway |
||
=== |
===Pharmacokinetics and Pharmacodynamics=== |
||
* |
*Non-linear pharmacokinetics |
||
* |
*58% protein-bound |
||
* |
*CSF 50% of plasma concentration |
||
* |
*Less than 5% excreted unchanged in the urine |
||
=== |
===Spectrum of Activity=== |
||
* |
*Active against [[Aspergillus]] (including [[Aspergillus terreus]]), [[Scedosporium species]], [[Fusarium species]], and [[Candida species]] |
||
* |
*Possibly active against [[Cryptococcus species]], [[Blastomyces dermatitidis]], [[Coccidioides immitis]], and [[Histoplasma capsulatum]] |
||
* |
*Less active against [[Sporothrix schenckii]] |
||
===Breakpoints=== |
===Breakpoints=== |
||
Line 112: | Line 112: | ||
|} |
|} |
||
== |
==Dosing== |
||
* |
*Voriconazole 6 mg/kg IV q12h x2 followed by 4 mg/kg PO/IV q12h |
||
*Voriconazole 200 mg PO q12h if weight >40 kg, or 100 mg PO q12h if weight <40 kg |
|||
**Give at least 1 hour before or after a meal |
|||
**Can be preceded by a loading dose of twice the maintenance for 24 hours |
|||
===Therapeutic Drug Monitoring=== |
===Therapeutic Drug Monitoring=== |
||
Line 137: | Line 140: | ||
|} |
|} |
||
== |
==Safety== |
||
*Elevated levels predict neurotoxicity, but ''not'' hepatotoxicity |
*Elevated levels predict neurotoxicity, but ''not'' hepatotoxicity |
||
Line 155: | Line 158: | ||
*Headache, nausea and vomiting, diarrhea, abdominal pain |
*Headache, nausea and vomiting, diarrhea, abdominal pain |
||
=== |
===Drug-Drug Interactions=== |
||
* |
*Voriconazole is metabolised by CYP450 enzymes |
||
* |
*Voriconazole also inhibits CYP3A4 and CYP2C9 |
||
{| class="wikitable" |
{| class="wikitable" |
Revision as of 00:36, 6 September 2020
Background
- Azole antifungal derived from fluconazole to improve mold coverage
- Indications include Alternaria, Blastomyces dermatitidis, Coccidioides immitis, Exophiala, Exserohilum, Fungal endocarditis, Histoplasma capsulatum, Rasamsonia
Mechanism of Action
- Like all azoles, inhibits Erg11/Cyp51p lanosterol 14-α-demethylase in the ergosterol synthesis pathway
Pharmacokinetics and Pharmacodynamics
- Non-linear pharmacokinetics
- 58% protein-bound
- CSF 50% of plasma concentration
- Less than 5% excreted unchanged in the urine
Spectrum of Activity
- Active against Aspergillus (including Aspergillus terreus), Scedosporium species, Fusarium species, and Candida species
- Possibly active against Cryptococcus species, Blastomyces dermatitidis, Coccidioides immitis, and Histoplasma capsulatum
- Less active against Sporothrix schenckii
Breakpoints
Species | ECV (μg/mL) | Breakpoints (μg/mL) | Breakpoints (mm) | ||||||
---|---|---|---|---|---|---|---|---|---|
S | I | SDD | R | S | I | SDD | R | ||
Candida albicans | 0.3 | ≤0.12 | 0.25-0.5 | — | ≥1 | ≥17 | 15-16 | — | ≤14 |
Candida glabrata | 0.25 | — | — | — | — | — | — | — | — |
Candida krusei | 0.5 | ≤0.5 | 1 | — | ≥2 | ≥15 | 13-14 | — | ≤12 |
Candida parapsilosis | 0.03 | ≤0.12 | 0.25-0.5 | — | ≥1 | ≥17 | 15-16 | — | ≤14 |
Candida tropicalis | 0.12 | ≤0.12 | 0.25-0.5 | — | ≥1 | ≥17 | 15-16 | — | ≤14 |
Cryptococcus neoformans | 0.25 | ||||||||
Cryptococcus gattii | 0.5 | ||||||||
Aspergillus flavus | 2 | ||||||||
Aspergillus fumigatus | 1 | ||||||||
Aspergillus niger | 2 | ||||||||
Aspergillus terreus | 2 |
Dosing
- Voriconazole 6 mg/kg IV q12h x2 followed by 4 mg/kg PO/IV q12h
- Voriconazole 200 mg PO q12h if weight >40 kg, or 100 mg PO q12h if weight <40 kg
- Give at least 1 hour before or after a meal
- Can be preceded by a loading dose of twice the maintenance for 24 hours
Therapeutic Drug Monitoring
- Measure trough within 7 days of starting, and at regular intervals or following dose adjustment
- Target trough > 1 mg/L for prophylaxis and treatment
Trough (mcg/mL) | Recommendation |
---|---|
0.0 to 0.6 | Increase dose by 100 mg and recheck trough on day 5 of new regimen |
0.7 to 0.9 | Increase dose by 50 mg and recheck trough on day 5 of new regimen |
1.0 to 4.0 | At target, no dose adjustment needed |
4.1 to 5.5 | Decrease dose by 50 mg and recheck trough on day 5 of new regimen |
5.6 to 7.9 | Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 100 mg. Recheck trough on day 5 of new regimen. |
≥8.0 | Hold dose. Follow daily trough levels, then restart when trough is ≤2.5 at a dose decreased by 50%. Recheck trough level on day 5 of new regimen. |
Safety
- Elevated levels predict neurotoxicity, but not hepatotoxicity
Adverse Drug Reactions
- Visual, which tend to improve after the first week of therapy and are reversible
- Floaters (photopsia) that usually improves with time (30%)
- Visual hallucinations (5%)
- Colour vision loss, blurred vision, photophobia
- Dermatologic
- Rashes, usually mild
- Stevens-Johnson syndrome and toxic epidermal necrolysis (rare)
- Photosensitivity
- Hepatotoxicity, proportional to serum levels
- QTc prolongation
- Headache, nausea and vomiting, diarrhea, abdominal pain
Drug-Drug Interactions
- Voriconazole is metabolised by CYP450 enzymes
- Voriconazole also inhibits CYP3A4 and CYP2C9
Drug | Recommendation |
---|---|
Decreases voriconazole levels | |
carbamazepine | contraindicated |
long-acting barbiturates | contraindicated |
rifampin | contraindicated |
Levels increased by voriconazole | |
astemizole | contraindicated |
cisapride | contraindicated |
cyclosporine | reduce cyclosporine dosage 50% and monitor levels |
ergot alkaloids | contraindicated |
omeprazole | reduce omeprazole by 50% |
quinidine | contraindicated |
sirolimus | contraindicated |
tacrolimus | reduce tacrolimus levels to 33% and monitor levels |
terfenadine | contraindicated |
warfarin | monitor INR |
Decreases voriconazole levels, and levels increased by voriconazole | |
rifabutin | contraindicated |
phenytoin | double voriconazole, and monitor phenytoin levels |
Levels likely increased by voriconazole | |
sulfonylureas | monitor for side effects of drug and consider decreasing dosage |
statins | |
vinca alkaloids | |
calcium channel blockers | |
benzodiazepines |
Further Reading
- Voriconazole Dose Modification Guideline to Optimize Therapeutic Levels in Patients With Hematologic Malignancies. Open Forum Infect Dis. 2015;2(S1):810. doi: 10.1093/ofid/ofv133.527