Cryptococcosis medical therapy: Difference between revisions
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==Overview== | ==Overview== | ||
The standard regimen of treatment in non-[[AIDS]] patients intravenous [[Amphotericin B]] combined with oral [[flucytosine]]. [[HIV AIDS|AIDS]] patients often have a reduced response to [[Amphotericin B]] and [[flucytosine]], therefore after initial treatment as above, oral [[fluconazole]] can be used. | The standard regimen of treatment in non-[[AIDS]] patients [[Intravenous therapy|intravenous]] [[Amphotericin B]] combined with [[oral]] [[flucytosine]]. [[HIV AIDS|AIDS]] patients often have a reduced response to [[Amphotericin B]] and [[flucytosine]], therefore after initial treatment as above, [[oral]] [[fluconazole]] can be used. | ||
==Medical Therapy== | ==Medical Therapy== | ||
The standard regimen of treatment in non-[[HIV AIDS|AIDS]] patients [[intravenous]] [[Amphotericin B]] combined with [[ | The standard regimen of treatment in non-[[HIV AIDS|AIDS]] patients [[intravenous]] [[Amphotericin B]] combined with [[oral]] [[flucytosine]]. | ||
AIDS patients often have a reduced response to [[Amphotericin B]] and [[flucytosine]], therefore after initial treatment as above, oral [[fluconazole]] can be used. | AIDS patients often have a reduced response to [[Amphotericin B]] and [[flucytosine]], therefore after initial treatment as above, [[oral]] [[fluconazole]] can be used. | ||
===Antimicrobial Regimens=== | ===Antimicrobial Regimens=== | ||
* '''1. Cryptococcus neoformans''' | * '''1. Cryptococcus neoformans''' | ||
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::* '''1.1.1 Induction and consolidation''' | ::* '''1.1.1 Induction and consolidation''' | ||
:::*Preferred regimen: ([[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV q24h for 2 weeks {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | :::*Preferred regimen: ([[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV q24h for 2 weeks {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | ||
:::*Preferred regimen (renally impaired): ([[Liposomal AmB]] 3-4 mg/kg IV q24h {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | :::*Preferred regimen ([[Renal impairment|renally impaired]]): ([[Liposomal AmB]] 3-4 mg/kg IV q24h {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | ||
:::*Preferred regimen (renally impaired): ([[Amphotericin B]] lipid complex (ABLC) 5 mg/kg IV q24h {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | :::*Preferred regimen ([[Renal impairment|renally impaired]]): ([[Amphotericin B]] lipid complex (ABLC) 5 mg/kg IV q24h {{and}} [[Flucytosine]] 100 mg/kg/day PO/IV q6h for 2 weeks) {{then}} [[Fluconazole]] 400 mg (6 mg/kg) PO qd for ≥8 weeks | ||
:::*Alternative regimen (1): [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV q24h {{or}} [[Liposomal AmB]] 3-4 mg/kg IV q24h {{or}} | :::*Alternative regimen (1): [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV q24h {{or}} [[Liposomal AmB]] 3-4 mg/kg IV q24h {{or}} [[amphotericin B]] lipid complex 5 mg/kg IV q24h for 4-6 weeks | ||
:::*Alternative regimen (2): ([[Amphotericin B]] deoxycholate 0.7 mg/kg IV q24h {{and}} [[Fluconazole]] 800 mg PO qd for 2 weeks) {{then}} [[Fluconazole]] 800mg PO qd for ≥8 weeks | :::*Alternative regimen (2): ([[Amphotericin B]] deoxycholate 0.7 mg/kg IV q24h {{and}} [[Fluconazole]] 800 mg PO qd for 2 weeks) {{then}} [[Fluconazole]] 800mg PO qd for ≥8 weeks | ||
:::*Alternative regimen (3): [[Fluconazole]] 800-1200 mg PO qd {{and}} [[Flucytosine]] 100 mg/kg/day PO qid for 6 weeks | :::*Alternative regimen (3): [[Fluconazole]] 800-1200 mg PO qd {{and}} [[Flucytosine]] 100 mg/kg/day PO qid for 6 weeks | ||
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::* '''1.1.2 Maintenance and prophylactic therapy''' | ::* '''1.1.2 Maintenance and prophylactic therapy''' | ||
:::*Preferred regimen: [[Fluconazole]] 200 mg PO qd {{and}} HAART 2-10 weeks after initiation of antifungal therapy | :::*Preferred regimen: [[Fluconazole]] 200 mg PO qd {{and}} HAART 2-10 weeks after initiation of [[Antifungal medication|antifungal therapy]] | ||
:::*Alternative regimen (1): [[Itraconazole]] 200 mg PO bid | :::*Alternative regimen (1): [[Itraconazole]] 200 mg PO bid | ||
:::*Alternative regimen (2): [[Amphotericin B]] deoxycholate 1 mg/kg IV qw | :::*Alternative regimen (2): [[Amphotericin B]] deoxycholate 1 mg/kg IV qw | ||
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::*'''1.3. Cryptococcus neoformans meningitis in HIV negative patients''' | ::*'''1.3. Cryptococcus neoformans meningitis in HIV negative patients''' | ||
:::*Preferred regimen: [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV qd {{plus}} [[Flucytosine]] 100mg/kg/day PO or IV qid for at least 4 weeks (which may be extended to 6 weeks if there is any neurological complication) followed by [[Fluconazole]] 400mg PO qd for 8 weeks. If there's toxicity to | :::*Preferred regimen: [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV qd {{plus}} [[Flucytosine]] 100mg/kg/day PO or IV qid for at least 4 weeks (which may be extended to 6 weeks if there is any [[neurological]] complication) followed by [[Fluconazole]] 400mg PO qd for 8 weeks. If there's toxicity to [[amphotericin B]] deoxycholate , consider changing to [[liposomal AmB]] in the second 2 weeks. | ||
:::*Note (1): After induction and consolidation therapy, start [[Fluconazole]] 200mg (3mg/kg) PO qd for 6-12 months. | :::*Note (1): After induction and consolidation therapy, start f[[Fluconazole]] 200mg (3mg/kg) PO qd for 6-12 months. | ||
:::*Note (2): If [[Flucytosine]] is not given, consider lengthening the induction therapy for at least 2 weeks. | :::*Note (2): If [[Flucytosine]] is not given, consider lengthening the induction therapy for at least 2 weeks. | ||
::*'''1.4. Cryptococcus neoformans pulmonary disease - immunosupressed''' | ::*'''1.4. Cryptococcus neoformans pulmonary disease - immunosupressed''' | ||
:::*Mild-moderate symptoms, without severe immunosupression and absence of diffuse pulmonary infiltrates: | :::*Mild-moderate symptoms, without severe [[immunosupression]] and absence of diffuse [[pulmonary]] infiltrates: | ||
::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ||
:::*Severe [[pneumonia]] or [[disseminated disease]] or [[CNS]] infection: | :::*Severe [[pneumonia]] or [[disseminated disease]] or [[CNS]] infection: | ||
::::*Preferred regimen: treat like CNS [[cryptococcosis]]. | ::::*Preferred regimen: treat like [[CNS]] [[cryptococcosis]]. | ||
:::*Note (1): In [[Human Immunodeficiency Virus (HIV)|HIV]]- infected patients, treatment should be stopped after 1 year if [[CD4]] count is >100 and a cryptococcal antigen titer is <1:512 and not increasing. | :::*Note (1): In [[Human Immunodeficiency Virus (HIV)|HIV]]- infected patients, treatment should be stopped after 1 year if [[CD4]] count is >100 and a [[Cryptococcal infection|cryptococcal]] [[antigen]] [[titer]] is <1:512 and not increasing. | ||
:::*Note (2): Consider [[corticosteroid]] if [[ARDS]] is present in a context which it might be attributed to IRIS. | :::*Note (2): Consider [[corticosteroid]] if [[ARDS]] is present in a context which it might be attributed to IRIS. | ||
::*'''1.5 Cryptococcus neoformans pulmonary disease - non-immunosupressed''' | ::*'''1.5 Cryptococcus neoformans pulmonary disease - non-immunosupressed''' | ||
:::*Mild-moderate symptoms, without severe immunosupression and absence of diffuse pulmonary infiltrates: | :::*Mild-moderate symptoms, without severe [[immunosupression]] and absence of diffuse [[pulmonary]] infiltrates: | ||
::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ||
::::*Alternative regimen: if [[Fluconazole]] is unavailable or contraindicated, [[Itraconazole]] 200mg PO bid, [[Voriconazole]] 200 mg PO bid, and [[Posaconazole]] 400mg PO bid | ::::*Alternative regimen: if [[Fluconazole]] is unavailable or contraindicated, i[[Itraconazole]] 200mg PO bid, [[Voriconazole]] 200 mg PO bid, and [[Posaconazole]] 400mg PO bid | ||
:::*If there's severe [[pneumonia]], disseminated disease or CNS infection: | :::*If there's severe [[pneumonia]], [[disseminated disease]] or [[Central nervous system infection|CNS infection]]: | ||
::::*Preferred regimen: treat like CNS [[cryptococcosis]] for 6-12 months. | ::::*Preferred regimen: treat like [[CNS]] [[cryptococcosis]] for 6-12 months. | ||
::*'''1.6 Cryptococcus neoformans non-lung, non-CNS infection''' | ::*'''1.6 Cryptococcus neoformans non-lung, non-CNS infection''' | ||
:::*Cryptococcemia or disseminated cryptococcic disease (involvement of at least 2 noncontiguous sites or cryptococcal antigen titer >1:512): | :::*Cryptococcemia or disseminated cryptococcic disease (involvement of at least 2 noncontiguous sites or [[Cryptococcal infection|cryptococcal]] [[antigen]] [[titer]] >1:512): | ||
::::*Preferred regimen: treat like CNS infection. | ::::*Preferred regimen: treat like [[Central nervous system infection|CNS infection]]. | ||
:::*If infection occurs at a single site and no immunosupressive risk factors | :::*If infection occurs at a single site and no [[Immunosuppressive drug|immunosupressive]] risk factors | ||
::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ::::*Preferred regimen: [[Fluconazole]] 400mg PO qd for 6-12 months | ||
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::::*Alternative regimen: patients with renal dysfunction: change [[Amphotericin B]] deoxycholate by [[Liposomal AmB]] 5mg/kg IV qd or [[Amphotericin B]] lipid complex (ABLC) 5mg/kg IV qd | ::::*Alternative regimen: patients with renal dysfunction: change [[Amphotericin B]] deoxycholate by [[Liposomal AmB]] 5mg/kg IV qd or [[Amphotericin B]] lipid complex (ABLC) 5mg/kg IV qd | ||
::::*Preferred regimen for maintenance: [[Fluconazole]] 6mg/kg PO qd. Discontinuation of maintenance therapy is poorly studied and should be individualized. | ::::*Preferred regimen for maintenance: [[Fluconazole]] 6mg/kg PO qd. Discontinuation of maintenance therapy is poorly studied and should be individualized. | ||
:::*Cryptococcal pneumonia: | :::*[[Cryptococcal infection|Cryptococcal]] [[pneumonia]]: | ||
::::*Preferred regimen [[Fluconazole]] 6-12mg/kg PO qd for 6-12 months | ::::*Preferred regimen [[Fluconazole]] 6-12mg/kg PO qd for 6-12 months | ||
::*'''1.8. Cryptococcosis in Pregnant Women''' | ::*'''1.8. Cryptococcosis in Pregnant Women''' | ||
:::*Preferred regimen for induction and consolidation: [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV qd (consider using lipid formulations for patients with renal dysfunction - [[Liposomal AmB]] 3-4mg/kg IV qd {{or}} [[Amphotericin B]] lipid complex (ABLC) 5mg/kg IV qd. Consider using [[Flucytosine]] in relationship to benefit risk basis, since it is a | :::*Preferred regimen for induction and consolidation: [[Amphotericin B]] deoxycholate 0.7-1.0 mg/kg IV qd (consider using lipid formulations for patients with [[renal dysfunction]] - [[Liposomal AmB]] 3-4mg/kg IV qd {{or}} [[Amphotericin B]] lipid complex (ABLC) 5mg/kg IV qd. Consider using [[Flucytosine]] in relationship to benefit risk basis, since it is a category C drug for pregnancy. Start [[Fluconazole]] after delivery. Avoid use during first trimester and consider use in the last 2 trimesters with the need for continuous antifungal therapy during pregnancy. | ||
:::*Note: If pulmonary cryptococcosis: perform close follow-up and administer [[fluconazole]] after delivery. | :::*Note: If [[pulmonary]] [[cryptococcosis]]: perform close follow-up and administer [[fluconazole]] after delivery. | ||
:*'''2. Cryptococcus gatti''' | :*'''2. Cryptococcus gatti''' | ||
::*Disseminated cryptococcosis or CNS disease: | ::*[[Disseminated disease|Disseminated]] [[cryptococcosis]] or [[CNS]] disease: | ||
:::*Preferred regimen: treatment is the same as [[Cryptococcus neoformans|C. neoformans]]. | :::*Preferred regimen: treatment is the same as [[Cryptococcus neoformans|C. neoformans]]. | ||
::*Pulmonary disease: single and small cryptococcoma: | ::*[[Pulmonary]] disease: single and small cryptococcoma: | ||
:::*Preferred regimen: [[Fluconazole]] 400mg per day PO for 6-18months | :::*Preferred regimen: [[Fluconazole]] 400mg per day PO for 6-18months | ||
::*Pulmonary disease: Very large or multiple cryptococcomas: | ::*[[Pulmonary]] disease: Very large or multiple cryptococcomas: | ||
:::*Preferred regimen: administer [[Flucytosine]] {{and}} [[ | :::*Preferred regimen: administer [[Flucytosine]] {{and}} [[amphotericin B]] deocycholate for 4-6 weeks, followed by [[fluconazole]] for 6-18 months. | ||
:::*Note: Surgery should be considered if there is compression of vital structures {{or}} failure to reduce the size of the cryptococcoma after 4 weeks of therapy | :::*Note: Surgery should be considered if there is compression of vital structures {{or}} failure to reduce the size of the cryptococcoma after 4 weeks of therapy | ||
Revision as of 18:26, 25 July 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Serge Korjian M.D.; Yazan Daaboul, M.D.
Overview
The standard regimen of treatment in non-AIDS patients intravenous Amphotericin B combined with oral flucytosine. AIDS patients often have a reduced response to Amphotericin B and flucytosine, therefore after initial treatment as above, oral fluconazole can be used.
Medical Therapy
The standard regimen of treatment in non-AIDS patients intravenous Amphotericin B combined with oral flucytosine. AIDS patients often have a reduced response to Amphotericin B and flucytosine, therefore after initial treatment as above, oral fluconazole can be used.
Antimicrobial Regimens
- 1. Cryptococcus neoformans
- 1.1 Meningoencephalitis in HIV infected patients[1]
- 1.1.1 Induction and consolidation
- Preferred regimen: (Amphotericin B deoxycholate 0.7-1.0 mg/kg IV q24h for 2 weeks AND Flucytosine 100 mg/kg/day PO/IV q6h for 2 weeks) THEN Fluconazole 400 mg (6 mg/kg) PO qd for ≥8 weeks
- Preferred regimen (renally impaired): (Liposomal AmB 3-4 mg/kg IV q24h AND Flucytosine 100 mg/kg/day PO/IV q6h for 2 weeks) THEN Fluconazole 400 mg (6 mg/kg) PO qd for ≥8 weeks
- Preferred regimen (renally impaired): (Amphotericin B lipid complex (ABLC) 5 mg/kg IV q24h AND Flucytosine 100 mg/kg/day PO/IV q6h for 2 weeks) THEN Fluconazole 400 mg (6 mg/kg) PO qd for ≥8 weeks
- Alternative regimen (1): Amphotericin B deoxycholate 0.7-1.0 mg/kg IV q24h OR Liposomal AmB 3-4 mg/kg IV q24h OR amphotericin B lipid complex 5 mg/kg IV q24h for 4-6 weeks
- Alternative regimen (2): (Amphotericin B deoxycholate 0.7 mg/kg IV q24h AND Fluconazole 800 mg PO qd for 2 weeks) THEN Fluconazole 800mg PO qd for ≥8 weeks
- Alternative regimen (3): Fluconazole 800-1200 mg PO qd AND Flucytosine 100 mg/kg/day PO qid for 6 weeks
- Alternative regimen (4): Fluconazole PO 800-2000 mg PO qd for 10-12 weeks
- 1.1.2 Maintenance and prophylactic therapy
- Preferred regimen: Fluconazole 200 mg PO qd AND HAART 2-10 weeks after initiation of antifungal therapy
- Alternative regimen (1): Itraconazole 200 mg PO bid
- Alternative regimen (2): Amphotericin B deoxycholate 1 mg/kg IV qw
- Note (1): Consider discontinuing therapy if CD4 count is higher than 100 cells/uL AND undetectable OR very low HIV RNA level for > 3 months
- Note (2): Consider reinstitution of maintenance therapy if CD4 count <100 cells/uL
- 1.2. Cerebral cryptococcomas
- Preferred regimen for induction and consolidation: (Amphotericin B deoxycholate 0.7-1.0 mg/kg IV qd (consider using lipid formulations for patients with renal dysfunction) OR Liposomal AmB 3-4mg/kg IV qd OR Amphotericin B lipid complex (ABLC) 5mg/kg IV qd) PLUS Flucytosine 100mg/kg/day PO or IV qid for at least 2 weeks followed by Fluconazole 400mg (6mg/kg) PO qd for at least 8 weeks
- Note: Consider surgery if lesions are larger than 3cm, accessible lesions with mass effect or lesions that are enlarging and not explained by IRIS.
- 1.3. Cryptococcus neoformans meningitis in HIV negative patients
- Preferred regimen: Amphotericin B deoxycholate 0.7-1.0 mg/kg IV qd PLUS Flucytosine 100mg/kg/day PO or IV qid for at least 4 weeks (which may be extended to 6 weeks if there is any neurological complication) followed by Fluconazole 400mg PO qd for 8 weeks. If there's toxicity to amphotericin B deoxycholate , consider changing to liposomal AmB in the second 2 weeks.
- Note (1): After induction and consolidation therapy, start fFluconazole 200mg (3mg/kg) PO qd for 6-12 months.
- Note (2): If Flucytosine is not given, consider lengthening the induction therapy for at least 2 weeks.
- 1.4. Cryptococcus neoformans pulmonary disease - immunosupressed
- Mild-moderate symptoms, without severe immunosupression and absence of diffuse pulmonary infiltrates:
- Preferred regimen: Fluconazole 400mg PO qd for 6-12 months
- Severe pneumonia or disseminated disease or CNS infection:
- Preferred regimen: treat like CNS cryptococcosis.
- Note (1): In HIV- infected patients, treatment should be stopped after 1 year if CD4 count is >100 and a cryptococcal antigen titer is <1:512 and not increasing.
- Note (2): Consider corticosteroid if ARDS is present in a context which it might be attributed to IRIS.
- 1.5 Cryptococcus neoformans pulmonary disease - non-immunosupressed
- Mild-moderate symptoms, without severe immunosupression and absence of diffuse pulmonary infiltrates:
- Preferred regimen: Fluconazole 400mg PO qd for 6-12 months
- Alternative regimen: if Fluconazole is unavailable or contraindicated, iItraconazole 200mg PO bid, Voriconazole 200 mg PO bid, and Posaconazole 400mg PO bid
- If there's severe pneumonia, disseminated disease or CNS infection:
- Preferred regimen: treat like CNS cryptococcosis for 6-12 months.
- 1.6 Cryptococcus neoformans non-lung, non-CNS infection
- Cryptococcemia or disseminated cryptococcic disease (involvement of at least 2 noncontiguous sites or cryptococcal antigen titer >1:512):
- Preferred regimen: treat like CNS infection.
- If infection occurs at a single site and no immunosupressive risk factors
- Preferred regimen: Fluconazole 400mg PO qd for 6-12 months
- 1.7. Cryptococcosis in Children
- Preferred regimen for induction and consolidation: Amphotericin B deoxycholate 1.0 mg/kg qd IV PLUS Flucytosine 100mg/kg PO or IV qid for 2 weeks followed by Fluconazole 10-12mg/kg PO qd for 8 weeks
- Alternative regimen: patients with renal dysfunction: change Amphotericin B deoxycholate by Liposomal AmB 5mg/kg IV qd or Amphotericin B lipid complex (ABLC) 5mg/kg IV qd
- Preferred regimen for maintenance: Fluconazole 6mg/kg PO qd. Discontinuation of maintenance therapy is poorly studied and should be individualized.
- Preferred regimen Fluconazole 6-12mg/kg PO qd for 6-12 months
- 1.8. Cryptococcosis in Pregnant Women
- Preferred regimen for induction and consolidation: Amphotericin B deoxycholate 0.7-1.0 mg/kg IV qd (consider using lipid formulations for patients with renal dysfunction - Liposomal AmB 3-4mg/kg IV qd OR Amphotericin B lipid complex (ABLC) 5mg/kg IV qd. Consider using Flucytosine in relationship to benefit risk basis, since it is a category C drug for pregnancy. Start Fluconazole after delivery. Avoid use during first trimester and consider use in the last 2 trimesters with the need for continuous antifungal therapy during pregnancy.
- Note: If pulmonary cryptococcosis: perform close follow-up and administer fluconazole after delivery.
- 2. Cryptococcus gatti
- Disseminated cryptococcosis or CNS disease:
- Preferred regimen: treatment is the same as C. neoformans.
- Pulmonary disease: single and small cryptococcoma:
- Preferred regimen: Fluconazole 400mg per day PO for 6-18months
- Pulmonary disease: Very large or multiple cryptococcomas:
- Preferred regimen: administer Flucytosine AND amphotericin B deocycholate for 4-6 weeks, followed by fluconazole for 6-18 months.
- Note: Surgery should be considered if there is compression of vital structures OR failure to reduce the size of the cryptococcoma after 4 weeks of therapy
References
- ↑ Perfect JR, Dismukes WE, Dromer F, Goldman DL, Graybill JR, Hamill RJ; et al. (2010). "Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of america". Clin Infect Dis. 50 (3): 291–322. doi:10.1086/649858. PMID 20047480.