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 Guide Editors
 Editor In Chief
    Joel E. Gallant, MD, MPH

Pharmacology Editor
    Paul Pham, PharmD, BCPS

Zambia Guideline Team
   Peter Mwaba MMed PhD FRCP
   Alywn Mwinga MMed
   Isaac Zulu MMed MPH
   Velepie Mtonga MMed
   Albert Mwango MBChB
   Jabbin Mulwanda MMed FCS



Diagnosis>Opportunistic Infections>
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Cryptococcal Meningitis

Amita Gupta, M.D. and Karen Wendel, M.D.

  • Cryptococcus is ubiquitous fungus and considered endemic in Zambia.
  • Epidemiology of cryptococcosis unclear in Zambia, but generally reported as significantly more prevalent in sub-Saharan Africa vs. developing world.
  • One Zambian study of patients with cryptococcal meningitis at the University Teaching Hospital in Lusaka reported that it was AIDS -defining illness in 91% of patients and 4th most common reason for medical admission. Mortality rate was 100%, despite use of fluconazole monotherapy in approximately half of pts (given at lower than currently recommended doses).
  • Recommendations for Dx and management of cryptococcal meningitis in Zambia largely similar to those in developed world.
  • Azole (fluconazole or itraconazole) primary prophylaxis, generally not recommended in developed world, may be beneficial in areas where cryptococcosis common and could be considered for patients in severely immunocompromised in Zambia (WHO Stage 4 or CD4 <100) whether or not they are on ART.
  • Clinical trials and more definitive recommendations for primarily azole prophylaxis in Africa currently in progress.
  • Liposomal amphotericin preparations, voriconazole, posaconazole, and 5-FC not readily available in Zambia.


Zambia Information Author: Larry William Chang, MD, MPH


  • Cryptococcus neoformans var. neoformans (serotypes A and D).
  • Cryptococcus neoformans var. gattii (serotypes B and C, rare in HIV).
  • Cryptococcus neoformans var. grubii (has been used to designate serotype A).


  • Infection via inhalation of fungus. Pneumonia can occur (focal infiltrates, nodules or rarely, cavitary lesions accompanied by low grade fever). Most pts with meningitis have no history of pneumonia and usually have CD4 <100.
  • Skin lesions resembling molluscum contagiosum can occur in the setting of disseminated cryptococcosis.
  • Sx of cryptococcal meningitis include gradually increasing headache with low grade fever. However, may also present with seizure, confusion, progressive dementia, fever without localizing signs, or bizarre behavior. Evidence of meningeal irritation often absent.
  • Reported mortality rate of meningitis 6-25%.
  • CNS mass lesions or cryptococcomas usually accompanied by meningitis.
  • Elevated intracranial pressure (>200 mm H20) common and may be accompanied by evidence of cerebral edema: blurred vision, diplopia, hearing loss, severe headaches, confusion, and papilledema.
  • Hydrocephalus can occur in more indolent cases and may require placement of CSF shunt.
  • Pts who initiate HAART are at risk for cryptococcal IRIS (either unmasking type or exacerbation of partly treated disease). Presentations can be atypical, such as lymphadenitis.


  • Cx for fungus: sputum, skin Bx, blood, and CSF.
  • Serum cryptococcal antigen (CrAg) positive in >99% of AIDS pts with cryptococcal meningitis, less often with isolated pulmonary disease.
  • CSF CrAg important tool to diagnose meningeal disease but can be negative in nonmeningeal cryptococcosis.
  • Pts with evidence of pulmonary or systemic cryptococcosis by CrAg or Cx should undergo LP to rule out meningitis. Pts with focal signs or evidence of cerebral edema should have a head CT or MRI prior to LP to assure no mass effect or risk of herniation.
  • CSF evaluation should include: opening pressure, fungal Cx, CrAg, glucose, protein, cell count and differential. CSF CrAg and fungal Cx positive in >95%. India ink less sensitive (60-80%).


Mild to moderate pulmonary disease or nonmeningeal cryptococcosis.

  • First line: fluconazole 400 mg PO qd x10 wks followed by 200 mg PO qd lifelong.
  • Second line: itraconazole (liquid formulation preferred) 400 mg PO qd for 10 wks then 200 mg qd lifelong; fluconazole 400 mg PO qd with flucytosine 100-150 mg/kg/d PO divided over 4 doses for 10 wks (toxicity limits utility of this regimen).
Severe pulmonary disease or nonmeningeal cryptococcosis

  • First line: amphotericin B 0.7-1.0 mg/kg/day IV; lipid formulation of amphotericin - 5mg/kg/day IV. Continue until pt improved clinically and stable for conversion to oral azole.
  • Second line: In pts who can not tolerate amphotericin, fluconazole 400 mg PO qd x 10 wks followed by 200 mg PO qd lifelong; itraconazole (liquid formulation preferred) 400 mg PO qd for 10 wks then 200 mg qd lifelong; fluconazole 400 mg PO qd with flucytosine100-150 mg/kg/day PO divided over 4 doses for 10 wks (toxicity limits utility of this regimen).
Cryptococcal meningitis: Induction/consolidation

  • First line: amphotericin B 0.7-1 mg/kg/day IV +/- flucytosine (5-FC) 100 mg/kg/day PO divided over 4 doses x2 wks, then fluconazole 400 mg/day x8 wks.
  • Second line: amphotericin B 0.7-1 mg/kg/day IV plus flucytosine100 mg/kg/day PO divided over 4 doses for 6-10 wks; amphotericin B 0.7-1 mg/kg/day for 6-10 wks; fluconazole 400-800 mg/day PO for 10-12 wks; fluconazole 400-800 mg/day PO with 5-FC 100-150 mg/kg/day PO divided over 4 doses for 6 wks; lipid formulation of amphotericin B 4-5 mg/kg/day IV for 6-10 wks. Itraconazole 400 mg/day PO (liquid formulation preferred) for 10-12 wks can be given but is less effective than fluconazole.
Cryptococcal meningitis: Maintenance

  • First line: fluconazole 200 mg PO qd.
  • Second line: itraconazole 200 mg PO bid; amphotericin B 1 mg/kg IV 1-3 times/wk. Intermittent amphotericin therapy associated with higher rate of relapse and greater toxicity compared to fluconazole.
  • ART may improve immunology control and decrease rates of relapse. See follow-up section regarding recommendations for discontinuing maintenance therapy.
Elevated intracranial pressure (ICP)

  • If ICP >250 mm and signs of cerebral edema present, do daily LP to reduce pressure until pt is improved.
  • If clinical signs of cerebral edema do not improve after about 2 wks of daily LPs, consider placement of a lumbar drain or ventriculoperitoneal shunt.
  • Pts with hydrocephalus may or may not have increased ICP and rarely have cerebral edema.
Primary prevention

  • Primary prevention with azoles not recommended due to the relative infrequency of infection, low attributable mortality, risk of toxicity and resistance, and no evidence of survival benefit.

Drug Comments

Amphotericin B Gold standard for initial therapy. Intrathecal amphotericin should only be used in cases refractory to standard IV amphotericin +/- flucytosine.
Fluconazole Drug of choice for maintenance therapy. Fluconazole superior to itraconazole in preventing relapse. All azoles should be avoided during pregnancy. If a women has active cryptococcosis during pregnancy, consider a switch to IV amphotericin B.
Flucytosine Can be used in combination with amphotericin for initial therapy. Favor use of this drug in severe cases characterized by increased ICP or change in mental status. Therapy should be monitored with peak levels drawn 2 hrs after oral dose (50-100 mcg/mL). No IV formulation.
Itraconazole Uncommonly used in place of fluconazole for maintenance therapy. Multiple drug-drug interactions require caution when prescribing this medication. Liquid formulation preferred due to improved bioavailability. Liquid formulation should be taken on empty stomach. Capsule formulation should be taken with food. Drug levels should be monitored with peak level drawn 2 hrs after dosing after >5 days of therapy with goal of >1 ug/mL (native drug).
Voriconazole  Limited data specific to cryptococcal meningitis. Given substantial risk of drug-drug interactions with ART and lack of data to support use over fluconazole for this indication; would avoid its use.
Posaconazole  May have a role for complex, refractory CNS fungal infections but data supporting its use for this indication are limited. Other options are cheaper and better studied.


Discontinuation of maintenance therapy

  • In pre-HAART era, risk of relapse was 4% in on maintenance therapy but up to 37-60% in those who discontinued therapy.
  • Pts should remain on maintenance therapy until they are asymptomatic, have had >6 mos with CD4 >100-200 on HAART and have completed initial course of antifungal therapy.
  • If after discontinuation of maintenance therapy, the CD4 falls to <100-200, reinitiate maintenance therapy.

  • Monitor for treatment related toxicity on bi-weekly schedule during induction phase and every other wk on consolidation phase.
  • 5-FC: severe colitis, leukopenia, thrombocytopenia, rash, or hepatitis. Dosage should be reduced for cytopenias or colitis and levels monitored to limit toxicity. Addition of 5-FC to amphotericin B provides only marginal benefit at most. 5-FC may be held if toxicity encountered that cannot be controlled with dosing changes.
  • Azoles: liver toxicity.
  • Amphotericin B: electrolyte imbalances, renal insufficiency, anemia, acute infusion-related toxicity and may require close monitoring. Liposomal formulation less toxic.
Diagnosis of relapse

  • Perform fungal Cx. Serum CrAg not reliable to evaluate pts for relapse of cryptococcal disease. If convalescence CSF CrAg titer available for comparison, an increase in titer of 2 dilutions suggests relapse.
  • Fungal Cx may help differentiate between relapse and IRIS. IRIS after initiation of ART can include worsening meningitis with elevated ICP, lymphadenitis, sterile abscess, or cavitation of pulmonary lesions.


  • Antifungal resistance testing should be limited to pts with multiple recurrences or disease in setting of adherence to standard therapy.




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