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Leishmaniasis

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18 64. The Panel recommends administering secondary prophylaxis (chronic maintenance therapy) to decrease the risk for posttreatment relapse of VL in persons with HIV/AIDS-associated immunosuppression (eg, CD4 T-lymphocyte cell counts <200 cells/mm 3 ) (S-M). 65. Persons with VL-HIV/AIDS coinfection should be monitored indefinitely (until effective immune reconstitution) for evidence of posttreatment relapse. ART and secondary prophylaxis provide only partial protection against relapse. Antileishmanial treatment is indicated for persons who have clinical and parasitologic evidence of recurrence (S-L). HIV/AIDS-ASSOCIATED CL or ML in North America 66. In HIV/AIDS-associated CL/ML, systemic antileishmanial therapy is recommended, particularly in persons who are moderately to severely immunosuppressed (eg, have CD4+ T-lymphocyte cell counts <200–350 cells/mm 3 ), who may be at increased risk for suboptimal therapeutic responses, for posttreatment relapses, and for cutaneous, mucosal, or visceral dissemination (S-VL). 67. The systemic regimens used for CL/ML in otherwise comparable immunocompetent persons typically are recommended for the initial treatment of coinfected persons, taking into account the potentials for drug interactions and toxicity (Tables 3 and 4) (S-VL). Remark: Whether coinfected persons who experience multiple posttreatment relapses of CL/ML would benefit from secondary prophylaxis (chronic maintenance therapy) has not yet been established. 68. Antiretroviral therapy (ART) should be initiated or optimized in accordance with standard practice for HIV/AIDS; no evidence- based, CL/ML-specific recommendations regarding ART have been established (S-L). Immunocompromised Hosts With Solid Organ Transplant, Persons With Lymphatic-Hematologic Malignancies, or Persons Receiving Immunosuppressive Therapy for Other Reasons 69. Liposomal amphotericin B (L-AmB) is recommended as the drug of choice for immunosuppressed persons with VL (Table 3) (S-L). Remarks: The FDA-approved regimen is 4 mg/kg/day IV on days 1–5, 10, 17, 24, 31, and 38 (total dose of 40 mg/kg ). Higher doses and longer durations of therapy may be needed depending in part on the level of immunosuppression. 70. Doses of immunosuppressive drugs should be decreased in persons with VL during antileishmanial therapy whenever possible (S-VL). Treatment

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