Leishmaniasis in Emergency Medicine Treatment & Management
- Author: Jennifer J Lee, MD; Chief Editor: Rick Kulkarni, MD more...
Emergency Department Care
- Cutaneous leishmaniasis
- Treatment of cutaneous leishmaniasis differs according to the etiology and geographic location of the infection. For certain types of cutaneous leishmaniasis where the potential for mucosal spread is low, topical paromycin can be used.
- For more invasive lesions (eg, those failing to respond to topical treatment; metastatic spread to the lymph nodes; or large, disfiguring, and multiple skin lesions, especially those on the face, near mucosal surfaces, or near joints), sodium stibogluconate or pentamidine can be used.
- Other reported treatments include meglumine antimonite in addition to topical imiquimod cream, cryotherapy, heat therapy (radiofrequency), ketoconazole, itraconazole, allopurinol, or miltefosine (not available in the US).
- Mucosal leishmaniasis
- Pentavalent antimony for a course of 4 weeks has been recommended.
- Amphotericin B deoxycholate may be first-line therapy for advanced mucosal disease.
- Visceral leishmaniasis
- Be alert for complications related to reticuloendothelial system failure. Patients may have bleeding or neutropenia leading to infectious conditions such as pneumonia or diarrhea. Transfusions may be necessary for severe bleeding or anemia. Antibiotics are indicated to treat intercurrent infectious conditions.
- Outside of India, treatment with a pentavalent antimonial compound usually is effective. The use of an alternative parenteral agent should be considered even for first-line therapy in areas where resistance to pentavalent antimony therapy is prevalent, as it is in India, or if nonantimonial therapy would be advantageous for other reasons (eg, toxicity profile, duration of therapy).
- A major advance has been the advent of liposomal formulations of amphotericin B, in which various alternative lipids have replaced deoxycholate. These formulations, which passively target amphotericin to macrophage-rich organs, are much more costly than conventional amphotericin B (making them cost-prohibitive in poor countries) but are associated with less nephrotoxicity and can be given in considerably shorter courses. Although visceral leishmaniasis is traditionally treated with multiple doses of amphotericin B deoxycholate, it appears, based on a single randomized trial, that a single dose of liposomal amphotericin B may be just as effective and cheaper.[2]
- Other parenteral alternatives that have merit include amphotericin B (not only in deoxycholate form but also in liposomal forms) and have generally replaced pentamidine. Miltefosine, a chemotherapeutic agent, is the first extremely effective oral agent for visceral leishmaniasis but is not currently available in the United States. Injectable paromycin has also been reported to be noninferior to amphotericin B but also is not currently FDA approved.
Consultations
- Infectious disease consultation can offer the most effective antiprotozoal regimen.
- Although cutaneous leishmaniasis can heal on its own, early lesions can also be treated with physical measures, such as local cryotherapy, heat therapy, electrocoagulation, or surgical removal.
- Surgical consultation may be necessary for adjunctive splenectomy.
Update: Cutaneous leishmaniasis in U.S. military personnel--Southwest/Central Asia, 2002-2004. MMWR Morb Mortal Wkly Rep. Apr 2 2004;53(12):264-5. [Medline].
[Best Evidence] Sundar S, Chakravarty J, Agarwal D, Rai M, Murray HW. Single-dose liposomal amphotericin B for visceral leishmaniasis in India. N Engl J Med. Feb 11 2010;362(6):504-12. [Medline].
Alrajhi AA, Ibrahim EA, De Vol EB, Khairat M, Faris RM, Maguire JH. Fluconazole for the treatment of cutaneous leishmaniasis caused by Leishmania major. N Engl J Med. Mar 21 2002;346(12):891-5. [Medline].
Berman J. Current treatment approaches to leishmaniasis. Curr Opin Infect Dis. Oct 2003;16(5):397-401. [Medline].
Berman JD. Human leishmaniasis: clinical, diagnostic, and chemotherapeutic developments in the last 10 years. Clin Infect Dis. Apr 1997;24(4):684-703. [Medline].
Braunwald E. Harrison's Principles of Internal Medicine. Online Update: McGraw-Hill.
Centers for Disease Control and Prevention. Cutaneous leishmaniasis in U.S. military personnel--Southwest/Central Asia, 2002-2003. MMWR Morb Mortal Wkly Rep. Oct 24 2003;52(42):1009-12. [Medline]. [Full Text].
Centers for Disease Control and Prevention (CDC). The Yellow Book, Health Information for Travelers, CDC 2003-2004. 2004.
Committee on Infectious Disease, American Academy of Pediatrics. Report of the Committee on Infectious Diseases. 24th ed. Red Book; 1997:321-323.
Davies CR, Kaye P, Croft SL, Sundar S. Leishmaniasis: new approaches to disease control. BMJ. Feb 15 2003;326(7385):377-82. [Medline]. [Full Text].
Foti G. [Treatment of visceral leishmaniasis]. Minerva Med. Aug 2001;92(4):245-9. [Medline].
Freedberg IM, Eisen AZ, Wolff K, Austen KF, Goldsmith LA, Katz S. Fitzpatrick's Dermatology in General Medicine. 6th ed. New York: McGraw-Hill; 2003.
Guerin PJ, Olliaro P, Sundar S, et al. Visceral leishmaniasis: current status of control, diagnosis, and treatment, and a proposed research and development agenda. Lancet Infect Dis. Aug 2002;2(8):494-501. [Medline].
Kafetzis DA. An overview of paediatric leishmaniasis. J Postgrad Med. Jan-Mar 2003;49(1):31-8. [Medline].
Lee SA, Hasbun R. Therapy of cutaneous leishmaniasis. Int J Infect Dis. Jun 2003;7(2):86-93. [Medline].
Magill AJ. Cutaneous leishmaniasis in the returning traveler. Infect Dis Clin North Am. Mar 2005;19(1):241-66, x-xi. [Medline].
Micromedex Healthcare Series. Thomson Healthcare, Inc [database online]. Vol 124. 2004.
Minodier P, Retornaz K, Horelt A, Garnier JM. Liposomal amphotericin B in the treatment of visceral leishmaniasis in immunocompetent patients. Fundam Clin Pharmacol. Apr 2003;17(2):183-8. [Medline].
Olliaro PL, Guerin PJ, Gerstl S, Haaskjold AA, Rottingen JA, Sundar S. Treatment options for visceral leishmaniasis: a systematic review of clinical studies done in India, 1980-2004. Lancet Infect Dis. Dec 2005;5(12):763-74. [Medline].
Pagliano P, Carannante N, Rossi M, et al. Visceral leishmaniasis in pregnancy: a case series and a systematic review of the literature. J Antimicrob Chemother. Feb 2005;55(2):229-33. [Medline].
Paredes R, Munoz J, Diaz I, Domingo P, Gurgui M, Clotet B. Leishmaniasis in HIV infection. J Postgrad Med. Jan-Mar 2003;49(1):39-49. [Medline].
Rogers ME, Ilg T, Nikolaev AV, Ferguson MA, Bates PA. Transmission of cutaneous leishmaniasis by sand flies is enhanced by regurgitation of fPPG. Nature. Jul 22 2004;430(6998):463-7. [Medline]. [Full Text].
Schwartz E, Hatz C, Blum J. New world cutaneous leishmaniasis in travellers. Lancet Infect Dis. Jun 2006;6(6):342-9. [Medline].
Sundar S, Jha TK, Thakur CP, et al. Oral miltefosine for Indian visceral leishmaniasis. N Engl J Med. Nov 28 2002;347(22):1739-46. [Medline].
Sundar S, Pai K, Kumar R, et al. Resistance to treatment in Kala-azar: speciation of isolates from northeast India. Am J Trop Med Hyg. Sep 2001;65(3):193-6. [Medline].
Sundar S, Rai M. Laboratory diagnosis of visceral leishmaniasis. Clin Diagn Lab Immunol. Sep 2002;9(5):951-8. [Medline]. [Full Text].
Tatro DS, Borgsdorf LR, Lopez JR, et al. A To Z Drug Facts. In: Facts and Comparisons. 5th ed. April 2005.
Tierney LM, McPhee SJ, Papadakis MA. Current Medical Diagnosis & Treatment 2005. 44th ed. New York: McGraw-Hill; 2004.
World Health Organization (WHO). Weekly epidemiological record No. 44. Vol 77. 2002:365-372.

