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Introducing Single Dose Liposomal Amphotericin B for the Treatment of Visceral Leishmaniasis in Rural Bangladesh: Feasibility and Acceptance to Patients and Health Staff

DOI: 10.1155/2014/676817

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Abstract:

Background. For the treatment of visceral leishmaniasis in Bangladesh, single dose liposomal amphotericin B (ambisome) is supposed to be the safest and most effective treatment. Specific needs for application and storage raise questions about feasibility of its implementation and acceptance by patients and health staff. Methods. The study was carried out in the most endemic district of Bangladesh. Study population includes patients treated with ambisome or miltefosine, hospital staff, and a director of the national visceral leishmaniasis program. Study methods include direct observation (subdistrict hospitals), open interviews (heath staff and program personnel), structured questionnaires, and focus group discussions (patients). Results. Politicalcommitment for ambisome is strong; the general hospital infrastructure favours implementation but further strengthening is required, particularly for drug storage below 25°C (refrigerators), back-up energy (fuel for generators), and supplies for ambisome administration (like 5% dextrose solution). Ambisome created high satisfaction in patients and hospital staff, less adverse events, and less income loss for patients compared to miltefosine. Conclusions. High political commitment, general capacities of subdistrict hospitals, and high acceptability favour the implementation of ambisome treatment in Bangladesh. However, strengthening of the infrastructure and uninterrupted supplies of essential accessories is mandatory before introducing sLAB in Bangladesh. 1. Background Visceral leishmaniasis (VL), also called Kala-azar (KA), is a vector borne neglected disease ranked by the WHO as the infectious disease with the ninth highest burden worldwide [1]. More than 70?per cent of the cases worldwide occur in India, Bangladesh, and Nepal [2]. The annual incidence for Bangladesh has recently been estimated to be between 12,400 and 24,900 cases [2]. Out of the 64 districts and 493 subdistricts of Bangladesh, 45 districts and 105 subdistricts are affected [3]. L. donovani causing VL in the region has no other reservoir than humans and no other vector other than Phlebotomus argentipes. There are new rapid diagnostic tests [4] and different treatment options so that the elimination of the disease was envisaged. In 2005 a Memorandum of Understanding was signed by Bangladesh, India, and Nepal to eliminate VL from the Indian subcontinent aiming for less than one case per 10,000 people in the endemic districts by 2015 [5]. One important element in the elimination strategy is early diagnosis and complete treatment. Within the

References

[1]  World Health Organisation, “Control of the leishmaniasis,” Report of a Meeting of the WHO Expert Committee on the Control of Leishmaniases, Geneva, Switzerland, 2010, http://whqlibdoc.who.int/trs/WHO_TRS_949_eng.pdf.
[2]  J. Alvar, I. D. Vélez, C. Bern et al., “Leishmaniasis worldwide and global estimates of its incidence,” PLoS ONE, vol. 7, no. 5, Article ID e35671, 2012.
[3]  N. Kshirsagar, R. Ferner, B. A. A. Figueroa, H. Ghalib, and J. Lazdin, “Pharmacovigilance methods in public health programmes: the example of miltefosine and visceral leishmaniasis,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 105, no. 2, pp. 61–67, 2011.
[4]  F. Chappuis, S. Sundar, A. Hailu et al., “Visceral leishmaniasis: what are the needs for diagnosis, treatment and control?” Nature Reviews Microbiology, vol. 5, no. 11, pp. 873–882, 2007.
[5]  World Health Organisation and South-East Asia Regional Office, “Regional strategic framework for elimination of Kala-azar from the South-East Asia Region (2005–2015),” WHO Project: IND CRD 714, http://209.61.208.233/LinkFiles/Kala_azar_VBC-85_Rev_1.pdf.
[6]  S. Sundar, J. Chakravarty, D. Agarwal, M. Rai, and H. W. Murray, “Single-dose liposomal amphotericin B for visceral leishmaniasis in India,” The New England Journal of Medicine, vol. 362, no. 6, pp. 504–512, 2010.
[7]  World Health Organisation, “Regional Technical Advisory Group on Kala-azar elimination,” Report of the 3rd Meeting, Dhaka, Bangladesh, 2009, http://209.61.208.233/catalogue/2005-2011/pdf/kala-azar/sea-cd-204.pdf.
[8]  C. Bern and R. Chowdhury, “The epidemiology of visceral leishmaniasis in Bangladesh: prospects for improved control,” Indian Journal of Medical Research, vol. 123, no. 3, pp. 275–288, 2006.
[9]  L. Lingard, M. Albert, and W. Levinson, “Grounded theory, mixed methods, and action research,” British Medical Journal, vol. 337, article a567, 2008.
[10]  D. Anoopa Sharma, C. Bern, B. Varghese et al., “The economic impact of visceral leishmaniasis on households in Bangladesh,” Tropical Medicine and International Health, vol. 11, no. 5, pp. 757–764, 2006.
[11]  I. O. Ajayi, E. N. Browne, B. Garshong et al., “Feasibility and acceptability of artemisinin-based combination therapy for the home management of malaria in four African sites,” Malaria Journal, vol. 7, article 6, 2008.
[12]  Pan American Sanitary Bureau, Tuberculosis Control: A Manual on Methods and Procedures for Integrated Programs, Pan American Health Organization, Pan American Sanitary Bureau, Regional Office of the World Health Organization, Washington, DC, USA, 1986.
[13]  WHO, “Regional Technical Advisory Group on Kala-azar elimination,” Report of the 1st Meeting, Manesar, Haryana, 2004, http://209.61.208.233/LinkFiles/Kala_azar_VBC-88.pdf.
[14]  M. Balasegaram, K. Ritmeijer, M. A. Lima et al., “Liposomal amphotericin B as a treatment for human leishmaniasis,” Expert Opinion on Emerging Drugs, vol. 17, pp. 493–510, 2012.
[15]  T. P. C. Dorlo, M. Balasegaram, J. H. Beijnen, and P. J. de Vries, “Miltefosine: a review of its pharmacology and therapeutic efficacy in the treatment of leishmaniasis,” Journal of Antimicrobial Chemotherapy, vol. 67, no. 11, pp. 2576–2597, 2012.
[16]  F. Meheus, M. Balasegaram, P. Olliaro et al., “Cost-effectiveness analysis of combination therapies for visceral leishmaniasis in the Indian subcontinent,” PLoS Neglected Tropical Diseases, vol. 4, no. 9, article e818, 2010.
[17]  M. R. Banjara, S. Hirve, N. A. Siddiqui et al., “Visceral leishmaniasis clinical management in endemic districts of India, Nepal, and bangladesh,” Journal of Tropical Medicine, vol. 2012, Article ID 126093, 8 pages, 2012.
[18]  J. Alvar, S. Yactayo, and C. Bern, “Leishmaniasis and poverty,” Trends in Parasitology, vol. 22, no. 12, pp. 552–557, 2006.
[19]  D. Mondal, J. Alvar, M. G. Hasnain et al., “Efficacy and safety of single-dose liposomal amphotericin B for visceral leishmaniasis in a rural public hospital in Bangladesh: a feasibility study,” The Lancet Global Health, vol. 2, no. 1, pp. e51–e57, 2014.

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