Abstract
Lymphatic filariasis afflicts 68 million people in 73 countries, including 17 million persons living with chronic lymphedema. The Global Programme to Eliminate Lymphatic Filariasis aims to stop new infections and to provide care for persons already affected, but morbidity management programs have been initiated in only 24 endemic countries. We examine the economic costs and benefits of alleviating chronic lymphedema and its effects through a simple limb-care program. For Khurda District, Odisha State, India, we estimated lifetime medical costs and earnings losses due to chronic lymphedema and acute dermatolymphangioadenitis (ADLA) with and without a community-based limb-care program. The program would reduce economic costs of lymphedema and ADLA over 60 years by 55%. Savings of US$1,648 for each affected person in the workforce are equivalent to 1,258 days of labor. Per-person savings are more than 130 times the per-person cost of the program. Chronic lymphedema and ADLA impose a substantial physical and economic burden on the population in filariasis-endemic areas. Low-cost programs for lymphedema management based on limb washing and topical medication for infection are effective in reducing the number of ADLA episodes and stopping progression of disabling and disfiguring lymphedema. With reduced disability, people are able to work longer hours, more days per year, and in more strenuous, higher-paying jobs, resulting in an important economic benefit to themselves, their families, and their communities. Mitigating the severity of lymphedema and ADLA also reduces out-of-pocket medical expense.
Highlights
Lymphatic filariasis (LF) afflicts an estimated 68 million people in 73 countries of Africa, Asia, Oceania, and the Americas[1] and is one of the diseases targeted for elimination by the World Health Assembly
Using Microsoft Excel (Microsoft Corporation, Redmond, WA), we estimated the economic cost of morbidity and disability over the working lives of affected persons without lymphedema management and the projected reduction in those costs that would result from implementation of a community-based lymphedema management program
Lymphedema and episodes of acute dermatolymphangioadenitis (ADLA) in filariasis-endemic areas diminish the quality of life of affected persons due to pain, stigma, numerous days of illness each year, restricted mobility, and reduced participation in family and community life
Summary
Lymphatic filariasis (LF) afflicts an estimated 68 million people in 73 countries of Africa, Asia, Oceania, and the Americas[1] and is one of the diseases targeted for elimination by the World Health Assembly An estimated 36 million people live with the disabling effects of LF, including about 17 million persons with chronic lymphedema, primarily of the legs, and of the arms, breasts, and scrotum, and 19 million men with hydrocele.[1] The remaining LF-infected persons are at risk of developing lymphedema or hydrocele. Programs to manage morbidity and prevent disability among infected persons, the second pillar of the GPELF, had been initiated in only 24 of the 73 endemic countries by 2014.4 This article examines the economic costs and benefits of one such program of morbidity management and disability prevention (MMDP) for alleviating the causes and effects of chronic lymphedema. Interventions for hydrocele differ from those for lymphedema and are not included in this study
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