Abstract

Lymphedema is a life-long sequelae to several neglected tropical diseases (NTD). In Bangladesh the main cause is lymphatic filariasis (LF) and Ethiopia is endemic for both LF and podoconiosis. The World Health Organization (WHO) recommends daily self-care including meticulous washing and drying of affected skin and attention to entry lesions, limb exercises and elevation. Adherence to this regime reduces secondary infections which cause disabling episodes of acute dermato-lymphangitis (ADL). Self-care practices must be integrated into family life, supported by community and monitored by health staff; however, little is known about the influence of personal and socio-demographic factors on adherence. People affected by lymphedema (n=272), adult caregivers (n=272), and health workers (n=68) in Bangladesh and Ethiopia were trained in lymphedema management according to WHO recommendations. Surveys on the causes and management of lymphedema were collected at baseline and 24-weeks, and patients completed a daily journal of self-care activities and symptoms. At baseline knowledge on causes and management of lymphedema was greater among health workers (>70%) than patients and caregivers (<20%) in both countries, and there were significant between-country differences in patient reported use of limb washing (Bangladesh = 7.7%. Ethiopia = 51.1%, p = 0.001). At 24-weeks knowledge on lymphedema causes and management had increased significantly among patients and caregivers, there was <70% adherence to limb washing and exercises, but lesser use of limb elevation in both countries. A range of patient characteristics were associated with significant variation in self-care, except for limb washing. Performance of fewer leg exercises was significantly associated with increased age or severe lymphedema in Bangladesh, and with being female or in paid work in Ethiopia. Patient journals recorded ADL symptoms and working days lost due to lymphedema more frequently than were reported by recall during the 24-week survey. Core elements of lymphedema self-care education, training and monitoring are the same for multiple etiologies. This creates opportunities for cross-cutting implementation of integrated service delivery across several skin NTDs. Sustainability will depend on community level ownership and research on factors affecting adherence to lymphedema self-care are urgently needed.

Highlights

  • The World Health Organization (WHO) Roadmap to End Neglected Tropical Diseases (NTD) includes the elimination of lymphatic filariasis (LF) as a public health problem in at least 58 of the 72 LF-endemic countries by 2030

  • There is no requirement to report on the number of people who are trained in lymphedema selfmanagement, or the frequency of their self-care practice [8]

  • Results presented here from both Bangladesh and Ethiopia showed that while most health workers had good knowledge on lymphedema causes (>90%) and the need for limb hygiene (>70%), knowledge among the end-users, the patients and their caregivers was much lower, less than 25% for either population. This knowledge gap must be addressed, and the goal to reduce the suffering of people affected by lymphedema requires that effective tools are placed in the hands of those affected and their families [23]

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Summary

Introduction

The World Health Organization (WHO) Roadmap to End Neglected Tropical Diseases (NTD) includes the elimination of lymphatic filariasis (LF) as a public health problem in at least 58 of the 72 LF-endemic countries by 2030. Elimination of LF as a public health problem is defined as 1) an infection rate sustained below transmission thresholds, and 2) the availability of an essential package of care for people with existing clinical disease [1]. The clinical manifestations of LF are hydrocele and lymphedema, and these conditions are exacerbated by secondary infections causing acute dermato-lymphangitis (ADL). Hydrocelectomy surgery offers a permanent cure for people affected by hydrocele, but lymphedema cannot be cured and treatment entails lifelong self-management by affected persons with the support of their family and broader community [3]. The WHO recommends similar self-management interventions for people affected by podoconiosis [4], which causes lower limb lymphedema after bare-foot exposure to irritant soils [5]. Together LF- and podoconiosis-related lymphedema cause pain, disfigurement, disability, and social exclusion for 20 million people globally [6, 7]

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