The Impact of the COVID-19 Pandemic on People With Lymphedema in an Endemic Area for Lymphatic Filariasis in Brazil.

Objectives: To investigate the repercussions of the COVID-19 pandemic on lymphedema patients from an endemic area of lymphatic filariasis. Methods: The study descriptive compared sociodemographic and clinical aspects, risk of falling and quality of life, prior and during the COVID-19 pandemic in 28 lymphedema patients, older than 18 years old and under investigation of filarial infection. For the evaluation of functional mobility, the Time Up and Go test and The Medical Outcome Study Short Form-36 Health for quality of life, was used. Results: An increase in interdigital and dermal lesions, a higher frequency of acute dermatolymphangioadenitis crises and risk of falling, worsening of quality of life in the domains of physical functioning, general health, vitality, and mental health during the pandemic was observed. Conclusion: Our findings of clinical worsening and quality of life of patients during the COVID-19 pandemic indicate the need to reinforce the goal of the Lymphatic Filariasis Program regarding the follow-up of these patients in the actions of the Global Program for the Elimination of Lymphatic Filariasis, due to the discontinuity in the care during the pandemic.

Functionality and quality of life of patients with unilateral lymphedema of a lower limb: a cross-sectional study.

BACKGROUND: Lymphedema of the lower limbs is a chronic disease caused by damage to the lymphatic system that influences people's mobility, functionality, and quality of life. Questionnaires and physical test are very practical, easy to apply, and low cost methods that provide important data for evaluation of these patients. OBJECTIVES: To evaluate the influence of unilateral lower limb lymphedema on functionality and quality of life, correlating 3 assessment tools. METHODS: This was a descriptive study investigating 25 patients of both sexes with unilateral lymphedema in a lower limb. Limb volume was assessed using circumferential tape measurements, the Medical Outcomes Study Short Form-36 Health Survey (SF-36) was used to assess quality of life, the Lymphoedema Functioning, Disability and Health Questionnaire for Lower Limb Lymphoedema (Lymph-ICF-LL) was used to assess physical, mental, and social skills related to lymphedema, and the Timed Up and Go (TUG) test was used for functional assessment. RESULTS: Lymphedema was present throughout the affected lower limb of participants. The domains most affected by lymphedema were physical aspects (25.0 ± 31.4) and emotional aspects (36.0 ± 42.9) from the SF-36 and the mobility domain (6.0 ± 2.6) from the Lymph -ICF-LL. Patients performed the TUG in 9.88 ± 1.98 seconds. The TUG was correlated with the questionnaires and the questionnaires were correlated with each other. CONCLUSIONS: People with unilateral lower limb lymphedema exhibited negative impacts on quality of life and functionality, as evaluated by questionnaires, which were correlated with each other. TUG performance was within normal limits, but results correlated with the questionnaires used.

Perfil de pacientes com linfedema atendidos no serviço de referência nacional em filarioses da Fundação Oswaldo Cruz, Pernambuco, Brasil / Profile of lymphedema patients attended at the national center of lymphatic filariasis of the Oswaldo Cruz Foundation, Pernambuco, Brazil

A filariose linfática é uma parasitose endêmica em 73 países e afeta, aproximadamente, 120 milhões de pessoas em todo o mundo. Este trabalho buscou traçar o perfil de pacientes com linfedema que residem em áreas endêmicas de filariose, com ou sem diagnóstico comprovado de doença prévia. Trata-se de um estudo transversal que envolveu pacientes com linfedema, cadastrados no SRNF-CPqAM-FIOCRUZ-PE, residentes nas principais cidades da região metropolitana de Recife, capital do estado de Pernambuco, aos quais foi aplicado um questionário para avaliação do perfil sociodemográfico e epidemiológico. Foram selecionados 35 pacientes, sendo 80% do sexo feminino, a maioria com idade entre 40 e 59 anos (48,6%). Do total examinado, 40% apresentaram linfedema bilateral de membros inferiores e presença de dor moderada no membro afetado. Além disso, dos indivíduos atendidos, apenas 20% receberam diagnóstico de filariose e 68% relataram morar em ruas pavimentadas com disponibilidade de coleta regular de lixo e acesso à água potável. Os resultados deste estudo propiciaram um conhecimento mais abrangente do perfil dos pacientes com linfedema atendidos pelo serviço de referência e poderão auxiliar no aprimoramento das políticas públicas de saúde.