Leprosy-Related Stigma and Social Representations Among Persons Affected by Leprosy and Primary Healthcare Professionals: A Structural Analysis in the Brazilian Amazon

Leprosy remains a persistent public health challenge not only because transmission continues in endemic settings, but also because stigma remains embedded in social relations, institutional practices, and historical forms of exclusion. This study analyzes the social representations of leprosy among persons affected by leprosy and primary healthcare professionals in a historically endemic area of the Brazilian Amazon, with particular attention to how these representations shape disease recognition, stigma, and care. An exploratory mixed-methods design combined structured questionnaires with a Free Word Association Test to investigate shared meanings of leprosy among 34 persons affected by leprosy (age available for 23 participants; range, 20-85 years) and 19 primary healthcare professionals. Findings show that leprosy is socially understood less through biomedical curability than through stigma, visible bodily damage, and exclusionary meanings, reflected in candidate central elements such as "prejudice", "deformity", and "pain". Although most affected participants recognized that leprosy is curable, substantial knowledge gaps were identified, particularly regarding transmission pathways. Similar limitations were observed among healthcare professionals, indicating weaknesses in diagnostic preparedness within primary healthcare. These results suggest that stigma in leprosy cannot be reduced to insufficient knowledge alone, but should instead be understood as a biosocial phenomenon produced through the interaction of social meanings, embodied experience, and institutional conditions. These dynamics may contribute to delayed diagnosis and reinforce the continued neglect of the disease, requiring integrated strategies that go beyond biomedical control, strengthen primary healthcare, and transform the social and institutional conditions that sustain stigma, diagnostic delay, and exclusion.

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Publication Details

Journal
Journal of Community Health
Published
2026-07-25
DOI
https://doi.org/10.1007/s10900-026-01618-2
Primary Topic
Leprosy Research and Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Leprosy-Related Stigma and Social Representations Among Persons Affected by Leprosy and Primary Healthcare Professionals: A Structural Analysis in the Brazilian Amazon

Luíz Carlos de Abreu, Francisco Albino de Araújo, Ítalla Maria Pinheiro Bezerra, Woska Pires da Costa et al.
Journal of Community Health
Leprosy Research and Treatment
article

Leprosy-Related Stigma and Social Representations Among Persons Affected by Leprosy and Primary Healthcare Professionals: A Structural Analysis in the Brazilian Amazon

Luíz Carlos de Abreu, Francisco Albino de Araújo, Ítalla Maria Pinheiro Bezerra, Woska Pires da Costa, Eloiza Toledo Bauduina, Vinícius Silva dos Santos
article en

Abstract

Leprosy remains a persistent public health challenge not only because transmission continues in endemic settings, but also because stigma remains embedded in social relations, institutional practices, and historical forms of exclusion. This study analyzes the social representations of leprosy among persons affected by leprosy and primary healthcare professionals in a historically endemic area of the Brazilian Amazon, with particular attention to how these representations shape disease recognition, stigma, and care. An exploratory mixed-methods design combined structured questionnaires with a Free Word Association Test to investigate shared meanings of leprosy among 34 persons affected by leprosy (age available for 23 participants; range, 20-85 years) and 19 primary healthcare professionals. Findings show that leprosy is socially understood less through biomedical curability than through stigma, visible bodily damage, and exclusionary meanings, reflected in candidate central elements such as "prejudice", "deformity", and "pain". Although most affected participants recognized that leprosy is curable, substantial knowledge gaps were identified, particularly regarding transmission pathways. Similar limitations were observed among healthcare professionals, indicating weaknesses in diagnostic preparedness within primary healthcare. These results suggest that stigma in leprosy cannot be reduced to insufficient knowledge alone, but should instead be understood as a biosocial phenomenon produced through the interaction of social meanings, embodied experience, and institutional conditions. These dynamics may contribute to delayed diagnosis and reinforce the continued neglect of the disease, requiring integrated strategies that go beyond biomedical control, strengthen primary healthcare, and transform the social and institutional conditions that sustain stigma, diagnostic delay, and exclusion.

Journal of Community Health
Universidade Federal do Acre (BR), Universidade de São Paulo (BR), University of Limerick (IE), Florida Gulf Coast University (US), Instituto Federal Goiano (BR), Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória (BR), Faculdade de Medicina do ABC (BR), Universidade Federal do Espírito Santo (BR), Universidade Federal do Pará (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Universidade de São Paulo
Reduced inequalities
Openalex Percentile: Top 8%
Leprosy Research and Treatment
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