ISSN: 2332-0877

感染症と治療ジャーナル

オープンアクセス

当社グループは 3,000 以上の世界的なカンファレンスシリーズ 米国、ヨーロッパ、世界中で毎年イベントが開催されます。 1,000 のより科学的な学会からの支援を受けたアジア および 700 以上の オープン アクセスを発行ジャーナルには 50,000 人以上の著名人が掲載されており、科学者が編集委員として名高い

オープンアクセスジャーナルはより多くの読者と引用を獲得
700 ジャーナル 15,000,000 人の読者 各ジャーナルは 25,000 人以上の読者を獲得

抽象的な

Improving leprosy treatment outcomes in Pernambuco, Brazil: A qualitative study exploring the experiences, perceptions, and beliefs of retreatment patients and their carers

Divya Khanna

Brazil has a high leprosy burden and poor treatment outcomes (TOs). Pernambuco, an impoverished Brazilian state, has ‘hyperendemic’ leprosy. While current literature focuses on treatment compliance, inadequate research exists on other factors influencing TOs. This qualitative study explores the views of leprosy patients and their careers in Pernambuco,Brazil, identifying location-specific factors influencing TOs. Semi-structured, in-depth interviews were conducted with 14 patients and 13 carers, recruited using purposive and snowball sampling from three clinics in Petrolina, Pernambuco.Transcripts and field notes were analyzed using conventional thematic and deviant case analysis. The University of Birmingham and the Instituto Lauro de Souza Lima, Brazil provided ethical approval.Two sets of four interdependent themes emerged: ‘personal factors’; ‘external factors’; ‘clinical factors’; and ‘the HCPpatient- carer relationship’. Inadequate participant knowledge and symptomatic relief caused distrust in treatment. However, HCPs effectively persuaded participants to adhere to pharmaceutical treatments. Better participant education facilitated treatment engagement, by encouraging evidencebased medicine belief and dispelling health myths and stigma. Healthcare was occasionally perceived as disorganized, particularly in resource-scarce suburbs and psychiatric care.
Participants experienced ineffective diagnosis and contact tracing. Leprosy’s negative socio-economic impact, effect on
interpersonal relationships, and stigma unfavorably caused altered senses of identity. Dialogue between patients, HCPs and
carers facilitated individualized patient support This study highlights the importance of evidence-based leprosy education; communication between HCPs, patients and carers; state funding; and healthcare resource distribution. These findings inform location-specific leprosy-targeting strategies, and if ignored may hinder regional elimination. Future research should evaluate the effectiveness of newly implemented leprosy-targeting strategies.