Abstract

BackgroundLeprosy is a leading cause of preventable disability worldwide. Delay in diagnosis of patients augments the transmission of infection, and allows progression of disease and more severe disability. Delays in diagnosis greater than ten years have been reported in Brazil. To reduce this delay, it is important to identify factors that hinder patients from presenting to doctors, and those that delay doctors from diagnosing patients once they have presented. This study aimed to explore factors associated with the delayed diagnosis of leprosy in Brazil.Methodology/ Principal FindingsThis is an exploratory study using a self-constructed questionnaire delivered to patients attending three leprosy referral clinics across three states in Brazil. Data were analysed to determine associations between variables and the time taken for participants to present to the health-service, and between variables and the time taken for doctors to diagnose participants once they had presented. Participants who suspected they had leprosy but feared community isolation were 10 times more likely to wait longer before consulting a doctor for their symptoms (OR 10.37, 95% CI 2.18–49.45, p = 0.003). Participants who thought their symptoms were not serious had a threefold greater chance of waiting longer before consulting than those who did (OR 3.114, 95% CI 1.235–7.856, p = 0.016). Forty-two point six per cent of participants reported initially receiving a diagnosis besides leprosy. These had a three times greater chance of receiving a later diagnosis of leprosy compared to those not misdiagnosed or not given a diagnosis (OR 2.867, 95% CI 1.288–6.384, p = 0.010).Conclusions/ SignificanceThis study implies a need for patient education regarding leprosy symptoms and the reduction of stigma to encourage patients to present. The high rate of misdiagnosis reported suggests a need to increase clinician suspicion of leprosy. Further education regarding disease symptoms in medical school curriculums may be advisable.

Highlights

  • Leprosy (Hansen’s disease) is one of the world’s Neglected Tropical Diseases and is recognised as ‘a disease of the poor’[1,2,3]

  • The deformities that the disease causes are largely preventable through early detection of the disease

  • In this study we observed that many patients were ignorant to the early symptoms of leprosy, and that the negative image surrounding leprosy within communities can hinder patients from seeking treatment due to the fear of being isolated

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Summary

Introduction

Leprosy (Hansen’s disease) is one of the world’s Neglected Tropical Diseases and is recognised as ‘a disease of the poor’[1,2,3]. Brazil was not predicted to achieve the WHO’s ‘Final push’ goal for 2015. This was to reduce the number of new cases with grade 2 disability that were detected in 2010 by 35% (grade 2 disability is defined as visible damage or deformity) [7,8,9]. Leprosy is a leading cause of preventable disability worldwide. Delays in diagnosis greater than ten years have been reported in Brazil. To reduce this delay, it is important to identify factors that hinder patients from presenting to doctors, and those that delay doctors from diagnosing patients once they have presented. This study aimed to explore factors associated with the delayed diagnosis of leprosy in Brazil

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