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Understanding reasons for delay in diagnosis of leprosy in Pakistan: A qualitative study

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  • Anil Fastenau
  • Maxwell Oliver Beresford
  • Matthew Willis
  • Sophie CW Stuetzle
  • Fabian Schlumberger
  • Heleen Neeltje Willemijn Duighuisen

Abstract

Background: Recent epidemiological data shows significant rates of grade 2 disability at point-of-diagnosis among new leprosy cases in Pakistan. This indicates a feature of extensive diagnostic delay; the disability burden appears unmoving and disproportionate to the falling leprosy incidence rates. Therefore, this study was required to understand reasons for delay in diagnosis and treatment of leprosy. Methods: A qualitative design of 7 semi-structured interviews was employed to reveal perceptions and understandings of various leprosy stakeholders in Pakistan, termed “leprosy experts”. Subsequent inductive analysis was used to identify themes and subthemes concerned with delay in the diagnosis and treatment of leprosy. Results: Leprosy experts identified three main areas, or domains, to which delay can be attributed: 1. Awareness and beliefs about leprosy, within the general population, 2. Knowledge and clinical experience of leprosy, among healthcare professionals, 3. Leprosy control program infrastructure, allocation of resources and institutional funding. These domains were each viewed as consequent to the larger theme of ‘low-endemicity’. Strong correlations between diagnostic delay and socioeconomic status, gender, geography and health system challenges, were also mentioned, and which intersected the three major themes. Conclusion: Reasons for diagnostic delay are evident in all tiers of the healthcare hierarchy in Pakistan. Thus, an approach at multiple levels is justified, to improve the general awareness of leprosy, education of healthcare professionals, and organizational structuring. Additionally, cultural features relevant to different communities in Pakistan which might be different from other care access frameworks demonstrated a need for further study into the health beliefs of Pakistani patients in a wide range of communities. Author summary: This study addresses the persistent issue of diagnostic delay in leprosy cases in Pakistan, where grade 2 disability remains prevalent at the point of diagnosis, despite declining incidence rates. Through qualitative analysis, seven semi-structured interviews with key stakeholders, termed "leprosy experts," were conducted to explore the underlying factors contributing to these delays.

Suggested Citation

  • Anil Fastenau & Maxwell Oliver Beresford & Matthew Willis & Sophie CW Stuetzle & Fabian Schlumberger & Heleen Neeltje Willemijn Duighuisen, 2025. "Understanding reasons for delay in diagnosis of leprosy in Pakistan: A qualitative study," PLOS Neglected Tropical Diseases, Public Library of Science, vol. 19(1), pages 1-12, January.
  • Handle: RePEc:plo:pntd00:0012764
    DOI: 10.1371/journal.pntd.0012764
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    References listed on IDEAS

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    1. Mary Henry & Noêmi GalAn & Katherine Teasdale & Renata Prado & Harpreet Amar & Marina S Rays & Lesley Roberts & Pedro Siqueira & Gilles de Wildt & Marcos Virmond & Pranab K Das, 2016. "Factors Contributing to the Delay in Diagnosis and Continued Transmission of Leprosy in Brazil – An Explorative, Quantitative, Questionnaire Based Study," PLOS Neglected Tropical Diseases, Public Library of Science, vol. 10(3), pages 1-12, March.
    2. Yudhy Dharmawan & Ahmad Fuady & Ida Korfage & Jan Hendrik Richardus, 2021. "Individual and community factors determining delayed leprosy case detection: A systematic review," PLOS Neglected Tropical Diseases, Public Library of Science, vol. 15(8), pages 1-17, August.
    3. Mull, J. Dennis & Wood, Corinne Shear & Gans, Lydia P. & Mull, Dorothy S., 1989. "Culture and 'compliance' among leprosy patients in Pakistan," Social Science & Medicine, Elsevier, vol. 29(7), pages 799-811, January.
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