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Adverse reactions in leprosy patients who underwent dapsone multidrug therapy: a retrospective study

Authors Guragain S, Upadhayay N, Bhattarai BM

Received 28 February 2017

Accepted for publication 30 May 2017

Published 29 June 2017 Volume 2017:9 Pages 73—78

DOI https://doi.org/10.2147/CPAA.S135846

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Akshita Wason

Peer reviewer comments 3

Editor who approved publication: Professor Arthur Frankel


Sanjeev Guragain,1 Namrata Upadhayay,2 Bishwa Mohan Bhattarai3

1Department of Pharmacology, Gandaki Medical College Teaching Hospital and Research Centre, Lekhnath, 2Department of Physiology, Gandaki Medical College Teaching Hospital and Research Centre, Lekhnath, 3Dermatology Department, Green Pastures Hospital and Rehabilitation Centre, Pokhara, Nepal

Objective: To investigate the occurrence and clinical characteristics of dapsone-related adverse drug reactions (ADRs) among leprosy patients who underwent multidrug therapy (MDT) from 2010 to 2013 in the western region of Nepal.
Methods: A retrospective review was carried out in the rehabilitation center. Data were collected from the record files of the hospital.
Results: From 2010 to 2013, there were 18 patients reported to have dapsone ADRs, with an occurrence rate of 0.82% in the 4-year duration. The maximum incidence of ADRs (1.043%) was in 2010 and the minimum incidence of ADRs (0.26%) was in 2013. Among two types of bacterial infections, 94.44% were of multibacillary and 5.56% were of paucibacillary type. The age range of patients with dapsone ADRs was 11–68 years. The male-to-female ratio was 1.25. The onset of dapsone ADRs after taking MDT was within a minimum of 3 weeks and a maximum of 21 weeks. There were 14 (77.77%) patients who presented with jaundice, 8 (44.44%) with exfoliative dermatitis, 5 (27.77%) with hemolytic anemia and 4 (22.22%) with fever and headache. The rare side effects (5.5%) found were agranulocytosis or toxic epidermal necrolysis. Three patients were cured; some were still on the treatment. Four patients died with dapsone ADRs.
Conclusion: The common dapsone ADRs present in leprosy patients were jaundice, exfoliative dermatitis and hemolytic anemia in MDT-treated patients. Patients could be cured by managing the dapsone ADRs effectively on time. Some patients may die of dapsone ADRs if clinicians fail to manage the side effects on time.

Keywords: dapsone, dermatitis, anemia, minocycline, ofloxacin

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