AI Article Synopsis

  • The study focuses on leprosy reactions during multidrug therapy, emphasizing the importance of monitoring to prevent disability.
  • The research involved 211 leprosy patients, finding that the majority experienced reactions within the first three months of treatment, with type one reactions being the most common.
  • Results indicated a positive correlation between bacillary load markers and the number of reactions, suggesting further investigation into the impact of antigenic load on these reactions is warranted.

Article Abstract

Introduction:: The occurrence of leprosy reactions, a common event during treatment, may be mostly related to the action of multidrug therapy on Mycobacterium leprae. The clinical and laboratory monitoring of patients with reactions is important, since collecting data that assists in predicting the risk of reactions may help to prevent disability.

Methods:: This was a sectional study, in order to correlate clinical and laboratory diagnosis with the number of reactions during treatment. Spearman's correlation was used to verify the degree of association between the assessed variables.

Results:: This study was conducted with 211 patients with leprosy reactions during treatment of M. leprae. The borderline tuberculoid group was the most prevalent clinical form (74/211; 35.1%) and the type one reaction showed the highest frequency (136/211; 64.5%). It was observed that 73.5% (155/211) of reactions occurred within 3 months of the initiation of multidrug therapy. The diagnostic values, including the bacterial indices (BIs) of dermal smears (r = 0.21, p < 0.05) and skin biopsies (r = 0.20; p < 0.05), showed a positive correlation with the number of reactions during treatment.

Conclusions:: This research showed a positive correlation between bacillary load markers and the number of leprosy reactions. This study provided scientific support to future research aiming to elucidate the influence of antigenic load on the number of leprosy reactions during treatment.

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Source
http://dx.doi.org/10.1590/0037-8682-0440-2015DOI Listing

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