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Confirmation of preclinical data on tioureidoiminomethylpyridinium perchlorate in treatment of MDR-TB

Maria Pavlova, Tatiana Vinogradova, Anna Starshinova, Piotr Yablonskii, Irina Chernokhaeva, Ludmila Archakova, Nadezda Sapozhnikova
European Respiratory Journal 2015 46: PA2711; DOI: 10.1183/13993003.congress-2015.PA2711
Maria Pavlova
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
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Tatiana Vinogradova
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
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Anna Starshinova
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
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Piotr Yablonskii
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
2Phthisiopulmonology Department, University of St. Petersburg, Saint-Petersburg, Russian Federation
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Irina Chernokhaeva
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
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Ludmila Archakova
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
2Phthisiopulmonology Department, University of St. Petersburg, Saint-Petersburg, Russian Federation
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Nadezda Sapozhnikova
1Phthisiopulmonology Department, Research Institute Phthisiopulmonology, Saint-Petersburg, Russian Federation
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Abstract

Introduction: In accordance to international classification Tioureidoiminomethylpyridinium perchlorate (Perchlozon) belongs to thioacetazone group [D.Tomas, 2014].

Objective: to confirm data on safety and efficacy of Tioureidoiminomethylpyridinium perchlorate (Pch) in treatment of multidrug resistant (MDR) lung tuberculosis.

Materials and methods: in vitro Pch demonstrated significant inhibiting effect on viability of drug-resistant mycobacteria strains of TB. Wherein MIC of the substance varied from 0.78 to 6.25 ug/ml. In the reported clinical study, which was performed in 2013-2014, 49 patients with MDR lung tuberculosis were enrolled. The patients were divided in two groups: Group 1 (main) 25 patients were administered Pch in addition to 6 other anti-tuberculosis drugs; in Group II (comparison) 24 patients received 6 anti-tuberculosis drugs. Duration of treatment in both groups was 6 months. After that in both groups 5 drugs in 6 mohth. Statistical analysis was peformed using SPSS 16.0.

Results and their discussion: In Group 1 the most common adverse drug reactions were endocrine disorders (18.4% (9) vs (0), p<0,01) and fever (8.2% (4) vs (0), p<0,05) – which were not observed in Group 2. Other adverse drug reactions were recorded in equal measures in both groups. Efficacy of treatment (which was assessed by cessation of bacterial excretion in sputum) was higher in Group 1 vs. Group 2 - both after 3 months (68.0 % (17) vs 37.5% (9) and after 6 months (80.0% (20) vs 62.5% (15) of study treatment start, after 12 month (88.0% (22) vs 66.7% (16).

Conclusion: Efficacy of treatment with Pch was 88.0% in complex with other anti-tuberculosis drugs.

  • Treatments
  • Tuberculosis - management
  • Pharmacology
  • Copyright ©ERS 2015
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Confirmation of preclinical data on tioureidoiminomethylpyridinium perchlorate in treatment of MDR-TB
Maria Pavlova, Tatiana Vinogradova, Anna Starshinova, Piotr Yablonskii, Irina Chernokhaeva, Ludmila Archakova, Nadezda Sapozhnikova
European Respiratory Journal Sep 2015, 46 (suppl 59) PA2711; DOI: 10.1183/13993003.congress-2015.PA2711

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Confirmation of preclinical data on tioureidoiminomethylpyridinium perchlorate in treatment of MDR-TB
Maria Pavlova, Tatiana Vinogradova, Anna Starshinova, Piotr Yablonskii, Irina Chernokhaeva, Ludmila Archakova, Nadezda Sapozhnikova
European Respiratory Journal Sep 2015, 46 (suppl 59) PA2711; DOI: 10.1183/13993003.congress-2015.PA2711
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