FIELD: medicine.
SUBSTANCE: invention relates to medicine and is a method of evaluating the effectiveness of therapy of genital tuberculosis comprising control Immunoassays, characterized in that at the end of the initial phase of therapy is carried out 1st control, which comprises determining the stimulation index of interferon-gamma (IFN-γ) with purified tuberculin (PPD-L), the definition of the levels of specific immunoglobulins (IgA, IgM) for mycobacterium tuberculosis (MBT) by enzyme-linked immunosorbent assay (ELISA), and the 2nd control is carried out through the 6-11 months after the end of the main course of therapy, In the case when a stimulation index IFNγ with PPD-L at the end of the intensive phase of TB treatment was higher than 7, 8 - only IFNγ with PPD-A, if the optical density IgM to MBT has a 0.600 - only IgM to MBT, when the optical density at MBT to IgA was more than 0.450 - control is performed only to IgA; while the results of controlled studies recommend an extension or correction, or the end of therapy.
EFFECT: invention provides a more accurate assessment of TB therapy.
1 cl, 2 ex, 1 tbl
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Authors
Dates
2016-03-20—Published
2014-07-10—Filed