FIELD: medicine.
SUBSTANCE: method involves determining antibodies IgG and/or IgM to retinal S-antigen. Optical density difference between test sera under test and reference one is taken into consideration. The values being equal to or greater than 0.2 and/or 0.15, available antibodies of corresponding class relative to retinal S-antigen are detected, respectively. High risk of complications is predicted. The values being less than 0.2 and/or 0.15, conclusions are drawn concerning absence of said antibodies and low risk of complications is predicted.
EFFECT: high accuracy of prognosis; wide range of applications.
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