FIELD: medicine.
SUBSTANCE: level of aspartate aminotransferase is determined in the blood serum in the acute period of the disease, linear discriminant functions of LDF1 (absence of development of gastroenterological pathology) and LDF2 (presence of development of gastroenterological pathology) are calculated according to formulas LDF1 = -6.03+2.40X1+0.83X2+0.64X3-1.42X4+0.64X5; LDF2 = -12.63+2.75X1+1.13X2+0.93X3+2.02X4+5.09X5, where X1 is the nature of fever in the first day of the disease (1 - subfebrile: 37.0-37.9°C; 2 - febrile: 38.0-38.9°C; 3 - high febrile: 39.0-39.9°C; 4 - hyperpyretic: 40.0°C and more); X2 is the frequency of liquid stool on the first day of the disease; X3 is the number of episodes of vomiting on the first day of the disease; X4 is the level of aspartate aminotransferase in serum in the acute period of the disease (0 - normal, 1 - elevated); X5 is the use of antibacterial drugs for prehospital treatment (0 - no, 1 - yes). LDF1 and LDF2 values are compared, and the development of post-infection functional gastroenterological pathology is predicted if LDF2>LDF1.
EFFECT: method application will increase the efficiency of prevention and prevent formation of post-infectious diseases of the digestive organs of a functional nature, reduce the number of adverse outcomes of rehabilitation.
2 ex, 3 tbl
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Authors
Dates
2017-06-21—Published
2016-06-23—Filed