FIELD: medicine.
SUBSTANCE: for correction, a course of three procedures is performed, including the introduction of thrombocytic autoplasm (TAP) into tissues. Before each procedure, sampling of blood in a volume of 9-36 ml is performed, which is centrifuged to obtain a native form of TAP. In carrying out the first two procedures 4 ml of the obtained native TAP form are taken into 4 sterile syringes by 1 ml in each syringe and placed in a thermostat at a temperature of 56°C and exposure for 5 minutes to obtain a fibrin form of TAP. The fibrin TAP form is mixed with 4 ml of native TAP form through the connector, connecting each syringe with the fibrin TAP form to the syringe with the native TAP form and making 5-10 passes from one syringe to the other. The resulting mixture is introduced into the upper layer of the dermis with a needle with a diametre of 30G and a size of 0.3×12 mm or with a cannula with a diametre of 2×5G and a length of 50 mm by papular, tubercular, linear-retrograde, fanning or bolus techniques of mesotherapy. When carrying out the third procedure 4 ml of the native TAP form is taken into 4 sterile syringes by 1 ml in each syringe and placed in a thermostat at a temperature of 75-80°C and exposure for 10 minutes to obtain a protein form of TAP. After cooling for 2 minutes, syringes with the protein TAP form are connected by a connector with an empty syringe and 10-15 passes are made from the syringe with a protein form into each empty syringe and back. The mixture is introduced into the deep layers of the dermis, the hypodermis and the periosteum by means of a cannula with a diametre of 22G and a length of 57 mm by linear-retrograde, fanning or bolus technique. If necessary, the course is repeated 2 weeks after.
EFFECT: increased efficiency.
4 cl, 2 ex
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Authors
Dates
2017-08-29—Published
2016-12-07—Filed