FIELD: medicine.
SUBSTANCE: method for face and/or neck soft tissue augmentation involving venous blood sampling in an amount of 9-36 ml; thereafter, the blood is centrifuged with acceleration of 1000 G for 5 minutes; the produced platelet-rich autoplasma is taken from the test tube in an amount of 3.0 ml by means of luer-lock syringes. The syringes containing the platelet-rich autoplasma are placed into a thermostat and kept there to produce gel. To introduce into a periorbital and neck region, the platelet-rich autoplasma is kept at 45°C for 5 minutes, or at 85°C for 6 minutes if it is necessary to introduce it into the other face regions. The produced gel is cooled down in a sterile tray for 2 minutes. By means of a connector, the syringe with the produced gel is attached to an empty sterile syringe; the produced gel is transited from one syringe into the other through 5-10 passages and introduced into the face region, avoiding the periorbital region, by means of a short-bevel needle 21G×3.8 cm. Before introduced into the periorbital and/or neck region, the produced gel of the platelet-rich autoplasma is mixed with untreated and platelet non-enriched autoplasma taken from the same patient, in ratio 2:1 and introduced into the periorbital and/or neck tissues by means of a short-bevel needle 27G×13 mm.
EFFECT: method provides ensuring the uniform distribution and adequate correction of the desired regions.
3 cl, 1 ex
