Body detoxification procedure
SUBSTANCE: first, Fraxiparine is inhaled for 5-10 minutes. A dialysis solution for peritoneal dialysis containing extranyl is administered into the abdominal cavity 1-1.5 hours later through a catheter. The solution additionally contains: albumin in the concentration of 35-40 g/l, heparin in the concentration of 500-750 Unit/l and papaverine in the concentration of 50-100 mg/l. Every 6-8 hours after the beginning of exposure of the dialysis solution in the abdominal cavity, the Fraxiparine inhalations are repeated. The time of a single exposure of the dialysis solution in the abdominal cavity makes 12-18 hours.
EFFECT: method provides effective body detoxification in the given category of patients by providing a high toxin clearance owing to a continuous high osmotic concentration of the solution and the dilatation of pre-capillary peritoneal arterioles, prevented inspissation of the albumin solution to the colloidal state and its inactivation that reduces a rate of the dialysis solution exchanges.
The invention relates to the field of medicine, to methods intracorporeal detoxification, and can be applied in stationary conditions.
One of the most common methods of detoxification is peritoneal dialysis (BT the Bikbov, N.A. Tomilin. Nephrology and dialysis. - 2011. - V.13. No. 3, s).
It is known that the possibility of applying this method of detoxification can be significantly limited as a result of the development of dialysis peritonitis, due to the need 4-5-fold replacement solution in the abdominal cavity and the associated high risk of infection dialysis solution, and frequently overweight patients, as well as features of the transport properties of the peritoneum, causing treatment failure peritoneal dialysis.
The closest is a way of detoxifying used in the treatment of kidney and liver failure, as well as endo - and exogenous intoxications, including peritoneal dialysis performed by introduction through the catheter into the abdominal cavity of the dialysis solution containing albumin in a concentration of 65-75 g/l and Fraxiparine 0,3-0,6 ml; the latter 2 components are pre-mixed together in 3-5 minutes, and then through the infusion system is introduced into a standard dialysis solution, PR is varicella warmed up to t 38-40°C. Exposure of this solution into the abdominal cavity occurs within 5-7 hours (RF Patent 2325194, IPC A61M 1/28, publ. 2008).
The disadvantages of this method include the risk of dialysis peritonitis and high cost of implementation due to the impossibility prolonged exposure dialysis solution and the need for 4-6-fold replacement dialysis solution into the abdominal cavity, which leads to increased risk of infection and the emergence of dialysis peritonitis.
The objective of the proposed method is to increase the efficiency of detoxification of the body by applying the composition solution for peritoneal dialysis, reduction in the incidence of dialysis peritonitis due to a significant reduction in the number of exchanges of dialysis solution, and improving the quality of life and survival of patients; reduction in the cost of treatment patients receiving treatment for peritoneal dialysis; reduction in bed-days due to the quick effect of dialysis therapy.
The task in the way of detoxification is due to the fact that first made by the inhalation of fraxiparina for 5-10 minutes. Then after 1-1,5 hours exercise introduction through the catheter into the abdominal cavity of the dialysis solution for peritoneal dialysis containing EXTRANEAL, in which BB is completed with albumin at a concentration of 35-40 g/l, heparin at a concentration of 500-750 IU/l papaverine at a concentration of 50-100 mg/L. thus every 6-8 hours after start of exposure dialysis solution into the abdominal cavity again inhalation of fraxiparina. During a single exposure dialysis solution into the abdominal cavity 12-18 hours.
That apply this dialysis solution provides high ground clearance of toxins through maintaining a constant high osmolarity of the solution, as well as dilatation precapillary arterioles peritoneum. This also contributes to the long exposure time of the proposed solution in the abdominal cavity. Inhalation of fraxiparina and content of heparin in solution to prevent the precipitation of albumin to a colloidal state and its inactivation. Reduces the number of exchanges of dialysis solution 2-6 times, namely up to 1.5-2 times per day.
The proposed method intracorporeal detoxification and characteristics that distinguish it from known, in the medical and patent literature is not found.
The method is as follows.
Is inhalation introduction of fraxiparina for 5-10 minutes in 1-1,5 hours, followed by infusion through the catheter into the abdominal cavity of the dialysis solution, mainly within the 2 liter Solutions of albumin, heparin and papaverine mixed between the Wallpaper in 3-5 minutes, and then through the infusion system is injected into dialyzing solution - EXTRANEAL. Exposure of this solution into the abdominal cavity occurs within 12-18 hours.
The proposed method was successfully applied in the Department of transplantation, Nephrology and surgery hemocorrection.
The implementation of the method is demonstrated on specific clinical examples.
Patient D., born in 1981, was admitted to the hospital with a diagnosis of poisoning with alcohol substitutes. Acute renal failure, anuria stage.
Upon receipt marked edema of the lower extremities, puffiness of the face, arterial hypertension, evidence of severe overhydration. Creatinine was 900 µmol/l, urea - 34 mmol/l, the critical hyperkalemia - 6.8 mmol/L.
Extra implantation of peritoneal catheter initiated treatment of peritoneal dialysis on the proposed method: in 2.0 l of 7.5% solution of EXTRANEAL put 1500 IU of heparin solution, 200 mg of a solution of papaverine and 80 g of albumin. The prepared solution was injected into the abdominal cavity of the patient within 1 hour after inhalation of fraxiparina within 5 minutes (repeated inhalation was performed every 6 hours). Dialysate drained after 12 hours in the volume of 3.1 l, controlled completely hyperkalemia. Repeated infusion of a solution with the same composition.
Chere is C day treatment peritoneal dialysis has managed to significantly reduce the overload, to reduce the creatinine level up to 450 mmol/l, urea to 20.3 mmol/L. Subsequently, the treatment of peritoneal dialysis in the same pattern held for two weeks until full recovery of renal function.
It should be noted that as a result of treatment the patient's proposed method of peritoneal dialysis managed to achieve restoration of diuresis after 2 weeks, which is considerably less than when using the standard treatment. This is due to effective detoxification and relief of factors contributing to necrosis of the renal tubules.
Was discharged in good condition after 17 days.
Patient O., born in 1970, was in outpatient treatment with a diagnosis of diabetes mellitus, type 2, insulin, asthma, heavy flow. Diabetic nephropathy. Diabetic angio-retinopathy. Chronic renal insufficiency, end-stage. Continuous ambulatory peritoneal dialysis.
Was admitted to hospital because of the development of dialysis peritonitis. Conducted antibacterial therapy. When examined, among other complications were identified deterioration of the transport properties of the peritoneum, which was reflected in the failure of ultrafiltration, reducing weekly index of the adequacy of treatment of peritoneal dialysis Kt/V of 1.2, as well as red eye reduction the Sri index weekly creatinine clearance up to 42 HP
In order to achieve effective treatment peritoneal dialysis was used in the proposed method: pre-prepared solution containing 2.0 l of a solution of EXTRANEAL, a solution of heparin in a dose of 1200 IU, albumin, 70 g, the solution of papaverine 150 mg
1.5 hours after inhalation of fraxiparina within 10 minutes, the mixed solution is introduced into the abdominal cavity 18 hours, repeated inhalation of fraxiparina was performed every 8 hours.
As a result of treatment under the scheme for 1.5 weeks on a background of antibacterial therapy were able to achieve edema dialysis peritonitis, terminate overload, increase weekly index, Kt/V to 2.3 and weekly creatinine clearance up to 75 litres per week, which contributed to the achievement of the necessary dose of dialysis.
The patient was discharged to outpatient treatment after 12 days.
Patient T., born in 1963, in connection with the transferred dialysis peritonitis observed treatment failure peritoneal dialysis according to the standard schema.
Therefore, it was decided to conduct the treatment by the proposed method with the use of a new dialysis solution.
Inhalation of fraxiparina for 7 minutes, followed after 1 hour by infusion into the abdominal cavity 2.0 l of EXTRANEAL with the addition of the solutions in the concentration of albumin 80 g of papaverine 100 mg/l, gaari is and 500 IU/L. Inhalation of fraxiparina repeatedly carried out every 7 hours. After 14 hours was drained dialysate in a volume of 3.5 liters To treat peritoneal dialysis under the proposed method, the serum creatinine was 1.25 mmol/l, urea 32.5 mmol/l after treatment - 0.65 mmol/l and 12.3 mmol/l, respectively.
The treatment in this way was carried out within 3 weeks, this was achieved prolonged use of peritoneal dialysis for conversion to hemodialysis without additional unscheduled medical measures to prolong hospitalization and extended periods of rehabilitation patients.
In General, application of the developed method of peritoneal dialysis in 82 patients made it possible to improve the results of the application of peritoneal dialysis by reducing the time of recovery of renal function in acute poisoning and acute renal failure due to effective detoxification.
The method allows to prolong the treatment of peritoneal dialysis in chronic renal failure, improve the quality of life and survival of patients with dialysis peritonitis, to reduce the number of bed-days, and to increase the economic efficiency of the treatment of these categories of patients.
The way de is oxical body, including peritoneal dialysis is injected into the abdominal cavity of the dialysis solution, which is injected albumin, the introduction of fraxiparina, characterized in that as a dialysis solution using EXTRANEAL, while albumin injected into the dialysis solution at a dose of 35-40 g/l, optionally add heparin at a dose of 500-750 IU/l and papaverine in a dose of 50-100 mg/l, exposure dialysis solution into the abdominal cavity is carried out for 12-18 hours, and Fraxiparine administered by inhalation for 5-10 minutes for 1-1,5 hours before the introduction of the dialysis solution, and then every 6-8 hours after start of exposure dialysis solution into the abdominal cavity.
FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to pharmaceutical industry, namely to an immunomodulatory composition for injection into a mammal. The immunomodulatory composition for injection into a mammal containing a hydrolysate prepared by acid and/or enzymatic hydrolysis of one or more bioresources specified in a group consisting of bivalve molluscs, annelids, leeches, and water taken in certain proportions. A method for preparing the immunomodulatory composition for injection into a mammal. A method of treating a pathological condition in a mammal in need thereof involving the injections of the immunomodulatory composition into the above mammal. Using the composition for normalising metabolism into the mammal in need thereof.
EFFECT: composition enables extending the range of products with immunomodulatory activity for injections.
19 cl, 7 tbl, 7 ex
FIELD: veterinary medicine.
SUBSTANCE: method of treatment of calves with Simuliidotoxicosis is that 40% solution of urotropine is administered intravenously to calves at a dose of 1.5 ml per 10 kg of animal body weight.
EFFECT: improvement of efficiency of the method.
SUBSTANCE: group of inventions relates to veterinary and medicine, in particular to obtaining and application of biopreparations for immunotherapy of ecopathologies. The group of inventions includes obtaining a protein antigen from a mixture of anatoxins from three enteropathogenic virulent strains of a pathogen of escherichiosis of calves E.coli No. 378, 379, 380 by their growing on Hottinger medium with further addition of 0.4-0.5% formalin, following thermostating for 10-12 days and cooling the mixture of anatoxins with a sterile solution of aluminium hydroxide, after that obtaining radioantigen from E.coli "PL-6" by growing cultures on a meat infusion agar with further washing away a biomass by a physiological solution and irradiation of the obtained suspension with a concentration of 1.2·1010 m.c./cm3 on a gamma-installation in a dose of 140-150 Gr with following thermostating and extraction of radiotoxin with 70% acidified with 0.05% hydrochloric acid to pH 5.5 ethanol, following evaporation of the exractant to the initial volume, after that, obtaining protein-cadmium radioantigen first by preliminary dechlorination of cadmium chloride, obtaining cadmium hydroxide, addition into the obtained 2.7% solution of the antigen of 0.77% solution of cadmium hydroxide in a ratio of 1:1 with following thermostating at a temperature of 37°C for 30 minutes, evaporation and dissolution of the residue to 12.8% concentration, further obtaining protein-cadmium radioantigen by an addition of 1.2% solution of a mixture of three anatoxins of E.coli and 12.8% solution of cadmium radioantigen in a ratio of 1:9, conjugation of components at room temperature for 8-10 hours, standardisation by a dry substance to 10% concentration and pouring into vials, and storage at a temperature of 4-6°C. The group of inventions also relates to a method of treating radiation, chemical and/or bacteriological damage to an organism by introduction of 10% solution of complex protein-cadmium radioantigen.
EFFECT: application of the group of inventions is effective in treatment of radiation, chemical and/or biological damage.
4 cl, 6 ex
FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to medicine and particularly to preparations for a therapy of oncological diseases, treatment of allergy, prevention and health improvement. The invention represents a method for preparing fraction 4 (ADP-f4) and fraction (ADP-f5) adaptogenic Dorogov's preparations, characterised by the fact that a primary product is a fraction 2 antiseptic Dorogov's stimulator (ADP-f2) to be thermally treated.
EFFECT: implementing the given invention provides the more effective prevention and eliciting anti-stress reactions for the purpose of improving the functional state of organism and increasing a resistance in an activation therapy.
SUBSTANCE: invention refers to medicine and veterinary science and aims at increasing the radioresistance in mammals. In the period of 12 hours to 20-30 minutes before a radiation exposure and immediately thereafter, 0.11% oil preparation of chlorophyll is introduced into the mammals. Linseed oil is used as an oil base. The preparation is introduced in a dose of 11-12 mg/kg intramuscularly.
EFFECT: method enables increasing the radioresistance and survival rate in the mammals.
1 tbl, 1 ex
FIELD: medicine, pharmaceutics.
SUBSTANCE: composition for treating oxidative stress comprises ball-shaped lipoic acid or one of salts thereof, and at least one lipophilic medium. The lipoic acid balls represent particles consisting of an inert core (a nucleus) coated with lipoic acid which is coated with a first layer of an isolating polymer, and with a second polymer layer resistant (stable) at gastric pH. What is also described is a preparation for treating oxidative stress with an unified dose containing the above composition. The preparation is presented in the form of a soft gelatin capsule.
EFFECT: compositions according to the invention are stable in the lipophilic medium.
22 cl, 15 ex
FIELD: medicine, pharmaceutics.
SUBSTANCE: group of inventions refers to medicine, particularly toxicology and radiology, to drug preparations based on antioxidant proteins and methods of using them. The pharmaceutical composition for treating toxic conditions wherein the therapeutic effect is ensured by the action of antioxidant, antimicrobial, antitoxic human lacroferrin protein on the human body contains non-replicating nanoparticles of human adenovirus serotype 5 genome with inserted human lactoferrin expressing human lactoferrin in the therapeutically effective amount in the body, and an expression buffer with the particle content not less than 2.33×1011 of physical particles per ml of the expressing buffer. The method of therapy involves administering the composition in the therapeutically effective dose of 7×1011 of physical particles to 7×1013 of physical particles per ml of the expressing buffer per an individual; the composition is administered intravenously.
EFFECT: invention provides the stable therapeutic effect after the single administration of the composition.
17 cl, 14 ex, 4 dwg
FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to medicine, and concerns a pharmaceutical composition for the therapy of acute toxic conditions. The composition for the therapy of acute toxic conditions contains a protein - human lactoferrin, and additionally contains non-replicating nanoparticles with an inserted gene of human lactoferrin, and an expressing buffer in the following proportions per a dose: human lactoferrin 50 to 100 mg; non-replicating nanoparticles - 7×1011 of physical particles; the expressing buffer - the rest, ml. Human lactoferrin is either donor breast milk lactoferrin, or any human lactoferrin.
EFFECT: invention provides fast onset and prolonged antitoxic action.
4 cl, 8 ex, 2 dwg
FIELD: medicine, pharmaceutics.
SUBSTANCE: invention relates to medicine and pharmacy and can be applied in production and application of solutions for intravenous introduction in treatment of conditions, associated with endogenous intoxication. Disintoxication solution contains components in the following ratio (wt %): sodium hypochlorite 0.04-0.08, sodium chloride 0.50-1.00, aminoethane sulfonic acid 0.02-1.20.
EFFECT: novel infusion solution is claimed.
4 ex, 1 tbl
FIELD: medicine, pharmaceutics.
SUBSTANCE: invention refers to pharmaceutical industry, namely an agent possessing anti-inflammatory action. The agent possessing anti-inflammatory action contains as active ingredient in the form of a complex prepared of a coelomic fluid of sea urchins containing peptides and amino acids at a certain ratio of the ingredients.
EFFECT: agent possesses a manifested anti-inflammatory effect.
2 cl, 2 tbl, 10 ex
SUBSTANCE: group of inventions relates to medical equipment. Respiratory mask contains mask frame, forming slot; lining, made from first material; and holding element, made from second material, which is more rigid than first material. Holding element is imbedded inside lining and made with possibility of detachable fixation to mask frame. Pad and holding element are located inside slot in such a way that lining is outside in slot. Method of assembling respiratory mask, determining mask casing, forming slot for reception of gas flow, and cross connection, originating from mask casing and determining first and second slots, is described. Lining unit includes lining and holding element, imbedded into lining. Holding element includes tongues for fixation of lining to mask casing and first and second forehead pads, located in first and second slots of cross connection. First and second forehead pads are made with possibility of independent regulation with respect to each other and with respect to mask frame both in horizontal and in vertical directions.
EFFECT: provision of convenience of assembling and sealing mask elements to user's face.
16 cl, 8 dwg
SUBSTANCE: invention refers to medicine, namely to anaesthesiology, resuscitation and otorhinolaryngology, and can be used if it is necessary to provide the anaesthetic management in the patients with terminal tracheostomy. For this purpose, pre-oxygenation, assisted and forced lung ventilation are conducted before tracheal intubation through a laryngeal mask with an inflated cuff tightly adjoining a tracheostomy opening. Then, an intubation tube is inserted into the tracheostomy, and volumetric induced ventilation is conducted through the above tube.
EFFECT: method provides the prevention of hypoxia in such patients at the stages of intravenous premedication, the induction of anaesthesia and the introduction of muscle relaxants due to the stability of hemodynamics and gas exchange due to the continuous ventilation through a terminal tracheostomy.
SUBSTANCE: invention refers to medicine, namely physiology and experimental medicine, and may be used for preventing and relieving a chemical liver injury in a living body. That is ensured by an atmospheric hypoxic exposure which is started with standard 21% air oxygen to be gradually reduced to 12% at 3±0.25% a minute. That is followed by a -minute pause at 12% oxygen to be gradually increased to 30% at 3±0.25% a minute. That is followed by another 5-minute pause at 30% oxygen. Then, the oxygen content is gradually reduced to 21% at 3±0.25% a minute. The procedure is daily for 10-14 days.
EFFECT: method provides higher body adaptation ensured by the gradual variations of gas mixture oxygen.
SUBSTANCE: group of inventions refers to medicine. A respiratory mask has a receiving nose chamber, and at least three fastening loops to fasten the mask to the user's head. Each of the first and second fastening loops is located in the appropriate section of the nose chamber corresponding to a wing of nose, and the third fastening loop is placed in the area of the nose chamber corresponding to a base of nose. What is also presented is a respiratory device consisting of a mask, a cap and fasteners which are interfaced with fastening loops and the cap thereby fastening the mask on the patient's head. What is also presented is a respiratory system comprising the respiratory device with the mask and a respiratory unit that generates constant high air pressure. What is also presented is a packaging unit accommodating the respiratory mask having a fringe with a peripheral groove, a sealant placed in the groove (21) to seal a border between the mask and the patient's face, as well as a protective film covering the sealant prior to the use of the mask.
EFFECT: group of inventions enables avoiding the mask leakage when in use.
13 cl, 6 dwg
SUBSTANCE: group of inventions refers to medicine. A mask comprises a body with a nose space; an interface portion attached to the body by a connection system having a side channel formed across an upper wall. The connection system is flexible. The interface portion is movable with respect to the body, and comprises a patient's port and an elongated hollow rod inserted in nostrils, projecting from the nose space and forming a gas passage for gas delivery into the patient's nose. The rod is rigidly connected to the patient's port of the interface portion. The interface portion is connected to a universal interface comprising a feed passage, a pressure passage and an inhalation port. The rod has proximal and distal ends. The proximal end is inserted into the nose space, while the distal end has a female end hermetically inserted into one of the patient's nostrils. The rod comprises a pear-shaped portion; it is fixed inside the patient's nose thereby attaching a nasal mask with using no head belt. What is also disclosed is the version of the nasal mask differing by the implementation.
EFFECT: lower risk of leakage.
17 cl, 10 dwg
SUBSTANCE: invention refers to medicine, namely paediatrics, cardiology, somnology, and may be used for treating adolescents with essential arterial hypertension with obstructive sleep apnoea/hypnoea syndrome. For this purpose, nasal non-invasive lung ventilation by nocturnal nasal continuous positive airway pressure (nCPAP-therapy) and light therapy with a therapeutic health-improving lamp with underlying standard therapeutic regimens. The nCPAP-therapy involves 10 monthly procedures for three months with a session length of 8 hours. The light therapy are performed once a day during a first hour after wakening up, a length of procedure is 30 minutes; the therapeutic course is 10 days for a first month of therapy.
EFFECT: method provides normalising the blood pressure level ensured by correcting obstructive respiratory sleeping disorders and normalising the circadian rhythm system.
FIELD: textiles, paper.
SUBSTANCE: material comprises fibrous layers of a mixture of viscose, polypropylene and bicomponent fibers, bonded with the back-up substrate, in the following ratio of components: viscose fibers (0.17-0.33) tex - (20-40) wt.% polypropylene fibers (0.33-0.67) tex - (30-45) wt %, polypropylene fibers 1.7 tex - (5-10) wt.%, bicomponent fibers (0.22-0.40) tex (20 - 30) wt %, calcium chloride (15-50) wt %. The surface density of the obtained filter material is (100-500) g/m2, air permeability (550-850) dm3/m2s, hygroscopicity (25.0-47.5)%. The objects of the invention are also variants of the method of manufacturing non-woven filter material, the first of which involves the processing of viscose and polypropylene fibers with an aqueous solution of calcium chloride with the mass concentration (100-500) g/dm3 at processing module (1:2÷1:5) of weight parts for viscose fibers, at processing module (1:1.5÷1:3) of weight parts for polypropylene fibers. The version 2 of the claimed method provides for the processing of the whole filtering material with a solution of calcium chloride, which mass concentration is (100-500) g/dm3 at processing module (1:1.15÷1:3) of weight parts. In both versions, drying of the treated material is carried out at a temperature not exceeding 80°C and heat treatment with hot air at a temperature of (120-145)°C.
EFFECT: obtaining a porous hydrophilic filter material with a high air permeability and stability of shape, providing moisture and warming of air entering the patient's lungs through a breathing filter when endotracheal anesthesia and mechanical lungs ventilation.
18 cl, 1 dwg, 5 ex
SUBSTANCE: group of inventions refers to medicine. An inflatable face seal comprises a ring air-tight hollow portion. The face seal in its cross-section section of the ring hollow portion comprises an adhesive joint which connects two overlapped boards glued together so that a surface of the first board facing inside from the two overlapped boards contact with a surface of the second board facing outside from said overlapped boards. The surface of the first board facing inside is pressed to surface of the second board facing outside due to initial stress in the inflatable face seal. There are disclosed a method for making the inflatable face seal with using a mould and extending a part of the section, and a workpiece for making the face seal.
EFFECT: cutting production costs.
9 cl, 9 dwg
SUBSTANCE: invention refers to medicine, namely therapy and surgery, and can be used for treating metabolic syndrome, including in patients suffering cardiovascular and respiratory insufficiency, and also obstructive sleep apnea. That is ensured by brief noninvasive continuous positive pressure assisted ventilation for 3 days (CPAP-therapy). The compensation is followed by inserting an intragastric cylinder and continuing the long-term CPAP-therapy to eliminate sleep apnea completely.
EFFECT: method provides compensating metabolic syndrome by manifested body weight reduction ensured by enabled insertion of the intragastric cylinder together with a reduced risk of developing complications accompanying the insertion due to the advance compensation of the detected disorders.
1 ex, 4 dwg
SUBSTANCE: invention refers to medicine, namely to anaesthesiology and resuscitation, and can be used if placing of a flexible reinforced laryngeal mask airway required. That is ensured by preoxygenation through a face mask for two minutes. Then a patient is placed in a "sniffing" position with a head supported by a cotton roll. The laryngeal mask airway is placed with its aperture upwards and arranging a mask tip on the centre of front incisors on an internal surface of a patient's mouth with pressing it to a hard palate with a third finger. After that, the mouth cavity is examined, and the LMA is moved downwards with pressing within a tube and mask junction to enable the mask passing near a tongue and falling in a pharynx. If observing resistance behind the tongue, the mask is turned around 90° with the aperture to the left and placed back into the initial position after passing the obstacle. Mask cuff is inflated with making sure that a black line is directed backwards and found in the middle.
EFFECT: method allows providing easy placing of the laryngeal mask airway with simultaneously reduced risk of hypoxia and laryngopharynx damages during mask placing.
7 tbl, 2 ex
SUBSTANCE: group of inventions relates to medicine. Flow system of portable dialysis device includes dialysate channel, made with possibility of connection with abdominal cavity for transfer of liquids and provision of liquid transfer with flow line. Flow line serves for flowing of dialysate from patient's body to sorbent, which serves for removal of polluting substances, which are in dialysate in outflow and inflow mode, with returning dialysate, practically free from polluting substances, to patient's body. Pump serves for transfer of dialysate by flow line both in inflow mode and in outflow mode. System of valves is located on flow line and makes it possible for dialysate to flow from dialysate channel to sorbent in outflow mode to remove polluting substances there, and in inflow mode making it possible for dialysate, practically free from polluting substances, to flow back to dialysate channel for transfer to patient's body. Accumulating chamber provides connection for transfer of liquids with flow line. Accumulating chamber is used for storing dialysate, practically free from polluting substances, removed by sorbent. Portable dialysis device and its application for treating renal disorder are described.
EFFECT: provision of flow dialysis without increase of size, weight and electricity consumption.
66 cl, 14 dwg