Reverse evaporator

FIELD: medicine.

SUBSTANCE: invention refers to medicine, particularly to medical equipment. It can be used for surgeries and postoperative care of wounds (including injuries, burns, freezing injuries and trophic ulcers), as well as soft tissues and mucous membranes for bleeding control, prevention and treatment of suppurative complications, infectious and dermatologic diseases. The object of the presented device is providing the local, targeted haemostatic and/or antiseptic preparation of biological tissues with an ozone-oxygen mixture in a combination with the effective aspiration and deactivation of ozone from the used gas mixture, staying within the maximum permissible ambient ozone concentration. The assigned object is solved by the fact that the device additionally comprises a motor and storage portions combined together into a one-piece working circuit. A tip in the form of an ozone handle and peripheral aspiration and release pumps connected by a plastic retainer; pump inlets and outlets are presented in the form of junction pipes provided with conical nozzles with adapters, are parts of the motor portion. The storage portion comprises a chain of cross-pieces coupled in the same direction by supplying pipes and provided on each side from each cross-piece with a pair of hermetic ozone-oxygen packages on the opposite crossarms.

EFFECT: presented reverse evaporator enables avoiding sophisticated, bulky, immobile treatment apparatuses and using the aggressive gas media, like ozone-oxygen mixtures.

3 cl, 4 dwg

 

The invention relates to medicine, in particular for medical applications, and can be used in the field of surgery, post-surgical and other wounds (trauma, burns, frostbite, trophic ulcers), and soft tissue, mucous membranes and wounds to stop bleeding, prevention and treatment of septic complications, infectious and dermatological diseases.

Known portable device for treating ozone / Application No. 2004137619, AN 33/14, BIPM No. 16, 10.06.2006, / containing communicated consistently ozone generator, a gas pipeline therapeutic camera aeration with a device for sealing the space processing and deactivator ozone in the form of bystroumova cartridge. Ozone generator, a gas pipeline and therapeutic Luggage aeration is performed in a separate, portable, compact, ozonostoyky devices, while the ozone generator includes a controller ozone concentrations in ozonopause mixture at the outlet of the gas conduit is made in the form of hose with quick connect and disconnect of the ozone generator and therapeutic gas chambers, and the latter is in the form of a nozzle designated processing desactivation ozone and out into the atmosphere and has the shape of a bell or overalls. However, this device does not provide accelerated filing sonobond what's mixture to the place of processing and active aspiration of waste gas mixture, and also functions only when the pressurized contact of the successive parts with the treated surface, and not able to work offline from your ozone generator.

A device for ozone/NO-ultrasonic treatment of the tonsils in the conservative treatment of chronic tonsillitis / Patent No. 76804, A61N 7/00, AM 37/00 BIPM No. 28, 10.10.2008,/ containing the ultrasonic generator, an acoustic node, the applicator with removable funnel, the waveguide-tool, two branches of the hydraulic system, interfacing socket, dip crane, electroejaculation, the ozone generator/NO-containing gas mixture, the mixer gaseous and liquid medicinal substances and a pneumatic system with a regulating valve. When the waveguide is a tool provided with a beveled radiant face pointing towards voiced tonsils, and through the Central channel of the applicator is in communication with the cavity removable funnel, one branch of the hydraulic system delivers the original drug solution into the Central channel of the applicator and a removable funnel, and the other branch diverts exhaust medicinal solution of the removable funnel applicator using electroadhesive and has a two-position valve, the mixer is equipped with a perforated grille and on the one hand connected with the branch that supplies the source of the medicinal solution into the Central channel of the applicator is removable funnel, and on the other, with the pneumatic system, connecting the mixer through a regulating valve ozone generator/NO-containing gas mixture. In addition, the ozone generator/NO-containing gas mixture and regulating valve for pneumatic system is installed above the level of the branches of the hydraulic system, feeding the medicinal solution into the Central channel of the applicator and a removable funnel. However, this device is intended only for the ozone treatment of the tonsils in the conservative treatment of chronic tonsillitis and has no forced feeding of the working substance, which uses ozonated medicinal solution.

Closest to the present invention is an apparatus for producing ozone/inventor's certificate SU # 1505553 A1, AM 16/00, bull. No. 33, 07.09.1989, / containing the ozone generator, the open end of the hemispherical chamber, an internal cavity which communicates with the outlet of the ozone generator, air compressor, two adjustable throttle, secondary camera, covering the main camera with the education they open with their common end of the annular cavity communicated with the suction cavity of the compressor with the formation of a vacuum gripper along the perimeter of the skirts. The input of the first adjustable inductor is connected to the pumping cavity of the compressor, its output to the input of the ozone generator, and the flap of the first adjustable throttle mechanically connect the on with the flap of the second adjustable inductor, an input connected to the pumping cavity of the compressor, and an exit to the atmosphere. The apparatus also includes sequentially connecting the annular cavity with the compressor coil, immersed in chilled water, a filter with a disinfectant and the adsorber activated carbon. The technical result consists in the exclusion of uncontrolled escape of ozone designated treatment that increases the stability of the regime ozonation at all periods of treatment, the decrease of the concentration of ozone in the air we breathe, reducing the absolute pressure ozonoterapia air to increase ozonoterapia without danger of hitting ozonoterapia air in the operating atmosphere, and thereby to increase the efficiency of ozone treatment.

However, this device does not provide the capabilities of local, directional processing of the biological object contains devices for sealing the zone of influence (spherical camera-"skirts"), which makes it impossible to use on biological objects with a rough surface, and also in the internal body cavities. The objective of the proposed device is the provision of local, aimed hemostatic and/or aseptic processing of biological tissues ozone-oxygen mixture with simultaneous eff is active aspiration and disposal of waste ozone gas mixture without exceeding the maximum allowable ozone concentration in the external environment.

The task to solve due to the fact that the device further includes a motor and cumulative portions, which are combined into a single work path, and the tip in the form of ozone handles and centrifugal, fastened with a plastic clamp suction and throwing pumps, inputs and outputs are in the form of pipes, provided with a conical nozzles with adapters, part of the motor portion; in the cumulative portion includes a chain of crosses, connected in one direction by means supplying tube and provided on each side of each cross pair of sealed packages for ozone-oxygen mixture at opposite lateral parts, containing a hollow cylindrical the insert so that the hollow cylindrical insert are equal to the diameters of openings within each of the crosses, but distinguished by the diameter of the lumen at different crosses with a consistent reduction in the diameters of openings from one extreme crosses, provided on the free longitudinal part of the nipple valve, containing the gasket to the other extreme of the cross, is supplied to the free longitudinal side of the exhaust valve, the chain crosses separated in place of articulation of one of the supply tubes with one of the crosses, respectively hemostatic and anti-Christ. Opticheskie modules communication consisting of moving the tee connected to one end of its longitudinal part with supplying tube hemostatic module, supplying tube with a release valve connected to the opposite end of the longitudinal part of the shunting tee and connected through the straddle crane with the longitudinal part of the cross antiseptic module, and the feeding tube is connected to a median portion moving the tee through the stopcock; collector in the composition of the motor portion includes a coupling with two cylindrical channels, one with the rear base of the coupling runs right along it contains a sleeve with an inner part of the giver fitting, inserted into the sleeve through its minor external segment on the back the basis of the coupling, and in the middle of the length of the clutch smoothly into a wide, flattened rectangular cavity with a gutter on the front of the base of the coupling containing a pair of afferent ports, which, entering the sleeve through his soft fixing Windows form its wide fitting on the bottom of the rectangular cavity, and the second cylindrical channel from the rear base of the coupling runs parallel to its lateral surface and contains a nozzle with the interior of the receiving fitting it with an external segment on the back of the base for coupling direction of poluchayutsia in the channel in order to fix it, but at the front base of the coupling of the second cylindrical channel arcuately curved toward the center and is in communication with the hollow rectangular cavity through its wide wall, passing back mounted on the tapered end of the nozzle efferent port where it passes between the afferent ports, diluting them to the narrow side walls of the rectangular cavity, removing the short outer segment of the efferent port of the gutters on the front of the base of the clutch, while the clutch is immersed to the bottom of the protective sleeve, where the notch corresponding to the groove on the front of the base coupling and bushing on top of a fitted cap with threaded through the holes receiving and giving fitting; ozone the handle is in the composition of the motor portion is made in the form of a hollow cylindrical body equipped trapezoidal flaps on the sides, open front substrate and the partition wall, which, with its sharp edge at a distance from the front of the base, is equal to the third length of casing parts on the center of the lumen parallel to the discharge valves on two Crescent as thickening of the septum and the wall of the casing gradually pass into the nozzle and then into the slots, with the inserted them from the back of the case base removes the needle and guide tube, sequentially passing between the grooves from the center of the rear base body through qi is andrijeski channel, passage and a rectangular slot in the wall to the middle of its sharp edges with making outside into the lumen of the housing front end of the guide tube, not reaching 0.5 to 1 cm to the front of the case base, and the protrusion of the rear end of the guide tube, which is included in short outer segment efferent port manifold from the rear base housing by a distance 2 times less compared to the end removes the needle within the afferent ports of the manifold; the adapter conical nozzle suction producing pump comprising motor portion connected in series short connecting tube, the longitudinal part of the mixing tee, the median part of which serially equipped with long halter tube, control valve and diffuser with air-bacterial filter, and then the intake tube, the longitudinal part of the return tee and efferent tube connected to the outlet tap accumulation portion; the adapter cone nozzles issuing nozzle expelling pump comprising motor portion through a short connecting tube connected in series to the longitudinal part two of the clip tees, median part with a reducing tubes connected to combine the tee, which departs from asiausa tube, combined with the median part of the return tee and from the longitudinal part of the extreme shut-off the tee consistently goes a long, but narrow discharge tube, the longitudinal portion separating the tee and narrow, short feed tube connected with the receiving fitting of the manifold; the adapter is tapered nozzle of the suction pipe of the suction pump in the composition of the motor portion of the serially connected second long intake tube, the longitudinal part of the host of the tee, the median of which is associated with a median separating part of the tee through two narrow, short skateline tube, a split release valve with restrictor, and then a short outlet tube connected with the giver fitting manifold; adapter conical nozzle outstanding suction pipe of the pump in the composition of the motor portion of the serially connected second pressure tube, the longitudinal part of the output of the tee, the median portion of which is provided with excretory tube connected to it through the cover with the tip of the neck body protivogaznyh box, supplied with a plug in the outer hole, and then narrow bearing tube with an inlet valve which is connected with the nipple valve cumulative portion; besides, all tees devices consist of the boom is hollow, perpendicularly interconnected cylindrical parts, in addition to combining the tee, which is several times larger than the others and is made in the shape of a hollow sphere whose wall is transferred in three hollow cylindrical branches, two of which are reducing tube and depart at an acute angle to each other in one plane at a small angle to which the opposite side of the ball departs the third branch with a connecting tube, and the pressure applying, generating, and skateline tube motor portion is made at least 3 times already, all other tubes of the device; external short period of efferent port manifold with14longer or14shorter protruding from the rear base of the housing of the ozone handles rear end of the guide tube; separating and receiving the tees are placed on the same level and parallel to each other and to one of megaclinic tubes attached to the free end of the tightening tube with a regulating valve and diffuser; in addition, centrifugal electric pumps that use as the working substance ozone-oxygen mixture, made of durable ozone materials, onionskin nozzle adapter, and all tees and valves of the device, bushing, cap, coupling, receiving, giving fittings and injector manifold, diffuser and ozone pen, crosses, and nipple valve cumulative portion - of the solid ozone plastic; all handsets and devices, ports and sleeve collector, a hollow cylindrical insert and tight the cumulative portion of the circuit from soft, supple ozone polymer, and seal nipple valve from an elastic ozone polymer.

Parts and materials

Reverse Gastor (Fig.1) consists of a motor and cumulative portions, which are combined into a single work path. The device is made teams of the simplest available ozone parts that can be easily cleaned, sterilized, repaired or replaced by new ones, which makes the device compact, mobile (disassembled placed in a nursing bag) and practical in the Russian Federation. Most miniature and complex of them are collector (5) and ozone handle (4), shows part of the device and in expanded form separate spatial figures figure 1, a more complete and detailed drawing with additional designations presented in figures 2 and 3 in the three standard planes. Cumulative dose in the built-in device in the de is presented in figure 1 and a separate device shown in figure 4.

The motor portion of the device (Fig.1) is basic and includes two centrifugal electric pump (suction pump (1)which emit pump (2)), suction connections which have conical heads (1A, 2A) with adapter (1B, 2B), and outstanding nipples - cone nozzles (1B, 2B) with adapter (1G, 2G). Pumps (1, 2) fasten together using durable plastic retainer (3), having them means to each other. Centrifugal pumps (1, 2) associated with the storage portion and the external air by means of tubes: intake (15, 22), connecting (16, 17, 21), pressure (18, 24), which reduces (19, 23), halter (20), binding (25), excretory (26), bearing (27), efferent (28), megaclinic (29, 30)applying (32) and outlet (31); tees: mixing (7), shut-off (8, 9), outputs (10), return (11)host (12)dividing (13) and combining (14); cranes: bleeding (33) with stroke limiter (33), control (34) and the inlet (35); collector (5); cone (36); ozone handles (4); protivogaznyh box (6). Pressure (24)applying (32), bearing (27) and skateline (29, 30) tube performed at least 3 times already, all other tubes. Direct interaction of the motor portion with the air of the atmosphere through the diffuser (36) with air-bacterial filter (36A), ozone knob (4) and protivogaza the box (6), supplied with a plug (6A) in the outer hole of the casing and cover (6B) with a tip (6V) on his neck. Collector (5) (Fig.1, 2) consists of a sleeve (5) with the cap (5), coupling (S), receiving (I) and the giver (5D) fittings, two afferent ports (5B, 5C), one efferent port (5A), nozzles (5E) and sleeves (5G) with locking Windows (5P) and wide fitting (5G"). When this coupling (53) collector (5) contains two cylindrical channel (5L, 5M) and a rectangular cavity (5H) chute (5P), bushing (5) - cut (5P), cap (5K) - hole (5S, 5C), and the efferent port (5A), nozzles (5E) and sleeves (5G) of the assembled manifold (5) allocate segments (5A', 5E', 5G").

Ozone handle (Fig.1, 3) consists of two drop needle (4L, 4M) and one guide tube (4H), and also provided with two dampers (4B, 4C) of the hollow cylindrical body (4A) with unevenly thickened wall (4A') and having a sharp edge (4P) partition (4G), which form in the lumen of the housing (4A) the following cavities: a couple of crescents (4D, 4E), a pair of nozzles (I, S) and a pair of grooves (4I, 4K), rectangular slot (4P), pass (4P) and a cylindrical channel (4C).

In the cumulative portion (Fig.1) includes a hemostatic (38) and antiseptic (37) modules containing brackets (39) with two hollow cylindrical inserts (39A, 39B)supplying tube (41) and sealed packages (40). Hemo is catechesi module (38) is further provided with an exhaust valve (43), and antiseptic module (37) - nipple valve (42)containing the gasket (42A), easily replaceable when worn. Cumulative portion has an integrated communication node, consisting of two tubes: the feeding (46) and the supplier (45); two valves: gate (48) and divisive (47); move tee (44).

Centrifugal electric pumps (1, 2) made of durable ozone materials, their conical nozzle (1A, 2A, 1B, 2B) with adapter (1B, 2B, 1G, 2G), as well as all tees (7-14, 44) and cranes (33-35, 43, 47, 48) motor and accumulating portions, the sleeve (5), cap (5), coupling (S), receiving (I), the giver (5D) fittings and nozzle (5E) collector (5), the diffuser (36) and ozone handle (4), crosses (39) and the nipple valve (42) funded portion - of the solid ozone plastic. All tubes (15 to 32, 41, 45, 46) motor and accumulating portions ports (5A, 5B, 5C) and the sleeve (5G) collector (5), a hollow cylindrical insert (39A, 39B) and sealed packages (40) cumulative portion made of a soft, elastic ozone polymer (e.g. polyvinyl chloride or silicone), and seal (42A) nipple valve (42) is of an elastic ozone polymer (for example, elastomers based on silicone and/or ethylene-propylene-diene-monomer).

Device and Assembly

When assembling the motor portion of the offer is on the device (Fig.1) on the nozzles emit pump (2) wear a conical nozzle (2A, 2B), the ends of which are inserted adapter (2B, 2G)intended for fastening of the connecting tubes (16, 17). From adapter (2V) departs short connecting tube (16)which is connected to one end of the longitudinal part of the mixing tee (7) and match it with a long halter tube (20) and an intake pipe (22). Halter tube (20)connected to the median part of the mixing tee (7), at the end of the report with the external air through the diffuser (36) with an adjusting valve (34), forming the air intake. In the funnel cone (36) for cleaning atmospheric air insert similar form of air-bacterial filter (36A). Intake tube (22)connected to the other end of the longitudinal part of the mixing tee (7), is connected to the longitudinal part of the recoil tee (11), from which the other end assign efferent tube (28), which serves as the main unifying knee for two servings. The adapter (2G) via a short connecting tube (17, 21) sequentially connect the longitudinal parts of the two shut-tees (8, 9), each of which is in the perpendicular direction through the median part of the assign by reducing the tube (19, 23), which combine at the ends by means combining tee (14). Combining tee (14) differs from all other tees device, consisting of the boom hollow cylindrical portions, perpendicularly connected to each other. He is several times larger than the others and is made in the shape of a hollow sphere whose wall is transferred in three hollow cylindrical branches, two of which are reducing tube (19, 23) and depart at an acute angle to each other in one plane at a small angle to which the opposite side of the ball departs the third branch (it is attached connecting tube (25)). The free end of the connecting tube (25) is connected to the edge of untapped median part of the recoil tee (11), closing the circuit between the incoming and out-emitting pump (2) lines motor portion. From the free end of the longitudinal portion at cut-off tee (9) assign a long, but narrow discharge tube (24), ending the connection with one end of the longitudinal part of the separating tee (13), the other end of which sochinyayut with narrow, short feed pipe (32)connected to the receiving socket (G) collector (5). Accordingly, by giving the fitting (5D) collector (5) connect a short discharge tube (31), ending the connection with the adjacent end of the longitudinal part of the host tee (12)located at the same level and in parallel with the separating tee (13). From the other end of the longitudinal part of the host tee (12) assign long second intake pipe (15), the cat is too late to pull the suction pump (1). Nozzle suction pump (1) (similar to throwing a pump (2)) pre-wear conical nozzle (1A, 1B)with adapter (1B, 1D). Intake tube (15) is connected to the suction pump (1) via an adapter (1B) one of the tapered nozzles (1A). Dividing (13) and receiving (12) tees connect with each other through two narrow, short megaclinic tubes (29, 30), each of which is attached to a free-median part of the corresponding tee (12, 13), and then the tube (29, 30) sochinyayut with each other using bleeding crane (33) with stroke limiter (33A), forming a connecting bridge. Thus, match the incoming and outgoing lines of different pumps (1, 2) motor portion. To improve the compactness of the links of the motor portion and facilities management gas flow tees (12, 13), communicating among themselves, it is desirable to seal as close as possible to each other, giving their median parts functionally advantageous for megaclinic tubes (29, 30) and bleeding crane (33) position. Long halter tube (20) of the air intake away from the incoming line throwing pump (2) to place the pair facing the line-emitting pump (2) with the incoming line of the suction pump (1) and having its free end with a diffuser (36) and control valve (34) for cepraga is a walking bridge, attaching it to one of megaclinic tubes (29, 30). Next to the adapter (1G) of the second conical nozzle (1B) of the suction pump (1) attach the second discharge pipe (18), the opposite end of which is connected to the longitudinal portion of output tee (10). On the other side of the longitudinal part of the excretory tee (10) assign narrow bearing tube (27), which provide the inlet valve (35) at the end. Bearing tube (27) with an inlet valve (35) is the final part of the opening line of the suction pump (1) and an additional unifying knee for two servings. To the median part of the excretory tee (10) attach the urinary tube (26), bearing protivogaznye box (6). Last, not removing the tube (6A) of the external hole of her body, connected to the urinary tube (26) with tip (6B), which is posted on the cover (6B), screwed to the neck of the housing protivogaznyh box (6). During operation of the device is when you need to replace the used or damaged protivogaznyh boxes (6), Sfintu cover (6B) and immediately installing in its place a new one.

Collector (5) (Fig.1, 2) is the link between the conductors of the motor portion and the ozone handle (4) and made in the form of a collapsible design with the aim of easy washing, sterilization and replacement Melk the x worn parts in conditions of long-term ozone aggression. On purpose all the parts of the manifold (5) can be classified on the carrier section (coupling (S) and bushing (5) from cap (5)), direct the transmitting element (efferent port (5A), the nozzle (5E), the receiving socket (G)) and reverse the transmitting element (afferent ports (5B, 5C), sleeve (5G), giving the fitting (5D)). When forming the collector (5) part details collected on assignment to the individual transmitting elements, packing them with parts of the supporting section. Direct mounting to the transmitting portions in the bearing section is clutch (S), through which one (back) of the Foundation are two cylindrical channel (5L, 5M), designed to accommodate transmitting elements. The first cylindrical channel (5L), containing part of the reverse of the transmitting element, with the rear base runs right along the coupling (S) and at the middle of its length smoothly into a wide, flattened rectangular cavity (5H), ending with a groove (5P) on the opposite (front) under coupling (S). The second cylindrical channel (5M)that allow direct transmitting element from the rear base of the sleeve (53) runs parallel to its lateral surface, but the front of the base coupling arcuate curved toward the center and communicates with the hollow rectangular cavity (5H) through its wide wall.

The collector (5) (Fig.1, 2) first collected about the feats of the transmitting element, inserting the ends of both afferent ports (5B, 5C) in the lumen of the sleeve (5G) through a soft fixing Windows (5P) at its end and forming a wide connecting portion (5G) sleeve (5G). The obtained flexible tee is inserted into the groove (5P) the free end of the sleeve (5G) and push the inside of the coupling (S), flowing sleeve (5G) through the first cylindrical channel (5L) until it stops its wide fitting (5G) in the bottom of the rectangular cavity (5H). Small, out of the rear base coupling (S) outer segment (5G"') of the free end of the elastic sleeve (5G) used for the introduction of one end of the giver fitting (5D) inside the sleeve (5G), limited to direct wall of the cylindrical channel (5)where leave the inner part of the fitting (5D). Then collect direct the transmitting element, hooking one end of efferent port (5A) on the tapered end of the nozzle (5E). The block is dipped with the rear base coupling (S) in the second cylindrical channel (5M) the free end of efferent port (5A) to lock them in touch at the center of the rectangular cavity (5H) afferent ports (5B, 5C). They then bred for protruding from the groove (5P) the free ends of the narrow side walls of the rectangular cavity (5H), which serves the free end of the efferent port (5A), pushing it into the gap between the afferent ports (5B, 5C). While the free ends of afferent ports (5B, 5B) is almost completely sink in a rectangular cavity (5H), and the free end of efferent port (5A) is removed from the gutter (5P), leaving a short outer segment (5A') on the front of the base sleeve (S). This inequality do with the purpose of tiny, closely spaced to each other removes the cannula (4L, 4M) and guide tube (4H) ozone handle (4) can easily consistently included in the formed socket ports (5A, 5B, 5C) of the manifold (5). Forming a collector (5) complete the stringing one end of the receiving nozzle (J) extending from the rear base of the coupling (S) outer segment (5E') injector (5E), in which the fitting (G) guide for fixing the second cylindrical channel (5M)where leave its inner part. Then come transmitting coupling elements (S) mounted on the bottom of the protective sleeve (5), where the tenderloin (5P), corresponding to the trench (5P) on the front of the base sleeve (S), fittings (5D, E) which pass through holes (5S, 5C) of the cap (5), Sasakawa on the top of the sleeve (5).

Ozone pen (4) (Fig.1, 3) is a hollow cylindrical body (4A), one of the grounds of which (the front) is open on the sides and goes into a trapezoidal flap (4B, 4C), designed to deter excessive gas ahead of the ozone handles (4). Valve (4B, 4C) you can also use the AMB as a support ozone handle (4) on the treated surface. Here, inside the ozone handles (4), at a distance from the front of the base, is equal to the third length of casing (4A), the lumen is divided at the center into two Crescent (4D, 4E) sharp edge (4') of the partition (4G) in parallel with the discharge valves (4B, 4C). As thickening of the septum (4G) and wall (4A') of the housing (4A) the Crescent (4D, 4E) gradually pass into the nozzle (G, Z), which in turn pass into the grooves (4I,4K) to the opposite (back) to the base (4A). The interior partitions (4G) from the middle of its sharp edges (4P) is rectangular slot (4P), blending smoothly into the passage (4P), closing in the structure of the partition (4G) in a cylindrical channel (4C)extending through the center of the rear base housing (4A) between the slots (4I, 4K).

Collect ozone knob (4) (Fig.1, 3), successively inserting first removing the cannula (4L, 4M) in the grooves (4I, 4K) on the back of the base (4A), and then the guide tube (4H) - in a cylindrical channel (4C) partition (4G) through the back of the base (4A) by pushing it along the septum (4G) via the passage (4P) and a rectangular slot (4P) and passing beyond the sharp edge (4') of the partition (4G) into the lumen of the housing (4A) the front end of the guide tube (4H), not reaching 0.5 to 1 cm to the front of the Cabinet base (4A). The length of the guide tube (4H) rely on the assumption that its rear end, a part of the short outer segment (5A') efferent port (5A) of the collector (5), must protrude out of the rear base housing (4A) by a distance 2 times less as compared with removing needle (4L, 4M)within the afferent ports (5B, 5C) of the manifold (5). In addition, the short outer segment (5A') efferent port (5A) should be longer than ¼ or¼ shorter protruding from the back of the case base (4A) of the rear end of the guide tube (4H). This is to ensure soft, smooth, consistent docking ports (5A, 5B, 5C) removing the cannula (4L, 4M) and guide tube (4H) when connecting to the manifold (5) ozone handles (4), than complete the motor portion of the Assembly.

Cumulative portion (Fig.4) collect, connecting brackets (39) in one direction through supply tubes (41), the ends of which are put in parallel, opposite side crosspieces (39). Next, perpendicular to the direction of the received circuit crosses (39) with two sides provide hermetic packages (40), connecting the past to the protruding transverse parts of the cross-pieces (39). The Assembly is completed by connecting to the free longitudinal parts at crossings (39) chain nipple valve (42) and exhaust valve (43). Prior to the Assembly in the lateral parts of each of the crosses (39) is placed on a hollow cylindrical insert (39A, 39B). This hollow cylindrical insert (39A, 39B) within the Ah each of the crosses (39) are equal to the diameters of openings, but distinguishing the diameter of the lumen at different crosses (39), located in the order of the pair of the diameter reduction of gaps from crosses (39) with nipple valve (42) to the crossbar (39) with the exhaust valve (43). Reducing the diameter of openings of the hollow cylindrical inserts (39A, 39B) is due to the thickening of their walls. The d-pad (39) with nipple valve (42) can not provide a hollow cylindrical inserts (39A, 39B), and place them, starting with the following crosses (39). The modular design allows you to change the gas capacity of the accumulating portion by adding or reducing the number of consecutive blocks in the chain. In order cumulative dose did not create any obstacles in medical facilities, it is more convenient to place around their perimeter.

The need to create a cumulative portion is dictated by the inability of the existing medical ozone generators to ensure that the necessary work of the motor portion of the flow rates of gas, meet medical needs, and need not bulky, portable depot gas for independent ozonizers operation of the device. When this cumulative portion performs the function of mobile, but roomy gas depot for ozone-oxygen mixture (ACS)produced by medical ozone, providing a stable work release pump () at the speed he creates ozone jet of at least 3 l/min

Collected cumulative portion (Fig.4) is connected to the medical ozone generator, connecting the free end of the nipple valve (42) to the efferent line medical ozonator. While the exhaust valve (43) on the opposite end of the circuit must be closed. Then make filing ACS with the desired ozone concentration. However, ozone is an unstable substance with a half-life in the undissolved state for about half an hour, and offer the device for even small exposure requires several liters of pre-stored gas. For filling the cumulative portion of at least this amount OAKS medical ozone generators, most of which is not given the hemostatic ozone concentrations above 40 mg/l) flow rate of more than 0.3 liters per minute, it will take time for which the at least one fourth of ozone in the gas depot will decompose to oxygen and dialed the ACS will not be usable for the desired procedure. The design of the cumulative portion allows to solve the problem of a significant decline in the concentration of ozone in the dialed ACS due to a significant increase in time refills from low-medical ozone generators when the need for large stock OAKS that becomes more relevant with increasing concentration of the ozone supplied OAKS, accompanied by a proportional reduction of its source of Finance for the and. Cumulative portion uses a common property of medical ozone generators to raise the ozone concentration in their discharge chamber when an obstacle at the outlet of the ozone generator in proportion to the degree of obstacles, the initial value of ozone concentration and time of trapping the gas. As serial, fresh reducing the diameter of openings of the hollow cylindrical inserts (39A, 39B) gradually narrows the channels of the transverse parts of the cross (39) with nipple valve (42) to the crossbar (39) with the exhaust valve (43), while promoting the QSR chain in this direction increases the time interval between the filling of successive pairs of sealed packages (40) due to problems with the gas flow into them. When this certain pair of sealed packages (40) is filled much faster subsequent and lock channels transverse parts of their crosses (39) due to the elastic resistance to the flow OAKS, sending the ozone flow down the chain, in the following pair of sealed packages (40). With each inflated by a pair of sealed packages (40) on the one hand gradually increasing shortage of ways outflow OAKS of the Central trunk of the cumulative portion, and on the other hand increases the resistance to the flow of ACS due to the constant increase of the distance to the functioning channels and consistently reduce the deposits. This creates the necessary increasing the compression ratio, forcing medical ozonator gradually increase the ozone concentration in the feed ACS in accordance with the time of filling the cumulative portion. In addition, each of the consecutive chain of pairs of sealed packages (40) accumulates ACS with different concentrations of ozone, which increases along the chain from the nipple valve (42) to the exhaust valve (43). After filling all pair of sealed packages (40) ACS gas supply from medical ozonator off, if necessary, removing the nipple valve (42) cumulative portion from passing line of medical ozone. Full filling the storage portion comes at the moment when the OAKS of medical ozone generator inflates the last couple of sealed packages (40) on the crossbar (39) with the exhaust valve (43) to a volume equal to the volume of all predlagash pairs of sealed packages (40). Immediately after this filing OAKS medical ozone generator should be stopped to prevent tearing and premature wear sealed packages (40) from overflow.

Return OAKS from the accumulation portion (Fig.4) is performed after connecting the free end of the exhaust valve (43) to the transmitting line of the consumer. Despite the unequal distance from the exit of the cumulative portions of the same volume, but the difference is, which is ozone in the ACS pairs of sealed packages (40), their evacuation occurs evenly on the amount of gas in a common trunk, where there is a constant mixing of equal amounts of the ACS of all sealed packages (40) under the action of the force vector of the consuming device. This is due to the consecutive pair of the thinning of the walls of the hollow cylindrical inserts (39A, 39B) from brackets (39) with the exhaust valve (43) to the crossbar (39) with nipple valve (42), which extends the channels of the transverse parts of the cross-pieces (39) in this direction as they move farther from the exhaust valve (43). At the same time over the entire period of the return gas does not flow change and ozone OAKS, leaving a chain accumulating portion through the exhaust valve (43), as the devastation sealed packages (40) ends at the same time. After the exhaust valve (43) overlap and, if necessary, disconnect from the consumer. Return gas can be conducted from disabled from medical ozone accumulation portion, and extending it from medical ozone generator to the consumer. In the second case, the return gas to the consumer can be performed sequentially or simultaneously with the filling of funded portion of the medical ozonator. In both cases, the nipple valve (42) performs the function of a reliable separator environments, not dependent on pressure changes in the circuit of the cumulative portion, the E. releasing stored OAKS in the external environment or back in medical ozone generator, and not letting external air or ACS in the cumulative portion occurs when the active negative thrust of consumers, from which the nipple valve (42) prevents the nodes of medical ozone. If during operation it is necessary to get rid of a certain number of stored UCN, the cumulative portion connecting blocked exhaust valve (43) to the tube going into the catalytic chamber of medical ozone, and by opening the valve (43), cumulative release portion from the gas, manually squeezing out unnecessary number of ACS from sealed packages (40), or use an active hood.

Cumulative portion is made in the specified form for the following reasons:

1) the need for instant, safe and economical replacement of fast moving gas reservoirs in terms of ozone aggression without violating the integrity of the systems ozone generator-tank, tank-consumer, ozone-tank-consumer;

2) the need for early leak detection OAKS from the gas tank when the pressure loss for one reason or another. The presence of a large number of tanks of small capacity (up to 3 liters) allows you to detect and fix a gas leak, preventing a significant release of toxic doses of ozone in the atmosphere.

3) preference is not bulky, portable gas tanks in copper is Ty premises, part or continuation of the efferent line medical ozonator;

4) the need for technology that compensates the significant drop in the concentration of ozone accumulated in the ACS during long refilling gas tanks from existing low-medical ozone generators. When using the cumulative portion of the ozone concentration in the accumulated ACS does not substantially decreases as the filling process is an increase in the concentration of ozone supplied OAKS, proportional to the time of refueling.

Thus, the cumulative dose allows to maintain the desired concentration of ozone in the ACS inside the gas tank during their long filling ozonizers low productivity and is an independent device that is used as the receiver needs large amounts of ACS, however, when operating within the framework of the invention the last man by the communication node for it.

The communication node (Fig.1) gather, wearing supplying tube (45) with release valve (47) at one end of the longitudinal part of the shunting tee (44), to the median part of which by means of a shut-off valve (48) connect the feeding tube (46).

Cumulative portion (Fig.1) equip a communication node, disconnecting the circuit in place of articulation of one of the supply tubes (41) with the od of the Oh of the crosses (39) into two unequal segment, one of which (the hemostatic module (38)) remains at the ends of the exhaust valve (43) and distribution pipe (41)connected to the communication node through the free end of the longitudinal part of the shunting tee (44), and the other segment (antiseptic module (37)is equipped with nipple valve (42) and a spare longitudinal part of the at crosses (39)connected to the communication node through the straddle crane (47). The communication is intended for the separation of the cumulative portion into two independent modules (37, 38), characterized by the system of filing them in the OAKS.

Equipped with a communication node of the cumulative portion (Fig.1) connected to the motor portion, connecting the free end of the exhaust valve (43) hemostatic module (38) with the efferent tube (28), and the free end of the nipple valve (42) antiseptic module (37) - inlet valve (35). Interfaces modules (37, 38) with the communication and knees motor portion indicated in figure 1, an adjustable pairs of arrows.

Hemostatic module (38) during refueling receives ACS in a closed system passive supply, formed after connecting the feeding tube (46) to the efferent line medical ozonator, closing straddle (47) and the outlet (43) of the valve and opening the shut-off valve (48), which closed immediately after filling hemostatic module (38), works on the same principle the imps, as a cumulative dose. When the need for refueling hemostatic module (38) during operation of the motor portion instead of a shut-off valve (48) can be installed nipple valve (42), took it with antiseptic module (37). Antiseptic module (37) is similar hemostatic module (38) can work as a cumulative portion, and also passively receive the ACS from the ozonizer through the nipple valve (42), then passing it hemostatic module (38) through the open release valve (47) for supplying the tube (45) and the longitudinal part of the shunting tee (44) with a closed shut-off valve (48). So antiseptic module (37) use when you want to use all sealed packages (40) cumulative portion without removal from its chain of communication. In the case of two-way connection accumulating portion from the communication node to the motor portion of the nipple valve (42) antiseptic module (37), it is necessary to switch the intake valve (35) motor portion for introducing a line of medical ozone. Medical ozone antiseptic module (37) should not be refilled through the feeding tube (46) of the communication node, as in this case the motion of the ACS in its circuit will occur in the direction of extension of the channels of the transverse parts of the cross-pieces (39), not providing the necessary increasing the comp is essay in efferent line of ozone and increase the concentration of ozone supplied to the ACS.

However, the main method of filling antiseptic module (37) is the return to him of gas from the additional unifying knee motor portion through the inlet valve (35). This antiseptic module (37) receives ACS during operation of the motor portion in its open system active supply, forced two centrifugal electric pumps (1, 2), taking the ACS with ozone handles (4) through the atmosphere together with the external air. In this case, through the motor portion antiseptic module (37) becomes dependent on the external environment and hemostatic module (38), from which delimit covered straddle crane (47).

Work and its modes

The device has three independent modes: hemostasis, hemostatic-antiseptic and antiseptic.

When the hemostatic mode after refueling cumulative portion of ACS with hemostatic ozone concentration (above 40 mg/l), directly before starting the motor portion of the external openings protivogaznyh boxes (6) remove plug (6A) and open only the exhaust valve (43) cumulative portion, and then include both the pump (1, 2), pre-connected to the power source. Using emit pump (2) motor portion actively tighten the ACS through the outlet edge is (43) and can consume it as soon as hemostatic module (38), and from all the cumulative portion with the communication or without him, emptying evenly paired sealed packages (40). In the motor portion of the movement of the OX begins with the incoming line throwing pump (2), in which it sequentially passes through the efferent tube (28), the longitudinal part of the return tee (11), suction tube (22), the longitudinal part of the mixing tee (7), a connecting tube (16), the adapter (2B) and a conical nozzle (2A), in doing throwing the pump (2). Last accelerates and delivers the ACS in its opening line, consistently pushing the gas through a conical nozzle (2B) with adapter (2G), alternating connecting tube (17, 21) and the longitudinal part of the clip tees (8, 9), discharge tube (24), the longitudinal part of the separating tee (13), feed tube (32), collector (5) and ozone knob (4). In direct transmitting element collector (5) the ACS of the receiving fitting (G) is adjudged to be in an injector (5E), which creates a stream of the Oxus, compensating the loss of gas pressure in the previous guides. Breaking away from the tapered end of the nozzle (5E), the OX turns in efferent port (5A) to the opposite edge of the front of the base manifold (5), moving in a perpendicular plane relative to the reverse of the transmitting element, and enters direct the second tube (4H) ozone handles (4). In the process of entering the OAKS in the external environment of the front end of the guide tube (4H) gradual braking and return gas through the open front of the base into the lumen of the housing (4A) of the ozone handles (4) under the action of the suction force of the suction pump (1) motor portion. In addition, the ACS is the aspiration of atmospheric air with further mixing of the two media inside the housing (4A) of the ozone handles (4) as the reverse movement through it. To ensure full reuptake ACS ozone handle (4) without exceeding the maximum permissible concentration (MPC) of ozone in the external workplace air (0.1 mg/m3) stream OAKS decrease in the initial section facing the line-emitting pump (2), successively cutting off a large part of the gas jet two tees (8, 9) with the promise of her coming in the line of the same pump (2) through the shunt of paired reducing tubes (19, 23)combining tee (14)connecting tube (25) and return tee (11). Combining tee (14) made in the specified form (see "structure and Assembly")in order to enroll in it by squeezing the tube (19) a large part of the clip stream from the tee (8) did not interrupt next reducing the tube (23) a lower part cut off flow from the tee (9). Moreover, further promotion of ACS on a narrower pressure 24) and feeding (32) of the tube significantly reduces the flow of ACS in the opening lines of one pump (2), making aspiration in comes another pump (1) superior over the supply of OAKS in the ozone knob (4) a total of at least 10 times, in spite of the identity of the two pumps (1, 2) power. In addition, for holding the OAKS along the edges of the plane of intersection of two vectors suction created by partitions (4G), where there is a deficiency of the suction force on the front of the base of the ozone handle (4) on opposite sides place a trapezoidal flap (4B, 4C). Partition (4G) breaks sinking deep into the ozone of the handle (4) ACS with air in two parallel streams, which are sequentially pass through the pair of crescents (4D, 4E), nozzles (I, S), and removing the cannula (4L, 4M) in afferent ports (5B, 5C) of the collector (5), uniting in his sleeve (5G), and a single stream into the wires coming to the suction line of the pump (1) through giving fitting (5D) of the manifold (5). Thus, the collector (5) is a redistribution of the mixed gas flows to implement full-fledged reverse circulation OAKS in the front under the ozone handles (4). Further waste gas mixture containing 4-8% of the ozone output of the ozone handles (4) ACS, sequentially passes through the discharge pipe (31), the longitudinal part of the host tee (12), suction tube (15) and enters the suction pump (1) via the th conical nozzle (1A) with adapter (1B). Suction pump (1) dispersing waste gas mixture and makes it through the second conical nozzle (1B) with adapter (1G) in its opening line, passing the gas through a pressure tube (18) in deducing tee (10), through the median part of which is spent gas mixture takes place in protivogaznye box (6) through the urinary tube (26).

Directly from the longitudinal part of the excretory tee (10) further generating tube (27) waste gas mixture can get, as an additional unifying the knee motor portion when the hemostatic mode blocked inlet valve (35). Inside protivogaznyh box (6) on the surface of particles of activated carbon is catalyzed decomposition reaction of ozone incoming waste gas mixture with the release into the environment air mixture enriched with oxygen. To improve elimination of ozone and increase service life protivogaznyh boxes (6) it is possible to provide hopcalite cartridge, inserting it into the outer housing bore protivogaznyh box (6). In the described technological processes achieve effective local, directional processing ACS desired area of the human body with full return capture and neutralization of ozone in the absence exceeding its MPC in the external environment. Work finished or priostanavili the Ute at the time, turning off both the pump (1, 2), and blocking the exhaust valve (43) hemostatic module (38). Hemostatic mode works well to counter the capillary stop, parenchymal and venous bleeding associated with an antiseptic effect.

Antiseptic mode works well for killing microorganisms and different from the hemostatic mode only in that the depot before working device download ACS with antiseptic ozone concentration (above 2-3 mg/l).

Hemostatic-antiseptic mode is used when there is a need for additional antiseptic effect after the primary hemostatic treatment. This mode involves equipping the cumulative portion of the site with the division of hemostatic (38) and antiseptic (37) modules straddle crane (47). From hemostatic mode, it differs in that after filling only hemostatic module (38) ACS with hemostatic ozone concentration immediately before the start of pumps (1, 2) motor portion along with the exhaust valve (43) cumulative servings open the inlet valve (35) motor portion. After starting the motor portion of this leads to a rapid filling of the sealed package (40) antiseptic module (37) through the open intake valve (35) part from Abtenau gas mixture, directly passing through the longitudinal part of the excretory tee (10) and narrow-generating tube (27), to reuse it with antiseptic purposes. In the circuit antiseptic module (37) receives no more than 1/6 of the opening of the suction pump (1) waste gas mixture, most of which comes in protivogaznye box (6), as the bearing tube (27) at least 3 times already excretory tube (26). Thus, when the hemostatic-antiseptic mode during the entire period of operation of the device within the opening of the suction line of the pump (1) is dominated by the flow of the waste gas mixture is directed to protivogaznyh box (6), above the flow going for additional unifying the knee motor portion. Moreover, in the process forced dressings antiseptic module (37), when gradually increasing the resistance in its circuit, the gas flow by an additional unifying the knee motor portion progressively decreases up to a full stop is inversely proportional to the simultaneous increase of the gas flow in a more easy way into the environment. These technological properties necessary to prevent early wear sealed package (40) of the funded portion of the flow speed of the aggressive gas mixture high pressure of aspiration the first pump (1) in the absence of needs in compression inside his opening line. Given the unequal ratio of spending OAKS, ozone produced by the handle (4), and aspirating the spent gas mixture, irregularly splitting in the opening line of the suction pump (1) throughout the period of operation of the motor portion, it should be noted that during the full devastation of the hemostatic module (38) in antiseptic module (37) must be received on average 2 times more waste gas mixture in comparison with the number of ACS initially charged hemostatic module (38). Therefore, the cumulative portion before working with the device it is desirable to divide the communication node on the antiseptic (37) and hemostatic (38) modules in the ratio of at least 2:1, respectively, for a maximum of storing the waste gas mixture in antiseptic module (37) without the threat of overflow. In addition to much less wear nipple valve (42) forced flow of the waste gas mixture and free refills antiseptic module (37) of the bearing tube (27) can be connected with the longitudinal part of its extreme crosses (39), separating from her nipple valve (42). Optionally, the inlet valve (35) can be open at any time of the motor portion of the work, and in varying degrees depending on the quantity requirements for ozone, as in antiseptic. After emptying hemostatic the RCM module (38), without turning off the pumps (1, 2), the work will involve antiseptic module (37), closing the inlet valve (35) and opening the release valve (47), after which there is a uniform emptying of the pair of sealed packages (40) antiseptic module (37). The device operates on the same principle that when the hemostatic and antiseptic modes, but before get from antiseptic module (37) in the main unifying the knee motor portion of the spent gas mixture must pass through a common trunk devastated hemostatic module (38). After the devastation of the antiseptic module (37) and/or at the end of the procedure pumps (1, 2) shut down, blocking the straddle crane (47). When between modules (37, 38) need some break, after the devastation of the hemostatic module (38) for the required period of time to produce the stopping of pumps (1, 2) closing the inlet valve (35) to prevent retrograde release of waste gas mixture from inflated antiseptic module (37) into the atmosphere through an opening of the housing (4A) of the ozone handles (4) and protivogaznye box (6), and antiseptic module (37) enables to resume the pumps (1, 2), opening the release valve (47). When there is need for the suspension of the operation of the device during operation of the individual modules (37 38) it is necessary to do such manipulation with the stopping of pumps (1, 2), only with the inlet valve (35) when emptying the hemostatic module (38) should be blocked exhaust valve (43), and when emptying antiseptic module (37) is the straddle crane (47) to prevent their contents into the environment from the guide tube (4H) ozone handles (4). If antiseptic module (37) do not clean the nipple valve (42), then the stop time of the pump (1, 2) inlet valve (35) can not overlap. Re-running the pumps (1, 2), valves (43, 47) of the respective modules (38, 37) open, if necessary, continuing the filling antiseptic module (37) part of the waste gas mixture by opening the inlet valve (35) while working with hemostatic module (38).

However, the pumps (1, 2) it is impractical to turn off if you use the above modes of operation need to pause briefly and often. In these situations provides a dummy load, creating a free communication between the output line of the suction pump (1) and coming line-emitting pump (2) via a common trunk cumulative servings. When used within the hemostatic or antiseptic modes without removing the nipple valve (42) with extreme crosses (39) antiseptic module (37) is necessary to fully open the inlet valve (35) motor portion, libpri removing the nipple valve (42) to open the exhaust valve (35) is only 2/3. In the elastic resistance of the sealing lip (42) or partially closed discharge valve (35) inhibit double in comparison with the outflow coming in the line-emitting pump (2) loose the flow of gas from the opening line of the suction pump (1). This creates a slight but constant positive pressure within the common trunk of the cumulative portion, locking the ACS in the pair of sealed packages (40), and on the working circuit device gradually begins to circulate the air. Idle load off full back overlap of the intake valve (35), renewing the exemption OAKS pair of sealed packages (40). When idling the load must be applied when the device is in hemostatic-antiseptic mode, the method of its switching on and off different during operation of the individual modules (37, 38), and also depends on the availability of nipple valve (42) in the antiseptic composition module (37). When you enable idle load during operation of the hemostatic module (38) either before engaging antiseptic module (37) facing the suction line of the pump (1) report to the incoming line throwing pump (2) the opening of the straddle crane (47). The inlet valve (35) leave it completely open in the presence of nipple valve (42) on Rainey frog (39) antiseptic module (37) or overlap by 1/3 in its absence. During operation of the hemostatic module (38) idle load off only in the presence of ACS, renewing the return of gas from its sealed package (40) reverse overlap straddle crane (47) with the regulation of the supply part of the waste gas mixture in antiseptic module (37) by means of an inlet valve (35). If haemostatic module (38) completely devastated, the idle load can be turned off, only through the involvement of antiseptic module (37) full overlap of the intake valve (35). During operation antiseptic module (37) idle load turns on and off as well as when it is used in the framework of the hemostatic or antiseptic modes, only the withdrawal of the gas comes from sealed packages (40) antiseptic module (37). For more simple and clear description of the operation of the device all of the content accumulation portion in the further text will be equal and called the OAKS.

Idle load is indispensable for numerous, repeated ozone treatments within one procedure, when the intervals between impacts ACS can to minimize its expenditure from the depot without turning off the pumps (1, 2). While it provided a point airtight processing ACS necessary when the problem area available for contact with the facial Foundation is receiving ozone handles (4), you need to create an amplified voltage OAKS. While pressing the front grounds of the ozone handle (4) to the biological tissue completely stops the flow of air from the external environment in the motor portion, which leads to a sharp gas shortages in the conductors in a single working circuit device and forcing pumps (1, 2) actively use the ACS of the pair of sealed packages (40). In contrast to emit pump (2), easily costing some stocks ACS from the accumulation portion, and the suction pump (1) for the sealing of the ozone handles (4) becomes totally dependent on supplies from ACS emit pump (2)that in case of equality of capacity of both pumps (1, 2) completely stops cutting off the excess thread ACS in the opening lines emit pump (2). Shunt between the outgoing and incoming lines emit pump (2) is a secondary highway feeding suction pump (1) missing number of ACS from the accumulation portion, as due to the large resistance of the facing line throwing pump (2) and the incoming line suction pump (1) loses the last ACS applied only emit pump (2). This leads to the fact that, as a result of contact of the ozone handle (4) with the surface, its front occurs under moderate vacuum, pressive the total ozone knob (4) to the biological tissue with a tight hold on it and more than 10 times increases the voltage passing through the front base of the ozone handles (4) flow OAKS in accordance with the maximum capacity of the pumps (1, 2), greatly improve the efficiency of the procedure. However, despite a substantial increase in the flow of ACS in a single working circuit device, its flow from the depot at idle load is much lower consumption of both pumps (1, 2) in connection with the cyclical return of the greater part thereof with a minimum of emissions into the environment through protivogaznye box (6). But when using spot airtight processing ACS idle without load consumption ACS from the depot significant, as equal to its consumption by the pumps (1, 2) with the full release it into the atmosphere through protivogaznye box (6) during the hemostatic and antiseptic modes or partial admission antiseptic module (37) during the haemostatic-antiseptic mode. When the hemostatic-antiseptic mode idle without load in moments of pressure ozone handle (4) to the surface system, the sensing point, sealed processing ACS as difficulties hemostasis begins directly be supplied with clean OAKS of hemostatic module (38) in antiseptic module (37), raising the concentration of ozone in the latter proportional to the contact time between the ozone handle (4) with the surface of the, to compensate for the large flow OAKS of hemostatic module (38) waste gas mixture with a high content of ozone during operation antiseptic module (37).

After the formation of the ozone handle (4) from the treated surface at a single load instantly decreases the vacuum in the conductors in a single working circuit device, stopping the flow OAKS pair of sealed packages (40). When this suction pump (1) begins to consume the gas already in the atmosphere, and release the pump (2) is fully covered by its gas needs through direct gas flow from the suction pump (2)and through the removal of gas through the shunt, additionally connecting the incoming and outgoing lines. As a result of strong pressure in the ozone the handle (4) practically vanishes, and the remaining part of the ACS in the conductors in a single working circuit device quickly dilutes the air coming back into the motor portion through the ozone knob (4).

When during the next pressing of the facial Foundation of the ozone handle (4) to the surface of the OAKS in the pair of sealed packages (40) comes to an end, the gas deficit in a single working circuit device is returned, and as it is grown pumps (1, 2) have to drain the external air retrograde talk through protiva the EIT box (6), while a closed system of two pumps (1, 2) will not receive the necessary volume of air to fully meet the gas needs dictated by their technical characteristics. This protivogaza box (6) becomes an external air filter. As a result, in a single working circuit device gradual substitution of residue OAKS on atmospheric air through the recirculation of the gases in protivogaznyh box (6).

When during operation of the device without idle load in the accumulation portion ends OAKS, and gradually increases the load on throwing out the pump (2), the shunt between the incoming and outgoing lines emit pump (2) prevents premature wear of its parts. The entire tributary of the Oxus to emit pump (2) gradually moves from its incoming line shunt conductors, and decreasing the flow of ACS in the opening lines emit pump (2) more returns on the shunt in his line coming under increasing gas demand emit pump (2), gradually reducing the stream of the Oxus from the handle (4) to zero. Rapidly increasing gas deficit in coming lines emit pump (2) in critical decline in ACS in the opening line throwing pump (2) leads to a sharp NARAS is aniu of depression in the past with further retrograde movement to the external air, withdrawn through the guide tube (4H) ozone handles (4). Throwing the pump (2) tighten the outer air, consistently going in the opposite direction through its opening line, the shunt and the adjacent area of the incoming line, and then dispersing it, forcing the gas cycle in shut-tees (8, 9).

During operation of the device in hemostatic-antiseptic mode using idle load or without it is not desirable to use antiseptic module (37), while not completely devastated hemostatic module (38), and use point airtight processing ACS when at idle load, the gas contained in both units (37, 38), as in the common trunk of the funded portion will be mixing the waste gas mixture from sealed packages (40) antiseptic module (37) with ACS from sealed packages (40) hemostatic module (38). In the result, the ozone concentration in the stream directed at the biological surface, will vary and is not constant.

In case significant in relation to the maximum permissible concentration of ozone accumulation of ACS in the air of the treatment area for forced downward beyond the ozone concentration in the air below acceptable limits resort to irreversible aspiration OAKS. It provides for aspiration of air with ACS from the external environment with the destruction of what she protivogaznyh box (6) in the absence of jet OAKS of the guide tube (4H) ozone handles (4). To do this, turn off just throwing the pump (2) or include only the suction pump (1) with the prior closing of the intake valve (35) (if not closed). Irreversible aspiration can be used preventively after each ozone treatment.

Flow control and ozone concentration.

The flow control ACS, forming a jet from the front end of the guide tube (4H), produced near the manifold (5) ozone handles (4), in place of the pair facing the line-emitting pump (2) with the incoming line of the suction pump (1), with bleeding crane (33) (refer to "design and build"). Because of the direct, pregliasco external environment communication between the output line throwing pump (2) and the incoming line suction pump (1) reducing jet OAKS of ozone handle (4) is directly proportional to the opening degree of bleeding of the valve (33). With the side facing the line-emitting pump (2) there is an active message OAKS, and from the side of the incoming line of the suction pump (1) is an energetic her aspiration. Reduced at least 10 times the flow of the ACS at the end facing the line-emitting pump (2) can be completely absorbed by the suction pump (1) via its incoming line via a connecting bridge, providing a wide range of regulation article the AP OAKS of ozone handle (1) from the maximum to zero. However, with the full opening of bleeding crane (33) aspiration coming in the suction line of the pump (1) in place of the pair will dominate several times over the reduced flow OAKS of the output lines emit pump (2), forcing the latter to send the part going into the shunt ACS on the discharge tube (24) connecting the bridge to supply her suction pump (1), which may increase the consumption of OAKS from the accumulation portion while reducing jet OAKS of ozone handles (4). Therefore, when assembling the connecting bridge, you must use narrow skateline tube (29, 30) and installed on the movable part of the release of the crane (33) stroke limiter (33A). Regulation jet OAKS of ozone handle (4) in the desired direction by a certain amount using bleeding crane (33) changes in the appropriate direction by the same amount and aspirate the spent gas mixture due to the emergence of a small, additional, active gas source to the suction pump (1) along with the main source of gas from the atmosphere. The flow control ACS as appropriate during the point, sealed processing OAKS, and during non-contact processing OAKS. In the latter case, in spite of the direct discharge of clean ACS from the depot in the incoming line suction pump (1), the ozone concentration in the waste gas is a mixture does not significantly change due to mixing is insignificant in comparison with its part number ACS per unit time.

The device also provides for regulation of concentration of ozone in the stream of the Oxus from the ozone handles (4) without the participation of medical ozone by reducing the concentration of already produced ozone through thinning OAKS from the accumulation portion cleaned outside air coming in the line-emitting pump (2). For this near-emitting pump (2) in its line coming embed intake (see "design and build"). When during operation of the device OAKS from the accumulation portion actively consumes emit pump (2), the message of his coming line with the external environment through the air vent allows up to two times to reduce the concentration of ozone in the stream of ACS due to the emergence of equivalent prelease part of the incoming line path for absorption of external air. The degree of dilution of the ACS cleaned outside air coming in the line-emitting pump (2), which determines the fall in the concentration of ozone in the stream of the Oxus, install the adjusting valve (34) of the air intake. At lower ozone concentrations in the stream of ACS during operation of the device in hemostatic-antiseptic mode is directly proportional to decreases in ozone concentration in the waste gas mixture fed to the antiseptic module (37) cumulative servings. Flow control and end what Tracia ozone provides the operator when working with ozone handle (4).

The advantages of the present invention is the ability Autonomous from the ozone generator work, mobility, ability to use on any on biological objects, including the exterior, with a rough surface, and also in the internal cavities of the body.

1. Reverse Gastor containing two pushers working substance electric pump, each of which has decorated the input and output associated with the adjacent unit so that the input and output of different pumps communicated through tubes with a single device in the form of a tip, characterized in that it further includes a motor and cumulative portions, which are combined into a single work path, and the tip in the form of ozone handles and centrifugal, fastened with a plastic clamp suction and throwing pumps, inputs and outputs are in the form of pipes, provided with a conical nozzles with adapters, part of the motor portion; cumulative portion includes a circuit crosspieces connected in one direction by means supplying tube and provided on each side of each cross pair of sealed packages for ozone-oxygen mixture at opposite lateral parts, containing a hollow cylindrical insert so that the hollow cylindrical insert are of equal diameters, the issue is billing purposes within each of the crosses, but distinguishing the diameter of the lumen at different crosses with a consistent reduction in the diameters of openings from one extreme crosses, provided on the free longitudinal part of the nipple valve, containing the gasket to the other extreme of the cross, is supplied to the free longitudinal side of the exhaust valve, the chain crosses separated in place of articulation of one of the supply tubes with one of the crosses, respectively hemostatic and antiseptic modules, the communication node comprising moving the tee connected to one end of its longitudinal part with supplying tube hemostatic module, supplying tube with a release valve connected to the opposite end of the longitudinal part of moving the tee and connected through the straddle crane with the longitudinal part of the cross antiseptic module, and the feeding tube is connected to a median portion moving the tee through the stopcock; collector in the composition of the motor portion includes a coupling with two cylindrical channels, one with the rear base of the coupling runs right along it contains a sleeve with an inner part of the giver fitting, inserted into the sleeve through its minor external segment on the back of the base of the coupling, and in the middle of the length of the clutch smoothly transition is in a wide, flattened rectangular cavity with a gutter on the front of the base of the coupling containing a pair of afferent ports, which, entering the sleeve through the soft fixing Windows form its wide fitting on the bottom of the rectangular cavity, and the second cylindrical channel from the rear base of the coupling runs parallel to its lateral surface and contains a nozzle with the interior of the receiving fitting it with an external segment on the back of the base for coupling direction of the receiving fitting in the channel in order to fix it, but at the front base of the coupling of the second cylindrical channel arcuately curved toward the center and is in communication with the hollow rectangular cavity through its wide wall passing down mounted on the tapered end of the nozzle efferent port where it passes between the afferent ports, diluting them to the narrow side walls of the rectangular cavity, removing the short outer segment of the efferent port of the gutters on the front of the base of the clutch, while the clutch is immersed to the bottom of the protective sleeve, where the notch corresponding to the groove on the front of the base coupling and bushing on top of a fitted cap with threaded through the holes receiving and giving fitting; ozone pen in the composition of the motor portion is made in the form of a hollow cylindrical body equipped typelevel the mi flaps on the sides, open the front substrate and the partition wall, which, with its sharp edge at a distance from the front of the base, is equal to the third length of casing parts on the center of the lumen parallel to the discharge valves on two Crescent as thickening of the septum and the wall of the casing gradually pass into the nozzle and then into the slots, with the inserted them from the back of the case base removes the cannula guide tube, sequentially passing between the grooves from the center of the rear base housing through a cylindrical channel, passage, and a rectangular slot in the wall to the middle of its sharp edges with making outside into the lumen of the housing front end of the guide tube, not reaching 0.5 to 1 cm to the front of the case base, and the protrusion of the rear end of the guide tube, which is included in short outer segment efferent port manifold from the rear base housing by a distance 2 times less compared to the end removes the needle within the afferent ports of the manifold; the adapter conical nozzle suction producing pump comprising motor portion connected in series short connecting tube, the longitudinal part of the mixing tee, the median part of which is sequentially supplied with long halter tube, the adjusting valve is m and a cone with air-bacterial filter, and then the intake tube, the longitudinal part of the return tee and efferent tube connected to the outlet tap accumulation portion; the adapter cone nozzles issuing nozzle expelling pump comprising motor portion through a connecting tube connected in series to the longitudinal part two of the clip tees, median part with a reducing tubes connected to combine the tee from which departs a connecting tube connected with the median part of the return tee and from the longitudinal part of the extreme shut-off the tee consistently leaves the discharge tube, the longitudinal portion separating the tee and a feed tube connected with the receiving fitting of the manifold; the adapter conical nozzle suction pipe suction pump in the composition of the motor portion of the serially connected second intake tube, the longitudinal part of the host of the tee, the median of which is associated with a median separating part of the tee through two skateline tube, a split release valve with restrictor, and then a discharge tube connected with the giver fitting manifold; the adapter cone nozzles issuing nozzle of the suction pump in the composition of the motor portion connected in series in ora pressure tube, the longitudinal part of the output of the tee, the median portion of which is provided with excretory tube connected to it through the cover with the tip of the neck body protivogaznyh box, supplied with a plug in the outer hole, and then bringing the tube with an inlet valve which is connected with the nipple valve cumulative servings.

2. Reverse Gastor under item 1, characterized in that all the tees devices consist of two hollow perpendicularly interconnected cylindrical parts, in addition to combining the tee, which is several times larger than the others and is made in the shape of a hollow sphere whose wall is transferred in three hollow cylindrical branches, two of which are reducing tube and depart at an acute angle to each other in one plane at a small angle to which the opposite side of the ball departs the third branch with a connecting tube, and the pressure applying, generating, and skateline tube motor portion is made at least 3 times already all of the other tubes of the device; the outer segment of the efferent port manifold with14longer or14shorter protruding from the rear base is orpus ozone handles rear end of the guide tube; separating and receiving the tees are placed on the same level and parallel to each other and to one of megaclinic tubes attached to the free end of the tightening tube with a regulating valve and diffuser.

3. Reverse Gastor under item 1, characterized in that the centrifugal electric pumps that use as the working substance ozone-oxygen mixture, made of durable ozone materials, their conical nozzle adapter, and all the tees and valves of the device, bushing, cap, coupling, receiving, giving fittings and injector manifold, diffuser and ozone pen, crosses, and nipple valve cumulative portion - of the solid ozone plastic; all handsets and devices, ports and sleeve collector, a hollow cylindrical insert and sealed cumulative servings of soft, elastic ozone polymer and sealing cuff nipple valve from an elastic ozone polymer.



 

Same patents:

FIELD: medicine.

SUBSTANCE: invention relates to medical equipment. Device contains cylindrical case element, plunger and cover, made with possibility f travel between closing position and dispensing position. Cover includes hole, which has specified dimensions to provide leaking of medication through cover, when cover is in dispensing position. Cylindrical case element has multitude of internal thread coils. Connection of cover and case is realised due to the fact that cover includes external wall and column, extending towards cylindrical case element, column includes external thread coils, or cylindrical case element includes multitude of external thread coils, and cover includes multitude of internal thread coils, which have such dimensions that they are capable of mating in thread coils of external thread of cylindrical case element, and/or cylindrical case element includes multitude of internal thread coils, and cover includes multitude of cogs, which have multitude of external thread coils, which have such dimensions that it is capable of mating in thread said coils of internal thread of cylindrical case element (12), or cylindrical case element includes flange part, passing from distal end, projection, formed near distal end, first groove and second groove, with cover including first holding bead, which has such dimensions that it is capable of interaction with flange part, and second holding bead, which has such dimensions that is capable of snapping shut in first groove, when cylindrical case element is in closing position, and has such dimensions that it is capable of snapping shut in second groove, when first holding bead interacts with flange part, in order to place cover in dispensing position. Device additionally contains holding means to hold cover on cylindrical case element, when cover is in dispensing position.

EFFECT: providing delivery of specified dose at any moment due to travel of case element between closing and dispensing position without separating cover from device.

13 cl, 14 dwg

FIELD: medicine.

SUBSTANCE: group of inventions refers to medicine, namely to gynaecology, and can be used in treating such diseases as dysfunctional uterine bleeding, menorrhagia, dysmenorrhoea, endometriosis, uterine fibroid, menopausal disorders, osteoporosis and urogenital atrophy. That is ensured by presenting an urogenital system comprising a frame forming an internal cavity enclosing an insert with a therapeutically effective dose of a biologically active compound. The insert is form-stable and damage-resistant when in use. The frame has an open structure providing access to a main portion of an external portion of the insert. The frame comprises one or more retaining element for frame holding in the uterine. What is also presented is a method for making the above intrauterine system.

EFFECT: group of inventions provides an effective controlled release drug delivery for a long period of time, as well as easy and safe administration and proper removal of the preparation.

14 cl, 9 dwg

FIELD: medicine.

SUBSTANCE: invention refers to medicine, namely traumatology, orthopaedics, and can be used for supporting treatment in large joint replacement. That is ensured by determining a volume of involved joint contracture six months before the operation. That is followed by X-ray and magnetic resonant examination of the involved and collateral joints to specify their state. Besides, a quality of the bone tissue is assessed by osteodensitometry. If observing changes in the bone tissue quality, the complex of the drug therapy is added with the preparations Bivalos and Calcemin. A pain syndrome intensity is assessed by the visual analogue scale three months before the operation. That is followed by the complex therapy aiming at optimising the state of extremity joints with added local injection therapy (LIT). That is ensured by preliminary exposing the biologically active periarticular zones in the proximal and distal direction from the involved joint to the focused infrared laser light. A mixture containing solutions of the therapeutic preparations: chondroprotectors, Contrykal, Lidocaine, vitamin B12 is injected into the same zones. Besides, Arthrofoon is administered for the whole preoperative period. If the pain syndrome intensity is less than 4 points, Arthrofoon is administered in a dose of 4 tablets a day. If the intensity value is more than 4 points, the preparation is administered in a dose of 8 tablets a day in a complex with a short course of a non-steroidal anti-inflammatory preparations and a chondroprotector. The replacement operation is immediately followed by fixing a collateral joint with an orthesis for the period of 3 months. The complex of the postoperative supporting therapy started three weeks after the operation is added with a single intravenous introduction of the preparation Aklasta, the preparation Arthrofoon in a dose of 4 tablets a day for three months, alpha calcidole and Calcemin continuously. A pectoral girdle of the extremities is reinforced by means of an individually specified set of therapeutic exercises and electric walking myostimulation. The LIT of the collateral joint is performed three months after the operation. If observing a degenerative process in the adjacent joints, the LIT is performed alternatively in these regions. Vasodilators, chondroprotectors, and the preparation Milgamma are administered with underlying LIT. If observing psychoemotional changes in the patient, the preparation Tenoten is additionally administered. A postoperative medication regimen, including the LIT is repeated 3-4 times every 6 months.

EFFECT: method provides optimising the effect of the surgical management and preventing developing complications both in the operated joint, and in the adjacent and symmetrical joints after the replacement, preventing developing instability of the endoprosthesis components, preventing developing or aggravating degenerative process in the symmetrical and adjacent joints that reduces a risk of the recurrent operations.

1 ex

FIELD: medicine.

SUBSTANCE: after a colocolonic anastomosis is created 10-12 cm in a proximal direction from the anastomosis, a double tube is inserted into an intestinal lumen. After a transanal insertion of the tube, an infusion pump is used for dosed introduction of a rifaximin suspension at 0.01 mcg of an active substance per 1 kg of a patient's body weight a minute through one channel and a passive outflow through the second channel. The rifaximin suspension is introduced continuously for the first days, then 3 times a day for 3 hours until observing active intestinal peristalsis.

EFFECT: method provides effective prevention of colocolonic anastomotic leakage, reduces a probability of postoperative complications ensured by avoiding microbial contamination, infection and development of anastomositis, as well as promotes reducing the length of treatment and postoperative stay in hospital.

2 ex

FIELD: medicine.

SUBSTANCE: invention relates to medicine, namely to gynaecology, reflexotherapy and pelotherapy. A method includes carrying out a course of antibacterial and/or antiviral therapy, which is started on 5-7 day of a menstrual cycle. From 5-7 day of the following menstrual cycle a course of pharmacopuncture is performed by introduction of homeopathic preparations into acupuncture points (AP). On 1, 3, 5, 7, 9, 11 and 13 days of the course Traumel C is introduced into points E36 (2), V31 (2), V32 (2), V33 (2), V34 (2). On 2, 4, 6, 8, 10, 12, 14 days of the course Ovarium compositum is introduced in AP Rp6 (2). Simultaneously with the course of pharmacopuncture or starting from 5-7 day of the following menstrual cycle a course of pelotherapy is carried out. Introduction of gel, based on the Dead Sea mud, is performed rectally for 30 minutes, 1 time per day.

EFFECT: method ensures recovery of the two-phase menstrual cycle due to normalisation of endometrium and vagina biocenosis, improvement of local immune and vegetative status, increases duration of remission.

4 cl, 2 ex

FIELD: medicine.

SUBSTANCE: invention relates to the field of medicine, in particular to vascular surgery, and is intended for transfer of medications onto an internal surface of a vessel wall. A device for transfer of medications onto the internal surface of the vessel wall contains a matrix, made in the form of a polymer film, covered with medication and placed on a flexible framework. The matrix and the framework have specified standard sizes. They are made with a possibility of placement in them of a cellular knitted metal temporary stent and with a possibility to be inside the temporary stent of an inflatable balloon with a fixed diameter and length and a cylindrical or conic shape when blowing under high pressure or a latex balloon with a possibility of filling the entire internal space of the temporary stent when blowing under low pressure.

EFFECT: invention makes it possible to simultaneously perform long-term efficient transfer of medication into the vessel wall with preservation of blood flow and efficient diameter of the affected vessel.

4 cl, 1 dwg

FIELD: medicine.

SUBSTANCE: there are performed beam therapy, intracavitary therapy and chemotherapy. For 5-7 days before the beginning of the radiation, Colagel-Beta with 1 β-interleukin 20 ml is introduced into a vaginal tube daily. Each session of the intracavitary therapy is preceded by introducing Colegel with 5-fluoruracil 20-25 ml into an uterine cavity and exposed for 30-40 minutes. Besides, from the beginning of the beam therapy 40-50 minutes after the radiation session, sodium alginate gel 20 ml containing methyluracil, dimethyl sulphoxide and hydrocortisone are introduced into a rectum and a bladder in a therapeutically effective amount. 5-10 procedures are performed.

EFFECT: providing faster regression of the tumour, reducing the rate and severity of radiation injuries of the rectus and bladder adjacent with the uterus with no risk of severe systemic toxic manifestations, including in senior patients with comorbid inoperable diseases and extended tumours.

3 ex

FIELD: medicine.

SUBSTANCE: invention refers to medicine, namely to traumatology and biotechnology, and may be used for the biocompatible polymeric structure formation in bone tissues. That is provided by a puncture approach to a filled cavity in the bone tissues. That is followed by filling the cavity with a polymeric gel compound containing 55-97.7 wt % of the biocompatible polymer polylactide of a particle size of 50 to 100 mcm, 0.3-45 wt % of magnetic nanoparticles of ferric oxide of a particle size of 10 to 100 nm, the gelling agent maltodexrin in the amount of 0.5 to 50 wt % of the weight of mixed polymer and magnetic nanoparticles, as well as distilled water in the amount of 0.5 to 100 wt % of the weight of a dry mixture of the polymer, magnetic nanoparticles and gelling agent. A solid three-dimension structure is formed. That is accompanied with heating the compound throughout by exposing to an alternating magnetic field at frequency 500 kHz and amplitude 500 E for 3-5 minutes. Where appropriate slow down the process of heating the compound, it is additionally exposed to a direct magnetic field at amplitude 1000 E applied either to the whole formed volume, or locally depending on the problem to be solved.

EFFECT: method enables forming the biocompatible three-dimension structure in the specified cavity of the bone tissue with minimum surgical intervention.

1 dwg

FIELD: medicine.

SUBSTANCE: invention refers to medicine, namely to neurosurgery, resuscitation and neurology, and may be used for treating the permanent unconscious vegetative state. That is ensured by intratympanic streptomycin treatment with underlying common drug therapy of the state. The completion of the above is followed by the electric transcranial exposure on the brain. For the intratympanic treatment, streptomycin 1 g is dissolved in physiologic saline 1 ml. The preparation is introduced once a day from one side, and on the other day from the opposite side. The therapeutic course is 5-10 days. The electric transcranial exposure is presented by transcranial DC micropolarisation of intensity 200-400 mcA for 30-40 minutes daily for 16-24 days. The exposure is performed through 3-4 electrodes places on the areas of temporo-caudal projections and posterior associated cortical areas from both sides. For the first 6 days, such exposure covers the temporo-caudal projections, while on the other days the posterior associated cortical area projections are exposed. If required, the above therapeutic courses are repeated not earlier than in 3 months until the clear consciousness is reached.

EFFECT: method provides an immediate and convincing clinical effect without brain invasiveness, an ability to recover the clear consciousness in these patients, as well as a significant reduction of the pathologically increased muscle tone and as a result, achieved satisfactory level of the patient's self-service.

2 ex

FIELD: medicine.

SUBSTANCE: invention refers to medicine, gynaecology and concerns treating non-specific cervicitis in nulliparae. What is involved is an etiotropic therapy according to the microscopic and bacterioscopic findings in a combination with a 10-day course of laser photophoresis started in the first phase of menstrual cycle for two menstrual cycles. For this purpose, the involvement area is coated with the balneological product 'Elton-gel' with the uterine cervix to be thereafter exposed to laser light at wavelength 0.9 nm, pulse power 5 Wt, pulse repetition frequency 600 Hz. The length of exposure for each locus makes: 2 minutes in first cervicitis, 3 minutes in the process of more than 1 year or the disease suffered for more than one year and the presence of more than two episodes of recurrence.

EFFECT: method provides reducing the length of treating subsacute and chronic non-specific cervicitis (SANC and CNC) in the given category of patients from 6-9 to 2-3 months, reducing the rate of the disease, providing noninvasiveness, safety and availability of the treatment.

3 ex, 2 tbl

FIELD: medicine, surgery, coloproctology.

SUBSTANCE: one should introduce gelatin-based colloids: gelatinol or gelofusin and crystalloids at 1:1 ratio at total volume of 40-50 ml/kg patient's body weight daily; additionally, since the 2nd to the 7th d after operation it is necessary to conduct enteral nutrition in the form of hypercaloric mixtures by increasing their volume at higher rate of injection starting from 25 ml/h/kg body weight on the 2nd and 3d d up to 100 ml/h on the 6th-7th d. The present innovation enables to improve nutrition of intestinal endothelium, decrease pathogenic and conditionally pathogenic microflora, prevents appearance of postoperational intestinal paresis and restores its function in more shortened terms.

EFFECT: higher efficiency.

1 ex, 3 tbl

FIELD: medicine.

SUBSTANCE: method involves introducing cauterizing necrotizing composition like paste containing silver nitrate and dextrane into uterine cavity. Paste contact to target tissue is supported during time enough for reaching chemical necrosis. Then cauterizing composition is brought in contact with deactivating agent like aqueous solution of sodium chloride and removed from the uterine cavity later on. It is proposed to protect non-target tissue by supplying protection agent to it and carrying out previously described steps.

EFFECT: enhanced effectiveness of cauterization controlled in time and action intensity degree; avoided other tissue injuries.

30 cl, 8 dwg

FIELD: medicine.

SUBSTANCE: method involves forming urinary bladder from retained walls after having done subtotal resection. 20-40 ml of physiologic saline and 10 ml dioxidine is introduced at the twenty first day after surgical operation for 2-3 h 3-4 times a day to cause marked vesical tenesmus. Spasmex is applied at a dose of 20 mg 3 times a day during 12 weeks.

EFFECT: enhanced effectiveness of treatment.

FIELD: medicine, medicinal parasitology.

SUBSTANCE: the present innovation deals with affecting the helminthes with curative mixture made out of eucalyptus leaf at addition of eucalyptus essential oil. Curative mixture at the quantity of 1 l at 40-42 C should be daily introduced into patient's rectum with enemas for 5-7 d at intestinal keeping for 15-20 min. Before introducing the curative mixture it is necessary to apply purifying enema. The method suggested provides removal of different types of helminthes at excluding toxic action upon human body.

EFFECT: higher efficiency of helminthic removal.

3 ex

FIELD: medical procedures.

SUBSTANCE: patients preliminarily undergo endoscopic papillo-sphincterotomy, whereupon stone in common bile duct is dissolved and removed by way of supplying stone-dissolving therapeutic mixture, in particular 1:1 solution of diethyl ether in olive oil, directly to bile stone. Therapeutic mixture creates, in the lumen of bile duct, hydrostatic pressure 200 mm water head. More specifically, 120 ml of therapeutic mixture is supplied during one day at a rate of 10 drops/min, while performing 5 to 16 daily sessions of stone-dissolving therapy.

EFFECT: increased efficiency in removal of sparingly soluble stones in common bile duct.

2 ex

FIELD: medicine, in particular, rectal dosed transportation of medicinal drugs into straight intestine.

SUBSTANCE: dosing apparatus has casing adapted for introduction into hollow organ and made in the form of continuous rod. Cavities for treating ointments on cylindrical outer part of rod are formed as slots. Rear end of rod has reduced diameter in comparison with maximal diameter of rod. Guiding pipe loosely put onto said end has outer diameter exceeding maximal diameter of casing. Figures are applied in equally spaced relation along length of pipe. Flexible cord with round restricting member is fixed at rear end of rod.

EFFECT: increased efficiency in transporting of high-density medicinal drugs, in particular, treating ointments, immediately to point of application.

2 cl, 2 dwg

FIELD: medicine, arthrology.

SUBSTANCE: the present innovation deals with treating arthritis of different etiology. For this purpose one should introduce medicinal preparation into articular cavity and immediately after introduction one should periodically change spatial articular position at the interval of 20-30 min. The present innovation provides efficient and safe treatment of arthritis due to steady distribution of medicinal substance along the whole area of articular surface.

EFFECT: higher efficiency of therapy.

1 cl, 2 ex

FIELD: oncology.

SUBSTANCE: invention provides a chemotherapy method that can be used in treatment of patients with widespread abdominal tumors. When performing laparotomy, sub-peritoneal infiltration with autoblood solution containing chemical agent is effected on zones of tumor infiltrates (supraperitoneal paraaortic tissue) and root of mesentery region.

EFFECT: expanded tumor treatment possibilities.

FIELD: medicine.

SUBSTANCE: method involves beginning disinvagination with mask narcosis by pumping air into large intestine under X-ray control. The invaginate remaining unstretched, the air is discharged from the intestine by massaging abdomen along the large intestine and pressing abdomen flanks. Next to it, air is pumped into the large intestine and invaginate stretching is carried out with an additional coercion by squeezing invaginated head out towards the neck part. No success being achieved, the procedure is repeated with mask narcosis to eight times. The invaginate remaining unstretched, endotracheal narcosis is given to the patient and myorelaxant drug of transitory action is introduced. Air volume introduced into the intestine is increased. The invaginate-stretching procedure is repeated with endotracheal narcosis to five times.

EFFECT: enhanced effectiveness of treatment.

FIELD: medicine.

SUBSTANCE: method involves administering triple injections of medicament mixture composed of Lidase 32 units, Anicaine 4ml, Dexamethazon 4 mg, Alflutop 1 ml, into Hoff fat pad.

EFFECT: reduced pain and knee joint edema manifestations; increased joint range of motions.

5 tbl

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