30 results about "Flow limitation" patented technology

A flow restriction system may include an implantable controller system for controlling an implantable flow restrictor. The controller system may include: an implantable housing, an actuator at least partially disposed within the implantable housing, the actuator having a first configuration corresponding to the implantable flow restrictor being in the low profile state and a second configuration corresponding to the implantable flow restrictor being in the high profile pressure restricting state, an internal power source configured to supply current to the actuator, and a processor configured to control operation of the actuator using power from the internal power source.

A cardiac microperfusion device is disclosed that includes an integrated flow restrictor and a diverter from the left atrium to modulate flow within the blood vessel, particularly flow within the coronary sinus. Related methods and systems are also disclosed.

A flow control component is provided for a patient interface for the supply of fluid to a surgical site. The flow control component includes an inlet, an outlet, and a flow restriction with a first opening and a second opening. The first opening and second opening are configured to alter a fluid characteristic of fluid passing therethrough. The patient interface may include an outer layer configured to enclose at least a portion of the flow control component, with the outer layer configured to contain the flow of fluid through the flow control component and / or along a portion of the flow path of the patient interface.

A tracheal connector is connected to a respiratory gas generator and a tracheal tube. The tracheal connector includes a tracheal connector body connected to the tracheal tube, a connector tube connected to the tracheal connector body and the respiratory gas generator, and a restriction mechanism configured to narrow a respiratory gas flow path configured to allow the respiratory gas to flow therein. The tracheal connector body includes a tracheal port connected to the tracheal tube, an exhaust port facing the tracheal port and configured to discharge at least expired air of the subject, and a respiratory port connected to the connector tube. The restriction mechanism is provided on the respiratory gas flow path between the respiratory port and the tracheal port.

The invention relates to a fluid compression apparatus (1) comprising a sealed enclosure (13) for containing a cryogenic fluid bath (16), a first (3) and a second compression chamber (4), an inlet system (2) for the first chamber (3), a transfer system (6) from the first (3) to the second (4) chamber, the apparatus (1) further comprising a communicating discharge port (7) for the outlet of compressed fluid from the second chamber, the apparatus (1) further comprising a discharge port equipped with a valve (9) for the discharge of the first compression chamber (3) into the bath (16) to allow excess liquid to escape during fluid compression in the first chamber (3), the discharge port communicating with the enclosure (13) via at least one flow restrictor (10) configured to attenuate the velocity and / or intensity of the discharged liquid flow by limiting its pressure drop. Abstract figure: Fig. 1

System and method for deploying a flow restriction device in patient vascular and recapturing and repositioning the flow device after full or partial deployment. Disclosed systems and methods permit confirmation of device placement, such as by measuring a pressure drop across the partially or fully deployed device in the coronary sinus before release of the device and permanent implantation.

An apparatus for controlling a flow rate of a gas is disclosed herein, including a flow restriction element configured to restrict a flow rate of a gas; a pressure regulator coupled to an inlet of the flow restriction element, wherein the pressure regulator is configured to control a pressure of the gas between the pressure regulator and the flow restriction element; a flow meter coupled to an outlet of the flow restriction element, wherein the flow meter is configured to measure the flow rate of the gas at the outlet of the flow restriction element; and a controller operatively coupled to the pressure regulator and the flow meter, wherein the controller receives the flow rate measurement of the flow meter, determines a pressure setting associated with a target flow rate, and causes the pressure regulator to have the pressure setting.

To provide a flow restriction device.SOLUTION: A housing forming a fluid flow path with an elastic valve positioned between a first section and a second section of the fluid path; A section of the fluid pathway includes a helical or involute shape, and the elastic valve is responsive to changes in pressure along the fluid pathway such that the elastic valve can move or deflect toward the fluid pathway to restrict fluid flow through the fluid pathway, thereby reducing the flow rate and pressure of the fluid, but if the fluid is blood, reducing the rate of hemolysis of the blood, and in some instances the elastic valve stops fluid flow through the fluid flow pathway to reduce the rate of hemolysis of the blood in response to excessive pressure along the fluid pathway.SELECTED DRAWING: Figure 5

This application discloses various systems, devices, components, and methods for controllably and selectively occluding, restricting, and / or shunting blood flow within a patient's vascular system. The flow restriction system may include an implant with a flow restrictor and an implantable controller with an actuator for actuating the flow restrictor. The implant may be separable from its respective controller and actuator. The implant may include a dual-frame configuration to prevent tissue growth into at least one frame.

A hemodialysis device including a replacement fluid passage between a dialysate circuit and a blood circuit, the dialysate circuit and the replacement fluid passage being respectively provided with first and second flow rate restriction devices. Also provided is a connection portion pressure sensor for measuring a pressure of a connection portion between a dialysate supply passage and the replacement fluid passage, and a vein-side pressure sensor for measuring a pressure of the blood circuit. A control device adjusts an opening degree of the second flow rate restriction device multiple times based on the measured pressure of the connection portion pressure sensor, and the measured pressure of the vein-side pressure sensor, for one round, being from when a supply compartment of a chamber provided to the dialysate circuit is filled with a fresh dialysate until all of the fresh dialysate in the supply compartment has been discharged.

A present ventilator system for detecting and treating concurrent chronic obstructive pulmonary disease (COPD) and overlap syndrome of obstructive sleep apnea (OSA events) includes a pressure generator for generating a pressurized flow of breathable gas for delivery to an airway of a subject, a sensor(s) for generating an output signal conveying information related to a parameter of the breathable gas, and a processor(s) operably connected to the sensor(s) and the pressure generator, configured to detect the presence of an OSA event and / or expiratory flow limitation (EFL) in the subject based on the output signal. In response to detecting the concurrent presence of an OSA event and EFL, the processor is configured to determine an OSA event therapy parameter for treating the detected OSA event in the subject, determine an EFL therapy parameter for treating the detected EFL in the subject, determine a priority treatment based on a comparison between the OSA event therapy parameter and the EFL therapy parameter, and control the pressure generator to deliver the determined priority treatment.

Methods and apparatuses for detecting full waste canister and / or fluid flow path blockage conditions are disclosed. Also disclosed are methods and apparatuses for controlling a pump. In some embodiments, flow of fluid can be restricted in a portion of the fluid flow path. A controller can be configured to compare a difference in pressure values upstream and downstream of a fluid flow restrictor to a pressure difference threshold, and determine based on the comparison whether to activate an alarm indicating the full waste canister condition or the fluid flow path blockage condition. The controller can be additionally or alternatively configured to determine a fluid flow using a flow meter, open a selectable valve in response to a comparison of the fluid flow with a fluid flow threshold, determine fluid flow after opening the valve, and determine based on the fluid flow after opening the valve whether to activate the alarm.

Mass flow controllers and associated methods are provided. A mass flow controller includes a control valve configured to control flow of a fluid in a flow path and first and second flow sensors. The second flow sensor includes a pressure sensor adjacent a flow restrictor disposed in the flow path. A controller is configured to control actuation of the control valve. The controller is configured to determine a first mass flow rate based on one or more first fluid flow parameters detected by the first flow sensor, determine a second mass flow rate based on one or more second fluid flow parameters detected by the second flow sensor, calculate an orifice area of the flow restrictor based on the determined first mass flow rate, and compare a nominal orifice area of the flow restrictor with the calculated orifice area to assess a condition of the second flow sensor.

A negative pressure wound treatment apparatus can include a negative pressure source configured to be connected to a wound by a fluid flow path, a valve in the fluid flow path and configured to allow supply of negative pressure from the negative pressure source upstream of the valve in an open state and to block supply of negative pressure from the negative pressure source upstream of the valve in a closed state, a flow restrictor in the fluid flow path, and a pressure sensor configured to measure a pressure differential across the flow restrictor. The apparatus can include a control circuit configured to cause the valve to be in the open state in a normal operating mode and to perform at least one of a leak test, a flow test, or an overpressure test in a test mode.

A method for providing therapeutic treatment to reduce pre-load may be provided. The method may include placing a ventricular assist device (VAD) at least partially within a left ventricle or a right ventricle of a patient, and placing a catheter-based device including an adjustable flow limiting element (FRE) such that the FRE is disposed within a superior vena cava (SVC) of the patient. The method may include receiving information from the VAD and / or conduit-based FRE device, determining a first determination value based on the information, and controlling at least one performance parameter of the VAD and / or conduit-based device based on the first determination value.

Disclosed are cardiac micro-perfusion devices including integrated flow restrictor and flow diversion from the left atrium to modulate flow within the vessel, in particular within the coronary sinus. Related methods and systems are also disclosed.

Provided is a leadless flow restriction system, which comprises an intravascular housing, a control unit and a flow restrictor assembly. An actuator configured to rotate a first shaft and a driving element connected with one end of the first shaft are encapsulated in the intravascular housing. The control unit is arranged in the intravascular housing or connected with the intravascular housing and the actuator. The flow restrictor assembly comprises an inflatable body, a flow restrictor and a transmission shaft assembly. In use, the activation of the actuator causes the transmission shaft in the transmission shaft assembly to rotate or move linearly, so that the flow restrictor adjustably blocks the inner cavity.

A device for regulating pressure, the device comprising: a body having: an inlet; the inner cavity is communicated with the inlet; and one or more flow features including a flow restrictor for restricting airflow through the lumen wherein downstream of the flow restrictor is a protective portion that helps protect the restrictor from damage.

Mass flow controllers and associated methods are provided. A mass flow controller includes a control valve configured to control flow of a fluid in a flow path and first and second flow sensors. The second flow sensor includes a pressure sensor adjacent a flow restrictor disposed in the flow path. A controller is configured to control actuation of the control valve. The controller is configured to determine a first mass flow rate based on one or more first fluid flow parameters detected by the first flow sensor, determine a second mass flow rate based on one or more second fluid flow parameters detected by the second flow sensor, calculate an orifice area of the flow restrictor based on the determined first mass flow rate, and compare a nominal orifice area of the flow restrictor with the calculated orifice area to assess a condition of the second flow sensor.

The present invention relates to a tracheal coupling comprising a patient port 33, an outlet port 36, an inlet port 31 between the patient port and the outlet port, such that flow 34 from the inlet port can go to the patient port or direct to the outlet port, and a flow restriction e.g. 32 between the inlet port and the outlet port, or at the outlet port.

The present invention relates to a tracheal coupling comprising a patient port 33, an outlet port 36, an inlet port 31 between the patient port and the outlet port, such that flow 34 from the inlet port can go to the patient port or direct to the outlet port, and a flow restriction e.g. 32 between the inlet port and the outlet port, or at the outlet port.

To provide a portable respiration system.SOLUTION: A portable respiration system includes a housing, a partitioning material, a flow rate sensor, an elastic member, hardware, an air blower, and a flow rate limitation part. By arranging the partitioning material inside the housing, the system is partitioned into an upper chamber and a lower chamber, the flow rate sensor is located in the upper chamber and the elastic member is located in the lower chamber. The hardware is fixed to the lower chamber and defines an intake flow path, a lateral flow path, a transport flow path, and an air blow flow path. The air blower is arranged inside the elastic member and is used to receive an air flow from the transport flow path to generate a positive pressure air flow. The flow rate limitation part includes a plurality of tubular bodies and is located inside the lateral flow path. The portable respiration system is compact, lightweight, and portable, and has a flow rate monitoring function, and can improve comfort and therapeutic effect by adjustment of the flow rate of the air flow according to needs of a user.SELECTED DRAWING: Figure 1

In the present invention, hemodialysis is continued even if a flow restricting means is blocked.　The present invention relates to a hemodialysis device (1) in which a first flow rate restricting means (MV1) is provided in a dialysate supply passage (14), a second flow rate restricting means (MV2) is provided in a replacement fluid passage (5), and first and second dialysate filters (21, 22) are provided in the dialysate supply passage (14).　Provided is a bypass passage (second flushing passage (24), bypass passage (32)) that communicates the branching position between the first dialysate filter (21) and the replacement fluid passage (5) in the dialysate supply passage (14) with the first flow rate restricting means (MV1) and a dialyzer (2), and a bypass on-off valve (tenth on-off valve (V10), supply fluid connection valve (V14)) that opens and closes the bypass passage, and if an abnormality occurs in either the first flow rate restricting means (MV1) or the second flow rate restricting means (MV2), the bypass on-off valve is opened to supply dialysate to the dialyzer (2) through the bypass passage.

Fluid flow limitation assembly (10) in a conduit, including: a body (12) defining an internal cavity, the body having a wall portion (18) extending from an end portion (20) of the body, the wall portion and the end portion defining the internal cavity (16), the wall portion having an outwardly flared portion (22) extending away from the internal cavity at an open end (24) of the body, the open end being opposite the end portion of the body, the wall portion having a corrugation (26) near the outwardly flared portion, the corrugation extending towards the internal cavity;and a fluid flow-limiting element (14) retained in the internal cavity of the body, wherein the fluid flow-limiting element (14) reduces or prevents the flow of fluid through the internal cavity and the corrugation (26) prevents the fluid flow-limiting element (14) from being removed from the internal cavity. Figure for abbreviation: Figure 4;

A flow restrictor includes a flexible tube held in a housing and a linear actuator connected through an intermediate link to a distal link via a first revolute joint proximate the linear actuator and a second revolute joint connecting the intermediate and distal links. The distal link has a distal end adjacent the flexible tube and the intermediate and distal links are constrained to move such that when the linear actuator moves the first revolute joint toward the linear actuator, the distal end of the distal link is driven into the side of the tube thereby progressively occluding the flexible tube.

A catheter has a jacket (10, 11, 5) defining a lumen and a helical support (6). The catheter has a proximal portion (4) and a distal portion (3), the distal portion having for at least some of its length a corrugated outer surface. A transition portion has a flexural stiffness which is less than that of the distal portion and more than that of the proximal portion. The transition portion provides an optimum transition in flexural stiffness by way of features of the jacket including geometry of jacket corrugations (15), or overlapping tubular layers (1073, 1074). The distal end of the distal portion may have an extension of liner material folded over (1072, 1082) to provide a particularly soft tip. In other examples the liner is terminated (763) before the distal tip. The catheter is particularly suited to an aspiration device (1350) with a flow restrictor (1353) and the distal portion distal of the flow restrictor. An aspiration system (3500) may employ the catheter with a pump which dynamically applies negative or positive pressure to optimally aspirate a clot.

A method of restricting fluid flow through a pipe. The method comprising installing an anchor through an opening in a wall of the pipe, engaging a portion of the wall with a foot of an anchor, securing a head of the anchor to the pipe, placing a saddle between a bottom surface of the head and an outer surface of the wall of the pipe, and inflating an inflatable plug coupled to the anchor. When securing the head of the anchor to the pipe, the head remains partially outside the pipe.

A vascular access system includes a catheter adapter having a body and a catheter configured to be inserted into a patient's vasculature, with the body having a distal end and a proximal end positioned opposite the distal end, and a blood collection device in fluid communication with the catheter. The blood collection device including a flow restriction device configured to reduce a blood collection flow rate to be equal to or less than a blood supply flow rate of a patient's blood vessel.

The utility model belongs to the technical field of medical instruments, and particularly relates to a fiberoptic bronchoscope with a pressure flow limiting mechanism, which comprises a display. A fixing block is fixedly connected to the bottom of the displayer, a control button is arranged on the front face of the fixing block, a handle is fixedly connected to the bottom of the fixing block, a pressure control device is fixedly connected to the back face of the displayer, an insertion hose is fixedly connected to the bottom of the pressure control device, and an occlusion device is movably connected to the surface of the insertion hose. Saliva collecting devices are fixedly connected to the front face and the back face of the occlusion device, a camera is arranged at the other end of the insertion hose, and illuminating lamps are arranged on the two sides of the top and the two sides of the bottom of the camera. Through the arrangement of the saliva collecting device, a large amount of saliva generated by long-time stimulation of instruments of a patient in the fiber bronchoscopy process can be effectively collected, the saliva is prevented from being accumulated in the oral cavity, and therefore the discomfort of the patient is reduced.