107 results about "Pleural cavity" patented technology

A biopsy needle and method of using the same. The biopsy needle includes a pair of articulating members that can be moved between a retracted position where the articulating members are contained within the biopsy needle and an extended position where the articulating members extend outwardly from the distal end of the biopsy needle into the pleural cavity of a patient. Once extended, the articulating members have operative surfaces that contact the parietal pleura of the patient such that a biopsy sample can be obtained as the operative surfaces are moved in contact with the parietal pleura. The operative surfaces may be a brush blade or a knife blade. A passageway within the interior of the biopsy needle allows removal of fluids from the patient.

An apparatus for use in insufflation of a body cavity 5, such as through a trocar 6 is described. One such application is laparoscopic surgery. The device is also suitable for use in any situation involving insufflation of a body cavity such as in arthroscopies, pleural cavity insufflation (for example during thoracoscopy), retroperitoneal insufflations (for example retroperitoneoscopy), during hernia repair, during mediastinoscopy and any other such procedure involving insufflation. The apparatus comprises a reservoir 1 for storing an liquid solution, an aerosol generator 2 for aerosolising the solution, and a controller 3 for controlling operation of the aerosol generator 2. Aerosolised liquid solution (which main contain a pharmaceutical) is entrained with insufflation gas using a T-piece connector or housing 30 having an insufflation gas inlet 31 and an outlet 32. The connector 30 also comprises an aerosol supply conduit 34 for delivering the aerosol from the aerosol generator 2 into a mixing chamber 33 in which the aerosol is entrained with insufflation gas. The aerosol insufflation gas mixture passes out of the connector 30 through the outlet 32 and is delivered along the insufflation gas conduit 15 to the trocar 6 for delivery into a body cavity 5. The connector 30 causes a substantial sudden reduction in the velocity of the insufflation gas from the insufflation gas inlet as it enters the mixing chamber 33. The connector 30 also causes a gradual increase in the velocity of the insufflation gas with entrained aerosol between the mixing chamber 33 and the outlet 32.

The present invention provides thoracentesis systems composed of an insertion needle, a thoracentesis catheter with self-sealing valve, and a valve opening device which are utilized in the removal of fluid or gases from a pleural cavity. The insertion needle is utilized to insert the thoracentesis catheter into the pleural cavity. The thoracentesis catheter provides automatic closure of the flow path from the pleural cavity by automatic closure of the self-sealing valve upon removal of the insertion needle from the thoracentesis catheter. The self-sealing valve prevents drainage of fluid from the pleural cavity and introduction of air into the pleural cavity when the needle is withdrawn from the thoracentesis catheter and a valve opening device is not in place. A drainage flow path from the pleural cavity is established by insertion of a valve opening device into the self-sealing valve of the thoracentesis catheter, thus opening the self-sealing valve. With the self-sealing valve opened by a valve opening device, fluid or gases can be removed from the pleural cavity.

A percutaneous single-phase surgical procedure is disclosed for creating a pneumostoma to treat chronic obstructive pulmonary disease. A pneumostomy instrument is introduced percutaneously through the thoracic wall, parietal membrane, visceral membrane and into the parenchymal tissue of the lung. The pneumostomy instrument crosses the pleural cavity between the parietal membrane and visceral membrane there being no pleurodesis between the membranes prior to passage of the pneumostomy instrument. A pneumoplasty device at the distal end of the pneumostomy instrument displaces and engages the parenchymal tissue of the lung and the pneumostomy instrument is used to secure the lung and visceral membrane in contact with the parietal membrane and chest wall. The pneumostomy instrument is left in place while a pneumostoma tract heals and pleurodesis occurs between the pleural membranes surrounding the pneumostomy instrument.

A method and device are provided for simultaneously or near-simultaneously diagnosing and treating tension pneumothorax and/or hemothoraxA Veress-type needle portion includes a hollow needle for puncturing the chest wall over a blunt hollow probe biased by one or more springs to extend distally into the pleural cavity. Openings in the blunt hollow probe connect via a pathway to an automatic check valve, which permits the flow of air and/or fluid only in a proximal direction. Pressure from within the pleural cavity is transmitted to the interior surface of a pressure documenter. If pressure greater than atmospheric pressure is present in the pleural cavity, the pressure documenter will be automatically urged proximally to simultaneously allow air and/or fluid to escape from the pleural space through the device, thus treating the tension pneumothorax and/or hemothorax, as well as providing a stable indicator to positively document the diagnosis of increased pressure.

This invention relates to a shield member for shielding the lens of a flexible or rigid surgical endoscope from body fluid, tissue debris, and condensation deposited on a working port valve as the lens passes through the working port lumen in a posterior direction to gain access to the intra-abdominal or pleural cavity regions. The shield member has a shield lumen and is telescopically and slidably carried within the lumen. The shield member is so dimensioned and proportioned such that the distal end of the shield member may be selectively positioned posteriorly of the working port valve thereby permitting the lens to advance axially within the shield lumen and by-pass the working port valve without coming in physical contact with the working port valve.

The invention discloses an intelligent breathing machine and a weaning method for the intelligent breathing machine. A ventilation effect can be automatically realized by the intelligent breathing machine before weaning is carried out. The weaning method includes examining variation delta V of the volumes of the pulmonary alveoli of a patient, variation delta P of the internal pressure of the pleural cavity of the patient and the spontaneous breathing frequency f of the patient at first; computing work W of breathing and a rapid-shallow-breathing index RSBI of the patient by the aid of examined values; monitoring a numerical value of the blood oxygen saturation degree SpO2 of the patient and a numerical value of end-tidal carbon dioxide EtCO2 of the patient; comparing computed values and the monitored values to weaning standards of the breathing machine; implementing weaning if the weaning standards of the breathing machine are met; implementing secondary weaning judgment if the weaning standards of the breathing machine are not met. The intelligent breathing machine, the weaning method and a weaning device have the advantages that various key indexes of vital signs of the patient are monitored automatically, so that whether weaning is implemented or not can be comprehensively judged, and the weaning judgment accuracy can be improved; a good clinical effect can be realized by the weaning method, and the weaning method and the weaning device bring convenience for medical staff to accurately implement weaning operation according to weaning information.

An improved method and device are provided for forming and/or maintaining a percutaneous access pathway. The device generally comprises at least one of three type of components: access pathway, insertion device, and attachment device. In one embodiment, the device is used to form and/or maintain a percutaneous access pathway into the pleural cavity (i.e. tube thoracostomy). The provided assembly substantially reduces the possibility of iatrogenic infection while accessing and/or re-accessing a body space.

A chest seal for treating an open pneumothorax that is low profile and thus unobtrusive so that the chest seal can be effectively maintained in position to seal a chest wound while allowing the pleural cavity to vent.

A fluid management system for moving bodily fluid accumulated due to ascites, pleural effusion or pericardial effusion is provided including an implantable pump coupled to an inflow catheter, an outflow catheter, and optionally an anti-clog catheter. The fluid management system facilitates removal of fluid from a body region, such as the peritoneum, pleural cavity or pericardial sac, where drainage is desired to another body region, such as the urinary bladder or the peritoneal cavity. The system includes clog resistant mechanisms such as clog resistant catheters and/or programmed routines for cycling fluid through inlet catheters in predetermined time intervals and/or responsive to sensed conditions to minimize the risk that inlet catheters become clogged due to, for example, tissue ingrowth and/or solid objects within accumulated fluid.

The invention provides a hybrid variation bioelectrical impedance imaging method, relating to the measurement on the conductivity of the pleural cavity of the body. According to the method, the potential spatial distribution condition is simulated by adopting a finite element method, a numerical model of the bioelectrical impedance imaging technology is established, a numerical model with large size is dispersed into small units, certain boundary conditions are applied and boundary voltage is calculated, a two-dimensional thoracic cavity numerical model and a three-dimensional thoracic cavity numerical model are respectively established, after the objective function of the hybrid variation algorithm is determined, the inverse problem solving is carried out by adopting the steepest descent method, the electrical impedance image reconstruction of the thoracic cavity is carried out, so that the resolution ratio of the reconstructed image is improved, therefore, the problems in the existing bioelectrical impedance imaging technology, the influences of noises and errors exist during the process of reestablishing the image with high resolution ratio, consequently, the excessive smooth and staircase effect are caused, and the accurate electrical impedance reconstructed image of the lung can not be obtained are solved.

A single stage instrument is used to insert a chest drainage tube into the inter-pleural space to facilitate drainage. The instrument is scissor-like with cylinder-like channels to slidably enclose the distal section of the tube therein when closed. The tip of the instrument is curved to enter the skin incision and the offset pleural incision whereafter the instrument is rotated 180 degrees to align the curved tip with the pleural space. The curved tip facilitates sliding the chest drainage tube through the instrument to effect sufficient insertion length. Once the instrument is in place, the tube is slid along the instrument to ensure that all drainage holes in the chest drainage tube are within the pleural cavity. Thereafter, the instrument is withdrawn leaving the chest drainage tube in place. After withdrawal of the instrument, it is opened laterally for lateral disengagement with the chest drainage tube.

Devices and to methods for thoracic drainage for a patient having an air fistula. A vacuum is produced in the pleural cavity of the patient by means of a suction device. In order to adjust the vacuum on the basis of objective criteria, a suitable size measure for the air fistula is determined and the vacuum produced by the suction device is controlled according to said size measure. An adaptive algorithm includes: (a) determining a first value of a size measure for the air fistula; (b) changing the vacuum by a first difference value; (c) determining a second value of the size measure after a first waiting period; (d) changing the vacuum by a second difference value having the opposite sign if the second measure is greater than the first measure; (e) repeating steps (a) to (d) after a second waiting period.

A chest drainage system includes a collection device and a fluid pathway configured to extend from the collection device to a patient. A pressure source is configured to selectively provide sub-atmospheric pressure to the fluid pathway. The system is configured to introduce sub-atmospheric pressure from the pressure source at a substantially constant target pressure and at a dynamic pressure that varies from the target pressure. A method is also disclosed for draining a pleural cavity of a patient. The method involves applying dynamic pressure to the pleural cavity of a patient by changing sub-atmospheric pressure applied to the patient such that the patient's pleura moves without any or limited patient activity, thus facilitating removal of loculated fluid from the pleural cavity. The method may involve the use of the chest drain system.

The invention relates to a medical device that is in the form of a catheter (3) for supplying fluid to but in particular removing fluid from body cavities. The catheter head (1) on the proximal end (4) comprises an inlet (5) that is provided with one or more sealing and/or blocking elements (6, 7) and that is used to introduce a hollow or Verres needle (18) into the catheter (3). In the region between the sealing or blocking element(s) and the region of the catheter shaft (2) that is introduced into the body, a branch connection (8) is arranged, said branch connection being connected to a suction pump arrangement (10) via a branch tube (9). Said branch tube (9) leads to a suction valve (11) that enables a fluid to flow in the direction of the suction device, but blocks the flow in the counter direction. The outlet of the suction valve (11) opens into a forked area (12), from which one branch (16) leads to a suction device connection, in particular an injection connection (13) that is embodied, preferably, as a Luer-lock, and the other branch thereof (17) leads to a secretion bag connection (14). A non-return valve (15) that blocks the return flow of the secretion bag is arranged between said branch (17) and the secretion bag connection (14).

The invention relates to a device for curing pneumothorax. The device ensures that a pneumothorax patient is not restricted in motion in a pleural cavity drainage period. The device is characterized by having the functions of initiative exhaust, passive exhaust, storage of liquid and pressure monitoring and alarming. The device structurally and mainly comprises a drainage connecting pipe, a pressure monitoring and alarming device, a one-way vent valve, an air driving handle, a motor, an exhaust ball bag, and a liquid storage bag. Gas of the pneumothorax patient is passively exhausted out of the body of the patient sequentially through the drainage connecting pipe, the one-way vent valve, the exhaust ball bag and the one-way vent valve. When the motor is driven by power to rotate, the air driving handle extrudes the exhaust ball bag so as to initiatively exhaust gas in the ball bag out of the body. Rotation speed of the motor can be controlled through the pressure monitoring and alarming device. The pressure monitoring and alarming device monitors air pressure value and adjusts the rotation speed of the motor. Pleural cavity liquid can be stored in the liquid storage bag, and is exhausted out through the liquid storage bag one-way vent valve.

Brachytherapy treatment of a patient's lung tissue following resection is effected using a balloon applicator which is inserted, normally through the same opening used for the surgery, through the chest wall and into the cavity. The lung and chest openings are closed around the applicator and generally sealed around the applicator. A suction port is provided, in a suction circuit of the applicator, to withdraw fluid from the pleural cavity, at intervals as needed, to assure that the lung can be inflated. Different embodiments of suction circuits are disclosed. A bronchial applicator and method are also disclosed.

A thorax drainage device for aspirating fluids from a pleural cavity of a patient using underpressure has a fluid collection container for collecting the aspirated fluids and a drainage tube for connecting the fluid collection container to the pleural cavity of the patient. The fluid collection container is connectable to a vacuum source, in order to generate an underpressure in the fluid collection container. The thorax drainage device has an adjustable mechanism for attenuating pressure differences during the respiration of the patient, this mechanism being adjustable independently of a suction capacity of the vacuum source. This device permits a gradual expansion of the lung without risk of injury and thus prepares the lung for the completion of the drainage.

The present invention is directed to a method and a device for accurately guiding a chest tube to an intended position within a pleural cavity of an animal or human being. There is also provided a kit-of-parts comprising a catheter and a catheter guiding device according to the present invention.

The invention discloses a left ventricle auxiliary blood pump, which comprises a cardiac apex sleevelet and a blood pump body fixedly connected with the cardiac apex sleevelet, wherein the cardiac apex sleevelet comprises a suture ring and a flexible skirt edge which is sleeved at the periphery of the suture ring; the suture ring comprises a suture ring inner hole and a convex edge which is convexly arranged in the radial direction; the blood pump body comprises an inlet pipe; the inlet pipe is convexly arranged on a rear cover of the blood pump body; a peripheral ring slot is formed between the convex edge and the flexible skirt edge; a sliding sheet which can only move in the radial direction relative to the blood pump body is arranged on the rear cover of the blood pump body and is stretched into the peripheral ring slot in a movable way; the convex edge is positioned between the sliding sheet and the bottom surface of a settling tank; and the cardiac apex sleevelet and the blood pump body are relatively axially fixed. In the invention, the sliding sheet is used for fixing the cardiac apex sleevelet and the blood pump, so that the cardiac apex sleevelet can be more conveniently and reliably connected with the blood pump; simultaneously, the axial dimension of the inlet pipe of the blood pump is reduced, so that the implantation of the left ventricle auxiliary blood pump in a pleural cavity is facilitated without damages to a diaphragm, and the success rate of a surgery is greatly improved.

The invention discloses a pleural cavity puncturing device having a function of sucking liquid at a uniform speed, for department of respiration. The pleural cavity puncturing device having a functionof sucking liquid at a uniform speed, for department of respiration comprises a base, a liquid sucking puncturing unit and a driving unit, wherein a protrusion platform is integrally arranged on oneside of the upper part of the base; the liquid sucking puncturing unit is mounted at the upper part of the protrusion platform; the driving unit is mounted at the upper part of the base; and the driving unit is in transmission connection with the liquid sucking puncturing unit. Through the adoption of the pleural cavity puncturing device having a function of sucking liquid at a uniform speed, fordepartment of respiration disclosed by the invention, hydrops in the pleural cavity of a patient can be sucked at the uniform speed, so that the situation that when some nurses or doctors which are insufficient in experience suck the hydrops, the speed is too high or too low, and the puncturing effect is influenced can be effectively avoided, the situation that the nurses or the doctors can suck the hydrops in the pleural cavity of the patient at a uniform speed can be guaranteed, and the working strength of the nurses or the doctors can also be effectively reduced; and a protection layer is arranged, so that the functions of anticorrosion, antisepsis, skid resistance and aging resistance of the base are effectively improved, more importantly, the situation that a large quantity of bacteria are bred on the surface of the base can be avoided, and the hygienic condition is good.