Patent Application
20200397956
The present invention relates to wound and surgical drainage.
All publications and patent applications mentioned in this specification are herein incorporated by reference to the same extent as if each such individual publication or patent application were specifically and individually indicated to be so incorporated by reference.
Chest tubes are required any time air and/or liquid accumulates in the chest cavity, disrupting normal pulmonary or cardiac function. Suction is commonly applied continuously to remove excess air and/or fluid from the chest until the internal wounds have healed, at which point the chest tubes can be removed. One of the most common uses of chest tubes is to drain the area around the heart after cardiac surgery.
Despite their benefits, current chest tube systems suffer from two major flaws. First, as liquid drains from the chest toward the suction container, it can pool in the drainage tubing and prevent the applied negative pressure from being transmitted to the chest. When this occurs, the pressure in the chest can be reduced to zero or even become positive, preventing proper drainage. Second, clogs can form in the chest tube which can obstruct the chest tube, which prevents the negative pressure from being transmitted to the chest and inhibits drainage. In fact, 36% of cardiac surgery patients experience chest tube clogging. When proper drainage is inhibited due to these factors, patients are at increased risk for accumulation of fluid around the heart, known as pericardial tamponade, which results in shock and can be fatal. Additionally, the lungs may be compressed, which can lead to respiratory compromise and can be fatal as well.
Pooling of liquid in the drainage line can theoretically be remedied by keeping the tubing straight from the patient to the collection container. However, this is nearly impossible in practice, as some slack is required to prevent accidental dislodging of the tube from the body. To combat clogging, clinicians use two methods known as milking and stripping. Milking refers to line manipulations such as lifting, squeezing, or kneading. Stripping refers to a pulling along the length of the tube with the thumb and forefinger to increase the amount of suction at the end of the tube. However, these methods have not been shown to be effective at improving chest tube suction or drainage. In fact, stripping has actually been discouraged because it is possible to create extremely high negative pressures (up to −370 cmH2O) that may damage the tissue.
In addition to these functional flaws, current systems also measure collected fluid volume and rate of chest air leak inaccurately and/or subjectively. As a result, clinicians make cautious clinical decisions based on these measurements, keeping patients in the hospital longer than necessary.
A chest drainage system is needed which reduces or eliminates pooling of blood/liquid and/or clogging/clotting in the drainage tube and/or chest tube, and provides objective and accurate measures of collected fluid volume and chest/thoracic air leak.
In one embodiment, a drainage system may generally comprise a chest tube having a chest tube drainage lumen and a drainage reservoir in fluid communication with the chest tube drainage lumen. A pump may be in fluid communication with the chest tube drainage lumen and a pressure sensor may be positioned proximal to the chest tube and in communication with the chest tube drainage lumen. Furthermore, a controller may be in communication with the pressure sensor and the pump, wherein the controller is configured to actuate the pump at a first suction level sufficient to drain a fluid from the chest tube drainage lumen, and wherein the controller is further configured to actuate the pump at a second suction level which is different from the first suction level such that an absence of attenuation in the second suction level over time is indicative of an obstruction in the chest tube.
In one embodiment for a method of draining, the method may generally comprise receiving a fluid through a chest tube having a chest tube drainage lumen, and applying a first suction level to the chest tube drainage lumen sufficient to drain the fluid from the chest tube. A pressure may be monitored within a drainage pathway from the chest tube drainage lumen via a pressure sensor in communication with a controller. Furthermore, a second suction level may be applied to the chest tube drainage lumen which is different from the first suction level such that an absence of attenuation in the second suction level over time is indicative of an obstruction in the chest tube.
Disclosed is a chest drainage system which reduces or eliminates pooling of blood/liquid and/or clogging/clotting in the drainage tube and/or chest tube, and provides objective and accurate measures of drained fluid volume and chest air leak.
The chest drainage system continuously monitors chest tube and drainage tube status and clears pooled liquid in the drainage tube, and/or a clogged chest tube when necessary to restore negative pressure to the chest, allowing it to drain. The system may include active and/or passive valve functions, as well as a controller (also referred to herein as a monitor) for monitoring the pressures in the system. The controller may control a pump for assisting in clearance of pooled liquid and/or clots in the drainage tube and/or chest tube. The controller may also control any active valves and/or suction device in response to measured pressure signals. The controller may also measure and communicate collected fluid volume and air leak information. The chest drainage system performs at least six primary functions:
Functions:
1. Drainage Tube Blockage Detection
The chest drainage system detects pooled liquid in the drainage tube by monitoring the pressure at or near the chest tube-drainage tube interface (the tube-tube interface or junction area). Pooled liquid in the drainage tube is indicated by a decrease in vacuum (increasing pressure) at the tube-tube interface. The chest drainage system may measure pressure with a sensor incorporated into the controller. The sensor may be in fluid communication with the tube-tube interface area via a fluid filled lumen (the relief lumen). The relief lumen may be open to atmosphere on the other end, and be filled with air. A valve (drainage tube valve, drainage tube relief valve or drainage tube relief lumen valve) may be used to open the relief lumen, exposing the tube-tube interface to atmospheric pressure. The drainage tube relief valve may also close the relief lumen, and may include a vent which prevents the transmission of bacteria and viruses from the atmosphere into the relief lumen. The drainage tube relief valve may be opened and closed by the controller based on the measured pressure at the tube-tube interface area.
Alternatively, the pressure sensor may be placed at the tube-tube interface area, connected directly to atmosphere. In this embodiment, the pressure sensor is in communication with the controller. Alternatively, the drainage tube relief valve may be passive, either with or without a relief lumen. Alternatively, the drainage tube relief valve may be operated manually.
Alternatively or additionally, a pressure sensor may be placed in the chest fluid collection chamber/reservoir/cassette/receptacle/canister. At a time when the vacuum pump is running, whether to perform a chest tube clearance, a drainage line clearance, or simply to regulate the suction, pressure in the canister may become more negative if a clog in the drainage line is present. A preset pressure (vacuum) threshold may be set by the user or the controller, the exceeding of which, indicates a blocked drainage lumen.
Alternatively, pressure sensors may be present both in the canister and at or around the tube-tube interface. The controller may continuously monitor the pressure differential between these two pressure sensors and detect a blocked drainage tube if the difference exceeds a pre-set threshold for the pressure difference.
2. Drainage Tube Blockage Clearance
When a blocked drainage line is detected (or at timed intervals), the chest drainage system clears the drainage tube by opening the drainage tube relief lumen valve which is in fluid communication with the tube-tube interface area. Opening the drainage tube relief lumen valve allows air to sweep away the liquid, and any blockage, in the drainage tube into the drainage container/reservoir. A pump which may be integrated with the controller, applies negative pressure to the drainage tube (via a collection reservoir/cassette/chamber). Optionally the pump may also apply positive pressure to the relief lumen (rather than its being open to atmospheric pressure) to help clear the blockage. Proper negative pressure at the chest is then restored. Optionally, the system may apply negative pressure (or an increased negative pressure) to the drainage tube without opening the relief lumen valve, or in addition to opening the relief lumen valve to restore proper suction. This measure may be performed when the controller senses a blockage in the drainage tube, or may be performed at set intervals. Pressure measured at the tube-tube interface may drive the controller to initiate a drainage tube clearance cycle The pressure measured at the tube-tube interface may also or alternatively drive the pump so that a desired suction level is maintained at the tube-tube interface during a clearance cycle.
3. Chest Tube Blockage Detection
Clots or clogs may form in the chest tube. To detect a blocked chest tube, the controller pulls suction intermittently to a level that exceeds the crack pressure of the chest tube relief valve. Once it hits this first pre-set threshold the pump turns off or reduces the suction (to a more positive pressure level). At this point, if there is no blockage, or if the blockage is able to be cleared via the transfer of the increased suction, the valve will open and the measured vacuum will attenuate down to a second pre-set threshold (more positive than the first threshold). If the controller does not sense this attenuation over a specified time interval, the controller determines that the chest tube is blocked and may issue an alarm, or attempt alternative measures of clearing the chest tube, such as increasing the suction applied to the chest tube to a third threshold. Pressure may be measured at the tube-tube junction or in the canister or elsewhere in the system.
4. Chest Tube Blockage Clearance
To clear blockages in the chest tube, the suction magnitude applied at the tube-tube interface may be increased by the controller. A passive chest tube relief valve, in fluid communication with a chest tube relief lumen, may be configured to open when the pressure in the tube-tube interface drops below a set level. The chest tube relief valve may be open to atmospheric pressure and include a filter or vent to prevent bacteria etc. from entering the system. Once the chest tube relief valve is open, the chest tube will be cleared. The chest tube relief valve may be configured to close at a pressure differential which is less than that of the opening pressure, to ensure the valve stays open long enough for the chest tube to be cleared and to minimize the flow resistance of the valve. Alternatively, the chest tube relief valve, may be an active valve, which the controller opens and closes based on pressures measured in the tube-tube interface area and/or in the chest tube relief lumen. An active chest tube relief valve may open and close at the same pressure differential or open and close at different pressure differentials.
Alternatively, the chest tube relief valve may be connected to the drainage line relief lumen and either controlled directly by the controller via a connection to the controller, or via pressure changes introduced through the drainage line relief lumen by the controller.
In some embodiments, one or more of the valves are passive and set to open at a set pressure and stay open until the same, or another, set pressure is reached. In some embodiments, one or more of the valves are active and directly controlled by the controller. In either case, one or more valves may be set to open at one pressure, and close at another pressure.
The intervals for clearing the chest tube may be different than the intervals for clearing the drainage line.
5. Chest Air Leak Detection
To detect air leaks from the patient's chest, the controller monitors the flow of air pumped from the canister to maintain the prescribed level of suction within the canister. This is done with a flow meter and/or measuring the revolutions of the pump necessary to evacuate the air.
6. Drainage Fluid Volume Measurement
The controller may measure the volume (or flow) of drained chest fluids that is collected within the canister. Collected fluid volume measurements are preferably made with a non-contact capacitive sensor, but may alternatively be made with optical sensors, pressure sensors, acoustic (such as ultrasonic) sensors, a camera, or any other liquid level sensing methods known in the art.
In some embodiments, the drainage tube relief lumen may be in fluid communication with the chest tube relief lumen.
Chest tube relief valve 112 may be incorporated into the chest tube, or a separate adapter designed to connect to the chest tube, for example, into chest tube connection barb 114. In this embodiment, the chest tube has at least two lumens, chest tube drainage lumen and chest tube relief lumen, as shown in
Controller 122 may include pump 124, pressure sensor 116, drainage tube relief lumen valve 118, filter/vent 120 (which may be on either side of valve 118 and pressure sensor 116), and fluid reservoir (or suction canister) 128, which is in fluid communication with drainage tube 108 via drainage tube drainage lumen connector 130 and drainage tube relief lumen connector 132. However, the drainage line relief lumen may connect to the controller directly, without connecting through the canister. The controller may also include display 134, which may receive input, for example via a touch screen, in addition to displaying information.
Controller 122 may include a suction device, such as pump 124 to create a negative pressure, or suction, force on the drainage tube (possibly via collection canister 128) which is in fluid communication with the chest tube and the chest tube relief valve. In this way, suction may be maintained on the chest cavity to promote chest fluid drainage and aid with patient breathing. The mechanism for creating the negative pressure may be a pump or any other suitable mechanism. The controller and the suction device may be incorporated or may be separate. Any communication between the controller and the suction device and/or any of the valves may be wired or wireless.
Controller 122 may also include pressure sensor 126 on the canister side of the pump, to measure and/or monitor the pressure within the canister. The controller may also include a flow sensor or flow meter on either side of the pump, and/or one-way valve on either side of the pump to measure air/gas pumped out of the canister. The air flow may also or alternatively be measured by measuring the pump revolutions.
Pressure sensor 116 senses the pressure in tube-tube interface area 105 (via drainage tube relief lumen 106). When the drainage tube is blocked or restricted, the pressure in the tube-tube interface area increases. When this pressure increases to a set pressure (generally, a negative pressure), controller 122 opens drainage tube relief valve 118 (which is normally closed) to allow filtered atmospheric pressure air to enter drainage tube relief lumen 106. This influx of air, in combination with the negative pressure in the drainage tube caused by pump 124, acts to clear the drainage tube of blockages/restrictions. Once the pressure in the tube-tube interface area returns to normal, and/or after a set time, the controller closes drainage tube relief valve 118. Alternatively, the drainage tube valve may be a passive valve set to open and close at set pressures.
Alternatively, the controller may be configured to open the drainage tube relief valve periodically, regardless of the pressure measured in the tube-tube interface.
The monitor/controller may monitor pressure in the drainage tube relief lumen and may pull additional suction in the fluid reservoir/suction canister as needed to maintain the suction pressure in the proper range at the tube-tube interface area. For example, when the desired pressure is set to −20 cmH2O, the monitor may activate the suction pump to keep the pressure at the tube-tube interface area between −15 cmH2O and −25 cmH2O or between −18 cmH2O and −22 cmH2O. In another embodiment, the monitor may activate the pump and drainage tube relief valve 118 at regular temporal intervals as a preventative measure to clear any pooled liquid from the drainage line. This is done by the controller activating suction pump 124 while simultaneously opening drainage tube relief valve 118 to allow air to sweep accumulated liquid into the suction canister via the drainage tube.
The chest tube may become blocked or restricted. To clear restrictions, the suction magnitude applied by the controller to the drainage tube and experienced by the tube-tube interface may be increased. When the pressure in the tube-tube interface reaches a set low level (i.e. high level of suction), chest tube relief valve 112 opens and allows filtered atmospheric air to enter the relief lumen of the chest tube (see
The chest tube relief valve may have a different opening pressure and closing pressure. For example, the chest tube relief valve may open at a higher pressure differential (i.e. a more negative pressure in the tube-tube interface area), and close at a lower pressure differential. This allows the valve to stay closed until a clear chest tube blockage is present and to minimize the flow resistance of the valve. Once the valve is open, this allows the valve to stay open to completely clear the chest tube blockage, even if the tube-tube interface area pressure increases so that the pressure differential across the chest tube valve drops below the valve opening pressure. In other words, the pressure within the tube-tube interface area may be more negative when a chest tube blockage is created, but less negative, as the chest tube blockage is being cleared.
When a drainage line purge cycle is initiated, the pump will turn on or increase and the drainage line relief valve will open to allow atmospheric air to enter the drainage tube relief lumen after passing through a filter membrane (for example, a 0.2-micron filter membrane). This air is pulled to drainage barb 502 and swept down the drainage lumen of the drainage tubing, along with other fluids, to the drainage canister. The pressure within the system during this process is affected by the pump RPM and the smallest inner diameter of the drainage tube relief valve (for example, a solenoid valve) and other tubing or channels that make up the drainage relief lumen. The pump may operate at a specified rate to maintain suction within the system without ramping up to dangerous levels.
During this process, pressure is also monitored at canister 128 to reduce the frequency of solenoid valve activation due to its proximity to barb 502.
System Diagnosis Using Pressure Readings
Additionally, the two pressure sensor readings (at barb 502 and at canister 128) may be used and/or compared and analyzed by the controller and used to diagnose various situations occurring within the system:
1. If the canister sensor is reading the prescribed suction level and the barb pressure is reading a lower suction level (a less negative pressure) than the prescribed suction level, the system will initiate a drainage line clearance cycle.
2. If the controller pulls additional (up to 100 cmH2O) suction and the canister pressure sensor reading shows a more negative pressure while the barb pressure reading does not change, the system will alert for an obstruction in the drainage line.
3. If the controller initiates a drainage line clearance cycle by pulling additional (up to 100 cmH2O) suction and the barb suction level reading increases (pressure level decreases) past a set threshold, the controller may determine that the chest tube relief valve did not open to clear the chest tube and therefore the system will alert for a clog in the chest tube drainage line.
4. If the controller is being triggered to correct the system suction level frequently (more frequently than a set frequency threshold), a drainage line clearance or chest tube clearance cycle may be performed to clear any fluid buildup in the line and/or chest tube.
5. If the controller is being triggered to correct the system suction level frequently, it may be indicative of an active air leak, in which case the current air leak rate will be displayed on the controller display screen and/or an alert may sound.
Pressure sensor(s) may reside at various locations in the system. A pressure sensor may be incorporated within the chest tube valve device near chest tube, and/or near the controller, in the receptacle, or within or near the tube-tube interface area. Pressure sensors may also be located in other places in the system, for example, near the chest. Pressure sensed at one or more location may be used to determine whether there is a change in pressure anywhere in the system, which may be used to identify drainage tube blockages and/or chest tube blockages. If an impediment is detected, an audible alarm may sound, and/or the controller may automatically clear the drainage tube and/or chest tube.
Chest Tube Detail
During successful chest drainage, chest tube relief valve 202 is in the closed position. In this position, fluid draining from the chest generally does not enter chest tube relief lumen 206 because of the fluid column in the chest tube relief lumen. A smaller diameter chest tube relief lumen may help prevent fluid from entering the chest tube relief lumen. The pressure in chest tube relief lumen 206 is slightly negative during chest tube drainage due to the negative pressure exerted by the pump on the drainage line, the chest tube drainage lumen, and to some extent, the chest tube relief lumen. The chest tube may become blocked or restricted, because of blood clots etc.
When a chest tube clog clearance cycle is initiated, the pump generates additional suction above the set level (to a more negative pressure) to open the chest tube relief valve. As this negative pressure drops to a set valve opening pressure, chest tube relief valve 202 opens, allowing atmospheric (i.e., more positive pressure) air to enter the chest tube relief lumen of the chest tube by passing through filter membrane 604. The air is pulled to the distal tip of the chest tube, through opening 612, and into the chest tube drainage lumen, where the air and other fluids are swept through the chest tube drainage lumen towards the drainage canister. This clearing is shown in
The chest tube relief valve is normally closed, as shown in
Once the pressure in the chest tube relief lumen increases back to a set valve closing pressure, chest tube relief valve 202 closes and normal drainage continues. The chest tube relief valve opening pressure may be different than the chest tube relief valve closing pressure. For example, the chest tube relief valve opening pressure may be at a higher pressure than the chest tube relief valve closing pressure.
For example, the chest tube relief valve may open when the pressure differential across the valve is about −10 cmH2O, about −20 cmH2O, about −30 cmH2O, about −40 cmH2O, about −50 cmH2O or as even high as about −100 cmH2O. Or for example, the chest tube relief valve may open when the pressure differential across the valve is within a range of about −10 cmH2O to about −20 cmH2O, or within a range of about −20 cmH2O to about −30 cmH2O, or within a range of about −30 cmH2O to about −30 cmH2O, or within a range of about −40 cmH2O to about −40 cmH2O, or within a range of about −50 cmH2O to about −100 cmH2O.
The chest tube relief valve may close at the same range, or at a lower differential than the opening pressure. For example, the chest tube relief valve may close at a pressure differential of about to 0 cmH2O, about −5 cmH2O, about −10 cmH2O, about −15 cmH2O, or about −20 cmH2O. Or for example, the chest tube relief valve may close at a pressure differential range of about to 0 cmH2O to about −5 cmH2O, or a range of about −5 cmH2O to about −10 cmH2O, or a range of about −10 cmH2O to about −15 cmH2O, or a range of about −15 cmH2O to about −20 cmH2O.
The chest tube relief valve may take a variety of known forms, including but not limited to a check valve, umbrella valve, ball valve, Belleville valve, X-fragm valve, cross-slit valve, or dome valve. The valve system preferably has a filter in place to prevent the entrance of bacteria or viruses from the atmosphere into the patient.
In another embodiment of the chest tube, chest tube relief valve is active, not passive, and is controlled directly by the controller. In some embodiments of the chest tube, chest tube relief valve is operated manually.
In some embodiments of the chest tube, chest tube relief valve is incorporated into the chest tube. In some embodiments, the chest tube relief valve is incorporated into a connecter which is connected to the chest tube. In some embodiments of the chest tube, both the chest tube relief lumen and the chest tube relief valve are incorporated into a connecter which may be connected to a chest tube.
In some embodiments, chest tube relief valve 202 takes the form of a magnetic check valve that has a substantial difference in the pressure differential required to open the valve, and the pressure differential required to keep the valve open (or close the valve), thereby amplifying the toggling effect of the valve. This is preferable to increase the effectiveness of the clog clearance cycle, because it allows for a greater pressure differential when the air is sweeping the chest tube drainage lumen via the chest tube relief lumen than if the valve opened and closed at the same pressure. The valve is normally closed in order to maximize drainage of liquid as it enters the chest tube and to reduce the need for continuous pumping.
Chest Tube Relief Valve
Frequency of clog clearance function activation at the controller may be 5 minutes or may be longer such as every 10 or 15 minutes. Air leak measurements may be temporarily suspended during the clog clearance cycle. The clog clearance cycle (either chest tube clearing or drainage tube clearing) frequency may be set by the user via the display/input interface.
Another embodiment of the chest tube relief valve may allow for selectable crack pressures. The activation mechanism may take the form of a button, switch, dial, or similar implement that mechanically alters the crack pressure by adjusting the stand-off distance of the magnetic seal allowing either higher or lower transmitted suction levels to open the valve. The adjustment can be a permanent alteration to the activation level of the relief valve or as a temporary override. A similar outcome may be achieved by altering the electromagnetic field in the proximity of the valve.
In yet another embodiment of the chest tube relief valve the clinician may temporarily open the chest tube relief valve allowing for the inflow of air to the chest tube relief lumen. This can either open the internal valve of the chest tube relief valve or bypass the chest tube relief valve by opening a separate bypass port in communication with the chest tube relief lumen. The activation mechanism may take the form of a button, switch, dial, or similar. The function can be used to assist in the activation of, or be used in place of, a chest tube clog clearance cycle. For example, the temporary or bypass function may be used to initiate clog clearance on a more frequent interval than that of the controller, to ensure clear chest tubes and drainage lines prior to measurement of fluid output, in place of the automated clog clearance feature, or for use with a different type of suction system. The bypass or adjustment can be a permanent alteration to the activation level of the relief valve or as a temporary override.
The controller can identify impediments to fluid drainage via a measured absolute pressure, change in pressure, pressure differential between or among 2 or more locations, or at one location. When an impediment to fluid drainage is identified, an alarm may sound and/or the controller may initiate clearing procedures, including opening and/or closing valve(s) in the chest drainage system, as described elsewhere herein. The negative pressure in the drainage tube may be increased, or changed in other ways, such as pulsed, reversed etc.
For example, if pressure measured at the tube-tube interface area is reading around −10 cmH20 to around −20 cmH20 and the reading changes to zero to −5 cmH20, the controller may open the drainage tube valve to filtered atmospheric air. The controller may leave the valve in this open position for a set period of time, for example, 5-10 seconds or 10-30 seconds and then may return the valve to its regular closed position. Alternatively, the controller may close the valve when a set pressure is measured at the tube-tube interface area or elsewhere. The controller may then check the pressure readings and if they have returned to normal, do nothing more. If they have not returned to normal, indicating a blockage or slowing condition is still present, the controller may repeat the clearing procedure. This may be done repeatedly until the tubing is cleared. Alternatively or additionally, the procedure may change if repeat clearings are necessary. For example, the magnitude of negative pressure used by the suction device to clear the tubing may be increased, and/or the negative pressure may be pulsed. The clearing procedure may be performed in response to the pressure readings and/or it may be done automatically on a periodic basis.
Section A of
Section D shows the magnitude of the negative pressure decreasing as a result of a reduction in suction being pulled by the controller/monitor. When the pressure in the system reaches the valve's set closing pressure, the valve closes (or is closed) and fluid drainage continues in a normal manner. The valve closing pressure may be at a lower magnitude negative pressure than that of the opening pressure, as shown here. The valve closing pressure may be at or near normal drainage negative pressure.
However, if there is a significant clog in the chest tube, the chest tube relief valve may not open, even with the increased suction. This case is represented by the solid line. The controller of the chest drainage system may increase and reduce the suction multiple times during the clog detection process. Section D shows the pump increasing the suction if suction attenuation has been sensed (i.e., an increase in pressure, or a reduction in suction in the canister or at the tube-tube interface)
If no chest tube clog is present, or if the increased suction level has cleared the chest tube, the suction will attenuate back down to the valve closing pressure after the suction is reduced. This is shown in section E. Alternatively, if a chest tube clog remains, the measured suction (negative pressure) will remain relatively un-attenuated, as shown by the solid line, and the controller may trigger an alarm or alert to notify the user that a chest tube clog is still present.
In some embodiments of the chest drainage system, the chest tube and/or drainage tubing clog detection techniques described herein may be used to confirm the patency of the chest tube prior to removing the tube from the patient. This may be particularly valuable, for example, when the air leak value has diminished to zero or near zero for a prolonged period of time, at which point the system may either automatically or manually activate a drainage tubing and/or chest tube clog clearance cycle in order to confirm patency of the chest tube. In doing so, the system provides confirmation that the cessation of air leak is due to actual physiological healing and not because the tube itself has become obstructed.
In some embodiments, the chest drainage system may include a pH sensor. Post-surgery infection and empyema are of particular concern to clinicians. The pH of fluid drained from the body can be useful in diagnosing these, and other, conditions. To aid in the diagnosis, the chest drainage system may include a pH monitor in the controller, with a sensor in the reservoir, in the tubing, the pump, the valve device, or anywhere in the system. The results may be displayed on the display device. The system may also include a sampling port to sample the fluid drained from the chest. The system may also include an infusion port to infuse an additive into the drainage fluid. These ports may be in the reservoir, tubing, controller, valve device, or elsewhere in the system, for example at the tube-tube interface.
In some embodiments, pH of the drained fluid is measured to monitor for infections. Additional parameters, such as conductance, spectroscopic signatures, protein content, and specific gravity of the drained fluid may also be measured to monitor patient recovery. Any of these measurements may be one time measurements or measurements made over time. For measurements made and collected over time, the controller may analyze these data for trends. These data may be integrated with the hospital's electronic medical record system (either communicated to, or data may be obtained from) and/or displayed on a screen on the device or on a connected monitor, which may be connected either by wire or wirelessly. In some embodiments, alarms or notifications may be activated by the controller when the parameters surpass certain thresholds, which may be preset or set by the user. These may be visual and/or audible alarms or notifications. These data may also provide input to the line-purging and clog-clearing functions of the device, such that, for example, line purging is activated when the suction at the chest drops below a certain level, or clog clearing is activated when tidal oscillations are diminished.
Air Leak
In some embodiments, the system is capable of measuring the flow rate of air evacuated from the canister/reservoir, in addition to pressure in the canister and pressure in the drainage tube relief lumen. Evacuation flow rate may be used to determine the presence and rate of an air leak from the chest cavity. The evacuation flow rate necessary to maintain the system at the prescribed suction level is equivalent to the flow rate of air entering the system (air leak), as the flows of air into and out of the system must be equal in the presence of steady pressure. Evacuation flow rate may be determined by the flow rate of the air being evacuated from the canister via the integrated suction pump and the volume of liquid in the canister. These parameters may be tracked over time by the controller to determine chest air leak presence and other parameters, such as air leak rate and changes to the air leak rate over time. Flow rate measurements can be made with any number of off-the-shelf sensitive air flow sensors that are known in the art. Flow rate may alternatively or additionally be measured by measuring the revolutions of the pump motor necessary to keep the suction at a prescribed level via a tachometer.
To determine the air leak rate within the system, the may utilize the pump tachometer to count the rotations that the pump is undertaking in creating the suction within the system. The rotation number, as well as pressure measurements and time measurements may be used to identify and quantify air leaks. The quantification of air leak rate to milliliters per minute may be achieved by the controller by using a transfer function to convert pump revolutions per minute (RPM), and canister pressure, to milliliters per “tick” of the pump rotation counter. This transfer function may depend on the suction level of the system and the speed of the pump. The number of “ticks” may then be multiplied by the milliliters per “tick” metric (based on the current RPM and pressure) and divided by the time over which the “ticks” occurred, resulting in an average air leak rate in milliliters per minute.
In some embodiments, the volume and/or flow rate of an air leak (from the patient's lung) is measured to monitor wound healing.
Drained Fluid Volume Measurement
Collected fluid (either gas, liquid, or both) volume and/or flow rate measurements may be made over time, and the data stored and/or displayed and/or shared with other systems. The volume measurements may be made with a non-contact capacitive sensor, but may alternatively be made with optical sensors, pressure sensors, acoustic (such as ultrasonic) sensors, or any other liquid level sensing methods known in the art.
To determine the drainage fluid volume collected in the drainage canister, the controller may utilize a built-in capacitive level sensor that senses changes in capacitance between two electrodes as the height of fluid in the drainage canister changes. The controller may utilize a transfer function to convert capacitance and directional tilt (measured by accelerometers, gyroscope, camera, etc.) of the controller/monitor into fluid volume in milliliters or other appropriate units.
In some embodiments, a capacitive sensor is mounted on the inside of the controller and may use out-of-phase techniques to reduce interference from within the proximity, such as a human hand near or in contact with the container. Such a technique uses a level electrode, reference electrode, environment electrode, ground electrode, and two shield electrodes. In some embodiments, the drainage volume is calculated by dividing the change in capacitance of the level electrode by the change in capacitance of the reference electrode and multiplying by the known volume that corresponds to the height of the reference electrode. In this embodiment, the height of reference electrode is a fraction of the height of the level electrode, for example but not limited to 1/10th, 1/20th or 1/50th of the height of the level electrode. In another embodiment, a compliant layer of material is present on either the controller or the suction canister in the area of the capacitive electrode in order to minimize or eliminate any air gaps between the controller and the suction canister.
Drainage fluid volume may be measured and tracked in the presence or absence of air leak determination.
In some embodiments, the controller is connected to a network, either wired or wireless, in order to transmit data for example to and/or from the patient's electronic medical record (EMR). The controller may also provide notifications of patient status on the controller/monitor itself and/or by transmitting notifications and/or safety alarms to the EMR or the clinician's phone, tablet, watch, etc.
In some embodiments, the chest drainage system includes the monitor/controller shown in
In some embodiments, the suction canister/reservoir is protected from liquid egress by means of a tortuous path created by the internal geometry of the suction canister/reservoir as shown in
In some embodiments, an accelerometer is used to monitor orientation of the monitor and the controller provides an alert when the monitor is in a position that may compromise the suction port. In this example embodiment, the drainage tubing is first connected to the drainage canister and the drainage canister is then connected to the monitor. Alternatively, the drainage tubing drainage lumen and/or drainage tube relief lumen may be connected to the monitor itself, and/or the two tubes (drainage tube drainage lumen and drainage tube relief lumen) may be connected separately. In the embodiment shown, the canister/reservoir is connected to the front of the monitor, but in other embodiments may be connected to the back or either side of the monitor, or be separate. In one embodiment, the suction canister/reservoir has a latching hinge that mates with a latch on the controller as shown in
In another embodiment of the device shown in
Multiple Chest Tubes
Embodiments of the chest drainage system may include the ability to support more than one chest tube. For example, the system may support up to 2 chest tubes. Alternatively, the system may support up to 3 chest tubes. Alternatively, the system may support up to 4 chest tubes. Alternatively, the system may support up to 5 chest tubes. Alternatively, the system may support up to 10 chest tubes. Some embodiments include the ability to configure the system to be used with one or more “off the shelf” chest tubes. “Off the shelf” (OTS) chest tubes may not include a chest tube relief lumen or a chest tube relief valve. For example, in a system which supports 3 chest tubes simultaneously, the controller may be configured to support any combination of OTS chest tubes and proprietary chest tubes (chest tubes with a chest tube relief lumen and a chest tube relief valve) (P). For example, a 3 chest tube system may be configured for:
P P P
P P OTS
P OTS OTS
OTS OTS OTS
The system may alternatively be configured to be used with fewer than the maximum number of chest tubes it supports.
The controller may pull additional suction sufficient for activating/opening multiple chest tube relief valves simultaneously, or in succession, for example as shown in
P OTS OTS
OTS OTS
P P OTS OTS
Note that in configurations where the chest drainage system is used with OTS chest tubes without a chest tube relief lumen/valve, the drainage lines connected to the OTS chest tubes may still be cleared using devices and methods disclosed herein. In other words, an OTS chest tube may be connected to a drainage line which has a drainage line relief lumen and drainage line relief valve.
In embodiments where the chest drainage system is used with a standard OTS chest tube without a chest tube relief lumen, the drainage tube relief lumen and drainage tube lumen may join together at a connection barb between the drainage tube and the chest tube. An example of this type of connection barb is shown in
User Interface
In some embodiments, a graphical user interface is displayed on the display of the controller. In some embodiments, the Graphical User Interface (GUI) may include the screens depicted in
Next, the system prompts the user to complete a self-check, which requires the user to confirm that the canister is firmly attached (
As part of the system initialization and drainage canister replacement processes, the controller may check for the presence and proper connection of a drainage canister before continuing to normal operation. The drainage canister may be equipped with a highly-reflective tab. The controller utilizes a built-in, infrared reflectivity sensor to detect the proper installation of the drainage canister using the reflective tab. The reflectivity of the reflective tab is acutely sensitive to the relative angle of the reflective tab to the sensor and can determine whether the drainage canister is fully seated or not. The controller may verify that the canister attached is an authentic drainage canister.
If the system check is successful, the controller then allows the user to begin using the system (
If the user presses the suction level on the main screen, he/she is taken to the suction setting screen, where it can be adjusted (
In addition, the controller may display a screen and/or sound an alarm when the canister is full if the capacitive sensor detects that the drainage canister has reached its maximum capacity. The controller will alert and prompt the attending physician to replace the canister. If the alert is ignored or an attempt to use a full canister is made, the controller may not allow normal operation until a new, or empty, drainage canister is attached.
In addition, the controller may display a screen and/or sound an alarm if the canister is disconnected from the controller. This may be determined using IR sensor(s) which determine when the drainage canister is no longer connected or not fully connected, to the controller. The controller will alert and/or prompt the attending physician to re-attach the canister. If the alert is ignored or not addressed properly, the controller may not allow normal operation until the drainage canister is properly attached.
In addition, the controller may display a screen and/or sound an alarm if the battery level is below a set threshold. The controller may prompt the user to plug the device into wall power to recharge the battery. If the alert is ignored and the battery level approaches dangerously low levels, the controller may place the system in a safe state before power is lost. The controller may display remaining battery life as a time or percentage. The battery icon may also implement color coding to indicate battery level.
In addition, the controller may display a screen and/or sound an alarm if the air leak rate is above a set threshold. The controller may alert and prompt the attending physician of the leak presence and prompt the physician to check the system for signs of leaks coming from tubing connections, chest tube drainage hole placement, etc. The controller may continue to alert until the air leak is resolved.
In addition, the controller may display a screen and/or sound an alarm if the drainage volume rate has exceeded the acceptable value as defined by the attending physician in the settings. The controller may alert and prompt the attending physician to verify the volume in the drainage canister using physical graduations or other means. The controller may continue to alert until the issue is resolved.
In addition, the controller may display a screen and/or sound an alarm if an obstruction is detected in the chest tube. If the controller attempts to run a clog clearance cycle and the pressure readings at the tube-tube interface exceed the maximum suction threshold, it will alert and prompt the attending physician to check the chest tube for any kinks or obstructions within the tube. The controller may continue to alert until the issue is resolved.
In addition, the controller may display a screen and/or sound an alarm if an obstruction is detected in the drainage line. If the controller attempts to draw suction and the suction level in the drainage canister increases (the pressure becomes more negative) but the suction level at the tube-tube interface doesn't change significantly, it will alert and prompt the attending physician to verify that the tubing clamp is disengaged and check for any kinks or obstructions within the drainage tubing. The controller may continue to alert until the issue is resolved.
In addition, the controller may display a screen and/or sound an alarm if the device is knocked over. If the controller detects a change in position of the system beyond the acceptable range, it will alert and prompt the attending physician to return the device to its upright position. The position detection may be done with accelerometers, a gyroscope, camera, etc. The controller may continue to alert and place the system in a safe state until the issue is resolved.
Also accessible on the main screen are the air leak and drainage volume trend buttons (graph icons next to respective text). When the user presses these buttons, they are taken to screens displaying historical data over the past 6, 12, or 24 hours, depending on the user selection (
The battery icon is shown with a lightning bolt in its center when it is plugged in, and becomes red when critically low. On screens other than the patient selection screen, the patient ID number may be displayed.
In another embodiment, the system may display an icon or alert when the patient has met predetermined criteria for air leak rate and/or drainage volume that indicate the chest tube is ready to be removed.
Software
In some embodiments of the system, the location of a clog can be determined to be either in the chest tube or the drainage tubing. When the system attempts to clear a clog in the chest tube, it temporarily increases the level of suction by running the pump. If, after the pump is turned off, this increased suction (which may be measured at the canister) does not attenuate substantially within a set time period, this indicates that the chest tube relief valve has not opened and air has not entered the system. This means that a clog has been detected. As a result of this condition, the controller may open the drainage tube relief valve connected to the relief lumen of the drainage tubing. If the suction (negative pressure) measured in the canister still has not attenuated substantially (become less negative), the controller may determine that the clog is likely in the drainage tubing. If adequate attenuation of the pressure measured in the canister does occur after opening the drainage tube relief valve, the controller may determine that the clog is likely in the chest tube.
In some embodiments, the controller can determine the clog location based on pressures sensed in both the drainage canister and at the tube-tube interface. In these embodiments, suction is increased in order to clear the chest tube. If the suction (negative pressure) measured in the drainage canister increases (becomes more negative) above a set threshold, including but not limited to −40, −60, −80, −100, −120, −140, or −160 cmH2O, while the pressure at the tube-tube junction remains at a lower (less negative) suction value, the controller may determine that the clog is in the drainage tubing. If the canister suction does not differ substantially relative to pressure at the tube-tube junction after increased suction is pulled, and attenuation of suction in the system does not occur after the pump has been turned off or decreased, the controller may determine that the clog is in the chest tube. The controller may also be able to determine what type (size, brand, configuration, etc.) or quantity of chest tube(s) is connected to the system based on the measured pressure(s) within the system.
In some embodiments of the system, the minimum suction necessary to keep up with the patient's air leak rate is used to minimize the differential pressure between the inside and outside of the patient's lung in order to expedite healing of the site of the air leak. In this mode, the user is not required to choose a specific suction level, as the system controller will automatically maintain the minimum level necessary to keep the patient's lung inflated.
In some embodiments, the system may have pre-set recommendations for drainage volume or air leak rates which indicate when it is appropriate for removing the patient's chest tube. The system may indicate when the air leak rate and/or drainage volume values are within acceptable levels, or may instruct the user to remove the patient's chest tube. In some embodiments, these recommendations may be based on the historical trends of data from a specific patient, or from aggregated patient data. These data are not limited to drainage volume and air leak rate data, other data collected, or associated with a patient or patient population, may be used.
Connectivity and Additional Functionality
Some embodiments of the system may transfer data either to or from the chest drainage system controller via hard wire connection or wirelessly. Wireless connections may include wi-fi, NFC, Bluetooth, cellular transmission, proprietary RF channel, or similar methods. Information transmission may be one-way or two-way. Communication may be with computers including servers, personal devices (phones, tablets, watches, etc.), other medical devices, cloud/remote based software, or electric systems.
Data may include, but are not limited to, any one or more of the following:
Data collected by the system: fluid drainage rate, system status, alarm notifications, air leak rate, system usage levels, system usage duration, battery level, average suction, applied changes, maintenance requirements, other programmed notifications, etc.
Data in other systems: patient health data, patient demographic data, aggregated patient data, etc.
Data may be transmitted actively or passively. Recipients of the data may have the option to view data or make system operating changes or both, either manually or defined by an algorithm. Data transmission may be collated for transmission into different sub-groups based on predefined user groups, access level, or allowable remote inquiry.
In some embodiments, the patient's drainage volume output as measured by the device is transmitted to an infusion pump and/or feeding pump, and the amount of fluids being administered are automatically adjusted accordingly. In this manner, the system may be part of a closed-loop fluid balance system, which may include, for example, systems for measuring fluids such as urine output, fecal output, wound drainage, perspiration, and moisture lost during respiration, and systems for administering fluids, such as infusion pumps and feeding pumps.
In some embodiments, the system is capable of communicating with other control modules, hospital monitoring systems, electronic health records, electronic medical systems, or other devices to either share and display information to physicians (e.g. air leak rate or drainage volume over the past hour), to receive information about the patient to be used for various actions (e.g. heart rate, body temperature, or O2 levels to gain insight on patient stability), or to send information about the patient to other devices for various actions (e.g. drainage volume output to inform autotransfusion machine of necessary input to compensate).
In some embodiments, the controller has the capability of wireless charging, for example but not limited to, exposed electrodes that engage with the charging electrodes of a charging station or dock; integrated wireless charging functionality in bedside or floor mount.
In some embodiments, the system makes use of mechanisms to prevent tampering or re-use of disposable components. In one such embodiment, the system may require authorization via PIN or swiping an RFID enabled badge, for example, in order to enable or disable device settings or functionality. In another embodiment, the system requires a specific set of screen touches in order to unlock the device and modify settings or functionality. The disposable components may become unusable after being removed from the controller, for example but not limited to a break-away latch connector that snaps off when the drainage canister is removed from the controller.
In some embodiments, the system has a “check for air leak” mode in which the system monitors various characteristics, including but not limited to, pump activation and pressure, to help identify the presence of an air leak as a final check before removing the chest tube from the patient. One embodiment of this functionality may include a 1-minute data collection period during which the patient coughs, sits up, or does some other action as cause for an air leak to show up; afterwards, the controller screen may indicate the results, for example but not limited to, a plot of chest pressure over time, pump activation over time, air leak in mL/min over time, or an info screen that displays the results in a text or graphic format.
Depending on the physician and/or patient, the desired length of drainage holes or channels may vary; therefore, it may be desirable for the chest tube to have a modular drainage area length to adapt to each clinical situation. In one embodiment of the chest tube, a sheath, such as silicone sheath 2002, is preinstalled, or may be installed by the user, along the length of chest tube 104. The sheath may be moved or removed as desired to expose additional drainage holes as shown in
In another embodiment, the chest tube may come with an excessive drainage area length to allow the physician to cut the drainage area to the desired length, by cutting the chest tube to length. This is shown in
In another embodiment of the chest tube, various drainage area lengths may be offered, for example, 4″, 5″, or 6″, less than 4″ or longer than 6″.
In another embodiment of the chest tube kit, an additional component, such as connecting, or holding, component 2202 is included with the system. Component 2202 holds more than one chest tube together such that the effective hole length is increased, as shown in
In yet another embodiment of the chest tube, a silicone, or other material, sheath is incorporated at the proximal end of the chest tube and can be pulled toward the distal end (the patient end), or in the opposite direction, to cover or uncover exposed holes, until the desired drainage area length is achieved as shown in
In another embodiment of the chest tube kit, a silicone, or other material, tape is included to cover drainage holes until the desired drainage area length is achieved.
In yet another embodiment of the chest tube, heat-shrink tubing 2402 may be placed over the undesired drainage areas, as shown in
In another embodiment of the chest tube kit, a mandrel and punch are included to allow physicians to punch additional holes as desired. Pad-printed markers may indicate where surgeon-generated hole creation is acceptable and where it should not be cut.
In yet another embodiment of the chest tube, the drainage holes are not completely punched, leaving thin film 2602 attaching hole slug 2604 to chest tube 2606. The physicians would then pull or punch out the desired number of slugs to create an appropriate drainage hole length or number as shown in
In another embodiment of the chest tube, drainage area length may be exposed using a silicone-based zipper.
In another embodiment of the chest tube, the dual-lumen extrusion has continuous drainage channel opening 2702 along one or more sides, with additional holes along the sides, as shown in
In another embodiment, the chest tube profile (dual-lumen with a channel on the side) is rotated during the extrusion process, so that the drainage area is present in all directions at some point along the extrusion, as shown in
In yet another embodiment of the chest tube, the extrusion consists of a channel drain with independent relief lumen 3002 running down the center, shown in
In another embodiment of the chest tube, a single channel is cut into the bottom of the extrusion; then twisted axially and heat set to generate a similar result as described above.
In some embodiments, the canister, or other components of the system, may include a hydrophobic, or other suitable, coating to repel body fluids. For example, if the drainage canister gets tipped over or knocked around, blood may coat the inside of the canister and leave a film, creating the potential for drainage volume measurement interference. In one embodiment of the device, a hydrophobic chemical coating may be applied to the inner surface of the drainage canister to repel bodily fluids. The coating may be on the entire canister, or on only certain areas. For example, for example, the coating may be placed on the inner wall nearest to the volume sensing mechanism.
In some embodiments, a thin film may be applied to the canister to repel bodily fluids. The film may comprise polypropylene, polycarbonate, PTFE, Teflon, or other materials. In another embodiment, modified surface finishes may be utilized to prevent blood and other particulate from sticking to the inner surface of the drainage canister. Any of the aforementioned methods for preventing adhesion of blood and other particulate may also be applied to other components of the system, for example, the chest tube, drainage tube, relief valve, and drainage barb.
In some embodiments, anti-foaming mechanisms and/or chemicals may be incorporated into the drainage system, and in particular, into the canister. For example, an anti-foaming additive may be added to the canister to reduce bubbling of drained fluid. In another embodiment, the drainage canister material itself may provide anti-foaming functionality. Hydrophobic and/or oleophobic materials and/or additives may be used for different applications throughout the system. For example, in another embodiment, a blood-repellant barrier may be utilized at the entrance to the drainage tube relief line of the drainage barb to prevent ingress of fluid. The anti-foaming mechanism may be in the form of an anti-foaming tablet, which is incorporated into the canister. The tablet may comprise simethicone, or other anti-foaming ingredient(s).
In another embodiment, a blood-repellant barrier may be incorporated within the drainage canister at the entrance to the suction inlet to act as a protection mechanism to the suction source, in the event of an overfilled canister. In yet another embodiment, blood-repellant barrier 3102 may be incorporated within the drainage canister at the drainage inlet to allow blood and other fluids to pass through into the canister while being repelled from passing through the opposite direction, out of the drainage inlet, as shown in
In another embodiment of the device, the system may allow for autotransfusion of blood to be re-introduced to the patient. For example, the drainage canister may feature a luer lock valve, stopcock, or other port that can be connected to an autotransfusion machine. This port may also be used to remove contents of the drainage canister during use, if so desired by the physician.
In some embodiments, the drainage canister may consist of a single chamber for collecting the drainage fluid. In some embodiments, one or more rib(s) or support(s) may be added to the drainage canister main body or front plate to provide additional rigidity and strength to the canister. In some embodiments, the drainage canister may comprise two or more separate chambers to collect draining fluid(s) as shown in
In some embodiments, the drainage canister may function as either a single chamber or dual chamber device as shown in
In yet another embodiment of the drainage canister, the suction port may automatically seal off when disconnected from the controller, for example, by using an umbrella valve, diaphragm valve, or duckbill valve to allow flow out of the canister but not in, making it possible for patient ambulation with the drainage canister alone. In this embodiment, the suction within the canister is maintained even when disconnected from the controller. The drainage tubing remains connected to the canister the entire time, making the use of this functionality simple and easy.
In another embodiment, the drainage tubing may be clamped via a mechanism incorporated into the drainage tubing, such as a valve, switch, or manifold. The clamping mechanism may be internal to, or external to, the drainage tubing. This clamping device may be activated manually by the attending physician or automatically by the controller. In another embodiment of the drainage canister, the drainage canister is offered in a variety of sizes with different volumetric capacities, for example 800 mL, 1600 mL, and 2000 mL.
In some embodiments of the drainage canister, the controller is able to detect specific information about the drainage canister in use, such as total volumetric capacity, relevant features (for example, anti-foaming, hydrophobic, etc.), and patient identification information (to prevent cross-contamination of bodily fluids when used in conjunction with autotransfusion). This information may be provided to the controller by, for example, RFID detection, color detection, or magnetic field detection.
In another embodiment of the drainage canister, data may be stored on the canister (stored to EPROM) in the event that a controller needs to be swapped out, to prevent data loss.
Alarms
In yet another embodiment, the device has alarms for various conditions that may affect the performance of the device and/or the safety of the patient, such as when the canister is full, the battery is low, or the chest tube is clogged. Some of these alarms and the user actions to be taken to resolve them are shown in
In some embodiments of the chest drainage system, the monitor provides pulsatile suction (whether via the valve device or via the pump in the monitor to maintain chest tube patency. This suction may be in the form of a sine wave, square wave, or any other suitable oscillatory waveform, and may oscillate between, for example but not limited to 0 to −40 cmH2O, 0 to −60 cmH2O, 0 to −80 cmH2O, 0 to −100 cmH2O, −10 to-40 cmH2O,-20 to-60 cmH2O, and so on. These embodiments may or may not include a chest tube relief lumen.
Some embodiments of the chest drainage system may include a fluid sample port to allow for easy access to draining fluids, for sampling, testing, etc. The port may include a luer-lock valve for the purposes of sampling. The sampling port may be anywhere in the system where drained or draining fluids may be accessed. For example, at the tube-tube junction, along the drainage tube, within the collection chamber, at connection point(s) along the system, etc. The system may provide intuitive, step-by-step sampling instructions via the controller display screen. These instructions may include how to properly clamp the drainage tubing, attach a syringe to the sampling port, and collect a fluid sample. The controller may be placed (or place itself) in standby mode during the sampling process, which may pause normal operation and hold the system in a safe state until the sample is collected.
Some embodiments of the chest drainage system may include an integrated drainage tubing clamp. This claim may slide along all or part of the length of the drainage tubing set and may be pre-installed.
Some embodiments of the chest drainage system may include a positive pressure relief valve. The drainage canister may include an overpressure valve designed to provide an outlet for positively pressurized air to escape the system, for example, when a patient coughs.
Some embodiments of the chest drainage system may include a canister plug for easy disposal of the drainage canister. For example, the drainage canister may have an integrated slot designed to hold a silicone rubber plug, which can be used to close off the drainage canister inlet port after use.
Some embodiments of the chest drainage system may include allow for the use of multiple drainage canisters per patient. Step-by-step instructions may be displayed on the monitor by the controller. These steps may include disconnecting the drainage tubing from the drainage canister, removing and disposing of the drainage canister, installing and attaching a new drainage canister, re-connecting the drainage tubing, etc. During this process, the controller may be placed, or place itself, in standby mode which pauses normal operation and holds the system in a safe state until the drainage canister is replaced.
Some embodiments of the chest drainage system may include physical graduations on the drainage canister, for example, graduation markings on the front face of the canister, ranging from 20-1200 ml in increments of 10 mL.
Some embodiments of the chest drainage system may include drainage canister overfill protection. In some embodiments, the drainage canister includes a filter membrane assembly which acts as a physical barrier to prevent fluid from entering the controller in the case of an overfilled drainage canister or if the system is tipped over. The “filter cage” may be a rigid structure that supports a filter membrane (for example but not limited to 0.2, 1.2, or 5 micron pore size) and is located inside the body of the drainage canister. In addition to the physical, filter membrane barrier in the drainage canister, the controller may utilize the built-in capacitive sensor to pre-emptively disable the pump from pulling fluid into the canister, and potentially into the pump of the controller/monitor, when the volume in the drainage canister reaches its capacity. This capacity may be sensed by the controller or preset by the user.
Some embodiments of the chest drainage system may automatically adjust the suction level based on a measured parameter, such as the air leak rate or drainage volume. In some embodiments, the controller may adjust the suction from, for example,-20 cmH2O when the patient has an air leak in excess of, for example, 500 mL/min, and then decrease the suction to a lower level, for example-8 cmH2O, when the air leak diminishes below, for example, 500 mL/min. A similar approach may be taken using drainage volume as the input parameter, whereby the suction level is higher as drainage volume output is higher and then decreases as the patient's drainage output diminishes. These techniques may depend on pre-defined thresholds at which the suction level is adjusted, or may be based on a continuous scale, whereby the suction level is adjusted continuously based on the air leak and/or drainage volume values.
Some embodiments of the chest drainage system may include a battery which allows the system to be portable. For example, the system may include a battery with a 4-hour battery life. Or, for example, the system may include a battery with a 1-hour battery life. Or, for example, the system may include a battery with a 2-hour battery life. Or, for example, the system may include a battery with a 3-hour battery life. Or, for example, the system may include a battery with a 5-hour battery life. Or, for example, the system may include a battery with a 24-hour battery life. Or, for example, the system may include a battery with a greater than 1-hour battery life.
In some embodiments, the system possesses a body contacting, or non-body contacting, sensor system or biological component with a physicochemical detector incorporated into the chest tube (
Example of Data Processing System
As shown in
Typically, the input/output devices 3610 are coupled to the system through input/output controllers 3609. The volatile RAM 3605 is typically implemented as dynamic RAM (DRAM) which requires power continuously in order to refresh or maintain the data in the memory. The non-volatile memory 3606 is typically a magnetic hard drive, a magnetic optical drive, an optical drive, or a DVD RAM or other type of memory system which maintains data even after power is removed from the system. Typically, the non-volatile memory will also be a random access memory, although this is not required.
While
Some portions of the preceding detailed descriptions have been presented in terms of algorithms and symbolic representations of operations on data bits within a computer memory. These algorithmic descriptions and representations are the ways used by those skilled in the data processing arts to most effectively convey the substance of their work to others skilled in the art. An algorithm is here, and generally, conceived to be a self-consistent sequence of operations leading to a desired result. The operations are those requiring physical manipulations of physical quantities.
It should be borne in mind, however, that all of these and similar terms are to be associated with the appropriate physical quantities and are merely convenient labels applied to these quantities. Unless specifically stated otherwise as apparent from the above discussion, it is appreciated that throughout the description, discussions utilizing terms such as those set forth in the claims below, refer to the action and processes of a computer system, or similar electronic computing device, that manipulates and transforms data represented as physical (electronic) quantities within the computer system's registers and memories into other data similarly represented as physical quantities within the computer system memories or registers or other such information storage, transmission or display devices.
The techniques shown in the figures can be implemented using code and data stored and executed on one or more electronic devices. Such electronic devices store and communicate (internally and/or with other electronic devices over a network) code and data using computer-readable media, such as non-transitory computer-readable storage media (e.g., magnetic disks; optical disks; random access memory; read only memory; flash memory devices; phase-change memory) and transitory computer-readable transmission media (e.g., electrical, optical, acoustical or other form of propagated signals—such as carrier waves, infrared signals, digital signals).
The processes or methods depicted in the preceding figures may be performed by processing logic that comprises hardware (e.g. circuitry, dedicated logic, etc.), firmware, software (e.g., embodied on a non-transitory computer readable medium), or a combination of both. Although the processes or methods are described above in terms of some sequential operations, it should be appreciated that some of the operations described may be performed in a different order. Moreover, some operations may be performed in parallel rather than sequentially.
This application is a continuation of International Application No. PCT/US2019/020809 filed Mar. 5, 2019, which claims the benefit of priority to U.S. Provisional Application No. 62/639,326 filed Mar. 6, 2018, U.S. Provisional Application No. 62/728,585 filed Sep. 7, 2018 and U.S. Provisional Application No. 62/798,379 filed Jan. 29, 2019, each of which is incorporated herein by reference in its entirety.
| Number | Date | Country | |
|---|---|---|---|
| 62639326 | Mar 2018 | US | |
| 62728585 | Sep 2018 | US | |
| 62798379 | Jan 2019 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | PCT/US2019/020809 | Mar 2019 | US |
| Child | 17007314 | US |
