Many of the medical products today are controlled by software. The process of documenting, testing, verifying, and updating the software is becoming more mature. The methods that are used to assure proper operation of the software, and therefore the proper operation of the medical product are time consuming. As the software becomes more and more complex, the required testing and documentation grows dramatically. The off-the-shelf software and operating systems (such as the operating system available from Microsoft under the trademark Windows) have grown in complexity and flexibility. It is possible to interface with data bases, LAN systems, WAN systems, Internet, application programs, and literally tens of thousands of third party software packages. This flexibility is a great advantage to medical products but the complexity of the software, and the inability of the manufacturer to know what other software products might be added at a later date, make complete testing of the software virtually impossible.
For this reason, most medical products do not use standard operating systems such as the Windows operating system. They incorporate their own operating systems or put huge restrictions on the operating system they do use to limit the complexity and changeability, and therefore the flexibility of the system. These restrictions are imposed to assure the proper operation of the medical product. One example of this problem is seen with a prior art endoscope reprocessing system controlled by a standard computer, typically a PC (personal computer). This allows the flexibility to use standard data base programs to track the endoscopes and their reprocessing history. Modem computer and communications technology provide the ability to network systems together and interface directly with hospital computer systems. The capability exists to incorporate off-the-shelf bar code readers for tracking products (to reduce human error) and use endoscope identification features so the endoscope type is automatically transmitted to both the reprocessing machine and to one or more computers which store data about the endoscopes and their reprocessing. One problem with using a standard computer is the inability to completely test the software code to assure that no software bugs or errors exist in that code. Even if one were to spend the time it would take to test the code in every conceivable condition, the testing would need to be repeated as soon as new software (even an upgrade) was installed on the system.
With the proliferation of software viruses, this problem becomes even more critical. It would be possible to have perfect code when the system was installed only to have a virus get into the code and change it to a condition that would cause improper operation of the medical product.
One possible solution to this problem is to have a second computer monitoring the first computer to assure that everything it is doing is correct. This complicates the situation as it is then necessary to program and test a second system, and take steps to prevent the second system from also being exposed to a virus.
The present invention solves this problem by having a separate monitor system between the main operating computer and the actual hardware of the medical product, in this case the endoscope reprocessor. This monitor system can be as simple as a PLC (programmable logic controller) with some intelligence or as complicated as a second microprocessor operating on imbedded software (i.e. non-Windows operating system software or equivalent). The main function of the monitor system software is to monitor the critical steps or parameters of the medical reprocessor product (or other medical product, it being understood that the present invention is not limited to reprocessing endoscopes, but is suitable for and encompasses processing other medical products requiring satisfactory performance of a series of critical steps in the processing or reprocessing of the medical device). For instance (in the endoscope reprocessor example) the monitoring system would insure that the correct steps were performed to disinfect, clean and rinse the endoscope.
By “cleaning” is meant the removal of physical debris from the endoscope. By “disinfecting” is meant the inactivation of biologically active material from the endoscope to a predetermined degree. An example of disinfection is the killing, inhibition, or removal of microorganisms that cause disease. Disinfection may not necessarily eliminate spores or all of the microorganisms from an object or environment. By “sterilizing” is meant the inactivation of biologically active material to a predetermined degree greater than disinfecting. An example of sterilization is a process in which all living cells, spores and viruses are completely destroyed or removed from an object or environment. It is to be understood that while the present invention is described herein with respect to disinfecting and disinfection, the present invention may be used to perform a process that includes only cleaning, or cleaning and disinfecting or disinfecting without cleaning. Furthermore, the present invention may also be used with a process that performs or includes sterilizing, either alone or in combination with cleaning.
In the practice of the present invention, the monitor system has the ability to take control of the hardware performing the processing or reprocessing. In particular with respect to the endoscope reprocessing example, the monitor system will keep the lid (or other access) of the reprocessor closed and not allow it to open (or provide access) until the endoscope is properly reprocessed, or (in the event of an error, access will be denied until the computer acknowledges the error and alerts the operator). It is to be understood that “lid” refers to a means of controlling access to the medical device being processed or reprocessed according to the present invention. If the computer code gets lost or causes improper critical commands (or an improper sequence of commands) to be sent to the reprocessor hardware, the monitor system will provide a warning to the operator that the endoscope has not been properly reprocessed. The monitor system has the ability to communicate directly with the operator. One or more human perceptible indicators, such as visual indicator lights or audible indicator annunciators may be used in the practice of the present invention to indicate normal and or abnormal operating conditions or status of the reprocessing, or that the monitor system has detected a problem.
This arrangement allows the PC or other computer to use its flexibility to the maximum. It can be connected to networks, the web, and any extra software that is needed. The monitor will assure that the medical device works properly. With this arrangement, the monitor system code can go through extensive testing and validation in a reasonable time as it is self-contained and controlled by the manufacturer. The integrity of the medical device and its operation is able to be controlled by well-tested software and the flexibility and upgradability of the computer is not lost.
As mentioned above, while it is possible to use a redundant computer to monitor the operation of the first system, such redundant computer systems often become as complicated as the original system, require extensive testing and are therefore impractical for an application such as endoscope reprocessing.
In contrast, the present invention allows complete software validation of that software that controls the critical aspects of a system without requiring complete validation of a general operating system or applications programs that may be present and active.
The aspects of the invention which are believed to be different from and preferred over known products, machines, processes, or business methods are, in particular, the separation of the critical steps to assure the fact of execution of each critical step and the proper performance of each such step by monitoring with a system that has the ability to directly control the hardware in the event it observes an improper condition.
The present invention has applicability to medical products beyond endoscopes. It could be used for any software controlled system that controls critical steps or processes in relation to a medical device.
One example of a system for cleaning, disinfecting and/or drying endoscopes is shown in U.S. Pat. No. 6,641,781 B2, issued Nov. 4, 2003, and the entire contents thereof are hereby incorporated by reference.
Another example of a device and method for cleaning and/or disinfecting endoscopes is shown in U.S. Pat. No. 6,260,560 B1, issued Jul. 17, 2001, and the entire contents thereof are hereby incorporated by reference.
Still another example of a device and method for cleaning and/or disinfecting endoscopes is shown in European Patent Application EP 0 709 056 A1, published Jan. 5, 1996, and the entire contents thereof are hereby incorporated by reference.
Referring now most particularly to
Referring now also to
The connection block 38 is arranged fixedly in the rack. This connection block is provided with passages and ports 52 which are connected to the passages and can be connected to the passages of the endoscope 36 by means of flexible tubes 54. On its underside (not visible in
Referring now to
Referring now to
Block 88 is a monitor system that observes the commands from the computer 82 through the master control 84. Blocks 84 and 88 together make up a monitor and control system. Monitor system 88 preferably has an embedded computer software program that mimics and monitors each of the critical steps performed by the applications program in the computer 82 as it instructs and receives data from the MDS 86 through the master control 84. The monitor system 88 takes control of the MDS 86 in the event that an error condition occurs, either in the commands sent by the computer 82 or in the data received from the MDS, or in the event communication is lost with the computer 82. The monitor system 88 prevents the reprocessor 30 from allowing access to an improperly or incompletely processed endoscope 36 contained in basin 31 or 32. This is accomplished by providing a human perceptible signal to the operator of the reprocessor 30, preferably by a visual alarm, such as illuminating a red LED 90 to alert the operator to the less than successful reprocessing of the endoscope then undergoing disinfection and cleaning. The system 80 will continue operation to reach a condition allowing-opening a lid 92 (see
Referring now to
In the event an error condition occurs in any of the critical steps, the monitor system 88 will override any commands from the computer 82 and drive the system to an error state 116 corresponding to an ERROR condition 990, as indicated by paths 118, 120 and 122. It is to be understood that state 116 can be reached from any critical step state, whether shown in
Once an error condition occurs, the monitor system 88 will await acknowledgement of the error condition by the computer 82, indicated by the path 124. At this time, the monitor system prevents opening the lid or otherwise providing access to the medical device such as the endoscope undergoing reprocessing. Once acknowledgment is received, the system passes to an ERROR (Lid open) condition 991, indicated by state 126. At this time, the computer 82 proceeds to clear itself to an idle condition preferably after logging the error condition, and the system returns along path 128 to the STANDBY state 102.
In the event that communication is lost between master control 84 and the computer 82, the monitor system 88 will take control of the MDS 86 until communication with computer 82 is re-established.
Referring now to
Referring now also to
Inputs
Referring now to
Outputs
Still referring to
Although in some instances reference has been made to certain operating elements in one of FIGS. 8 or 9, it is to be understood that the same description applies to corresponding elements in the other of FIGS. 8 or 9.
Key for
Critical Steps
The following is an itemization of one example of a series of critical steps of the MDS 86 carried out by instructions from the computer 82 and monitored by the monitor system 88. Instructions from computer 82 are received as OUTPUTS by master control 84 and acted upon by commands sent to the MDS 86 with consequent action taken in device 30. Signals as INPUTS from the sensors are transmitted from the MDS 86 to the master control 84 and computer 82, with both OUTPUTS and INPUTS monitored by monitor system 88.
The following general checks are performed in steps 1 through 83:
The following general checks are performed in steps 1 though 991:
The following are checks performed in all steps except 0, 900 and 991:
Example critical steps performed by the MDS are as follows:
1. Start Leaktest (FL-SL)
The step time is between a minimum of zero and a selected predetermined maximum time. The endoscope is tested in this step to determine if there are any leaks in the channels of the endoscope. Lower pressure air is introduced to the interior of the endoscope, i.e., to the space between the casing and the channels. If a leak is found, the endoscope is not suitable for reprocessing and an indication thereof is given by the system 80 to the operator to remove the endoscope from the reprocessing queue.
11. Pre Rinse (FS-ST)
The step time is between a minimum of zero and a selected predetermined maximum time. The endoscope is rinsed with water in this step to flush debris from the endoscope.
12. Drain (FS-SD)
The step time is between a minimum of zero and a selected predetermined maximum time.
The basin is drained in this step.
21. Dosing Soap (FV-SD)
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
23. Fill Basin (FV-SV)
The step time is between a minimum of zero and a selected predetermined maximum time.
24. Rinse Channels (FV-SS)
The step time is between a minimum time equal to a selected predetermined time less the Step 23 time and a selected predetermined maximum time.
25. Check Channels (FV-SC)
The step time is between a minimum of zero and a selected predetermined maximum time.
26. Drain (FV-SR)
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
In steps 21 through 26, soap and water are supplied to the endoscope and basin, filling the endoscope channels and supplying the basin with the solution, after which the channels are rinsed and the endoscope and basin are drained.
31. Pre Rinse (FS-ST)
The step time is between a minimum of zero and a selected predetermined maximum time.
32. Drain (FS-SR)
The step time is between a minimum of zero and a selected predetermined maximum time.
Pre rinsing is repeated in step 31 and the basin emptied in step 32.
41. Dosing disinfectant (FD-SD) Until Pressure Switch is Satisfied
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a minimum time equal to a selected predetermined time less the Step 43 time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
In steps 41 through 46, the endoscope and basin are supplied with a solution of disinfectant and water which fills and recirculates through the channels of the endoscope and a flow through check or test is performed on the channels, after which the endoscope and basin is drained.
51. Pre Rinse (FS-ST)
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
A further pre rinse and drain with water is performed in steps 51 and 52.
61. Fill Channels (FS-SK)
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a minimum time equal to a selected predetermined time less the Step 62 time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
In steps 61 through 65 the channels of the endoscope and the basin are supplied with water and rinsed, checked and drained.
71. Fill Channels (FN-SK)
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a minimum time equal to a selected predetermined time less the Step 72 time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
In steps 71 through 75 the channels of the endoscope and the basin are again supplied with water and rinsed, checked and drained.
81. Drain (FA-SB)
The step time is between a minimum of zero and a selected predetermined maximum time.
The step time is between a selected predetermined minimum time and a selected predetermined maximum time.
The step time is between a minimum of zero and a selected predetermined maximum time.
In steps 81 through 83, the basin is kept in an open drain condition, and the endoscope is flushed with air.
900. Correct, (Lid open)
Once the reprocessing is successfully completed, the lid is opened and the green LED is switched from a continuous illumination to a flashing mode, indicating reprocessing is complete.
990. Error LIO Acknowledgement
The red LED is continuously illuminated to indicate an error condition.
991. Error, (Lid Open)
When an error condition exists, after acknowledgement by the computer (and operator, if desired) the lid is opened to allow removal of the incompletely reprocessed endoscope. The red LED is illuminated.
0 Standby
In the standby state, both the red and green LEDs are not illuminated, and the system is waiting to commence reprocessing.
LIO disconnected (refers to loss of communication with computer 82)
The heart beat refers to a form of hand-shake signal between the computer 82 and the master control 84 repeatedly made to confirm that two-way communication between the computer 82 and the master control 84 is present. The red LED is illuminated for this condition.
Although not described above, it is within the operation of the system 80 and device 30 to perform self-disinfecting, according to a set of critical steps similar to those for endoscope reprocessing, if desired, and such a self-disinfecting process may be monitored by the monitor system 88 and be within the scope of the present invention.
It may thus be seen that the present invention is a method and apparatus for monitoring critical steps of a process, more particularly, a medical device process, and even more particularly, an endoscope reprocessing process wherein the endoscope is cleaned and disinfected. Alternatively, the process of sterilization may replace disinfection. Furthermore, the present invention may be used with a process that includes only one, or two or three of these activities of cleaning and disinfecting and sterilizing. During the process, a monitor system checks both inputs and outputs with respect to a computer which may have a conventional operating system. The monitor system 88 has a custom embedded version of software to monitor the critical steps to be sure they are performed and performed correctly. The monitor system 88 allows for changes in the operating systems and applications programs in the computer 82 (and or in any networks connected to the computer 82) while not requiring a failure mode and criticality analysis to be performed on the operating system of computer 82 or applications programs of the computer 82. The embedded software in the monitor system 88 checks the operation of the overall system 80 normally under control of the computer 82 and overrides or takes control when an error occurs in a critical step of the operation. The critical steps are determined in advance of operation. In an alternative embodiment, the monitor system 88 and master control 84 may be combined together.
In one aspect, the present invention is an apparatus for monitoring critical steps in the reprocessing of endoscopes in a system of the type having a computer (which may be a personal computer or any other type of reprogrammable computer) controlling a reprocessing device through a master control, which may be a programmable logic controller. The apparatus for monitoring critical steps includes a monitor system having an embedded monitoring program which tracks the critical steps in the reprocessing. The embedded monitoring program may be a “mirror” or image of the program containing the reprocessing critical steps. In the practice of one embodiment of the present invention, the monitor system compares the actual reprocessing step to the corresponding step in the monitor image program, and verifies whether the step is correct or not. If it is correct, the reprocessing is allowed to continue. If an error in a critical step is observed, the monitor system will take control of the reprocessing and signal the personal computer that an error has occurred. A perceptible indication is also preferably given to the operator of the reprocessing device, to signal the operator that the endoscope has not been properly reprocessed. Access to the endoscope during normal reprocessing and during an error condition is controlled by a means for providing selectively operable access such as a lid on a basin containing the endoscope in question. Once successful reprocessing has occurred, or the error reported appropriately, the lid is allowed to be opened (or the alternative means for providing access are selectively operated or enabled) to allow access to the endoscope (or other medical device being processed).
The present invention is particularly applicable to reprocessing medical and other devices that are thermolabile, i.e., that would be subject to breakdown or degradation if heat were to be applied to raise the temperature sufficient to sterilize such devices.
In one aspect of the present invention a predetermined set of critical steps (e.g., steps corresponding to states 104, 106 and 112) must each be completed and completed in a specified predetermined order. In other words in this aspect, the monitor system 88 looks to see that each of the predetermined critical steps is performed, and performed satisfactorily (i.e., within specified parameter limits, if applicable) and performed in a desired sequence. The monitor will only allow the overall system to reach the last step indicating successful completion of the process related to the critical steps (e.g., successfully reprocessing an endoscope, indicated by step 900 in the endoscope reprocessing example process described above) after the system successfully completes all of the previous critical steps and in the correct order. However, it is to be further understood that “non-critical” steps may be performed (with or without specified parameters) or omitted (or possibly performed in a different order) while still remaining within the spirit and scope of the present invention, as long as the critical steps aspect of the present invention is practiced.
In the practice of the present invention as applied to endoscope reprocessing, it is to be understood that only one basin and control system and apparatus may be used, or that more than two basins and control systems may be used. Furthermore, additional or fewer or different critical steps may be used while practicing the present invention, either for endoscope reprocessing or for another “critical steps” process or apparatus.
This invention is not to be taken as limited to all of the details thereof as modifications and variations thereof may be made without departing from the spirit or scope of the invention.
This application claims the benefit of U.S. Provisional Application No. 60/550,129 filed Mar. 4, 2004, the entire contents of which are hereby expressly incorporated by reference.
Number | Date | Country | |
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60550129 | Mar 2004 | US |