CN116705231A - Configuration method of infusion pump and infusion equipment - Google Patents
Configuration method of infusion pump and infusion equipment Download PDFInfo
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- 238000001802 infusion Methods 0.000 title claims abstract description 382
- 238000000034 method Methods 0.000 title claims abstract description 92
- 239000003814 drug Substances 0.000 claims description 164
- 229940079593 drug Drugs 0.000 claims description 149
- 238000001514 detection method Methods 0.000 claims description 27
- 238000009434 installation Methods 0.000 claims description 22
- 238000012423 maintenance Methods 0.000 claims description 19
- 238000010200 validation analysis Methods 0.000 claims description 5
- 239000012530 fluid Substances 0.000 claims description 2
- 238000012544 monitoring process Methods 0.000 description 31
- 238000012790 confirmation Methods 0.000 description 20
- 238000011282 treatment Methods 0.000 description 12
- 238000010586 diagram Methods 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 238000012986 modification Methods 0.000 description 11
- 230000004048 modification Effects 0.000 description 11
- 230000000474 nursing effect Effects 0.000 description 10
- 239000004973 liquid crystal related substance Substances 0.000 description 9
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- 206010002091 Anaesthesia Diseases 0.000 description 3
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
- G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H40/00—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices
- G16H40/20—ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the management or administration of healthcare resources or facilities, e.g. managing hospital staff or surgery rooms
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H70/00—ICT specially adapted for the handling or processing of medical references
- G16H70/40—ICT specially adapted for the handling or processing of medical references relating to drugs, e.g. their side effects or intended usage
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Abstract
The application provides a configuration method of an infusion pump and infusion equipment, which relate to the technical field of medical appliances and comprise the following steps: determining one set mode from at least two set modes provided by the infusion pump as a target set mode; wherein, a setting mode corresponds to a configuration flow, and the configuration flow defines configuration parameters, configuration steps and execution sequence of the configuration steps; and controlling the infusion pump to sequentially execute corresponding configuration steps according to the determined target setting mode and the configuration flow corresponding to the target setting mode. The application reduces the complexity of the configuration operation of the infusion pump, improves the configuration efficiency of the infusion pump and reduces the risk of configuration errors.
Description
The present application claims priority from the chinese patent office filed at 2023, 5 and 12, with application number 202310541357X, entitled "method for configuring infusion pump", the entire contents of which are incorporated herein by reference.
Technical Field
The application relates to the technical field of medical equipment, in particular to a configuration method of an infusion pump and infusion equipment.
Background
The intelligent infusion pump is a digital and intelligent medical instrument, is mainly used for realizing high-precision injection and infusion timing and quantitative liquid medicine clinically, has the characteristics of wide market application range and multiple application departments, and can be used for not only ICUs of hospitals but also various clinical departments.
The intelligent infusion pump is frequently applied in various departments (such as ICU and anesthesia department), and for nurses in different departments, the various departments have different requirements and use habits, the operation is different, most infusion pumps in the market at present do not decompose the work flow in the main flow, so that the information configuration operation of the infusion pump is complex and complicated, the efficiency is low, and the configuration error is easy to occur.
Disclosure of Invention
The application provides a configuration method and infusion equipment of an infusion pump, which are used for solving the problems that the information configuration operation of the current infusion pump is complex and tedious, the efficiency is low, and the configuration error is easy to occur.
The application provides a configuration method of an infusion pump, which comprises the following steps:
determining one set mode from at least two set modes provided by the infusion pump as a target set mode; wherein, a setting mode corresponds to a configuration flow, and the configuration flow defines configuration parameters, configuration steps and execution sequence of the configuration steps;
And controlling the infusion pump to sequentially execute corresponding configuration steps according to the determined target setting mode and the configuration flow corresponding to the target setting mode.
In the above scheme, the configuration step includes a necessary step, or the configuration flow includes a necessary step and an unnecessary step;
the necessary steps include configuration of infusion parameters, starting, infusion detection and ending infusion;
optional steps include one or more of drug library selection, device maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview validation, consumable installation prompting, consumable selection, and return to standby.
In the above scheme, the target setting mode is determined according to one or more of departments, usage scenes, setting configurations and user types.
In the above scheme, the configuration steps corresponding to different configuration flows and/or the execution sequence of the configuration steps are different.
In the above scheme, the infusion parameter configuration includes: one or more of infusion parameter input, infusion parameter update, and infusion parameter confirmation.
In the above solution, the device maintenance configuration includes: equipment maintenance prompts and/or equipment maintenance selections.
In the above-described aspect, the patient information configuration includes: patient information selection, patient information update, and patient information input.
In the above scheme, the configuration of infusion parameters in the necessary steps includes: one or more of a speed mode parameter setting, a dose control mode parameter setting, a plasma target infusion mode parameter setting and a custom parameter setting;
the starting in the necessary steps comprises: starting transfusion;
the infusion detection in the necessary steps includes: and (5) monitoring transfusion.
In the above scheme, the parameter setting of the speed mode includes: one or more of infusion rate, preset amount, remaining time;
the parameter settings of the dose control mode include: one or more of dose rate, infusion volume;
parameter settings for plasma target infusion mode include: plasma drug concentration and infusion rate based on plasma drug concentration.
In the above scheme, the configuration flow includes: minimal flow and/or simplified flow,
The steps of the simplest flow include infusion parameter configuration, start, infusion detection and end of infusion, which may be performed sequentially. Of course, the specific order can also be set according to actual needs.
The steps of the simplified flow include infusion mode selection, infusion parameter configuration, starting, consumable installation prompt, infusion detection and ending infusion, which can be sequentially performed. Of course, the specific order can also be set according to actual needs.
In the above scheme, the configuration flow includes: based on the main flow of the drug library; the steps of the main flow based on the drug library comprise: patient information configuration, drug library selection, infusion parameter configuration, starting, infusion detection and ending infusion; wherein the patient information configuration includes: newly building a patient, selecting the patient again and scanning codes to acquire one or more of patient information; the newly built patient includes: selecting new patients and filling in relevant information of the patients; the patient was again selected including: selecting the last patient, scanning the code to acquire the patient comprises: the order is closed loop and scanned, patient information and drug information are checked, and an order list is checked.
In the above scheme, the main flow based on the drug library comprises: a first drug library-based main flow, a second drug library-based main flow, and a third drug library-based main flow;
the steps of the first drug library-based main flow include: patient information configuration, drug library selection, infusion mode selection, infusion parameter configuration, infusion parameter preview confirmation, starting, consumable installation prompt, infusion detection, infusion ending and standby state returning; wherein the patient information configuration in the first drug library-based main flow includes: newly-built patients;
The steps of the second drug library-based main flow include: drug library selection, patient information configuration, infusion parameter configuration, starting, consumable installation prompt, infusion detection, infusion ending and standby state returning; wherein the patient information configuration of the second drug library includes re-selecting the patient;
the third drug library-based main flow step comprises: drug library selection, patient information configuration, infusion mode selection, infusion parameter configuration, starting, consumable installation prompt, infusion detection, ending infusion and returning to a standby state; wherein the patient information configuration in the third drug library-based main flow includes a scan code to obtain the patient.
In the above-described arrangement, the first and second embodiments,
the patient information configuration in the optional steps is set to be enabled or disabled according to one or more of department, application scenario, and user type.
In the above-mentioned scheme, the drug library selection in the unnecessary step is to pre-establish at least one drug library;
before determining one of the at least two setting modes provided by the infusion pump as the target setting mode, the method further comprises:
issuing at least one drug library to an infusion pump and synchronizing parameters of the drug library to the infusion pump; wherein parameters of the drug library define the drugs and drug limitations of the drug library.
The application also provides infusion equipment, which comprises a liquid medicine driving device, a shell, a storage device and a processor which are arranged in the shell, and a display device and an information input device which are arranged on the shell;
the processor executes the configuration method.
The application provides a configuration method of an infusion pump and infusion equipment, wherein at least one setting mode is determined according to departments, use scenes, setting configuration and user types, and each setting mode is used for setting a flow; determining a target setting mode selected by a user, and sequentially feeding back setting parameters of a flow corresponding to the target setting mode according to the setting sequence of the target setting mode; the technical effects of creating different setting modes and flows thereof based on different departments, use scenes, setting configurations and user types are achieved, so that a user can configure response information according to the selected setting modes and steps fed back in sequence according to the setting modes to configure the infusion pump, complexity of configuration operation of the infusion pump is reduced, configuration efficiency of the infusion pump is improved, and risk of configuration errors is reduced.
Drawings
The accompanying drawings, which are incorporated in and constitute a part of this specification, illustrate embodiments consistent with the application and together with the description, serve to explain the principles of the application.
FIG. 1 is a flow chart of an embodiment of a method of configuring an infusion pump;
FIG. 2 is a page of a start-up in a simplified flow in an embodiment of a method of configuring an infusion pump;
FIG. 3 is a page of speed mode parameter settings in an infusion parameter configuration in a simplest flow in an embodiment of a method of configuring an infusion pump;
FIG. 4 is a diagram of infusion monitoring in a simplified flow chart in an embodiment of a method of configuring an infusion pump;
FIG. 5 is a diagram of a page ending infusion in a simplified flow in an embodiment of a method of configuring an infusion pump;
FIG. 6 is a page of startup in a main flow with profile in an embodiment of a configuration method of an infusion pump;
FIG. 7 is a diagram showing a page of device maintenance prompts in a startup screen in a main flow with profile in an embodiment of a configuration method of an infusion pump;
FIG. 8 is a page of a new patient selected in the main flow with profile in an embodiment of a method of configuring an infusion pump;
FIG. 9 is a page with profile for filling out patient-related information in a main flow in an embodiment of a method of configuring an infusion pump;
FIG. 10 is a page of profile for selecting care units in a main flow with profile in an embodiment of a method of configuring an infusion pump;
FIG. 11 is a diagram showing a configuration of an infusion pump according to an embodiment of a method for selecting an infusion mode in a main flow with profile;
FIG. 12 is a page of a configuration of infusion parameters in a main flow with profile in an embodiment of a method of configuring an infusion pump;
FIG. 13 is a page of a main flow preview with profile in an embodiment of a method of configuring an infusion pump;
FIG. 14 is a diagram showing a main flow with profile for monitoring consumable loading and consumable selection in an embodiment of a configuration method of an infusion pump;
FIG. 15 is a page of in-flow infusion monitoring with profile in an embodiment of a method of configuring an infusion pump;
FIG. 16 is a diagram showing a main flow with profile for ending infusion in an embodiment of a method of configuring an infusion pump;
FIG. 17 is a page of a start-up in a main flow with profile in an embodiment of a method of configuring an infusion pump;
FIG. 18 is a page of another in-process selection profile with profile in an embodiment of a method of configuring an infusion pump;
FIG. 19 is a page of a previous patient selected from another main flow with profile in an embodiment of a method of configuring an infusion pump;
Fig. 20 is a page of another main flow Cheng Zhongshang with profile infusion information in an embodiment of a method of configuring an infusion pump;
FIG. 21 is a page of another in-process infusion monitoring with profile in an embodiment of a method of configuring an infusion pump;
FIG. 22 is a diagram showing a main flow with profile for ending infusion in an embodiment of a method of configuring an infusion pump;
FIG. 23 is a diagram showing a further configuration of an infusion pump in a main flow on-line page with profile;
FIG. 24 is a page of a selected profile in a main flow with a profile in an embodiment of a method of configuring an infusion pump;
FIG. 25 is a diagram of a still further embodiment of a method of configuring an infusion pump with profile for closed loop scanning of orders in a main flow;
FIG. 26 is a page of a still further in-process view order list with profile in an embodiment of a method of configuring an infusion pump;
FIG. 27 is a page of speed mode parameter settings in a master flow infusion parameter configuration with profile in an embodiment of a method of configuring an infusion pump;
FIG. 28 is a page of still another in-process infusion monitoring with profile in an embodiment of a method of configuring an infusion pump;
FIG. 29 is a diagram showing a main flow with profile for ending an infusion in an embodiment of a method of configuring an infusion pump;
FIG. 30 is a page of profile in an embodiment of a method of configuring an infusion pump;
FIG. 31 is a page of infusion mode selection of profile in an embodiment of a method of configuring an infusion pump;
fig. 32 is a block diagram schematically illustrating the structure of an infusion device.
Specific embodiments of the present application have been shown by way of the above drawings and will be described in more detail below. The drawings and the written description are not intended to limit the scope of the inventive concepts in any way, but rather to illustrate the inventive concepts to those skilled in the art by reference to the specific embodiments.
Detailed Description
Reference will now be made in detail to exemplary embodiments, examples of which are illustrated in the accompanying drawings. When the following description refers to the accompanying drawings, the same numbers in different drawings refer to the same or similar elements, unless otherwise indicated. The implementations described in the following exemplary examples do not represent all implementations consistent with the application. Rather, they are merely examples of apparatus and methods consistent with aspects of the application as detailed in the accompanying claims.
The following examples are now provided:
referring to fig. 1, an embodiment of the present application provides a method for configuring an infusion pump, the method including:
s101: determining one set mode from at least two set modes provided by the infusion pump as a target set mode; wherein, a setting mode corresponds to a configuration flow, and the configuration flow defines configuration parameters, configuration steps and execution sequence of the configuration steps;
s102: and controlling the infusion pump to sequentially execute corresponding configuration steps according to the determined target setting mode and the configuration flow corresponding to the target setting mode.
Preferably, the configuring step includes a necessary step, or the configuring flow includes a necessary step and an unnecessary step;
the necessary steps include configuration of infusion parameters, starting, infusion detection and ending infusion;
optional steps include one or more of drug library selection, device maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview validation, consumable installation prompting, consumable selection, and return to standby.
Specifically, the infusion parameter configuration includes: one or more of infusion parameter input, infusion parameter update, and infusion parameter confirmation. Further, the contents of the infusion parameter input, the infusion parameter update, and the infusion parameter confirmation include: comprises one or more of concentration, fast forward preset quantity, fast forward dosage, fast forward speed, infusion flow rate, first dosage, background dosage flow rate, automatic control quantity, locking time, limit time and limit quantity.
Specifically, the device maintenance configuration includes: equipment maintenance prompts and/or equipment maintenance selections.
Specifically, the patient information configuration includes: patient information selection, patient information update, and patient information input.
Specifically, the configuration steps corresponding to different configuration flows and/or the execution sequence of the configuration steps are different.
Preferably, the target setting mode may be determined according to one or more of a department, a usage scenario, a setting configuration, and a user type.
Preferably, the configuration parameters corresponding to different configuration flows are different.
In this embodiment, the infusion parameters are configured to configure and confirm the infusion parameters in the infusion pump;
starting an infusion pump to trigger the infusion pump to perform infusion according to the infusion parameters;
the infusion detection is used for monitoring the variation condition of infusion parameters in the infusion parameter configuration in the execution process;
ending the infusion to indicate that the infusion pump has completed the infusion;
drug library selection is that a user or infusion pump selects a drug library of a care unit from at least one drug library previously established, acquired or stored;
the device maintenance configuration is used to reflect that the infusion pump needs maintenance and/or to reflect the manner in which the infusion pump may be maintained and to present options for the manner in which maintenance may be performed.
The patient information is configured to perform a selection operation, an update operation, and an input operation on the patient information.
Infusion-molded option for setting a treatment regimen for a patient, comprising: selecting a treatment scheme of a patient for setting, setting an intelligent shunt mode and the like;
the infusion parameter preview confirmation is used for displaying the infusion parameters, wherein the infusion parameter preview confirmation can use a non-editable display page for displaying the infusion parameters;
the consumable installation prompt is used for displaying whether the monitored consumable is loaded or not;
the consumable selection is used for displaying the consumable brand, and a user selects the required consumable brand and consumable usage amount;
the return to the standby state is used to instruct the infusion pump to enter the standby state.
For example, the intelligent infusion pump is frequently applied in various departments (such as ICU and anesthesia department), for nurses in different departments, different requirements and usage habits are provided for each department, the operation is different, most of infusion pumps in the market at present do not decompose the workflow in the main flow, the flow is simplified or the special flow setting can improve the convenience of user operation, the efficiency is improved, the user can easily use the pump, the operation flow is vital to them, the timely safe infusion and safe medication of the patient are ensured, different flows are set according to different users, departments, application scenes and the like, and thus the clinical operation flow is more met:
1) A plurality of interaction flows can be selected to adapt to different use scenes, and the operation steps are simplified to the greatest extent;
2) The simpler the flow or the more familiar the user is, the user error rate can be reduced;
3) The design flow is reasonably disassembled, and the strategy is proper;
4) The innovation of the task flow is relatively large-scale innovation, so that the user efficiency is directly and quickly improved;
therefore, at least two setting modes are configured in the infusion pump, each setting mode corresponds to different configuration processes, and each configuration process has different steps; configuration flows and/or steps are associated with one or more of departments, usage scenarios, setup configurations, user types, etc.; different configuration flows and/or steps correspond to different setting parameters, sequences, etc., and the steps in the configuration flows may include: drug library selection, equipment maintenance prompt/selection, patient information selection/input, infusion model selection, infusion parameter preview confirmation, consumable installation prompt, consumable selection, starting, infusion detection, ending infusion, and returning to a standby state, wherein the infusion parameter input/confirmation, starting, infusion detection, ending infusion are necessary steps; the selection of different configuration procedures and/or steps may be selected or preset by the user himself or may be determined according to one or more of the patient, the medical order, the department, the degree of informatization of the hospital, the drug library system, etc.
Specifically, the infusion main flow of the intelligent infusion pump at least comprises 2 sets of different configuration flows, and according to different usage scenarios, departments, user types, hospital informatization degrees and drug library system management degrees, one or more sets of different interaction schemes can be corresponding, so that the most simplified operation flow is supported, the flows of emergency treatment, ICU rescue, ICU common use, common departments and the like are met, information interconnection and intercommunication are supported, the intelligent infusion pump is connected with a hospital DERS system, different profiles are established for specific diseases or patient groups (such as pediatric or oncology patients), hospital areas and nursing areas (such as emergency critical sickrooms), profiles are supported to be issued to the pump, parameters are synchronously updated to the pump, the setting errors of infusion can be prevented, manual input parameters of users are reduced, the operation flow is simplified, medication errors are reduced, medication safety reminding and limitation are supported, the user efficiency is rapidly improved, the operation is reduced, the specificity is high, and the safety is higher.
In one embodiment, the configuration flow includes: the simplest flow and/or the simplified flow;
the steps of the simplest flow include configuration of infusion parameters, starting, infusion detection and ending infusion;
the simplified flow includes infusion mode selection, infusion parameter configuration, start-up, consumable installation prompting, infusion detection, and end of infusion.
Specifically, the starting includes, corresponding to the necessary steps: starting up and transfusion;
infusion detection includes: monitoring transfusion;
infusion parameter configuration includes: one or more of speed mode parameter setting, dose control mode parameter setting, plasma target infusion mode parameter setting, custom parameter setting, etc.;
the starting comprises the following steps: starting transfusion;
infusion detection includes: and (5) monitoring transfusion.
Wherein, for different infusion modes, infusion parameters to be set are different, specifically, the parameter setting of the speed mode includes: one or more of infusion rate, preset amount, remaining time, etc.; infusion mode refers to: for each drug, there are different infusion modes (including fast forward, dose control, speed, PCA, TCI mode, etc.), default values and adjustment values for the corresponding infusion parameters (including concentration, fast forward preset, fast forward dose, fast forward speed, infusion flow rate, first dose, background dose flow rate, self-controlled amount, lock-in time, limit amount, etc.) in each mode are included in the steps of the infusion parameter configuration, wherein the default values and adjustment values include: upper and lower limits of softness and hardness, etc.
The parameter settings of the dose control mode include: one or more of dose rate, infusion volume;
Parameter settings for plasma target infusion mode include: plasma drug concentration and/or infusion rate based on plasma drug concentration.
Further, the configuration flow includes: a simplest flow;
the steps in the simplest flow include: start-up, parameter setting, start-up, infusion monitoring and end infusion.
In particular, a parameter setting (doscontrol) of the dose control mode is used to control the infused drug dose according to the drug type; for example: certain drugs are toxic or susceptible to allergy in patients, and the dosage of the drug needs to be tightly controlled.
The parameter setting of the speed mode is used for controlling the speed of infusing the medicine according to the type of the medicine; for example: some drugs are too strong and if infusion rates are too fast, which can cause discomfort or even allergy to the patient, the infusion rate of the drug needs to be tightly controlled.
The parameter settings of the plasma target infusion mode (TCI mode) are used to select the desired (target) plasma drug concentration and to calculate the infusion rate required to achieve that concentration using a pharmacokinetic model.
The automatic control analgesic mode (PCA) is a novel analgesic technology and is widely applied to clinic at present. The automatic control pain relieving (PCIA) of intravenous patient means that when the patient feels pain, he presses the start key (bolus) in PCA pump to make intravenous injection of medicine with set dosage into body by means of micropump controlled by computer.
The parameter settings of the custom mode (other modes) are used to define one or more of the infusion rate, infusion dose, preset amount, infusion amount, etc. of each drug according to the actual needs of the user (e.g., patient condition, patient height weight, etc.).
Further, the parameter setting of the speed mode includes: one or more of infusion rate, preset amount, and remaining time, etc.;
the parameter settings of the dose control mode include: one or more of a dose rate and an infusion volume;
parameter settings for plasma target infusion mode include: plasma drug concentration and infusion rate based on plasma drug concentration.
For example, the configured infusion parameters may be different for different configuration procedures or infusion modes, e.g., for a simplest procedure, only the infusion rate, infusion volume, etc. need be configured in the parameter settings of the speed mode to increase the efficiency of execution of the simplest procedure. For simplifying the flow and based on the main flow of the drug library, one or more of the parameter settings of the dose control mode, the parameter settings of the speed mode, the parameter settings of the plasma target infusion mode and the parameter settings of the custom mode can be determined as required, so that the technical effect of setting different infusion parameters under different flows is realized.
Optionally, the infusion parameter configuration further comprises: parameter setting confirmation and modification;
the parameter setting confirmation and modification is also used for determining parameters in the infusion parameter configuration according to the received confirmation instruction;
the parameter setting confirmation and modification is also used to modify parameters in the infusion parameter configuration in accordance with the received modification instructions.
Illustratively, the steps in the simplest flow include: start-up, parameter setting, start-up, infusion monitoring and end infusion. For example: referring to fig. 2-5, the simplest flow is: start > parameter set > start > infusion monitor > end infusion.
The simplified flow includes infusion mode selection, infusion parameter configuration, start-up, consumable installation prompting, infusion detection, and end-of-infusion, wherein,
specifically, the patient information configuration is to configure basic information of the infusion subject, corresponding to an unnecessary step, and may include: selecting a new patient;
infusion mold selection includes: one or more of a dose control mode, a speed mode, a plasma target control infusion mode, a custom mode, an automatic pain relief mode and a treatment mode selection; consumable installation prompt includes: monitoring whether consumable materials are loaded;
for example: the steps of the simplified flow include: starting up, selecting a new patient, selecting a main menu, selecting a new infusion, selecting a treatment mode, setting parameters, starting infusion, monitoring whether consumable materials are loaded, monitoring infusion, ending infusion, and returning to the new patient. Wherein, returning to the new patient is referred to as returning to the step of "selecting a new patient".
It should be noted that, the profile mentioned in the present application is a drug library.
Preferably, one or more unnecessary steps of drug library selection, equipment maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview confirmation, consumable installation prompt, consumable selection can be configured to have an activation switch respectively;
if a start switch of an unnecessary step is turned on, the unnecessary step is inserted into the configuration flow;
if the start switch of an unnecessary step is turned off, the unnecessary step is removed from the configuration flow.
Illustratively, links of the flow can be freely configured, for example, patient information and maintenance period are independent modules, and are opened to different users according to departments.
Determining whether a starting switch of an unnecessary step in the configuration flow is on or off according to a department; when the infusion system is started, the page is added into a main flow, and a user is prompted to perfect patient information and perform safe infusion; when the system is closed, the page is not displayed in the main flow, so that the steps of the department are simplified, and the system is switched on or off according to the configuration of the system.
The drug library selection in the optional step is to pre-establish, acquire or store at least one drug library;
Before determining one of the at least two setting modes provided by the infusion pump as the target setting mode, the method further comprises:
issuing at least one drug depot to an infusion pump; wherein the drug library defines one or more of preset infusion parameters, medication limits, patient types, etc. for different drugs.
In one embodiment, the step of configuring the flow based on the master flow of the drug library may comprise: patient information configuration, drug library selection, infusion parameter configuration, starting, infusion detection and ending infusion; wherein the patient information configuration includes: newly building a patient, selecting the patient again and scanning codes to acquire one or more of patient information; the newly built patient includes: selecting new patients and/or filling in relevant information of the patients; the patient was again selected including: selecting the last patient; scanning the sign indicating number to acquire the patient includes: the order closed loop scan code, check patient information and medication information, and view one or more items in the order list.
In the example, in the main flow based on the drug library, different patient information configuration methods can be adopted, and corresponding controls are displayed on the display interface corresponding to different configuration modes; the scanning and obtaining can be to obtain patient information from a remote device such as a server by scanning images such as two-dimensional codes on a patient's bracelet through a scanning component of an infusion pump after clicking a corresponding control.
Further, the parameter setting of the speed mode includes: one or more of infusion rate, preset amount, remaining time;
the parameter settings of the dose control mode include: one or more of dose rate, infusion volume;
parameter settings for plasma target infusion mode include: plasma drug concentration and infusion rate based on plasma drug concentration.
For example, the configured infusion parameters may be different for different configuration procedures or infusion modes, e.g., for the simplest procedure, it may be sufficient to configure only infusion rate, infusion volume, but for the other procedure, a more paired configuration may be provided; in addition, the infusion parameters may also be related to infusion molds, infusion of medications, etc., corresponding to different infusion parameters, as well as settings.
Optionally, the infusion parameter configuration further comprises: parameter setting confirmation and modification;
the parameter setting confirmation and modification is also used for determining parameters in the infusion parameter configuration according to the received confirmation instruction;
the parameter setting confirmation and modification is also used to modify parameters in the infusion parameter configuration in accordance with the received modification instructions.
In another embodiment, in order to enable infusion of a new patient directly using a selected drug library, to reduce manual user input parameters, simplify the operation procedure, reduce medication errors, support medication safety reminders and restrictions, quickly improve user efficiency, reduce operational errors, improve safety, the steps of the configuration procedure including the first drug library-based main procedure include: patient information configuration, drug library selection, infusion mode selection, infusion parameter configuration, infusion parameter preview confirmation, start-up, consumable installation prompt, infusion detection, end of infusion, return to standby state.
Wherein the step of first drug library-based master flow patient information configuration comprises: is a newly built patient; the drug library selection can be based on different usage scenes, departments, user types, informatization degrees of hospitals and management degrees of drug library systems, and corresponds to a plurality of sets of interaction schemes, so that the operation flow is supported to be simplified, emergency treatment, ICU rescue and ICU common flow are met, information interconnection and intercommunication are supported, the drug library selection is connected with a hospital DERS system, different drug libraries are established for specific diseases or patient groups (such as pediatric or oncology patients), hospital areas and nursing areas (such as emergency critical illness wards), the drug libraries are supported to be issued to pumps, parameters are synchronously updated to the pumps, infusion setting errors can be prevented, manual input parameters of users are reduced, the operation flow is simplified, medication errors are reduced, medication safety reminding and limitation are supported, user efficiency is improved rapidly, operation errors are reduced, the specificity is high, and safety is higher.
The drug library-based master flow patient information configuration includes: selecting a new patient and filling in relevant information of the patient;
the drug library selection step includes: selecting a drug library of a care unit;
wherein, the drug library for selecting the nursing unit is a drug library for selecting the nursing unit from at least one drug library which is pre-established, acquired or stored; the care unit characterizes the administrative department and/or administrative scenario of the infusion pump for the patient undergoing the infusion, such as: the emergency department, ICU are responsible for departments, departments for specific diseases or patient groups (such as pediatric or oncology patients), hospital regional scenes and nursing ward (such as emergency critical sickrooms) scenes, therefore, selection of drug libraries is achieved based on different nursing units, and according to different usage scenes, departments, user types, informatization degrees of hospitals and management degrees of drug library systems, a plurality of sets of interaction schemes are correspondingly achieved, the simplest operation flow is supported, different drug libraries are established to support drug libraries to be issued to pumps, parameters are synchronously updated to the pumps, infusion setting errors can be prevented, manual input parameters of users are reduced, operation flow is simplified, medication errors are reduced, medication safety reminding and limitation are supported, user efficiency is rapidly improved, operation errors are reduced, the specificity is high, and the safety is higher.
The infusion parameter configuration mode is a selected infusion mode;
consumable installation prompt includes: monitoring whether consumable materials are loaded;
returning to the standby state includes: returning to the new patient;
the steps of the first drug library-based main flow include: starting up, selecting a new patient, filling in relevant information of the patient, selecting a medicine library of a nursing unit, selecting an infusion mode, configuring infusion parameters, previewing, starting infusion, monitoring whether consumable materials are loaded or not, monitoring infusion, ending infusion, and returning to the new patient.
For example: referring to fig. 6-16, the first drug library-based main process is set as a main process with profile: starting up > selecting new patient > filling in patient related information > selecting profile (drug library) of care unit > selecting infusion mode > infusion parameter configuration > previewing > infusion start > monitoring consumable loading > infusion monitoring > ending infusion > returning to new patient.
In another exemplary embodiment, to achieve the ability to infuse new patients directly using a selected drug library without re-filling patient information, to reduce manual user input parameters, simplify the operational flow, reduce medication errors, support medication safety reminders and restrictions, quickly improve user efficiency, reduce operational errors, improve safety, the configuration flow includes a second drug library-based main flow, the steps of the second drug library-based main flow include: drug library selection, patient information configuration, infusion parameter configuration, starting, consumable installation prompt, infusion detection, infusion ending and standby state returning.
Wherein the step of patient information configuration of the second drug library-based main flow includes re-selecting the patient;
the master drug library selection based on drug libraries includes: selecting a drug library of a care unit;
the patient information configuration includes: the last time the patient was;
consumable installation prompt includes: monitoring whether consumable materials are loaded;
returning to the standby state includes: returning to the new patient;
the steps of the second drug library-based main flow include: starting up, selecting a drug library of a nursing unit, confirming and modifying the last patient, starting transfusion, monitoring whether consumable materials are loaded, monitoring transfusion, ending transfusion and returning to a new patient.
For example: referring to fig. 17-22, the second drug library-based main flow is set as another main flow with profile: start > select profile of care unit > last patient > parameter set confirmation and modification > infusion start > monitor consumable loading > infusion monitor > end infusion > return to new patient.
In yet another exemplary embodiment, to achieve that patient information need not be refilled again, patient information need only be obtained by scanning a code, and infusion is directly performed on a new patient using a selected drug library according to the information, so as to reduce manual input parameters of a user, simplify an operation procedure, reduce medication errors, support medication safety reminding and limitation, quickly improve user efficiency, reduce operational errors, and improve safety, the configuration procedure includes a third drug library-based main procedure, and the third drug library-based main procedure includes: drug library selection, patient information configuration, infusion mode, infusion parameter configuration, starting, consumable installation prompt, infusion detection, ending infusion and returning to a standby state; wherein the step of patient information configuration in the third drug library-based main flow includes code scanning to acquire the patient.
A drug library-based main flow wherein drug library selection comprises: selecting a drug library of a care unit;
the patient information configuration includes: the method comprises the steps of performing closed loop code scanning on medical orders, checking patient information and drug information, and checking a medical order list;
infusion mold selection includes: one or more of a dose control mode, a speed mode, a plasma target control infusion mode, a custom mode, an automatic pain relief mode and a treatment mode selection; the method comprises the steps of carrying out a first treatment on the surface of the
Consumable installation prompt includes: monitoring whether consumable materials are loaded;
returning to the standby state includes: returning to the new patient;
the configuration flow includes a third drug library-based main flow, and the step of the third drug library-based main flow includes: starting up, selecting a medicine library of a nursing unit, closing a medicine order closed loop, scanning codes, checking patient information and medicine information, checking a medicine order list, selecting a treatment mode, setting parameters, starting transfusion, monitoring whether consumable materials are loaded, monitoring transfusion, ending transfusion, and returning to a new patient.
For example, referring to fig. 23-29, the third drug library-based main flow is set to be a further main flow with profile: starting up > selecting profile (drug library) of care unit > doctor's order closed loop scan code > checking patient information and drug information > checking doctor's order list > selecting treatment mode > parameter setting > infusion start > monitoring consumable loading > infusion monitoring > ending infusion > and returning to new patient.
Of course, in different configuration flows, the implementation manners of different steps can be exchanged and combined according to actual requirements.
In the application, links of the flow can be freely configured, for example, patient information is an independent module, the patient information is opened to different users according to different departments, when the patient information is opened, the page is added into the main flow to prompt the users to perfect the patient information and perform safe infusion, and if the patient information is closed, the page is not displayed in the main flow, so that the steps of the departments are simplified, and the patient information is started according to whether a system configuration switch is started or not.
Specifically, the infusion main flow of the intelligent infusion pump has at least 2 sets of different configuration flows/step flows, and according to the difference of usage scenes, departments, user types, hospital informatization degrees and drug library system management degrees, a plurality of sets of interaction schemes are corresponding, the operation flow is supported to be simplified, emergency treatment and ICU rescue are met, ICU common flows are supported, information interconnection and intercommunication are also supported, the intelligent infusion pump is connected with a hospital DERS system, different profiles are established for specific diseases or patient groups (such as pediatric or oncology patients), hospital areas and nursing areas (such as emergency critical illness wards), profile is supported to be issued to the pump, parameters are synchronously updated to the pump, infusion setting errors can be prevented, manual input parameters of users are reduced, operation flows are simplified, medication errors are reduced, medication safety reminding and limitation are supported, user efficiency is improved rapidly, operation errors are reduced, the specialty is strong, and the safety is higher.
1) Main flow with profile (drug library): starting up > selecting new patient > filling in patient related information > selecting profile (drug library) of care unit > selecting infusion mode > infusion parameter configuration > previewing > infusion start > monitoring consumable loading > infusion monitoring > ending infusion > returning to new patient.
2) Main flow with profile: start > select profile of care unit > last infusion information > parameter set confirmation and modification > infusion start > monitor consumable loading > infusion monitor > end infusion > return to new patient.
3) Main flow with profile: starting up > selecting profile (drug library) of care unit > doctor's order closed loop scan code > checking patient information and drug information > checking doctor's order list > selecting treatment mode > parameter setting > infusion start > monitoring consumable loading > infusion monitoring > ending infusion > and returning to new patient.
4) The simplest flow is as follows: start > parameter set > start > infusion monitor > end infusion.
5) The simplified flow: start > select new patient > main menu > select new infusion > select treatment mode > parameter set > infusion start > monitor consumable loading > infusion monitor > end infusion > return to new patient.
Preferably, the patient information configuration in the optional step is set to be enabled or disabled according to one or more of department, application scenario and user type. And starting or closing according to the department and the user type. Furthermore, links of the flow can be freely configured, for example, patient information and maintenance periods are independent modules, the pages are opened to different users according to different departments, when the pages are opened, the pages are added into the main flow to prompt the users to perfect the patient information and perform safe infusion, and if the pages are closed, the pages are not displayed in the main flow, so that the steps of the departments are simplified, and the pages are started or not according to the configuration switch of the system.
Preferably, the drug library selection in the optional step is to pre-establish at least one drug library;
before determining one of the at least two setting modes provided by the infusion pump as the target setting mode, the method further comprises:
issuing at least one drug library to an infusion pump and synchronizing parameters of the drug library to the infusion pump; wherein parameters of the drug library define the drugs and drug limitations of the drug library. For example, referring to fig. 30 and 31, the profile may be customized according to some parameters of different departments, or one department may have several profiles, which may be fully customized and selected. A profile may be followed by a plurality of medications, with each medication having different infusion modes (including fast forward, dose control, speed, PCA, TCI mode, etc.), default values for infusion parameters (including concentration, preset fast forward, fast forward dose, fast forward speed, infusion flow rate, first dose, background dose flow rate, automatic control, lock-in time, limit amount, etc.), upper and lower limits, etc. for each mode.
The icms platform is a central station informatization, and can pack a parameter set in advance in a department, namely profile, and transmit the parameter to the infusion pump, and after the infusion pump receives the parameter, the parameter can be identified by selecting the profile, so that the infusion can be started easily without setting the parameter.
profile flow (drug library based main flow), simplest infusion flow, more in line with clinical operation flow of department:
1) A plurality of interaction flows can be selected to adapt to different use scenes, and the operation steps are simplified to the greatest extent;
2) The simpler the flow is, the user error rate can be reduced;
3) The design flow is reasonably disassembled, and the strategy is proper;
4) The innovation of the task flow is relatively large-scale innovation, so that the user efficiency is directly and quickly improved.
Referring to fig. 32, another embodiment of the present application further provides an infusion device 32, including a liquid medicine driving means 321, a housing 322, a storage means 323 and a processor 324 disposed in the housing 322, and a display means 325 and an information input means 326 disposed on the housing 322;
the processor 324 is configured to perform the configuration method in the above-described embodiment.
In use, an infusion set, including a syringe pump, infusion tube, etc., containing the fluid to be infused is connected to the infusion device 32.
The liquid medicine driving device 321 is a mechanical or electronic control device acting on the infusion accessory to achieve the purpose of controlling the infusion speed of the infusion accessory to deliver the liquid medicine to be infused to the patient, so as to strictly control the infusion speed and/or the infusion quantity, and particularly, when the pressure boosting medicine, the antiarrhythmic medicine, the infant intravenous infusion or the intravenous anesthesia is applied, the infusion speed and/or the infusion quantity are more required to be precisely controlled.
The housing 322 is a case for protecting the chemical driving device 321, the storage device 323, and the processor 324.
The storage device 323 may store computer-executable instructions that when executed by the processor 324 perform corresponding functions. The computer-readable storage medium of the present embodiment is used to store computer-executable instructions that implement the configuration method, which when executed by the processor 324 implement the configuration method of the above embodiment. Such as flash memory, hard disk, multimedia card, card memory (e.g., SD or DX memory, etc.), random Access Memory (RAM), static Random Access Memory (SRAM), read Only Memory (ROM), electrically Erasable Programmable Read Only Memory (EEPROM), programmable Read Only Memory (PROM), magnetic memory, magnetic disk, optical disk, server, app application store, etc.
The storage 323 may be implemented by any type or combination of volatile or non-volatile memory devices, such as Static Random Access Memory (SRAM), electrically erasable programmable read-only memory (EEPROM), erasable programmable read-only memory (EPROM), programmable read-only memory (PROM), read-only memory (ROM), magnetic memory, flash memory, magnetic disk, or optical disk. A storage media may be any available media that can be accessed by a general purpose or special purpose computer.
An exemplary storage 323 is coupled to the processor 324 such the processor 324 can read information from, and write information to, the storage medium. Of course, the storage medium may be integral to processor 324. The processor 324 and the storage medium may reside in an application specific integrated circuit (Application Specific Integrated Circuits, ASIC for short). Of course, the processor 324 and the storage medium may reside as discrete components in an electronic device or a host device.
The processor 324 is a computer-executable instruction stored by the memory device 323 to implement the configuration methods described above, and the processor 324 may be a central processing unit 324 (Central Processing Unit, CPU), controller, microcontroller, microprocessor, or other data processing chip in some embodiments. The processor 52 is typically used to control the overall operation of the computer device. In this embodiment, the processor is configured to execute the program code or process data stored in the storage device 323, for example, execute the configuration device, so as to implement the configuration method of the above embodiment. The processor may be a central processing unit (Central Processing Unit, CPU for short), or other general purpose processor, digital signal processor (Digital Signal Processor, DSP for short), application specific integrated circuit (Application Specific Integrated Circuit, ASIC for short), etc. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. The steps of a method disclosed in connection with the present application may be embodied directly in a hardware processor for execution, or in a combination of hardware and software modules in a processor for execution. The memory may comprise a high-speed RAM memory, and may further comprise a non-volatile memory NVM, such as at least one magnetic disk memory, and may also be a U-disk, a removable hard disk, a read-only memory, a magnetic disk or optical disk, etc.
The display device 325 is connected to the processor 324, and is configured to display a setting mode provided by the infusion pump, where one setting mode corresponds to one configuration procedure, and the configuration procedure defines one or more of configuration parameters, configuration steps, and execution sequence of the configuration steps; the display device 325 is further configured to display a configuration step, where the configuration step includes a necessary step, or the configuration flow includes a necessary step and an unnecessary step; the necessary steps include configuration of infusion parameters, starting, infusion detection and ending infusion; optional steps include one or more of drug library selection, device maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview validation, consumable installation prompting, consumable selection, and return to standby.
When the display device 325 has an input function (e.g., a touch screen display), the display device 325 is further configured to receive a selection of a user input to determine one of at least two setting modes provided by the infusion pump as a target setting mode;
the display device 325 includes: one or more of a liquid crystal display, a touch screen display, a nixie tube display and a holographic display.
The liquid crystal display uses liquid crystal material as basic component, and fills liquid crystal material between two parallel plates, and uses voltage to change the arrangement state of internal molecules of liquid crystal material so as to attain the goal of shading light and transmitting light to display images with different depth and different places.
The touch screen display is also called a touch panel, and is an inductive liquid crystal display device 325 capable of receiving input signals such as contacts, and when the touch screen is touched with graphic buttons, the on-screen haptic feedback system can drive various connecting devices according to a preprogrammed program, and can be used to replace a mechanical button panel and produce vivid audio/video effects by means of a liquid crystal display.
A nixie tube display is an output device that can display numbers or simple digital words. Nixie tube displays have several light emitting diodes or liquid crystals for displaying content, which are most commonly used on calculators and watches at present. Is a simple and basic display. In addition, a large number of LEDs or liquid crystals are paved and formed in high density, and the luminous sequence and position are controlled by the chip, so that an image which can be watched in a long distance can be formed, and the outdoor advertisement display screen of many shopping malls is the technology.
Holographic displays are a generic term for holographic display devices comprising a plurality of different modalities. Including holographic display screens, holographic display helmets, and the like. The hologram technology is a technology of recording and reproducing a real three-dimensional image of an object using interference and diffraction principles.
An information input device 326 is coupled to the processor 324, the information input device 326 being configured to receive a selection of a user input to determine one of at least two setting modes provided by the infusion pump as a target setting mode and to operate the setting mode provided by the infusion pump; wherein, a setting mode corresponds to a configuration flow, the configuration flow defines one or more of configuration parameters, configuration steps and execution sequence of the configuration steps;
the information input device 326 is further configured to receive an operation instruction input by a user, so as to configure steps, where the configuring steps include necessary steps, or the configuring flow includes necessary steps and unnecessary steps; the necessary steps include configuration of infusion parameters, starting, infusion detection and ending infusion; optional steps include one or more of drug library selection, device maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview validation, consumable installation prompting, consumable selection, and return to standby.
The information input device 326 includes: one or more of a keyboard, an optical mark reader, an optical character reader, a mouse, a joystick, a light pen, a digital camera, a scanner, a facsimile machine and a language analog-digital conversion recognition system.
Other embodiments of the application will be apparent to those skilled in the art from consideration of the specification and practice of the application disclosed herein. This application is intended to cover any variations, uses, or adaptations of the application following, in general, the principles of the application and including such departures from the present disclosure as come within known or customary practice within the art to which the application pertains. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the application being indicated by the following claims.
It is to be understood that the application is not limited to the precise arrangements and instrumentalities shown in the drawings, which have been described above, and that various modifications and changes may be effected without departing from the scope thereof. The scope of the application is limited only by the appended claims.
Claims (10)
1. A method of configuring an infusion pump, comprising:
determining one set mode from at least two set modes provided by the infusion pump as a target set mode; wherein, a setting mode corresponds to a configuration flow, and the configuration flow defines configuration parameters, configuration steps and execution sequence of the configuration steps;
And controlling the infusion pump to sequentially execute corresponding configuration steps according to the determined target setting mode and the configuration flow corresponding to the target setting mode.
2. The method of configuring an infusion pump according to claim 1, wherein the configuring step includes a necessary step, or the configuring flow includes a necessary step and an unnecessary step;
the necessary steps include configuration of infusion parameters, starting, infusion detection and ending infusion;
optional steps include one or more of drug library selection, device maintenance configuration, patient information configuration, infusion mode selection, infusion parameter preview validation, consumable installation prompting, consumable selection, and return to standby.
3. The method of configuring an infusion pump according to claim 1, wherein the target setting mode is determined according to one or more of a department, a use scenario, a setting configuration, and a user type.
4. The method for configuring an infusion pump according to claim 1, wherein configuration parameters corresponding to different configuration procedures are different.
5. The configuration method of an infusion pump according to claim 1, wherein the configuration steps corresponding to different configuration flows and/or the execution order of the configuration steps is different.
6. The method of configuring an infusion pump of claim 2, wherein the configuration flow comprises: minimal flow and/or simplified flow,
The steps of the simplest flow include configuration of infusion parameters, starting, infusion detection and ending infusion;
the simplified flow includes infusion mode selection, infusion parameter configuration, start-up, consumable installation prompting, infusion detection, and end of infusion.
7. The method of configuring an infusion pump of claim 2, wherein the configuration flow comprises: based on the main flow of the drug library; the steps of the main flow based on the drug library comprise: patient information configuration, drug library selection, infusion parameter configuration, start, infusion detection, and end of infusion.
8. The method of configuring an infusion pump according to claim 2, wherein the patient information configuration in the optional step is set to be enabled or disabled according to one or more of a department, an application scenario, and a user type.
9. The method of configuring an infusion pump according to claim 2, wherein the drug library selection in the optional step is to pre-establish at least one drug library;
before determining one of the at least two setting modes provided by the infusion pump as the target setting mode, the method further comprises:
Issuing at least one drug library to an infusion pump and synchronizing parameters of the drug library to the infusion pump; wherein parameters of the drug library define the drugs and drug limitations of the drug library.
10. An infusion device comprising a medical fluid drive means, a housing, a memory means and a processor disposed within said housing, and a display means and an information input means disposed on said housing;
the processor performs the configuration method of claims 1-9.
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