MXPA06005795A - Medical treatment management systems - Google Patents

Abstract

A medical treatment process and system, in which a patient fluid is subjected to extracorporeal handling and treatment prior to administration to the patient, is provided. The system includes two or more treatment units which successively handle the fluid, and a token associated with the patient. The token includes a patient identification and, as the treatment proceeds, more information is added to the token as the fluid moves around the system until the token contains a record of the treatment conducted on the sample, the times of various treatments, and a verification that treatment has been conducted in accordance with pre-determined criteria. The token, provided it contains information verifying the identity of the patient and treatment according to specification, allows administration of the treated fluid to the patient and provides an audit record of the treatment.

Description

MAN EJO SYSTEMS OF MEDICAL TREATMENT Reference with Co-pending Application The subject subject of the Provisional application of E. U. series number 60/482725 filed on June 27, 2003 and labeled MEDICAL TREATMENT CONTROL SYSTEM is incorporated for reference.

BACKGROUND OF THE INVENTION 1. FIELD OF THE I NVENTION The present invention refers to the handling of medical treatments. 2. DISCUSSION OF RELATED MATTER There have been, in recent years, enormous changes in the way in which the patients were treated. Most social health care systems have changed to improve productivity. However, these changes have not occurred without problems. A recent heart lung transplant surgery was terribly wrong because of a difference in the blood type of the donor and the recipients. This eventio is overshadowed by the death of patients who receive the wrong medication. Esio suggests the need for improved monitoring of patients and that their traffickers make sure they give the medicines and / or appropriate medical procedures, given the specific and perhaps unique needs of each patient. An object of the present invention is to provide a novel medical treatment management system.

BRIEF DESCRIPTION OF THE INVENTION The term "processing device", used herein below, is intended to mean a device used directly or indirectly in the course of a traffic. It may include provisions that actually conduct a medical evaluation in the patient or a modification or management of treatment in a sample derived from the patient, or alternatively be an article to perform functions associated with operations, such as transferring or otherwise transferring. the sample towards or from a shop and process the sample. Several examples of the disposal of irrigation systems are described in the following pages. In one of its aspects, the present invention provides a method for controlling and recording the process of a patient material sample for a patient, comprising the steps of: equipping the patient with a machine-readable patient data record; provide a first trailing device; provide a first data sheet for the processing, readable by machine, to the first user device; provide at least one correlation unit; transferring at least one of the damage records between the patient and the first treatment device; record temporary data associated with control and processing; allowing the correlation unit to perform a correlation function between the patient data record and the first data sheet of data; automatically allow the tracking device to perform a scan only if a correlation has been made between the patient's data sheet and the first treatment data sheet; and taking into account that the stages occur within predetermined periods of time through analysis of the temporary data. In another of its aspects, the present invention includes, in particular, the steps of: providing a second method of treatment; provide the second layout device with a second treatment data sheet, machine-readable: - provide at least one correlation unit, allow the correlation unit to perform a correlation function between the data sheet of the page and the minus one of the damage files of the treatment; allow at least one of the framing devices to carry out a corresponding processing only when a correlation has been drawn between the patient data sheet and the corresponding treatment data sheet. In yet another of its aspects, the present invention provides a method for controlling patient registration records, comprising the steps of: associating the patient with a patient data record, machine-readable; associating a first processing device with a first processing data sheet, machine readable; - transfer the patient's data sheet to the first disposition of treatment; conducting a treatment on a patient material sample with the first delivery device; providing a second processing device with a second, machine readable data record; transferring the patient data sheet and the first tracing data sheet from the first treatment device to the second treatment device; conduct a treatment either on the patient or on the material sample of the patient with the second delivery device; and transferring the patient data sheet, the first treatment data sheet and the second treatment data sheet to a registration station after the second treatment.

In yet another of its aspects, the present invention provides a method for controlling patient treatment records, comprising the steps of: associating the patient with a machine-readable patient data record; forming a packet of treatment data in order to record one or more treatment in the patient or a patient material sample, including the damage packet the patient data sheet; - providing a first treatment device with a first treatment data sheet, readable by machine; monitor a first operation with the first irradiation device; add the first traffic data sheet to the damage dailies packet; provide a second layout device with a second record of date, machine-readable treatment: monitor a second route with the second route device; - add the second damage datasheet to the damage packet; and transferring the treatment data packet to a registration station after the second day. From a further aspect, the present invention provides a system for controlling patient record records, comprising: a patient-readability record, machine-readable, for associating a patient data record with a patient; at least one treatment device for conducting a treatment on the patient or on a material sample of the patient; at least one machine data file, machine-readable, associated with the corresponding information by means of at least one delivery device; a card transfer unit for exchanging the patient data sheet and / or the patient data sheet between the patient and at least one treatment device; an accountant to record temporary damages associated with the business; a correlation unit to determine a predefined relationship between the patient's damage record and the at least one of the damage datasheets, so that the at least one year-long device carries out the analysis in an auimomical manner only if the predetermined relationship has been established, and the process occurs within a predetermined period of time through analysis of the temporary data from the meter, otherwise the process is automatically terminated irreversibly; wherein the package data package forms a portion of the patient's tracking records. In one embodiment, the machine-readable record means of the patient includes an arycle configured for use, transported by or within, or attached to the patient. The processing means includes a first processing device and a second processing device, while the machine-readable processing data card means are operable to associate each treatment to be carried out by each driving device. From an additional aspect, the present invention provides a device for recording patient injury data, comprising a portable article for associating with a patient, the article including machine readable data card data means for associating a data record with a patient. patient with the patient and means of transfer for data sheet operable in a phase to supply the data sheet of the patient to a device of traffic or an initial device, and in another phase to receive at least one data sheet of damage from the same . Also, according to another of its aspects, the present invention provides a computer product for controlling one or more trays in a plurality of material samples of patient, having the computer program production: a computer readable medium that is stored in a computer. the same instructions that, when executed by a computer, cause the computer to carry out a plurality of computer executable steps in order to control one or more operations in a plurality of patient samples, comprising the steps of: ) encode a plurality of patient data cards, to associate each with a plurality of patients; (b) processing instructions for conducting a trait in a plurality of patients or in a plurality of material samples of the patients; (c) coding a plurality of data sheets of tramadol, to associate each damage datasheet with each of the treatments; (d) coding a packet of damage data for each of the patients, including each damage packet or deriving from the trafficking data sheet and the patient data sheet; and (e) associating each package of data with the corresponding patient. Preferentially, the plan includes the task of loading the damage packet into a portable array for transpor- tation, convention, use by or attach to, or be associated with, the packet. In another aspect of the invention, the present invention provides a method for reconciling and recording the processing of a donor's maferial sample for administration to a recipient, comprising the steps of: equipping the donor with a first patient data record, readable by machine; equip the container with a second patient data sheet, machine-readable; - providing at least one trailing device; providing the at least one conveyor device with a machine damage datasheet, machine-readable, corresponding; - proportional to at least one correlation unit; record timeless damage associated with conírol and processing; allowing the correlation unit to perform a correlation function between the donor data sheet and any of the container data sheets and / or the at least one treatment data sheet; allow the correlation unit to analyze the temporal data to determine if the steps occur within predetermined time periods; and - allowing the at least one treatment device to carry out a treatment of the donor sample material only when a correlation has been made between the first patient-readable data record, and any of the patient data sheet. , readable by machine, reclpienie and / or the at least one data sheet of treatment; and taking into account that the stages occur within predetermined periods of time. In still other aspects, a computer program product encoded in a computer-readable medium is provided which includes a plurality of computer executable steps for a computer in order to control one or more devices in a plurality of patients or a plurality. of material samples thereof, comprising: a) executing a step to encode a plurality of patient data tokens, each to be associated with one of a plurality of patients; b) executing a step to conduct a tramage in a plurality of material samples of the patients; c) executing a step to encode a plurality of tracing data tokens, each treatment data token to associate with each of the tramamieníos; d) execute a stage to codify a package of damages for each of the patients, including each damage packet or derivative of the damage datum card and the patient damage record; and e) associating each package of damage with the corresponding patient. Preferably, step e) includes the step of loading each bundle of tracing data into a portable article to be transposed by, transpired into, used by being attached to, or associated with, the corresponding patient. Another aspect of the present invention is a computer-readable damage structure for controlling patient registration records, comprising a patient data record that encodes a given patient and at least one disclosure data sheet that encodes at least one patient. trayement conducted in the patient or a maferial sample of the same. In yet another of its aspects, a signal propagated in a vehicle means is provided, the signal including a patient data card element encoding a given patient and at least one treatment data card element encoding at least the patient-driven treatment. or a maerial sample of it. Thus, in one example, the system is capable of transferring a patient data sheet from an article that is used by or associated with a patient (such as a wrist band or its equivalent) to the one or more devices of the patient. The procedure will continue as the treatment proceeds, before the procedure begins or after the treatment is completed, as the case may be. The data sheet of the patient can also be represented in a password or access word in order to obtain permission for a traficing to occur in parficular. This permission may involve the collection of untreated blood, or the supply of treated blood or the like. In this case, the data sheet of the patient may be different from the data in relation to the records recorded, measured or accumulated in the same way during the treatment. In this case, the trait data sheet can be represented with hearing damage which, after the treatment procedure, can be used to review a particular patient treatment program, as the case may be.

In addition, this permitting function may also give priority to the supply to the patient of a treated sample, or a unit or means of transfer of record, or one or more of the data sheets therein. In other words, the final supply of the trafada sample or one or more of the cards may proceed only in this case, taking into account that a positive correlation or verification is made between the patient of origin and the sample or the data sheet. . If a positive correlation can not be made, supply is avoided. This can also apply to ordering and dispensing drugs where a container or record can be dispensed to a pharmacy or other drug store and then filling the required prescription and delivered to the patient only after a positive correlation is made.

BRIEF DESCRIPTION OF THE DRAWINGS Some preferred embodiments of the present invention will now be described, by way of example only, with reference to the accompanying drawings in which: Figure 1 is a schematic view of a medical handling system; and Figure 2 is a schematic view of an alternating medical treatment management system.

DESCRIPTION OF THE PREFERRED MODALIDS Figure 1 illustrates a system 10 for management of fratamienlo and care of a patient. As will be explained more fully below, system 10 is based on the principle that one or more "damage tokens", machine-readable, eikinies or data are available to identify the patient and one or more other events or events. Procedures for the patient. Each data sheet provides sufficient coordinated information in order to identify the patient or the treatment that was conducted on the patient or a sample derived from the patient. According to the above, if the patient is subjected to an audited system, then the system tracks two damage tokens, a patient's datasheet and a first treatment data file. Together, these cards provide a useful audit trail for the process carried out. However, in perhaps more frequent cases, the patient is subject to many treatments and procedures. Under the 1 0 system, then, an audit trail may be established to record the relevant patient coordinate data as well as one or more or all of the treatments and / or procedures. In addition, the system 10 can be used to ensure that the correct procedure is conducted on the correct patient or sample derived from the patient. By doing so, system 10 can be used to perform a correlation function between the patient data sheet and the patient's damage record. In such a case, the system can be configured to allow a particular procedure to be carried out only when a correlation has been made between the patient data record and the data record of the treatment. Damage tokens can be collected in various ways, for example, in a number of discrete forms, such as mechanically prepared labels, such as bar codes and the like. Alternatively, each damage token can be packaged and transferred to a vehicle signal, for example, through an optical vehicle wave, transmitted over a fiber network, an RF vehicle signal transmitted over an RF network, or other forms. The data sheets can be maintained, stored or otherwise retained in a "package" of data cards, for example, a sub file or sector in a database or memory device, such as a microcircuit of data. memory, a magnetic memory band, a hard drive or the like. In the system 1 0 shown in Fig. 1, there exists a packet of machine-readable damage tokens per machine 12 represented by representation 12, which has four discrete areas. Each of the four areas or sections 12a, 12b, 12c and 12d constitutes a sector of chip contention that receives a discrete "chip"or information package, in the form of electronic data received and stored directly in one of the sections, or in a physical form such as a microcircuit that transports data, a unique physical object such as a key or the like. The patient data sheet and the data card pack 12 can be transported, for example, in an RFID microcircuit 14a which is located on itself in a wrist band 14b. In this case, the RFID microcircuit also provides the function of a chip transfer unit, since the RFID microcircuit is capable of transmitting the chip to an appropriately tuned RFID receiver. The RFID microcircuit can be, for example, of the active or passive type available in Microchlp Technology Inc. under the serial number MCR 45X, as described in the RFID Design Guide Sysíem microl D 1 3.56 MHz. The chip transfer unit 14 is enabled to collect, retrieve and / or store the data sheet of the patient in relation to the patient, upon receipt of the packet of data sheets 12 that transports the patient data sheet as electronic data in sector 12a. In this case, the chip transfer unit 14 may be operable to receive the patient data record from an RFID writing unit at the time the patient enters medical facilities. The RFID microcircuit can be energized externally or externally by such energy sources, such as a battery or an internal power generation module, such as a solar energy generator operating in the presence of microwave or RF radiation. The power supply portion can include a conductive path to an external power source. The system 10 includes a first treatment device generally shown at 16, a second focusing device generally shown at 18, and a third moving device shown generally shown at 20. Three such treatment units are shown in the present for illustrative purposes, and that the system may be applicable to a treatment device, two treatment devices or any number of treatment devices as required. The first, second and third treatment devices 16, 18 and 20 may each comprise one or more syringes, IV bottles, fluids and / or inhalant gas dispensers, implant dispensing dispensers, ventilators, syringe pumps , intubation tubes, gastrointestinal feeding tubes or a plurality and / or a combination thereof. One of the trapping devices may also comprise a blood circulation device as disclosed in International Publication No. WO 01 19318141 entitled APPARATUS AND PROCESS FOR CONDITIONING MAMMAL BLOOD, published on March 22, 2001. Alternatively, a radiation device can be equipped to carry out a range of invasive and non-invasive procedures, such as surgeries, treatments for diseases such as cancer, as well as exploratory or diagnostic investigations, such as X-rays, CAT scans. , MRI's and the like. The treatment devices, first, second and third, 16, 18 and 20, are each provided with tracing data sheets, readable by machine, first, second and third, respectively, showing the first record of data of tramadol in the sec. 12b of data packet 12, showing the second data sheet of data in sector 12c and displaying the third data record of traffing in sector 12d. The first and third raid devices 16 and 20 are enabled to exchange one or more data tokens with the chip transfer unit 14 together with data paths 22a, 22c, respectively. Optionally, the second processing device 1 8 is enabled to exchange one or more data cards with the data transfer unit 14 along the data path 22b. The treatment devices, first and second, 16 and 18, are enabled to exchange one or more pieces of damage between themselves along the path of damage 22d, while the second, third and third devices, 18 and 20, are enabled to exchange one or more data cards with each other along the data path 22e. Optionally, the first and third order devices, 16 and 20, are enabled to exchange one or more data cards with each other along the data path 22f. Although the data paths are illustrated by being discrete and separated from one another, they can be provided or included in one or more vehicle signals between the various processing devices and the chip transfer unit. If desired, any of the transfer devices, the chip transfer device or an intermediate device, can be equipped with a correlation unit, for example, as shown in 16a, 18 and 20 in Figure 1, in order to carry out a correlation function between the patient data sheet and at least one of the second treatment data sheets or the third treatment data sheet, in order to execute the treatment stage or the stage of injecting the patient with the treated blood, only after an appropriate concordance or correlation, as described, for example, in the Provisional Application of US series number 60 / 428,942, filed on November 26, 2002 and tiíulada BLOOD TREATMENT CONTROL SYSTEM. The correlation unit can also be a separate device from the other tracking devices (ie, a separate unit). In such a case, the condition of transferring the bodily fluid from the ferrous delivery device to the patient is permitted only when a correlation has been made between the patient's damage record and the corresponding damage datasheets. This may be vitally important in normal procedures such as blood and other procedures, where the reorientation of the sample to the patient's home (eg, blood testing) is essential. In addition to providing this essential safety feature, the modalities of the invention can be adapted to provide a complete audit trail of the patient's treatments during the entire course of treatments, to record medical progress, efficacy, suitability of the treatment regimen. , frequency of treatments, billing, adverse events, etc. There may be cases where the correlation function occurs indirectly between the patient data sheet and the data tracing data sheets. For example, the correlation can be made between the patient data sheet and the first data sheet of the patient, and after that, enter the first data sheet of data and the second data record of the patient once it has been adequately verified. the previous damage file. The chip transfer unit 14 is thus operable to receive the datasheet pack 12 of the third tracking device 20. It will be understood that the function of the chip transfer unit 14 (i.e., the transmission of the patient data record). in the first case and the reception of the data sheets accumulated in the data package in the final case), it also resides in each of the planning devices, in order to allow the package of accumulated data cards to be transferred from one processing device to the next and finally to the chip transfer unit 14. However, for reasons of brevity, only the chip transfer unit 14 will be identified. On the other hand, there may be cases where the function of the unit of chip transfer 14 does not reside in each of the processing devices, but rather in one of the devices or in an intermediate unit, for example. Thus, in one example, the pack of data cards 12 is transferred from the chip transfer unit 14 to the first processing device 16 with the first sector 12a containing the patient data sheet. The pack of data sheets 12, in this case, it is shown with four secfores in order to correspond to the patient data and to the three treatments, it being understood that the package of data cards may contain as many sections as necessary to accommodate the files of the treatment devices used in any given application. If applicable, the correlation unit 16a performs a correlation function between the patient data sheet and the first treatment data sheet and, if the correction is made, the first treatment is carried out. The pack of data cards 12 is then transferred from the first processing device 16 to the second transport device 18 with the sections 12a, 12b by transferring their corresponding patient data cards, with the corresponding correlation function carried out, if is applicable. The data chip pack 12 is then transferred from the second trailing device 1 8 to the third trailing device 20, translating the sections, 12a, 12b and 12c its corresponding patient damage cards, as well as the data sheets. of treatment, first and second, with the correlation function again carried out between the second treatment data sheet and the patient's damage record, if applicable. The pack of damage cards 12 is finally transferred to the chip transfer device 14, the sectors 12a, 12b, 12c and 12c carrying their corresponding patient data cards, as well as the traffic data sheets, first, second and second. With the new correlation function carried out between the third damage datasheet and the patient's damage datasheet, if applicable. In this case, the data card packet 12 can be transferred to the card transfer device only if a positive correlation is made between the patient of origin and the patient data card confented in the packet of Damage Cards 12. In this way, in system 10, the damage tokens are accumulated in a way to form an audit trail or repository that returns to the patient or an intermediate device, in the form of a packet of data cards containing all or cards of selective data in relation to the treatments that are conducted in the patient in a period of treatment in paríicular. For example, a packet of data cards can be accumulated for each series of blood runs during several periods of treatment or for a single blood treatment. Desirably, one or more of the treatment devices are operable for registration when the treatment occurred by associating a time count with the corresponding treatment data sheet. In this way, one or more of the data sheets may also include a time stamp or some other time count indicating the time and / or date of the processing. Figure 2 illustrates an alternate system 50 having, as before, treatment units, first, second and third, of the unit of transfer of cards usable by the patient, 54, 56 and 58, all of which are enabled to communicate with an intermediate registration station 60. In this case, the intermediate registration station 60 may be provided with a memory portion, such as a write memory microcircuit or a writing medium, such as a hard disk drive, so as to storing the data sheets received from the data transfer unit as well as from one or more of the treatment devices 54, 56 and 58, by means of a wireless data link or wired to each other, as shown in 62a, 62b, 62c and 62d, respectively. The intermediate registration station 60 may include a data processing station 60a operable to exchange data with a central database 64. In this way, in system 50, the packet of data cards shown at 66 was collected and stored at or by the intermediate registration station 60, but is not passed from a processing device to the other as in system 10. However, the System 50 does not provide an effective audit trail or repository for the treatments to be carried out on the patient during a given treatment period. The data sheets can be found in electronic, graphic, mechanical or nuclear form, machine readable, and / or transferred through a vehicle wave. The vehicle wave may include radio frequency waves, microwaves or waves or signals of other frequencies or frequency ranges, with the signal transporized by frequency modulation, amp modulation, wave superposition or a combination thereof. The patient datasheet cards may also include, for example, data representative of or derived from a retinal scanning image provided by a biometrical sensor, a damage code provided by an optical character reader, a bar code reader, a magnetic strip reader, or a combination thereof. In this case, the chip transfer unit may include a signal emitter and / or receiver to send and / or receive remarks on the visible or invisible frequency spectrums. In applications where one or more treatment devices are a syringe or a similar device, the data sheets may be embedded in or printed on an empty surface or a surface of the syringe with or without additional identifying indicia printed thereon. If desired, the patient data sheet and at least one of the treatment data sheets, first, second or third, may include mechanical elements of mutual interference between the first chip transfer unit and at least one of the second chip transfer unit, the first processing device, or the second transfer device or the third irradiation device, as shown, for example, in International Publication No. WO 2004 / 095379A1, published on April 23, 2004 , entitled "DISTRIBUTION SYSTEMS" The card transfer unit or the first, second and / or third treatment devices may include a programmed logic controller or some other form of controller. It can be included in a software program configured to run on a general purpose computer, such as a personal computer, or in a more substantial computer structure, which is operable to work within a network, so that the data on the files of patient data are loaded into a central database, or the transfer devices or the card transfer unit are conirled or downloaded remotely with data from recent patient data sheets. The network of work can thus involve various general-purpose computers, for example, those sold under the trade names APPLE ™ or IBM ™, or clones thereof, which are programmed with operating systems known by the trade names WINDOWS ™, LINUX or you will hear equivalences of these well known or less known. The system may involve pre-programmed software through the use of several possible languages or a client-designed version of a programming soflware sold under the ACCESS ™ trademark or similar programming software. The computer network can be a local area network connected by cable or a wide area network such as Internet, or a combination of the two with or without security protocols, authentication, aggregates, or under networked architectures of network. "equal to equal" or "client-server". The network can also be a wireless network or a combination of wireless or wired networks. The wireless network can operate under frequencies such as those called 'radio frequency' or 'RF' through the use of protocols such as 802.1 1, TCP / IP, BLUE TOOTH and similar, or other Internet protocols, wireless, satellite or cell phone, well known. The system can also include a single client construction computer that is dedicated to the function of the system. The operation of the system 10 will be explained in the following example of blood circulation. In this case, the first irradiation device 1 6 is a syringe that is used to separate a sample or aliquot of bodily material, in the form of blood, from the patient. Either before, during, or after the separation step, the card transfer unit 14 transfers the damage token packet 12 that contains the patient's damage tokens and which includes patient identification information, to the syringe 1 6. The patient identification information is also referenced in unit 14 on the wrist band. A first time stamp is also added to the syringe correlation unit 16a as to the wrist band unit 14, recording the time at which the aliquot of blood was collected. The syringe correlation unit 16a may not contain information initially, except perhaps an identifier that is proposed for use in the system, until the wrist band unit 14a reads the patient ID information for it. The blood sample is then transferred from the syringe 16 to a blood tracing device 18, while the pack of data cards is transferred from the syringe 16 to the blood treatment device 1 8 containing the patient data sheet. and a datasheet of "separation of samples". The blood treatment unit 18 contains the correlation unit 18a which in this mode is an RFID reader-writer. Unit 18a interrogates unit 16a on the syringe to verify that it is in fact a proposed sample for treatment and that it is being received by unit 18 within an appropriate pre-determined time structure. Once this has been verified, the syringe 16 can be allowed to deliver its contents to the delivery unit 18. All the information coming from the syringe unit 16a, including the patient idenification information and the first time stamp, it is read and stored in the RFID Reader-Writer 18a. To this is added, in the lecturer-writer 18a, information on the condition of the weather in order to allow verification that the pre-determined treatment conditions were followed, denoting a second stage of time the start time of the train and denoting a third time stamp the time of conclusion of the traisamiento. Alternatively, the step of separating blood can be considered as a step that does not need to be audited, in which case, the transfer of the packet of damage cards can occur between the card transfer unit 14 and the blood treatment device 18 directly, by using the data path 22b, with a "blood treatment" data sheet that includes a first time stamp indicating when the sample was transferred and a second time stamp indicating when the stage was carried out of blood circulation in the sample, taking into account that a correlation is made between the data sheet of "blood treatment" and the data sheet of the patient. With the blood treatment completed, the sample of blood drawn was transferred from the blood treatment device 18 to a second return syringe 20, constituting the third treatment unit. The blood treatment device 18 transfers the pack of data cards 12 to the correlation unit 20a, an RFID microcircuit, of the second syringe 20 together with the patient's datasheet, the "sample separation" data sheet ( yes it is included) and the data sheet of "blood circulation". At this point, a "blood supply" sample is added to the pack of data cards 12. Accordingly, taking into account that a positive correlation is made between the patient data sheet and the "blood supply" data sheet, the data record pack 12 is transferred from the second syringe 20 to the card transfer unit 14 and the blood sample can exit the return syringe 20 for delivery to the patient only if the wrist band 14 and the unit 20a verify the patient's identity, the appropriate treatment conditions and the appropriate time lapses. All accumulated data is recorded in the chip transfer unit 14a, which thus provides a complete audit trail of the transfer process.

Ideally, the packet of patient data cards may be directly or indirectly addressed to a central database for subsequent handling procedures or to a local memory device, such as a memory microcircuit embedded in a patient's chart or the like. Blood irradiation can be carried out in a portion of or on the blood sample per year and may include the blood sample with oxidative stress, where the oxidative stress is a gas mixture of ozone / oxygen bubbled through, with or without UV radiation, heat or a combination of the same. Alternatively, the blood treatment device can transfer the data record pack directly to the chip transfer unit 14, together with the patient data sheet 12a, the "sample separation" data sheet 12b (if included). ) and the "blood treatment" data sheet 12c, thereby diverting a transfer of data cards to the second syringe 20. It is also contemplated that a number of iterative treatments may be conducted in a sample derived from the patient or the patient, which it may involve a number of sub-treatments each of which may include the detection of one or more conditions, vital parameters of the patient or the sample (or environmental conditions, such as temperalure, intensity of travail, characteristic measures of the sample or the patient) during the sub-treatment. In this case, the data accumulated in the datasheet package 12 may include the results of the sub-raids and the conditions that prevailed in each stage. As an additional illustration, a treatment step may involve a feedback function, which detects the condition of an aliquot and treatment of the aliquot, while measuring parameters such as blood density, treatment parameters themselves such as ozone or other stressing densities. , gas mixtures and the like. The feedback function can then provide improved traffings while the packet of data records records one or more of those iterative stages. In addition to the autologous blood samples, it will be understood that the system, its components and alternates thereof can be used for autologous samples other than blood samples, such as bone marrow or lymphatic fluids, semen, mixtures of ova-fluids, other body fluids or Other medical fluids that may or may not be "auiologists", for example, mixtures of fluids that may contain a desired solid sample of the patient such as from organs, body cells and cell tissue, skin cells and skin samples, spinal cords . All fluids, June with blood, are encompassed by the term "patient material" used in the present. The system can also be used for medical examination where it is important to ensure that the test results of a particular test can be transferred to the patient of origin.

Claims (39)

1. CLAIMS 1. A method to control and record the processing of a patient material sample for a patient, characterized in that it comprises the steps of: - equipping the patient with a patient's damage sheet, readable by machine; provide a first treatment device; providing the first tampering device with a first tampering record, machine readable; - provide at least one correlation unit; transfer at least one of the data sheets between the patient and the first trauma card; record temporary data associated with control and processing; - allowing the correlation unit to perform a correlation function between the patient data sheet and the first treatment data sheet; allow the correlation unit to analyze temporal data to determine if stages occur within predetermined time periods; and automatically allow the patient's device to perform a procedure only if a correlation has been made between the patient data record and the first treatment data sheet and taking into account that the data occur within predetermined periods of time. through analysis of the temporary data, otherwise the transfer terminates irreversibly automatically. The method according to claim 1, characterized in that it further comprises the steps of: - providing a second radiating device; provide the second processing agent with a second treatment data sheet, machine readable; provide at least one correlation unit; transfer the patient data sheet and at least one of the treatment data sheets between the patient and at least one of the treatment devices, or between the treatment devices; allow the correlation unit to perform a correlation function on the patient's damage sheet and on at least one of the trait data cards; automatically allow at least one of the treatment devices to carry out a corresponding treatment only when a correlation has been made between the data sheet of the patient and the corresponding damage datum card, otherwise the treatment is irreversibly terminated in a manner automatic 3. A method as defined in claim 2, characterized in that the first irradiation device is a dispenser for the patient's primary sample. 4. A method as defined in claim 3, characterized in that the material sample of the patient includes a body fluid. A method as defined in claim 4, characterized in that it further comprises the step of transferring the body fluid from the first framing device to the second treatment device. 6. A method as defined in claim 4, characterized in that the second treatment device conducts the circulation in the body fluid. 7. A method as defined in claim 6, characterized in that it further comprises the steps of: providing a random disposition device; and provide the disposer of treatment with a third treatment data sheet, machine readable. 8. A method as defined in claim 7, characterized in that the first, second or third treatment devices include a syringe, a bottle IV, a syringe pump, and / or a combination thereof. 9. A method as defined in claim 8, characterized in that after following the treatment of the material sample of the patient by the second scanning device, the method further comprises the step of transferring the material sample of the patient from the second treatment device. towards the eventual representative of the rally. A method as defined in claim 9, characterized in that it further comprises the steps of: allowing the correlation unit to perform a correlation function between the patient data sheet and the third treatment data sheet; and - opening the third treatment device in order to allow the confinement output thereof only when a correlation has been made between the patient data sheet and the corresponding treatment data sheet in order to correlate the patient with the material sample of the patient. eleven . A method as defined in claim 9, characterized in that it further comprises the step of providing a chip transfer unit to each of the patient treatment devices, first, second or third, or an intermediate device, thereby Transfer units are operable to exchange data cards with each other. 12. A method as defined in claim 1, characterized in that the patient data record includes indicia associated with the patient and any of the treatment damage tokens include indicia associated with the treatment. 13. A method as defined in claim 12, characterized in that at least one of the data cards is invented over a wireless or wired data link, or a combination thereof. A method as defined in claim 13, characterized in that the data link is established on a radio frequency signal. 15. A method as defined in claim 12, characterized in that the indicia of the patient data record include at least one bar code. 16. A method as defined in claim 13, characterized in that the intermediate device includes an operable data processing station for exchanging data with a central database. 17. A method as defined in claim 1, characterized in that the patient data record or at least one of the treatment data sheets, first, second or third, are associated with mechanical elements of mutual internal adjustment between the chip transfer unit and at least one of the first processing device, the second disposal device or the third radiating device. 18. A method as defined in any of claims 7 to 17, characterized in that an aliquot of whole blood is found in the material sample of the patient. 19. A method as defined in claim 18, characterized in that the first traffic device is a syringe for receiving the aliquot. 20. A method as defined in claim 19, characterized in that the third treatment device is a second syringe. twenty-one . A method as defined in claim 18, characterized in that the blood was brought simulataneously with at least two UV, oxygen / ozone and heat. 22. A method to confirm patient treatment records, characterized in that it comprises the steps of: - associating the patient with a patient-readable data record by machine; provide a first treatment device with a first data sheet of treatment, readable by machine; transfer the damage tab of the paclenfe to the first treatment device; conducting a treatment either on the patient or on a material sample of the patient with the first delivery device; provide a second treatment document with a second data sheet of Irrigation, machine-readable; transferring the patient's damage sheet and the first treatment data sheet of the first treatment device to the second delivery device; conduct a procedure either on the patient or on the patient's physical sample with a second treatment device; and transferring the patient data sheet, the first treatment data sheet and the second damage data sheet to a registration station after the second treatment. 23. A method for controlling patient registration records, characterized in that it comprises the steps of: associating the patient with a patient data record, machine-readable; - forming a packet data packet to record one or more traits in the patient or a material sample of the patient, including the data packet the patient data sheet; providing a first treatment device with a first treatment data sheet, readable by machine, monitoring a first treatment with the first delivery device; add the first trafficking data sheet to the treatment data package. - providing a second disposal device with a second data sheet of machine-readable data; monitor a second train with the second train device; add the second trafficking data sheet to the damage datas pack; and transferring the treatment data package to a registration station after the second treatment. 24. A method as defined in claim 22 or 23, characterized in that the registration station is included in the first treatment device, the second treatment device or a recording device is separated from the first treatment device and the second treatment device. 25. A method as defined in claim 24, characterized in that the recording station is included in an article by associating with the patient. 26. A method as defined in claim 25, characterized in that the article can be used by the patient. 27. A method as defined in claim 26, characterized in that it further includes the steps of associating a period of time with one or more of the fractions and adding representative data of the time count to the one or more corresponding tracing tokens. 28. A system for controlling patient registration records, characterized in that it comprises: a means of patient datasheets, machine-readable, to associate a data record of the patient with a patient; at least one treatment device to conduct a treatment on the patient or on a patient's physical sample; at least one treatment data sheet, machine readable, associated with the corresponding treatment by the at least one treatment device; the at least one delivery device and the patient, each having a file transfer unit for exchanging the patient data records and / or the patient data records between the patient and the at least one treatment device; a counter to record temporary data associated with the treatment; a correlation unit for determining a predetermined relationship between the patient data sheet and the at least one of the treatment data cards, so that the at least one treatment device automatically carries out the treatment only if the predetermined relation has been established and the processing occurs within a predetermined period of time through the analysis of the temporary data of the counter, otherwise, the treatment is irreversibly terminated automatically; - a data generating means for generating a fraizing data package, the processing data package having the patient data record and the at least one data sheet for machine-readable data, having the data package for processing data related to the patient and the corresponding patient's pathology or the patient's maferial sample, and temporal data; wherein the treatment data package forms a portion of the patient's treatment records. 29. A system as defined in claim 28, characterized in that the patient-readable dataset medium, machine readable, includes an item configured to be used by, transported by or inside, or attached to the patient. 30. A system as defined in claim 29, characterized in that the at least one trailing device includes a first radiating device and a second reeling device, the processing data medium being machine-readable for operation. Associate a data sheet of treatment with each of the treatments to be carried out by the treatment devices, first and second. 31 A device for recording data of patient treatment, characterized in that it comprises a portable article to be associated with the patient, the article including means of a patient data record, readable by machine, to associate a data sheet of the patient with the patient and means of transferring tokens operable in a phase to deliver the patient's damage record to a disposal device or an intermediary device, and in another phase to receive at least one data sheet of treatment originating therefrom. 32. A computer product for controlling one or more items in a plurality of material samples of the patient, having the computer program product: a computer-readable medium which is stored in the same instructions as, when executed by a computer, cause the computer to perform a plurality of computer executable steps in order to control one or more treatments on a plurality of material samples of the patient, the steps comprising: a) encoding a plurality of patient data records, each by associate with one of a plurality of patients; b) processing instructions to conduct a treatment on a plurality of patients or on a plurality of material samples of the patients; c) coding a plurality of treatment data cards, each treatment data card to be associated with each of the treatments; d) coding a treatment data package for each of said patients, including each data packet or deriving from the treatment data sheet and the patient data sheet; and e) associate each data package with the corresponding patient. 33. A computer product as defined in claim 32, characterized in that the step e) includes the loading of each packet of processing data into a portable article to be transposed by, transported in, used by or appended to, or associated with. with the corresponding patient. 34. A method for controlling and recording the processing of a donor's maternal sample for administration to a recipient, characterized in that it comprises the steps of: equipping the donor with a first, machine-readable patient data record; equip the container with a second data sheet of the patient, readable by machine; provide at least one treatment device; providing the at least one trailing device with a corresponding, machine-readable treatment data sheet; provide at least one correlation unit; record temporary dafos associated with control and processing; enabling the correlation unit to perform a correlation function between the data sheet of the donor and any of the data sheet of the recipient and / or the at least one data sheet of the trader; enable the correlation unit to analyze the temporary data in order to determine if the stages occur within predetermined time periods; automatically enable the at least one treatment device to carry out a sample donor sample transfer only when a correlation has been made between the first patient-readable data record of the patient and any of the patient data record; readable by machine, container and / or the at least one treatment data sheet; and taking into account that the stages occur within predetermined periods of time, otherwise the treatment ends irreversibly in an automatic way. 35. The method according to claim 34, characterized in that the at least one treatment device includes a device for carrying out a medical treatment on the material sample of the patient, or for processing the material sample of the patient, a device for altering the composition of the patient material, a device for carrying out functions associated with the procedure, a device for transferring the material sample of the patient to and from other devices and a device is a dispenser for the patient's physical sample. 36. The method according to claim 35, characterized in that the at least one delivery device is a syringe. 37. The method according to claim 35, characterized in that each of the donor, recipient and at least one delivery device includes a transfer of tokens to send and receive the first data sheet of the patient, machine-readable, the second data record of the patient, machine-readable and / or at least one data sheet of the patient. 38. The method according to claim 37, characterized in that each of the transfer unit accumulates any of the data cards received in such a way that the received datasheet cards are correlated by the correlation unit in various stages of the processing. 39. The method according to claims 34 to 38, characterized in that the donor and the container are the same entity.