METHOD AND SAFETY MODULE FOR AN AUTOMATIC OR SEMI-AUTOMATIC DETECTION WHETHER AN MR EXAMINATION OF A PERSON IS APPROVED WITH A PREDETERMINED MR SYSTEM

Abstract

The invention relates to a method for an automatic or semi-automatic detection whether an MR examination of a person (12) is approved with a predetermined MR system (10), which MR system (10) includes at least one coil (14, 16, 18) for generating a magnetic field. According to the invention the method comprises the following steps: Step 1: providing information whether and which contra-indication for such an MR examination is present for this person (12) (S1); Step 2: providing information about a location of a cause (30) of the contra-indication within the person (12) (S2); Step 3: a determination of a position of this cause (30) during the MR examination of said person with respect to the at least one coil (14, 16, 18) (S3); Step 4: a determination of at least one characteristic parameter of the magnetic field generated by said coil (14, 16, 18) at said position of the cause (30) during the MR examination (S4); and Step 5: an automatic check, whether the MR examination is approved for the combination of the determined cause (30) of the contra-indication and the determined characteristic parameter of the magnetic field at the location of said cause (30) (S5). The invention relates to a corresponding safety module (26) for an MR system (10) and a corresponding MR system (10).

Claims

1. A method for an automatic or semi-automatic detection whether an MR examination of a person is approved with a predetermined MR system, which MR system includes at least one coil for generating a magnetic field, wherein the method comprising: providing information whether and which contra-indication for such an MR examination is present for the person; providing information about a location of the cause of the contra-indication within the person; a determination of a position of this cause during the MR examination of said person with respect to the at least one coil; a determination of at least one characteristic parameter of the magnetic field generated by said coil at said position of the cause during the MR examination; and an automatic check, whether the MR examination is approved for the combination of the determined cause of the contra-indication and the determined characteristic parameter of the magnetic field at the position of said cause, wherein the determination of the characteristic parameter of the magnetic field at the location of the cause of the contra-indication is automatically derived from a selected examination protocol.

2. The method according to claim 1, wherein the information about at least one of the potential contra-indication for an MR examination of the person; the location of the cause of the contra-indication within the person; and the position of this cause during the MR examination of said person with respect to the at least one coil is/are provided by use of a manual input via a user interface and/or a manual selection from a list presented by said user interface.

3. The method according to claim 2, wherein the user interface requests the information automatically by means of a request routine.

4. The method according to claim 1, further comprising: an automatic release of the MR examination of the person in case the MR examination is approved and an automatic blocking of the MR examination of the person in case the MR examination is not approved.

5. The method according to claim 1, including specification of the person's identity before determining the contra-indication.

6. The method according to claim 1, wherein the characteristic parameter of the magnetic field generated by the at least one coil is a field gradient.

7. The method according to claim 1, wherein the cause of the contra-indication is an implant or a pregnancy of the person.

8. A computer program product for executing the method according to claim 1.

9. A safety module for an MR system, which MR system includes at least one coil for generating a magnetic field, wherein the safety module has access to the technical characteristics of the predetermined MR system and is established to perform: a receipt of information whether and which contra-indication for such an MR examination is present for this person; a receipt of information about a position of a cause of the contra-indication during the MR examination of said person with respect to the at least one coil; or about a location of the cause of the contra-indication within the person followed by an automatic determination of a position of this cause during the MR examination of said person with respect to the at least one coil; a determination of at least one characteristic parameter of the magnetic field generated by said coil at said position of the cause during the MR examination; and an automatic check, whether the MR examination is approved for the combination of the determined cause of the contra-indication and the determined characteristic parameter of the magnetic field at the position of said cause, wherein the determination of the characteristic parameter of the magnetic field at the location of the cause of the contra-indication may be automatically derived from a selected examination protocol.

10. The module according to claim 9, wherein the receipt of information about the position or the location of this cause is performed by use of a manual input and/or a manual selection from a list presented by a user interface.

11. The module according to claim 10, wherein the information about potential contra-indications for an MR examination of the person is requested by a request routine, which is performed automatically on the user interface.

12. The module according to claim 9, wherein the module is further established to send a control signal to a control unit of the MR system to perform an automatic release of the MR examination of the person in case the MR examination is approved and an automatic blocking of the MR examination of the person in case the MR examination is not approved.

13. The module according to claim 7, wherein the characteristic parameter of the magnetic field generated by the at least one coil is a field gradient.

14. A MR system for performing an MR examination of a person, the MR system including a control unit; at least one coil for generating a magnetic field; and a safety module according to claim 9.

15. An MR system of claim 14, comprising a gradient system to apply a gradient magnetic field in an examination zone, in which the safety module includes a user interface, and the safety module being configured to display the gradient strength distribution on the user interface, in particular to highlight regions in which the gradient strength exceeds a pre-set safety level.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0030] These and other aspects of the invention will be apparent from and elucidated with reference to the embodiments described hereinafter.

[0031] In the drawings:

[0032] FIG. 1 shows a schematic representation of a MR system including a safety module;

[0033] FIG. 2 shows a kind of process flow chart of a process for a semi-automatic detection whether an MR examination of a person is approved with a given MR system according to preferred embodiments of the invention;

[0034] FIG. 3 shows a first request-mask of a request routine presented by a user interface (UI) for performing the process presented in FIG. 2;

[0035] FIG. 4 shows a second request-mask of the request routine;

[0036] FIG. 5 shows a third request-mask of the request routine;

[0037] FIG. 6 shows a fourth request-mask of the request routine; and

[0038] FIG. 7 shows a file system for the corresponding data.

DETAILED DESCRIPTION OF EMBODIMENTS

[0039] FIG. 1 shows a schematic representation of a MR system 10 for performing an MR (MR: Magnetic Resonance) examination of a person (in general a patient) 12, the system 10 comprises a plurality of coils 14, 16, 18 including a field coil 14, a gradient field coil 16 and an RF coil 18 (RF: Radio Frequency), a patient bed 20, a corresponding control unit 22 for controlling the MR examination, a personal computer 24 with a processor (not shown), a memory (not shown) and at least one user interface 26 (including the necessary hardware: display, keyboard, mouse, etc.). A safety module 28 of said MR system 10 is made up of said computer 24. The person 12 to be MR examined has got an unsafe implant, which is a cause 30 of a contra-indication for such an MR examination.

[0040] In the following discussion reference is made to a method for a semi-automatic detection whether an MR examination of a person is approved with a predetermined MR system 10, which method is performed by use of the user interface (UI) 26. The invention is however applicable with other devices for providing adequate information either. The use of the UI 26 is selected as a preferred example.

[0041] FIG. 2 shows a kind of process flow chart of a process for a semi-automatic detection whether an MR examination of a person is approved with the MR system 10.

[0042] The process comprises the following steps:

[0043] Step 1 (S1): the person 12 to be examined provides information whether and which contra-indication for an MR examination is present. A typical contra-indication is an implant or a pregnancy of the person 12. The operator of the MR system 10 enters the corresponding data of the person and the contra-indication to the user interface 26 of the safety module 28.

[0044] Step 2 (S2): the person 12 to be examined provides information about a location of a cause 30 of the contra-indication within his body.

[0045] Step 3 (S3): the operator of the MR system 10 determines a position of this cause 30 during the MR examination with respect to the at least one coil 14, 16, 18 and enters the corresponding data to the user interface 26.

[0046] Alternatively, in step 3 (S3) the operator of the MR system 10 enters the corresponding data to the user interface 26 and the safety module 28 determines a position of this cause 30 during the MR examination with respect to the at least one coil 14, 16, 18 automatically.

[0047] Step 4 (S4) is an automatic determination of at least one characteristic parameter of the magnetic field generated by said coil 14, 16, 18 at said position of the cause 30 during the MR examination. The automatic determination is performed by the safety module 28. In general the spatial gradient field (measured e.g. in Gauss/cm) is the most relevant parameter of the magnetic field.

[0048] Step 5 (S5) is an automatic check, whether the MR examination is approved for the combination of the determined cause 30 of the contra-indication and the determined characteristic parameter of the magnetic field at the location of said cause 30. The automatic check is performed by the safety module 28 either.

[0049] Step 6 (S6) is an automatic release of the MR examination of the person 12 in case the MR examination is approved and an automatic blocking of the MR examination of the person 12 in case the MR examination is not approved.

[0050] Preferably, the information about the potential contra-indications and the information about the location/position of the cause 30 of the contra-indication is requested by a request routine, which is performed automatically on the user interface 26.

[0051] FIGS. 3 to 6 show different request-masks of said request routine. FIG. 3 shows the request-mask of step 1. Personal data and data about the contra-indication for the MR examination are requested. In other words: Patient conditions that require a restriction of the MR scanner output are offered as input fields of the Patient Administration UI 26. FIG. 4 shows an additional request-mask of step 1 requesting a status flag of the implant (status safe/unconditional/unsafe). The input fields for the Implant conditions are aligned to standards like ASTM F2503-8 used by implant manufacturers. FIG. 5 shows the request-mask of a request for a look-up table of possible implants. Resource like implant manufacturer database could be integrated with the UI 26 for quick access to implant information. This could be used as reference, or direct input of MR conditions into the scanner to eliminate operator workflow steps.

[0052] FIG. 6 shows the request-mask of step 3 and 4. The spatial gradient field in relation to the implant position is graphically and interactively visualized. Spatial gradient fields are complex to interpret by MR operators, yet the majority of static implants require evaluation of this MR conditions. Currently this is achieved by the operator having to retrieve this information from the technical documentation and interpret Gradient Plots. The UI 26 offers an interactive method where the operator indicates the implant location by a mouse click and inputs the maximum value as stated in the implant labeling. The Implant UI will indicate to the user of that spatial gradient field condition is met.

[0053] FIG. 7 shows a file system for the corresponding data. An icon indicates which of the suggested ExamCards adhere to the MR restrictions dictated by the Implant conditions.

[0054] While the invention has been illustrated and described in detail in the drawings and foregoing description, such illustration and description are to be considered illustrative or exemplary and not restrictive; the invention is not limited to the disclosed embodiments. Other variations to the disclosed embodiments can be understood and effected by those skilled in the art in practicing the claimed invention, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word comprising does not exclude other elements or steps, and the indefinite article a or an does not exclude a plurality. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.