Method and device for optimizing magnetic resonance system operating sequences with respect to physiological limiting values

1. A method for establishing a protocol for a measurement sequence for operating a magnetic resonance tomography system comprising:

providing a measurement sequence to a computer and, in said computer automatically segmenting said measurement sequence into a plurality of different groups of partial modules, with all partial modules in each different group performing a similar function in said measurement sequence;

in said computer, identifying a partial module that produces a greatest physiology altering exposure to patient;

in said computer testing said identified partial module with respect to a modeled function of the function performed by the identified partial module, to determine whether physiological limiting values, which limit an amount of said physiology altering, are observed by said measurement sequence for the identified partial module;

in said computer, if said testing determines that said physiological limiting values are not being observed in said measurement sequence, modifying parameters that influence said measurement at least once in order to obtain modified parameters that cause said physiological limiting value to be observed by said measurement sequence for the partial module with the modified parameters; and

in said computer, generating an operating protocol from said measurement parameters with said modified parameters for said identified partial module, and making said protocol available in electronic form at an output of said computer in a form for operating said magnetic resonance tomography system.

2. A method as claimed in claim 1 comprising, in said computer, determining parameters for the identified partial module that cause said measurement sequence to observe hardware limits of said magnetic resonance tomography system.

3. A method as claimed in claim 2 comprising determining said parameters for said partial module that cause said measurement sequence to observe said hardware limits before said testing.

4. A method as claimed in claim 2 comprising, in said computer, determining together whether said hardware limits are observed and testing whether said physiological limiting values are observed.

5. A method as claimed in claim 1 comprising:

if said testing determines that said physiological limiting values are observed by the measurement sequence with the identified partial module, determining whether said partial module can be repeated at a specified repetition rate while still causing said physiological limiting values to be observed; and

if said partial module cannot be repeated at said specified repetition rate without still observing the physiological limiting values, repeating said testing after performing at least one of reducing said repetition rate and further modifying said parameters of said partial module in order to obtain modified parameters that cause said physiological limiting value still to be observed.

6. A method as claimed in claim 5 comprising reducing said repetition rate by introducing pauses between respective partial modules of said measurement sequence.

7. A method as claimed in claim 6 comprising selecting a duration of said pauses as a function of said physiological limiting values.

8. A method as claimed in claim 1 comprising identifying and testing multiple partial modules that exhibit said greatest physiological exposure for said patient.

9. A method as claimed in claim 1 wherein said protocol designates a slice orientation from which magnetic resonance data are to be obtained by operating said magnetic resonance tomography system, and using said slice orientation in said testing as to whether said physiological limiting values are observed.

10. A method as claimed in claim 1 comprising employing, as said physiological limiting values, at least one of stimulation by gradient fields and exposure to radio-frequency fields.

11. A method as claimed in claim 1 wherein said parameters that are modified are selected from the group consisting of gradient slew rate, time to echo, and repetition time.

12. A method as claimed in claim 1 wherein each of said partial modules of said measurement sequence comprises radiation of a radio-frequency (RF) pulse having an associated RF energy, and wherein said physiology altering exposure is a specific absorption rate (SAR) of the patient.

13. A method as claimed in claim 1 wherein each of said partial modules of said measurement sequence comprises activation of a gradient pulse, and wherein said physiology altering exposure is peripheral nerve stimulation caused by said gradient pulse.

14. A device to establish a protocol to operate a magnetic resonance tomography system, said device comprising:

a computer having an input interface that receives a measurement sequence;

said computer being configured to automatically segment said measurement sequence into a plurality of different groups of partial modules, with all partial modules in each different group performing a similar function in said measurement sequence;

said computer being configured to identify a partial module that produces a greatest physiology altering exposure to patient;

said computer being configured to test said identified partial module with respect to a modeled function of the function performed by the identified partial module, to determine whether physiological limiting values, which limit an amount of said physiology altering, are observed by said measurement sequence for the identified partial module;

said computer being configured, if said testing determines that said physiological limiting values are not being observed in said measurement sequence, to modify parameters that influence said measurement at least once in order to obtain modified parameters that cause said physiological limiting value to be observed by said measurement sequence for the partial module with the modified parameters;

an output interface; and

said computer being configured to generate an operating protocol from said measurement parameters with said modified parameters for said identified partial module, and to make said protocol available in electronic form at said output interface of said computer in a form for operating said magnetic resonance tomography system.

15. A device as claimed in claim 14 wherein each of said partial modules of said measurement sequence comprises radiation of a radio-frequency (RF) pulse having an associated RF energy, and wherein said physiology altering exposure is a specific absorption rate (SAR) of the patient.

16. A device as claimed in claim 14 wherein each of said partial modules of said measurement sequence comprises activation of a gradient pulse, and wherein said physiology altering exposure is peripheral nerve stimulation caused by said gradient pulse.

17. A magnetic resonance apparatus comprising:

a computer having an input interface that receives a measurement sequence;

said computer being configured to automatically segment said measurement sequence into a plurality of different groups of partial modules, with all partial modules in each different group performing a similar function in said measurement sequence;

said computer being configured to identify a partial module that produces a greatest physiology altering exposure to patient;

said computer being configured to test said identified partial module with respect to a modeled function of the function performed by the identified partial module, to determine whether physiological limiting values, which limit an amount of said physiology altering, are observed by said measurement sequence for the identified partial module;

said computer being configured, if said testing determines that said physiological limiting values are not being observed in said measurement sequence, to modify parameters that influence said measurement at least once in order to obtain modified parameters that cause said physiological limiting value to be observed by said measurement sequence for the partial module with the modified parameters;

an output interface; and

said computer being configured to generate an operating protocol from said measurement parameters with said modified parameters for said identified partial module, and to make said protocol available in electronic form at said output interface of said computer in a form for operating said magnetic resonance scanner.

18. A magnetic resonance apparatus as claimed in claim 17 wherein each of said partial modules of said measurement sequence comprises radiation of a radio-frequency (RF) pulse having an associated RF energy, and wherein said physiology altering exposure is a specific absorption rate (SAR) of the patient.

19. A magnetic resonance apparatus as claimed in claim 17 wherein each of said partial modules of said measurement sequence comprises activation of a gradient pulse, and wherein said physiology altering exposure is peripheral nerve stimulation caused by said gradient pulse.

20. A non-transitory, computer-readable data storage medium encoded With programming instructions, said storage medium being loaded into a control computer of a magnetic resonance tomography system, and said programming instructions causing said control computer to:

receive a measurement sequence to a computer and automatically segment said measurement sequence into a plurality of different groups of partial modules, with all partial modules in each different group performing a similar function in said measurement sequence;

identify a partial module that produces a greatest physiology altering exposure to patient;

test said identified partial module with respect to a modeled function of the function performed by the identified partial module, to determine whether physiological limiting values, which limit an amount of said physiology altering, are observed by said measurement sequence for the identified partial module;

if said testing determines that said physiological limiting values are not being observed in said measurement sequence, modify parameters that influence said measurement at least once in order to obtain modified parameters that cause said physiological limiting value to be observed by said measurement sequence for the partial module with the modified parameters; and

generate an operating protocol from said measurement parameters with said modified parameters for said identified partial module, and make said protocol available in electronic form at an output of said computer in a form for operating said magnetic resonance tomography system.

21. A storage medium as claimed in claim 20 wherein each of said partial modules of said measurement sequence comprises radiation of a radio-frequency (RF) pulse having an associated RF energy, and wherein said physiology altering exposure is a specific absorption rate (SAR) of the patient.

22. A storage medium as claimed in claim 20 wherein each of said partial modules of said measurement sequence comprises activation of a gradient pulse, and wherein said physiology altering exposure is peripheral nerve stimulation caused by said gradient pulse.