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Register 5English
Print No.: SPB7-230.898.01.01.02Doc. Gen. Date:04.00
Replaces: n.a.
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MAMMOMAT 1000/3000Register 5SPB7-230.898.01Page 2 of 4Siemens AG
MAMMOMAT 1000/3000Register 5SPB7-230.898.01Page 4 of 4Siemens AG
Rev. 0104.00TD SD 24Medical Engineering
F
Functional description1
Overview1
This document describes the control model of the AEC unit for M1000/3000. A view of the
function of the Mammomat is given together with a summary of possible exposure settings, their effects and characteristics of Mammomat performance. The function of dose
control is described together with an explanation of measurements done during the exposure, on which it is based.
Main function of the MAMMOMAT1
Picture below gives a schematic view of the exposure system.
X-rayTube
ilter
1-1
Target- Breast
Object Table
ScreenandFilm
Detector
Schematic view of the Mammomat
The generator supplies a voltage across the x-ray tube. The resulting radiation is filtered
before it reaches the target. Then it passes through an object table and reaches the fluorescent screen, which emits visible light giving the desired picture on the film. The part of
the radiation, which is not attenuated in the screen, reaches finally the detector and
results in a signal measured by the AEC unit. The main purpose of the AEC unit is to stop
the exposure so that the resulting picture is given the desired average optical density
based on current exposure settings and the measured signal from the detector.
Tube1
When a voltage is applied acrossthe x-ray tube, the electrons, hitting the anode, initiate
radiation. The tube contains two different anode materials - molybdenum and tungsten giving different kind of x-ray spectra. There are actually two different anodes for each
mentioned material, used to give large and small focus for the x-ray beam. Small focus is
usedtogether with magnifying objecttables. Large focus is used for all other object tables.
Siemens AGRegister 5SPB7-230.898.01Page 1 of 8MAMMOMAT 1000/3000
Medical EngineeringRev. 0104.00TD SD 24
1 - 2Functional description
Theoperator isallowedto choosea desiredtubevoltagefrom a rangebetween23 and35
kV with 1 kV resolution. The voltage influences the energy spectrum and gives the operator a control of how hard x-rays are used during the exposure. The current through the
tube, which is directly proportional to the overall intensity of the beam, is a function of the
chosen voltage, the maximum power setting and the maximum current limit.
Neither the energy spectrum of the beam nor it's intensity are constantduring the exposure, due to raising and falling times for the voltage and the tube current. The voltage has
typical raising timesof app. 50 ms and the tube current 5 ms.
Filter1
Different filtering is used to give the beam desired energy spectrum. For the molybdenum
anode, two filter selections are possible: molybdenum and rhodium. For the tungsten
anode, only rhodium is used as the filter material. This gives three possible anode/filter
combinations - Mo/Mo, Mo/Rh and W/Rh - resulting in three main kinds of x-ray beam.
Within each, a fine adjustment of the energy spectrum, i.e. the hardness of the beam, is
possible by adjusting the voltage.
Object Table1
There are totally 7 different kinds of object tables that can be used described in the table
below.
NameTypeUsed beam focusSizeMagnification
Grid 18 x 24GridLarge18 x 24 cmGrid 24 x 30GridLarge24 x 30 cmNoGrid 18 x 24Grid-lessLarge18 x 24 cmNoGrid 24 x 30Grid-lessLarge24 x 30 cmMag 1.5MagnificationSmall-1.5
Mag 1.8MagnificationSmall-1.8
Biopsy
table
According to their x-ray characteristics and use, the object tables are ordered into four
groups: grid, grid-less, magnification and biopsy:
The biopsy table, also called stereotactictable, isvery similar to the grid-less tables.
Itis equippedwitha biopsyunit thattogether withstereotacticsisusedto identify the
3D-position of the biopsy target within the breast and perform the biopsy. The pictures
are smaller and can be taken from a direction not perpendicular tothe object table.
Angles of+
MAMMOMAT 1000/3000Register 5SPB7-230.898.01Page 2 of 8Siemens AG
10° are used.
Rev. 0104.00TD SD 24Medical Engineering
Functional description1 - 3
Film and Screen1
A considerable part of the radiation, which passes the target and possibly the grid of the
object table, is attenuated in the fluorescent screen. The energy is than emitted as visible
light and gives the desired picture on the film. The film is also sensitive to the x-rays, however the x-rays do not contribute to the picture significantly, compared to the visible light
emitted by the screen.
Detector1
After passing the filter, the breast, the object table with screen and film, the radiation
finally reaches the detector. It is a semiconductor device that acts as a current source
supporting a current proportional to the overall intensity of the attenuated radiation. The
attenuation of the detector varies of course with the energy of the radiation, which makes
the generated current dependent on the energy spectrum of the beam. The generated
current is amplified and converted to a voltage level, which is the signal received from the
detector by the AEC unit.
Measured Signal1
The signal from the detector is amplified on the AEC board and than converted to pulses
with a frequency proportional to the voltage level of the signal. The AEC unit contains a
PLD (Programmable Logic Device), programmed to register the detector signal by counting the pulses that the signal is conver ted to.
Gain1
Before every exposure, there is a possibility to alter the gain applied to the detector signal
by the AEC board. Higher gain gives stronger signal to the V/F-converter, i.e. more pulses
and better precision in the counters of the PLD. There is however an upper bound for the
voltage level of the amplified signal - the V/F-converter functions for signals up to 10 V
and all voltages above this limit does not contribute to larger frequency of out-coming
pulses.
Dose Measuring1
ThedoseismeasuredbycountingthepulsesfromtheV/F-converterduringatimeof
interest. This dose measure is not comparable to any conventional dose units because it
gives varying responses depending strongly on the energy spectrum of the radiation registered by the detector. However, for the same anode, filter, tube voltage, object table,
screen and object, this dose measure is directly proportional to the dose received by the
screen.
A logarithmic scale for the dose is also used. It is based on the usual definition of relative
exposure and the unit exposure points (EP).
Dose
ΕΦ
DoseDoseEP
01
log10loglog10
1
Dose
0
The used logarithmic scale is however absolute in the sense that 0 EP is defined to be
equal to 100 counts:
Dose
EP
10
Dose
counts
Siemens AGRegister 5SPB7-230.898.01Page 3 of 8MAMMOMAT 1000/3000
Medical EngineeringRev. 0104.00TD SD 24
10100
i.e.
Dose
EP
log10
Dose
100
counts
1 - 4Functional description
Dose Rate Measuring1
In order to measure the dose rate, the pulses are counted during a period of time and the
resultingdoseisthendividedbythelengthofthetimeperiod.Theresultingdoserateis
an average over the chosen time interval.
Time Dependency1
Due to the raising and falling times of the tube voltage and current, the detector signal is
also time dependent and has typical raising times of 50 ms.
Two Wings1
The Mammomat can have one or two wings using separatedetectors.
User Choices1
The following table summarises possible user choices affecting the exposure:
User choiceRangeChange consequence
Anode/ filterMo/Mo, Mo/Rh, W/Rh Rough change of spectral properties of the
beam, possibly affecting power settings and
automatic choice of tube current.
Tube voltage23 - 35 kVFine change of spectral propertiesof the
beam, possibly affecting power settings and
automatic choice of tube current.
SpeedH or DChoice between two sets of parameters for
two different film/ screen-combinations.
Density correction-24/8 to + 24/8 EPRelative adjustment of exposurelength,
0 = nominal AEC exposure.
Object tableOne of 7See section Object Table
Wing1 or 2Different detectors in both wings.
Exposure control1
Thecontrolmodelforthe AEC-unitis typically subdividedinto twoparts.Firstpart handles
the control of a single exposure with one set of exposure settings such as kV, anode/filter
etc. It is based on the knowledge of these parameters before the start and measurements
done during the exposure. Second part puts the control model for one exposure into a
systematic approach to all possible exposure settings for the Mammomat. It explains how
the entire set of control parameters for the AEC-unit is build up in order to cover all possible combinations of kV, object tables, anode/filter choices and up to 2 film/screen combinations.
MAMMOMAT 1000/3000Register 5SPB7-230.898.01Page 4 of 8Siemens AG
Rev. 0104.00TD SD 24Medical Engineering
Functional description1 - 5
Ε
Φ
Control of One Exposure1
Before start of exposure, the AEC-unit is only aware of exposure settings chosen by the
operator and has no knowledge of thickness or density of the actual breast. This implies a
two step approach to control of the entire exposure. First step is done before the exposure
start and contains calculation of an initial dose that will be executed before the AEC will
decide what to do next. During the execution of the initial dose, the unit measures the
dose rate and uses it to calculate a correction dose that has to be executed before the
exposure stops. When the AEC-unit has registered a total dose being equal to the sum of
the initial dose and the correction dose, it will stop the exposure.
Initial Dose1
The initial d ose is chosen in EP. It co nsists of an estimated dose, a sensitivity, a sensitivity
correction and a density correction:
DcScSDoseDose
ΗΗΗΖ
EPEPEPEPestimatedEPinitial
,,,,,
where:
Dose
estimated,EP
- the estimated dose, a value specifically chosen for the used film/screen
combination, anode/filter combination, object table group and tube voltage.
- the sensitivity, a value controlling an overall level of target optical density for all
S,
EP
AEC-exposures.
SC,
- the sensitivity correction, chosen as a part of the calibration of specific equipment
EP
(Mammomat, object tables).
DC,
- the density correction, a value that is chosen by the operator for each exposure.
EP
The estimated dose is usually chosen, so it will give an OD = 1,5 for a 5 mm thick PMMAphantom.
Dose Correction1
In order to measure the dose rate with the detector, the following procedure is used. The
initial dose is subdivided into a 60%-part and a 40%-part. Both parts are handled in the
AEC-unit by two separate counters, implemented in the PLD. At the exposure start, the
60% counter starts counting down at the rate of pulses from the V/F-converter that handles the amplifiedsignal from the detector. During counting down the 60% of the initial
dose, time is measuredby a time monitor. Whenthe 60% counterhas reached 0, the time
is read and used together with the actual value of 60 % of the initial dose as an average
dose rate:
Dose
Dr
6,0
%60
ΕΦ
DoseTime
6,0
countsinitial
,
countsinitial
,
where
DoseTime,6,0
Siemens AGRegister 5SPB7-230.898.01Page 5 of 8MAMMOMAT 1000/3000
Medical EngineeringRev. 0104.00TD SD 24
- time as a function of 60 % of initial dose in counts.
countsinitial
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