Breast cancer is considered emotional and biological
It is one of the most treatable cancers when detected early
Efforts have been focused on developing breast cancer screening and early detection methods
Mammography is a crucial innovation in breast cancer control, aiming to detect breast cancer before it is palpable
The combination of early detection, diagnosis, and treatment has led to increased survival rates
In 1924, male radiologists in Rochester, NY speculated about x-raying the breast to locate tumors
Dr. Soloman, a German physician in 1913, reported the radiographic appearance of breast cancers
Otto Kleinschmidt made the first published radiograph of a living person's breast in 1927
In the 1930s, publications on mammography appeared in South America, the United States, and Europe
Xerography was introduced in the 1960s, lowering radiation doses and improving image quality
The duPont Company introduced higher resolution, faster-speed x-ray film, and an intensifying screen in the 1960s
The Breast Cancer Detection Demonstration Project (BCDDP) in 1973 demonstrated the effectiveness of screening methods
The Mammography Quality Standards Act (MQSA) was implemented in 1992 to maintain high-quality breast cancer screening programs
Risk factors for breast cancer include age, hormonal history, and family history
The breasts are lobulated glandular structures located within the superficial fascia of the thorax
Male breasts are rudimentary and without function, rarely subject to abnormalities
Female breasts function as accessory glands to the reproductive system by producing and secreting milk during lactation
The adult female breast consists of 15 to 20 lobes, each divided into many lobules
The radiographer must consider breast anatomy and patient body habitus for successful imaging
The glandular and connective tissues of the breast are soft tissue density structures
During pregnancy, significant hypertrophy of glands and ducts occurs within the breast
Analog mammography units require proper space, portability, electrical requirements, and ergonomics for optimal performance
CompressionDeviceto-Receptor Distance:
Should allow adequate space when positioning an obese woman for an oblique view
When magnifying an area in a large breast
When raising the compression device over the needle during preoperative localizations
TubeHousingorFaceShield:
Should remain as small as possible to facilitate positioning of the client’s head for the craniocaudal view and during magnification views
Foot Controls:
Remote foot controls for vertical movement of the C-arm and the compression device free the hands of the technologist while positioning
The amount of compression exerted by the foot pedal control should be minimal
The final compression of the breast should be done using a hand-controlled device
IRSD (ImageReceptorSupportDevice):
Permit fast and easy exchange of different size film Buckys or cassettes
Both 18 x 24 cm and 24 x 30 cm imaging systems should be available to match the size of the receptor to the size of the breast being imaged
ControlPanel:
Should be easy to read and to adjust
All units must have automatic exposure control (AEC)
When the exposure has ended, the control panel should indicate the exposure factors used
Density Selection:
At least nine density adjustment steps should be available
There should be a 10% to 15% difference in optical density between steps
Kilovoltage:
Molybdenum Target Units: range of at least 24 to 32 kVp in no greater than 1 kVp increments
Rhodium Target Units: range of at least 28 to 38 kVp in no greater than 1 kVp increments
Lower settings may be used in specimen radiography and higher settings for special views
MilliamperageSelection:
May be fixed or variable
If the mA value automatically decreases while increasing the kVp, it should occur outside the range of settings routinely used for screen–film mammography: the 25 to 30 kVp range
TimeSelection:
Short exposures: the grid is not “caught in motion” when using a grid on a thin adipose-replaced breast
Long exposures: the time setting must surpass the reciprocity law failure of the recording system
Source-Image Detector Distance:
Standard imaging SID: 55 cm
Magnification imaging SID: 60 cm
Collimators:
Fixed apertures
Interchangeable cones of various sizes
Internal set of collimating blades
NeedleLocalizationCapability:
Aside-loading cassette holder or Bucky is required if the equipment has preoperative needle localization capabilities
The compression device for needle localization either has a series of concentric holes or a large rectangular cutout
FieldLight:
The brightness of the light source should be 160 LUX or higher
Misalignment of the x-ray/light field can be a maximum of 2% of the SID
BreastThicknessScale:
Separate scales for grid versus non-grid versus magnification imaging should be available
The scales should be accurate to within 0.5 cm
Alignment:
The focal spot, compression device, and image receptor must align perfectly at the chest wall edge to ensure that all posterior breast tissue is included
Automatic Technique Selection:
Units must have a postexposure display that indicates the technical factors used
This mode aims to produce an image using an acceptable length of exposure time to reduce motion blurring and/or client dose, without compromising image quality
Exposure Control:
The operator can make an exposure only when completely outside of the X-ray field
RadiationShield:
Equivalent attenuation to at least 0.08 mm of lead at 35 kVp or the maximum kVp
This is to limit operator exposure to well below 0.1 mSv/week based on 40 patients/day, 5 days/week