ACR Electronics L-32 FIELD MARKER LIGHTING SYSTEM Technické informace

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AAPM REPORT NO. 25
PROTOCOLS FOR THE RADIATION
SAFETY SURVEYS OF
DIAGNOSTIC RADIOLOGICAL
EQUIPMENT
Published for the
American Association of Physicists in Medicine
by the American institute of Physics
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AAPM REPORT NO. 25PROTOCOLS FOR THE RADIATIONSAFETY SURVEYS OFDIAGNOSTIC RADIOLOGICALEQUIPMENTPublished for theAmerican Association of Physicists in M

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I-3. Beam on Controls and IndicatorsVerify the availability of a positive indicator ofx-ray production when the x-raytube is energized, suchas:(a) mA-

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The surveyorshielding devices.should verify the presence and use ofThe surveyor should check or monitorthe checking ofprotectiveapparel. Theshieldinga

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devices have been developed to expedite this. Hendee andRossi, for example,employ aplasticcylinder formeasuring SID (Reference #3).Localization of the

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3)4)5)6)8)TheSet a standard x-ray field size, 18 x 24 cm(8 x 10"), using the appropriate numericalindicator scale on the collimator.Turn on the c

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on the x-ray tube assembly.X-ray Field/Numerical Indicator Size:I-6(c)Measure the length and width of the x-ray field oneach film.These dimensionsshou

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Three differenttestmethods which require nospecial instrumentation are described below.Test Method I1)Place the collimator in automatic mode.2)Center

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Caution:Some PBL collimators do not have a key designedto-disable their automatic sizing as required in step 3of Method II.If this key is not provided

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lock out exposuresuntilthe operator has manuallyadjusted the x-ray field to be smaller or equal to thesize of the image receptor.The function and sizi

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the HVL measurement.The test protocolsof the following two sectionsdescribe methods to measurethe HVL todeterminecompliance with minimum filtration re

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concerning compliance with minimumfiltrationrequirements. For example.if the actual kV is lowerthan indicated on the operator's console,the measu

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AAPM REPORT NO. 25PROTOCOLS FOR THE RADIATIONSAFETY SURVEYS OFDIAGNOSTIC RADIOLOGICALEQUIPMENTA REPORT OF THE DIAGNOSTICX-RAY IMAGING COMMITTEETASKGRO

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7) Compare the measured HVL against "Table I-Minimum HVL Requirement" to determinecompliance.Test Method II: Units With No Manual TimingPlac

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filtration may be necessary as discussed in Section 1-7-A.This abbreviated test method can also be applied tostep #8 in Test Method II in section I-7-

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(g) X-ray tube age.If the measured radiation output deviates more than40-50% from the appropriate value suggested in Table III,the generator may need

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high voltage cables contributes to the actual output ofeach exposure (Reference #21).While this contributionto the measured mR/mAs is less than 5-10%

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items should beincluded on the survey forms. Arecommendation or a suggestion should accompany each itemin an effort to bring the unit into full compli

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Checklist Outline forRadiographic InstallationsI-2.SYSTEM INFORMATIONA.Installation2.1. Date of surveyRoom number3.Department/Building4.InstitutionUn

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E.Other Specialized DevicesI-5.SOURCE-TO-IMAGE RECEPTOR DISTANCEA.Focal Spot Localization (when x-raytube is replaced)B.SID indicators2.1. Accuracy

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(at least annually or as in I-7.A)I-8.RADIOGRAPHIC TECHNIQUE CHARTA.AvailabilityB.UseC.CompletenessI-9.IDENTIFICATION OF PERSON CONDUCTING EVALUATIONA

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Part II. Medical Fluoroscopic InstallationsII-l. IntroductionPages 34-37 contain a checklist of the physicalparameters which require evaluation and th

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the completion of the elapsed preset time. Re-initiationof the fluoroscopic exposure without resetting the timershall restart the audible warning (Ref

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DISCLAIMER: This publication is based on sources andinformation believed to be reliable, but the AAPM and theeditors disclaim any warranty or liabilit

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capabilities. The 38 cm SSD also applies to lateralplane x-ray tubes found in biplane fluoroscopic systems.Since automatic collimators required on cer

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II-6. Radiation Beam Restriction and AlignmentThis sectiondescribestheevaluation of thecollimator's ability to automatically restrict the x-rayfi

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3)4)5)6)7)8)9)10)11)12)During fluoroscopy, center the test tool.This process is normally easier if one ofthe two pair of collimator blades is closedto

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19) If any question concerning alignment as afunction of SID exists, steps 13-18 shouldbe repeated with the tower positioned verticallyat the maximum

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intersecting at the center of the field of view shall notexceed 4 percent of the SID (Reference #1).II-6-C. Evaluation of Spotfilm AlignmentSteps 13-1

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II-6-E. Alternate Test MethodsThe test method briefly described in II-6-A is onlyone of many. While the test equipment required for thismethod is mini

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HVLs for Units With Manual Exposure Rate ControlsFluoroscopic systemswith manual exposureratecontrols allow use of Test Method I in Section I-7-A with

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7) Complete steps #8-#12 of Test Method IIfound in Section I-7-A.HVL Test Method II: Noninvasive, Maximum kVp Test Point1) Use identical geometry desc

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for the high exposure rate mode.considered good practice to However, it islimit this mode to 10 R/min(2.6 mC/(kgmin)) unless a specific clinical need

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assembly. When the maximumis measured, theentrance exposure of a unitlead plate protects theintensifier from excessiveimageentrance exposure rates.Als

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ContentsIntroduction and General ClarificationsIntroduction ------------------------------- 1General Clarifications---------------------1Part I.Medica

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II-l.II-2Checklist Outline forFluoroscopic InstallationSYSTEM INFORMATION (See Section I-2)A. Installation1. Date of survey2. Room number3. Department

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II-3.FLUOROSCOPIC TIMERA. Five Minute Maximum SettingB. Audible Warning FunctionalC. Accuracy of Elapsed Exposure time (at leastannually or after repa

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B. Fluoroscopic Mode Alignment and Sizing(Maximum SID, auto and/or manual mode)1. Large FOV (14", 13, 12", 11", 10", or 9")2.

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C. Qualitative Evaluation of AERC Device (samefrequency as II-7.BII-8.IDENTIFICATION OF PERSON CONDUCTING EVALUATIONA. NameB. TitleC. Professional Cer

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III. Dental Radiographic InstallationsIII-l. IntroductionMany items discussed in the Medical RadiographicInstallation Section, Section I, are applicab

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SSD shall be 10 cm (4") (Reference #L). The distancebetween the end of the cone attached to the tube headassembly and focalspot usually can be me

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an appropriate image receptor which is larger than the x-ray field placed at the distal end of the cone. The imagereceptor can be film, fluorescent sc

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these interchangeable cones. or apertures shall havepermanent labels which indicate the image receptor sizeand SID for which the beam restrictor is de

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for Devices and Radiological Health (CDRH) of the USDepartment of Health and Human Services (USDHHS), hasdocumented that dental film development is a

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The general commentsof Section I-7-C on measuringradiation exposures apply to dental x-ray units. Theionization chamber and electrometer described in

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Radiographic Installation Checklist -------- 19Part II.Medical Fluoroscopic InstallationsII-l. Introduction---------------------------- 22II-2. Exposu

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The mechanical support of the x-ray tube on Cephalometricand Panoramic units shall be designedso that the x-raytube housing assembly remains stable du

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Checklist Outline ForDental Radiographic InstallationsIII-1.SYSTEM INFORMATION (See Section I-2)A.Installation2.1. Date of surveyRoom number4.3. Dep

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III-5.III-6.III-7.III-8.III-9.RADIATION BEAM RESTRICTORSA.Intraoral System (at least annually or afterremoval of cone)1.X-ray field diameter at SSDB.P

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III-12. IDENTIFICATION OF PERSON CONDUCTING EVALUATION(See Section I-9)A.NameB.TitleC.Professional CertificationIII-13. RECOMMENDATIONS AND SUGGESTION

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IV. Measurement of Area Radiation LevelsIV-l. IntroductionParts I,II, and III, have concentrated on equipmentrelated radiation safety matters.In addit

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(b) The lowest tube current station availableon the control panel exceeds the maximumcontinuous rated current for the maximumrated tube potential, and

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6) Select positions on the surface of animaginary sphere of 1 meter radius withits-center located at the focal spot.Include points at a height equal t

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(b) Orientation of the x-ray beam in the room,(c) Workload of the x-ray unit,(d) Size of the room and the equipment layout, and(e) Degree of occupancy

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following factors must be considered when quantitativemeasurements are completed:(a) Meter's energy response(b) Meter's directional response

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Checklist OutlineMeasurement of Area Radiation LevelsIV-2.LEAKAGE RADIATION (prior to first patient use oranytime damage to the tube housing is suspec

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III-2.Beam-on Controls and Indicators ------ 38III-3.Minimum Source-Skin Distance:Intraoral Unit----------------------- 38III-4.Source to Image Recept

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1.2.3.4.5.6.7.8.9.10.11.12.REFERENCES"Part 1020-PerformancestandardsforRadiation Emitting Products", 21 Code ofIonizingFederal Regulations,

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13.14.15.16.17.18.19.20.21.22.24.Personal Communication with Thomas Mosely concerningFDA Compliance Policy Guide issued to manufacturers,assemblers, a

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Introduction and General ClarificationsIntroductionThe task group:"Protocols on The Radiation SafetySurvey of Diagnostic Radiological Equipment&q

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2.Determine typical patient exposure levelsfor standard radiographic exams and fluoroscopy,3. Assess fluoroscopic contrast and spatialresolution,5.4.

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Part I:Medical Radiographic InstallationsI-l. IntroductionPages 19-21 contain a checklist of the physicalparameters to be evaluated and the informatio

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