Revision History
All ACR Nuclear Medicine accredited facilities and those applying for accreditation must maintain a documented quality control (QC) program and must comply with the minimum frequencies of testing outlined in the 2024 ACR NM Quality Control Manual. As part of the accreditation process, facilities must demonstrate compliance with the ACR requirements for QC. Documentation showing compliance of all QC including the most recent NRC and/or state inspection results (report) for the facility and documentation of written responses to any violations noted must be available for review during Validation Site Surveys. In addition, facilities must demonstrate compliance by providing:
The most recent physicist report for each unit including the annual performance tests described below and the most recent dose calibrator linearity and accuracy testing
Documentation of corrective action (if the physicist report indicates areas where corrective action is needed)
Acceptance Testing
Acceptance tests must be performed on systems when they are installed. Initial testing of imaging equipment must be performed upon installation and should be completed before clinical use. This testing should be more comprehensive than periodic performance testing and should be consistent with current acceptance testing practice.
Annual Physics Survey
A physics survey must be performed on each nuclear medicine unit at least annually. Blank Equipment Evaluation Summary Forms (PDF and Excel versions) are attached below. The ACR realizes that surveys cannot usually be scheduled exactly on the anniversary date of the previous survey; therefore, a period of up to 14 months between surveys is acceptable. These tests do not need to be as rigorous as acceptance tests but must be a comprehensive suite of individual measurements that ensure adequate sensitivity for detecting detrimental changes in performance. A practicing qualified medical physicist (QMP) may perform these tests. Alternatively, the tests may be performed by properly trained individuals approved by the medical physicist using National Electrical Manufacturers Association (NEMA) protocols and/or other appropriate testing protocols developed and approved by the QMP. The test results must be reviewed by the QMP and documented in the annual survey report. As a part of this annual survey the QMP should meet with the supervising physician and the QC technologist to review the results of the survey and the effectiveness of the technologist QC program, and to recommend any corrective action or repairs that are needed. The supervising physician is responsible for assuring compliance with the recommendations of the medical physicist.
All QC testing must be carried out in accordance with the methods outlined in the 2024 ACR NM Quality Control Manual. The annual physicist survey must include, but not be limited to, the following:Sty
Nuclear Medicine Performance Tests | |
Test | Description |
Intrinsic Uniformity | Performed to ensure that the intrinsic detector integral and differential uniformity are sufficient to minimize the production of artifacts and ensure that patient abnormalities can be visualized without interference from the imaging system. These tests also monitor a scintillation unit for electronic problems and crystal deterioration (hydration). |
System Uniformity | Performed to check all commonly used collimators for defects that might produce artifacts in planar and tomographic studies. |
Intrinsic or System Spatial Resolution | Performed to ensure that the detector resolution is sufficient to provide satisfactory detection of lesions and delineate detail in clinical images. |
System Sensitivity/Relative Sensitivity | Performed to measure the count rate per time and ensure the results between the detectors is within 5%. |
Energy Resolution | Performed to verify that scatter rejection is sufficient to provide optimal contrast in clinical studies. Note: On some systems, energy resolution is very difficult to measure precisely. |
Count Rate Parameters | Performed to measure the max count rate. |
Processing Monitor | Performed to ensure that systems used to produce hard copy and monitors that are used for processing of clinical studies provide satisfactory image quality. |
Safety Evaluation | Performed to ensure that the mechanical and electrical systems are working correctly and safely. |
Overall System Performance for SPECT Systems | Performed to quantitatively verify that SPECT systems provide satisfactory tomographic uniformity, contrast, and spatial resolution. |
Camera Interlocks | Performed to verify that all system interlocks (i.e., touch pads and collision rails) are operating as designed and that the system is safe and reliable for the nuclear medicine technologist to operate and for imaging patients. |
Dose Calibrators | Performed to verify that readings from this instrument are accurate. All basic measurements of performance must be done at the time of installation and repeated after major repair. This test must be done according to protocols accepted by the appropriate state regulatory agencies or the NRC.
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Thyroid Uptake and Counting Systems (if applicable) | Performed to verify energy calibration, energy linearity, energy resolution, sensitivity, and reliability (Chi-squared test) for the measurement of organ function and the assay of patient samples.
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Continuous Quality Control
The nuclear medicine technologist is responsible for verifying day-to-day operation of instruments and performing a few additional tests on a quarterly basis. These requirements represent the standard of practice and are in compliance with requirements and recommendations of The Joint Commission (TJC) and state and federal agencies. Documentation of compliance with all quality control tests and corrective action is required as part of the application process.
The technologist QC program must include, but not be limited to, the following:
Nuclear Medicine Technologist's Quality Control Tests | ||
Test | Description | Frequency |
Intrinsic or System Uniformity | Performed to verify that components are properly functioning and provide a uniform image in response to a uniform flux of radiation | Each day of use |
Daily CT Check (if applicable) | Per manufacturer recommendations | Each day of use |
Intrinsic or System Spatial Resolution | Performed to quantitatively verify that detector spatial resolution is satisfactory for clinical imaging – The weekly resolution phantom is not necessary on cameras with pixilated detectors | Weekly |
Center of Rotation | Performed to maintain ability to resolve details in clinical SPECT studies | Monthly |
High-Count Floods for Uniformity Correction | Performed to correct for residual detector and collimator non-uniformity and to minimize the production of artifacts in clinical studies | As recommended by a qualified medical physicist |
Overall System Performance for SPECT Systems | Performed to qualitatively verify that the system has maintained its capabilities with respect to tomographic uniformity, contrast, and spatial resolution that maximize the benefit in clinical studies. Technetium must be done at least semiannually; other radionuclides may be tested on alternate quarters. | Semiannually (quarterly recommended) |
Dose Calibrators | Tests are performed to verify that the calibrator is accurate and reliable for the assay of doses administered to patients | Daily |
Thyroid Uptake and Counting Systems (if applicable) | Standards are measured to verify energy calibration and sensitivity for the measurement of organ function and the assay of patient samples | Each day of use |
Preventive Maintenance
Preventive maintenance must be scheduled, performed, and documented by a qualified service engineer on a regular basis. Service performed to correct system deficiencies must also be documented and service records maintained by the facility.
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