Introduction Phantoms are elements used in radiological services for quality control tests. In the case of equipment with ionizing radiation, quality control tests focus on image quality and dosimetry. These phantoms are made with materials that resemble human tissues internally but are high-cost and difficult to access for radiology services.
Objectives To design a methodology for creating an anthropomorphic radiology phantom with materials correlating to human tissues of the pelvis for various uses, using Hounsfield Units (HU) as a comparison.
Methodology Data from 34 female patients with bone pelvis exams were collected. HU was measured in bone, muscle, and adipose tissue of the hip. Simultaneously, HU of different material mixtures was measured to correlate data between patients and materials for the creation of a right hip phantom.
Results HU values of the materials match human tissues except for adipose tissue, which is slightly increased. The costs for phantom creation were low.
Discussion and Conclusion HU estimates of materials and human tissue mostly align with those estimated in the sample and reported in the literature, achieving the creation of a low-cost phantom easily accessible for institutions or educational centers requiring quality, dosimetry, or educational tests.
Competing Interest StatementThe authors have declared no competing interest.
Funding StatementThis study did not receive any funding
Author DeclarationsI confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained.
Yes
The details of the IRB/oversight body that provided approval or exemption for the research described are given below:
Undergraduate Scientific Ethics Committee Alemana Clinical Medicine Faculty Desarrollo University From Chile
I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals.
Yes
I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance).
Yes
I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable.
Yes
Data AvailabilityAll data produced in the present study are available upon reasonable request to the authors
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