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Dosimetric perturbations due to an implanted cardiac pacemaker in MammoSite® treatment
Author(s) -
Sung Wonmo,
Kim Siyong,
Kim Jungin,
Lee Jaegi,
Shin YoungJoo,
Jung JaeYong,
Ye SungJoon
Publication year - 2012
Publication title -
medical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 180
eISSN - 2473-4209
pISSN - 0094-2405
DOI - 10.1118/1.4752088
Subject(s) - balloon , brachytherapy , nuclear medicine , medicine , dose profile , ionization chamber , materials science , dosimetry , biomedical engineering , radiology , radiation therapy , ion , surgery , chemistry , organic chemistry , ionization
Purpose: To investigate dose perturbations for pacemaker‐implanted patients in partial breast irradiation using high dose rate (HDR) balloon brachytherapy. Methods: Monte Carlo (MC) simulations were performed to calculate dose distributions involving a pacemaker in Ir‐192 HDR balloon brachytherapy. Dose perturbations by varying balloon‐to‐pacemaker distances (BPD = 50 or 100 mm) and concentrations of iodine contrast medium (2.5%, 5.0%, 7.5%, and 10.0% by volume) in the balloon were investigated for separate parts of the pacemaker (i.e., battery and substrate). Relative measurements using an ion‐chamber were also performed to confirm MC results. Results: The MC and measured results in homogeneous media without a pacemaker agreed with published data within 2% from the balloon surface to 100 mm BPD. Further their dose distributions with a pacemaker were in a comparable agreement. The MC results showed that doses over the battery were increased by a factor of 3, compared to doses without a pacemaker. However, there was no significant dose perturbation in the middle of substrate but up to 70% dose increase in the substrate interface with the titanium capsule. The attenuation by iodine contrast medium lessened doses delivered to the pacemaker by up to 9%. Conclusions: Due to inhomogeneity of pacemaker and contrast medium as well as low‐energy photons in Ir‐192 HDR balloon brachytherapy, the actual dose received in a pacemaker is different from the homogeneous medium‐based dose and the external beam‐based dose. Therefore, the dose perturbations should be considered for pacemaker‐implanted patients when evaluating a safe clinical distance between the balloon and pacemaker.