Table 2.
Quality item | Detectability |
Uncertainty level5,40 | Error probability and effect (authors' opinion) |
||
---|---|---|---|---|---|
Real-time IVD | Real-time imaging | Probability of error | Effecta | ||
Source calibration | ✔b | 2% | Low | Low–high | |
Afterloader source positioning and dwell time (non-patient specific)c | ✔d | 4% | – | – | |
Afterloader malfunction | ✔d | – | Low | Low–high | |
Patient identification | ✔e | – | Low | High | |
Correct treatment plan | ✔f | – | Low | High | |
Intra- and interfraction organ/applicator movementc | ✔d,g | ✔ | 10–25% for organs at risk; >10–25% for target if high-dose-rate needle movements uncorrected | – | – |
Applicator reconstruction and fusion errors | ✔d,h | ✔ | 4% | Intermediate | Low–intermediate |
Applicator length/source indexer length | ✔d,i | – | Intermediate | Low–high | |
Source step size (patient specific) | ✔d,i | – | Low | High | |
Interchanged guide tubes | ✔d | – | Intermediate | Low–high | |
Recording of dosec | ✔j | 3–5% | – | – |
The table is a complement to Table 1 by Tanderup et al.11 The uncertainty levels are taken from Tanderup et al5 and Kirisits et al.40 The probabilities and effects were estimated by the authors.
Refers to the potential effect on dose administration.
If the dosemeter calibration is independent from the actual source.
Quality item that corresponds to an uncertainty in the treatment, which is always present and therefore does not have an occurrence likelihood, rather than an error.
Quality items for which detectability strongly would benefit from two or more point detectors, as stated or indicated in Andersen et al,14 Therriault-Proulx et al,17,18 Cartwright et al,20 Kertzscher et al,21 Reniers et al,22 Kertzscher et al,25 Cherpak et al46 and Nakano et al.99
Wrong patient identification could be detected, for example, by comparing the patient's anatomy acquired during the treatment with the anatomy from the treatment plan.
If digital imaging and communications in medicine (DICOM) was exported independently to the afterloader and the IVD data acquisition system (see second paragraph in the Automation section.).
If IVD dosemeter probe is not attached to source applicator (see last paragraph in the Dosemeter placement tools section).
May be detected with source localization and applicator reconstruction (see Source localization and real-time applicator reconstruction section), dedicated algorithms for real-time IVD (see fourth paragraph in the Knowledge of dosemeter position section) and positioning technology (see third paragraph in the Knowledge of dosemeter position section).
May be detected by means of comparisons between measured and expected dose rates or source positions.
Relevant if treatment planning system dose calculations are inaccurate, for example, if significant tissue heterogeneity and/or dose field perturbation effects are insufficiently accounted for by TPS (see seventh paragraph in Dosimeter placement tools section).