Abstract

Use of radiation for medical examinations and tests is the largest manmade source of radiation exposure. No one can doubt the immense clinical and scientific benefits of imaging to the modern practice of medicine. Every radiological and nuclear medicine examination confers a definite (albeit low) long-term risk of cancer, but patients undergoing such examinations often receive no or inaccurate information about radiological dose exposure and corresponding risk directly related to the radiological dose received. Too detailed information on radiological dose and risk may result in undue anxiety, but information "economical with the truth" may violate basic patients' rights well embedded in ethics (Oviedo convention 1997) and law (97/43 Euratom Directive 1997). Informed consent is a procedure needed to establish a respectful and ethical relation between doctors and patients. Nevertheless, in an "ideal" consent process, the principle of patient autonomy in current radiological practice might be reinforced by making it mandatory to obtain explicit and transparent informed consent form for radiological examination with high exposure (≥ 500 chest x-rays). The form may spell-out the type of examination, the exposure in effective dose (mSv), derived from reference values in guidelines or – better – from actual values from their department. The dose equivalent might be also expressed in number of chest radiographs and the risk of cancer as number of extra cases in the exposed population, derived from most recent and authorative guidelines (e.g., BEIR VII Committee, release 2006). Common sense, deontological code, patients'rights, medical imaging guidelines, Euratom law, all coherently and concordantly encourage and recommend a justified, optimized, responsible and informed use of testing with ionizing radiation. Although the idea of informed consent for radiation dose does not seem to be on the immediate radar screen at least in the US, the current practice clashes against these guidelines and laws.

Highlights

  • Every radiological and nuclear medicine examination confers a definite long-term risk of cancer, but patients undergoing such examinations often receive no or inaccurate information about these risks, directly related to the radiological dose received [1,2,3,4,5]

  • A too detailed information on radiological dose and risk may result in undue anxiety, but an information "economical with the truth" may violate basic patients' rights well embedded in ethics (Oviedo convention 1997) [6] and law (97/43 Euratom Directive 1997) [7]

  • One of the three fundamental principles of the "charter of medical professionalism" in the new millennium is the principle of patient autonomy: "Physicians must empower their

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Summary

Background

Every radiological and nuclear medicine examination confers a definite (albeit low) long-term risk of cancer, but patients undergoing such examinations often receive no or inaccurate information about these risks, directly related to the radiological dose received [1,2,3,4,5]. The clinical information provided by the 4 protocols is basically the same, and can be obtained with no radiation exposure by ultrasound or magnetic resonance imaging [24] This simple, evidence based communication strategy, if used when obtaining informed consent, will increase the currently suboptimal level of radiological awareness among doctors and patients. Radiological informed consent : towards the perfect legal storm Patients undergoing common imaging examinations involving significant exposure have little or no awareness about radiological dose exposure (and corresponding risk). This ineffective communication poses significant ethical problems, with high litigation potential.

Valentin J
26. Gibbons RJ
Findings
28. Redberg RF
Full Text
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