2009
DOI: 10.1016/j.jvir.2009.04.037
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Guidelines for Patient Radiation Dose Management

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Cited by 386 publications
(280 citation statements)
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References 33 publications
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“…This difference may not have been as pronounced if GA had been used in both groups. Radiation doses for both procedures were well within safe ranges (\3% of accepted Dose Area Product threshold of 500 Gy cm 2 ) [25]. The site of disc prolapse was similarly distributed in both treatment arms.…”
Section: Discussionmentioning
confidence: 68%
“…This difference may not have been as pronounced if GA had been used in both groups. Radiation doses for both procedures were well within safe ranges (\3% of accepted Dose Area Product threshold of 500 Gy cm 2 ) [25]. The site of disc prolapse was similarly distributed in both treatment arms.…”
Section: Discussionmentioning
confidence: 68%
“…The number of procedures performed annually throughout the world has increased over the past 20 years [1]. The benefits of interventional radiology to patients are both extensive and beyond dispute, but many of these procedures also have the potential to produce patient radiation doses high enough to cause radiation effects and occupational doses to interventional radiologists high enough to cause concern [1][2][3][4]. A joint SIR-CIRSE guideline on patient radiation management has addressed patient issues [3].…”
Section: Introductionmentioning
confidence: 99%
“…If meaningful changes appear, proper medical treatment should be provided and DAP dose area product, CAG coronary angiography, PCI percutaneous transluminal coronary intervention continuous trace investigation with hospital consultation is needed. If a patient who has exceeded action levels receives additional radiation exposure within 60 days, the total dose of all exposures should be evaluated [18]. Particular caution is needed in coronary angiography when additional exams to check prognosis are performed because of the additional exposure of the same area.…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, the US FDA requires that all angiographic equipment that has been sold in the USA after June 2006 must measure, indicate and record reference doses including air kerma rate and cumulative air kerma [10]. The cumulative dose is an especially useful index for evaluating risk of deterministic radiation effect in patients [11]. The cumulative data represent the total entrance dose from the angiography equipment to patients.…”
Section: Radiation Dose Monitoringmentioning
confidence: 99%