Abstract
Prussian blue (PB) is an antidote used to treat patients with confirmed or suspected internal contamination with radioactive cesium (137Cs), radioactive thallium (201Tl), or nonradioactive thallium. PB was introduced as an antidote in the USA for drug preparedness over concerns of the possibility of bioterrorism (e.g., radiologic dispersing device or “dirty bomb”) and other radiation event. The dosing for adolescents over 12 years old and adults is 3 g taken orally three times daily. In critically ill patients who cannot swallow the capsules, these may be opened and administered by orogastric or nasogastric tube. PB should be used with caution in patients with a history of gastrointestinal obstruction, peptic ulcer disease, preexisting cardiac arrhythmias, or electrolyte imbalances.
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Grading System for Levels of Evidence Supporting Recommendations in Critical Care Toxicology, 2nd Edition
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I.
Evidence obtained from at least one properly randomized controlled trial.
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II-1
Evidence obtained from well-designed controlled trials without randomization.
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II-2
Evidence obtained from well-designed cohort or case–control analytic studies, preferably from more than one center or research group.
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II-3
Evidence obtained from multiple time series with or without the intervention. Dramatic results in uncontrolled experiments (such as the results of the introduction of penicillin treatment in the 1940s) could also be regarded as this type of evidence.
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III
Opinions of respected authorities, based on clinical experience, descriptive studies, and case reports, or reports of expert committees.
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Dubé, PA., Gosselin, S. (2016). Prussian Blue. In: Brent, J., Burkhart, K., Dargan, P., Hatten, B., Megarbane, B., Palmer, R. (eds) Critical Care Toxicology. Springer, Cham. https://doi.org/10.1007/978-3-319-20790-2_167-1
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