Source:http://linkedlifedata.com/resource/pubmed/id/14627852
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
12
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pubmed:dateCreated |
2003-11-20
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pubmed:abstractText |
Due to its high success rate and non-invasive character, an increasing demand for radioiodine therapy can be seen. This study was conducted to determine whether standardized 131I activities can be used to facilitate management of patients with hyperthyroid disorder or whether a pre-therapeutic radioiodine test is advisable to determine an adequate therapeutic activity. The therapeutic uptake of 218 patients with benign thyroid disorders were determined and compared with 24 h and 48 h test uptake measurements as well as with calculated standard uptake values. Since there is a linear relationship between iodine uptake and delivered radiation dose, the effect of the different therapeutic approaches on the latter parameter was analysed. Special care was taken to assess possible differences between the various thyroid disorders. A mean deviation between pre-therapeutic test uptake and actual therapeutic uptake of 14.7% was observed in contrast to one of 29.1% when using disease specific standard values per millilitre of thyroid tissue. Furthermore, the proportion of patients with large deviations of more than 40% increased drastically when using standard uptake values (with radioiodine test, 4.1%; with standard values, 18.8%). In conclusion, the dosimetric approach with a pre-therapeutic radioiodine test proved to be the most accurate therapeutic procedure. Both the 24 h and 48 h test uptake measurements gave analogous results and yielded a correlation coefficient of 0.91 when compared with the therapeutic uptake. While it may be tempting to use standard activities to facilitate patient management, the findings of this study confirm that, for precise therapy planning, a pre-therapeutic radioiodine test is advised. Since no significant difference could be found between the 24 h and 48 h test uptake values, an early measurement 24 h after administration of the test activity is recommended.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0143-3636
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
24
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1247-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:14627852-Female,
pubmed-meshheading:14627852-Humans,
pubmed-meshheading:14627852-Hyperthyroidism,
pubmed-meshheading:14627852-Iodine Radioisotopes,
pubmed-meshheading:14627852-Male,
pubmed-meshheading:14627852-Middle Aged,
pubmed-meshheading:14627852-Radiometry,
pubmed-meshheading:14627852-Radiopharmaceuticals,
pubmed-meshheading:14627852-Radiotherapy Dosage,
pubmed-meshheading:14627852-Radiotherapy Planning, Computer-Assisted,
pubmed-meshheading:14627852-Reproducibility of Results,
pubmed-meshheading:14627852-Sensitivity and Specificity
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pubmed:year |
2003
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pubmed:articleTitle |
Radioiodine therapy in patients with hyperthyroid disorder: standard versus dosimetric activity application.
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pubmed:affiliation |
Department of Nuclear Medicine, University Hospital Aachen, Aachen, Germany. preinhartz@compuserve.com
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Comparative Study,
Controlled Clinical Trial,
Validation Studies
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