EANM Dosimetry Committee guidance document: good practice of clinical dosimetry reporting. (Articolo in rivista)

Type
Label
  • EANM Dosimetry Committee guidance document: good practice of clinical dosimetry reporting. (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Alternative label
  • Lassmann M, Chiesa C, Flux G, Bardiès M; EANM Dosimetry Committee. (2010)
    EANM Dosimetry Committee guidance document: good practice of clinical dosimetry reporting.
    in European journal of nuclear medicine and molecular imaging (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Lassmann M, Chiesa C, Flux G, Bardiès M; EANM Dosimetry Committee. (literal)
Pagina inizio
  • 192 (literal)
Pagina fine
  • 200 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 38 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • -Department of Nuclear Medicine, University of Würzburg, Oberdürrbacher Str. 6, 97080, Würzburg, Germany. -Institute of Neurobiology and Molecular Medicine-ARTOV, CNR via Fosso del Cavaliere 100, 00133-Rome, Italy. (literal)
Titolo
  • EANM Dosimetry Committee guidance document: good practice of clinical dosimetry reporting. (literal)
Abstract
  • Many recent publications in nuclear medicine contain data on dosimetric findings for existing and new diagnostic and therapeutic agents. In many of these articles, however, a description of the methodology applied for dosimetry is lacking or important details are omitted. The intention of the EANM Dosimetry Committee is to guide the reader through a series of suggestions for reporting dosimetric approaches. The authors are aware of the large amount of data required to report the way a given clinical dosimetry procedure was implemented. Another aim of this guidance document is to provide comprehensive information for preparing and submitting publications and reports containing data on internal dosimetry. This guidance document also contains a checklist which could be useful for reviewers of manuscripts submitted to scientific journals or for grant applications. In addition, this document could be used to decide which data are useful for a documentation of dosimetry results in individual patient records. This may be of importance when the approval of a new radiopharmaceutical by official bodies such as EMA or FDA is envisaged. (literal)
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