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more on capsules!
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From: Bass, Billy G.[SMTP:bgb3@mhg.edu]
Sent: Wednesday, October 01, 1997 10:37 AM
To: Multiple recipients of list
Subject: Re: I-131 procedure bioassay requirement
Regarding the bioassay requirement, we had a case where a
technologist
transferred I-131 capsules from the shipping container to the
dosing
container without using the hood (capsules are sealed, right?).
That
individual received an elevated thyroid burden of iodine. I
don't remember
the exact level, but the effective dose was estimated at about 1
rem. Since
then all handling of capsules (diagnostic or therapeutic) are
performed in
an approved hood. In a related incident, some of our nuclear
physicians
felt that they did not have to get the bioassays because "they
did not
participate directly in the administration of the iodine". The
NRC
disagreed, and a number of us got an invitation to
King-of-Prussia for an
enforcement conference, a fine, and some very unpleasant
publicity which the
Board of Directors did no appreciate. To quote the old adage "a
word to the
wise..."
Bill Bass
RSO Washington Hospital Center
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From: radsafe%romulus.ehs.uiuc.edu
To: Multiple recipients of list
Subject: Re: I-131 procedure bioassay requirement
Date: Tuesday, September 30, 1997 5:54PM
Dear Radsafers,
The discussions on the need for bioassays when using I-131
capsules has been
restricted purely to the legal requirements under the various US
legislation.
No one has mentioned whether they have ever detected a
significant internal
contamination problem from the administration of I-131 capsules,
from their
routine bioassays.
Bioassays after I-131 administration are not legally required in
NSW,
Australia, and are not routinely performed. Does any one have
data which
would suggest that we should be doing bioassays routinely?
Regards
Richard
Richard Smart PhD
Department of Nuclear Medicine
St. George Hospital
Kogarah, NSW 2217
Australia
Tel:61 2 9350 3112
Fax:61 2 9350 3991
Email:R.Smart@unsw.edu.au