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Category:Report
MONTHYEARML24221A1452024-08-0808 August 2024 ACMUI Subcommittee on Financial Assurance Draft Report, August 8 2024 ML24185A2682024-07-0303 July 2024 ACMUI Training and Experience (T&E) for All Modalities Subcommittee Final July 3, 2024 ML24170A3162024-06-18018 June 2024 Advisory Committee on Medical Uses of Isotopes (ACMUI) Subcommittee on Extravasations Final Report June 17 2024 ML24163A4042024-06-11011 June 2024 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Extravasations, Draft Report, June 11, 2024 ML24177A1532024-06-11011 June 2024 ACMUI, Subcommittee on Extravasations, Draft Report, June 11, 2024 ML24116A2662024-04-25025 April 2024 Subcommittee on Yttrium-90 Microsphere Brachytherapy Eye90 Microspheres Device, Final Report, Dated April 25, 2024 ML24115A1402024-04-24024 April 2024 ACMUI Spring 2024 Liberty Vision Y-90 Disc and Iwand Ophthalmic System Subcommittee Final Report Dated April 24 2024 ML24120A2452024-04-24024 April 2024 ACMUI Spring 2024 Eye90 Subcommittee Final Report, Dated April 24 2024 ML24116A2632024-03-16016 March 2024 Subcommittee on Yttrium-90 Microsphere Brachytherapy Eye90 Microspheres Device, Draft Report, Dated March 16 2024 ML24101A4082024-03-14014 March 2024 Medical Events Subcommittee Report ACMUI 2024 Spring ML24115A0752024-03-11011 March 2024 ACMUI Spring 2024 Liberty Vision Y-90 Disc and Iwand Ophthalmic System Subcommittee Draft Report Dated March 11 2024 ML24093A0762024-03-0606 March 2024 Advisory Committee on the Medical Use of Isotopes (Acmui), Subcommittee Onakesis Galaxy Rti Draft Licensing Guidance, Draft Report, March 6, 2024 ML24068A0492024-02-0909 February 2024 ACMUI Fall 2023 Medical Events Subcommittee Report Final February 9 2024 ML24040A1292023-10-23023 October 2023 ACMUI Fall 2023 Medical Events Subcommittee Report Final October 23, 2023 ML24040A1032023-09-21021 September 2023 ACMUI Fall 2023 Medical Events Subcommittee Report Draft September 21, 2023 ML23136A4582023-05-17017 May 2023 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on the Decommissioning Financial Assurance for Sealed and Unsealed Radioactive Materials, Final Report, May 17, 2023 ML23136A4592023-05-17017 May 2023 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Training and Experience for All Modalities, Final Report, May 17, 2023 ML22353A0542022-12-19019 December 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Y-90 Medical Events, Final Report, December 19, 2022 ML22353A0532022-12-19019 December 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Emerging Medical Technologies/Rubidium-82 Generator Rulemaking Draft Regulatory Basis, Final Report, December 19, 2022 ML22322A1832022-11-18018 November 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Y-90 Medical Events, Draft Report, November 18, 2022 ML22322A1572022-11-18018 November 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Emerging Medical Technologies/Rubidium-82 Generator Rulemaking Draft Regulatory Basis, Draft Report, November 18, 2022 ML22021B2982022-01-21021 January 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Alpha Dart, Review and Comment on Draft Licensing Guidance Alpha Tau Alpha Dart Manual Brachytherapy, Final Report ML22021B2992022-01-21021 January 2022 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on RG 8.39, Release of Patients Administered Radioactive Materials, Review and Comment on the Draft Civaderm Device Licensing Guidance, Final Report, January 21, 2022 ML22021B3002022-01-21021 January 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on RG 8.39, Release of Patients Administered Radioactive Material, Review and Comment on Draft Proposed Revision 2 to Regulatory Guide 8.39, Final Report, January 21, ML21287A6312021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Emerging Radiopharmaceutical Therapy Knowledge Requirements in Theranostics Subcommittee, Final Report, October 14, 2021 ML21288A1262021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Radionuclide Generator Knowledge and Practice Requirements, Final Report, October 14, 2021 ML21288A1272021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommitee on Medical Events, Final Report, October 14, 2021 ML21264A0772021-10-0404 October 2021 Me Subcommittee Report 10-4-21 Final ML21288A1252021-09-16016 September 2021 Advisory Committee on the Medical Uses of Isotopes (Acmui), Final Report, Subcommittee Review and Comments on NRC Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting ML21287A0742021-07-30030 July 2021 Advisory Committee on the Medical Uses of Isotopes (Acmui), Final Report, Subcommittee Review and Comments on NRC Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting ML21223A0852021-07-30030 July 2021 U.S. Nuclear Regulatory Commission Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting for ACMUI Review ML21227A0012021-06-0101 June 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Abnormal Occurrence Subcommittee, Proposed Revisions to Abnormal Occurrence Medical Event Criteria, Final Report, June 1, 2021 ML20279A8032020-09-24024 September 2020 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Medical Events, Final Report, September 24, 2020 ML20279A6792020-08-11011 August 2020 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Medical Events, Draft Report, August 11, 2020 ML20125A1482020-05-0404 May 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) COVID-19 Subcommittee, Final Report, May 4, 2020 ML20118D0142020-04-30030 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) April 30, 2020 Teleconference Meeting Ebinder ML20125A1452020-04-27027 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) COVID-19 Subcommittee, Draft Report, April 27, 2020 ML20097F4762020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Patient Intervention, Final Report, April 6, 2020 ML20097F5322020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Bylaws Subcommittee, Final Report, April 6, 2020 ML20097F6252020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Interventional Radiology Subcommittee, Final Report, April 6, 2020 ML20085H2672020-03-25025 March 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Regulatory Guide 8.39, Release of Patients Administered Radioactive Material, Draft Final, Revision 1 (Phase 1), Final Report, March 25, 2020 ML20075A0282020-03-0505 March 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Patient Intervention, Draft Report, March 5, 2020 ML20075A0302020-02-25025 February 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Interventional Radiology Subcommittee, Draft Report, February 25, 2020 ML19325E6712019-11-18018 November 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Annual Report FY2019 ML19316E0672019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Extravasation, Final Report, October 23, 2019 ML19296D1462019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on ACMUI Institutional Memory, Final Report, October 23, 2019 ML19297E9492019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Medical Event Reporting, Review of FY2018, Final Report, October 23, 2019 ML19309D4022019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Xcision Gammapod Licensing Guidance, Final Report, October 23, 2019 ML19297E8332019-08-19019 August 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Xcision Gammapod Licensing Guidance, Draft Report, August 19, 2019 ML19297H3162019-08-15015 August 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Extravasation, Draft Report, August 15, 2019 2024-08-08
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MONTHYEARML24163A4042024-06-11011 June 2024 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Extravasations, Draft Report, June 11, 2024 ML24115A1402024-04-24024 April 2024 ACMUI Spring 2024 Liberty Vision Y-90 Disc and Iwand Ophthalmic System Subcommittee Final Report Dated April 24 2024 ML24120A2452024-04-24024 April 2024 ACMUI Spring 2024 Eye90 Subcommittee Final Report, Dated April 24 2024 ML23136A4592023-05-17017 May 2023 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Training and Experience for All Modalities, Final Report, May 17, 2023 ML22353A0542022-12-19019 December 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Y-90 Medical Events, Final Report, December 19, 2022 ML22322A1832022-11-18018 November 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Y-90 Medical Events, Draft Report, November 18, 2022 ML22322A1572022-11-18018 November 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Emerging Medical Technologies/Rubidium-82 Generator Rulemaking Draft Regulatory Basis, Draft Report, November 18, 2022 ML22021B2992022-01-21021 January 2022 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on RG 8.39, Release of Patients Administered Radioactive Materials, Review and Comment on the Draft Civaderm Device Licensing Guidance, Final Report, January 21, 2022 ML22021B3002022-01-21021 January 2022 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on RG 8.39, Release of Patients Administered Radioactive Material, Review and Comment on Draft Proposed Revision 2 to Regulatory Guide 8.39, Final Report, January 21, ML21288A1272021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommitee on Medical Events, Final Report, October 14, 2021 ML21287A6312021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Emerging Radiopharmaceutical Therapy Knowledge Requirements in Theranostics Subcommittee, Final Report, October 14, 2021 ML21288A1262021-10-14014 October 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Radionuclide Generator Knowledge and Practice Requirements, Final Report, October 14, 2021 ML21288A1252021-09-16016 September 2021 Advisory Committee on the Medical Uses of Isotopes (Acmui), Final Report, Subcommittee Review and Comments on NRC Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting ML21287A0742021-07-30030 July 2021 Advisory Committee on the Medical Uses of Isotopes (Acmui), Final Report, Subcommittee Review and Comments on NRC Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting ML21223A0852021-07-30030 July 2021 U.S. Nuclear Regulatory Commission Staff Preliminary Evaluation of Radiopharmaceutical Extravasation and Medical Event Reporting for ACMUI Review ML21227A0012021-06-0101 June 2021 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Abnormal Occurrence Subcommittee, Proposed Revisions to Abnormal Occurrence Medical Event Criteria, Final Report, June 1, 2021 ML20279A8032020-09-24024 September 2020 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Medical Events, Final Report, September 24, 2020 ML20279A6792020-08-11011 August 2020 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on Medical Events, Draft Report, August 11, 2020 ML20125A1482020-05-0404 May 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) COVID-19 Subcommittee, Final Report, May 4, 2020 ML20118D0142020-04-30030 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) April 30, 2020 Teleconference Meeting Ebinder ML20125A1452020-04-27027 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) COVID-19 Subcommittee, Draft Report, April 27, 2020 ML20097F4762020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Patient Intervention, Final Report, April 6, 2020 ML20097F5322020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Bylaws Subcommittee, Final Report, April 6, 2020 ML20097F6252020-04-0606 April 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Interventional Radiology Subcommittee, Final Report, April 6, 2020 ML20075A0282020-03-0505 March 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Patient Intervention, Draft Report, March 5, 2020 ML20075A0302020-02-25025 February 2020 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Interventional Radiology Subcommittee, Draft Report, February 25, 2020 ML19316E0672019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Extravasation, Final Report, October 23, 2019 ML19296D1462019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (Acmui), Subcommittee on ACMUI Institutional Memory, Final Report, October 23, 2019 ML19297E9492019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Medical Event Reporting, Review of FY2018, Final Report, October 23, 2019 ML19309D4022019-10-23023 October 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Xcision Gammapod Licensing Guidance, Final Report, October 23, 2019 ML19297E8332019-08-19019 August 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Xcision Gammapod Licensing Guidance, Draft Report, August 19, 2019 ML19171A2222019-06-19019 June 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Draft Proposed Regulatory Guide 8.39, Release of Patients Administered Radioactive Material, Revision 1 (Phase 1), Final Report, June 19, 2019 ML19143A3672019-05-23023 May 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Draft Proposed Regulatory Guide 8.39, Release of Patients Administered Radioactive Materials, Revision 1 (Phase 1), Draft Report. May 23, 2019 ML19130A1032019-05-0909 May 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on Yttrium-90 Microsphere Brachytherapy Sources and Devices Licensing Guidance, Revision 10, Final Report, May 9, 2019 ML19126A2962019-05-0606 May 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Germanium-68/Gallium-68 Generator Licensing Guidance, Revision 1, Final Report, May 6, 2019 ML19126A2972019-04-10010 April 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the ACMUI Bylaws, Final Report, April 10, 2019 ML19091A2422019-03-25025 March 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Appropriateness of Medical Event Reporting, Interim Report, March 25, 2019 ML19091A2402019-03-11011 March 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Draft Revision 10 of the Yttrium-90 Microspheres Brachytherapy Sources and Devices Therasphere and SIR-Spheres Licensing Guidance, Draft Report, March 11, 2019 ML19091A2382019-03-0707 March 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the ACMUI Bylaws, Draft Report, March 7, 2019 ML19058A5982019-02-27027 February 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee Report on Training and Experience (T&E) Requirements for All Modalities, Final Report, February 27, 2019 ML19039A1132019-02-0707 February 2019 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee Report on Training and Experience (T&E) for All Modalities, Draft Report, February 7, 2019 ML19091A2562018-11-30030 November 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Subcommittee on the Germanium-68/Gallium-68 Generator Licensing Guidance, Revision 1, Draft Report, November 30, 2018 ML18253A1242018-08-31031 August 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Comments on the Draft Revision to the Leksell Gamma Knife Perfexion and Leksell Gamma Knife Icon Licensing Guidance, Draft Report, August 31, 2018 ML18186A5172018-07-0505 July 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Comments on the Draft T&E Secy Paper, Draft Report, July 5, 2018 ML18177A4512018-06-26026 June 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Nursing Mother Guidelines for Medical Administration of Radioactive Materials, Final Report, June 26, 2018 ML18071A4132018-02-27027 February 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Physical Presence Requirements for the Leksell Gamma Knife Icon, Final Report, February 27, 2018 ML18033B0332018-02-0101 February 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Physical Presence Requirements for the Leksell Gamma Knife Icon, Revised Draft Report, February 1, 2018 ML18033B0342018-02-0101 February 2018 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Nursing Mother Guidelines for Medical Administration of Radioactive Materials, Revised Draft Report, February 1, 2018 ML17293A2482016-09-13013 September 2016 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Comments on the Yttrium-90 Microsphere Brachytherapy Licensing Guidance, Draft Report, September 13, 2016 ML17293A2492016-09-0808 September 2016 Advisory Committee on the Medical Uses of Isotopes (ACMUI) Comments on the Draft Northstar Molybdenum-99/Technetium-99m Generator (Radiogenixtm) Licensing Guidance, Draft Report, September 8, 2016 2024-06-11
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U.S. Nuclear Regulatory Commission (NRC)
Advisory Committee on the Medical Use of Isotopes (ACMUI)
Subcommittee Review and Comments on Draft Proposed Regulatory Guide 8.39, Release of Patients Administered Radioactive Materials, Revision 1 (Phase 1)
Final Report Submitted: June 19, 2019 Subcommittee Members:
Dr. Vasken Dilsizian Ms. Melissa Martin Dr. A. Robert Schleipman Mr. Michael Sheetz (Chair)
Ms. Megan Shober Ms. Laura Weil NRC Staff Resource: Dr. Said Daibes-Figueroa Charge During the September 20-21, 2018 ACMUI Meeting, ACMUI Chairman, Dr. Christopher Palestro, established a subcommittee to review the NRC staffs draft proposed revision to Regulatory Guide (RG) 8.39, Release of Patients Administered Radioactive Materials.
Background
The NRCs current RG 8.39, Revision 0, was issued in April 1997, following the rule change in 10 CFR 35.75 to allow the release of patients administered radioactive material on a solely dose-based basis. Since that time, there have been several challenges to the appropriateness of the release criteria and the associated precautions that are required to be provided to minimize radiation exposure to other individuals from the released patient. The NRC requested public comments on the Patient Release Program in 2017 (Docket ID NRC-2017-0094). The NRC also created a webpage to provide potential patients with information on radioactive iodide (RAI) treatment procedures so that the patients will understand the reason for the procedures, the process, and how to reduce radiation exposure to others (https://www.nrc.gov/materials/miau/patient-release.html).
NOTE: RG 8.39 is being revised in two phases. This Phase 1 revision of RG 8.39, updates the patient release guidance, including information for patient instructions and updates to Table 3, Activities of Radiopharmaceuticals that Require Instructions and Records When Administered to Patients who are Breast-Feeding an Infant or Child. In Phase 2, the dosimetric equations, methodologies, and tables used to calculate dose to members of the public from released patients will be updated. The following Subcommittee comments and recommendations only pertain to the Phase 1 revision.
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Changes and Recommendations to Regulatory Guidance Considered by the Subcommittee General Comment:
The Subcommittee supports the addition of a Table of Contents to the RG and expanding the section on Content of Instructions to include subsections on Pretreatment Discussions, Patient Precautions, Patient Instructions, and Patient Acknowledgement of Instructions.
Specific Comments:
Pg 1, Under
Introduction:
Change the heading Applicable Regulations to Regulations.
Pg 2, Under Purpose of Regulatory Guide, 1st sentence: Replace the words and to provide guidance to applicants with and to provide guidance to licensees.
Pg 4, Under Reason for Revision: Change 2nd sentence By updating the NRC guidance with this information, the patient will be better informed and can make better choices when following the instructions to read By updating the NRC guidance with this information, the licensee will be better informed on what instructions and options should be provided to the patient.
Pg 5, Under Background, last sentence: Delete reference to Staff Regulatory Guidance Position 2.3, as it does not pertain to breastfeeding infants or children.
Pg 6, Section 1.1 Release of Patients Based on the Administered Activity, last paragraph: Delete reference to Staff Regulatory Guidance Position 1.1, as it does not pertain to breastfeeding infants or children.
Pg 7, Table 1. Activities and Dose Rates for Authorizing Patient Release: This table should be updated to include the new and potential radionuclides used in medicine.
Pg 9, Table 2. Activities and Dose Rates above Which Instructions Should be Given When Authorizing Patient Release: This table should be updated to include the new and potential radionuclides used in medicine.
Pg 9, Table 2. Activities and Dose Rates above Which Instructions Should be Given When Authorizing Patient Release, Notes: Delete the sentences Although the NRC does not regulate nonbyproduct material, this RG includes information on nonbyproduct material for the licensees convenience. Agreement State regulations may vary.
Pg 10, Section 2.2 Additional Instructions for Release of Patients Who Could be Breastfeeding after Their Release, 2nd paragraph: Change the sentence The patient should also be informed if breastfeeding would have no consequences on the infant or child. to read The patient should also be informed if breastfeeding would not likely result in consequences to the infant or child.
Pg 11, Table 3. Activities of Radiopharmaceuticals That Require Instructions and Records When Administered to Patients Who Are Breastfeeding an Infant or Child: This table should be 2 of 6
updated to include the radionuclides, activities, and recommended duration of interruption of breastfeeding as contained in the ACMUI Subcommittee report on Nursing Mother Guidelines for the Medical Administration of Radioactive Materials, Final Report, January 31, 2019.
Pg 11, Table 3. Activities of Radiopharmaceuticals That Require Instructions and Records When Administered to Patients Who Are Breastfeeding an Infant or Child, Notes: Delete the sentences Although the NRC does not regulate nonbyproduct material, this RG includes information on nonbyproduct material for the licensees convenience. Agreement State regulations may vary.
Pg 12, Section 2.3 Content of Instructions, 2nd paragraph: Add currently after I-131 is. Add iodine before (I)-125. Delete the sentence None of these radioisotopes have the high-energy gamma emission and volatility of I-131; therefore they present a lower external radiation hazard than I-131 does. Add the treating before physician.
Change the last sentence The instructions should include the name of a knowledgeable person and his or her telephone number, to contact if the patient has any questions to read The instructions should include a telephone number, to contact if the patient has any questions.
Pg 13, Section 2.3.1 Pretreatment Discussions on the Administration of Radiopharmaceuticals:
Change the 1st paragraph to read Engaging the patient early in the treatment process (i.e.,
during treatment planning) may help the licensee better familiarize the patient and caregiver with the treatment procedures, posttreatment radiation safety precautions and protective measures to minimize radiation exposure to other individuals. This discussion should also include medical issues such as complications, side effects, dietary and medication changes, as appropriate. Additionally, early engagement with the patient allows the patient to ask the licensee questions that will help him or her comply with the release instructions. It also allows the licensee to determine whether the patient will be able to follow the release instructions.
Pg 13, Section 2.3.1, i: Add hotel to the list of examples of post treatment lodging the patient may use.
Pg 13, Section 2.3.1, ii: Delete 2. If the patient is driving, will he or she be too impaired to drive?
Pg 13, Section 2.3.1, ii: Delete 3. If the patient is driving, will he or she be driving alone (preferred)?
Pg 13, Section 2.3.1, ii: 4: Add the sentence Emphasis should be made to minimize the number of traveling companions.
Pg 13, Section 2.3.1, iv: Delete i. Are there any concerns about breastfeeding or pregnancy?
Pg 13, Section 2.3.1: Add the pretreatment discussion topic Potential restrictions on burial or cremation should the patient passes away within a certain period of time following treatment.
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Pg 14, Section 2.3.1, last paragraph: Add the sentence It will also allow the licensee to assess the patients capacity to understand the procedure and precautions.
Pg 14, Section 2.3.2 Patient Precautions, a: Add the precaution If the patient is traveling with other individuals to the post treatment lodging location, emphasis should be made to minimize the number of traveling companions and to maximize the distance from the patient.
Pg 14, Section 2.3.2, a. (7): Separate the patient precaution Emphasize abstention from all forms of intimate contact. Advise the patient on the recommended length of time he or she should wait before becoming pregnant to minimize radiation exposures to a developing fetus. into two different instructions.
Pg 14, Section 2.3.2, a. (8): Replace the word breast milk with urine.
Pg 14, Section 2.3.2, a. (9): Replace the word Emphasize with Evaluate.
Pg 14, Section 2.3.2, a. (9): Change the last sentence Holding trash to allow for radioactive decay is important because the landfill may detect the radiation and send the trash back to the patient. To read Holding trash to allow for radioactive decay may be important if the landfill will detect the radiation and send the trash back to the patient.
Pg 15, Section 2.3.2, b.: Add the sentence Provide information to a family member or caregiver to contact the treating medical facility if the patient has a medical emergency or passes away.
Pg 15, Section 2.3.2, 1st paragraph, last sentence: Add the word likely before exceed 5 mSv (0.5 rem).
Pg 15, Section 2.3.2, 2nd paragraph, last sentence: Change the word key to important.
Pg 15, Section 2.3.2, 4th paragraph, first sentence: Change the words 3 months or more to several weeks or months.
Pg 15, Section 2.3.3 Patient Instruction, 1st paragraph, Change the last two sentences to read The list below provides some basic posttreatment instructions that the patient may need to follow for managing radiation exposure to other individuals. The instructions should always be tailored to the specific patient situation and type and amount of radioactive material administered or implanted.
Pg 16, Section 2.3.3: Add Minimize the amount of time spent near other people, especially children and pregnant women to the list of instructions.
Pg 16, Section 2.3.4 Patient Acknowledgement of Instructions, c. (4): Delete in accordance with NRC, State, and local requirements.
Pg 16, Section 2.3.4, c. (6): Change the sentence contact information (i.e., the name and telephone number of a knowledgeable person) in the event that questions arise during the recovery 4 of 6
period to contact information in the event that questions arise about the radiation safety instruction.
Pg 17, Section 2.4 Death of a Patient Following Radiopharmaceutical Administration or Implants, 1st paragraph: Add the word therapeutic before quantity of radioactive material. Add a second sentence to read The RSO should perform an assessment of the type and amount of retained activity, based on the patient records.
Pg 17, Section 2.4, 1st paragraph: Begin a new paragraph with If the death occurs in a hospital to read If the death occurs in a hospital, access to the room occupied by the deceased should be controlled until the room has been surveyed, and decontaminated if necessary. A specified form of identifier (e.g., bracelet, badge) should be used to identify the radioactive body. A body bag may need to be used to contain the leakage of radioactive material. To minimize external radiation, the body may need to be retained in a secured area. Radiation safety procedures to be applied in practice for handling the body should be determined in close consultation with the RSO at the facility where the therapy was administered.
Pg 17, Section 2.4, 3rd paragraph: Begin a new paragraph after the sentence Wearing a face shield or eye protection and a face mask can prevent an intake of airborne material inadvertently released during the cutting or movement of radioactive tissue or organs. to read The RSO should notify the morgue or funeral home that the body contains therapeutic quantities of radioactive material and provide precautions to minimize radiation exposures and radioactive contamination for embalming and burial. These include the use of gloves and protective clothing and proper cleaning of equipment.
Pg 17, Section 2.4: Begin a new paragraph after the one above to read If the body is to be cremated, the RSO should provide precautions on handling the body to crematorium employees who may receive external exposure from the radioactive body or from contamination of the crematorium or internal exposure from inhalation of radioactive particles while handling the ashes. A proportion of the activity retained will appear in cremated remains and may be a concern, particularly in the case of long-lived radionuclides, that will require specified controls. The main concern is in regard to the scattering of ashes, although contact dose rates with the container may have to be considered if cremation takes place shortly after administration of the treatment.
Pg 17, Section 2.4, 4th paragraph: Delete the sentences Bodies that contain gamma-emitting radionuclides will result in some external exposure to crematorium employees. and Each crematorium should maintain records of the type and activity in bodies cremated, when known (Ref. 9).
Pg 17, Section 2.4, last paragraph: Change the last paragraph to read The RSO should be consulted to determine the amount of activity remaining in the deceased patient and a determination should be made if there are any state or municipal restrictions on cremation.
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Pg 18, Section 2.5 Precautions for Long-Lived Contaminants in Radiopharmaceutical Therapy, 1st sentence: Change the words radioactive decay to their method of production.
Other Recommendations
- 1. In the Patient Precautions and Instructions Sections, it should be emphasized that the major source of radiation dose to other individuals will be from external exposure from the patient (Ref 1). After completion of the Phase II revisions, these sections should also include the recommended time period for following the precautions.
- 2. While there is adequate guidance on the precautions to take to minimize radiation exposure for post mortem activities of a patient who has died after being administered a therapeutic quantity of radioactive material (Ref 2, 3), there is little or no consistent guidance on what retained activity or time period when the precautions should be followed. The Subcommittee recommends that a dose based model be developed to provide guidance on when precautions or restrictions would be appropriate following the death of a patient administered a therapeutic quantity of radioactive material.
References
- 1. ICRP Publication 94, Release of Patients After Therapy with Unsealed Radionuclides, 2004
- 2. NCRP Report No. 155, Management of Radionuclide Therapy Patients, 2006
- 3. Canadian Nuclear Safety Commission, Radiation Protection Guidelines for Safe Handling of Decedents, Regulatory document REGDOC-2.7.3, 2018 The ACMUI unanimously approved this report, during its public teleconference meeting on June 10, 2019.
Respectfully submitted, June 19, 2019, Subcommittee on Regulatory Guide 8.39 Release of Patients Administered Radioactive Materials, Advisory Committee on the Medical Use of Isotopes (ACMUI),
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