Regulatory Guide 8.35

(Draft Was Issued as DG-8008), Planned Special Exposures

ML003739507
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Issue date:	06/30/1992
From:	Office of Nuclear Regulatory Research
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RG-8.35
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U.S. NUCLEAR REGULATORY COMMISSION June 1992 REGULATORY GUIDE OFFICE OF NUCLEAR REGULATORY RESEARCH REGULATORY GUIDE 8.35 (Draft was issued as DG-8008) PLANNED SPECIAL EXPOSURESA. INTRODUCTION In the revised 10 CFR Part 20, "Standards for Protection Against Radiation," paragraphs 20.1201(b) and 20.1206 provide the conditions and limits for planned special exposures (PSEs) of adult workers, i.e., doses in addition to and accounted for separately from the doses received under the limits specified in 10 CFR 20.1201. In addition, 10 CFR 20.2104(b) and 20.2104(e)(2) specify the requirements for obtaining prior occupational dose information, and 10 CFR 20.2105 and 20.2106 specify the requirements for exposure and monitoring records applicable to PSEs. The requirements for reporting PSEs are in 10 CFR 20.2202(e) and 20.220 PSEs have been included in the revised 10 CFR Part 20 to provide for exceptional situations when alternatives that might avoid the special exposure are unavailable or impractical. The previous rule's 5(N-18) provision, which permitted accumulating unused annual exposures for use in dose averaging (or a dose bank), has been deleted. Under the revised rule, if the worker's exposure is under the 5-rem annual dose limit, there is no way to recapture the difference between the actual dose and the limit for use in future year The PSE rule is designed to provide occupational dose flexibility similar to that provided by the previous 5(N-18) rule. Thus, even though doses cannot be "banked" or saved as before, the revised rule will al-low 5 rems occupational exposure and 5 rems PSE for a total of 10 rems for the year, which is similar to the maximum amount of 12 reins allowed under the previous 5(N-18) rule. The difference is that there are additional conditions that must be satisfied prior to allowing the special exposure. These conditions are detailed in 10 CFR 20.1206, and this provision is intended to be used only under very special circumstances, not as a routine measure for extending dose limits applicable to routine exposures. In addition, there are requirements for recording and reporting the PS This regulatory guide provides guidance on the conditions and prerequisites for permitting PSEs allowed by the revision to 10 CFR Part 20, the associated specific monitoring and reporting requirements, and examples of acceptable means of satisfying these requirement Any information collection activities mentioned in this regulatory guide are contained as requirements in 10 CFR Part 20, which provides the regulatory basis for this guide. The information collection requirements in 10 CFR Part 20 have been cleared under 0MB Clearance No. 3150-001 B. DISCUSSION PSEs are restricted to those special situations that could result in a higher exposure than allowed by the normal limits of 10 CFR 20.1201 and that, if not provided for, could create a severe problem in theUSNRC REGULATORY GUIDES The guides are issued in the following ten broad divisions: Regulatory Guides are issued to describe and make available to the public methods acceptable to the NRC staff of Implementing specific parts of the Commission's regulations, to delineate techniques used by the 1. Power Reactors 6. Products staff in evaluating specific problems or postulated accidents, or to pro- 2. Research and Test Reactors 7. Transportation vide guidance to applicants. Regulatory Guides are not substitutes for 3. Fuels and Materials Facilities 8. Occupational Health regulations, and compliance with them Is not required. Methods and 4. Environmental and Siting 9. Antitrust and Financial Review solutions different from those set out In the guides will be acceptable If 5. Materials and Plant Protection 10. General they provide a basis for the findings requisite to the issuance or continuance of a permit or license by the Commission. Copies of issued guides may be purchased from the Government Printing This guide was issued after consideration of comments received from Office at the current GPO price. Information on current GPO prices may the public. Comrments and suggestions for improvements in these be obtained by contacting the Superintendent of Documents, guides are encouraged at all times, and guides will be revised, as ap- Government Printing Office, Post Office Box 37082, Washington, DC propriate, to accommodate comments and to reflect new information or 20013-7082. telephone (202)275-2060 or (202)275-217 experienc Written comments may be submitted to the Regulatory Publications Issued guides may also be purchased from the National Technical InforBranch, DFIPS, ADM, U.S. Nuclear Regulatory Commission, Washing- mation Service on a standing order basis. Details on this service may be ton. DC 20555. obtained by writing NTIS, 5285 Port Royal Road, Springfield, VA 2216 licensee's operations. Problems might include unscheduled facility shutdowns, high radiation levels that impede operations important to safety. Accordingly, a special set of limitations and reporting and recordkeeping requirements apply if licensees decide to use PSEs. Approval of a PSE for an adult worker must be in writing before the exposure occurs and, once it occurs, the exposure cannot be treated as a routine occupational exposure. Furthermore, minors are not allowed to participate in PSE In planning for a PSE, the licensee is permitted to assign a portion of the dose to routine exposure and the rest to the PSE. However, when the postexposure evaluation is made, the dose amount planned to be assigned to PSE must be recorded as PSE. If the total dose received is less than the planned PSE, the actual dose received must be recorded as PSE dose. If the total dose received is more than the planned PSE, but not an overexposure, the extra portion may be recorded as PSE or routine dose. In other words, the planned PSE dose cannot be reassigned, postexposure, to routine exposure if it is later determined that a PSE was not needed. The intent of the PSE was that it would be used infrequently. Once a licensee decides to conduct a PSE, all the unique limitations and reporting and recordkeeping requirements are to apply, even if the doses actually received fall within the dose limits for routine operations. For example, if a job planned with a PSE of 5 rems and a routine dose of 2 reins to an individual actually results in a dose of 4 reins, the entire 4-rem dose must be recorded as PSE dos In determining the amount to assign to the PSE in advance of the exposures, licensees should be aware of the individual's current year exposure and lifetime PSE bank to avoid unnecessarily impacting a worker's employabilit C. REGULATORY POSITION 1. USE OF PLANNED SPECIAL EXPOSURES PSEs are only to be used under exceptional circumstances, not as a routine method of increasing dose limits applicable to routine exposures. However, licensees may consider the use of PSEs to permit workers who have critical skills and who are necessary for a particular job to receive an exposure in addition to the routine occupational exposure limi The rule does not require that participation in PSEs be voluntary on the part of the individual workers. However, licensees may establish a program of voluntary PSEs. In any case, consideration should be given to the potential benefits of involving the worker in the planning and preparation for the PSE. The NRC believes that the risk of suffering health effects from these limited exposures is small and that the use of PSEs may be necessary for licensees to accomplishimportant tasks vital to continued safe operation The issue of a worker accepting the risks associated with an assigned task is discussed in Regulatory Guide 8.29, "Instruction Concerning Risks from Occupational Radiation Exposure." Exposures in excess of the routine occupational dose limits received during accident or emergency situations that require immediate action to save human lives or to prevent the failure of equipment important to safety are not PSEs. However, if conditions associated with an accident or emergency permit complying with the conditions specified in 10 CFR 20.1206(a) through (e), a PSE can be used. However, all exposures in excess of the routine occupational dose limits received during accident and emergency situations must be determined and subtracted from the annual 5-remn PSE limit and the 25 reins allowed for lifetime PSEs (see 10 CFR 20.1206(e)). 2. CONDITIONS FOR USE OF PSEs There are seven conditions listed in 10 CFR 20.1206 that must be satisfied if a licensee authorizes an adult worker to receive a PSE. These conditions are presented in Figure 1 and are discussed belo FIGURE 1 Conditions for Planned Special Exposures Exceptional SituationPrior Written Authority Individual Informed and Instructed Doses from Previous PSEs and Doses in Excess of Annual Dose Limits DeterminedPSEs Plus All Occupational Exposures Over Annual Limits Must Be: <Dose Limits for 1 Year and <5 x Annual Dose Limits for a Lifetime Records Maintained of Conduct of PSE, Written Report of PSE to NRC PSE Dose Recorded and Individual Informed of Dose Within 30 Days8.35-21-.t!.'

2.1 Exceptional Situations Authorization for PSEs should only be given for exceptional situations. The use of PSEs must be justified and well documented (see 10 CFR 20.2105). PSEs should not be used as a routine method of increasing a worker's routine exposure limits. The justification for the PSE will be reviewed by the NRC staff when the licensee's records of the PSE are examine If a licensee would like an NRC review prior to initiating a PSE, the licensee may contact the appropriate regional office directl The following are examples of exceptional situations in which a PSE might be justified: The work is to be performed by one individual rather than several. A source becomes disconnected during radiography. It may not be practical or feasible for the source to be recovered in two or three steps by different persons. Authorization for one person to receive up to 5 rems total effective dose equivalent, in addition to his or her routine occupational exposure, may be reasonable for the recover The licensee is permitted to use previously approved procedures in carrying out work under a PS For example, the licensee could have an approved generic procedure for source retrieval that, among other things, addresses all the administrative and recordkeeping requirements of 10 CFR 20.1206. Provided the situation is exceptional and alternatives that might avoid higher exposures are unavailable or are impractical, an individual's exposure received during such a source retrieval may be considered as a PS All the conditions of 10 CFR 20.1206 must be met and documented prior to each exposur Use of dose-averting methods are not possibl Work must be performed on instrumentation in a high-radiation area where space is very limited and shielding or other dose-averting methods are not possible. It may be necessary to authorize a PSE to make the necessary repairs to the instrumentatio Collective dose to personnel may be reduce It may be more dose effective to keep certain skilled workers on a particular job because they will be able to perform the job rapidly and reduce the overall dose to personnel. For example, if two persons can weld in a high-radiation area and collectively receive 12 reins (6 reins per person, 2 reins under a PSE and 4 reins routine) while four less skilled workers would receive 16 reins (4 reins per person routine exposure), the collective dose would be reduced from 16 to 12 reins by using the two skilled workers. PSEs are not intended to be used only as a routine collective dose reduction technique. However, reducing collective dose could contribute to the justification of the need for a PSE.2.2 Prior Written Authority The licensee (and employer if the employer is not the licensee) must specifically authorize the PSE in writing before the exposure occurs. A contractor employer may authorize the use of PSEs by a licensee in advance to accommodate any urgent circumstances that may aris If, prior to initiating a PSE, it is found that a PSE is not needed, the resulting exposure can be recorded as routine if the PSE is cancele The procedures for the radiation protection program should specify the management level that may authorize a PSE. The responsible person'should be at a sufficiently senior level to ensure worker protection and to judge the appropriateness of the PSE for the exceptional circumstances. This person would normally be the RSO/radiation protection manager or someone in the organization with equivalent qualification .3 Individual Informed and Instructed Before a planned special exposure, the licensee must ensure that the individuals involved are (1) informed of the purpose of the planned operation, (2) informed of the expected radiation levels, estimated doses, and associated risks or other conditions that may be involved in performing the task, and (3) instructed in measures to be taken to keep the dose ALARA (as low as reasonably achievable) while considering other risks that may be presen To ensure that the intent of the plan is carried out, it is important that the workers who are to receive a PSE are fully informed and aware of the circumstances under which the PSE was authorize These workers must understand the importance of keeping their exposure ALARA. They must also understand the procedures and controls to be used in the particular PSE in order to keep their exposures ALARA. Licensees have an obligation to inform workers (before they receive a PSE) of the expected radiation levels, estimated doses, associated risks, or other significant conditions that might be involved in performing the task so that the individuals are aware of and understand the health and safety significance of the PSE. This information should also be included on the authorization for the PS .4 Determine Prior Doses According to 10 CFR 20.1206(d), prior to authorizing the PSE, all previous PSEs and all doses in excess of the routine occupational limits in effect at the time of the exposures (10 CFR 20.1201(1)(a) and the former 10 CFR 20.101) for the individual's lifetime must be determined from records for each individual who will participate in the PSE. Doses received in excess of routine occupational dose limits in effect at the time of the exposures during accidents and emergencies must also be determined and8.35-3r F subtracted from the limits for PSEs. (Accident doses are doses resulting from an unexpected event involving exposure to radiation or radioactive materia Emergency doses are doses resulting from any immediate action taken in response to a situation or occurrence of a serious nature developing suddenly and unexpectedly.) If complete records (including the provisions of 20.2104(c)) of the worker's current and previously accumulated occupational dose such as a completed NRC Form 4 are not available, it must be assumed that the individual is not eligible for PSEs, i.e., the person cannot be authorized to receive a PSE (see 10 CFR 20.2104(e)(2)). Guidance on records of occupational exposure is available in Revision 1 to Regulatory Guide 8.7, "Instructions for Recording and Reporting Occupational Radiation Exposure Data." 2.5 PSEs and Exposure Limits Individuals receiving PSEs can receive a maximum dose in 1 year of any or all of the following: 1. 10 reins total effective dose equivalent (5 reins from routine operations and 5 reins from PSEs); or 100 rems to any individual organ or tissue, including any deep-dose equivalent plus the committed dose equivalent for the organ or tissue (50 rems from routine operations and 50 rems from PSEs); and 2. 30 reins dose equivalent to the eye (15 rems from routine operations and 15 rems from PSEs); and 3. 100 rems to the skin or to any extremity (50 reins from routine operations and 50 reins from PSEs). Individuals can receive a lifetime dose from PSEs of any or all of the following: 1. 25 reins total effective dose equivalent; or 250 rems to any individual organ or tissue; and 2. 75 reins to the eye; and 3. 250 reins to the skin or to any extremit .6 Records and Written Reports The licensee must maintain records of the conduct of a PSE in accordance with 10 CFR 20.2105 and must submit a written report in accordance with 10 CFR 20.2204. In addition, 10 CFR 20.2106 requires that the records of doses received during PSEs be maintained for all individuals who participated in a PSE. These records should include all the information listed in 10 CFR 20.2105. A revised NRC Form 5 has been developed, along with guidance on its use,in Revision 1 to Regulatory Guide 8.7, "Instructions for Recording and Reporting Occupational Radiation Exposure Data." A written report of the PSE, notifying the Administrator of the appropriate NRC Regional Office, is due within 30 days after the PSE has occurred (see 10 CFR 20.2204). The report allows the NRC to assess the actual frequency of PSEs and determine whether followup inspections may be warranted. The information-in the records listed in 10 CFR 20.2105 must be included in any report filed under 10 CFR 20.220 .7 Recording Worker's PSE Dose and Informing the Worker The licensee must record its best estimate of the dose (dose of record) resulting from the PSE in each affected individual's record and inform the individual, in writing, of the dose within 30 days of the PSE (10 CFR 20.1206(g)). The dose from PSEs is not to be considered in controlling future occupational dose of the individual under 10 CFR 20.1201(a) but is to be included in evaluations required by 10 CFR 20.1206(d) and (e). The dose resulting from a PSE is to be included in the total for all PSEs for the individual, and it is to be used in determining the dose balance remaining for future PSE The 30-day time period for notifying the worker of the dose received is to allow sufficient time for the licensee to make its best estimate of internal and external exposures received as part of the PSE. The best estimate is understood to mean the dose of record as determined by accredited dosimetry, bioassay, air sampling, or other analyses such as time and motion studies. If the intake of Class Y material (i.e., materials that remain in the body for time periods on the order of years) is being assessed, the licensee may delay the recording and reporting of the results of its assessments for periods up to 7 months to allow for additional measurements necessary for the assessments (10 CFR 20.1204(d)). The internal dose reported within the 30 days may be identified as an initial best estimate pending completion of a final assessment after which the actual dose assigned should be recorded and reporte The dose from a PSE must be tracked separately from the routine occupational dose for the individua Thus, a person may have an accumulated routine occupational dose of 3 rems total effective dose equivalent for the year, receive a dose of 4 reins total effective dose equivalent from a PSE, and still be able to receive up to 2 more reins of routine occupational exposure for the year, even though the person has had a total dose of 7 rems for the yea . INTERNAL AND EXTERNAL EXPOSURE CONSIDERATIONS For PSEs, as well as for routine exposures, both internal and external doses are to be summed in8.35-4/

calculating the total effective dose equivalent. This requires controlling the total effective dose equivalent but permits tradeoffs between internal and external exposures to be made to achieve ALARA doses. The sum of external and internal doses during the PSE should be maintained ALARA. The conditions specified in 10 CFR 20.1502 should be used in making the determination of when monitoring is require . EXPOSURES OF MINORS AND DECLARED PREGNANT WOMEN The PSE provisions of 10 CFR 20.1206 do not apply to minors (10 CFR 20.1207) or to the embryo/ fetus (10 CFR 20.1208). The rule permits a licensee to authorize only an adult worker to receive PSEs. In addition, the dose limits in 10 CFR 20.1208 would normally preclude a declared pregnant woman from receiving a PSE since the 10 CFR 20.1208 limits are more restrictive than the annual dose limits in 10 CFR 20.1201. In general, declared pregnant women should not be considered candidates for PSEs. How-ever, the provisions of 10 CFR 20.1206 also apply to the dose limits for the lens of the eye, skin, and extremities. Therefore, in some situations it may be possible for a declared pregnant woman to receive a PSE to her extremities (or skin or eyes) that would not exceed the dose limits to the embryo/fetu D. IMPLEMENTATION The purpose of this section is to provide information to applicants and licensees regarding the NRC staff's plans for using this regulatory guid Except in those cases in which an applicant proposes an acceptable alternative method for complying with specified portions of the Commission's regulations, the methods described in this guide will be used in the evaluation of applications for new licenses, license renewals, and license amendments and for evaluating compliance with 10 CFR 20.1001-20.2401.8.35-5 REGULATORY ANALYSISA separate regulatory analysis was not prepared for this regulatory guide. The regulatory analysis prepared for 10 CFR Part 20, "Standards for Protection Against Radiation" (56 FR 23360), provides the regulatory basis for this guide and examines the costs and benefits of the rule as implemented by the guide. Acopy of the "Regulatory Analysis for the Revision of 10 CFR Part 20" (PNL-6712, November 1988) is available for inspection and copying for a fee at the NRC Public Document Room, 2120 L Street NW, Washington, DC, as an enclosure to Part 20./8.35-6

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