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MEDICAL SURVEILLANCE

LBNL provides free medical monitoring to all employees who face workplace risks.  The program is designed to monitor potential health hazards associated with research and development activity with recombinant DNA, Bloodborne pathogens, other etiologic agents, hazardous chemicals and heavy metals.  The program is coordinated by an occupational physician.

Persons with severe immunological deficiencies or persons undergoing treatment with immunosuppressive drugs and certain other medical disorders should be discouraged/prevented from working with potentially infectious organisms.  Persons undergoing treatments with antibiotics or steroids; persons with eczema, colitis, ileitis, active chronic diarrhea or other gastrointestinal disorders; and women during pregnancy must seriously consider whether or not they should participate in any research activities.  Consultation with a physician and other health and safety professionals (including biohazard specialists) is available.

Any changes in the health status of research personnel or illness which lasts four days or longer must be reported to the PI and Health Services.  If there is any suspicion of rDNA involvement a physician will be consulted.

Annually a review questionnaire will be sent to each worker known to use recombinant or carcinogenic materials.  Completed forms will be reviewed by our medical surveillance coordinator.  The physician will be monitoring for the incidence of unusual illnesses at LBNL.  All staff members are encouraged to cooperate with this survey, which is strictly confidential.  Personnel engaged in work with substantial hazards are urged to participate in the medical surveillance program.

If a safe and effective vaccine is available against an organism with which a person must work, LBNL will provide it free.  The most common example is Hepatitis B immunization.  Personnel using human source materials are urged to be immunized against Hepatitis B.  The vaccine currently used at LBNL is made from recombinant material and NOT from human source material (sera).  Participation in this program is voluntary and individuals should assess the risk/benefit ratio after consultations with health care providers.  The vaccination is administered by Health Services personnel.  Following the final injection, the IBC recommends that individuals submit a blood sample in order to evaluate the immunization effectiveness. 

If unusual treatments or vaccines are needed in case of an accident, Health Services should be apprised of the situation before work begins in order for the appropriate materials to be available for emergency treatment.

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