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E Party

Publications and source records attributed to E Party.

15 recordsLinked to original sources

Evaluation of a room for tuberculosis patient isolation using theatrical fog.

OBJECTIVE: To develop a method to evaluate directional airflow patterns, air dilution, and air mixing in facilities where tuberculosis patients are seen. DESIGN: A tuberculosis patient isolation room was evaluated by analyzing pressure differential between the room and the corridor and by using theatrical fog to visualize room air movement and impact of dilution and exchange, as well as air capture and displacement. Tracer gas was compared to fog results and used to calculate air exchange rates. SETTING: A small research hospital. RESULTS: By adding theatrical fog to the patient room at several locations, we quickly learned that most of the air entering the room through the transom and around the door to the corridor was exhausted through the three exhaust vents. Little air appeared to move toward the exhaust fan. For comparison and to confirm the room air exchange rate, tracer gas was distributed and sampled. The kinetics of decay were very similar whether the tracer gas and room air were mixed during sampling or not. CONCLUSIONS: The fog procedure allowed good visual confirmation of air mixing and airflow patterns and provided quantitative data for evaluating the efficacy of air capture and displacement or dilution and exchange.

Aerosols↗

Removable surface contamination at a biomedical research institution.

A rigorous, unannounced, campus-wide survey for removable surface contamination was performed at our institution. Wipe samples (n = 1,090) were collected from a variety of standardized locations in 45 large biomedical research laboratories that routinely use kBq-MBq (microCi-mCi) amounts of 3H, 14C, 32P, 35S, 51Cr, and 125I. The results showed a log-normal distribution for contamination, with about 90% of all samples below ten times background. Although working surfaces and equipment used in these laboratories can become contaminated with radioactive materials, especially by transfer from soiled gloves, the magnitude of the contamination is very small and typically restricted to surfaces, instruments, and equipment that are directly handled in the course of experimental work and which can be reasonably anticipated to be contaminated. These data suggest that contamination is not a significant problem in biomedical research laboratories at this institution and that the best protection from workplace contamination appears to continue to be the use of well-reviewed standard operating procedures and good work practices.

Carbon Radioisotopes↗

Elimination of tritiated thymidine from birds.

The kinetics with which tritiated thymidine is eliminated from birds and the concentration of radioactivity remaining in the carcass after 350-430 h were measured. Birds injected with tritiated thymidine eliminated 98% of the radioactivity injected within 28 h. Ninety-eight percent was identified in the excreta, and less than 2% of the radioactivity injected remained in the birds 28 h after injection.

Animals↗

Consensus radiation protection practices for academic research institutions.

Under the auspices of the Howard Hughes Medical Institute, a set of consensus guidelines for Radiation Protection Practices has been developed for biomedical research using radioactive materials. The purposes of the guidelines are (1) to promote good radiation protection practices consistent with the needs of biomedical research, the ALARA principle, and regulatory requirements; (2) to establish common goals and consistent practices within radiation safety programs; and (3) to build a meaningful partnership between radiation safety professionals and the biomedical research community. These practices are intended to enhance radiation protection and the efficiency of the research staff. The consensus guidelines will lessen the variability in radiation safety practices that is evident among many academic research institutions and will encourage better acceptance and regulatory compliance by users of radioactive materials in biomedical research.

Academies and Institutes↗

Biodegradation of radioactive animals.

The two most common disposal alternatives for animals contaminated with radioactive materials are incineration and burial. For most of the country burial has entailed shipping the carcasses to a commercial disposal facility at Barnwell, South Carolina, where it was landfilled along with other solid radioactive waste. Unfortunately, since 30 June 1994, this facility accepts waste generated by the states of the Southeast Compact only. Therefore, burial is no longer an option for most of the country's generators and incineration is an option only for those institutions which have, or have access to, an incinerator that is permitted to burn radioactive materials and that accepts animal carcasses with de minimis levels of radioactive contaminants. Many institutions, especially those in congested urban areas where the public does not support incineration, do not have viable outlets for radioactive animal carcasses. Interim, on-site storage poses problems of its own. Biodegradation of animal carcasses with dermestid beetles is an inexpensive approach to this waste management problem.

Animals↗

Virus penetration of examination gloves.

Examination gloves worn for protection from biohazards were sampled and evaluated for their ability to exclude virus particles. We found that thin gloves manufactured from polyethylene or polyvinyl chloride are ineffective barriers while gloves of thin latex are superior but not without failure. Polyethylene and polyvinyl chloride gloves had failure rates of 40% and 22%, respectively. Following exposure to the common disinfectant, 70% ethanol, these failure rates increased to 94% and 56% for polyethylene and polyvinyl chloride gloves, respectively. Latex, although permeable to ethanol, was penetrated by virus less than 1% of the time regardless of whether the latex had been pre-exposed to disinfectant or not. This study highlights the need for caution on the part of those who rely upon examination gloves for protection from infectious agents as well as the need for establishing more adequate standards and testing procedures for their manufacture.

Ethanol↗