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Experiences in setting up the first centralized radiopharmacy in Spain.

The centralized radiopharmacy set up in Spain by the Cetir Medical Group allows optimal use of radiopharmaceuticals and complies with laws (Directive 89/343/EEC and Royal Decree 479/1993/Spain) governing their use. More than 220,000 individual patient doses have been supplied since the unit was established in November 1995. In this paper, we describe the infrastructure of the centralized radiopharmacy, including the operations and procedures involved, and how we believe we have achieved our original objectives.

Drug Storage↗

A cc of prevention.

Rarely do saving money and saving lives fit so closely together as they do with sharps safety. Here's how to choose the best devices to reduce injuries in your hospital.

Accidents, Occupational↗

Select new, safer i.v. therapy equipment.

Learn how to select i.v. therapy safety equipment that complies with the Needlestick Safety and Prevention Act, which mandates the use of needlestick-prevention devices.

Accidents, Occupational↗

Management of spent sealed radioactive sources in Turkey.

Spent radioactive sources (SRS) have been generated from industrial applications, research, and medicine in Turkey. In this study, management of SRS (Co, Cs) at Cekmece Waste Processing and Storage Facility (CWPSF) is described. Eleven Cs sources (total 851 GBq) and four Co sources (total 27.75 GBq) that had been used as levels and density gauges were conditioned. Reinforced metal drums (200 L in volume) and cement matrix were used for conditioning of these sources. In this way, greater confinement was achieved for long-term storage. Maximum dose rates at the surface of the conditioned waste package were determined. In addition to information about conditioning stages of the sources, various calculations that have been done for shielding are presented. Surface dose rates of the waste packages were 1.60 mSv h for Cs and 1.63 mSv h for Co. Measurements of the final waste packages were presented to fulfill the requirements (<2 mSv h) of transportation according to regulations for the safe transport of radioactive material.

Cesium Radioisotopes↗

Complying with the Occupational Safety and Health Administration's Bloodborne Pathogens Standard: implementing needleless systems and intravenous safety devices.

Preventing the transmission of bloodborne pathogens to healthcare workers has been a mission and a challenge of the healthcare industry for over 20 years. The development of the Occupational Safety and Health Administration Bloodborne Pathogens Standard in 1991 and the passing of the Needlestick Safety Act in 2000 mandated hospitals to develop an Exposure Control Plan to protect workers from these pathogens. Children's Hospital Boston began implementation of a needleless system in 1993. Employees readily accepted these systems into practice, because they were convenient and easy to use. A marked decrease in exposures to bloodborne pathogens naturally followed, which is consistent with the national data. The transition to intravenous (i.v.) safety devices at Children's Hospital began in 2000 and proved to be more of a challenge. First, the clinicians must choose a safety product, which requires developing and implementing a trial plan with potential catheters. This selection process is especially difficult in pediatrics where successful placement of the smallest-gauge catheter, no. 24, is imperative. After choosing an i.v. safety product, successful transition is dependent upon the thoroughness of i.v. safety device training and a commitment by the clinicians to the use of these products. Although the number of needlestick injuries and subsequent transmission of bloodborne pathogens have been further reduced with the use of i.v. safety devices, needlestick injuries still occur. This results from a lack of familiarity with the engineering of the device and therefore poor technique or a failure to activate the safety mechanism. Staff resistance due to loss of expertise with the new device and patient care concerns are additional barriers to the use of these new products. Addressing these obstacles and providing adequate training for all clinicians were required for successful implementation of these i.v. safety devices.

Attitude of Health Personnel↗

Assessment of microwave-based clinical waste decontamination unit.

A clinical waste decontamination unit that used microwave-generated heat was assessed for operator safety and efficacy. Tests with loads artificially contaminated with aerosol-forming particles showed that no particles were detected outside the machine provided the seals and covers were correctly seated. Thermometric measurement of a self-generated steam decontamination cycle was used to determine the parameters needed to ensure heat disinfection of the waste reception hopper, prior to entry for maintenance or repair. Bacterial and thermometric test pieces were passed through the machine within a full load of clinical waste. These test pieces, designed to represent a worst case situation, were enclosed in aluminium foil to shield them from direct microwave energy. None of the 100 bacterial test pieces yielded growth on culture and all 100 thermal test pieces achieved temperatures in excess of 99 degrees C during their passage through the decontamination unit. It was concluded that this method may be used to render safe the bulk of of ward-generated clinical waste.

Aerosols↗

Effectiveness of wet and dry mercury vapour suppressant systems in a faculty of dentistry clinic.

The objective of this study was to determine the effectiveness of a liquid and a dry commercial mercury vapour suppressant system. Measurements were made in a student dental clinic, using a mercury vapour detector for periods up to 76 weeks. The two products examined were Mercon vap liquid in a stock jar and the Mercon tainer dry jar system. Amalgam scrap jars were removed from the study when the mercury vapour concentration in the jars exceeded the arbitrary cut-off criterion of 0.05 mg Hg m(-3). Results showed that the mercury vapour concentration in the liquid system exceeded the cut-off criterion in 44 weeks or less, whereas the dry system remained below the detection limit (0.01 mg Hg m(-3)) for the maximum measurement period of 76 weeks. It was concluded that the dry system is more effective and reliable than the liquid system. The reliability of the liquid system may be influenced by contact of amalgam scrap with the portion of the inner wall of the jar that is not covered by liquid. It is proposed that amalgam scrap contaminates the wall with mercury during its insertion.

Air Pollution, Indoor↗