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PubMed · 12974124

Standards update.

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Richard Moore. 2003. Standards update.. https://pubmed.ncbi.nlm.nih.gov/12974124/

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Development and application of a quality control procedure for short-wave diathermy units.

Short-wave diathermy (SWD) is a form of radiofrequency (RF) radiation, operating at 27.12 MHz, that is used therapeutically by physiotherapists. Although this form of therapy is widely available, the management of the equipment is not often addressed by either physiotherapists or by medical physics/clinical engineering. A quality control protocol for SWD units, examining power output and electrical and mechanical condition, was developed and applied to 20 units used in clinical practice. In addition, an environmental assessment of where the units were used was also included. Results showed that the power output was generally stable (coefficient of variation range 0-8.8%) and reproducible (coefficient of variation range 0-6.8%). When the outputs from 12 similar units were compared, it was found that the relationship between the units' intensity settings and power output measurements was non-linear. Two units with mechanical timers were found to have inaccuracies that could contribute, under a 'worst-case' scenario, to a dosage error of up to 45%. Environmental analysis found that all treatment plinths in use contained metal parts, which could constitute a fire hazard, and no department examined was equipped with an RF screened room, a facility that would ensure that other persons in the vicinity were not exposed to excessive stray radiation.

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Venturi systems are among the most widely used devices for delivering oxygen therapy. Nevertheless, rigorous quality control of their reliability is lacking. In this study we used mass spectrometry to evaluate Venturi systems sold by various companies in Spain. We also studied tolerance under various conditions (changes in oxygen flow and with increased system resistance). Fixed systems were found to comply well with recommendations, whereas none of the variable systems complied. One system (Oxigem Variable) was unable to provide an oxygen concentration below 31% when set to deliver at 24% to 28%. We conclude that the variable masks available in Spain do not comply with European Union recommendations and the range of error of one of them (Oxigem Variable) means it is not clinically useful. Fixed systems were the most reliable ones in our market, and airlife and intersurgical devices were the variable systems that best approximated the reliability of fixed systems.

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Impact resistance of common spectacle and safety lenses to airgun and rimfire projectiles.

PURPOSE: To evaluate the penetration resistance of common spectacle and safety lenses to high-velocity projectiles and to examine the current recommendations regarding the use of such lenses. METHODS: The penetration threshold of glass, high-index, and polycarbonate spectacle and safety lenses was determined by firing BBs, pellets, and 0.22-caliber projectiles. The mass, diameter, velocity, and energy of each projectile were measured, and the center thickness, mass, and refractive power of each lens were recorded. The penetration threshold for each lens type was calculated, and a comparison of impact resistance was made. RESULTS: The maximum velocity of the BB was measured at 221 m/s; pellets at 210 m/s; CB.22 rimfire projectiles at 204 m/s; and 0.22 rimfire projectiles at 290 m/s. The BB penetration thresholds were as follows: glass lenses = 84.0 m/s (2.4 J) and high-index lenses = 107.7 m/s (4.09 J). Polycarbonate spectacle and safety lenses were not penetrated by BBs regardless of their velocity; however, these lenses were penetrated by CB.22 rimfire projectiles (89.2 J). Review of the penetrated lenses showed that center thickness and refractive power was comparable between the various groups of projectiles. CONCLUSIONS: Polycarbonate offers a vastly superior degree of penetration resistance compared with other commonly used lens materials. The current recommendations regarding the use of polycarbonate in prescription and protective lenses, as endorsed by the American Academy of Ophthalmology and the American Academy of Pediatrics, must be reevaluated.

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