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Original Articles

Control of Methyl Methacrylate During the Preparation of Orthopedic Bone Cements

, &
Pages 272-280 | Published online: 31 Oct 2007
 

Abstract

The use of methyl methacrylate (MMA) bone cement during orthopedic procedures has been seen as a potential exposure hazard to health care professionals. However, that assessment is based on a number of investigations with problems in experimental design, analysis, and data interpretation. The current investigation quantified differences in MMA vapors produced during the preparation of competing bone cements using various methods of preparation. Unlike previous investigations, this effort employs modern validated sampling and analytical methods, and considers the affect of censored results. Measurements of sufficient quality and number were collected to allow for a statistical treatment of the data. The ability of two controlled preparation techniques to reduce MMA emissions were compared with a traditional open container. The results confirmed that the preparation of bone cement releases MMA vapors into the breathing zone of the preparer. One preparation technique (Stryker Bowl) controlled emissions during mixing and curing and affected a 73% reduction in measured MMA concentrations. In addition to mixing and curing, the second technique (UltraMix System) also controlled the MMA during pouring of the monomer and affected a 90% reduction in MMA concentrations. An ANOVA test of interaction indicates that the reductions are attributable to the preparation technique regardless of the type of cement being used. Both a Fisher's PLSD and Games/Howell post hoc test of the results indicate that the mean differences between the uncontrolled open container and the controlled preparation techniques are significant (p < 0.05).

ACKNOWLEDGMENTS

Funding for this investigation was provided through a contract with DePuy Orthopaedics, Inc., Warsaw, Indiana, a Johnson & Johnson Company.

Notes

A Berufsgenossenschaftliches Institute fur Arbeitsschutz.( Citation16 )

B A gas chromatograph equipped with a thermal conductivity detector.

C A gas chromatograph equipped with a flame ionization detector.

D Reference 15.

A Reference 15.

B Calculated as the auto sample volume of 0.014 L per sample divided by a sample time of 0.75 min, or 0.02 L/min.

C Calculated as the relative standard deviation × 100 and reported as a percentage.

A Significant at 5% level.

A Significant at 5% level.

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