Bioequivalence approach for whole effluent toxicity testing

被引:8
作者
Shukla, R [1 ]
Wang, Q
Fulk, F
Deng, CQ
Denton, D
机构
[1] Univ Cincinnati, Med Ctr, Dept Environm Hlth, Cincinnati, OH 45267 USA
[2] ABT Associates Inc, Clin Trials, Biostat & Epidemiol, Cambridge, MA 02138 USA
[3] US EPA, Natl Exposure Res Lab, Cincinnati, OH 45268 USA
[4] US EPA, San Francisco, CA 94105 USA
关键词
toxicity testing; bioequivalence testing; hypothesis testing; practically equivalent toxicity;
D O I
10.1002/etc.5620190120
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Increased use of whole effluent toxicity (WET) tests in the regulatory arena has brought increased concern over the statistical analysis of WET test data and the determination of toxicity. One concern is the issue of statistical power. A number of WET tests may pass the current hypothesis test approach because they lack statistical power to detect relevant toxic effects because of large within-test variability. Additionally a number of WET tests may fail the current approach because they possess excessive statistical power, as a result of small within-test variability, and detect small differences that may not be biologically relevant. The strengths and limitations of both the traditional hypothesis test approach and the bioequivalence approach for use in the National Pollutant Discharge Elimination System program were evaluated. Data from 5,213 single-concentration, short-term chronic WET tests with Ceriodaphnia dubia provided the database for analysis. Comparison of results between the current approach and the bioequivalence approach indicates that the current approach to WET testing is generally sound but that adopting the proposed bioequivalence approach resolves concerns of statistical power. Specifically, within this data set, applying the bioequivalence approach resulted in failure for tests with relatively large test variability and a pass for tests with relatively small within-test variability.
引用
收藏
页码:169 / 174
页数:6
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