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At least 19 recordsLinked to original sources
PubMed1975

[Paracoagulation tests in laboratory verification of intravascular coagulation. Comparative clinical evaluation of the SDPS test and of the ethanol test with serial dilution (SD ethanol test)].

The AA. remark that laboratory diagnosis of intravascular coagulation is a still alive methodological problem. The presence in the flowing blood of certain molecules (fdp) that derive from that alteration of fibrinogen metabolism, that is at the basis of any intravascular coagulation syndrome, can be detected by immunological methods. Paracoagulation tests allow on the contrary to detect fibrin monomers and fibrin degradation products (fdp) that are still clottable (nonenzymatic coagulation). The positivity of these ones constitutes therefore an indirect evidence of the effects of thrombin on fibrinogen and keeps us nearer to the pathogenetic moment which is the real basis of any I.C. syndrome. The AA. make here a parallel between the two principal paracoagulation tests that are S.D.P.S. test according to GUREWICH (1971 [7]) and Ethanol Gelation test according to GODAL (1966 [6]) whose details are given. These two tests were performed in parallel in 589 cases which showed clinical evidence or suspicion of I.C. mostly supported by the further clinical courses of the patients. The two tests are both positive only in 164 cases (27,8%); both non-positive in 109 cases (18,6%); S.D.P.S. test is positive alone in 306 cases (51,9%); Godal's test is positive alone in 10 cases (1,7%). These data, supported by clinical course, allow the AA. to think that S.D.P.S. test is more sensitive than Godal's test. Although the AA. make the hypothesis that S.D.P.S. test may be more sensitive owing to its serial diluitions method that allows it to achieve an optimal ratio between the paracoagulant agent and the molecules which are capable to be clotted (paracoagulated). So they modify Godal's test applying to it too the principle of serial diluitions. The details are given. This new Serial Diluition Ethanol Gelation test is therefore performed in parallel with S.D.P.S. test in 314 cases which showed clinical evidence or suspicion of I.C. mostly supported by further clinical courses of the patients. In this second series of 314 patients the two tests are both positive in 138 cases (43,9%); both non-positive in 33 cases (10,5%); S.D.P.S. test was positive alone in 108 cases (34,3%); S.D.E.G. test was positive alone in 35 cases (11,3%). As we can see in this second series S.D.P.S. test remains more sensitive showing positivities in 246 cases (78,2%) whereas S.D.E.G. test is positive in 173 cases (55,2%). In conclusion the application of serial diluitions also to Ethanol Gelation test increase its sensitivity (from 29,5% to 55,2%), but it does not reach S.D.P.S. test's one. S.D.E.G. test may be really useful in clinics because it gives informations within 10 min but its non-positivity must be supported by the results of S.D.P.S. test which on the contrary gives sure informations only after 24 hours.

Blood Coagulation Tests↗
PubMed1986

Quantitative determination of beta-lactamase production in Staphylococcus aureus strains compared to qualitative testing by a microbiological clover leaf test, a chromogenic cephalosporin test and a iodometric test.

One hundred and twelve beta-lactamase producing strains of Staphylococcus aureus with known quantitative production were investigated together with 45 non-beta-lactamase producing derivatives by three qualitative beta-lactamase tests: the microbiological clover leaf test, the iodometric tube test and a chromogenic cephalosporin disc test. For the beta-lactamase producing strains strong positive reactions in the qualitative tests were not correlated with high beta-lactamase production, large degree of extracellularity or high induction ratio in any of the tests. Low beta-lactamase production was not correlated to weak reactions. Best results in identifying beta-lactamase production were obtained using the iodometric test in which 109 of 112 beta-lactamase producing strains were positive and no false positive reactions were observed. Some strains had only weak positive reactions but they were easily read. The clover leaf test and the chromogenic cephalosporin test detected 105 and 107 of 112 strains, respectively. The chromogenic cephalosporin disc test had more weakly reacting strains, which were difficult to read, especially among strains of phage type 95. Three non-beta-lactamase producing strains of phage type 95 were positive in the clover leaf test. It is concluded that the iodometric tube test is the most useful one for qualitative determination of beta-lactamase production in S. aureus. It is recommended as control when normal susceptibility testing for penicillin has shown susceptibility or doubtful susceptibility. Furthermore, it is useful when no susceptibility testing has been carried out and a rapid result is needed.

Biological Assay↗
PubMed1989

[A study of caries activity test. 1. Comparison of MSBB test, Cariostat test, RD test].

In the present study, experiments were performed using three variations of the caries activity test: the modified MSBB test (MSBB test), Cariostat test and Resazurin Disk test (RD test). The subjects of experiment I consisted of 147 patients treated in Nippon Dental University Hospital and first- and second-year students of Affiliated School of Dental Hygiene. Those of experiment II consisted of 25 men and women, aged 14 to 28 years. Experiment I was performed to determine the influence of the subject's concept of dental hygiene, DMF rate, presence or absence of regular brushing and skill in brushing, on the scores of MSBB and Cariostat test, and to determine whether or not there was a correlation between these two test. In experiment II, the correlation between the MSBB and Cariostat tests was studied, using the RD test as a standard. In experiment I, a comparison of MSBB scores before and after practice in dental hygiene revealed significantly decreased caries activity in the first-year students. Similar results were obtained by the Cariostat test. There was a positive correlation between the scores of the MSBB and Cariostat tests. The second-year students, who were considered to have a relatively good sense of oral hygiene, had the lowest scores. Experiment II revealed a correlation between the scores of the RD and MSBB tests.

Adolescent↗
PubMed2002

Comparison of the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antibiotic Susceptibility Testing proposed standard and the E-test with the NCCLS broth microdilution method for voriconazole and caspofungin susceptibility testing of yeast species.

The proposed standard of the Antifungal Susceptibility Testing Subcommittee of the European Committee on Antibiotic Susceptibility Testing (AFST-EUCAST) and the E-test procedures were compared with the NCCLS reference broth microdilution method for voriconazole and caspofungin susceptibility testing of 102 clinical Candida species and Saccharomyces cerevisiae isolates. The voriconazole MIC at which 50% of strains were inhibited (MIC(50)) was < or =0.125 mg/liter for all yeast species except for Candida glabrata and Candida krusei, which yielded MIC(50) values of 0.25 to 1 mg/liter depending on the method. Caspofungin exhibited in vitro activity (MIC(50) of < or =0.125 to 2 mg/liter) against all yeast species except for Candida guilliermondii. The agreements between MICs within +/-2 dilutions obtained by the NCCLS method and the EUCAST standard were 97% for voriconazole and 96% for caspofungin. Intraclass correlation coefficients were statistically significant (P < 0.05). The agreements between voriconazole MICs provided by the E-test and the NCCLS and between the E-test and the AFST-EUCAST method were 100 and 90%, respectively. Because of lower caspofungin MICs provided by the E-test, the agreement was slightly poorer with the NCCLS method (89%) than with the AFST-EUCAST procedure (94%). Both the EUCAST and the E-test procedures can be reliable techniques for susceptibility testing of yeasts to voriconazole and caspofungin.

Anti-Bacterial Agents↗
PubMed2004

Frontal lobe damage and tests of executive processing: a meta-analysis of the category test, stroop test, and trail-making test.

The Category Test, Trails B, and the interference task of the Stroop Test are among the most commonly administered measures of frontal lobe functioning and are thought to tap different cognitive functions mediated by these brain regions. Two meta-analyses were conducted on these tests to determine their sensitivity to frontal and lateralized frontal brain damage. Study 1 compared participants with frontal lobe damage to those with damage to posterior brain regions, whereas Study 2 compared participants with left and right frontal lobe damage. For each study, effect sizes based on performance differences between the above groups were calculated for the Category Test, Trail-Making Test Parts A and B, and the Stroop Test, including Word, Color, and Color-Word subtests. In Study 1 significant differences between groups were found for Trails A and all Stroop tasks, but in Study 2 the only difference between left and right frontal participants was on the Stroop Color-Word task. Potential reasons why Trails A and the Stroop Test are sensitive to frontal lobe damage are discussed, such as novelty and processing speed, as are clinical implications of these findings. The challenges of research on assessment of frontal lobe functioning are discussed and new developments in this area are highlighted.

Adult↗
PubMed1985

Mutagenicity testing of ST-film with the Ames test, chromosome test in vitro and micronucleus test in female mice.

The mutagenicity of ST-film and its components polyoxyethylenenonylether (NP-10) and polyvinylalcohol (PVAL) were studied by a reverse mutation test in S. typhimurium (Ames test), a chromosome test in cultured Chinese hamster V 79 cells and a micronucleus test in female mice. The results obtained from these test systems were all negative. Thus, it may be concluded that ST-film is not mutagenic either in vitro or in vivo mutagenicity testing systems.

Animals↗
PubMed1982

Comparative study of three tests (dye test, indirect haemagglutination test, latex agglutination test) for the detection of antibodies to Toxoplasma gondii in human sera.

An evaluation has been made of a commercial latex agglutination test, Toxotest-MT (TMT) (Eiken, Japan), for the detection of antibodies to Toxoplasma gondii in human sera. In qualitative studies, 878 sera were examined in both the TMT and dye test (DT) and 96.6% agreement was found, In quantitative studies 339 sera were titrated in the TMT and DT, with 337 of these sera also titrated in the indirect haemagglutination test (IHAT). Agreement between the DT and TMT was best, 78% of the sera showing titres within +/- 1 dilution in the two tests. The IHAT and TMT gave 66% agreement, while the DT and IHAT showed least agreement, 40.9%. The results suggest that the pattern of antigenic determinants to which antibody levels are measured are different in the three test systems. The TMT is a better substitute for the DT than the IHAT.

Antibodies↗
PubMed1982

Mutagenicity and dominant lethal test of kojic acid--Ames test, forward mutation test in cultured Chinese hamster cells and dominant lethal test in mice.

The mutagenicity of kojic acid was studied by means of reversion mutation test in bacteria (Ames test), forward mutation test in cultured Chinese hamster cells and dominant lethal test in mice. A positive result was obtained only in Ames test (TA 98, 1535 and 100) which was not modified by the presence of S-9 fraction. Thus, it is concluded that although kojic acid is a weak mutagen in bacteria, it is nonmutagenic in eukaryotic systems either in vivo or in vitro.

Animals↗
PubMedDate not supplied

A direct immunofluorescence test for the detection of sperm surface bound antibodies. Comparison with sperm agglutination test, indirect IF test and MAR test.

A direct immunofluorescence (DIF) test using sperm suspensions and F (ab')2 antisera was carried out on 30 patients with sperm-agglutinating (SA) activity and on 25 negative controls. Its results were related with the occurrence of SA activity in serum and seminal plasma, with the results of the indirect IF test and those of the direct IgG-MAR test. DIF test gave positive results in all patients with significant serum SA activity, even when it was undetectable in seminal plasma, except in 2 cases with serum IF-reactivity for IgM, and negative results in all controls. IgG were involved in IF-reactivity in 88.4% of positive cases and IgA in 42.3%. IgA were always found in association with sustained SA activity in seminal plasma. In these cases the IgG-MAR test might not result strongly positive, in spite of the high titre of SA activity in semen.

Antibodies↗
PubMedDate not supplied

Can't miss: conquer any number task by making important statistics simple. Part 6. Tests of statistical significance (z test statistic, rejecting the null hypothesis, p value), t test, z test for proportions, statistical significance versus meaningful difference.

Healthcare quality professionals need to understand and use inferential statistics to interpret sample data from their organizations. Since in quality improvement and healthcare research studies all the data from a population often are not available, investigators take samples and make inferences about that population using inferential statistics. This series of six articles will give readers an understanding of the concepts of inferential statistics as well as the specific tools for calculating confidence intervals and tests of statistical significance for samples of data. This article, Part 6, merges the four concepts of the (1) standard error of the difference between sample means, (2) the z test statistic, (3) rejecting the null hypothesis, and (4) the p value to provide a comprehensive view of tests of statistical significance. This is followed by a description of t tests, statistical tests for comparing two sample proportions, and Type I and Type II errors. The series of articles concludes with a description of statistical significance versus meaningful difference.

Confidence Intervals↗
PubMed1997

[Exceptional Application of Content Uniformity Test and Weight Variation Test in the Japanese Pharmacopoeia 13 revision and usage of these tests for in-process tests].

The criteria of Content Uniformity test and Weight Variation test in JP 13 were greatly changed to reduce consumer's risk. The new criteria were set to keep the rate of defectives in lots passing the tests less than the acceptable rate. However, in some cases, the new criteria can not directly be applied to some formulations and several modifications are needed in the criteria. In this report, the several resolution of this problem are represented. The applicability of these tests for in-process tests is also discussed.

Japan↗
PubMed1999

A quantitative comparison of induction and challenge concentrations inducing a 50% positive response in three skin sensitization tests; the guinea pig maximization test, adjuvant and patch test and Buehler test.

The sensitivities of three skin sensitization tests such as the Guinea pig maximization test (GPMT), Adjuvant and patch test (APT) and Buehler test (BT), were quantitatively compared with reference to induction and challenge concentrations. Four chemical which had different physico-chemical properties (octanol-water partition coefficient (logP) and reactivity with NH2-group) were used in order to clarify the effect of the physico-chemical properties of chemicals on the sensitivity of the different methods. The induction concentrations inducing a 50% positive response (IC50) demonstrated extreme variation with the three methods. For example, the BT/GPMT ratio of IC50 values for 2,4-dinitrochlorobenzene was 33, whereas that for maleic anhydride was 300,000. The results were thought to be caused by difference properties such as the logP and reactivity of chemicals. This correlation was confirmed by using 2-dodecen-1-yl succinic anhydride, which had the same reactivity but higher logP than that of maleic anhydride. On the other hand, the challenge concentrations inducing 50% positive responses (CC50) were less affected by the methods and the BT/GPMT ratios for CC50 values were all within a 10-fold range. These results suggest that the sensitivity might be strongly different with reference to induction concentration, but not challenge concentration among the three methods.

Adjuvants, Immunologic↗
PubMed1993

Genotoxicity testing of the herbicide Roundup and its active ingredient glyphosate isopropylamine using the mouse bone marrow micronucleus test, Salmonella mutagenicity test, and Allium anaphase-telophase test.

The genotoxic potential of the herbicide Roundup and its active agent, glyphosate isopropylamine salt, was studied in three different assays. No clastogenic effects were found in the mouse bone marrow micronucleus test for either of the two agents. In the Salmonella assay only Roundup was tested. It showed a weak mutagenic effect for the concentrations 360 micrograms/plate in TA98 (without S9) and 720 micrograms/plate in TA100 (with S9). These concentrations are close to the toxic level. The anaphase-telophase Allium test showed no effect for the glyphosate isopropylamine salt, but a significant increase in chromosome aberrations appeared after treatment with Roundup at concentrations of 1.44 and 2.88 mg/l when calculated as glyphosate isopropylamine. The most frequent aberrations observed could be characterized as disturbances of the spindle.

Allium↗
PubMed2004

Comparison of Multi-Test II skin prick testing to intradermal dilutional testing.

OBJECTIVES/HYPOTHESIS: Intradermal dilutional testing (IDT) has been considered more sensitive than prick testing for detecting low-level allergies. Multi-Test II is one of the most sensitive and reproducible prick testing methods available. This study compares Multi-Test II prick testing with IDT. DESIGN: Retrospective chart review and data analysis on patients who had allergy testing with both Multi-Test II and IDT. SETTING: Outpatient allergy clinic in the otolaryngology department of an academic tertiary care medical center. POPULATION: Forty adult patients had complete allergy testing with both Multi-Test II and IDT for a standard panel of twelve antigens between January 2002 and April 2002. INTERVENTION: Analysis and comparison of test results on Multi-Test II and IDT for each antigen separately and across all antigen tests together. RESULTS: Forty patients had complete testing for all antigens during the time period for the study. Six of these patients did not react to the positive control on Multi-Test II and were eliminated from the main analysis. Of the 34 patients included in the main analysis, all were positive for at least one antigen on IDT; one half (17/34) were negative for all antigens on Multi-Test II. A significantly greater number of patients were positive on IDT than Multi-Test II for all antigens except dog (P < 0.05). There was a statistically significant correlation between IDT endpoint and Multi-Test II score for several antigens (P < 0.05). Of 408 total antigen tests performed, 339 (83.1%) were negative on Multi-Test II. Of these 339 negative Multi-Test II tests, 148 (43.7%) were negative on IDT and 191 (56.3%) were positive on IDT; 174/339 (51.3%) had an IDT endpoint of 2 or 3 and 17/339 (5.0%) had an IDT endpoint > or = 4. A significantly greater number of antigen tests were positive on IDT than on Multi-Test II (P < 0.001). The overall Spearman correlation coefficient between IDT endpoint and Multi-Test II score was 0.370 (P < 0.001). CONCLUSION: Patients were more likely to have a positive test on IDT than on Multi-Test II. IDT therefore may be a more sensitive testing technique for inhalant allergies than Multi-Test II prick testing. In addition, Multi-Test II score may not be a good predictor of IDT endpoint. Although a statistically significant correlation is demonstrated between Multi-Test II score and IDT endpoint, the correlation coefficient is low enough that clinical application may not always be safe or appropriate. The clinical significance of positive IDT results in the presence of negative Multi-Test II results is not known.

Adolescent↗
PubMed1968

Standardized ability tests and testing. Major issues and the validity of current criticisms of tests are discussed.

At the outset a distinction was made between criticisms directed at the validity of tests and criticisms not affected by the validity of the tests. It was noted further that all criticisms of tests must take into consideration the type of test and the use to which the test is put. Criticisms of the validity of tests involved the following issues: (i) tests may be unfair to certain groups and individuals, including the extremely gifted, the culturally disadvantaged, and those who lack experience in taking tests; (ii) tests are not perfect predictors of subsequent performance; (iii) tests may be used in overly rigid ways; (iv) tests may not measure inherent qualities of individuals; and (v) tests may contribute to their own predictive validity by serving as self-fulfilling prophecies. Criticisms that are more or less independent of test validity included the effects of tests on (i) thinking patterns of those tested frequently; (ii) school curricula; (iii) self-image, motivation, and aspirations; (iv) groups using tests as a criterion for selection or allocation, or both; and (v) privacy. Several concluding remarks are in order: 1) This paper has focused almost entirely on criticisms of tests. However, the positive value of standardized tests should not be ignored. Here we must keep in mind what possible alternative measures would be used if standardized tests were abandoned. 2) We must begin thinking about tests in a much broader perspective- one that includes consideration of the social effects of tests as well as their validity and reliability. 3) Finally, an effort should be made to develop rational and systematic policies on the use of tests with the culturally disadvantaged, the dissemination of test results, and the problem of invasion of privacy. Such policies can be formulated only if we are willing to take a long hard look at the role we want testing to play in the society. Standardized tests currently are a cornerstone in the edifice of stratification in American society. It is up to the social scientist to conduct research that will enable policy makers in education, business and industry, and government to determine in a consistent and rational way the ultimate shape of this edifice.

Achievement↗
PubMed1975

[Potency testing of inactivated rabies vaccines with the antibody binding test in comparison with the NIH and habel test(author's transl)].

The Antibody Binding Test, a new technique for the evaluation of inactivated Rabies vaccines, developed by Arko, Wiktor and Sikes, was compared with the NIH- and Habel Test. Various vaccines were tested with these methods with the following results and conclusions. 1. The Habel Test was useful for testing of Hempt vaccines. With highly potent vaccines however it was not possible to get exact protection values, for all vaccinated mice were protected against all virus dilutions. 2. The NIH Test seemed to have an advantage over the Habel Test, since animals are vaccinated only twice, instead of 6 times, within two weeks. But this test was less suitable for the evaluation of Hempt vaccines. The requested Antigenic Value was reached only rarely with these vaccines. Repeated, NIH Tests gave widely differing results with Hempt vaccines. Vaccines which passed the NIH Test also passed the Habel Test, but not always vice versa. Antigenic Values of highly potent vaccines could be determined exactly with the NIH Test. This method is much better standardized by using a Standard vaccine in the test. The NIH Test is preferable for inactivated Rabies vaccines, with the exception of vaccines containing brain tissue, like the Hempt vaccine. 3. The Antibody Binding Test is a useful technique for the examination of inactivated cell culture vaccines. Consistent results can be achieved by skilled and experienced laboratory personnel. To avoid irregularities in the mortality rates, at least 10 mice should be used for each dilution of vaccine. With this method only Rabies virus antigen is measured which is bound by serum antibody during an incubation period of 60 min. Other factors supporting immunization like adjuvant- or booster-effects are not evaluated. Compared with the Habel and NIH Test the Antibody Binding Test is the best method for the evaluation of the amount of antigen in a Rabies vaccine. Hempt vaccines reached - as they did in the NIH Test - only Antigenic Values in this test. Vaccines with an Antigenic Value of larger than or equal to 0,3 in the Antibody Binding Test gave positive results also in the Habel and NIH Test, Vaccines with a Protection Value of 10-3 in the Habel Test and an Antigenic Value of 0,3 in the NIH Test did not always reach an Antigenic Value of 0.3 in the Antibody Binding Test.

Animals↗