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Biomedical subjects

J E Murphy

Publications and source records attributed to J E Murphy.

129 records · Page 8Linked to original sources

Identification of Salmonella enteritidis from experimentally infected hens using a colorimetric DNA hybridization method.

Identification of Salmonella enteritidis from cloacally challenged commercial laying hens was studied by comparing bacterial isolations using conventional methods with detection by the use of the GENE-TRAK colorimetric DNA probe assay. More positive test results were obtained using the latter on days 14, 28, and 42 postchallenge, but the difference between the two methods was not statistically significant. Over the duration of the experiment, positive cloacal samples were statistically more frequent from a commercial strain of white leghorn hens when compared with a commercial brown egg-producing strain (28/60 vs. 9/57; chi-square 1 df = 12.9, P < 0.001). Eggs having various shell defects were produced by the infected hens only after Salmonella challenge. These defects included, in order of frequency, elongated shape, thin shells, off-white color (tints), small size, wrinkles, and pimples. No Salmonella could be recovered from 193 defective eggs, nor were positive isolates made from additional tests performed on 50 normal eggs. Proteus sp. was isolated from 10 eggs, however. Our observations demonstrate that the GENE-TRAK colorimetric method is comparable with conventional bacteriology for the identification of Salmonella in cloacal samples taken from laying hens. Moreover, the two methods demonstrate the existence of breed differences in susceptibility to S. enteritidis challenge.

Analysis of Variance↗

Clinical pharmacokinetic pearls: bolus versus infusion equations.

Using a nonprogrammed calculator to solve lengthy pharmacokinetic equations is time consuming and carries the potential for entry error. Shorter equations reduce both the time and the risk. The aminoglycosides and vancomycin are usually administered as short infusions. The pharmaco-kinetic equation describing multiple-dose administration of short infusions is much longer than the corresponding equation for bolus dosing. This study examined the percentage errors that would occur using the bolus equation instead of the infusion equation at various drug half-lives. When the half-life is 5 or more times the duration of infusion, the error in predicting concentration is 6.8% or less. Although clinicians should make their own decisions on how much error is acceptable and whether introducing guaranteed error is appropriate to save time and reduce risk of potential error, it appears that the simpler bolus equation may be used safely when the half-life is at least 5 times the duration of the infusion.

Aminoglycosides↗