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Biomedical subjects

R Coleman

Publications and source records attributed to R Coleman.

401 records · Page 23Linked to original sources

Overview of antiretroviral therapy.

All of the agents that are available for the treatment of human immunodeficiency viral infection belong to the class of drugs called nucleoside analogs that act on the virus's reverse transcriptase enzyme. As their use expanded for increasing cohorts of patients and stages of disease, it became clear that additional agents were required that would act at different points in the virus's life cycle. Several different classes of drugs have been identified and evaluated in the laboratory and the clinic. At this point, one of the most promising that is undergoing clinical trials is the proteinase inhibitors. It is important to assess the data for currently available drugs and use that information to determine the most appropriate role for proteinase inhibitors. To appreciate their potential role best, we must also glance over the horizon at other experimental treatments.

Drug Therapy, Combination↗

Direct comparison of three methods for predicting digoxin concentrations.

Three methods of determining digoxin population pharmacokinetic parameters were compared for their abilities to predict 118 measured serum digoxin concentrations (SDCs) in 49 patients. NONMEM software (version IV) was used to generate a residual and a weighted residual for each measured-concentration-predicted-concentration pair. Prediction error analysis was done by a maximum likelihood technique that accounted for several within-patient measures. Data analysis also included graphic observation of weighted residuals (WRES) and calculation of the mean WRES and median absolute prediction error. A further parallel analysis was also carried out on subpopulations with and without concurrent quinidine and congestive heart failure (CHF). Method III was without bias in all subpopulations studied and had the smallest WRES in all populations. Method I was without bias in the overall population, however, it underpredicted SDCs in patients receiving quinidine and in those with CHF. Method II underpredicted SDCs in the overall population, those receiving quinidine, and in patients without CHF. There were no between-method differences in precision as assessed by absolute prediction error.

Adult↗