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Biomedical subjects

A Pasquetti

Publications and source records attributed to A Pasquetti.

5 recordsLinked to original sources

Effects of thalidomide on HIV-associated wasting syndrome: a randomized, double-blind, placebo-controlled clinical trial.

OBJECTIVE: To evaluate the efficacy of thalidomide in treating wasting syndrome in patients with advanced HIV disease, and to assess the effects of thalidomide on circulating CD4+ T cells, and on HIV viral burden in peripheral blood mononuclear cells (PBMC). DESIGN: Randomized, double-blind placebo-controlled clinical trial. SETTING: Public tertiary care hospital in Mexico City. PATIENTS: Twenty-eight adults with advanced HIV disease being treated with antiretroviral therapy, and who had received antiretrovirals for at least 6 months, who did not have an active opportunistic infection, and who had 10% weight loss in the previous 6 months. INTERVENTIONS: Patients received thalidomide (100 mg by mouth, four times daily) or a matching placebo for the duration of the study (12 weeks). MAIN OUTCOME MEASURES: The main clinical endpoint for efficacy of thalidomide was weight gain or no progression of wasting. Secondary endpoints were Karnofsky performance status, CD4+ cell counts, and HIV viral burden in PBMC. RESULTS: Both groups were comparable in their baseline status. Therapeutic failure occurred in 10 out of 14 patients from the placebo group and in three out of 14 from the thalidomide group (P = 0.021). Weight gain occurred in one patient on placebo and in eight given thalidomide. The Karnofsky index was significantly higher by the end of the study in the thalidomide group (P = 0.003). Mild and transient somnolence and erythematous macular skin lesions were significantly more common in the thalidomide group. CD4+ T cell counts and HIV viral burden in PBMC did not change in either group. CONCLUSIONS: Results suggest that thalidomide not only impeded but also reverted the wasting syndrome, preserving the Karnofsky index in patients with advanced HIV disease. Thalidomide, at the dosage used in this study, had no effect on peripheral CD4+ T cells nor on HIV viral burden in PBMC.

Adult↗

Lactose digestion and clinical tolerance to milk, lactose-prehydrolyzed milk and enzyme-added milk: a study in undernourished continuously enteral-fed patients.

We investigated: (1) the capacity to digest and tolerate the lactose administered by continuous infusion of intact milk to undernourished tube-fed patients, and (2) the effectiveness of lactose-prehydrolyzed milk, and of the addition of exogenous lactase to milk at infusion time, to reduce lactose maldigestion and increase clinical tolerance. Carbohydrate digestion was evaluated in 10 subjects with the hydrogen breath analysis test during 8 hr of observation. Lactose intolerance was determined by evaluation of subject's symptoms. With the infusion of intact milk (IM), none of the subjects were able to efficiently digest the lactose infused (5.6 +/- 0.35 g/hr, mean +/- SEM) and 86% of them experienced major symptoms of intolerance. With the infusion of lactose-prehydrolyzed milk (HM) and enzyme-added milk (EM) there was a highly significant reduction in lactose maldigestion. More importantly, major symptoms were present in only 10% of subjects with EM, and were completely eliminated with HM. Lactose maldigestion and intolerance represent a major limitation for the application of milk-based polymeric formula for liquid diets in undernourished subjects. The use of exogenous beta-galactosidases represents an alternative to avoid such reactions.

Adult↗

[A model for evaluating internal accuracy].

OBJECTIVE: To provide an evaluation model of internal accuracy illustrating its use in a quality control program of clinical chemistry. METHODS: The model uses data transformed to percentage of assigned value (%AV) that allows the pooling of different controls. Precision is evaluated by the mean of the intracontrol coefficients of variation, and accuracy by the mean of means of the %VAs and its standard deviation. The model was used in 17,280 measurements of 23 analytes assayed in seven pairs of controls (medium and high concentration) during four years in two automated clinical chemistry analyzers. RESULTS: The model established inaccuracy of 5% to 25% in seven analytes, five of them enzymes. It also detected interanalyzer differences in accuracy of five analytes (22%) and an erroneous assigned value in 19 of 304 controls (6%). CONCLUSIONS: The model showed its capacity to dissect the sources of variation of accuracy. There was inaccuracy in 30% of the analytes but further studies are needed to validate these inaccuracies with controls of other sources. The model can be useful for control programs of any quantitative assay system. A summary description of the model's operation is given.

Chemistry, Clinical↗