PubMed Health⌕ Search

Biomedical subjects

J G Duarte

Publications and source records attributed to J G Duarte.

5 recordsLinked to original sources
PubMed1999

Chronic inhaled cocaine abuse may predispose to the development of pancreatic adenocarcinoma.

BACKGROUND: The acute and chronic effects of cocaine over various organ systems have been well documented. A more recent approach to the effects of this drug has focused on the immunological consequences of its exposure, with results that indicate a possible carcinogenic effect. METHODS: A chart review was made in order to search for young pancreatic adenocarcinoma patients (arbitrarily defined as younger than 40) who made use of inhaled cocaine. This age was chosen because of a higher probability of cocaine addiction than at older ages. RESULTS: Of the 198 patients with pancreatic adenocarcinoma, 13 were younger than 40 years (range 19 to 37) and 5 of these had abused inhaled cocaine for about a decade. One patient had abused marijuana, and there was no information on drug usage in the other 7 patient charts. CONCLUSION: Although this is a very small series, we believe there might be a possibility that chronic cocaine exposure predisposes to the development of pancreatic adenocarcinoma. Further studies are necessary.

Adenocarcinoma↗
PubMed1995

Respiratory mechanics and morphometry after progressive intraperitoneal effusion.

Respiratory mechanics and thoraco-abdominal morphometry were evaluated in anesthetized, paralyzed, mechanically ventilated rats before and after controlled intraperitoneal injection of warm (37 degrees C) saline. Respiratory system resistances and static elastance were determined in 9 animals using the end inflation occlusion method. Chest wall configuration at both functional residual capacity (FRC) and end inspiration (FRC + VT) was evaluated in: (a) 6 rats by measurements of lateral and anteroposterior diameters, and circumferences at four levels: 3rd intercostal space, xiphoid, subcostal plane and crista iliaca; and (b) 8 rats by measurements of thoracic cephalo-caudal diameter. In addition, FRC changes were measured in 6 rats. Resistances were not altered but static elastance increased progressively. Morphometric changes were similar at both FRC and FRC + VT: cephalo-caudal diameter diminished whereas all other diameters augmented; FRC decreased. In conclusion, intraperitoneal infusion of saline in rats augments elastance, and this is related to a cephalad deviation of the diaphragm plus an increase of the circumferences and diameters of the lower thorax.

Abdomen↗
PubMed1986

Potential of indium-111 to measure inflammatory arthritis.

Since an objective noninvasive method for measuring inflammation in arthritis is lacking, radioimaging experiments were conducted with 111indium-chloride (111InCl3) in the collagen model. A computer imaging index, reflecting uptake in the feet and ankles, was significantly greater in 16 rats immunized with collagen than in 6 nonimmunized rats (mean +/- SEM 1.18 +/- 0.04 vs 0.39 +/- 0.02, for the 2 groups, respectively, p less than 0.001). Additional analyses provided evidence that the 111InCl3 technique can be used to measure objectively progression of the arthritic response of rats of immunization with collagen, and pilot comparisons with conventional bone scintigraphy in 2 patients with rheumatoid arthritis suggested that the method is applicable to human arthritic disease.

Animals↗
PubMedDate not supplied

Toxicity of drugs used for treatment of rhinitis: a reminder to the otorhinolaryngologist.

We retrospectively studied files on toxicity of drugs used for treatment of rhinitis (nasal antihistamines, oral antihistamines, nasal vasoconstrictors, oral decongestants, nasal corticosteroids, nasal anticholinergic agent, nasal mast cell stabilizer, and respiratory antigen preparations for oral use) that occurred in São Paulo, Brazil, from 1 July 1996 to 30 June 1998. There were 823 cases of toxicity by these agents, with a predominance of oral decongestants (in combination with antihistamines) (53.4%). There was a significant incidence of toxicity within children aged 1 to 4 years (P < 0.05) and a preponderance among males aged 5-9 years and females aged 10-39 years. Accidental intake of medicines accounted for the majority of toxicity cases (57.2%).

Adolescent↗