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Biomedical subjects

M Atassi

Publications and source records attributed to M Atassi.

3 recordsLinked to original sources

In vivo interaction of ketoconazole and sucralfate in healthy volunteers.

Absorption of ketoconazole is impaired in subjects with an increased gastric pH due to administration of antacids, H2-receptor antagonists, proton pump inhibitors, or the presence of hypochlorhydria. Sucralfate could provide an attractive alternative in patients receiving ketoconazole who require therapy for acid-peptic disorders. Twelve healthy human volunteers were administered a single 400-mg oral dose of ketoconazole in each of three randomized treatment phases. In phase A, ketoconazole was administered orally with 240 ml of water. In phase B, ketoconazole and sucralfate (1.0 g) were administered simultaneously with 240 ml of water. In phase C, ketoconazole was administered with 240 ml of water 2 h after administration of sucralfate (1.0 g) orally with 240 ml of water. A 680-mg oral dose of glutamic acid hydrochloride was administered 10 min prior to and with each dose of ketoconazole, sucralfate, or ketoconazole plus sucralfate. Simultaneous administration of ketoconazole and sucralfate led to a significant reduction in the area under the concentration-time curve and maximal concentration of ketoconazole in serum (78.12 +/- 12.20 versus 59.32 +/- 13.61 micrograms.h/ml and 12.34 +/- 3.07 versus 8.92 +/- 2.57 micrograms/ml, respectively; P < 0.05). When ketoconazole was administered 2 h after sucralfate, the observed ketoconazole area under the concentration-time curve was not significantly decreased compared with that of ketoconazole alone. The time to maximal concentrations in serum and the ketoconazole elimination rate constant were not significantly different in any of the three treatment phases. In patients receiving concurrent administration of ketoconazole and sucralfate, doses should be separated by at least 2 h.

Absorption

[Reading epilepsy].

Reading epilepsy in many cases may be identified by clicking sensations or myoclonic jaw jerks, which are supposed to be prodromal symptoms to generalized epileptic convulsions. Although these prodromal symptoms were considered as characteristic by the first authors describing the illness, they were not observed in all the published cases. In this paper a modified classification following the original proposal of Bickford is suggested. It is now proposed to differentiate a primary specific respectively nonspecific form from a secondary type. Most of the cases described were between 15 and 28 years of age. Probably the disorder is only of transient nature. The pathogenic roots are multifactorial, and the seizures cannot be attached to typical focus-regions. Decoding mechanisms and disorders of speech as sensoric restraints are obviously of great importance in actual provocation.

Adolescent

[Primary reading epilepsy; a case report (author's transl)].

It is reported on a 21 years old patient with primary reading epilepsy. While reading various texts he suffered from involuntary jaw-jerks, which once a G.M. seizure caused. While reading on the EEG were synchronously 4--5/s bursts registered, once as vehement that the registration had to be stopped. As in two other publicated cases, the spinal fluid protein as well as a slightly pleocytosis, was elevated, which was thought to be inflammatory caused as the case in encephalomyelitis disseminata.

Adult