RÉSUMÉ
On 44 epileptic patients antiepileptic phenobarbital, finlepsin, diphenine, hexamidine were studied. The alterations in the level of free and bound fractions under the drug application in maximal tolerance daily doses, depending on changes in the administration frequency during the day, were recorded. It was established that level fluctuations of the total preparation occur mainly owing to level alterations in the fraction not bound to serum proteins. An increase in the drug administration frequency under the constant daily dose leads to a distinct reduction in the free fraction level fluctuations between doses, to a decrease in the intensity or removal of side effects, and makes it possible to further build up the daily dose to obtain the required effect.
Sujet(s)
Anticonvulsivants/administration et posologie , Épilepsie/traitement médicamenteux , Adolescent , Adulte , Anticonvulsivants/sang , Protéines du sang/métabolisme , Maladie chronique , Relation dose-effet des médicaments , Résistance aux substances , Épilepsie/sang , Femelle , Humains , Mâle , Adulte d'âge moyen , Liaison aux protéines , Comprimés , Facteurs tempsRÉSUMÉ
Overall 30 women in childbirth with preeclampsia and fetoplacental dysfunction received piracetam solution which was given initially in a dose of 5 g by intravenous drip, rapidly since the onset of labour and then every 2 hours till the end of labour in a dose of 2 g by jet injection. This made it possible to increase fetus resistance to hypoxic conditions. The concentrations of piracetam within the range of 60-80 g/l in the blood of women in childbirth should be viewed as minimum therapeutic. A single daily intramuscular injection of piracetam (50 mg/kg) into neonates with encephalopathies may build up blood concentrations equal to 25-60 mg/l after 2 hours. The drug is not detectable in the blood by the moment the next injection is given.
Sujet(s)
Surveillance des médicaments , Travail obstétrical/effets des médicaments et des substances chimiques , Piracétam/sang , Adolescent , Adulte , Asphyxie néonatale/sang , Asphyxie néonatale/prévention et contrôle , Chromatographie en phase liquide à haute performance , Maladie chronique , Femelle , Humains , Nouveau-né , Travail obstétrical/sang , Piracétam/administration et posologie , Insuffisance placentaire/sang , Insuffisance placentaire/traitement médicamenteux , Pré-éclampsie/sang , Pré-éclampsie/traitement médicamenteux , GrossesseSujet(s)
Anticonvulsivants/administration et posologie , Barbituriques/administration et posologie , Épilepsies partielles/traitement médicamenteux , Épilepsie généralisée/traitement médicamenteux , Adolescent , Adulte , Anticonvulsivants/sang , Barbituriques/sang , Chromatographie en phase liquide à haute performance , Maladie chronique , Évaluation de médicament , Épilepsies partielles/sang , Épilepsie généralisée/sang , Femelle , Humains , Mâle , Adulte d'âge moyen , Facteurs tempsRÉSUMÉ
Despite complete absorption of theophylline by CKH-4H and phi AC sorbents from the blood of patients one hour after hemosorption the blood drug level reached the values corresponding to the usual level of theophylline elimination. It is concluded that no correction of theophylline dosage is needed during treatment of patients with bronchial asthma by hemosorption, however, the initial blood content of the drug should be between medium and maximum drug level capable of causing therapeutic effect.
Sujet(s)
Asthme/thérapie , Hémoperfusion , Théophylline/administration et posologie , Adolescent , Asthme/traitement médicamenteux , Enfant , Association thérapeutique , Humains , Théophylline/sang , Théophylline/usage thérapeutiqueRÉSUMÉ
The treatment with primidone alone of 53 epileptic patients with generalized tonic-clonic seizures, partial attacks with elementary symptomatology, and partial fits with complex symptomatology removed them completely in 75, 64.2, and 36.9% of the patients, respectively. The number of attacks was decreased as a result by 50% and over in 90, 78.6, and 73.7% of the patients, respectively. The attainment of such high efficacy of the monotherapy (called by the author intensive in contrast to routine or inadequate therapy carried out, as a rule, in standard doses) appeared possible only under the conditions of individualization of the drug doses which ranged within 250-2500 mg/day. The concentration of phenobarbital, the main end metabolite of primidone, in the blood serum of patients, in whom the attacks were completely arrested and who developed no clinical side effects with no toxic action on the internal organs, ranged from 14 to 59.1 mg/l. In partial fits with complex symptomatology, primidone appeared least effective for those types of fits in the treatment of which it was viewed as most adequate.
Sujet(s)
Anticonvulsivants/administration et posologie , Épilepsies partielles/traitement médicamenteux , Grand mal épileptique/traitement médicamenteux , Adolescent , Adulte , Benzamidines/administration et posologie , Relation dose-effet des médicaments , Surveillance des médicaments , Épilepsie partielle complexe/traitement médicamenteux , Humains , Adulte d'âge moyen , PrimidoneSujet(s)
Asthme/traitement médicamenteux , Théophylline/administration et posologie , Adolescent , Asthme/métabolisme , Enfant , Enfant d'âge préscolaire , Rythme circadien , Résistance aux substances , Humains , Monitorage physiologique , Récidive , Théophylline/sang , Théophylline/pharmacocinétiqueRÉSUMÉ
The study of almagel effect on euphylline absorption in children with bronchial asthma showed a decrease of theophylline concentration by 10-15% ten days after the combined administration of the drugs. The absence of the change in the blood theophylline concentration three days after administration of almagel against the background of euphylline indicates that the reason for a decrease of euphylline absorption is not the absorbing and lubricating properties of almagel but probably almagel-induced reduction of the inflammation of the gastrointestinal tract mucosa (hyperemia, increased vascular permeability) caused by euphylline.
Sujet(s)
Hydroxyde d'aluminium/usage thérapeutique , Aminophylline/pharmacocinétique , Asthme/traitement médicamenteux , Benzocaïne/usage thérapeutique , Hydroxyde de magnésium/usage thérapeutique , Magnésium/usage thérapeutique , Absorption , Adolescent , Aminophylline/effets indésirables , Aminophylline/sang , Asthme/sang , Enfant , Enfant d'âge préscolaire , Association médicamenteuse/usage thérapeutique , Association de médicaments , Humains , Théophylline/sang , Facteurs tempsRÉSUMÉ
In spite of the appearance of the tolerance to phenibut in white rats at days 11-12 of its intraperitoneal administration (250 mg/kg), the drug injections (25 micrograms) into the lateral ventricles of the brain via permanent cannulas evoked, as before, a fall in the body temperature and synchronization of the electrocorticogram in rats. The tolerance to phenibut did not occur when the drug was injected daily (12 days) into the brain ventricles. A conclusion is made that the tolerance to phenibut has a peripheral character.