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1.
Article in Russian | MEDLINE | ID: mdl-11517472

ABSTRACT

Efficiency of Semax (synthetic derivative of ACTH-4-10) was studied in 30 patients in acute period of hemispherical ischemic stroke. Control group consisted of 80 patients with the strokes analogous in severity and location of the damages and which were treated by conventional therapy. Different clinical rating scales were used for both objectivization of the severity of the patients' state and estimation of the degree of neurological defect. The control of Semax influence on the functional state of the brain included monitoring of EEG with mapping, repeated analysis of somatosensory evoked potentials and their mapping. It was established that including of Semax in combined intensive therapy of acute ischemic stroke had some influence on the rate of restoration of the damaged neurological functions in terms of increasing the regress of general cerebral and focal, especially motor disorders. The most effective daily doses were 12 mg for patients with strokes of moderate severity and 18 mg for patients with severe strokes (treatment course--5 and 10 days).


Subject(s)
Adrenocorticotropic Hormone/therapeutic use , Neuroprotective Agents/therapeutic use , Nootropic Agents/therapeutic use , Peptide Fragments/therapeutic use , Stroke/drug therapy , Acute Disease , Adrenocorticotropic Hormone/administration & dosage , Adrenocorticotropic Hormone/analogs & derivatives , Aged , Amino Acids/administration & dosage , Amino Acids/therapeutic use , Brain Mapping , Electroencephalography , Evoked Potentials, Somatosensory , Female , Gangliosides/administration & dosage , Gangliosides/therapeutic use , Humans , Male , Neuroprotective Agents/administration & dosage , Nootropic Agents/administration & dosage , Peptide Fragments/administration & dosage , Severity of Illness Index , Stroke/diagnosis , Stroke/physiopathology , Time Factors
2.
Article in Russian | MEDLINE | ID: mdl-9424343

ABSTRACT

54 patients were treated by notropil (pyracetam). The results of therapy were evaluated statistically according to a number of clinical scales and neurophysiologic indices (EEG and evoked potentials with mapping of bioelectric activity). The results were compared with the data about 56 patients of the control group which were treated by traditional method without application of notropil. Notropil was applied by two ways: small doses (4-12 g daily) during 5 days or high doses (10-12 g daily) during 30 days from the moment when the patient admitted to the hospital. Intravenous injections of the drug were used in all cases as well as its internal administration. It was showed either efficiency of the drug, especially in high doses, in early beginning of the treatment and its duration for at least 30 days or good tolerance of the drug. Authors supposed that application of pyracetam is not adequate in strokes with severe disorders of consciousness and cerebral edema.


Subject(s)
Brain Ischemia/drug therapy , Neuroprotective Agents/administration & dosage , Piracetam/administration & dosage , Acute Disease , Brain Ischemia/diagnosis , Brain Ischemia/metabolism , Combined Modality Therapy , Dose-Response Relationship, Drug , Drug Evaluation , Electroencephalography/drug effects , Female , Humans , Male , Middle Aged , Time Factors
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