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1.
Nervenarzt ; 68(4): 324-30, 1997 Apr.
Article in German | MEDLINE | ID: mdl-9273461

ABSTRACT

Sixty-three patients with tick-borne encephalitis were studied for sequelae up to 5 years after the acute illness (median: 12 months, range: 1-44 months). Patients were examined clinically, by neuropsychological testing and by electroencephalography. The clinical presentation during the acute stage was as follows: Meningitis (M,n = 12), Meningoencephalitis (Me,n = 27), Meningoencephalomyelitis (My,n = 15), and Meningoencephaloradiculitis (R,n = 9). A total of 59 patients reported a neurasthenic syndrome after discharge, which correlated with the severity of the acute illness. Twenty patients were not able to work because of reduced stress tolerance, fatigue or an elevated emotional sensitivity, which lasted for 3 months at most. In some patients hypacusis (n = 7), severe dysarthria and dysphagia (n = 4) remained essentially unimproved for years following the acute illness. While in 8/9 patients with radiculitis paresis of the extremities improved well over months to years, improvement was quite limited in all patients with myelitis. In 41/55 patients, investigations by electroencephalography revealed normal findings even within months after acute illness. Persistent cognitive deficits were present only in 7/11 patients with a severe course of disease.


Subject(s)
Electroencephalography , Encephalitis, Tick-Borne/diagnosis , Neurologic Examination , Neuropsychological Tests , Adolescent , Adult , Aged , Aged, 80 and over , Brain Damage, Chronic/diagnosis , Brain Damage, Chronic/physiopathology , Cerebral Cortex/physiopathology , Child , Encephalitis, Tick-Borne/physiopathology , Female , Follow-Up Studies , Humans , Male , Middle Aged , Myelitis/diagnosis , Myelitis/physiopathology , Spinal Cord/physiopathology
3.
Dtsch Med Wochenschr ; 109(48): 1829-32, 1984 Nov 30.
Article in German | MEDLINE | ID: mdl-6209080

ABSTRACT

In a randomized double-blind cross-over trial, the effectiveness of lorcainide at a dosage of three times 100 mg/d by mouth was compared with that of a placebo for the treatment of subjectively disturbing stable ventricular extrasystoles (VES), using 48-hour continuous ECG monitoring. In 11 of 20 patients there was a regression in the VES rate to under 5%, in other 3 patients to under 50% of the initial values. Continuing the treatment, good therapeutic effect was still demonstrable 14 and 28 days later. However, only three patients had no side-effects. The others had sleep disturbances, hot flushes, sweating, restlessness, anxiety, dizziness, hallucinations and gastrointestinal symptoms. Lorcainide thus has a good anti-arrhythmic effect but, because of its side-effects, it should be used only in special circumstances.


Subject(s)
Anti-Arrhythmia Agents/therapeutic use , Benzeneacetamides , Cardiac Complexes, Premature/drug therapy , Piperidines/therapeutic use , Adult , Cardiac Complexes, Premature/physiopathology , Clinical Trials as Topic , Double-Blind Method , Electrocardiography , Female , Humans , Male , Middle Aged , Piperidines/adverse effects , Placebos , Time Factors
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