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Quantitative assessment of the electroencephalogram in renal disease.

Authors :
Bourne JR
Ward JW
Teschan PE
Musso M
Johnston HB Jr
Ginn HE
Source :
Electroencephalography and clinical neurophysiology [Electroencephalogr Clin Neurophysiol] 1975 Oct; Vol. 39 (4), pp. 377-88.
Publication Year :
1975

Abstract

EEGs wre recorded from renal patients to determine if there are quantifiable characteristic changes in the EEG was quantified by calculating the percentage of spectral power in the bandwidth 3-7 c/sec referrred to a frequency range of 3-13 c/sec and by computing the mean frequency of the dominant rhythm in the EEG. Blood urea nitrogen and creatinine concentrations, as well as a self-assessment of the patient's clinical condition, were recorded. The general finding of this research is that EEG slowing, as evaluated by power spectral techniques, is correlated with uremia-associated variables. 1. In a non-dialyzed patient population with renal failure, slowing in the EEG was found to be directly corelated with increased creatinine concentrations. 2. Quantitative measures of slow wave activity computed using power spectral techniques were found to be highly corelated with an estimate of slowing made by an electroencephalographer. 3. Compared with undialyzed azotemic patients, malignant hypertensive patients with comparable serum creatinine concentrations typically displayed increased slow wave activity, while slowing was generally reduced in the dialyzed patient population. 4. A series of EEGs recorded from one patient during the first three dialyses of her life revealed that slow wave activity decreased during each successive dialysis. In another patient, all quantified EEG values recorded prior to renal transplantation significantly improved after transplantation...

Details

Language :
English
ISSN :
0013-4694
Volume :
39
Issue :
4
Database :
MEDLINE
Journal :
Electroencephalography and clinical neurophysiology
Publication Type :
Academic Journal
Accession number :
51721
Full Text :
https://doi.org/10.1016/0013-4694(75)90101-7