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1.
Brain Inj ; 13(4): 229-43, 1999 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-10230524

RESUMO

Carbon monoxide (CO) poisoning has been shown to result in neuropathologic changes and cognitive impairments due to anoxia and other related biochemical mechanisms. The present study investigated brain-behaviour relationships between neuropsychological outcome and SPECT, MRI, and Quantitative magnetic resonance imaging (QMRI) in 21 patients with CO poisoning. Ninety-three per cent of the patients exhibited a variety of cognitive impairments, including impaired attention, memory, executive function, and mental processing speed. Ninety-five per cent of the patients experienced affective changes including depression and anxiety. The results from the imaging studies revealed that 38% of the patients had abnormal clinical MRI scans, 67% had abnormal SPECT scans, and 67% had QMRI findings including hippocampal atrophy and/or diffuse cortical atrophy evidenced by an enlarged ventricle-to-brain ratio (VBR). Hippocampal atrophy was also found on QMRI. SPECT and QMRI appear to be sensitive tools which can be used to identify the neuropathological changes and cerebral perfusion defects which occur following CO poisoning. Cerebral perfusion defects include frontal and temporal lobe hypoperfusion. Significant relationships existed between the various imaging techniques and neuropsychological impairments. The data from this study indicate that a multi-faceted approach to clinical evaluation of the neuropathological and neurobehavioural changes following CO poisoning may provide comprehensive information regarding the neuroanatomical and neurobehavioural effects of CO poisoning.


Assuntos
Encéfalo/diagnóstico por imagem , Encéfalo/patologia , Intoxicação por Monóxido de Carbono/complicações , Transtornos Cognitivos/induzido quimicamente , Transtornos Cognitivos/diagnóstico , Adulto , Atrofia/patologia , Encéfalo/irrigação sanguínea , Feminino , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Testes Neuropsicológicos , Índice de Gravidade de Doença , Tomografia Computadorizada de Emissão de Fóton Único
2.
J Rheumatol ; 24(12): 2353-7, 1997 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-9415641

RESUMO

OBJECTIVE: To investigate whether reduced circulating levels of ascorbic acid in patients with systemic sclerosis (SSc) are a result of malabsorption. METHODS: Eight patients with SSc, but with no evidence of bacterial overgrowth, and 8 healthy controls were recruited. On the first day of study, each subject was given orally an aliquot of [14C] ascorbic acid, which was then "flushed out" by oral intake of unlabeled ascorbic acid for the following 7 days. Plasma samples were collected at specified intervals and urine was collected continuously over the 8 day study period. [14C] content of plasma and urine were measured by scintillation counting. For each subject, a plasma [14C] decay curve was drawn. Each subject's ascorbic acid absorption was assessed using the area under the curve (AUC) and the apparent renal clearance (CLr[app]). Ascorbic acid intake was assessed using dietary history and food composition tables. RESULTS: There were no differences in the dietary intake of vitamin C (p = 0.16) and body mass indices (p = 0.91) between patients and controls. The plasma [14C] AUC and CLr(app) were similar between patients and controls [AUC patient mean (standard deviation, SD) = 37.1 (6.8), AUC control mean (SD) = 38.6 (9.9), p = 0.74; CLr(app) patient mean (SD) = 0.57 (0.24), CLr(app) control mean (SD) = 0.47 (0.27), p = 0.45]. CONCLUSION: There was no evidence of impaired absorption of ascorbic acid in patients with SSc without bacterial overgrowth compared to healthy controls.


Assuntos
Ácido Ascórbico/farmacocinética , Escleroderma Sistêmico/metabolismo , Absorção , Adulto , Ácido Ascórbico/sangue , Ácido Ascórbico/urina , Índice de Massa Corporal , Radioisótopos de Carbono , Feminino , Motilidade Gastrointestinal , Humanos , Intestinos/microbiologia , Síndromes de Malabsorção/metabolismo , Síndromes de Malabsorção/microbiologia , Masculino , Pessoa de Meia-Idade , Escleroderma Sistêmico/microbiologia
3.
J Urol ; 113(2): 258-60, 1975 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-1113423

RESUMO

Intrauterine fetal vesicoureteral reflux has been demonstrated in a 25-week fetus. A voiding cystourethrogram when the patient was 1 year old showed persistence of the bilateral reflux. No urinary tract infectious have been documented. A survey of other physicians performing fetal transfusions indicates that fetal cystograms are infrequently obtained and that vesicoureteral reflux has been observed by ourselves and one other contributing physician. The incidence of reflux in fetal cystograms reviewed appears to be higher than would be expected when compared to normal premature babies, newborns, infants and children. This procedure provides an unusual opportunity to document intrauterine fetal vesicoureteral reflux and later obtain followup cystourethrograms in these children to determine the resolution or progression of this urinary tract abormality.


Assuntos
Doenças Fetais , Refluxo Vesicoureteral , Adulto , Transfusão de Sangue Intrauterina , Eritroblastose Fetal/complicações , Eritroblastose Fetal/terapia , Feminino , Doenças Fetais/diagnóstico por imagem , Seguimentos , Humanos , Lactente , Recém-Nascido , Gravidez , Radiografia , Refluxo Vesicoureteral/diagnóstico por imagem
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