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Dive into the research topics where D. Wyper is active.

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Featured researches published by D. Wyper.


The Lancet | 1986

Use of magnetic resonance imaging to measure intracranial cerebrospinal fluid volume

Barrie Condon; D. Wyper; Robert M. Grant; James Patterson; Donald M. Hadley; Graham M. Teasdale; Jack Rowan

Magnetic resonance imaging was used to measure intracranial extraventricular and ventricular cerebrospinal fluid (CSF) volume. In 10 normal subjects lateral ventricular and extraventricular intracranial CSF volumes were 25.3 +/- 4.6 ml (mean +/- SD) and 97.6 +/- 6.6 ml, respectively (total 122.8 +/- 38.7). These volumes were measured in 4 patients and the results were: 11.0 ml ventricular volume, 68.7 ml total cranial CSF in the patient with benign intracranial hypertension; 606.6 ml ventricular, 174.1 ml total in the patient with hydrocephalus due to a blocked ventriculo-peritoneal (V-P) shunt; 83.4 ml ventricular, 108.5 ml total in the patient with normal pressure hydrocephalus; and 52.7 ml ventricular, 181.0 ml total in the patient with cerebral atrophy due to Alzheimers disease. The technique gave highly reproducible results (SD less than 5.7% of mean value). It may be useful in differential diagnosis and as an objective means of monitoring therapy or progress in conditions such as cerebral atrophy, hydrocephalus, and benign intracranial hypertension.


Journal of Neurology, Neurosurgery, and Psychiatry | 1990

CT, MR and SPECT imaging in temporal lobe epilepsy.

Roderick Duncan; Jim Patterson; Donald M. Hadley; P Macpherson; M J Brodie; Ian Bone; A P McGeorge; D. Wyper

Cranial computed tomography (CT) with modified temporal lobe technique, 0.15T magnetic resonance imaging (MRI) and single photon emission computed tomography (SPECT) were carried out on 30 patients with intractable temporal lobe epilepsy. Lateralising abnormalities were detected in 21/30 patients overall. Specific lesions were detected by CT in one patient and by MRI in seven patients (in one case bilateral). In addition CT detected asymmetry of the sylvian fissures or temporal horns in 10 patients, and MRI in eight patients. SPECT detected lateralising abnormalities in 19 patients (in five cases bilateral). It is concluded that low field MRI is superior to modified CT in demonstrating subtle structural lesions of the temporal lobe. Functional scanning with SPECT supports the evidence of origin of an epileptic focus in a substantial proportion of cases and may improve the selection of patients for surgery.


Acta Neurologica Scandinavica | 2009

Tc99m HM-PAO single photon emission computed tomography in temporal lobe epilepsy

Roderick Duncan; Jim Patterson; Donald M. Hadley; D. Wyper; A. P. McGeorge; Ian Bone

We present the results of single photon emission computed tomography (SPECT) in 40 patients with temporal lobe epilepsy and normal computed transmission tomography (CT). Abnormalities of regional cerebral blood flow were found in 26 patients. There was focal hypoperfusion alone in 14, focal hyperperfusion alone in 6, and both types of abnormality in 6. In 4 patients there were bilateral abnormalities. Repeat SPECT showed persistence of interictal hyperperfusion in 5/12 patients. There were no significant correlations between SPECT findings and clinical parameters, and no relation between the persistence of interictal hyperperfusion and time since last seizure or seizure frequency. Where SPECT and multiple surface EEG recordings were both lateralising, agreement between them was good. The results of this study support the usefulness of HMPAO SPECT in detecting lateralising abnormalities in temporal lobe epilepsy. Interictal hyperperfusion may be commoner than previous publications suggest, and may be persistent in some cases.


Journal of Computer Assisted Tomography | 1987

MR relaxation times of cerebrospinal fluid.

Barrie Condon; James Patterson; Alistair Jenkins; D. Wyper; Donald M. Hadley; Robert M. Grant; Jack Rowan; Graham M. Teasdale

A review of 15 recent publications purporting to provide the relaxation times of CSF reveals a considerable disparity in the quoted results, by a factor of five in terms of T1 (range 1,000 to 5,500 ms) and by a factor of 16 for T2 (range 166 to 2,640 ms). In this article measurements are performed independently on both a spectrometer and an imager. The results indicate that for CSF T1 is >3,000 ms and T2 is ∼2,000 ms at 6 MHz. The vast differences in relaxation behaviour between CSF and other body tissues have considerable clinical implications and present profound diagnostic opportunities. The application of this knowledge to ventriculography, myelography. and image contrast methodology is discussed.


Journal of Neurology, Neurosurgery, and Psychiatry | 1986

Accuracy of stereotaxic localisation using MRI and CT.

D. Wyper; J W Turner; James Patterson; Barrie Condon; K W Grossart; A Jenkins; Donald M. Hadley; J O Rowan

The accuracy of stereotaxic coordinates determined using the Leksell apparatus with CT and MRI was investigated using an Agar filled head phantom. Both imaging techniques were found to produce an accuracy of better than 2 mm with the exception of the Z coordinate as measured by CT (2.3 mm). This latter error is greater because of the 3 mm slice width used. Direct coronal views were used to determine Z more accurately using MRI. The measurement procedures are described and it is shown that the Leksell system of using orthogonal coordinates enables the scaling of images, which is particularly necessary with MRI, to be done easily.


Acta neurochirurgica | 1988

Intracranial CSF volumes: natural variations and physiological changes measured by MRI.

Graham M. Teasdale; Robert M. Grant; Barrie Condon; James Patterson; Audrey Lawrence; Donald M. Hadley; D. Wyper

Cranial CSF volumes, for the first time including CSF in the subarachnoid space, can be measured by Magnetic Resonance Imaging (MRI). The MRI sequence causes signal from the grey matter and white matter to cancel producing a contrast of 200: 1 between a unit of CSF and a unit of brain. We have assessed the variations between normal individuals and investigated some of the physiological factors that might influence cranial CSF volumes. Total CSF volumes were measured in 64 normal subjects, aged from 18-64 years (mean 38 years). Ventricular, cortical sulcal and posterior fossa volumes were also calculated separately. In 20 females with a normal menstrual cycle, CSF volumes were measured mid cycle and premenstrually; 10 post menopausal females and 10 males were rescanned after an interval of 2 weeks. Total cranial CSF volume were calculated before and during inhalation of 7% CO2 and before and during hyperventilation while breathing 60% O2, in 12 normal subjects. Total intracranial CSF volume ranged from 57.1-286.5 ml. Total intracranial and cortical sulcal CSF volumes increased more steeply with age than ventricular or posterior fossa CSF volumes. Males had more cranial CSF than females. Total CSF volume increased premenstrually in 19 females. Males and post-menopausal females did not have a significant change in CSF volume, on repeat examination. CO2 inhalation produced a mean increase of paCO2 of 17.2 mmHg and CSF volume decreased in all subjects (mean 9.4 ml). Cranial CSF volume increased in 11 subjects during O2 inhalation (range -0.5 to +26.7 ml mean 10.9 ml).(ABSTRACT TRUNCATED AT 250 WORDS)


Journal of Neurology, Neurosurgery, and Psychiatry | 1989

Changes in cranial CSF volume during hypercapnia and hypocapnia.

Robert M. Grant; Barrie Condon; James Patterson; D. Wyper; M. D. M. Hadley; Graham M. Teasdale

Magnetic resonance imaging was used to measure the effect of inhalation of 7% CO2 and hyperventilation with 60% O2 on human cranial cerebrospinal fluid volume. During CO2 inhalation there was a reduction in the cranial CSF volume ranging from 0.7-23.7 ml (mean 9.36 ml). The degree of reduction in cranial CSF volume was independent of the individual subjects increase in end-expiratory pCO2 or mean arterial blood pressure, in response to hypercapnia. During hyperventilation with high concentration oxygen the cranial CSF volume increased in all subjects (range 0.7-26.7 ml, mean 12.7 ml). The mean changes in cranial CSF volume, induced by hypercapnia and hypocapnia, were very similar to the expected reciprocal changes in cerebral blood volume.


Archive | 1989

Tomographic Mapping of CBF, CBV and Blood Brain Barrier Changes in Humans After Focal Head Injury Using SPECT-Mechanisms for Late Deterioration

R. Bullock; P. Statham; James Patterson; G. M. Teasdale; E. Teasdale; D. Wyper

Ischemic brain damage due to reduced global cerebral perfusion pressure is a major determinant of outcome after head injury, and its recognition has led to major changes in management over the last few years (Graham et al. 1978). However, the effects of focal injury upon the local cerebral microcirculation has received little attention despite experimental evidence that progressive abnormalities can occur and may account for the delayed deterioration which often occurs in patients with cerebral contusions, intracerebral or subdural hematomas (Bullock et al. 1984). Serial CT scanning in patients with focal injury have shown hematoma enlargement in under 10% of patients while progression of surrounding brain edema occurs in one third of cases, and may cause raised intracranial pressure (Kobayashi et al. 1983). Hyperaemia has also been cited as a cause of raised ICP after diffuse injury and has been demonstrated after focal injury, but its role in causing later deterioration is not known (Kuhl et al. 1980).


Acta neurochirurgica | 1990

The Time Course of Vasogenic Oedema After Focal Human Head Injury — Evidence from SPECT Mapping of Blood Brain Barrier Defects

R. Bullock; P. Statham; James Patterson; D. Wyper; Donald M. Hadley; E. Teasdale


The Lancet | 1987

Reversible cerebellar diaschisis in focal epilepsy.

Roderick Duncan; James Patterson; Ian Bone; D. Wyper

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James Patterson

Southern General Hospital

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Barrie Condon

Southern General Hospital

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Jim Patterson

Southern General Hospital

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Ian Bone

Southern General Hospital

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E. Teasdale

Southern General Hospital

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Jack Rowan

Southern General Hospital

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