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Biomedical subjects

J A da Silva

Publications and source records attributed to J A da Silva.

At least 19 recordsLinked to original sources

[Acute neurogenic pulmonary edema: a case report].

The authors report a case of acute neurogenic pulmonary edema in a 28-year-old woman who presented rupture of an internal carotid artery aneurysm and subarachnoid hemorrhage. The respiratory disorders started at the same time the patient's symptomatology aggravated. Some etiological and pathophysiological aspects on neurogenic pulmonary edema are revised.

Acute Disease

[Attitudes of professional nurses towards burn patients: elaboration and reliability tests of a measurement instrument].

In this study it was developed an Instrument for Measuring the Attitudes of Nursing Professionals toward Patients with Burns. 194 items, divided into subscales, expressing favorable and unfavorable attitudes toward patients with burns, were analyzed, concerning their apparent and context validity. Following this psychometric analysis 170 items were selected to compose the definitive scale. The confiability coefficient estimated by the split-half method for the different subscales ranged from 0.61 to 0.82. The confiability coefficient of the total scale was equal to 0.92.

Attitude of Health Personnel

Basilar impression and Arnold-Chiari malformation. Surgical findings in 209 cases.

The surgical findings observed in a series of 209 consecutive patients with craniovertebral anomaly are presented. The high prevalence of basilar impression in the Northeast of Brazil is noteworthy. There were 28 (13.3%) patients with basilar impression alone, 10 (4.7%) cases of pure Arnold-Chiari malformation and in 171 (81.8%) cases the basilar impression was associated with Arnold-Chiari malformation. This study reflects our surgical experience of the pathology in a 17-year period (1971-1987). It reflects also the peculiarities of neurosurgical practice in an undeveloped region of this Country. The literature is extensively reviewed.

Adolescent

[Acute cerebellar infarction simulating posterior fossa tumor].

We report a case of space-occupying infarction of the left cerebellar hemisphere with occlusive hydrocephalus and left to right shift of the fourth ventricle. The patient, a 58 years old man, underwent shunting and decompressive craniectomy of the posterior fossa and survived without neurological deficits.

Cerebellar Diseases

[Autonomic nervous system disorders in 230 cases of basilar impression and Arnold-Chiari deformity].

Within the period of 1971 to 1989 we operated on 230 cases of craniocervical malformations characterised by 189 cases of basilar impression associated with Arnold-chiari malformation, 28 cases of isolated basilar impression and 13 cases of Arnold-Chiari malformation. Autonomic disturbance was observed in 136 (59.1%) cases: sexual disorders like reduced potency and impotency were observed in 86 (60.9%) out of 141 male patients, urinary symptoms in 39 (17%) patients; and other autonomic features like dyspnea, anhidrosis, hyperhidrosis, Claude Bernard-Horner syndrome and constipation in 41 (17.8%) patients.

Adolescent

Measurement of visual acuity with logarithmic charts: comparison between methods of threshold estimation.

The variability of the repetition of visual acuity measurements with a log MAR acuity chart with five optotypes in each row of acuity was studied in four groups of subjects. In three groups the threshold was calculated by probability of seeing curves, but the optotypes were read in different orders. For the fourth group the acuity was taken as the smallest row discriminated. Estimating the threshold by a probability of seeing curve did not improve the threshold's stability. Poorer acuity was detected when the optotypes were read vertically. It is suggested that clinical visual acuity charts are not suitable tools for generating data points to be fitted by probability of seeing curves.

Adolescent

Agranulocytosis and liver damage associated with pyrazinobutazone with evidence for an immunological mechanism.

Agranulocytosis and liver injury is described in a patient with Reiter's syndrome of 3 years duration who received pyrazinobutazone for 6 weeks before the development of the clinical picture reported. Other causes of agranulocytosis and hepatic damage were excluded and a lymphocyte transformation test to the drug revealed significant lymphocyte proliferation in response to the drug. This suggests a hypersensitivity reaction as the mechanism for this previously unrecognized association of adverse effects to pyrazinobutazone.

Adult

[Basilar impression as a cause of trigeminal neuralgia: report of a case].

A case of basilar impression associated with Arnold-Chiari malformation and with trigeminal neuralgia is reported. The radiological examination of the skull showed marked asymmetry of the petrous bone with the tip of the odontoid apophysis located 30 mm above the McGregor line. Treatment consisted of craiectomy of the posterior fossa and cervical laminetomy (C1 to C3). The postoperative course was uneventful with total disappearance of the trigeminal neuralgia.

Arnold-Chiari Malformation

[Innocent murmurs].

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Heart Auscultation

Loxapine versus thioridazine in the treatment of organic psychosis.

Two double-blind trials comparing loxapine and thioridazine were conducted in hospitalized adult males diagnosed as having symptoms of chronic psychosis associated with organic brain syndrome or mental retardation. The drugs were administered orally in the ranges of loxapine 10--150 mg/day and thioridazine 150--750 mg/day for 13 weeks. In the first trial loxapine was found to be generally superior to thioridazine on the Brief Psychiatric Rating Scale, Nurses Observation Scale for In-Patient Evaluation and Clinical Global Impression. The second trial failed to confirm this superiority. The heterogeneity of diagnostic categories included may explain the discrepancy. Extra-pyramidal symptoms and sedative effects were common to both groups and consistent with the pharmacologic profiles of the study drugs.

Adolescent

[Ataxia-telangiectasia. Report of 4 cases].

The clinical, immunologic and radiologic aspects of 4 cases of ataxia telangiectasia are reported. Comparing with a large revision of literature, the authors justify the publication of the report by the scarse occurrence of the disease and by its incidency in 3 brothers of one same family.

Adolescent