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1.
Int J Stroke ; 17(5): 545-552, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-34282988

RESUMO

BACKGROUND: Literature is inconclusive regarding the association between antiplatelet agents use and outcome after aneurysmal subarachnoid hemorrhage. AIMS: To investigate the association between clinical outcome and prehemorrhage use in aneurysmal subarachnoid hemorrhage patients as well as the impact of thrombocyte transfusion on rebleed and clinical outcome. METHODS: Data were collected from prospective databases of two European tertiary reference centers for aneurysmal subarachnoid hemorrhage patients. Patients were divided into "antiplatelet-user" and "non-user" according to the use of acetylsalicylic acid prior to the hemorrhage. Primary outcome was poor clinical outcome at six months (Glasgow Outcome Scale score 1-3). Secondary outcomes were in-hospital mortality and impact of thrombocyte transfusion. RESULTS: Of the 1033 patients, 161 (15.6%) were antiplatelet users. The antiplatelet users were older with higher incidence of cardiovascular risk factors. Antiplatelet use was associated with poor outcome and in-hospital mortality. After correction for age, sex, World Federation of Neurosurgical Societies score, infarction and heart disorder, pre-hemorrhage acetylsalicylic acid use was only associated with poor clinical outcome at six months (adjusted OR 1.80, 95% CI 1.08-3.02). Thrombocyte transfusion was not associated with a reduction in rebleed or poor clinical outcome. CONCLUSION: In this multicenter study, the prehemorrhage acetylsalicylic acid use in aneurysmal subarachnoid hemorrhage patients was independently associated with poor clinical outcome at six months. Thrombocyte transfusion was not associated with the rebleed rate or poor clinical outcome at six months.


Assuntos
Acidente Vascular Cerebral , Hemorragia Subaracnóidea , Aspirina/uso terapêutico , Escala de Resultado de Glasgow , Humanos , Acidente Vascular Cerebral/complicações , Hemorragia Subaracnóidea/complicações , Hemorragia Subaracnóidea/tratamento farmacológico , Resultado do Tratamento
2.
J Pediatr Surg Case Rep ; 62: 101641, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32904556

RESUMO

The health emergency linked to the Sars-Cov-2 infection represented an absolutely new problem for all health professionals. In particular, the information regarding the spread of the virus in the pediatric field and its manifestations are still incomplete. In this paper we present a case of neonatal infection which, as far as we know, represents one of the few published cases and which occurred in a patient who came to our attention for acute abdomen from intestinal perforation. The perforation was caused by Meckel's diverticulum, an event considered infrequent in the first year of life and almost exceptional in the neonatal period. This case required particular management, putting pediatric surgeons in front of new and difficult to solve problems. New onset clinical events, such as this one described, represent an opportunity for sharing useful data for the creation of universal protocols for the management of patients with problems that are becoming common and of which little is known.

3.
Neurol Sci ; 41(4): 817-824, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31802342

RESUMO

BACKGROUND: Although most aneurysmal subarachnoid hemorrhage (aSAH) patients suffer from neuropsychological disabilities, outcome estimation is commonly based only on functional disability scales such as the modified Rankin Scale (mRS). Moreover, early neuropsychological screening tools are not used routinely. OBJECTIVE: To study whether two simple neuropsychological screening tools identify neuropsychological deficits (NPDs), among aSAH patients categorized with favorable outcome (mRS 0-2) at discharge. METHODS: We reviewed 170 consecutive aSAH patients that were registered in a prospective institutional database. We included all patients graded by the mRS at discharge, and who had additionally been evaluated by a neuropsychologist and/or occupational therapist using the Montreal Cognitive Assessment (MoCA) and/or Rapid Evaluation of Cognitive Function (ERFC). The proportion of patients with scores indicative of NPDs in each test were reported, and spearman correlation tests calculated the coefficients between the both neuropsychological test results and the mRS. RESULTS: Of the 42 patients (24.7%) that were evaluated by at least one neuropsychological test, 34 (81.0%) were rated mRS 0-2 at discharge. Among these 34 patients, NPDs were identified in 14 (53.9%) according to the MoCA and 8 (66.7%) according to the ERFC. The mRS score was not correlated with the performance in the MoCA or ERFC. CONCLUSION: The two screening tools implemented here frequently identified NPDs among aSAH patients that were categorized with favorable outcome according to the mRS. Our results suggest that MoCA or ERFC could be used to screen early NPDs in favorable outcome patients, who in turn might benefit from early neuropsychological rehabilitation.


Assuntos
Disfunção Cognitiva/diagnóstico , Disfunção Cognitiva/etiologia , Aneurisma Intracraniano/complicações , Testes Neuropsicológicos , Avaliação de Resultados em Cuidados de Saúde , Índice de Gravidade de Doença , Hemorragia Subaracnóidea/complicações , Idoso , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Testes Neuropsicológicos/normas , Hemorragia Subaracnóidea/etiologia
4.
Curr Genomics ; 17(1): 70-9, 2016 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-27013925

RESUMO

Vesicoureteral reflux (VUR) is the retrograde passage of urine from the bladder to the upper urinary tract. It is the most common congenital urological anomaly affecting 1-2% of children and 30-40% of patients with urinary tract infections. VUR is a major risk factor for pyelonephritic scarring and chronic renal failure in children. It is the result of a shortened intravesical ureter with an enlarged or malpositioned ureteric orifice. An ectopic embryonal ureteric budding development is implicated in the pathogenesis of VUR, which is a complex genetic developmental disorder. Many genes are involved in the ureteric budding formation and subsequently in the urinary tract and kidney development. Previous studies demonstrate an heterogeneous genetic pattern of VUR. In fact no single major locus or gene for primary VUR has been identified. It is likely that different forms of VUR with different genetic determinantes are present. Moreover genetic studies of syndromes with associated VUR have revealed several possible candidate genes involved in the pathogenesis of VUR and related urinary tract malformations. Mutations in genes essential for urinary tract morphogenesis are linked to numerous congenital syndromes, and in most of those VUR is a feature. The Authors provide an overview of the developmental processes leading to the VUR. The different genes and signaling pathways controlling the embryonal urinary tract development are analyzed. A better understanding of VUR genetic bases could improve the management of this condition in children.

5.
Eur J Pediatr Surg ; 17(2): 129-31, 2007 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-17503308

RESUMO

We report an unusual case of spontaneous haemothorax in a 13-year-old girl with isolated costal exostosis. Surgical excision of the exostosis was performed with complete resolution. Costal exostosis should be considered in the differential diagnosis of spontaneous haemothorax in children in order to avoid unnecessary investigation and to establish an adequate treatment plan.


Assuntos
Exostose/complicações , Exostose/cirurgia , Hemotórax/etiologia , Costelas , Adolescente , Exostose/diagnóstico por imagem , Feminino , Humanos , Derrame Pleural/química , Radiografia , Costelas/cirurgia
6.
Pediatr Res ; 50(5): 565-8, 2001 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11641448

RESUMO

Patients with cephalic neurocristopathy (an abnormality of neural crest differentiation) present a striking pattern of associated cardiovascular anomalies (CVA). Therefore, to support the hypothesis that esophageal atresia (EA) may be related to a defective contribution from the cephalic neural crest, we studied the pattern of CVA associated with EA. Medical records of 99 patients with isolated EA, 101 with isolated anorectal malformations (ARM) and 15 with both EA and ARM, consecutively admitted to our unit, were reviewed. The prevalence and pattern of CVA associated with isolated EA or isolated ARM were compared on the assumption that the cranial or caudal location of a major malformation is related to a different regional patterning of associated anomalies. The prevalence of CVA was 39% in patients with isolated EA and 7% in those with isolated ARM (p < 0.01). Neural crest-related CVA (aortic arch anomalies, conotruncal defects, and superior vena cava malformations) accounted for 72% of all CVA in patients with isolated EA versus 14% in those with isolated ARM (p < 0.02). In patients with isolated EA, anomalies of the fourth and sixth aortic arch derivatives accounted for 75% of all neural crest related CVA. The present pattern of CVA in infants with EA supports the concept that EA may be related to an abnormal contribution from caudal portion of cephalic neural crest.


Assuntos
Anormalidades Cardiovasculares/epidemiologia , Atresia Esofágica/patologia , Crista Neural/anormalidades , Faringe/anormalidades , Anormalidades Múltiplas/epidemiologia , Humanos , Prevalência , Estudos Retrospectivos
8.
G Batteriol Virol Immunol ; 76(7-12): 282-9, 1983.
Artigo em Italiano | MEDLINE | ID: mdl-6681022

RESUMO

The AA, taking the latest reports as a starting point, are attempting a first epidemiological reconsideration of Hepatitis, Virus B. They have found that the disease, which was generally thought not to be contagious, is actually deceptive in its potential for transmission from person to person. Hospital personnel, in particular, are greatly at risk as are their families.


Assuntos
Antígenos de Superfície da Hepatite B/análise , Hepatite B/imunologia , Saliva/imunologia , Ensaio de Imunoadsorção Enzimática , Hepatite B/epidemiologia , Hepatite B/transmissão , Antígenos de Superfície da Hepatite B/líquido cefalorraquidiano , Humanos , Imunoglobulinas/análise , Itália
9.
Patol Clin Ostet Ginecol ; 8(5): 378-82, 1980.
Artigo em Italiano | MEDLINE | ID: mdl-12310938

RESUMO

PIP: After examining 146 copper-improved IUD users and comparing the vaginal bacterioscopic reports and the appearance of the cytological drawings obtained either traditionally or by endocervical aspiration with those from a test-group, the authors found nonappreciable differences, except for a more marked incidence of mycosis (11% against 7%) and 3 cases of slight dysplasia in the endocervical aspiration of IUD carriers, which were not statistically significant. The observations made for a slight cervical dysplasia were identical in both groups considered (3.5%). (Author's)^ieng


Assuntos
Colo do Útero , Cobre , Histologia , Dispositivos Intrauterinos , Biologia , Fenômenos Químicos , Química , Anticoncepção , Serviços de Planejamento Familiar , Genitália , Genitália Feminina , Compostos Inorgânicos , Metais , Fisiologia , Sistema Urogenital , Útero
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