Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros











Base de dados
Intervalo de ano de publicação
1.
Curr Med Res Opin ; 34(10): 1809-1817, 2018 10.
Artigo em Inglês | MEDLINE | ID: mdl-29528246

RESUMO

INTRODUCTION AND OBJECTIVES: Statins have become an integral part of treatment to reduce cardiac events in patients with cardiovascular disease. However, their use within the public healthcare system in Brazil is unknown. Consequently, we sought to determine and characterize statin use in primary healthcare delivered by the public health system (SUS) in Brazil and evaluate associated patient factors to improve future use. METHODS: Cross-sectional study with a national representative sample from five Brazilian regions, derived from the National Survey on Access, Use and Promotion of Rational Use of Medicines using a multi-stage complex sampling plan. Patients over 18 years old were interviewed from July 2014 to May 2015. The prevalences of statin use and self-reported statin adherence were determined amongst medicine users. The associations between statin use and sociodemographic/health condition variables were assessed using logistic regression. RESULTS: A total of 8803 patients were interviewed, of whom 6511 were medicine users. The prevalence of statin use was 9.4% with simvastatin (90.3%), atorvastatin (4.7%) and rosuvastatin (1.9%) being the most used statins. Poor adherence was described by 6.5% of patients. Statin use was significantly associated with age ≥65 years old, higher educational level, residence in the South, metabolic and heart diseases, alcohol consumption and polypharmacy. CONCLUSIONS: This is the first population based study in Brazil to assess statin use in SUS primary healthcare patients. Addressing inequalities in access and use of medicines including statins is an important step in achieving the full benefit of statins in Brazil, with the findings guiding future research and policies.


Assuntos
Doenças Cardiovasculares , Inibidores de Hidroximetilglutaril-CoA Redutases/uso terapêutico , Hipercolesterolemia , Adesão à Medicação/estatística & dados numéricos , Atenção Primária à Saúde , Adulto , Idoso , Atorvastatina/uso terapêutico , Brasil/epidemiologia , Doenças Cardiovasculares/epidemiologia , Doenças Cardiovasculares/prevenção & controle , Estudos Transversais , Revisão de Uso de Medicamentos , Feminino , Equidade em Saúde/estatística & dados numéricos , Humanos , Hipercolesterolemia/tratamento farmacológico , Hipercolesterolemia/epidemiologia , Masculino , Pessoa de Meia-Idade , Atenção Primária à Saúde/métodos , Atenção Primária à Saúde/estatística & dados numéricos , Rosuvastatina Cálcica/uso terapêutico , Sinvastatina/uso terapêutico
2.
ACS Nano ; 11(11): 11041-11046, 2017 11 28.
Artigo em Inglês | MEDLINE | ID: mdl-29053921

RESUMO

Kidney transplant patients require life-long surveillance to detect allograft rejection. Repeated biopsy, albeit the clinical gold standard, is an invasive procedure with the risk of complications and comparatively high cost. Conversely, serum creatinine or urinary proteins are noninvasive alternatives but are late markers with low specificity. We report a urine-based platform to detect kidney transplant rejection. Termed iKEA (integrated kidney exosome analysis), the approach detects extracellular vesicles (EVs) released by immune cells into urine; we reasoned that T cells, attacking kidney allografts, would shed EVs, which in turn can be used as a surrogate marker for inflammation. We optimized iKEA to detect T-cell-derived EVs and implemented a portable sensing system. When applied to clinical urine samples, iKEA revealed high level of CD3-positive EVs in kidney rejection patients and achieved high detection accuracy (91.1%). Fast, noninvasive, and cost-effective, iKEA could offer new opportunities in managing transplant recipients, perhaps even in a home setting.


Assuntos
Técnicas Biossensoriais/métodos , Exossomos/imunologia , Rejeição de Enxerto/urina , Inflamação/urina , Vesículas Extracelulares/imunologia , Vesículas Extracelulares/patologia , Feminino , Rejeição de Enxerto/imunologia , Rejeição de Enxerto/fisiopatologia , Humanos , Inflamação/imunologia , Inflamação/fisiopatologia , Rim/imunologia , Rim/patologia , Transplante de Rim/efeitos adversos , Masculino , Proteômica/métodos , Linfócitos T/imunologia
3.
Neurosciences (Riyadh) ; 6(3): 188-91, 2001 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-24185369

RESUMO

Problems of Parkinson`s Disease within the Arab world are discussed and a number of solutions are presented that will help in the management of Idiopathic Parkinson`s Disease. The problems discussed are problems related to the diagnosis whereby no individual clinical feature has sufficient sensitivity and specificity to serve as the sole basis for distinguishing Parkinson`s disease from other diseases with Parkinsonian features. Problems related to the Unified Parkinson`s Disease Rating Scale are also discussed and convey a multitude of problems culturally distinct to the Arab world. Problems related to the medical treatment, selection of patients for surgery, the surgery itself and the surgeon, programming and rehabilitation are discussed in detail.

4.
Berl Munch Tierarztl Wochenschr ; 112(1): 18-23, 1999 Jan.
Artigo em Alemão | MEDLINE | ID: mdl-10028727

RESUMO

237 cattle of a dairy herd in Syria were tested for anti-BLV antibody by the ELISA. 194 animals were additionally examined by the agar gel immunodiffusions test (AGID) on BLV antibodies and 100 by polymerase chain reaction (PCR) for BLV provirus. BLV specific antibodies were determined by means of AGID and ELISA at 62.9% and 69.2% of the examined animals, respectively. Using the PCR method the BLV provirus was detected in 89% of the investigated cattle. Only one ELISA seropositive animal was negative for BLV provirus. The results show the high BLV contamination of this herd and lead to the presumption of wide spread enzootic bovine leukosis in Syria. In the case of the diagnosis of BLV-infection, the PCR-technique compared to the serological tests proved to be much more sensitive. By the detection of BLV antibody, the ELISA showed a higher sensitivity than the AGID and in this way, is advisable as a method of choice for screening investigations. Restriction enzyme and sequence analysis of PCR-amplificates demonstrate that different BLV provirus variants (A, B and C) in the examined herd occur, where the variant C which a high similarity to an Australian BLV provirus isolates showed, occurred most frequently at 92.5%.


Assuntos
Leucose Enzoótica Bovina/diagnóstico , Vírus da Leucemia Bovina/isolamento & purificação , Animais , Bovinos , Leucose Enzoótica Bovina/epidemiologia , Ensaio de Imunoadsorção Enzimática/métodos , Feminino , Imunodifusão/métodos , Reação em Cadeia da Polimerase/métodos , Testes Sorológicos/métodos , Síria/epidemiologia
5.
J Neurol Sci ; 96(2-3): 191-205, 1990 May.
Artigo em Inglês | MEDLINE | ID: mdl-2376751

RESUMO

An Arab family with an autosomal recessive form of spinocerebellar degeneration with slow eye movements is reported. Hitherto all the reported cases were either sporadic or of autosomal dominant inheritance. Associated are progressive intellectual impairment and extrapyramidal dysfunction as well as peripheral neuropathy and skeletal abnormalities. Muscle biopsy revealed non-specific mitochondrial abnormalities. The spectrum of eye movement abnormalities is discussed and the literature is reviewed. It is concluded that the hallmark of this syndrome (slow or even absent saccades) is one of a group of oculomotor abnormalities, all being characterized by delayed initiation and slow velocity. The syndrome seems to be related to the olivopontocerebellar degenerations, but differs in that there is in addition selective degeneration of certain tracts and nuclei in the mesencephalon and probably more rostral structures.


Assuntos
Ataxia/genética , Demência/genética , Movimentos Oculares , Doenças do Sistema Nervoso/genética , Degenerações Espinocerebelares/genética , Adolescente , Adulto , Ataxia/complicações , Demência/complicações , Feminino , Humanos , Masculino , Doenças do Sistema Nervoso/complicações , Linhagem , Degenerações Espinocerebelares/complicações , Síndrome
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA