Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 7 de 7
Filtrar
1.
J Wound Care ; 25(3): 154, 156-9, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26947696

RESUMO

OBJECTIVE: Negative pressure wound therapy (NPWT) is a widely accepted treatment modality for open or infected wounds. Premature ending of NPWT occasionally occurs due to negative effects on the quality of life (QoL), however, the actual impact on QoL is unknown. The aim of this review is to analyse the effect of NPWT versus standard wound care (SWC) on QoL when used for the treatment of open or infected wounds. METHOD: A systematic literature search in a range of databases (PubMed, CINAHL, Medline, Web of Science, Science Direct Freedom Collection, SwetsWise, PSYCArticles and Infrotrac Custom Journals) using the following search terms; 'standard wound care', 'wound dressing', 'dressing', 'treatment', OR 'negative pressure wound therapy [MESH]', OR 'vacuum assisted closure' AND 'quality of life [MESH]', 'patient-satisfaction', OR 'experiences' was performed. Methodological quality was assessed using the methodological index for non-randomised studies (MINORS) checklist. RESULTS: There were 42 studies identified, five matched the inclusion criteria: two randomised clinical trials (RCTs), one clinical comparative study, one exploratory prospective cohort study and one quasi experimental pilot study. Median MINORS-score was 75% (58%-96%). There were seven different questionnaires used to measure QoL or a subsidiary outcome. QoL in the NPWT group was lower in the first week, though no difference in QoL was observed thereafter. CONCLUSION: This systematic review observed that QoL improved at the end of therapy independent of which therapy was used. NPWT led to a lower QoL during the first week of treatment, possible due to aniexty, after which a similar or better QoL was reported when compared with SWC. It could be suggested that NPWT might be associated with increased anxiety. DECLARATION OF INTEREST: All authors of this publication have received no financial support or have personal interests conflicting with the objectivity of this manuscript.


Assuntos
Tratamento de Ferimentos com Pressão Negativa/métodos , Qualidade de Vida , Ferimentos e Lesões/terapia , Ansiedade , Humanos , Resultado do Tratamento , Cicatrização , Ferimentos e Lesões/psicologia
2.
Chem Commun (Camb) ; (9): 1010-1, 2002 May 07.
Artigo em Inglês | MEDLINE | ID: mdl-12123048

RESUMO

We describe in this paper the development of plugged hexagonal templated silicas (PHTS) which are hexagonally ordered materials, with internal microporous silica nanocapsules; they have a combined micro- and mesoporosity and a tuneable amount of both open and encapsulated mesopores and are much more stable than other tested micellar templated structures.

3.
Langmuir ; 20(1): 41-5, 2004 Jan 06.
Artigo em Inglês | MEDLINE | ID: mdl-15744997

RESUMO

In this paper, we show that water inside mesoporous cavities in zeolites can be supercooled to ca. -40 degrees C at which point homogeneous nucleation of the water takes place. The fundamental phenomena observed here are similar to those reported earlier in for example emulsion droplets or droplets in the vapor phase. However, as these zeolite materials are widely available, they may provide an easily accessible source for studies of supercooled liquids in confinements. Next to this, it is now possible to discriminate with thermoporometry between mesoporous cavities inside the zeolite crystals, in which homogeneous nucleation takes place, and mesopores that are connected to the external surface in which heterogeneous nucleation takes place.


Assuntos
Zeolitas/química , Porosidade , Propriedades de Superfície , Temperatura , Água/química
4.
Hum Genet ; 49(2): 199-208, 1979 Jun 19.
Artigo em Inglês | MEDLINE | ID: mdl-468251

RESUMO

Chromosomes were studied in a mentally retarded boy with microcephaly, growth retardation, facial erythema, café-au-lait spots, and IgA deficiency. In the lymphocytes there was a remarkable tendency to exchange parts of the chromosomes Nos. 7 and 14, the translocations almost exclusively taking place in bands 7p13, 7q32 and 14q11. Seven different types of rearrangements between Nos. 7 and 14, and some other chromosomal aberrations were found. No abnormalities could be detected in the bone marrow. The patient somewhat resembles those affected with ataxia-telangiectasia or with Bloom's syndrome, but on clinical and cytogenetic grounds these disorders could be excluded. 7/14 Translocations similar to those found in our patient's lymphocytes have been reported to occur very rarely in the lymphocyte cultures of individuals with apparently normal chromosome constitution. A relationship between these phenomena may exist.


Assuntos
Aberrações Cromossômicas , Cromossomos Humanos 13-15 , Cromossomos Humanos 6-12 e X , Criança , Disgamaglobulinemia/genética , Transtornos do Crescimento/genética , Humanos , Imunoglobulina A , Deficiência Intelectual/genética , Lentigo , Masculino , Microcefalia/genética , Síndrome
5.
J Med Genet ; 29(10): 739-41, 1992 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-1433237

RESUMO

A balanced complex chromosome rearrangement (CCR) involving four chromosomes is very rare and may lead to different types of aneuploid germ cells. We report a liveborn child with multiple congenital anomalies and an apparently balanced translocation, t(11;12). High resolution chromosome analysis in the mother showed a CCR involving chromosomes 5, 11, 12, and 16. In situ hybridisation showed that this CCR was the result of a five break rearrangement, and that the derivative chromosome 12 consisted of parts of chromosomes 5, 11, and 12. From this it could be deduced that the karyotype of the child was not balanced, but resulted in partial trisomy for 5q and partial monosomy for 12p. The clinical findings in the child were compatible with partial trisomy for 5q.


Assuntos
Anormalidades Múltiplas/genética , Cromossomos Humanos Par 12 , Cromossomos Humanos Par 5 , Monossomia/genética , Trissomia/genética , Deleção Cromossômica , Cromossomos Humanos Par 11 , Cromossomos Humanos Par 16 , Fissura Palatina/genética , Humanos , Recém-Nascido , Masculino , Microcefalia/genética
6.
J Microsc ; 205(Pt 2): 187-200, 2002 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-11879433

RESUMO

Electron tomography is a versatile method for obtaining three-dimensional (3D) images with transmission electron microscopy. The technique is suitable to investigate cell organelles and tissue sections (100-500 nm thick) with 4-20 nm resolution. 3D reconstructions are obtained by processing a series of images acquired with the samples tilted over different angles. While tilting the sample, image shifts and defocus changes of several microm can occur. The current generation of automated acquisition software detects and corrects for these changes with a procedure that incorporates switching the electron optical magnification. We developed a novel method for data collection based on the measurement of shifts prior to data acquisition, which results in a five-fold increase in speed, enabling the acquisition of 151 images in less than 20 min. The method will enhance the quality of a tilt series by minimizing the amount of required focus-change compensation by aligning the optical axis to the tilt axis of the specimen stage. The alignment is achieved by invoking an amount of image shift as deduced from the mathematical model describing the effect of specimen tilt. As examples for application in biological and materials sciences 3D reconstructions of a mitochondrion and a zeolite crystal are presented.


Assuntos
Imageamento Tridimensional/métodos , Tomografia/métodos , Animais , Células Dendríticas/ultraestrutura , Camundongos , Microscopia Eletrônica/métodos , Mitocôndrias/ultraestrutura , Zeolitas/química
7.
Clin Genet ; 12(2): 85-96, 1977 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-891017

RESUMO

The clinical and cytogenetic data are presented of four children with Bloom's syndrome, who belong to two unrelated Dutch families. The patients showed, in varying degrees, the clinical features most characteristic of the syndrome: stunted growth; telangiectatic facial erythema; sun-sensitivity of the skin; and decreased immuno-competence. In one child the skin lesions were only minor and the diagnosis would probably not have been made if her sib had not been recognized as having Bloom's syndrome. The cytogenetic characteristics of the syndrome were present in all patients. Each showed a high number of chromosomal aberrations and numerous sister-chromatid exchanges per cell.


Assuntos
Dermatoses Faciais/genética , Transtornos do Crescimento/genética , Síndromes de Imunodeficiência/genética , Transtornos de Fotossensibilidade/genética , Telangiectasia/genética , Anormalidades Múltiplas/genética , Adolescente , Criança , Pré-Escolar , Cromátides/ultraestrutura , Aberrações Cromossômicas , Feminino , Humanos , Imunidade Celular , Imunoglobulinas/análise , Masculino , Países Baixos , Síndrome
SELEÇÃO DE REFERÊNCIAS
Detalhe da pesquisa