RESUMO
The management of aortoiliac insufficiency has been improved considerably since the introduction of balloon-expandable stents in 1991. Although numerous studies have shown the safety and efficacy of balloon-expandable iliac artery stent placement, the procedure is not without potential complication. We report here a very unusual case of iliac artery stenting being complicated by deformation and elongation of the stent following balloon rupture at initial deployment with retention of the distal balloon marker and our successful approach to subsequent management with combined acetylsalicylic acid and clopidogrel. In conclusion, this conservative approach may be an alternative treatment of a partially deployed aortoiliac stent with a retained foreign body when further intervention is considered to be of high risk.
Assuntos
Angioplastia com Balão/efeitos adversos , Angioplastia com Balão/instrumentação , Arteriopatias Oclusivas/terapia , Catéteres , Artéria Ilíaca , Falha de Prótese , Stents , Arteriopatias Oclusivas/diagnóstico por imagem , Constrição Patológica , Desenho de Equipamento , Humanos , Artéria Ilíaca/diagnóstico por imagem , Masculino , Pessoa de Meia-Idade , Inibidores da Agregação Plaquetária/uso terapêutico , Desenho de Prótese , Tomografia Computadorizada por Raios X , Resultado do TratamentoRESUMO
In a RCT of family psychoeducation, 47 carers of 34 patients were allocated to one of three groups; Multifamily Group Psychoeducation, Solution Focussed Group Therapy or Treatment as Usual. Carers in both the MFGP intervention and the SFGP arm demonstrated greater knowledge and reduction in burden than those in the TAU arm.
Assuntos
Transtorno Bipolar/psicologia , Cuidadores/psicologia , Família/psicologia , Psicoterapia de Grupo , Transtorno Bipolar/terapia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Qualidade de Vida/psicologia , Resultado do TratamentoRESUMO
The innate immune system is believed to be important in the pathogenesis of psoriasis and natural killer (NK) have been found in increased numbers in psoriatic plaques. Alterations in the numbers of NK cells in peripheral blood have been reported. We investigated the effect of phototherapy on levels of peripheral NK cells and lymphocytes in patients with psoriasis. In nine patients whom we followed before, during and after narrowband ultraviolet B (UVB) treatment there were no differences in the numbers of circulating lymphocytes, lymphocyte subsets or cells expressing NK markers and controls. Treatment with narrowband UVB did, however, significantly lower circulating CD4 counts which gradually recovered posttreatment.
Assuntos
Movimento Celular , Células Matadoras Naturais/citologia , Células Matadoras Naturais/efeitos da radiação , Fototerapia , Psoríase/terapia , Linfócitos T/citologia , Linfócitos T/efeitos da radiação , Adulto , Movimento Celular/imunologia , Humanos , Células Matadoras Naturais/imunologia , Psoríase/imunologia , Linfócitos T/imunologiaRESUMO
The rpmA gene, which encodes 50S ribosomal subunit protein L27, was cloned from the extreme thermophile Aquifex aeolicus, and the protein was overexpressed and purified. Comparison of the A. aeolicus protein with its homologue from Escherichia coli by circular dichroism analysis and proton nuclear magnetic resonance spectroscopy showed that it readily adopts some structure in solution that is very stable, whereas the E. coli protein is unstructured under the same conditions. A mutant of E. coli that lacks L27 was found earlier to be impaired in the assembly and function of the 50S subunit; both defects could be corrected by expression of E. coli L27 from an extrachromosomal copy of the rpmA gene. When A. aeolicus L27 was expressed in the same mutant, an increase in the growth rate occurred and the "foreign" L27 protein was incorporated into E. coli ribosomes. However, the presence of A. aeolicus L27 did not promote 50S subunit assembly. Thus, while the A. aeolicus protein can apparently replace its E. coli homologue functionally in completed ribosomes, it does not assist in the assembly of E. coli ribosomes that otherwise lack L27. Possible explanations for this paradoxical behavior are discussed.
Assuntos
Proteínas de Bactérias , Escherichia coli/genética , Bacilos e Cocos Aeróbios Gram-Negativos/genética , Proteínas Ribossômicas/genética , Sequência de Aminoácidos , Dicroísmo Circular , Escherichia coli/crescimento & desenvolvimento , Espectroscopia de Ressonância Magnética , Proteínas de Membrana/genética , Dados de Sequência Molecular , Mutação , Proteínas Ribossômicas/isolamento & purificação , Ribossomos/química , Alinhamento de Sequência , Transformação BacterianaAssuntos
RNA Ribossômico/química , Proteínas Ribossômicas/química , Ribossomos/metabolismo , Ribossomos/ultraestrutura , Archaea/genética , Archaea/metabolismo , Escherichia coli/genética , Escherichia coli/metabolismo , Modelos Moleculares , Modelos Estruturais , Conformação de Ácido Nucleico , Biossíntese de Proteínas , Conformação Proteica , RNA Mensageiro/química , RNA Mensageiro/metabolismo , RNA Ribossômico/genética , RNA de Transferência/química , RNA de Transferência/metabolismo , Proteínas Ribossômicas/metabolismoRESUMO
This paper will present a brief review of the use of simulations in clinical reasoning research and education, followed by a case-study describing the development of a research tool which attempted to elicit the decision-making strategies of novice and competent hospital nurses. The central feature of this simulation was the degree of flexibility and control it gave to the nurse participants over their information seeking strategies. The ability of this interactive multimedia simulation to mimic a real ward environment has a great potential in the teaching of clinical reasoning skills to health professionals.
Assuntos
Educação em Enfermagem/métodos , Aprendizagem Baseada em Problemas , Interface Usuário-Computador , Simulação por Computador , Tomada de Decisões , Humanos , Design de SoftwareRESUMO
Genetics are coming to play an increasing role in biomedical understanding of common diseases. The implication of such findings is that at-risk individuals may be offered predictive genetic tests. How do individuals make decisions about predictive tests and what information do they need to make informed choices? Richards [Richards, M.P.M., 1993. The new genetics: some issues for social scientists. Sociology of Health and Illness 15, 567-586] has argued the first step in understanding and helping people to make these decisions is to investigate lay beliefs of genetics. This study examined mental models of inheritance in a sample of 72 lay people. Through analysis of open-ended questionnaires we found three mental models which loosely corresponded to three phases of historical development in the science of genetics. These we labelled the Constitutional, Mendelian and Molecular Models. Predictions for individuals holding each model are made for the comprehension of genetic information in a testing situation.
Assuntos
Doenças Genéticas Inatas , Genética Médica , Modelos Psicológicos , Feminino , Predisposição Genética para Doença , Humanos , Masculino , Modelos Genéticos , Fatores de Risco , Inquéritos e QuestionáriosRESUMO
Two important goals in allied health education are to prepare future allied health professionals to function as members of interdisciplinary teams and to increase their awareness of issues related to the growing older adult population. The responsibility for achieving these goals rests on the faculty and administrators of allied health education programs, who may not themselves be proficient in either of these domains. A multidisciplinary team of health educators and administrators was brought together to produce six problem-based learning (PBL) cases related to older adults. Members of the team represented a variety of disciplines in health care, diverse philosophies of educational development, a variety of roles in allied health education, and differing levels of knowledge of issues related to older adults--parameters similar to those found in the members of an interdisciplinary healthcare team. The methods by which this multidisciplinary group functioned and the dynamics in attaining the goals of the project are presented.
Assuntos
Pessoal Técnico de Saúde/educação , Geriatria/educação , Equipe de Assistência ao Paciente , Aprendizagem Baseada em Problemas/organização & administração , Idoso , District of Columbia , Feminino , Humanos , Masculino , Maryland , VirginiaRESUMO
Mucinous carcinoma may present at various sites, including the breast and the gastrointestinal tract. Rarely, such tumors arise within the skin. Comparatively, breast lesions are relatively common and usually associated with a good prognosis. When pure, they are typically estrogen (ER) and progesterone receptor (PR) positive and responsive to tamoxifen. The authors studied 12 mucinous carcinomas of the skin and compared the morphology with that of typical mammary lesions. The authors also evaluated for expression of estrogen receptor, progesterone receptor, and the mucus-associated peptides of the trefoil factor family (TFF), TFF1 (formerly pS2) and TFF2 (formerly SP), using immunohistochemistry. The localization of mRNAs for TFF1, TFF2, and TFF3 (formally ITF) was also studied in a subset of three tumors, using in-situ hybridization with S35 labeled riboprobes. The Grimelius stain was used to look for evidence of neuroendocrine differentiation. Eight resembled type A mucinous carcinomas of the breast, two resembled type B, and one had composite features. The 12th was a papillary neoplasm. The two type B tumors exhibited argyrophilia. All showed strong nuclear staining with the estrogen receptor antibody but a more varied pattern with antibodies to progesterone receptor and TFF1. None labeled for TFF2. The detection of TFF1 in mammalian skin is a novel finding. Cutaneous mucinous carcinoma shows strong similarities to its mammary counterpart, including expression of estrogen receptor, TFF1, and TFF3 mRNA. These observations suggest that some mucinous carcinomas of the skin might respond to antiestrogenic therapies.
Assuntos
Adenocarcinoma Mucinoso/metabolismo , Proteínas/metabolismo , Receptores de Estrogênio/metabolismo , Receptores de Progesterona/metabolismo , Neoplasias Cutâneas/metabolismo , Adenocarcinoma Mucinoso/patologia , Idoso , Idoso de 80 Anos ou mais , Neoplasias da Mama/metabolismo , Neoplasias da Mama/patologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Proteínas de Neoplasias/metabolismo , Neoplasias Cutâneas/patologia , Fator Trefoil-1 , Fator Trefoil-2 , Proteínas Supressoras de Tumor , Neoplasias Vulvares/metabolismo , Neoplasias Vulvares/patologiaRESUMO
Malignant rhabdoid tumors are morphologically characterized by the presence of sheets of large polygonal cells with abundant cytoplasm containing eosinophilic inclusions. They have vesicular nuclei, often with prominent central nucleoli. The term rhabdoid tumor was originally coined to describe a group of rare, aggressive renal neoplasms of childhood. Since then, similar lesions, so-called extrarenal malignant rhabdoid tumors have been increasingly reported. The evidence to date suggests that, at least in extrarenal locations, rhabdoid tumors do not constitute a homogeneous entity, but rather represent the shared morphological pattern of a diverse range of malignant neoplasms. Although such rhabdoid features are not uncommon in metastatic malignant melanoma, they have only once been briefly described in a primary lesion. We report three further cases of cutaneous primary malignant melanoma with rhabdoid morphology.
Assuntos
Melanoma/patologia , Tumor Rabdoide/patologia , Neoplasias Cutâneas/patologia , Adulto , Biomarcadores Tumorais/análise , Feminino , Humanos , Imuno-Histoquímica , Masculino , Melanoma/química , Pessoa de Meia-Idade , Tumor Rabdoide/química , Neoplasias Cutâneas/química , Vimentina/análiseRESUMO
As research in human genetics advances, genes for familial forms of cancer and heart disease will continue to be identified. The implication of such findings is that at-risk individuals will be offered a predictive genetic test. How do individuals make such decisions and what information do they need to make informed choices? Richards (1993) has argued that the first step in understanding and helping people to make these decisions is to investigate lay beliefs of genetics. This study examined illness representations of genetic disease, and predictive testing in a sample of 20 educated lay people. Through content analysis of open-ended interviews, we discovered that individuals have limited knowledge of late-onset genetic disorders and predictive testing. Most of the sample identified genetic diseases that manifest in childhood, and were more familiar with prenatal testing. They did not mention any treatment options for genetic disorders, which may indicate that lay people are more deterministic about diseases with a genetic component. Finally, they consistently raised concerns about the ethics of genetic testing and research. The implications of our findings for the provision of information in a genetic testing situation are discussed.
RESUMO
Beginning with known parameters that characterize the EMR spectra of several proteins containing high-spin ferric iron, the information content of the spectra has been examined by simulations that cover a range of magnetic fields and frequencies. Transitions between levels that are not Kramers doublet levels are particularly interesting when the applied frequency is approximately two to three times the value of the zero-field splitting parameter, D. In these cases, transitions at very low magnetic fields correspond to portions of interdoublet transitions that are well separated from all other transitions. The magnetic field is aligned at angles between the molecular principal axes for the portion of the molecules giving rise to the low-field interdoublet transitions. This provides an opportunity for unique angle-selection experiments.
Assuntos
Espectroscopia de Ressonância de Spin Eletrônica , Compostos Férricos/química , Proteínas/química , HumanosRESUMO
The rpmB,G operon of Escherichia coli codes for proteins L28 and L33 of the larger (50S) ribosomal subunit. Strains with mutations in this operon can help define the roles of these proteins in ribosome synthesis and function. One such strain, BM108, makes neither protein and is unable to synthesize completed ribosomes; instead ribonucleoproteins accumulate, in the form of '30S material' and '47S particles'. However, when protein L28 is supplied from a plasmid, the growth rate, the kinetics of ribosome synthesis and the coordination of ribosomal protein synthesis are no different from that in wild-type organisms even though protein L33 is missing. This suggests that the latter protein can be redundant for ribosome synthesis and function. Another mutant strain, BM81, has a frameshift mutation that gives rise to an oversized protein L28. This mutant accumulates 30S material and 47S particles during slow exponential growth. The composition of the 47S particles from strains BM81, BM108 and a third mutant strain, TP28, suggests that their defining feature is the absence of L28; this is further evidence for an important role for this protein in ribosome assembly. Accumulation of ribonucleoproteins in strains BM81 and BM108 leads to some loss of the ordinarily precise coordination of synthesis of ribosomal proteins. We describe and discuss the characteristic features of this unbalanced synthesis.
Assuntos
Compostos de Anilina , Proteínas de Bactérias , Proteínas de Escherichia coli , Escherichia coli/genética , Proteínas Ribossômicas/biossíntese , Ribossomos/genética , Fracionamento Celular , Escherichia coli/fisiologia , Genes Bacterianos , Mutação , Óperon , Plasmídeos , Proteínas Ribossômicas/fisiologia , Ribossomos/fisiologiaRESUMO
The rpmBG operon of Escherichia coli codes for ribosomal proteins L28 and L33. Two strains with mutations in the operon are AM81, whose ribosomes lack protein L28, and AM90, whose ribosomes are without protein L33. Neither strain showed major defects in ribosome assembly. However, when the mutations were transferred to other strains of E. coli, ribosome synthesis was greatly perturbed and precursor ribonucleoproteins accumulated. In the new backgrounds, the mutation in rpmB was complemented by synthesis of protein L28 from a plasmid; the rpmG mutation was not complemented by protein L33 because synthesis of protein L28 from the upstream rpmB gene was also greatly reduced. The results suggest that protein L33, in contrast to protein L28, has at best a minor role in ribosome assembly and function.
Assuntos
Compostos de Anilina , Proteínas de Bactérias , Proteínas de Escherichia coli , Escherichia coli/genética , Mutação/genética , Proteínas Ribossômicas/genética , Ribossomos/metabolismo , Sequência de Aminoácidos , Sequência de Bases , Mutação da Fase de Leitura , Teste de Complementação Genética , Dados de Sequência Molecular , Óperon/genética , Fenótipo , Proteínas Ribossômicas/biossíntese , Análise de Sequência , Especificidade da Espécie , Supressão Genética , Transdução GenéticaRESUMO
INTRODUCTION: An eight year retrospective analysis was conducted to determine the type and outcome of lawsuits related to the provision of 9-1-1 paramedic service in an urban environment. METHODS: For the evaluation period of May 1986 to March 1994, all litigation cases related to Ambulance Service or paramedics were collected and analyzed. This urban 9-1-1 Paramedic Service has an estimated call volume of > 60,000 assignments resulting in > 30,000 patient encounters during the evaluation period. RESULTS: Seven lawsuits were filed against the service. No lawsuits were related to tardy response, failure to transport, or patient care negligence of any kind. All of the litigation was related to motor vehicle collisions (MVC). CONCLUSIONS: The data suggest that motor vehicle collisions are a significant medical-legal risk to the EMS community. In addition, it was found that the use and lack of use of seatbelts was an important component in many of the suits.
Assuntos
Pessoal Técnico de Saúde/legislação & jurisprudência , Serviços Médicos de Emergência/legislação & jurisprudência , Imperícia/estatística & dados numéricos , Humanos , Incidência , Cidade de Nova Iorque , Estudos Retrospectivos , População UrbanaRESUMO
Strain BM108 of Escherichia coli has a chromosomal mutation in the rpmB,G operon that prevents synthesis of ribosomal proteins L28 and L33. The mutation was lethal unless synthesis of protein L28 was induced from a plasmid. Without protein L28, RNA and protein synthesis were linear rather than exponential. No 70S ribosomes were made. Instead, RNA accumulated in '30S material' and '47S particles'; the latter were distinct from 50S ribosomal subunits, lacked proteins L28 and L33 and had substoicheometric amounts of three other proteins. When L28 synthesis was induced (but protein L33 was still absent), the strain grew as well as, and assembled 70S ribosomes with similar kinetics to, a wild-type control. Thus, protein L28 is required for ribosome assembly in strain BM108 while protein L33 has no significant effect on ribosome synthesis or function.