995 resultados para 1995_01270355 TM-56 4302606
Resumo:
Aplicou-se ethephon nas dosagens de 0,2 e 3 l/ha em cana-de-açúcar NA 56-79, 31 dias antes da colheita. Dos colmos colhidos foram efetuadas avaliações referentes a: infestação da broca da cana; gemas danificadas,entumescidas e brotadas; altura dos colmos; comprimento do ápice; número total de gemas e por último, análises tecnológicas para Pol, Brix, pureza e teor de fibras. Os toletes obtidos desses colmos foram plantados combinando-se as três dosagens de ethephon com três densidades de plantio: colmos simples, cruzados e duplos. Foram coletados dados semanais e posteriormente mensais de brotação e dados mensais de altura dos colmos. Dados de produção e número de colmos produzidos foram tomados por ocasião do 1º, 2º e 3º cortes da cana-de-açúcar. Os resultados revelaram que a aplicação de ethephon 2 l/ha, no estágio que antecede a colheita, promoveu um aumento do número de gemas e na altura dos colmos, e a dosagem 3 l/ha reduziu o teor de fibras na região apical da cana-de-açúcar em relação ao controle. Observou-se um aumento na velocidade de emergência de gemas obtidas de colmos tratados com o produto na dosagem 2 l/ha, antes do início do perfilhamento. Quanto à densidade de plantio, colmos duplos possibilitaram maior velocidade de emergência, seguidos de colmos cruzados, com relação a colmos simples. O crescimento, perfilhamento e produção de três anos consecutivos da cana-de-açúcar proveniente de toletes obtidos de plantas tratadas com ethephon não diferiram do controle. Notou-se um maior número de colmos produzidos no 1º ano, na densidade de plantio colmos duplos, quando comparados a colmos simples, sem, contudo, haver um aumento correspondente na produção.
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É feita a análise de áreas com diferentes classes de declividade (A = 0-3%, B = 3-8%, C = 8-16% e D = 16-30%) sscom a fina1idade de se verificar a potencialidade de imagens TM/LANDSAT, na escala 1:100.000, para planejamento agrícola. Devido à ausência de visão tridimensional, o trabalho baseia-se nas relações quantitativas entre índices dedrenagem (freqüência de rios e densidade de drenagem) determinados a partir das imagens, e expressão do relevo (declividade média) extraída de cartas planialtimétricas, na escala 1:50.000. Fotografias aéreas na escala 1:35.000 são utilizadas para fins comparativos. Conclui-se que o uso dessas imagens para mapear classes de declividade através do padrão de drenagem é viável, embora as características regionais o tenham limitado para diferenciar mais facilmente áreas com declividades A e B de áreas com declividades C e D.
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Este estudo objetivou verificar a distribuição temporal e espacial de Eretmochelys imbricata (Linnaeus, 1766) e aspectos de sua biologia reprodutiva, tais como tempo de incubação, sucesso reprodutivo, biometria das fêmeas, número de ninhos e fecundidade. Os dados foram coletados de 2007 a 2010 nas praias de Muro Alto, Cupe, Merepe, Porto de Galinhas e Maracaípe, todas elas localizadas no município do Ipojuca, estado de Pernambuco, Brasil. Foram analisados comparativamente parâmetros relativos à biologia reprodutiva e áreas de nidificação da espécie. Eretmochelys imbricata foi registrada nidificando entre os meses de outubro a maio, totalizando 350 ninhos monitorados em três temporadas. Os picos de desova ocorreram de janeiro a março, revelando um padrão sazonal das desovas. Houve diferença significativa entre o número de ninhos nas temporadas. A praia de Merepe apresentou uma ocorrência elevada de ninhos (46 ninhos/km) em relação às demais praias monitoradas. Quanto aos aspectos da biologia reprodutiva, o sucesso reprodutivo foi 65,6%, e o intervalo do tempo de incubação de 54 a 56 dias. As medidas biométricas foram coletadas de 59 espécimes, e apresentaram média de 92,5 cm ± 4,5 para o comprimento curvilíneo da carapaça e de 83,4 cm ± 5 para a largura curvilínea da carapaça. Os resultados podem ser utilizados para subsidiar planos de conservação e demonstram que as praias registradas neste estudo têm relevância como áreas de nidificação para E. imbricata.
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This document is intended to be a practical clinical guideline for the control of pain in patients with cancer. Its target group is hospital staff, primary care team members and nursing home staff. It attempts to apply the clinical principles outlined in the document 'Control of Pain in Patients with Cancer' published by "Scottish Intercollegiate Guidelines Network" (SIGN). This document has been adapted with the permission of SIGN. Rigour of Development A full evidence based reference list is available with the SIGN document. This can be accessed at www.sign.ac.uk. Contents not based on the SIGN document are referenced separately. This document has been developed as one part of the recommendations identified in the Regional Review of Palliative Care Services, 'Partnerships in Caring'. The development of these Pain Guidelines was led by the Northern Ireland Group of the National Council for Hospice and Specialist Palliative Care, whose membership is detailed in Appendix 4. They will be reviewed and updated in two years. A wide consultation process with potential users was undertaken. åÊ åÊ
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Explanatory Memorandum
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The neuropsychological records of 56 patients operated for clipping were studied. Almost every patient remained autonomous and without invalidating motor defect. The present study was aimed at specifying the type and frequency of neuropsychological sequelae and, to a lesser extent, the role of various pathophysiological factors. A main concern was to examine to what extent and at what post-operative interval the neuropsychological assessment can predict the intellectual and socioprofessional outcome of each individual patient. The neuropsychological assessment performed beyond the acute phase showed evidence of intellectual sequelae in about two thirds of the patients. Only one case of permanent anterograde amnesia was observed, probably due to unavoidable inclusion of a hypothalamic artery in the clip during surgery. Transient anterograde amnesia and confabulations were occasionally observed, generally for less than three weeks. A common finding was impaired performance on memory and/or executive tests. In a minority of patients, language disorders, visuoperceptive and visuoconstructive disabilities were found, probably in relation with hemodynamic changes at distance from the aneurysm. Global impairment of intellectual function was not uncommon in the acute post-operative phase but it evolved in most cases towards a more selective impairment, for instance restricted to executive and memory functions, in the chronic phase. The neuropsychological investigation carried out 4 to 15 weeks post-operatively provided satisfactory information about possible long-lasting intellectual disturbances and professional resumption. In particular, persistent global intellectual impairment, persistent amnesia and confabulations 4-15 weeks post-operative were associated with cessation of professional activity; executive and memory impairment, behavioral disturbances such as those encountered in patients with frontal lobe damage were associated with a decreased probability of full-time employment. Pre- and post-operative angiography were not good predictors of long-term cognitive outcome: normal angiography was not necessarily followed by normal neuropsychological outcome, conversely abnormal angiography could be found together with normal neuropsychological outcome. By contrast, there was a relationship between left-lateralised abnormalities on post-operative angiography and occurrence of language disorders; similarly, there was a relationship between side of craniotomy and type of deficits, that is language disorders versus visuoperceptive-visuoconstructive impairments.
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The case of a patient with severe pulmonary hypertension whose etiology has remained unknown until an autopsy was performed is discussed in a symposium of pathological anatomy. This case helped to address the diagnostic and therapeutic management of pulmonary hypertension. The broad differential diagnosis of this disease requires a diagnostic strategy to be developped. Clinical reasoning leading to a probable diagnosis based on clinical biological and radiological information is not only a difficult task for the speaker but also a rich source of learning opportunities for our medical community.
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BACKGROUND Challenges exist in the clinical diagnosis of drug-induced liver injury (DILI) and in obtaining information on hepatotoxicity in humans. OBJECTIVE (i) To develop a unified list that combines drugs incriminated in well vetted or adjudicated DILI cases from many recognized sources and drugs that have been subjected to serious regulatory actions due to hepatotoxicity; and (ii) to supplement the drug list with data on reporting frequencies of liver events in the WHO individual case safety report database (VigiBase). DATA SOURCES AND EXTRACTION (i) Drugs identified as causes of DILI at three major DILI registries; (ii) drugs identified as causes of drug-induced acute liver failure (ALF) in six different data sources, including major ALF registries and previously published ALF studies; and (iii) drugs identified as being subjected to serious governmental regulatory actions due to their hepatotoxicity in Europe or the US were collected. The reporting frequency of adverse events was determined using VigiBase, computed as Empirical Bayes Geometric Mean (EBGM) with 90% confidence interval for two customized terms, 'overall liver injury' and 'ALF'. EBGM of >or=2 was considered a disproportional increase in reporting frequency. The identified drugs were then characterized in terms of regional divergence, published case reports, serious regulatory actions, and reporting frequency of 'overall liver injury' and 'ALF' calculated from VigiBase. DATA SYNTHESIS After excluding herbs, supplements and alternative medicines, a total of 385 individual drugs were identified; 319 drugs were identified in the three DILI registries, 107 from the six ALF registries (or studies) and 47 drugs that were subjected to suspension or withdrawal in the US or Europe due to their hepatotoxicity. The identified drugs varied significantly between Spain, the US and Sweden. Of the 319 drugs identified in the DILI registries of adjudicated cases, 93.4% were found in published case reports, 1.9% were suspended or withdrawn due to hepatotoxicity and 25.7% were also identified in the ALF registries/studies. In VigiBase, 30.4% of the 319 drugs were associated with disproportionally higher reporting frequency of 'overall liver injury' and 83.1% were associated with at least one reported case of ALF. CONCLUSIONS This newly developed list of drugs associated with hepatotoxicity and the multifaceted analysis on hepatotoxicity will aid in causality assessment and clinical diagnosis of DILI and will provide a basis for further characterization of hepatotoxicity.
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The objective of the current study was to compare two rapid methods, the BBL Mycobacteria Growth Indicator Tube (MGIT TM) and Biotec FASTPlaque TB TM (FPTB) assays, with the conventional Löwenstein-Jensen (LJ) media assay to diagnose mycobacterial infections from paucibacillary clinical specimens. For evaluation of the clinical utility of the BBL MGIT TM and FPTB assays, respiratory tract specimens (n = 208), with scanty bacilli or clinically evident, smear negative cases and non-respiratory tract specimens (n = 119) were analyzed and the performance of each assay was compared with LJ media. MGIT and FPTB demonstrated a greater sensitivity (95.92% and 87.68%), specificity (94.59% and 98.78%), positive predictive value (94.91% and 99.16%) and negative predictive value (96.56% and 90.92%), respectively, compared to LJ culture for both respiratory tract and non-respiratory tract specimens. However, the FPTB assay was unable to detect nontuberculous mycobacteria and few Mycobacterium tuberculosis complex cases from paucibacillary clinical specimens. It is likely that the analytical sensitivity of FPTB is moderately low and may not be useful for the direct detection of tuberculosis in paucibacillary specimens. The current study concluded that MGIT was a dependable, highly efficient system for recovery of M. tuberculosis complexes and nontuberculous mycobacteria from both respiratory and non-respiratory tract specimens in combination with LJ media.
Validation d'une version abrégée du TCI (TCI-56) sur un échantillon de jeunes fumeurs et non-fumeurs
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Introduction: The psychobiological seven-factor model proposed by Cloninger et al. (1993) takes into account temperament and character dimensions to describe personality. Four of the dimensions are linked with biological, genetic and neuroanatomic structures, whereas the three other dimensions are related to the degree of individual, social and spiritual development. A study conducted by Wills et al. (1994) with adolescents showed that substance abuse was associated with high scores on Novelty Seeking and low scores on Harm Avoidance and Reward Dependence. The aim of the present study was, firstly, to create a short form of Cloninger's (1993) Temperament and Character Inventory (TCI) and, secondly, to study the impact of nicotine dependence as well as demographic variables on a sample of young adults. Method: We created a short form of the TCI containing 56 items (TCI-56), 8 for each scale. Responses are made on a five-point Likert type scale. A Swiss sample (n=211), of 116 women and 95 men, aged from 15 to 30 years, participated in this study. Our population was divided into a group of 81 smokers and another of 130 non-smokers, according to their scores on the Fagerstörm test for nicotine dependence (1999). Results: The structural validation consisted of two separate factor analysis with varimax rotations, one for the temperamental items, and the other, for the character ones. The first factor analysis conducted on the items of the temperament scales allowed to extract 4 factors explaining 40.7% of the variance. The correlations between factors and scales are the following: r=.71 for Novelty Seeking, r=.69 for Persistence, r=.95 for Harm Avoidance, r=.94 for Reward Dependence. The second factor analysis conducted on the items of the character scales allowed to extract 3 factors explaining 41.5% of the variance. The correlations between factors and scales are the following: r=.94 for Self-Directedness, r=.91 for Cooperativeness and r=.99 for Self-Transcendence. The internal consistencies range from α=.65 to α=.75 for the temperament scales, and from α=.71 to α=.83 for the three character scales. Concerning, the impact of the nicotine dependence, we observed that smokers have significantly higher scores for Novelty seeking, than non-smokers (p=.01). We found no difference for Harm Avoidance and Reward Dependence. Nevertheless, smokers seem to have the tendency to score higher on Transcendence (p=.06). Moreover, people having smoked more than 100 cigarettes in their life have significantly higher scores on this scale (p.04) and the correlation between Transcendence and the Fagerstörm test is significant (r=.19). We also found gender differences: the women (N=116) obtain significantly higher scores for Harm Avoidance (p<.001), for Reward Dependence (p<.001) and for Cooperation (p=.01). We further found a significant correlation between age and Self-Directedness, r=.34. We observed no interaction between gender and smoking or age and smoking on the dimensions of the TCI-56. Discussion: The TCI short form (TCI-56) seems to be a valid and useful inventory to assess personality differences. Confirming the results of others about the relation between addiction and personality, we found that smokers have significantly higher scores for Novelty seeking, than non-smokers. But we were not able to find any significant differences for Harm Avoidance and Reward Dependence. This might be due to our sample that was made of young adults. This study also shows that Transcendence could be an interesting dimension for studies on Tobacco smoking to consider. Concerning the impact of demographic variables, we observed that age and gender have specific and coherent influence on personality.
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Infliximab es un anticuerpo monoclonal efectivo en la psoriasis. Métodos: Estudio retrospectivo de 56 pacientes tratados con infliximab. Resultados: El 82% y 91,1% de los pacientes alcanzaron respuestas PASI 75 en la semana 12 y al año.La probabilidad de supervivencia global del tratamiento fue de 40% a los 4 años. Conclusiones: Infliximab ha demostrado ser efectivo y seguro a corto y largo plazo. La intensificación fue el predictor positivo más importante de aumento de supervivencia del tratamiento, seguido por el tratamiento combinado. El factor predictor negativo de supervivencia más importante parece ser el fracaso previo a otros anti-TNF.