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2021 ◽  
Vol 16 ◽  
pp. e57485
Author(s):  
Jéssica Almeida Leite ◽  
Emilly Della Pasqua Pompeo ◽  
Luana Silva Monteiro ◽  
Ana Paula Muraro ◽  
Patrícia Simone Nogueira ◽  
...  

Objetivo: Revisar sistematicamente a associação entre composição domiciliar e consumo alimentar em adolescentes. Métodos: Trata-se de revisão sistemática da literatura. A busca dos artigos foi realizada nas bases de dados MEDLINE via PubMed, Scientific Electronic Library Online (SciELO), Web of Science, Biblioteca Virtual em Saúde, Embase e Scopus. Os artigos foram avaliados por meio do Research Triangle Institute (RTI) Item Bank sobre risco de viés e acurácia de estudos observacionais. Foram avaliados estudos observacionais com adolescentes (10-19 anos de idade). Resultados: Dos 2.324 artigos encontrados, 11 atenderam aos critérios de inclusão, 9 de delineamento transversal e 2 longitudinais. Quanto à avaliação do consumo alimentar, foram avaliadas as frequências de: jantar em família, consumo de café da manhã, consumo de refeições, omissão do café da manhã, consumo de grupos alimentares, número de refeições realizadas durante o dia, assim como densidade energética de grupos alimentares e o Índice de Alimentação Saudável. Observou-se que adolescentes que moravam com ambos os pais apresentaram maior frequência de consumo do café da manhã e maior consumo de vegetais. Preferências alimentares mais positivas e saudáveis foram mais frequentes entre adolescentes que residiam em famílias nucleares. Por outro lado, consumo irregular de café da manhã e consumo de marcadores de alimentação não saudável foram mais frequentes entre adolescentes residentes em domicílios monoparentais, com família reconstituída e famílias extensas. Conclusão: Adolescentes que moravam com ambos os pais apresentaram melhor consumo alimentar. Ressalta-se a necessidade de considerar a composição domiciliar ao planejar programas de promoção da alimentação saudável entre adolescentes.


Blood ◽  
2016 ◽  
Vol 128 (22) ◽  
pp. 1239-1239 ◽  
Author(s):  
Carol Mansfield ◽  
Anthony Masaquel ◽  
Jessie Sutphin ◽  
Elisa S Weiss ◽  
Meghan E. Gutierrez ◽  
...  

Abstract Background: Over 15,000 new cases of CLL are diagnosed each year in the U.S. Different treatment options exist, which vary in efficacy, side effects, and mode of administration. Little is known about the value patients place upon the different attributes of available CLL treatments. Objectives: To estimate patient preferences for CLL treatments and investigate the relationship between treatment preferences and cost. Methods: Patients with a self-reported physician diagnosis of CLL were recruited through a patient advocacy group to complete an online discrete-choice experiment (DCE) survey. The survey included 8 DCE questions in which respondents chose between pairs of hypothetical treatments for CLL. Each hypothetical treatment was defined by 5 attributes with several predefined levels; the attributes were progression-free survival (PFS; 10-60 months), diarrhea (none to severe), chance of severe infection (0-30%), chance of organ damage (0-8%), and mode and schedule of administration (pill versus intravenous administration). Treatment duration was not addressed independently and treatment cost was not included in the DCE. Random-parameters logit (RPL) was used to analyze the data and estimate patient preference weights for each attribute level in the survey. An importance score and minimum acceptable benefit score were calculated using results from the RPL model. Later, a cost attribute was added that included 2 hypothetical treatment profiles (Treatment A: 26 months of PFS, no diarrhea, 15% chance of serious infection, 8% chance of organ damage, IV once a month for 6 months, and lower cost; Treatment B: 60 months of PFS, mild/moderate diarrhea, 30% chance of serious infection, no chance of organ damage, daily pill for 60 months, and higher cost). Results from the RPL model were used to predict the share of respondents who would choose each treatment based on the DCE questions when cost was not a consideration, as compared with respondents' choices when cost was included. Results: 384 respondents recruited through LLS: 53% were female, 94% were white, and the mean age was 65 years. 57% had Medicare insurance, 53% of respondents had received financial aid and 40% reported difficulty in paying out-of-pocket costs for their medicines. In the DCE results, the attribute levels were ordered as expected, with respondents preferring better outcomes to worse. Within each attribute, all levels were statistically significantly different from each other (P ≤ 0.05). Attributes in the order of importance to patients as determined by DCE were PFS, chance of infection, chance of organ damage and the occurrence and severity of diarrhea. Mode of administration was the least important attribute. Although PFS had the highest importance score, the risk of adverse events was also highly important to patients; significant additional PFS was needed to offset patients' acceptance of worsening adverse events. For example, an increase in the chance of infection from 0% to 30% required an offset of 36 months of additional PFS. An increase in the chance of organ damage from 0% to 8% required an additional 26 months of PFS by the respondents. A tradeoff of 22 additional months in PFS is needed for a change from no diarrhea to severe diarrhea. Using results from the RPL model, it was predicted that 91% of respondents would choose Treatment B when cost is excluded from the treatment profile description. This was mainly driven by the better PFS attribute of Treatment B. When a modest cost difference was introduced ($75 more per month for treatment B), half of the patients chose treatment A. When this difference became larger ($400 more per month), the change in patient preference was even more pronounced; 74% chose option A. Conclusions: The most important attribute in the survey was PFS, however patients also indicated that increases in the risk of adverse events would require significant increase in PFS to offset that risk. Patients with CLL are sensitive to treatment costs and many reported difficulty in paying for their medications. Given the choice of treatments available to patients and the high cost of some treatments, physicians may want to explore their patients' preferences for different treatment features, including benefit-risk tradeoffs and out-of-pocket cost when selecting the best treatment strategies for patients. Disclosures Mansfield: RTI Health Solutions: Other: Research for this abstract was performed in the course of my employment at Research Triangle Institute d/b/a RTI Health Solutions, pursuant to a contract between my employer and the study sponsor, Genentech. RTI was compensated by the sponsor.. Masaquel:Roche: Equity Ownership; Genentech: Employment. Sutphin:RTI Health Solutions: Other: Research for this abstract was performed in the course of my employment at Research Triangle Institute d/b/a RTI Health Solutions, pursuant to a contract between my employer and the study sponsor, Genentech. RTI was compensated by the sponsor.. Li:Genentech: Employment; Roche: Equity Ownership. Reyes:Genentech: Employment; Roche: Equity Ownership.


2008 ◽  
Author(s):  
Kenneth Bowan ◽  
Ed Brooks ◽  
Walter Franzen ◽  
Frank Gulla ◽  
Walt Keays ◽  
...  

Author(s):  
S. Turner ◽  
E.B. Steel ◽  
O.S. Crankshaw

The National Voluntary Laboratory Accreditation Program (NVLAP) of the National Institute of Standards and Technology (NIST) has been accrediting laboratories for the analysis of asbestos by transmission electron microscopy since 1990. As part of the quality assurance procedures for the program, laboratories are required to determine k factors for Na, Mg, Si, Al, Ca and Fe. An interlaboratory study has been conducted by NIST and the Research Triangle Institute (RTI) in which laboratories analyzed thin film standards SRM 2063 or SRM 2063a. This work reports results of initial analysis of the data.


Curationis ◽  
1988 ◽  
Vol 11 (1) ◽  
Author(s):  
H.I.L. Brink

The purpose of this study was to explore and describe selected demographical, biographical, educational and professional background characteristics of the registered nurse tutors in the RSA and to construct a profile of the characteristics. Such a profile could provide a baseline for future studies and evaluation concerning registered nurse tutors. Data were collected from a random proportional stratified sample of 233 registered nurse tutors from a total of 1312 registered tutors whose names appeared on the SANC register. A questionnaire developed by the researcher and based on and adopted from a questionnaire from the Research Triangle Institute USA on the registered nurse in the USA, was used for data collection. The data were analysed and from the findings a profile of the registered nurse tutor in the RSA was constructed.


1982 ◽  
Vol 48 (6) ◽  
pp. 490-495 ◽  
Author(s):  
John N. Pyecha ◽  
Lucia A. Ward

During the spring of 1980, the Research Triangle Institute conducted a telephone survey to determine the extent to which a sample of 153 handicapped migrant children were identified as being handicapped—and had IEP's prepared—by schools in which they were enrolled from January 1978 through June 1979. The survey also was used to determine the extent to which IEP's and IEP-related information were transmitted between, and utilized by, staff of the various schools in which the students were enrolled. Findings indicate that: (a) the various schools in which students were enrolled were inconsistent in identifying these students as needing special education and in preparing their IEP's; (b) IEP's were developed less frequently for the most mobile than for the less mobile migrant students; (c) only a small percentage of the students had IEP's developed at more than one school; and (d) IEP's and IEP-related information were rarely transmitted between schools.


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