342 research outputs found

    EPIQR-TOBUS: a new generation of refurbishment decision aid methods

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    In a large majority of European countries, the amount of maintenance and refurbishment works represents nearly 50% of the total amount spent in the building sector. New requirements are being added to the necessity of maintaining or re-establishing the building stock's usage value. They are linked to the determination to reduce energy consumption, pollutant emissions, work site wastes, to improve the Indoor Environment Quality (IEQ) and all the modern conveniences inside buildings. Two European projects, EPIQR (réf. nr.: JOR3-CT96-0044) and TOBUS (réf. nr.: JOR3-CT98-Û235), developed in the IIIrd and IVth framework programs put the foundations of a new generation of refurbishment decision aid tools. A structured diagnosis scheme covering the state of deterioration of the building elements, energy performance, indoor environment quality, functional obsolescence offer a new concept which helps architects and engineers to approach the building refurbishment with a global view of the whole process, to take informed decisions, to construct coherent refurbishment scenarii and calculate a reasonable investment budget in the very first stage of the refurbishment project. EPIQR project addresses residential buildings and it has been finished in 1998, TOBUS addresses office buildings and it is still in course. The support of these methods is a multimedia computer program. Several modules help the users to treat the data collected during a diagnosis survey, to set up refurbishment scenarii and calculate their cost or energy performance, and finally to visualise the results in a comprehensive way and to prepare quality reports. This paper presents the structure and the main features of the method and softwar

    Ігор Степанович Флюнт - доктор медичних наук

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    23 грудня 2003 року на засіданні спеціалізованої вченої Д 26.198.01 при Інституті фізіології ім. О.О. Богомольця НАН України успішно захистив докторську дисертацію за спеціальністю 14.03.04 - патологічна фізіологія провідний бальнеолог України, лауреат премії ім. Т. Торосєвича в галузі бальнеології, член Нью-Йоркської АН, член Ради Асоціації учених міста Трускавця, керівник трускавецької групи клінічної бальнеології та фітотерапії Інституту фізіології ім. О.О. Богомольця, начмед санаторію “Весна” ЗАТ ЛОЗ “Трускавецькурорт” Ігор Степанович ФЛЮНТ

    Interdisciplinary Medication Adherence Program: The Example of a University Community Pharmacy in Switzerland.

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    The Community Pharmacy of the Department of Ambulatory Care and Community Medicine (Policlinique Médicale Universitaire, PMU), University of Lausanne, developed and implemented an interdisciplinary medication adherence program. The program aims to support and reinforce medication adherence through a multifactorial and interdisciplinary intervention. Motivational interviewing is combined with medication adherence electronic monitors (MEMS, Aardex MWV) and a report to patient, physician, nurse, and other pharmacists. This program has become a routine activity and was extended for use with all chronic diseases. From 2004 to 2014, there were 819 patient inclusions, and 268 patients were in follow-up in 2014. This paper aims to present the organization and program's context, statistical data, published research, and future perspectives

    Lack of Association between ABO, PPAP2B, ADAMST7, PIK3CG, and EDNRA and Carotid Intima-Media Thickness, Carotid Plaques, and Cardiovascular Disease in Patients with Rheumatoid Arthritis

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    Introduction. Rheumatoid arthritis (RA) is a polygenic disease associated with accelerated atherosclerosis and increased cardiovascular (CV) mortality. Recent studies have identified the ABO rs579459, PPAP2B rs17114036, and ADAMTS7 rs3825807 polymorphisms as genetic variants associated with coronary artery disease and the PIK3CG rs17398575 and EDNRA rs1878406 polymorphisms as the most significant signals related to the presence of carotid plaque in nonrheumatic Caucasian individuals. Accordingly, we evaluated the potential relationship between these 5 polymorphisms and subclinical atherosclerosis (assessed by carotid intima-media thickness (cIMT) and presence/absence of carotid plaques) and CV disease in RA. Material and Methods. 2140 Spanish RA patients were genotyped for the 5 polymorphisms by TaqMan assays. Subclinical atherosclerosis was evaluated in 620 of these patients by carotid ultrasonography technology. Results. No statistically significant differences were found when each polymorphism was assessed according to cIMT values and presence/absence of carotid plaques in RA, after adjusting the results for potential confounders. Moreover, no significant differences were obtained when RA patients were stratified according to the presence/absence of CV disease after adjusting for potential confounders. Conclusion. Our results do not confirm association between ABO rs579459, PPAP2B rs17114036, ADAMTS7 rs3825807, PIK3CG rs17398575, and EDNRA rs1878406 and subclinical atherosclerosis and CV disease in RA.European Union FEDER Funds and “Fondo de Investigación Sanitaria” (Grants PI06/0024, PS09/00748, and PI12/00060) from “Instituto de Salud Carlos III” (ISCIII, Health Ministry, Spain). It was also partially supported by RETICS Programs RD12/0009/0013 and RD12/0009/0004 (RIER) from “Instituto de Salud Carlos III” (ISCIII, Health Ministry, Spain) and in part by grants from the European IMI BTCure Program.Peer reviewe

    Expression of osteoprotegerin and its ligands, RANKL and TRAIL, in rheumatoid arthritis

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    Osteoprotegerin (OPG), receptor activator of nuclear factor-?B ligand (RANKL) and tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) have been involved in rheumatoid arthritis (RA) pathophysiology. In this study, we assessed messenger RNA (mRNA) expression of these molecules by qPCR in peripheral blood from 26 patients with RA (12 of them with ischemic heart disease -IHD) and 10 healthy controls. Correlation coefficients between OPG, RANKL and TRAIL expression levels in RA patients and their clinical and demographic characteristics were also evaluated. Whereas OPG and OPG/TRAIL ratio expression were significantly increased in RA patients compared to controls (fold change?=?1.79, p?=?0.013 and 2.07, p?=?0.030, respectively), RANKL/OPG ratio was significantly decreased (fold change?=?0.50, p?=?0.020). No significant differences were found between patients and controls in RANKL and TRAIL expression. Interestingly, TRAIL expression was significantly higher in RA patients with IHD compared to those without IHD (fold change?=?1.46, p?=?0.033). Moreover, biologic disease-modifying antirheumatic drugs (DMARDs) significantly decreased RANKL expression in RA patients (p?=?0.016). Our study supports an important role of OPG and TRAIL in RA. Furthermore, it highlights an effect of biologic DMARDs in the modulation of RANKL
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