25 research outputs found

    IT Enabled Service Innovation In E-Government: The Case Of Taiwan Drug Abuse Reduction Service

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    Drug abuse problem is one of the toughest issues faced by governments in the world. The typical solution is every time when the drug abuse offenders are under arrest, they are jailed for a while. There is high probability that they will repeat the offense after leaving the prison. Thus, such a solution wastes lots of administrative resources from the government, yet still cannot reduce the recidivism of drug abuse. Nowadays, most countries treat drug abuse offenders as patients, and offer them substitute treatment in order to reduce the dependence on drug and also reduce the risk of infecting AIDS. The patients will go to work as a normal person, live as a normal person, and keep their human dignity. In this study, we introduce the care of Taiwan drug abuse reduction service by service blueprinting method. The service integrates several ministries of Taiwan government in signal information system, and will be triggered automatically when the drug abuse offender is leaving the prison. Subsequently, we analyze the case by the framework of Service Open System View and then provide some suggestions for improvement of the existing service. This study share the case of Taiwan drug abuse reduction service and provide the best practice of improving existing service by the view point of service science to academics

    Analysis of the X(1835) and related baryonium states with Bethe-Salpeter equation

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    In this article, we study the mass spectrum of the baryon-antibaryon bound states ppˉp\bar{p}, ΣΣˉ\Sigma\bar{\Sigma}, ΞΞˉ\Xi\bar{\Xi}, ΛΛˉ\Lambda\bar{\Lambda}, pNˉ(1440)p\bar{N}(1440), ΣΣˉ(1660)\Sigma\bar{\Sigma}(1660), ΞΞˉ\Xi\bar{\Xi}^\prime and ΛΛˉ(1600)\Lambda\bar{\Lambda}(1600) with the Bethe-Salpeter equation. The numerical results indicate that the ppˉp\bar{p}, ΣΣˉ\Sigma\bar{\Sigma}, ΞΞˉ\Xi\bar{\Xi}, pNˉ(1440)p\bar{N}(1440), ΣΣˉ(1660)\Sigma\bar{\Sigma}(1660), ΞΞˉ\Xi\bar{\Xi}^\prime bound states maybe exist, and the new resonances X(1835) and X(2370) can be tentatively identified as the ppˉp\bar{p} and pNˉ(1440)p\bar{N}(1440) (or N(1400)pˉN(1400)\bar{p}) bound states respectively with some gluon constituents, and the new resonance X(2120) may be a pseudoscalar glueball. On the other hand, the Regge trajectory favors identifying the X(1835), X(2120) and X(2370) as the excited η(958)\eta^\prime(958) mesons with the radial quantum numbers n=3n=3, 4 and 5, respectively.Comment: 13 pages, 2 figures, revise a numbe

    Candida colonization and subsequent infections in critically ill surgical patients

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    OBJECTIVE. The authors determined the role of Candida colonization in the development of subsequent infection in critically ill patients. DESIGN. A 6-month prospective cohort study was given to patients admitted to the surgical and neonatal intensive care units in a 1600-bed university medical center. METHODS. Patients having predetermined criteria for significant Candida colonization revealed by routine microbiologic surveillance cultures at different body sites were eligible for the study. Risk factors for Candida infection were recorded. A Candida colonization index was determined daily as the ratio of the number of distinct body sites (dbs) colonized with identical strains over the total number of dbs tested; a mean of 5.3 dbs per patient was obtained. All isolates (n = 322) sequentially recovered were characterized by genotyping using contour-clamped homogeneous electrical field gel electrophoresis that allowed strain delineation among Candida species. RESULTS. Twenty-nine patients met the criteria for inclusion; all were at high risk for Candida infection; 11 patients (38%) developed severe infections (8 candidemia); the remaining 18 patients were heavily colonized, but never required intravenous antifungal therapy. Among the potential risk factors for candida infection, three discriminated the colonized from the infected patients--i.e., length of previous antibiotic therapy (p < 0.02), severity of illness assessed by APACHE II score (p < 0.01), and the intensity of Candida spp colonization (p < 0.01). By logistic regression analysis, the latter two who were the independent factors that predicted subsequent candidal infection. Candida colonization always preceded infection with genotypically identical Candida spp strain. The proposed colonization indexes reached threshold values a mean of 6 days before Candida infection and demonstrated high positive predictive values (66 to 100%). CONCLUSIONS. The intensity of Candida colonization assessed by systematic screening helps predicting subsequent infections with identical strains in critically ill patients. Accurately identifying high-risk patients with Candida colonization offers opportunity for intervention strategies

    Export from Pericentriolar Endocytic Recycling Compartment to Cell Surface Depends on Stable, Detyrosinated (Glu) Microtubules and Kinesin

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    A significant fraction of internalized transferrin (Tf) concentrates in the endocytic recycling compartment (ERC), which is near the microtubule-organizing center in many cell types. Tf then recycles back to the cell surface. The mechanisms controlling the localization, morphology, and function of the ERC are not fully understood. We examined the relationship of Tf trafficking with microtubules (MTs), specifically the subset of stable, detyrosinated Glu MTs. We found some correlation between the level of stable Glu MTs and the distribution of the ERC; in cells with low levels of Glu MTs concentrated near to the centriole, the ERC was often tightly clustered, whereas in cells with higher levels of Glu MTs throughout the cell, the ERC was more dispersed. The clustered ERC in Chinese hamster ovary cells became dispersed when the level of Glu MTs was increased with taxol treatment. Furthermore, in a temperature-sensitive Chinese hamster ovary cell line (B104-5), the cells had more Glu MTs when the ERC became dispersed at elevated temperature. Microinjecting purified anti-Glu tubulin antibody into B104-5 cells at elevated temperature induced the redistribution of the ERC to a tight cluster. Microinjection of anti-Glu tubulin antibody slowed recycling of Tf to the cell surface without affecting Tf internalization or delivery to the ERC. Similar inhibition of Tf recycling was caused by microinjecting anti-kinesin antibody. These results suggest that stable Glu MTs and kinesin play a role in the organization of the ERC and in facilitating movement of vesicles from the ERC to the cell surface
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