220 research outputs found

    A Morbidity Submodel of Infectious Diseases

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    Numbers of sick persons with infectious diseases in a country can be estimated by the morbidity submodel of infectious diseases. The input of the model is the population structure of the country and the outputs are numbers of sick, deaths and prevalence rates of infectious diseases. The model makes use of three disease specific rates which are assumed to be constant across developed countries, namely morbidity rate, recovery rate, and death rate per capita. For this paper values of these three rates were calculated from Japanese survey data describing disease specific prevalence rate, death rate, and duration of stay. The outputs of the model are in good agreement with WHO statistics from Japan and other developed countries

    Analysis and Future Estimation of Medical Demands Using a Health Care Simulation Model: A Case Study of Japan

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    A method of building a universal health care model was proposed in RM-77-006 (Kaihara, et al., An Approach to Building a Universal Health Care Model). This method is based on the calculation of essential parameters of health care from ordinary statistics. The essential parameters proposed in the previous report were population structure, morbidity rate, recovery rate, death rate, patient registration rate and awareness rate. The method was applied successfully to the analysis of medical demands at the national level of Japan. The results showed that in the past 15 years the awareness rate was the most important factor which contributed to the increase of the patients. But in the future, the model predicted that the change of population structure will be the main cause of the increase of the number of patients in Japan

    An Approach to Building a Universal Health Care Model: Morbidity Model of Degenerative Diseases

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    There have been many different approaches to building health care models. Because of these differences, it is sometimes difficult to relate the developed models to each other. We have therefore first defined the submodels of the health care system and clarified the relation of our approach to studies already undertaken. The submodels also show the steps in building the health care model. The first step was to construct the morbidity model of degenerative diseases. The validity of the model was tested for various countries, using statistics from the World Health Organization. The fit of the model to empirical data was satisfactory. The model was applied to an international comparison and estimation of trends in degenerative diseases. The study showed the feasibility of this type of approach in health planning

    Effect of sub- and supercritical water treatments on the physicochemical properties of crab shell chitin and its enzymatic degradation

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    This study examined the effects of sub- and supercritical water pretreatments on the physicochemical properties of crab shell α-chitin and its enzymatic degradation to obtain N,N′-diacetylchitobiose (GlcNAc)2. Following sub- and supercritical water pretreatments, the protein in the crab shell was removed and the residue of crab shell contained α-chitin and CaCO3. Prolonged pretreatment led to α-chitin decomposition. The reaction of pure α-chitin in sub- and supercritical water pretreatments was investigated separately; we observed lower mean molecular weight and weaker hydrogen bonds compared with untreated α-chitin. (GlcNAc)2 yields from enzymatic degradation of subcritical (350 °C, 7 min) and supercritical water (400 °C, 2.5 min) pretreated crab shell were 8% and 6%, compared with 0% without any pretreatment. This study shows that sub- and supercritical water pretreatments of crab shell provide to an alternative method to the use of acid and base for decalcification and deproteinization of crab shell required for (GlcNAc)2 production.ArticleCarbohydrate Polymers. 134:718-725 (2015)journal articl

    Circulating mucosal-associated invariant T cells identify patients responding to anti-PD-1 therapy

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    Immune checkpoint inhibitors are used for treating patients with metastatic melanoma. Since the response to treatment is variable, biomarkers are urgently needed to identify patients who may benefit from such therapy. Here, we combine single-cell RNA-sequencing and multiparameter flow cytometry to assess changes in circulating CD8+ T cells in 28 patients with metastatic melanoma starting anti-PD-1 therapy, followed for 6 months: 17 responded to therapy, whilst 11 did not. Proportions of activated and proliferating CD8+ T cells and of mucosal-associated invariant T (MAIT) cells are significantly higher in responders, prior to and throughout therapy duration. MAIT cells from responders express higher level of CXCR4 and produce more granzyme B. In silico analysis support MAIT presence in the tumor microenvironment. Finally, patients with >1.7% of MAIT among peripheral CD8+ population show a better response to treatment. Our results thus suggest that MAIT cells may be considered a biomarker for patients responding to anti-PD-1 therapy

    Microvascular engineering in perfusion culture: immunohistochemistry and CLSM findings

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    BACKGROUND: One of the most challenging problems in tissue engineering is the establishment of vascular supply. A possible approach might be the engineering of microvasculature in vitro and the supply by engineered feeder vessels. METHODS: An in vitro model for a small-diameter vessel was developed and made from adipose tissue stromal cells and human umbilical vein endothelial cells in a tube-like gelatine scaffold. The number of "branches" emerging from the central lumen and the morphology of the central lumen of the vessel equivalent were assessed after 16 days of either pulsatile perfusion culture or culture in rotating containers by evaluation of immunohistochemically stained sections (n = 6 pairs of cultures). Intramural capillary network formation was demonstrated in five experiments with confocal laser scanning microscopy. RESULTS: Perfused specimens showed a round or oval lumen lined by a single layer of endothelial cells, whereas following rotation culture the lumen tended to collapse. Confocal laser scanning microscopy showed more extended network formation in perfused specimens as compared to specimens after rotation culture. Partially highly interconected capillary-like networks were imaged which showed orientation around the central lumen. Perfused specimens exhibited significantly more branches emerging from the central lumen. There were, however, hardly any capillary branches crossing the whole vessel wall. CONCLUSION: Pulsatile perfusion supports the development of vascular networks with physiological appearance. Advances in reactor development, acquisition of functional data and imaging procedures are however necessary in order to attain the ultimate goal of a fully functional engineered supplying vessel

    The ability of contemporary cardiologists to judge the ischemic impact of a coronary lesion visually

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    Background: Landmark trials showed that invasive pressure measurement (Fractional Flow Reserve, FFR) was a better guide to coronary stenting than visual assessment. However, present-day interventionists have benefited from extensive research and personal experience of mapping anatomy to hemodynamics. Aims: To determine if visual assessment of the angiogram performs as well as invasive measurement of coronary physiology. Methods: 25 interventional cardiologists independently visually assessed the single vessel coronary disease of 200 randomized participants in The Objective Randomized Blinded Investigation with optimal medical Therapy of Angioplasty in stable angina trial (ORBITA). They gave a visual prediction of the FFR and Instantaneous Wave-free Ratio (iFR), denoted vFFR and viFR respectively. Each judged each lesion on 2 occasions, so that every lesion had 50 vFFR, and 50 viFR assessments. The group consensus visual estimates (vFFR-group and viFR-group) and individual cardiologists' visual estimates (vFFR-individual and viFR-individual) were tested alongside invasively measured FFR and iFR for their ability to predict the placebo-controlled reduction in stress echo ischemia with stenting. Results: Placebo-controlled ischemia improvement with stenting was predicted by vFFR-group (p < 0.0001) and viFR-group (p < 0.0001), vFFR-individual (p < 0.0001) and viFR-individual (p < 0.0001). There were no significant differences between the predictive performance of the group visual estimates and their invasive counterparts: p = 0.53 for vFFR vs FFR and p = 0.56 for viFR vs iFR. Conclusion: Visual assessment of the angiogram by contemporary experts, provides significant additional information on the amount of ischaemia which can be relieved by placebo-controlled stenting in single vessel coronary artery disease
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