236 research outputs found

    Economic burden and its associated factors of hospitalized patients infected with A (H7N9) virus: a retrospective study in Eastern China, 2013–2014

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    BACKGROUND: H7N9 continues to cause human infections and remains a pandemic concern. Understanding the economic impacts of this novel disease is important for making decisions on health resource allocation, including infectious disease prevention and control investment. However, there are limited data on such impacts. METHODS: Hospitalized laboratory-confirmed H7N9 patients or their families in Jiangsu Province of China were interviewed. Patients’ direct medical costs of hospitalization were derived from their hospital bills. A generalized linear model was employed to estimate the mean direct medical costs of patients with different characteristics. RESULTS: The mean direct cost of hospitalization for H7N9 was estimated to be ¥ 71 060 (95 % CI, 48 180–104 820), i.e., US10996(95 10 996 (95 % CI, 7 455–16 220), and was ¥12 060 (US 1 861), ¥136 120 (US21001)and¥218610(US 21 001) and ¥218 610 (US 33 728) for those who had mild or severe symptoms or who died, respectively. The principal components of the total fees differed among patients with different disease severity, although medication fees were always the largest contributors. Disease severity, proportion of reimbursement and family member monthly average income were identified as the key factors that contributed to a patient’s direct medical cost of hospitalization. CONCLUSIONS: The direct medical costs of hospitalized patients with H7N9 are significant, and far surpass the annual per capita income of Jiangsu Province, China. The influencing factors identified should be taken into account when developing related health insurance policies and making health resource allocation. TRIAL REGISTRATION: Not applicable. This is a survey study with no health care intervention implemented on human participants. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40249-016-0170-5) contains supplementary material, which is available to authorized users

    Excellent Performance of Fe78Si9B13 Metallic Glass for Activating Peroxymonosulfate in Degradation of Naphthol Green B

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    The functional application of metallic glasses in the catalytic field has widely attracted research attention due to its unique atomic structure compared to crystalline materials. It has been reported that metallic glasses can effectively activate H2O2 and persulfate, yet the activation of peroxymonosulfate by metallic glasses is not studied well. In this work, the metallic glass with atomic composition of Fe78Si9B13 was applied for investigating the peroxymonosulfate (PMS) activation on degradation of naphthol green B (NGB) dye. The change of surface morphology indicated the important role of oxide films during the dye degradation. The effects and first-order kinetics model of various reaction parameters were evaluated systematically, including PMS concentration, catalyst dosage, irradiation intensity, and dye concentration. The results showed that about 98% of the dye removal rate could be achieved only within 10 min under rational conditions. The reaction kinetics k of 0.1339 min−1 without ribbons was sharply improved to 0.3140 min−1 by adding 0.5 g/L ribbons, indicating the superior activation ability of Fe78Si9B13 metallic glass. The recycling experiment revealed that the Fe78Si9B13 ribbons exhibited the excellent surface stability and catalytic reusability for activating PMS even after reused for 10th run

    31st Annual Meeting and Associated Programs of the Society for Immunotherapy of Cancer (SITC 2016) : part two

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    Background The immunological escape of tumors represents one of the main ob- stacles to the treatment of malignancies. The blockade of PD-1 or CTLA-4 receptors represented a milestone in the history of immunotherapy. However, immune checkpoint inhibitors seem to be effective in specific cohorts of patients. It has been proposed that their efficacy relies on the presence of an immunological response. Thus, we hypothesized that disruption of the PD-L1/PD-1 axis would synergize with our oncolytic vaccine platform PeptiCRAd. Methods We used murine B16OVA in vivo tumor models and flow cytometry analysis to investigate the immunological background. Results First, we found that high-burden B16OVA tumors were refractory to combination immunotherapy. However, with a more aggressive schedule, tumors with a lower burden were more susceptible to the combination of PeptiCRAd and PD-L1 blockade. The therapy signifi- cantly increased the median survival of mice (Fig. 7). Interestingly, the reduced growth of contralaterally injected B16F10 cells sug- gested the presence of a long lasting immunological memory also against non-targeted antigens. Concerning the functional state of tumor infiltrating lymphocytes (TILs), we found that all the immune therapies would enhance the percentage of activated (PD-1pos TIM- 3neg) T lymphocytes and reduce the amount of exhausted (PD-1pos TIM-3pos) cells compared to placebo. As expected, we found that PeptiCRAd monotherapy could increase the number of antigen spe- cific CD8+ T cells compared to other treatments. However, only the combination with PD-L1 blockade could significantly increase the ra- tio between activated and exhausted pentamer positive cells (p= 0.0058), suggesting that by disrupting the PD-1/PD-L1 axis we could decrease the amount of dysfunctional antigen specific T cells. We ob- served that the anatomical location deeply influenced the state of CD4+ and CD8+ T lymphocytes. In fact, TIM-3 expression was in- creased by 2 fold on TILs compared to splenic and lymphoid T cells. In the CD8+ compartment, the expression of PD-1 on the surface seemed to be restricted to the tumor micro-environment, while CD4 + T cells had a high expression of PD-1 also in lymphoid organs. Interestingly, we found that the levels of PD-1 were significantly higher on CD8+ T cells than on CD4+ T cells into the tumor micro- environment (p < 0.0001). Conclusions In conclusion, we demonstrated that the efficacy of immune check- point inhibitors might be strongly enhanced by their combination with cancer vaccines. PeptiCRAd was able to increase the number of antigen-specific T cells and PD-L1 blockade prevented their exhaus- tion, resulting in long-lasting immunological memory and increased median survival

    Using Cellular Ant Colony Algorithm for Path-Planning of Robots

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    To overcome some shortcoming existed in the conventional ant colony algorithms, e.g. slow converging and trend for falling into local convergences, a novel method for robot path planning is introduced based on cellular ant colony. Firstly, two ant colonies were set to run with different strategies. Secondly, the existing ant colony paths were evolved by following the cellular rules, so that the ants could jump from the current region into the region with a solution. Experiment results showed that the proposed algorithm proved to be stable, and that the global optimal path was found in a short time in a number of iterations.</jats:p
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