15 research outputs found

    Additional file 1: of Cost-effectiveness of a cardiac output-guided haemodynamic therapy algorithm in high-risk patients undergoing major gastrointestinal surgery

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    Supplementary data describing costs and the findings of sub-group analyses and sensitivity analyses. The additional file 1 includes supplementary information on unit costs of resources, 6 months results (hospital costs, sub-group results, cost-effectiveness acceptability curves), Kaplan-Meier survival curves and parametric extrapolation of survival beyond trial period, results of sensitivity analysis and populationexpected value of perfect information

    Additional file 3: of Dynamic modulation of phosphoprotein expression in ovarian cancer xenograft models

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    Differential protein expression. Log fold changes of differentially expressed proteins over 14 days are shown in 4 worksheets, each for a xenograft-treatment condition: carboplatin treated OV1002; carboplatin treated HOX424; carboplatin-paclitaxel treated OV1002; carboplatin-paclitaxel treated HOX424. (XLS 57 kb

    Irish National ICU Audit Annual Report 2017

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    By the end of 2017, the Irish National Intensive Care Unit Audit (INICUA) run by the National Office of Clinical Audit (NOCA) covered 58% of Intensive Care Unit (ICU) activity in adult Health Service Executive (HSE) funded hospitals (12 Units in nine hospitals) and all ICU activity in both specialist paediatric hospitals in the Republic of Ireland (ROI).</div

    1,2,4-Triazolo-[1,5‑<i>a</i>]pyridine HIF Prolylhydroxylase Domain‑1 (PHD-1) Inhibitors With a Novel Monodentate Binding Interaction

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    Herein we describe the identification of 4-{[1,2,4]­triazolo­[1,5-<i>a</i>]­pyridin-5-yl}­benzonitrile-based inhibitors of the hypoxia-inducible factor prolylhydroxylase domain-1 (PHD-1) enzyme. These inhibitors were shown to possess a novel binding mode by X-ray crystallography, in which the triazolo N1 atom coordinates in a hitherto unreported monodentate interaction with the active site Fe<sup>2+</sup> ion, while the benzonitrile group accepts a hydrogen-bonding interaction from the side chain residue of Asn315. Further optimization led to potent PHD-1 inhibitors with good physicochemical and pharmacokinetic properties
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