8 research outputs found

    Massachusetts Depth to Bedrock Project

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    The depth to bedrock is perhaps one of the most important surfaces that is fundamental to many practical engineering and geological problems. Yet it is not well understood everywhere. Knowing the depth to bedrock for transportation projects not only influences cost but may also affect selection of the appropriate foundation system for a particular structure. Furthermore, estimates of the bedrock depth, along with the type of overburden (e.g., glacial till, varved clay, sand and gravel) help determine the most appropriate subsurface investigation method to use during project planning, and reduces construction delays and claims brought forward by contractors. Accordingly, there is some level of uncertainty in planning subsurface investigations for any transportation project when depth to bedrock information is lacking. This project is an attempt to reduce the uncertainty in highway project planning by providing interpolated statewide data layers of the depth to bedrock and bedrock altitude at 100-meter resolution based on currently available subsurface data. In addition, maps depicting the level of confidence in the estimate of the bedrock altitude and depth are also provided. The confidence is based on both the interpolated prediction standard error as well as the measurement uncertainties associated with the input data

    Implementation Plan of the National Cooperative Geologic Mapping Program Strategy—Northeast Region of the United States: New York and New England

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    Complexly deformed igneous, metamorphic, and sedimentary rocks form the bedrock of the Northeast region of the United States. Variably thick unconsolidated sediments deposited by glacial, fluvial, and eolian systems locally cover the bedrock. New geologic mapping focuses on areas lacking modern, detailed studies or syntheses, and contributes to existing framework research. This report addresses plans for the continued development of regionally and nationally consistent geologic maps and map databases, efforts to answer outstanding geologic questions, and societal concerns associated with related geologic topics, such as hazards, geologic and hydrologic resources, and environmental issues

    Edoxaban versus warfarin in patients with atrial fibrillation

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    Contains fulltext : 125374.pdf (publisher's version ) (Open Access)BACKGROUND: Edoxaban is a direct oral factor Xa inhibitor with proven antithrombotic effects. The long-term efficacy and safety of edoxaban as compared with warfarin in patients with atrial fibrillation is not known. METHODS: We conducted a randomized, double-blind, double-dummy trial comparing two once-daily regimens of edoxaban with warfarin in 21,105 patients with moderate-to-high-risk atrial fibrillation (median follow-up, 2.8 years). The primary efficacy end point was stroke or systemic embolism. Each edoxaban regimen was tested for noninferiority to warfarin during the treatment period. The principal safety end point was major bleeding. RESULTS: The annualized rate of the primary end point during treatment was 1.50% with warfarin (median time in the therapeutic range, 68.4%), as compared with 1.18% with high-dose edoxaban (hazard ratio, 0.79; 97.5% confidence interval [CI], 0.63 to 0.99; P<0.001 for noninferiority) and 1.61% with low-dose edoxaban (hazard ratio, 1.07; 97.5% CI, 0.87 to 1.31; P=0.005 for noninferiority). In the intention-to-treat analysis, there was a trend favoring high-dose edoxaban versus warfarin (hazard ratio, 0.87; 97.5% CI, 0.73 to 1.04; P=0.08) and an unfavorable trend with low-dose edoxaban versus warfarin (hazard ratio, 1.13; 97.5% CI, 0.96 to 1.34; P=0.10). The annualized rate of major bleeding was 3.43% with warfarin versus 2.75% with high-dose edoxaban (hazard ratio, 0.80; 95% CI, 0.71 to 0.91; P<0.001) and 1.61% with low-dose edoxaban (hazard ratio, 0.47; 95% CI, 0.41 to 0.55; P<0.001). The corresponding annualized rates of death from cardiovascular causes were 3.17% versus 2.74% (hazard ratio, 0.86; 95% CI, 0.77 to 0.97; P=0.01), and 2.71% (hazard ratio, 0.85; 95% CI, 0.76 to 0.96; P=0.008), and the corresponding rates of the key secondary end point (a composite of stroke, systemic embolism, or death from cardiovascular causes) were 4.43% versus 3.85% (hazard ratio, 0.87; 95% CI, 0.78 to 0.96; P=0.005), and 4.23% (hazard ratio, 0.95; 95% CI, 0.86 to 1.05; P=0.32). CONCLUSIONS: Both once-daily regimens of edoxaban were noninferior to warfarin with respect to the prevention of stroke or systemic embolism and were associated with significantly lower rates of bleeding and death from cardiovascular causes. (Funded by Daiichi Sankyo Pharma Development; ENGAGE AF-TIMI 48 ClinicalTrials.gov number, NCT00781391.)
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