12 research outputs found

    A Large Specific Deterrent Effect of Arrest for Patronizing a Prostitute

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    BACKGROUND: Prior research suggests that arrest, compared with no police detection, of some types of offenders does not decrease the chances they will reoffend. METHODOLOGY/PRINCIPAL FINDINGS: We assessed the specific deterrent effect of arrest for patronizing a street prostitute in Colorado Springs by comparing the incidence of arrest for clients of prostitutes first detected through public health surveillance with the incidence of rearrest for clients first detected by police arrest. Although these sets of clients were demographically and behaviorally similar, arrest reduced the likelihood of a subsequent arrest by approximately 70%. In other areas of the United States, arrest did not appear to displace a client's patronizing. CONCLUSIONS/SIGNIFICANCE: Our results suggest that apprehending clients decreases their patronizing behavior substantially

    An Analysis of the Open Architecture Warfare System Domain Model for surface time critical targets

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    This study's objective is to evaluate the Open Architecture Warfare System Domain Model (OAWSDM) against time critical targets with specific focus on command, control, and communication processes. A functional analysis of the OAWSDM was conducted and synthesized to create the Open Architecture Time Critical Target Engagement Process Model (OATCTEPM). This model represents the notional engagement cycle of a Navy cruiser. Two scenarios were developed to exercise the system: a surprise assault from a number of personal watercraft and a saturation assault in which approximately fifty craft of varying sizes attack. Results from these scenarios were analyzed for system bottlenecks and recommendations were made to improve decision making processes and reduce engagement time. This study concludes that while the OAWSDM may offer no technical flaws in its design, it fails to factor in the role of the human in the decision making and engagement processes. In doing so it overlooks a key factor in the effectiveness of the architecture against surface TCT engagements.http://archive.org/details/ananalysisofopen109456933N

    Creatine Kinase-Overexpression Improves Myocardial Energetics, Contractile Dysfunction and Survival in Murine Doxorubicin Cardiotoxicity

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    Doxorubicin (DOX) is a commonly used life-saving antineoplastic agent that also causes dose-dependent cardiotoxicity. Because ATP is absolutely required to sustain normal cardiac contractile function and because impaired ATP synthesis through creatine kinase (CK), the primary myocardial energy reserve reaction, may contribute to contractile dysfunction in heart failure, we hypothesized that impaired CK energy metabolism contributes to DOX-induced cardiotoxicity. We therefore overexpressed the myofibrillar isoform of CK (CK-M) in the heart and determined the energetic, contractile and survival effects of CK-M following weekly DOX (5mg/kg) administration using in vivo (31)P MRS and (1)H MRI. In control animals, in vivo cardiac energetics were reduced at 7 weeks of DOX protocol and this was followed by a mild but significant reduction in left ventricular ejection fraction (EF) at 8 weeks of DOX, as compared to baseline. At baseline, CK-M overexpression (CK-M-OE) increased rates of ATP synthesis through cardiac CK (CK flux) but did not affect contractile function. Following DOX however, CK-M-OE hearts had better preservation of creatine phosphate and higher CK flux and higher EF as compared to control DOX hearts. Survival after DOX administration was significantly better in CK-M-OE than in control animals (p<0.02). Thus CK-M-OE attenuates the early decline in myocardial high-energy phosphates and contractile function caused by chronic DOX administration and increases survival. These findings suggest that CK impairment plays an energetic and functional role in this DOX-cardiotoxicity model and suggests that metabolic strategies, particularly those targeting CK, offer an appealing new strategy for limiting DOX-associated cardiotoxicity
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