1,210 research outputs found
Flat-H Redundant Frangible Joint Design Evolution 2018: Feasibility Study Conclusions
This paper reports results of an investigation into developing a single failure tolerant pyrotechnic linear separation system which features completely redundant explosive trains suitable for human spaceflight. It is a follow up to Flat-H Redundant Frangible Joint Design Evolution 2017 and Flat-H Redundant Frangible Joint Evolution. The paper chronicles the history of the redundant frangible joint development program including testing, analysis, and design improvements from 2014 to the present culminating in a successful proof-of-concept prototype. The paper describes work done to address debris control and containment of combustion products. A performance optimization strategy is presented along with optimization results. Additionally a novel containment manifold design is presented with test results
Onset of occupational hand eczema among healthcare workers during the SARSâCoVâ2 pandemic: Comparing a single surgical site with a COVIDâ19 intensive care unit
Background
As a result of the COVIDâ19 outbreak, hygiene regulations have been revised and hand sanitation has been intensified.
Objective
To investigate the onset of hand eczema during the COVIDâ19 pandemic in healthcare workers (HCWs) directly involved in intensive care of COVIDâ19 patients and HCWs without direct contact with COVIDâ19 patients. Hereby, we aim at increasing awareness about occupational hand eczema and preventive measures that can be adopted.
Method
A survey was distributed amongst 114 HCWs at a single surgical centre and at a COVIDâ19 intensive care unit of the university hospital Ludwig Maximilian University Munich, Germany. Participants were questioned about the daily frequency of hand hygiene prior to and during the pandemic. Participants selfâreported the onset of hand eczema and associated symptoms.
Results
Our study revealed a significant increase in hand washing, disinfection, and use of hand cream across all participants (Pâvalue <.001), regardless of having direct contact with COVIDâ19 patients. A high prevalence of symptoms associated with acute hand dermatitis of 90.4% was found across all HCWs, whereas hand eczema itself was underreported (14.9%).
Conclusion
The increase in hand sanitation during the COVIDâ19 pandemic impairs the skin of the hands across all HCWs, independent of direct intensive care of affected patients
Race and sex differences in response to endothelin receptor antagonists for pulmonary arterial hypertension
Background
Recently studied therapies for pulmonary arterial hypertension (PAH) have improved outcomes among populations of patients, but little is known about which patients are most likely to respond to specific treatments. Differences in endothelin-1 biology between sexes and between whites and blacks may lead to differences in patients' responses to treatment with endothelin receptor antagonists (ERAs).
Methods
We conducted pooled analyses of deidentified, patient-level data from six randomized placebo-controlled trials of ERAs submitted to the US Food and Drug Administration to elucidate heterogeneity in treatment response. We estimated the interaction between treatment assignment (ERA vs placebo) and sex and between treatment and white or black race in terms of the change in 6-min walk distance from baseline to 12 weeks.
Results
Trials included 1,130 participants with a mean age of 49 years; 21% were men, 74% were white, and 6% were black. The placebo-adjusted response to ERAs was 29.7 m (95% CI, 3.7-55.7 m) greater in women than in men (P = .03). The placebo-adjusted response was 42.2 m for whites and â1.4 m for blacks, a difference of 43.6 m (95% CI, â3.5-90.7 m) (P = .07). Similar results were found in sensitivity analyses and in secondary analyses using the outcome of absolute distance walked.
Conclusions
Women with PAH obtain greater responses to ERAs than do men, and whites may experience a greater treatment benefit than do blacks. This heterogeneity in treatment-response may reflect pathophysiologic differences between sexes and races or distinct disease phenotypes
Discovery and Early Evolution of ASASSN-19bt, the First TDE Detected by TESS
We present the discovery and early evolution of ASASSN-19bt, a tidal
disruption event (TDE) discovered by the All-Sky Automated Survey for
Supernovae (ASAS-SN) at a distance of Mpc and the first TDE to be
detected by TESS. As the TDE is located in the TESS Continuous Viewing Zone,
our dataset includes 30-minute cadence observations starting on 2018 July 25,
and we precisely measure that the TDE begins to brighten days before
its discovery. Our dataset also includes 18 epochs of Swift UVOT and XRT
observations, 2 epochs of XMM-Newton observations, 13 spectroscopic
observations, and ground data from the Las Cumbres Observatory telescope
network, spanning from 32 days before peak through 37 days after peak.
ASASSN-19bt thus has the most detailed pre-peak dataset for any TDE. The TESS
light curve indicates that the transient began to brighten on 2019 January 21.6
and that for the first 15 days its rise was consistent with a flux power-law model. The optical/UV emission is well-fit by a blackbody SED,
and ASASSN-19bt exhibits an early spike in its luminosity and temperature
roughly 32 rest-frame days before peak and spanning up to 14 days that has not
been seen in other TDEs, possibly because UV observations were not triggered
early enough to detect it. It peaked on 2019 March 04.9 at a luminosity of
ergs s and radiated
ergs during the 41-day rise to peak. X-ray observations after peak indicate a
softening of the hard X-ray emission prior to peak, reminiscent of the
hard/soft states in X-ray binaries.Comment: 23 pages, 14 figures, 5 tables. A machine-readable table containing
the host-subtracted photometry presented in this manuscript is included as an
ancillary fil
Recommendations for the advancement of oil-in-water media and source oil characterization in aquatic toxicity test studies
During toxicity testing, chemical analyses of oil and exposure media samples are needed to allow comparison of results between different tests as well as to assist with identification of the drivers and mechanisms for the toxic effects observed. However, to maximize the ability to compare results between different laboratories and biota, it has long been recognized that guidelines for standard protocols were needed. In 2005, the Chemical Response to Oil Spills: Ecological Effects Research Forum (CROSERF) protocol was developed with existing common analytical methods that described a standard method for reproducible preparation of exposure media as well as recommended specific analytical methods and analyte lists for comparative toxicity testing. At the time, the primary purpose for the data collected was to inform oil spill response and contingency planning. Since then, with improvements in both analytical equipment and methods, the use of toxicity data has expanded to include their integration into fate and effect models that aim to extend the applicability of lab-based study results to make predictions for field system-level impacts. This paper focuses on providing a summary of current chemical analyses for characterization of oil and exposure media used during aquatic toxicity testing and makes recommendations for the minimum analyses needed to allow for interpretation and modeling purposes.publishedVersio
Statistical design of personalized medicine interventions: The Clarification of Optimal Anticoagulation through Genetics (COAG) trial
<p>Abstract</p> <p>Background</p> <p>There is currently much interest in pharmacogenetics: determining variation in genes that regulate drug effects, with a particular emphasis on improving drug safety and efficacy. The ability to determine such variation motivates the application of personalized drug therapies that utilize a patient's genetic makeup to determine a safe and effective drug at the correct dose. To ascertain whether a genotype-guided drug therapy improves patient care, a personalized medicine intervention may be evaluated within the framework of a randomized controlled trial. The statistical design of this type of personalized medicine intervention requires special considerations: the distribution of relevant allelic variants in the study population; and whether the pharmacogenetic intervention is equally effective across subpopulations defined by allelic variants.</p> <p>Methods</p> <p>The statistical design of the Clarification of Optimal Anticoagulation through Genetics (COAG) trial serves as an illustrative example of a personalized medicine intervention that uses each subject's genotype information. The COAG trial is a multicenter, double blind, randomized clinical trial that will compare two approaches to initiation of warfarin therapy: genotype-guided dosing, the initiation of warfarin therapy based on algorithms using clinical information and genotypes for polymorphisms in <it>CYP2C9 </it>and <it>VKORC1</it>; and clinical-guided dosing, the initiation of warfarin therapy based on algorithms using only clinical information.</p> <p>Results</p> <p>We determine an absolute minimum detectable difference of 5.49% based on an assumed 60% population prevalence of zero or multiple genetic variants in either <it>CYP2C9 </it>or <it>VKORC1 </it>and an assumed 15% relative effectiveness of genotype-guided warfarin initiation for those with zero or multiple genetic variants. Thus we calculate a sample size of 1238 to achieve a power level of 80% for the primary outcome. We show that reasonable departures from these assumptions may decrease statistical power to 65%.</p> <p>Conclusions</p> <p>In a personalized medicine intervention, the minimum detectable difference used in sample size calculations is not a known quantity, but rather an unknown quantity that depends on the genetic makeup of the subjects enrolled. Given the possible sensitivity of sample size and power calculations to these key assumptions, we recommend that they be monitored during the conduct of a personalized medicine intervention.</p> <p>Trial Registration</p> <p>clinicaltrials.gov: NCT00839657</p
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