681 research outputs found
Reporting ethics committee approval and patient consent by study design in five general medical journals.
BACKGROUND: Authors are required to describe in their manuscripts ethical approval from an appropriate committee and how consent was obtained from participants when research involves human participants. OBJECTIVE: To assess the reporting of these protections for several study designs in general medical journals. DESIGN: A consecutive series of research papers published in the Annals of Internal Medicine, BMJ, JAMA, Lancet and The New England Journal of Medicine between February and May 2003 were reviewed for the reporting of ethical approval and patient consent. Ethical approval, name of approving committee, type of consent, data source and whether the study used data collected as part of a study reported elsewhere were recorded. Differences in failure to report approval and consent by study design, journal and vulnerable study population were evaluated using multivariable logistic regression. RESULTS: Ethical approval and consent were not mentioned in 31% and 47% of manuscripts, respectively. 88 (27%) papers failed to report both approval and consent. Failure to mention ethical approval or consent was significantly more likely in all study designs (except case-control and qualitative studies) than in randomised controlled trials (RCTs). Failure to mention approval was most common in the BMJ and was significantly more likely than in The New England Journal of Medicine. Failure to mention consent was most common in the BMJ and was significantly more likely than in all other journals. No significant differences in approval or consent were found when comparing studies of vulnerable and non-vulnerable participants. CONCLUSION: The reporting of ethical approval and consent in RCTs has improved, but journals are less good at reporting this information for other study designs. Journals should publish this information for all research on human participants
Late follow-up after thoracic duct drainage in cadaveric renal transplantation
Thoracic duct drainage was added to conventional immunosuppression with azathioprine, prednisone and, sometimes, antilymphocyte globulin in 83 patients given cadaveric kidneys, including 65 primary graft recipients. The most effective use of thoracic duct drainage was for pretreatment. Optimal conditioning was at least four weeks duration, and when lymph drainage was this long, the incidence of rejection during the first three postoperative months was reduced to 4.5 per cent. Shorter pretreatment or institution of thoracic duct drainage contemporaneous with transplantation were less effective, but the one year results were still better than those with conventional immunosuppression alone. However, the advantage gained with thoracic duct drainage during the first year was diminished in all the treatment groups by graft losses in the second postoperative year. It was concluded that, without better maintenance therapy, the full value of temporary early lymphoid depletion procedures cannot be fully exploited
CSF lactate dehydrogenase activity in patients with Creutzfeldt-Jakob disease exceeds that in other dementias
The diagnosis of Creutzfeldt- Jakob disease (CJD) is still made by exclusion of other dementias. We now evaluated lactate dehydrogenase (LDH) in the cerebrospinal fluid (CSF) as a possible additional diagnostic tool. CSF LDH levels of patients with CJD ( n = 26) were compared with those in other dementias ( n = 28). LDH isoenzymes were determined in a subset ( n = 9). Total LDH and isoenzyme LDH-1 were significantly higher, whereas the fractions of LDH-2 and LDH-3 were significantly lower in CJD patients. We conclude that in addition to established CSF parameters, LDH and its isoenzymes might serve as a further help to discriminate between CJD and other dementias. Copyright (C) 2004 S. Karger AG, Basel
Enhanced transmission versus localization of a light pulse by a subwavelength metal slit: Can the pulse have both characteristics?
The existence of resonant enhanced transmission and collimation of light
waves by subwavelength slits in metal films [for example, see T.W. Ebbesen et
al., Nature (London) 391, 667 (1998) and H.J. Lezec et al., Science, 297, 820
(2002)] leads to the basic question: Can a light be enhanced and simultaneously
localized in space and time by a subwavelength slit? To address this question,
the spatial distribution of the energy flux of an ultrashort (femtosecond)
wave-packet diffracted by a subwavelength (nanometer-size) slit was analyzed by
using the conventional approach based on the Neerhoff and Mur solution of
Maxwell's equations. The results show that a light can be enhanced by orders of
magnitude and simultaneously localized in the near-field diffraction zone at
the nm- and fs-scales. Possible applications in nanophotonics are discussed.Comment: 5 figure
Geometry-induced asymmetric diffusion
Past work has shown that ions can pass through a membrane more readily in one
direction than the other. We demonstrate here in a model and an experiment that
for a mixture of small and large particles such asymmetric diffusion can arise
solely from an asymmetry in the geometry of the pores of the membrane. Our
deterministic simulation considers a two-dimensional gas of elastic disks of
two sizes diffusing through a membrane, and our laboratory experiment examines
the diffusion of glass beads of two sizes through a metal membrane. In both
experiment and simulation, the membrane is permeable only to the smaller
particles, and the asymmetric pores lead to an asymmetry in the diffusion rates
of these particles. The presence of even a small percentage of large particles
can clog a membrane, preventing passage of the small particles in one direction
while permitting free flow of the small particles in the other direction. The
purely geometric kinetic constraints may play a role in common biological
contexts such as membrane ion channels.Comment: published with minuscule change
1.68-angstrom crystal structure of endopolygalacturonase II from Aspergillus niger and identification of active site residues by site-directed mutagenesis
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