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51.
Geert Molenberghs Christel Faes Johan Verbeeck Patrick Deboosere Steven Abrams Lander Willem Jan Aerts Heidi Theeten Brecht Devleesschauwer Natalia Bustos Sierra Franoise Renard Sereina Herzog Patrick Lusyne Johan Van der Heyden Herman Van Oyen Pierre Van Damme Niel Hens 《Euro surveillance : bulletin européen sur les maladies transmissibles = European communicable disease bulletin》2022,27(7)
BackgroundCOVID-19 mortality, excess mortality, deaths per million population (DPM), infection fatality ratio (IFR) and case fatality ratio (CFR) are reported and compared for many countries globally. These measures may appear objective, however, they should be interpreted with caution.AimWe examined reported COVID-19-related mortality in Belgium from 9 March 2020 to 28 June 2020, placing it against the background of excess mortality and compared the DPM and IFR between countries and within subgroups.MethodsThe relation between COVID-19-related mortality and excess mortality was evaluated by comparing COVID-19 mortality and the difference between observed and weekly average predictions of all-cause mortality. DPM were evaluated using demographic data of the Belgian population. The number of infections was estimated by a stochastic compartmental model. The IFR was estimated using a delay distribution between infection and death.ResultsIn the study period, 9,621 COVID-19-related deaths were reported, which is close to the excess mortality estimated using weekly averages (8,985 deaths). This translates to 837 DPM and an IFR of 1.5% in the general population. Both DPM and IFR increase with age and are substantially larger in the nursing home population.DiscussionDuring the first pandemic wave, Belgium had no discrepancy between COVID-19-related mortality and excess mortality. In light of this close agreement, it is useful to consider the DPM and IFR, which are both age, sex, and nursing home population-dependent. Comparison of COVID-19 mortality between countries should rather be based on excess mortality than on COVID-19-related mortality. 相似文献
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Michele L. R. Heffernan Lee W. Herman Scott Brown Philip G. Jones Liming Shao Michael C. Hewitt John E. Campbell Nina Dedic Seth C. Hopkins Kenneth S. Koblan Linghong Xie 《ACS medicinal chemistry letters》2022,13(1):92
Ulotaront (SEP-363856) is a trace-amine associated receptor 1 (TAAR1) agonist with 5-HT1A receptor agonist activity in Phase 3 clinical development, with FDA Breakthrough Therapy Designation, for the treatment of schizophrenia. TAAR1 is a G-protein-coupled receptor (GPCR) that is expressed in cortical, limbic, and midbrain monoaminergic regions. It is activated by endogenous trace amines, and is believed to play an important role in modulating dopaminergic, serotonergic, and glutamatergic circuitry. TAAR1 agonism data are reported herein for ulotaront and its analogues in comparison to endogenous TAAR1 agonists. In addition, a human TAAR1 homology model was built around ulotaront to identify key interactions and attempt to better understand the scaffold-specific TAAR1 agonism structure–activity relationships. 相似文献
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1. Intramuscular dosage of antipneumococcus sera in a standard dermal pneumococcic infection in rabbits is as effective as intravenous dosage provided the degree of blood stream invasion be not unusually high. 2. The immediate bactericidal effect of doses of serum given intramuscularly is equal to that of the same doses given intravenously in the cases of mild and moderately severe bacteremias. 3. The intramuscular method of serum administration in human beings with lobar pneumonia deserves a carefully controlled clinical trial. 相似文献
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Dr. Herman Franken 《Journal of molecular medicine (Berlin, Germany)》1929,8(10):439-442
Ohne ZusammenfassungDie Arbeit wurde durchgeführt mit Unterstützung des Kuratoriums der Freiburger Wissenschaftlichen Gesellschaft, der auch an dieser Stelle gedankt sei. 相似文献