"Muzej primenjene umetnosti, Beograd, Belgrade, Serbia, May 19th - June 27th 2015. -- Porzellanikon - Staatliches Museum für Porzellan, Hohenberg a. d. Eger/Selb, Germany, July 31st - November 15th 2015. -- Museo Nacional de Cerámica y Artes Suntuarias "González Martí", Valencia, Spain, January 15st - April 10th 2016. -- Museo Internazionale delle Ceramiche in Faenza, Italy, April 23rd - September 11th 2016. -- The Potteries Museum and art Gallery, Stoke-on-Trent, United Kingdom, October 1st 2016 - January 6th 2017. -- Eesti Tarbekunsti- ja Disainimuuseum, Tallinn, Estonia, January 22nd - April 30th 2017"--Rub tit. l., Autoři: Wilhelm Siemen ... [et al.], and Pod názvem: Ceramics and its Dimensions. -- Co-funded by the Creative Europe Programme of the European Union
The purpose of this study was to evaluate the efficacy and safety of FDP in patients with ocular ischemic syndrome. Material and methods. The material for this study is based on results of a comprehensive examination and treatment of 53 patients with a diagnosis OIS. The average age of the patients was 57,8 ± 6,82 year. 19 of them women, 34 men. 27 patients entered to the main group (1) which received standard therapy in combination with intravenous FDP (fructose 1,6-bisphosphate). 26 patients in the control group (2) received standard treatment. Results. In applying the FDP combined with comprehensive therapy in the main group resulted in increased of visual acuity by 32.8%, parameters of retinal sensitivity by 17.8%, reducing the area of scotomas compared with patients of the control group. Optical coherence tomography registered significant changes in the dynamics in patients of the main group - reducing the edema and restoration of RNFL and ONH. Recovery of visual function may have contributed neuroprotective activity of the drug FDP by a protective effect on nerve tissue, reducing the effects of hypoxic stress. Conclusions. The use of standard therapy in combination with FDP in the treatment of ocular ischemic syndrome has a positive effect on the course of the disease, thereby, increase of visual acuity, a decrease in sectoral loss in vision fields, the positive dynamics OCT parameters, improving hemodynamic parameters at Doppler imaging in dynamics., Dilbar Makhkamova, and Literatura
Projekt PROFICIO zahrnuje 20 klinických studií hodnotících účinek evolokumabu na výskyt kardiovaskulárních onemocnění včetně jeho bezpečnostního profilu a tolerance. Většina zařazených studií sleduje průměrné procentuální snížení koncentrací LDL-cholesterolu za 10 a 12 týdnů podávání evolokumabu ve srovnání se vstupními hodnotami. První výsledky byly prezentovány na přelomu srpna a září 2015 na kongresu Evropské kardiologické společnosti (ESC) v Londýně. Do této subanalýzy bylo zařazeno 3 146 pacientů, kteří absolvovali jednu z vybraných studií 3. fáze klinického zkoušení a kterým byl evolokumab podáván v dávce 140 mg s.c. 1krát za 2 týdny nebo 420 mg s.c. 1krát za 4 týdny. Hodnoty LDL-cholesterolu se po evolokumabu snížily v jednotlivých studiích o 56,5–74,9 % ve srovnání s placebem a o 36,9–44,9 % oproti ezetimibu. Výskyt nežádoucích účinků se nelišil od skupiny užívající placebo. Klíčová slova: evolokumab – projekt PROFICIO – LDL-cholesterol – kardiovaskulární riziko, The PROFICIO project includes 20 clinical studies evaluating the effect of evolocumab on the incidence of cardiovascular disease including its safety profile and tolerance. Most of the included studies follow the average proportional decrease of LDL-cholesterol concentrations over 10 and 12 weeks of administering evolocumab as compared to the input values. The first results were announced at the congress of the European Society of Cardiology (ESC) in London at the end of August and beginning of September 2015. This subanalysis comprised 3146 patients, who underwent one of the selected studies of phase 3 clinical testing and who were administered a dose of 140 mg s.c. evolocumab once in 2 weeks, or 420 mg s.c. once in 4 weeks. LDL-cholesterol levels decreased after evolocumab by 56.5 – 74.9% in the individual studies as compared to placebo and by 36.9 – 44.9% compared to ezetimib. The incidence of adverse effects did not differ from the group which used placebo. Key words: evolocumab – PROFICIO project – LDL-cholesterol – cardiovascular risk, and Pavel Kraml