116 results on '"Nakov R"'
Search Results
2. Velingrad Hydrogeothermal System (Bulgaria): Geochemical Features and Heat Output
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Polyak, B. G., Kikvadze, O. E., Ermakov, A. V., Hristov, V., Kamenskii, I. L., Lavrushin, V. Yu., Nakov, R., and Deneva, B.
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- 2020
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3. Significant Differences in IBD Care and Education across Europe: Results of the Pan-European VIPER Survey.
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Kral, J., Nakov, R., Lanska, V., Barberio, B., Benech, N., Blesl, A., Brunet, E., Capela, T., Derikx, L.A.A.P., Dragoni, G., Eek, A., Frias-Gomes, C., Gîlcă-Blanariu, G.E., Gilroy, L., Harvey, P., Kagramanova, A., Kani, H.T., Konikoff, T., Lessing, M., Madsen, G., Maksimaityte, V., Miasnikova, M., Mikolasevic, I., Milivojevic, V., Noviello, D., Oliinyk, D., Patai, A., Pisani, A., Protopapas, A., Rodríguez-Lago, I., Schreiner, P., Skuja, V., Tran, F., Truyens, M., Włodarczyk, M., Zatorski, H., Verstockt, B., Segal, J.P., Kral, J., Nakov, R., Lanska, V., Barberio, B., Benech, N., Blesl, A., Brunet, E., Capela, T., Derikx, L.A.A.P., Dragoni, G., Eek, A., Frias-Gomes, C., Gîlcă-Blanariu, G.E., Gilroy, L., Harvey, P., Kagramanova, A., Kani, H.T., Konikoff, T., Lessing, M., Madsen, G., Maksimaityte, V., Miasnikova, M., Mikolasevic, I., Milivojevic, V., Noviello, D., Oliinyk, D., Patai, A., Pisani, A., Protopapas, A., Rodríguez-Lago, I., Schreiner, P., Skuja, V., Tran, F., Truyens, M., Włodarczyk, M., Zatorski, H., Verstockt, B., and Segal, J.P.
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Item does not contain fulltext, BACKGROUND: Inflammatory bowel disease (IBD) care and education might differ around Europe. Therefore, we conducted this European Variation In IBD PracticE suRvey (VIPER) to investigate potential differences between countries. METHODS: This trainee-initiated survey, run through SurveyMonkey®, consisted of 47 questions inquiring basic demographics, IBD training, and clinical care. Results were compared according to gross domestic product (GDP) per capita, for which countries were divided into 2 groups (low/high income, according to the World Bank). RESULTS: The online survey was completed by 1,285 participants from 40 European countries, with a majority of specialists (65.3%) working in academic institutions (50.4%). Significant differences in IBD-specific training (55.9% vs. 38.4%), as well as availability of IBD units (58.4% vs. 39.7%) and multidisciplinary meetings (73.2% vs. 40.1%), were observed between respondees from high and low GDP countries (p < 0.0001). In high GDP countries, IBD nurses are more common (85.9% vs. 36.0%), also mirrored by more nurse-led IBD clinics (40.6% vs. 13.7%; p < 0.0001). IBD dieticians (33.4% vs. 16.5%) and psychologists (16.8% vs. 7.5%) are mainly present in high GDP countries (p < 0.0001). In the current COVID era, telemedicine is available in 73.2% versus 54.1% of the high/low GDP countries, respectively (p < 0.0001). Treat-to-target approaches are implemented everywhere (85.0%), though access to biologicals and small molecules differs significantly. CONCLUSION: Much variability in IBD practice exists across Europe, with marked differences between high and low GDP countries. Further work is required to help address some of these inequalities, aiming to improve and standardize IBD care and training across Europe.
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- 2023
4. Development of a core descriptor set for Crohn's anal fistula
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Lee M. J., Williams K. M., Lamidi S., Coe P. O., Bordeianou L. G., Hart A. L., Hind D., Lindsay J. O., Lobo A. J., Myrelid P., Raine T., Sebastian S., Fearnhead N. S., Adams K., Almer S., Ananthakrishnan A., Bethune R. M., Block M., Brown S. R., Cirocco W. C., Cooney R., Davies J., Atici S. D., Dhar A., Din S., Drobne D., Espin-Basany E., Evans J. P., Fleshner P. R., Folkesson J., Fraser A., Graf W., Hahnloser D., Hager J., Hancock L., Hanzel J., Hargest R., Hedin C. R. H., Hill J., Ihle C., Jongen J., Kader R., Karmiris K., Katsanos K. H., Keller D. S., Kopylov U., Koutrabakis I. E., Lamb C. A., Landerholm K., Lee G. C., Litta F., Limdi J. K., Lopes E. W., Madoff R. D., Martin S. T., Martin-Perez B., Michalopoulos G., Millan M., Munch A., Nakov R., Noor N. M., Oresland T., Paquette I. M., Pellino G., Perra T., Porcu A., Roslani A. C., Samaan M. A., Sebepos-Rogers G. M., Segal J. P., de Silva S., Soderholm M., Spinelli A., Speight A., Steinhagen R. M., Stenstrom P., Tsimogiannis K. E., Varma M. G., Verma A. M., Verstockt B., Warden C., Yassin N., Zawadzki A., Carr P., Devlin B., Mannick S., Avery P., Gecse K. B., Goren I., Hellstrom P. M., Kotze P. G., McWhirter D., Naik A. S., Sammour T., Selinger C. P., Stein S. L., Torres J., Wexner S. D., Younge L. C., Lee, M. J., Williams, K. M., Lamidi, S., Coe, P. O., Bordeianou, L. G., Hart, A. L., Hind, D., Lindsay, J. O., Lobo, A. J., Myrelid, P., Raine, T., Sebastian, S., Fearnhead, N. S., Adams, K., Almer, S., Ananthakrishnan, A., Bethune, R. M., Block, M., Brown, S. R., Cirocco, W. C., Cooney, R., Davies, J., Atici, S. D., Dhar, A., Din, S., Drobne, D., Espin-Basany, E., Evans, J. P., Fleshner, P. R., Folkesson, J., Fraser, A., Graf, W., Hahnloser, D., Hager, J., Hancock, L., Hanzel, J., Hargest, R., Hedin, C. R. H., Hill, J., Ihle, C., Jongen, J., Kader, R., Karmiris, K., Katsanos, K. H., Keller, D. S., Kopylov, U., Koutrabakis, I. E., Lamb, C. A., Landerholm, K., Lee, G. C., Litta, F., Limdi, J. K., Lopes, E. W., Madoff, R. D., Martin, S. T., Martin-Perez, B., Michalopoulos, G., Millan, M., Munch, A., Nakov, R., Noor, N. M., Oresland, T., Paquette, I. M., Pellino, G., Perra, T., Porcu, A., Roslani, A. C., Samaan, M. A., Sebepos-Rogers, G. M., Segal, J. P., de Silva, S., Soderholm, M., Spinelli, A., Speight, A., Steinhagen, R. M., Stenstrom, P., Tsimogiannis, K. E., Varma, M. G., Verma, A. M., Verstockt, B., Warden, C., Yassin, N., Zawadzki, A., Carr, P., Devlin, B., Mannick, S., Avery, P., Gecse, K. B., Goren, I., Hellstrom, P. M., Kotze, P. G., Mcwhirter, D., Naik, A. S., Sammour, T., Selinger, C. P., Stein, S. L., Torres, J., Wexner, S. D., Younge, L. C., Gastroenterology and Hepatology, and AGEM - Amsterdam Gastroenterology Endocrinology Metabolism
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Crohn's disease ,anal fistula ,consensus ,methodology ,Gastroenterologi ,Gastroenterology ,consensu ,Gastroenterology and Hepatology - Abstract
Aim: Crohn's anal fistula (CAF) is a complex condition, with no agreement on which patient characteristics should be routinely reported in studies. The aim of this study was to develop a core descriptor set of key patient characteristics for reporting in all CAF research.Method: Candidate descriptors were generated from published literature and stakeholder suggestions. Colorectal surgeons, gastroenterologists and specialist nurses in inflammatory bowel disease took part in three rounds of an international modified Delphi process using nine-point Likert scales to rank the importance of descriptors. Feedback was provided between rounds to allow refinement of the next ratings. Patterns in descriptor voting were assessed using principal component analysis (PCA). Resulting PCA groups were used to organize items in rounds two and three. Consensus descriptors were submitted to a patient panel for feedback. Items meeting predetermined thresholds were included in the final set and ratified at the consensus meeting.Results: One hundred and thirty three respondents from 22 countries completed round one, of whom 67.0% completed round three. Ninety seven descriptors were rated across three rounds in 11 PCA-based groups. Forty descriptors were shortlisted. The consensus meeting ratified a core descriptor set of 37 descriptors within six domains: fistula anatomy, current disease activity and phenotype, risk factors, medical interventions for CAF, surgical interventions for CAF, and patient symptoms and impact on quality of life.Conclusion: The core descriptor set proposed for all future CAF research reflects characteristics important to gastroenterologists and surgeons. This might aid transparent reporting in future studies.
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- 2022
5. Pooled analysis of two randomized, double-blind trials comparing proposed biosimilar LA-EP2006 with reference pegfilgrastim in breast cancer
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Blackwell, K., Gascon, P., Jones, C. M., Nixon, A., Krendyukov, A., Nakov, R., Li, Y., and Harbeck, N.
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- 2017
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6. Additional file 1 of Superior physical and mental health of healthy volunteers before and five years after mobilized stem cell donation
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Heyn, J., Br��uninger, S., Dimova-Dobreva, M., Mathieson, N., Koptelova, N., Kolpakova, A., Seidl, C., Reinhardt, P., Tsamadou, C., Schrezenmeier, H., Nakov, R., Seifried, E., and Bonig, H.
- Abstract
Additional file 1: A supplement with additional detail about the study design (Supplemental methods) and tables comparing obeserved and expected case number for malignant tumors (Table S1), power analysis for detection of differences in cancer incidence (Table S2), analysis of association between likelihood to suffer AEs and QOL (Table S3), analysis of association of probability of suffering AEs and continued study participation (Table S4), analysis of association of apheresis number and QOL (Table S5). The supplement contains supplemental references.
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- 2022
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7. MODERN OF MIGRATION GAS IN MARGINAL FLEXURES THE DOBRUDZHІ
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Vergelska, N.V., primary and Nakov, R., additional
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- 2021
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8. Comparison of EP2006, a filgrastim biosimilar, to the reference: a phase III, randomized, double-blind clinical study in the prevention of severe neutropenia in patients with breast cancer receiving myelosuppressive chemotherapy
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Blackwell, K., Semiglazov, V., Krasnozhon, D., Davidenko, I., Nelyubina, L., Nakov, R., Stiegler, G., Singh, P., Schwebig, A., Kramer, S., and Harbeck, N.
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- 2015
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9. The public's attitude towards doctors' use of Twitter and perceived professionalism: an exploratory study
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Kilic, Y, Chauhan, D, Avery, P, Horwood, N, Nakov, R, Disney, B, Segal, JP, Kilic, Y, Chauhan, D, Avery, P, Horwood, N, Nakov, R, Disney, B, and Segal, JP
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INTRODUCTION: Medical professionals use social media to interact with other healthcare professionals, discuss medical issues and promote healthcare information. These platforms have tremendous power to promote healthcare messages but also have potential to damage the profession if used inappropriately. It is currently unknown how others perceive medical doctors' Twitter activity and, therefore, we conducted an online survey exploring these views. METHODS: We used a Google Forms questionnaire consisting of 21 questions, which we distributed on Twitter, exploring doctors', patients', the public's and other healthcare professionals' views of doctors' Twitter activities. We investigated factors that were associated with mistrust by univariate and multivariate analysis. RESULTS: Seven-hundred and twenty-six respondents completed the survey. By univariate analysis, a higher proportion of non-doctors reported witnessing unprofessional behaviour and potential breaches of patient confidentiality compared with doctors (p<0.01). In addition, a significantly higher proportion of non-doctors felt that doctors' Twitter accounts should be monitored by both their employer and regulator when compared with doctors. By multivariate analysis, the main predictor of mistrust in the profession were those that had previously witnessed unprofessional behaviour (odds ratio 2.70; 95% confidence interval 2.08-3.33; p<0.01). CONCLUSION: There are discrepancies in how doctors and non-doctors view Twitter activity and significant mistrust in the profession was brought about by doctors' Twitter activity. To help limit this, adherence to current guidelines set out by the General Medical Council and British Medical Association is vital and doctors should be cautious about how their Twitter activity is professionally perceived by others before posting.
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- 2021
10. A standardised model for stool banking for faecal microbiota transplantation: a consensus report from a multidisciplinary UEG working group
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Keller, J. J., Ooijevaar, R. E., Hvas, C. L., Terveer, E. M., Lieberknecht, S. C., Hogenauer, C., Arkkila, P., Sokol, H., Gridnyev, O., Megraud, F., Kump, P. K., Nakov, R., Goldenberg, S. D., Satokari, R., Tkatch, S., Sanguinetti, Maurizio, Cammarota, Giovanni, Dorofeev, A., Gubska, O., Laniro, G., Mattila, E., Arasaradnam, R. P., Sarin, S. K., Sood, A., Putignani, Lorenza, Alric, L., Baunwall, S. M. D., Kupcinskas, J., Link, A., Goorhuis, A. G., Verspaget, H. W., Ponsioen, C., Hold, G. L., Tilg, H., Kassam, Z., Kuijper, E. J., Gasbarrini, Antonio, Mulder, C. J. J., Williams, H. R. T., Vehreschild, M. J. G. T., Sanguinetti M. (ORCID:0000-0002-9780-7059), Cammarota G. (ORCID:0000-0002-3626-6148), Putignani L., Gasbarrini A. (ORCID:0000-0002-7278-4823), Keller, J. J., Ooijevaar, R. E., Hvas, C. L., Terveer, E. M., Lieberknecht, S. C., Hogenauer, C., Arkkila, P., Sokol, H., Gridnyev, O., Megraud, F., Kump, P. K., Nakov, R., Goldenberg, S. D., Satokari, R., Tkatch, S., Sanguinetti, Maurizio, Cammarota, Giovanni, Dorofeev, A., Gubska, O., Laniro, G., Mattila, E., Arasaradnam, R. P., Sarin, S. K., Sood, A., Putignani, Lorenza, Alric, L., Baunwall, S. M. D., Kupcinskas, J., Link, A., Goorhuis, A. G., Verspaget, H. W., Ponsioen, C., Hold, G. L., Tilg, H., Kassam, Z., Kuijper, E. J., Gasbarrini, Antonio, Mulder, C. J. J., Williams, H. R. T., Vehreschild, M. J. G. T., Sanguinetti M. (ORCID:0000-0002-9780-7059), Cammarota G. (ORCID:0000-0002-3626-6148), Putignani L., and Gasbarrini A. (ORCID:0000-0002-7278-4823)
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Background: Faecal microbiota transplantation is an emerging therapeutic option, particularly for the treatment of recurrent Clostridioides difficile infection. Stool banks that organise recruitment and screening of faeces donors are being embedded within the regulatory frameworks described in the European Union Tissue and Cells Directive and the technical guide to the quality and safety of tissue and cells for human application, published by the European Council. Objective: Several European and international consensus statements concerning faecal microbiota transplantation have been issued. While these documents provide overall guidance, we aim to provide a detailed description of all processes that relate to the collection, handling and clinical application of human donor stool in this document. Methods: Collaborative subgroups of experts on stool banking drafted concepts for all domains pertaining to stool banking. During a working group meeting in the United European Gastroenterology Week 2019 in Barcelona, these concepts were discussed and finalised to be included in our overall guidance document about faecal microbiota transplantation. Results: A guidance document for all domains pertaining to stool banking was created. This document includes standard operating manuals for several processes involved with stool banking, such as handling of donor material, storage and donor screening. Conclusion: The implementation of faecal microbiota transplantation by stool banks in concordance with our guidance document will enable quality assurance and guarantee the availability of donor faeces preparations for patients.
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- 2021
11. New therapeutic molecules and their metabolism in gastroenterology-part ii
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Nakov, R., Maida, M., Ianiro, Gianluca, Ianiro G. (ORCID:0000-0002-8318-0515), Nakov, R., Maida, M., Ianiro, Gianluca, and Ianiro G. (ORCID:0000-0002-8318-0515)
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N/A
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- 2021
12. DOP37 Large differences in IBD care and education across Europe, first results of the pan-European VIPER survey
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Král, J, primary, Nakov, R, additional, Lanska, V, additional, Barberio, B, additional, Benech, N, additional, Blesl, A, additional, Brunet, E, additional, Capela, T L, additional, Derikx, L A A P, additional, Dragoni, G, additional, Eek, A, additional, Frias-Gomes, C, additional, Gîlcă-Blanariu, G E, additional, Gilroy, L, additional, Harvey, P R, additional, Kagramanova, A, additional, Kani, H T, additional, Konikoff, T, additional, Lessing, M, additional, Madsen, G R, additional, Maksimaityte, V, additional, Miasnikova, M, additional, Mikolasevic, I, additional, Milivojevic, V, additional, Noviello, D, additional, Oliinyk, D, additional, Patai, A, additional, Protopapas, A A, additional, Rodríguez-Lago, I, additional, Schreiber, P, additional, Skuja, V, additional, Tran, F, additional, Truyens, M, additional, Włodarczyk, M, additional, Zatorski, H, additional, Verstockt, B, additional, and Segal, J P, additional
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- 2021
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13. GEODYNAMIC FEATURES OF DOBROGEA FORMATION
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Vergelska, N.V., Nakov, R., Kukovska, T.S., and Parуshev, O.O.
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Dobrogea, Pre-Dobrogea depression ,geodynamics ,migration of hydrocarbons ,УДК 662.83:553.98(477.7) ,Добруджа ,Переддобрудзький прогин ,геодинаміка, міграція вуглеводнів - Abstract
The formation of Dobrogea as a modern geographical unit dates back to the late Neogene. The complex tectonic structure indicates multiphase changes in this key area that are buried under sediment or reflected in outcrops. Separate outcrops to Mesozoic sedimentary rocks and Precambrian-Paleozoic crystalline basement have been identified, while the main part of the region is characterized by Paleogene-Neogene outcrops. According to the peculiarities of the tectonic structure of Dobrogea, it is divided into the Southern, Central and Northern parts, which are separated by faults of the north-western extension and the Pre-Dobrogea depression. The main part of Dobrogea is located in Romania, within Ukraine there is the Prut ledge of the Northern Dobrogea and the Pre-Dobrogea depression, and part of the Southern Dobrogea goes within the borders of Bulgaria - the southern slope of the Dobrogea massif.The geodynamics of the joint zone determined the stages of formation, which were accompanied by platform transformations and tectonic-magmatic processes, as well as the formation of sedimentary complexes with coal, coal seams and oil and gas reservoirs. Based on the factor of destruction of Cretaceous and, possibly, Jurassic and Triassic deposits and their transformation into younger, Paleocene and Maikop deposits, it can be said that large accumulations of gas on structures in Paleogene traps are unlikely.Modern gas migration is characteristic of both the sedimentary strata of the Pre- Dobrogea Depression, ie the northern part of the study region, and the south-eastern part of Southern Dobrogea in carbonate deposits., Формування Добруджі як сучасної географічної одиниці датовано пізнім неогеном. Складна тектонічна будова вказує на багатофазні зміни цієї ключової області, які поховані під осадовим покривом і відображені у відслоненнях. Визначено окремі відслонення мезозойських осадових порід і докембрійсько-палеозойського кристалічного фундаменту, тоді як основна частина регіону характеризується палеоген-неогеновими відслоненнями. За особливостями тектонічної будови Добруджа поділяється на Південну (ПдД), Центральну (ЦД) і Північну (ПнД) частини, що розділяються розломами північно-західного простягання, та Переддобрудзький прогин. Основна частина Добруджі розміщена в Румунії, у межах України простягається Прутський виступ ПнД і Переддобрудзький прогин, а частина ПдД заходить у межі Болгарії – Південний схил масиву Добруджі.Геодинаміка зони зчленування визначала етапність формування, що супроводжувалося трансформаціями платформ і тектономагматичними процесами, а також формуванням осадових комплексів із вугільними, вуглистими пластами та нафтогазовими колекторами. Зважаючи на чинник руйнування крейдових і, можливо, юрських та тріасових покладів і переформування їх у молодших, палеоценових і майкопських відкладах, попередньо можна стверджувати, що великі скупчення газу в структурних пастках палеогену малоймовірні.Сучасна газова міграція характерна як для осадових товщ Переддобрудзького прогину, тобто північної частини регіону досліджень, так і південно-східної частини Південної Добруджі в карбонатних відкладах.
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- 2020
14. Young GI Societies in Europe: 2019 update
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Heinrich, H., Rodríguez-Lago, I., Nakov, R., Skuja, V., Acedo, P., Nitsche, U., Mikolasevic, I., Herwaarden, Y.J. van, Heinrich, H., Rodríguez-Lago, I., Nakov, R., Skuja, V., Acedo, P., Nitsche, U., Mikolasevic, I., and Herwaarden, Y.J. van
- Abstract
Contains fulltext : 220034.pdf (Publisher’s version ) (Open Access), BACKGROUND: One of the aims of the Young Talent Group (YTG) is to make United European Gastroenterology (UEG) more attractive to young fellows interested in gastroenterology (GI), and to actively involve them in UEG activities and the activities of their respective national societies. In 2017, we conducted a survey among the Friends of the UEG YTG with the aim of identifying the state of organization and needs of Young GI Sections (YGISs) throughout Europe, highlighting areas for further development and improvement. AIMS: The aim of the current web-based survey was to assess the progress of YGISs over 1 year, and persisting hurdles in forming and running a YGIS. RESULTS: Overall, 38 of 42 Friends answered the survey (91%). The number of YGISs has increased significantly from 12 in 2017 to 25 in 2019. Young gastroenterologists remained supported, but not influenced, by national societies. Results of the survey suggest that a lack of dedicated and motivated fellows has replaced a lack of funding as the most prevalent hurdle in forming these types of sections. CONCLUSION: Our survey shows that the development of YGISs has improved markedly within the last 2 years. However, several limitations, like underrepresentation in subcommittees of national societies, remain and need to be addressed in order to involve young gastroenterologists in their respective national societies and within UEG, to pave the way for future research, education and excellent quality of care, and reduce health inequalities across Europe.
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- 2020
15. How to start a Young GI Section in your country: A cookbook
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Skuja, V., Nakov, R., Herwaarden, Y.J. van, Rodríguez-Lago, I., Acedo, P., Mikolasevic, I., Nitsche, U., Heinrich, H., Dignass, A., Skuja, V., Nakov, R., Herwaarden, Y.J. van, Rodríguez-Lago, I., Acedo, P., Mikolasevic, I., Nitsche, U., Heinrich, H., and Dignass, A.
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Contains fulltext : 220090.pdf (Publisher’s version ) (Open Access)
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- 2020
16. Microbiome: What intensivists should know
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Nakov, R., Segal, J. P., Settanni, C. R. S., Bibb, S., Barrini, A. G., Cammarota, Giovanni, Ianiro, Gianluca, Cammarota G. (ORCID:0000-0002-3626-6148), Ianiro G. (ORCID:0000-0002-8318-0515), Nakov, R., Segal, J. P., Settanni, C. R. S., Bibb, S., Barrini, A. G., Cammarota, Giovanni, Ianiro, Gianluca, Cammarota G. (ORCID:0000-0002-3626-6148), and Ianiro G. (ORCID:0000-0002-8318-0515)
- Abstract
The standard conditions of critical illness (including sepsis, acute respiratory distress syndrome, and multiorgan failure) cause enormous global mortality and a growing economic burden. Increasing evidence suggests that critical illness may be associated with loss of commensal microbes and overgrowth of potentially pathogenic and inflammatory bacteria. This state could be associated with poor outcomes. Therefore, microbiota-targeted interventions are potentially attractive novel treatment options. Although the precise mechanisms of microbiome-directed treatments such as prebiotics, probiotics, and fecal microbiota transplantation remain to be determined, they can be utilized in the Intensive Care Unit (IC U) setting. The current review aims to offer intensivists an evidenced-based approach on what we currently know about the role of the microbiome in critical illness and how the microbiome could be targeted in the clinical practice to improve IC U-related outcomes.
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- 2020
17. P217 The role of 7-alfa-hydroxy-4-cholesten-3-one (C4) as a biomarker for bile acid malabsorption in inflammatory bowel disease and microscopic colitis
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Lyutakov, I, primary, Lozanov, V, additional, Sugareva, P, additional, Nakov, R, additional, Valkov, H, additional, Dimov, A, additional, Vladimirov, B, additional, and Penchev, P, additional
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- 2020
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18. Stool for fecal microbiota transplantation should be classified as a transplant product and not as a drug
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Keller, J.J., Vehreschild, M.J.G.T., Hvas, C.L., Jorgensen, S.M.D., Kupciskas, J., Link, A., Mulder, C.J.J., Goldenberg, S.D., Arasaradnam, R., Sokol, H., Gasbarrini, A., Hoegenauer, C., Terveer, E.M., Kuijper, E.J., Arkkila, P., Gridnyev, O., Megraud, F., Kump, P.K., Nakov, R., Satokari, R., Tkatch, S., Sanguinetti, M., Cammarota, G., Dorofeev, A., Gubska, O., Ianiro, G., Mattila, E., Ooijevaar, R.E., Sarin, S.K., Sood, A., Putignani, L., Alric, L., Williams, H.R.T., Goorhuis, A., Verspaget, H.W., Hold, G.L., Tilg, H., Ponsioen, C.Y., Standards Guidelines Initiative, Leiden University Medical Center (LUMC), Goethe-University Frankfurt am Main, University of Cologne, Aarhus University Hospital, Hospital of Lithuanian University of Health Sciences Kauno Klinikos [Kaunas, Lithuania], Otto-von-Guericke University [Magdeburg] (OVGU), Free University Medical Center [Amsterdam], Guy's and St Thomas NHS Trust Foundation & King's College London School of Medicine, Haemostasis Research Unit, Centre for Haemostasis and Trombosis, Warwick Medical School, University of Warwick [Coventry], MICrobiologie de l'ALImentation au Service de la Santé (MICALIS), Institut National de la Recherche Agronomique (INRA)-AgroParisTech, CEREST-TC [CHU Saint-Antoine], Université Pierre et Marie Curie - Paris 6 (UPMC)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-CHU Saint-Antoine [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Sorbonne Université (SU), French Group of Fecal Microbiota Transplantation [Paris] (GFTF), Fondazione 'Policlinico Universitario A. Gemelli' [Rome], Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, University of Helsinki, UEG Standards and Guidelines Activity grant (2018)., and Gastroenterology and hepatology
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Drug ,medicine.medical_specialty ,[SDV]Life Sciences [q-bio] ,media_common.quotation_subject ,MEDLINE ,Transplants ,Feces ,03 medical and health sciences ,0302 clinical medicine ,Internal medicine ,medicine ,Humans ,030212 general & internal medicine ,Product (category theory) ,Letters to the Editor ,Enterocolitis, Pseudomembranous ,media_common ,Enterocolitis ,business.industry ,Gastroenterology ,Fecal bacteriotherapy ,Fecal Microbiota Transplantation ,3. Good health ,Oncology ,030211 gastroenterology & hepatology ,medicine.symptom ,business - Abstract
International audience; Fecal microbiota transplantation (FMT) or donor feces infusion is a therapy that aims to restore a perturbed gut microbiota composition and function. FMT is effective for treatment of patients with (multiple) recurrent Clostridioides difficile infections1–3 and recommended by current guidelines.4–6 In the near future, FMT may also become an accepted treatment option for other intestinal or extra-intestinal diseases.7FMT is performed using suspensions made of donor stool from carefully selected and screened healthy individuals.1,7 Donor screening is time consuming and costly. Before the establishment of stool banks, physicians and patients had to find their own donors. This resulted in uncontrolled application of FMT, and the logistical challenge made physicians reluctant to offer FMT to their patients. To overcome these problems, stool banks have been established.8,9 The mission of those stool banks is :to produce ready-to-use donor feces suspensions for treatment of patients,to improve the quality and safety of FMT by centralization and standardization,to increase the cost effectiveness of FMT, andto facilitate research.Stool banks are built in concordance with the model of blood banks and should follow quality standards applied to other transplantation products. Most stool banks are non-profit institutions, operating at a local (institution-based), national or international level. Recently, a UEG-funded working group was initiated to define quality standards for stool banking and FMT, which will result in further standardization of this new treatment approach. The current costs to deliver a ready-to-use stool suspension are €1050–1700 in Europe.9,10 There are also commercial initiatives,11 which may aim for much higher prices.Driven by the needs of patients, stool banks have emerged as new entities in a landscape without existing regulatory boundaries. This lack of guidance and National or European legislation may become a serious threat to providing the treatment for severely ill patients. This is also illustrated by the recent safety alert in the US about the transmission of multi-drug resistant organisms through FMT,12 which underlines the need for standardization, quality assurance, and a regulatory framework supporting the activities of stool banks. Legislation requires classification of stool as a product to treat patients. We strongly believe that stool should be considered a transplant product, or be regarded equivalent in status to blood products used for transplantation or transfusion purposes. The EU Tissue and Cells Directive (2004/23/EC) is best suited to guide FMT. Currently, this Directive does not cover FMT because the mechanism of action is not mediated by human cells. An adjustment to align this directive with the new reality of fecal transplantation is thus urgently needed. Only in the case of modification to the donated feces, other than those necessary for the conservation of the microbial community, does the product made of the donated feces become comparable to a drug and is best covered within the European directive for medicinal products intended for human use (2001/83/EC).Unfortunately, the misclassification of donor feces suspensions as a drug or pharmaceutical product, although difficult to imagine, is still one of the possible outcomes of the current discussion about classification. Currently, stool has already been classified as a drug in countries such as France, Germany, and the United Kingdom. Recently, companies have formed the “Pharmabiotic Research Institute” in Europe and the “Microbiome Therapeutics Innovation Group (MTIG)” in the US. The mission of those groups is “to improve market access,” and to “enhance the regulatory, investment, and commercial environment for microbiome therapeutic drug product development.” Both groups have published statements about the classification of FMT as a drug.13,14 MTIG actively collaborates with the Food and Drug Administration for the evaluation of safety parameters related to microbiota-based therapeutic products. Concern has been raised by the MTIG that the existence and accessibility of material from stool banks limits enrollment into clinical trials for microbiome therapeutics. This illustrates how companies are active to influence the current discussion about classification and regulation of FMT. In fact, this discussion has already been troubled by commercial interest in the US some years ago.15In this regard, it is important to mention the overall major disadvantages of classification as a drug, which will result in time-consuming and costly registration processes, and a sharp and unjustified rise in costs. Most importantly, this will negatively impact availability and innovation, obstructing, for example, the future development of single-donor individualized solutions due to the requirements for standardization of active substances. We postulate that stool treatment defined as drug treatment is counterproductive. Stool is not a standardized product that is produced in a factory, but a highly diverse and donor-specific substance of human origin (SoHO) delivered by healthy, usually unpaid, volunteer donors. Therefore, stool suspensions require suitable guidance of quality and safety measures comparable to guidance of other SoHO (blood, tissues, cells and organs) within the EU.If government authorities seek affordable and quality-assured FMT, a supportive regulatory framework, in combination with appropriate funding or reimbursement, is required for stool banks. This will not only guarantee broad access and safety of FMT, but also enable the future innovation of this new treatment strategy targeting the gut microbiota. If eventually future research results in the replacement of FMT by standardized mixtures of bacteria (or another yet undiscovered stool extract that could theoretically underly the clinical effects of FMT), these should indeed be regulated as a drug or pharmaceutical product.
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- 2019
19. UEG Young Talent Group: What do we do?
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Acedo, P., Heinrich, H., Herwaarden, Y.J. van, Nakov, R., Nitsche, U., Rodriguez-Lago, I., Salaga, M., Skuja, V., Acedo, P., Heinrich, H., Herwaarden, Y.J. van, Nakov, R., Nitsche, U., Rodriguez-Lago, I., Salaga, M., and Skuja, V.
- Abstract
Contains fulltext : 215335.pdf (publisher's version ) (Closed access)
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- 2019
20. Randomized, double-blind, cross-over phase I study comparing pharmacokinetics, pharmacodynamics, safety and immunogenicity of a biosimilar pegfilgrastim with EU and US references
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Velinova, M., primary, Bellon, A., additional, Nakov, R., additional, Schussler, S., additional, Schier-Mumzhiu, S., additional, Schelcher, C., additional, Koch, S.D., additional, Skerjanec, A., additional, Wang, J., additional, Krendyukov, A., additional, and Otto, G.P., additional
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- 2019
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21. PF353 PATIENTS WITH SEVERE CHRONIC NEUTROPENIA SUBTYPES TREATED WITH BIOSIMILAR FILGRASTIM: A STUDY BY THE EUROPEAN BRANCH OF THE SEVERE CHRONIC NEUTROPENIA INTERNATIONAL REGISTRY
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Zeidler, C., primary, Mellor-Heineke, S., additional, Nakov, R., additional, Natek, M., additional, Mathieson, N., additional, and Gattu, S., additional
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- 2019
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22. DIAGNOSTIC ACCURACY OF ACETIC ACID OR CRYSTAL VIOLET ENHANCED NARROW BAND IMAGING (NBI) FOR DETECTING GASTRIC INTESTINAL METAPLASIA (MAPS) USING EGGIM AND SIMPLIFIED NBI CLASSIFICATION
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Lyutakov, I, additional, Nakov, R, additional, Valkov, H, additional, Dimov, A, additional, Penchev, P, additional, and Vladimirov, B, additional
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- 2019
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23. Abstract P4-16-14: Meta-analysis of Phase I pharmacokinetic/pharmacodynamic results of proposed biosimilar pegfilgrastim
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Nakov, R, primary, Wang, J, additional, Chen, Y, additional, Bellon, A, additional, Gattu, S, additional, Krendyukov, A, additional, and Li, Y, additional
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- 2019
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24. P268 Eosinophil-derived neurotoxin (eosinophil protein x) showed higher specificity and positive predictive value for detecting disease activity in inflammatory bowel disease compare to faecal calprotectin
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Lyutakov, I, primary, Nakov, R, additional, Nakov, V, additional, Vladimirov, B, additional, Asenova, B, additional, Chetirska, M, additional, Dimov, A, additional, Vatcheva-Dobrevska, R, additional, and Penchev, P, additional
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- 2019
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25. P149 Searching for bile acid malabsorption using serum fibroblast growth factor 19 (FGF19) and faecal bile acids in patients with inflammatory bowel diseases, microscopic colitis and irritable bowel syndrome
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Lyutakov, I, primary, Nakov, R, additional, Nakov, V, additional, Vladimirov, B, additional, Dimov, A, additional, Asenova, B, additional, Chetirska, M, additional, Vatcheva-Dobrevska, R, additional, and Penchev, P, additional
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- 2019
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26. Establishment of the first stool bank in an Eastern European country and the first series of successful fecal microbiota transplantations in Bulgaria.
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NAKOV, R., LYUTAKOV, I., MITKOVA, A., GEROVA, V., PETKOVA, V., GIRAGOSYAN, S., VATCHEVA-DOBREVSKA, R., KANEVA, R., and NAKOV, V.
- Abstract
OBJECTIVE: For safe implementation and broader application of fecal microbiota transplantation (FMT), quality controlled stool banking is a must. Establishing a stool bank is a complex, time-consuming, and expensive process, making it a real challenge in an Eastern European country. We aimed to establish the first stool bank in Eastern Europe - in Bulgaria. SUBJECTS AND METHODS: A multidisciplinary team of gastroenterologists, microbiologists, infectionists, and geneticists was set up. We used a questionnaire based on the First European FMT Consensus in order to recruit possible stool donors. Laboratory blood and stool tests were performed on all potential donors. RESULTS: Between October 2018 and April 2019, 112 donor volunteers completed a questionnaire; 70 (62.5%) were excluded, mainly because of age above 50, an unhealthy BMI, and risk behavior. Fourty-two (37.5%) donor candidates were invited for laboratory testing of blood and feces, of which 12 (28.6%) passed this screening. Of 12 donors, 4 (33%) failed at the following screening test, which is performed every 3-6 months. Finally, 8 (7.14%) active donors were enrolled. Ten successful FMTs were performed on patients with recurrent Clostridium difficile infection. CONCLUSIONS: Even though we found many healthy volunteers, only a low percentage (7.14%) of them were suitable to become feces donors. Establishing a stool bank in an Eastern European country is essential for making FMT safe and more popular as a treatment method, finding further implementation and regulation of FMT and supporting physicians offering this treatment to their patients. [ABSTRACT FROM AUTHOR]
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- 2021
27. Intestinal barrier dysfunction in liver cirrhosis assessed by iohexol test.
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GEROVA, V. A., SVINAROV, D. A., NAKOV, R. V., STOYNOV, S. G., TANKOVA, L. T., and NAKOV, V. N.
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OBJECTIVE: To study gut barrier function in patients with liver cirrhosis (LC) by evaluating the intestinal permeability (IP) and its relationship with the severity and etiology of the disease. PATIENTS AND METHODS: The study included 31 patients with LC and 25 healthy controls. Child-Pugh score was used for evaluation of the LC severity. IP was assessed by the rise in levels of iohexol, which was administered orally (25 mL, 350 mg/mL) 2 h after breakfast. Three and six hours later serum (SIC mg/L) and urine (UIC g/mol) iohexol concentrations were determined by a validated HPLC-UV technique. RESULTS: Patients with LC had significantly higher mean SIC value compared with control group at 3 h (2.05 ± 1.67 vs. 1.25 ± 1.41 mg/L, p=0.021, as well as at 6 h (2.20 ± 2.65 vs. 1.11 ± 1.06 mg/L, p=0.001) after ingestion. No significant difference was found in mean SIC value of patients at 3 and 6 h. 23% of the patients had an increased IP. The mean iohexol urine recovery of patients was similar to that of the controls both at 3 h and at 6 h. Mean SIC values were significantly higher in patients with advanced Child C class than in healthy controls or the subgroup with Child B class, both at 3 h (2.54 ± 1.95 mg/L vs. 1.11 ± 1.06 mg/L, p=0.007) or (2.57 ± 1.85 mg/L vs. 1.35±1.32 mg/L, p=0.005) and at 6 h (2.57 ± 1.85 mg/L vs. 1.25 ± 1.40 mg/L, p=0.002) or 2.54 ± 1.95 mg/L vs. 1.07 ± 0.35 mg/L, p=0.02). Cirrhotic patients with ascites had significantly higher SIC in comparison with the controls, both at 3 h (2.31 ± 1.74 vs. 1.25 ± 1.41 mg/, p=0.009) and at 6 h (2.20 ± 1.87 vs. 1.11 ± 1.06 mg/l, p=0.007). In the subgroup of patients with alcoholic LC, the mean SIC values at 3 and 6 h (2.29 ± 1.80, 2.33 ± 1.85 mg/L, respectively) were significantly higher (p= 0.016, p=0.003) compared to the control group (1.25 ± 1.41, 1.11 ± 1.06 mg/L, respectively). CONCLUSIONS: Increased IP is found in 23% of cirrhotic patients. Permeability alterations are significantly more pronounced in patients with advanced LC with the presence of ascites and in those with alcoholic etiology. [ABSTRACT FROM AUTHOR]
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- 2020
28. A large multi-center, randomized, double-blind, crossover study in healthy volunteers to compare pharmacokinetics and pharmacodynamics of a proposed biosimilar pegfilgrastim with EU and US reference pegfilgrastim: Methodological approach
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Nakov, R., primary, Schussler, S., additional, Schier-Mumzhiu, S., additional, Skerjanec, A., additional, Bellon, A., additional, Wang, J., additional, Krendyukov, A., additional, and Otto, G., additional
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- 2018
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29. Overall survival and risk of second malignancies with cancer chemotherapy and G-CSF support
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Lyman, G.H., primary, Yau, L., additional, Nakov, R., additional, and Krendyukov, A., additional
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- 2018
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30. Abstract P3-14-10: Proposed biosimilar pegfilgrastim LA-EP2006 shows similarity in pharmacokinetics and pharmacodynamics to reference pegfilgrastim in healthy subjects
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Nakov, R, primary, Gattu, S, additional, Wang, J, additional, Velinova, M, additional, and Skerjanec, A, additional
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- 2018
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31. Abstract P2-11-05: Safety, immunogenicity and efficacy of proposed biosimilar pegfilgrastim (LA-EP2006) compared with reference pegfilgrastim in breast cancer: Pooled analysis of two randomized, double-blind, phase III trials
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Blackwell, K, primary, Gascon, P, additional, Jones, CM, additional, Nixon, A, additional, Nakov, R, additional, Mo, M, additional, Krendyukov, A, additional, and Nadia, H, additional
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- 2017
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32. LBA2 Proposed biosimilar pegfilgrastim (LA-EP2006) compared with reference pegfilgrastim in Asian patients with breast cancer receiving myelotoxic chemotherapy: Pooled subgroup analysis of two randomized trials
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Harbeck, N., primary, Gascon, P., additional, Jones, C.M., additional, Nixon, A., additional, Krendyukov, A., additional, Nakov, R., additional, Mo, M., additional, and Blackwell, K.L., additional
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- 2016
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33. Endorectal power Doppler ultrasonography is a reliable method for evaluation of rectal cancer angiogenesis.
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TANKOVA, L., NAKOV, R., STOILOV, G., GEGOVA, A., NAKOV, V., GEROVA, V., TERZIEV, I., and KOVATCHKI, D.
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OBJECTIVE: We aimed to assess the preoperative rectal cancer angiogenesis with Endorectal Power Doppler Ultrasonography by using the Power Doppler Vascularity Index (PDVI) calculated by imaging analysis software, and to compare it with the microvessel density (MVD) in surgical specimens PATIENTS AND METHODS: This study included 110 patients (39 females; mean age 61.5 years) with rectal cancer. Immunohistochemical staining of surgical specimens with anti-CD-31 antibody was used for MVD evaluation. The PDVI of each tumor was calculated using Endorectal Power Doppler with computer-assisted quantification of colour pixels. RESULTS: Mean MVD - 163 ± 69 microvessels/ mm
2 (50-328) was used as a cutoff point, differentiating two groups of tumors with high (> 160 mm2) and low (≤ 160 mm²) angiogenic activity. Mean PDVI of 8.9 ± 6.0% (0-27.3) was used as a cutoff point, dividing two groups of tumors with high (> 8%) and low (≤ 8%) PDVI. The MVD and the PDVI showed a good positive correlation (r = 0.438, p = 0.002). Patients with low PDVI had 25 months longer overall survival (p < 0.05) than patients with high PDVI. Patients with low MVD had 36 months longer survival (p < 0.05). CONCLUSIONS: Endorectal Power Doppler Ultrasonography is a reliable and noninvasive method for assessment of the extent of rectal cancer angiogenesis. Tumor angiogenesis assessed by the PDVI correlated with histological MVD determination and could predict survival rates. Endorectal Power Doppler examination is a useful and reproducible method for in vivo preoperative quantitative assessment of tumor vascularization. [ABSTRACT FROM AUTHOR]- Published
- 2019
34. Serum trefoil factor 3 predicts disease activity in patients with ulcerative colitis.
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NAKOV, R., NAKOV, V., GEROVA, V., TANKOVA, L., VELIKOVA, T., and IANIRO, G.
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OBJECTIVE: In this study, we aimed to evaluate the role of serum trefoil factor 3 (TFF3) as a biomarker of disease activity in patients with inflammatory bowel disease (IBD) and to compare TFF3 values with those of fecal calprotectin (FC). PATIENTS AND METHODS: 128 patients with IBD were divided into four groups: 1) active ulcerative colitis (UC); 2) quiescent UC; 3) active Crohn's disease (CD); 4) quiescent CD. The serum levels of TFF3 and FC levels were assessed in all patients and 16 controls. RESULTS: Patients with active UC had higher TFF3 levels than those with quiescent UC (p<0.001), those with active (p<0.001) or quiescent CD (p<0.001) and controls (p <0.001). We found a correlation between TFF3 and FC values in patients with active (r = 0.478, p = 0.006) and quiescent UC (r=0.528, p=0.002). TFF3 levels correlated with endoscopic activity in UC (evaluated by UC Endoscopic Index of Severity - UCEIS) (r=0.662, p<0.001). CONCLUSIONS: Serum TFF3 is able to identify patients with active UC. It could be used as a marker to predict disease activity in patients with UC. [ABSTRACT FROM AUTHOR]
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- 2019
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35. 1815P - Randomized, double-blind, cross-over phase I study comparing pharmacokinetics, pharmacodynamics, safety and immunogenicity of a biosimilar pegfilgrastim with EU and US references
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Velinova, M., Bellon, A., Nakov, R., Schussler, S., Schier-Mumzhiu, S., Schelcher, C., Koch, S.D., Skerjanec, A., Wang, J., Krendyukov, A., and Otto, G.P.
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- 2019
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36. Abstract P1-10-01: A randomized, double-blind trial to compare the efficacy and safety of proposed biosimilar pegfilgrastim (LA-EP2006) with reference pegfilgrastim in patients with breast cancer (PROTECT1)
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Harbeck, N, primary, Zbarskaya, I, additional, Lipatov, O, additional, Frolova, M, additional, Udovitsa, D, additional, Topuzov, E, additional, Ganea-Motan, DE, additional, Nakov, R, additional, Singh, P, additional, Rudy, A, additional, and Blackwell, K, additional
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- 2016
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37. 1796P - A large multi-center, randomized, double-blind, crossover study in healthy volunteers to compare pharmacokinetics and pharmacodynamics of a proposed biosimilar pegfilgrastim with EU and US reference pegfilgrastim: Methodological approach
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Nakov, R., Schussler, S., Schier-Mumzhiu, S., Skerjanec, A., Bellon, A., Wang, J., Krendyukov, A., and Otto, G.
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- 2018
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38. Role of Fecal Calprotectin as a Noninvasive Indicator for Ulcerative Colitis Disease Activity
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Nakov Radislav V., Nakov Ventsislav N., Gerova Vanya A., and Tankova Lyudmila T.
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UCEIS ,Mayo score ,fecal calprotectin ,ulcerative colitis ,Medicine - Abstract
Background: It is essential in clinical management to determine the disease activity in ulcerative colitis (UC) patients. At present, the most accurate way of evaluating the UC severity is endoscopy with biopsy. Fecal calprotectin (FCP) is a non-invasive biomarker that is frequently used for monitoring of intestinal inflammation.
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- 2019
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39. Acid suppression therapy, gastrointestinal bleeding and infection in acute pancreatitis - An international cohort study
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Péter Jenő Hegyi, Áron Vincze, Alexandra Demcsák, László Gajdán, Andrey Litvin, Andra Iulia Suceveanu, Eva Pijoan Comas, Riccardo Casadei, George I Papachristou, Vincenzo Cennamo, Yu-Ting Chang, Péter Hegyi, Ionut Negoi, Carlo Ingaldi, Vitor Nunes, Adriano Quiroga Castiñeira, Lihui Deng, Orestis Ioannidis, Ernő Bóna, Milene Raquel Ramos Moreira e Sá, Juan Armando Rodriguez-Oballe, Andrea Jardi Cuadrado, József Hamvas, Judit Bajor, Alexander Schneider, Tiago Cúrdia Gonçalves, Haluk Tarik Kani, Alexandra Soós, Serge Chooklin, Marcus Hollenbach, Claudio Ricci, Marta Freitas, Isabel Miguel Salas, Michael Hirth, Cristina Tocia, Dóra Illés, Daniel de la Iglesia Garcia, Amir Gougol, Patrícia Sarlós, Marco Marino, Emőke Miklós, Qing Xia, Valentina Negoita, Mihailo Bezmarevic, Radislav Nakov, Erika Darvasi, Deniz Güney Duman, Péter Kanizsai, Laura Mastrangelo, Vasile Sandru, Andrea Párniczky, Hubert Zatorski, Andrea Szentesi, Mária Papp, Mario Pelaez-Luna, Marcel Tantau, Yliya Rabotyagova, Ferenc Izbéki, Natalia V Shirinskaya, Cristian Gheorghe, Ewa Małecka-Panas, Giedrius Barauskas, Engin Altintaş, Wei Huang, Ali Kchaou, Povilas Ignatavicius, Cezar Ciubotaru, Stefania Bunduc, Jorge Paulino Pereira, Dong Wu, Sabite Kacar, Alina Tantau, António Pedro Gomes, Svetlana Turcan, Bálint Erőss, Sorin T. Barbu, Adriana Gherbon, Georgi Minkov, Júlio Constantino, Márk Félix Juhász, Jimin Han, Serhii Chuklin, Klementina Ocskay, Mila Kovacheva-Slavova, Eugen Tcaciuc, Elio Jovine, Lilla Barbara Kincses, Ines Capunge, Gabriel Constantinescu, Bogdan Mateescu, Eugen Dumitru, Ming-Chu Chang, Andrea Soriano Rios, Márta Varga, László Czakó, Volkan Gökbulut, Alexandra Mikó, Szilárd Váncsa, Ahmed Tlili, Demcsak, Alexandra, Soos, Alexandra, Kincses, Lilla, Capunge, Ines, Minkov, Georgi, Kovacheva-Slavova, Mila, Nakov, Radislav, Wu, Dong, Huang, Wei, Xia, Qing, Deng, Lihui, Hollenbach, Marcus, Schneider, Alexander, Hirth, Michael, Ioannidis, Orestis, Vincze, Aron, Bajor, Judit, Sarlos, Patricia, Czako, Laszlo, Illes, Dora, Izbeki, Ferenc, Gajdan, Laszlo, Papp, Maria, Hamvas, Jozsef, Varga, Marta, Kanizsai, Peter, Bona, Erno, Miko, Alexandra, Vancsa, Szilard, Juhasz, Mark Felix, Ocskay, Klementina, Darvasi, Erika, Miklos, Emoke, Eross, Balint, Szentesi, Andrea, Parniczky, Andrea, Casadei, Riccardo, Ricci, Claudio, Ingaldi, Carlo, Mastrangelo, Laura, Jovine, Elio, Cennamo, Vincenzo, Marino, Marco V., Barauskas, Giedrius, Ignatavicius, Povilas, Pelaez-Luna, Mario, Rios, Andrea Soriano, Turcan, Svetlana, Tcaciuc, Eugen, Malecka-Panas, Ewa, Zatorski, Hubert, Nunes, Vitor, Gomes, Antonio, Goncalves, Tiago Curdia, Freitas, Marta, Constantino, Julio, Sa, Milene, Pereira, Jorge, Mateescu, Bogdan, Constantinescu, Gabriel, Sandru, Vasile, Negoi, Ionut, Ciubotaru, Cezar, Negoita, Valentina, Bunduc, Stefania, Gheorghe, Cristian, Barbu, Sorin, Tantau, Alina, Tantau, Marcel, Dumitru, Eugen, Suceveanu, Andra Iulia, Tocia, Cristina, Gherbon, Adriana, Litvin, Andrey, Shirinskaya, Natalia, Rabotyagova, Yliya, Bezmarevic, Mihailo, Hegyi, Peter Jeno, Han, Jimin, Rodriguez-Oballe, Juan Armando, Salas, Isabel Miguel, Comas, Eva Pijoan, de la Iglesia Garcia, Daniel, Cuadrado, Andrea Jardi, Castineira, Adriano Quiroga, Chang, Yu-Ting, Chang, Ming-Chu, Kchaou, Ali, Tlili, Ahmed, Kacar, Sabite, Gokbulut, Volkan, Duman, Deniz, Kani, Haluk Tarik, Altintas, Engin, Chooklin, Serge, Chuklin, Serhii, Gougol, Amir, Papachristou, George, Hegyi, Peter, Demcsak A., Soos A., Kincses L., Capunge I., Minkov G., Kovacheva-Slavova M., Nakov R., Wu D., Huang W., Xia Q., Deng L., Hollenbach M., Schneider A., Hirth M., Ioannidis O., Vincze A., Bajor J., Sarlos P., Czako L., Illes D., Izbeki F., Gajdan L., Papp M., Hamvas J., Varga M., Kanizsai P., Bona E., Miko A., Vancsa S., Juhasz M.F., Ocskay K., Darvasi E., Miklos E., Eross B., Szentesi A., Parniczky A., Casadei R., Ricci C., Ingaldi C., Mastrangelo L., Jovine E., Cennamo V., Marino M.V., Barauskas G., Ignatavicius P., Pelaez-Luna M., Rios A.S., Turcan S., Tcaciuc E., Malecka-Panas E., Zatorski H., Nunes V., Gomes A., Goncalves T.C., Freitas M., Constantino J., Sa M., Pereira J., Mateescu B., Constantinescu G., Sandru V., Negoi I., Ciubotaru C., Negoita V., Bunduc S., Gheorghe C., Barbu S., Tantau A., Tantau M., Dumitru E., Suceveanu A.I., Tocia C., Gherbon A., Litvin A., Shirinskaya N., Rabotyagova Y., Bezmarevic M., Hegyi P.J., Han J., Rodriguez-Oballe J.A., Salas I.M., Comas E.P., Garcia D.D.L.I., Cuadrado A.J., Castineira A.Q., Chang Y.-T., Chang M.-C., Kchaou A., Tlili A., Kacar S., Gokbulut V., Duman D., Kani H.T., Altintas E., Chooklin S., Chuklin S., Gougol A., Papachristou G., and Hegyi P.
- Subjects
Male ,Endocrinology, Diabetes and Metabolism ,Gastroenterology ,Cohort Studies ,Feces ,0302 clinical medicine ,Risk Factors ,Surveys and Questionnaires ,Acid suppressing drug ,Acute pancreatitis ,Gastrointestinal bleeding ,Gastrointestinal infection ,Proton pump inhibitor ,Enterocolitis, Pseudomembranous ,Aged, 80 and over ,RISK ,ASSOCIATION ,Middle Aged ,Clostridium difficile ,CANCER ,3. Good health ,Hospitalization ,Treatment Outcome ,030220 oncology & carcinogenesis ,Acute Disease ,Female ,030211 gastroenterology & hepatology ,Gastrointestinal Hemorrhage ,Cohort study ,Adult ,medicine.medical_specialty ,GI bleeding ,medicine.drug_class ,Proton-pump inhibitor ,Infections ,PROTON-PUMP INHIBITORS ,03 medical and health sciences ,Internal medicine ,mental disorders ,medicine ,MANAGEMENT ,Humans ,DRUGS ,Acute pancreatiti ,Aged ,Retrospective Studies ,Hepatology ,Clostridioides difficile ,business.industry ,Proton Pump Inhibitors ,medicine.disease ,Pancreatitis ,Acid suppression ,business - Abstract
Background: Acid suppressing drugs (ASD) are generally used in acute pancreatitis (AP); however, large cohorts are not available to understand their efficiency and safety. Therefore, our aims were to evaluate the association between the administration of ASDs, the outcome of AP, the frequency of gastrointestinal (GI) bleeding and GI infection in patients with AP. Methods: We initiated an international survey and performed retrospective data analysis on AP patients hospitalized between January 2013 and December 2018. Results: Data of 17,422 adult patients with AP were collected from 59 centers of 23 countries. We found that 23.3% of patients received ASDs before and 86.6% during the course of AP. ASDs were prescribed to 57.6% of patients at discharge. ASD administration was associated with more severe AP and higher mortality. GI bleeding was reported in 4.7% of patients, and it was associated with pancreatitis severity, mortality and ASD therapy. Stool culture test was performed in 6.3% of the patients with 28.4% positive results. Clostridium difficile was the cause of GI infection in 60.5% of cases. Among the patients with GI infections, 28.9% received ASDs, whereas 24.1% were without any acid suppression treatment. GI infection was associated with more severe pancreatitis and higher mortality. Conclusions: Although ASD therapy is widely used, it is unlikely to have beneficial effects either on the outcome of AP or on the prevention of GI bleeding during AP. Therefore, ASD therapy should be substantially decreased in the therapeutic management of AP. (C) 2020 IAP and EPC. Published by Elsevier B.V.
- Published
- 2020
40. Significant Differences in IBD Care and Education across Europe: Results of the Pan-European VIPER Survey.
- Author
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Kral J, Nakov R, Lanska V, Barberio B, Benech N, Blesl A, Brunet E, Capela T, Derikx L, Dragoni G, Eek A, Frias-Gomes C, Gîlcă-Blanariu GE, Gilroy L, Harvey P, Kagramanova A, Kani HT, Konikoff T, Lessing M, Madsen G, Maksimaityte V, Miasnikova M, Mikolasevic I, Milivojevic V, Noviello D, Oliinyk D, Patai A, Pisani A, Protopapas A, Rodríguez-Lago I, Schreiner P, Skuja V, Tran F, Truyens M, Włodarczyk M, Zatorski H, Verstockt B, and Segal JP
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- Humans, Europe epidemiology, Surveys and Questionnaires, COVID-19, Inflammatory Bowel Diseases epidemiology, Inflammatory Bowel Diseases therapy, Biological Products
- Abstract
Background: Inflammatory bowel disease (IBD) care and education might differ around Europe. Therefore, we conducted this European Variation In IBD PracticE suRvey (VIPER) to investigate potential differences between countries., Methods: This trainee-initiated survey, run through SurveyMonkey®, consisted of 47 questions inquiring basic demographics, IBD training, and clinical care. Results were compared according to gross domestic product (GDP) per capita, for which countries were divided into 2 groups (low/high income, according to the World Bank)., Results: The online survey was completed by 1,285 participants from 40 European countries, with a majority of specialists (65.3%) working in academic institutions (50.4%). Significant differences in IBD-specific training (55.9% vs. 38.4%), as well as availability of IBD units (58.4% vs. 39.7%) and multidisciplinary meetings (73.2% vs. 40.1%), were observed between respondees from high and low GDP countries (p < 0.0001). In high GDP countries, IBD nurses are more common (85.9% vs. 36.0%), also mirrored by more nurse-led IBD clinics (40.6% vs. 13.7%; p < 0.0001). IBD dieticians (33.4% vs. 16.5%) and psychologists (16.8% vs. 7.5%) are mainly present in high GDP countries (p < 0.0001). In the current COVID era, telemedicine is available in 73.2% versus 54.1% of the high/low GDP countries, respectively (p < 0.0001). Treat-to-target approaches are implemented everywhere (85.0%), though access to biologicals and small molecules differs significantly., Conclusion: Much variability in IBD practice exists across Europe, with marked differences between high and low GDP countries. Further work is required to help address some of these inequalities, aiming to improve and standardize IBD care and training across Europe., (© 2022 S. Karger AG, Basel.)
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- 2023
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41. Prevalence and Risk Factors of Gastroesophageal Reflux Disease in Bulgaria: An Internet-Based Survey.
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Nakov R, Velikova T, Dimitrova-Yurukova D, Snegarova V, Nakov N, and Nakov V
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- Adult, Female, Humans, Male, Bulgaria, Prevalence, Risk Factors, Surveys and Questionnaires, Irritable Bowel Syndrome epidemiology, Gastroesophageal Reflux diagnosis, Dyspepsia diagnosis
- Abstract
Background: The global pooled prevalence of gastroesophageal reflux disease (GORD) is approximately 14% and varies significantly according to the country. More population-based studies are needed in regions lacking epidemiological data on the prevalence of GORD, such as Eastern Europe, particularly Bulgaria. This current study aimed to evaluate the prevalence of GORD in Bulgaria and assess the risk factors associated with this disorder., Methods: An internet-based health survey was sent to Bulgarian adults. Individuals were invited to complete an online questionnaire on general and gastrointestinal health. The aim of the study was not explicitly stated. The survey collected data on sociodemographic and behavioral characteristics, validated questions to assess GORD, diagnostic questions based on Rome IV criteria to assess irritable bowel syndrome (IBS) and functional dyspepsia (FD), and questions about antisecretory drugs usage., Results: Data were collected from 1,896 individuals (mean age = 35.5 years, SD = 11.7, 73.1% females). The prevalence of GORD in the study population was 27.5%, while 57.29% of all GORD patients taking PPIs had PPI-refractory GORD. Age (p = 0.02), body mass index (BMI) (p < 0.001), marital status (p = 0.03), occupation (p < 0.001), sexual problems (p < 0.001), FD (p < 0.001), and IBS (p < 0.001) were significantly associated with GORD prevalence. Patients with FD (p < 0.001; OR 5.38), IBS (p = 0.03; OR 1.07), and with higher BMI (p < 0.001, OR 1.05) were at an increased risk of having GORD., Conclusions: The first data on GORD prevalence in the adult population in Bulgaria have been reported. Disorders of gut-brain interaction have a significant impact on the prevalence of GORD., (© 2022 S. Karger AG, Basel.)
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- 2023
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42. Diagnosis and management of irritable bowel syndrome-like symptoms in ulcerative colitis.
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Dimitrova-Yurukova D, Boyanov N, Nakov V, and Nakov R
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- Humans, Irritable Bowel Syndrome, Colitis, Ulcerative
- Abstract
Both ulcerative colitis (UC) and irritable bowel syndrome (IBS) are chronic gastrointestinal (GI) conditions that show some typical features. Persistent GI symptoms typical for IBS are observed in patients with diagnosed UC. Both IBS and UC are characterised by dysregulation of the enteric nervous system, alterations in the gut flora, low-grade mucosal inflammation, and activation of the brain-gut axis. Therefore, it appears that there may be some overlap between the two conditions. It is rather difficult to tell if the lower gastrointestinal symptoms are secondary to coexisting IBS or a hidden UC condition., (This is an open access article distributed under the terms of the Creative Commons Attribution License (CC BY 4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
- Published
- 2022
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43. Coordinated Multi-Language Translation of A Validated Symptom Questionnaire for Carbohydrate Intolerances: A Practical Structured Procedure.
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Sonyi M, Hammer J, Basilisco G, Belei O, Benninga MA, Bordin DS, Dumitrascu D, Hauser B, Herszenyi L, Lopetuso L, Mion F, Mulak A, Nakov R, Nakov V, Tepes B, and Hammer HF
- Subjects
- Adult, Carbohydrate Metabolism, Inborn Errors, Child, Humans, Malabsorption Syndromes, Poland, Surveys and Questionnaires, Language, Translating
- Abstract
Background and Aims: Validated questionnaires help to minimize diagnostic bias, to standardize symptom assessment and to achieve comparability between studies and centers. In a recent European guideline the adult and the pediatric carbohydrate perception questionnaires (aCPQ and pCPQ), were recommended to be used for the diagnosis of carbohydrate intolerances in adult and pediatric patients. The implementation of this guideline into clinical practice makes availability of validated translations a necessity., Methods: Clinical experts who recognized the need for these questionnaires to be available in their own language participated in the translation process. The tasks were assigned and a workflow following a predefined procedure based on recommendations of the Rome foundation was developed. The procedure had 5 phases: foundation, nomination, translation, revision, cognitive debriefing., Results: Within eight months the aCPQ was translated into Bulgarian, French, Hungarian, Italian, Polish, Romanian, Russian and Slovenian language and the pCPQ into Dutch, French and Romanian. This expands the population which can be served with the aCPQ from 160 million to over 500 million Europeans. The reach of pCPQ expanded from 92 million to 193 million Europeans., Conclusions: We report the development and implementation of a centrally organized process of translation of validated questionnaires, following a predefined procedure based on recommendations of the Rome foundation. This structured procedure may aid future efforts to standardize and harmonize the translation of validated questionnaires.
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- 2022
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44. Functional bowel disorders with diarrhoea: Clinical guidelines of the United European Gastroenterology and European Society for Neurogastroenterology and Motility.
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Savarino E, Zingone F, Barberio B, Marasco G, Akyuz F, Akpinar H, Barboi O, Bodini G, Bor S, Chiarioni G, Cristian G, Corsetti M, Di Sabatino A, Dimitriu AM, Drug V, Dumitrascu DL, Ford AC, Hauser G, Nakov R, Patel N, Pohl D, Sfarti C, Serra J, Simrén M, Suciu A, Tack J, Toruner M, Walters J, Cremon C, and Barbara G
- Subjects
- Bile Acids and Salts therapeutic use, Diarrhea diagnosis, Diarrhea etiology, Diarrhea therapy, Gastrointestinal Agents therapeutic use, Humans, Gastroenterology, Irritable Bowel Syndrome diagnosis, Irritable Bowel Syndrome epidemiology, Irritable Bowel Syndrome therapy
- Abstract
Irritable bowel syndrome with diarrhoea (IBS-D) and functional diarrhoea (FDr) are the two major functional bowel disorders characterized by diarrhoea. In spite of their high prevalence, IBS-D and FDr are associated with major uncertainties, especially regarding their optimal diagnostic work-up and management. A Delphi consensus was performed with experts from 10 European countries who conducted a literature summary and voting process on 31 statements. Quality of evidence was evaluated using the grading of recommendations, assessment, development, and evaluation criteria. Consensus (defined as >80% agreement) was reached for all the statements. The panel agreed with the potential overlapping of IBS-D and FDr. In terms of diagnosis, the consensus supports a symptom-based approach also with the exclusion of alarm symptoms, recommending the evaluation of full blood count, C-reactive protein, serology for coeliac disease, and faecal calprotectin, and consideration of diagnosing bile acid diarrhoea. Colonoscopy with random biopsies in both the right and left colon is recommended in patients older than 50 years and in presence of alarm features. Regarding treatment, a strong consensus was achieved for the use of a diet low fermentable oligo-, di-, monosaccharides and polyols, gut-directed psychological therapies, rifaximin, loperamide, and eluxadoline. A weak or conditional recommendation was achieved for antispasmodics, probiotics, tryciclic antidepressants, bile acid sequestrants, 5-hydroxytryptamine-3 antagonists (i.e. alosetron, ondansetron, or ramosetron). A multinational group of European experts summarized the current state of consensus on the definition, diagnosis, and management of IBS-D and FDr., (© 2022 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC on behalf of United European Gastroenterology.)
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- 2022
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45. European guideline on indications, performance, and clinical impact of hydrogen and methane breath tests in adult and pediatric patients: European Association for Gastroenterology, Endoscopy and Nutrition, European Society of Neurogastroenterology and Motility, and European Society for Paediatric Gastroenterology Hepatology and Nutrition consensus.
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Hammer HF, Fox MR, Keller J, Salvatore S, Basilisco G, Hammer J, Lopetuso L, Benninga M, Borrelli O, Dumitrascu D, Hauser B, Herszenyi L, Nakov R, Pohl D, Thapar N, and Sonyi M
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- Adult, Breath Tests standards, Carbohydrate Metabolism, Child, Dietary Carbohydrates administration & dosage, Dietary Carbohydrates metabolism, Endoscopy, Digestive System, Europe, Gastroenterology, Gastrointestinal Microbiome, Gastrointestinal Transit, Humans, Intestine, Small microbiology, Nutritional Sciences, Societies, Medical, Symptom Assessment methods, Symptom Assessment standards, Breath Tests methods, Consensus, Dysbiosis diagnosis, Hydrogen analysis, Malabsorption Syndromes diagnosis, Methane analysis
- Abstract
Introduction: Measurement of breath hydrogen (H
2 ) and methane (CH4 ) excretion after ingestion of test-carbohydrates is used for different diagnostic purposes. There is a lack of standardization among centers performing these tests and this, together with recent technical developments and evidence from clinical studies, highlight the need for a European guideline., Methods: This consensus-based clinical practice guideline defines the clinical indications, performance, and interpretation of H2 -CH4 -breath tests in adult and pediatric patients. A balance between scientific evidence and clinical experience was achieved by a Delphi consensus that involved 44 experts from 18 European countries. Eighty eight statements and recommendations were drafted based on a review of the literature. Consensus (≥80% agreement) was reached for 82. Quality of evidence was evaluated using validated criteria., Results: The guideline incorporates new insights into the role of symptom assessment to diagnose carbohydrate (e.g., lactose) intolerances and recommends that breath tests for carbohydrate malabsorption require additional validated concurrent symptom evaluation to establish carbohydrate intolerance. Regarding the use of breath tests for the evaluation of oro-cecal transit time and suspected small bowel bacterial overgrowth, this guideline highlights confounding factors associated with the interpretation of H2 -CH4 -breath tests in these indications and recommends approaches to mitigate these issues., Conclusion: This clinical practice guideline should facilitate pan-European harmonization of diagnostic approaches to symptoms and disorders, which are very common in specialist and primary care gastroenterology practice, both in adult and pediatric patients. In addition, it identifies areas of future research needs to clarify diagnostic and therapeutic approaches., (© 2021 The Authors. United European Gastroenterology Journal published by Wiley Periodicals LLC. on behalf of United European Gastroenterology.)- Published
- 2022
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46. Increased prevalence of gastrointestinal symptoms and disorders of gut-brain interaction during the COVID-19 pandemic: An internet-based survey.
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Nakov R, Dimitrova-Yurukova D, Snegarova V, Nakov V, Fox M, and Heinrich H
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- Adult, Anxiety psychology, Bulgaria epidemiology, Female, Humans, Internet, Male, Middle Aged, Prevalence, SARS-CoV-2, Stress, Psychological complications, Stress, Psychological psychology, Surveys and Questionnaires, Brain-Gut Axis, COVID-19 psychology, Gastrointestinal Diseases epidemiology, Gastrointestinal Diseases psychology, Quarantine psychology
- Abstract
Background: Quarantine with social distancing has reduced transmission of COVID-19; however, fear of the disease and these remedial measures cause anxiety and stress. It is not known whether these events have impacted the prevalence of gastrointestinal (GI) symptoms and disorders of brain-gut interaction (DGBI)., Methods: An online platform evaluated the prevalence of GI symptoms during the COVID-19 pandemic. Data collection utilized validated questionnaires and was fully anonymized. Findings were compared with identical data acquired in 2019. The association of results with stress and anxiety was analyzed., Results: Data were collected from 1896 subjects May - August 2019 to 980 non-identical subjects May - June 2020. GI symptoms were reported by 68.9% during the COVID-19 lockdown compared with 56.0% the previous year (p < 0.001). The prevalence of irritable bowel syndrome (26.3% vs. 20.0%; p < 0.001), functional dyspepsia (18.3% vs. 12.7%; p < 0.001), heartburn (31.7% vs. 26.2%, p = 0.002), and self-reported milk intolerance (43.5% vs. 37.8% p = 0.004) was higher during the pandemic. Many individuals reported multiple symptoms. Anxiety was associated with presence of all GI symptoms. High levels of stress impacted functional dyspepsia (p = 0.045) and abdominal pain (p = 0.013). The presence of DGBI (p < 0.001; OR 22.99), self-reported milk intolerance (p < 0.001; OR 2.50), and anxiety (p < 0.001; OR 2.18) was independently associated with increased GI symptoms during COVID-19 pandemic., Conclusions: The prevalence of GI symptoms was significantly higher during the COVID-19 lockdown than under normal circumstances the previous year. This increase was attributable to increased numbers of patients with DGBI, an effect that was associated with anxiety., (© 2021 John Wiley & Sons Ltd.)
- Published
- 2022
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47. Biomarkers in Irritable Bowel Syndrome: Biological Rationale and Diagnostic Value.
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Nakov R, Snegarova V, Dimitrova-Yurukova D, and Velikova T
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- Biomarkers, Diagnosis, Differential, Feces, Humans, Irritable Bowel Syndrome diagnosis, MicroRNAs
- Abstract
Background: Patients with irritable bowel syndrome (IBS) usually suffer from nonspecific and overlapping signs that hamper the diagnostic process. In line with this, biomarkers specific for IBS could be of great benefit for diagnosing and managing patients. In IBS, the need is for apparent distinguishing features linked to the disease that improve diagnosis, differentiate from other organic diseases, and discriminate between IBS subtypes., Summary: Some biomarkers are associated with a possible pathophysiologic mechanism of IBS; others are used for differentiating IBS from non-IBS patients. Implementation of IBS biomarkers in everyday clinical practice is critical for early diagnosis and treatment. However, our knowledge about their efficient use is still scarce. Key Messages: This review discusses the biomarkers implemented for IBS diagnosis and management, such as blood (serum), fecal, immunological, related to the microbiome, microRNAs, and some promising novel biomarkers associated with imaging and psychological features of the disease. We focus on the most commonly studied and validated biomarkers and their biological rationale, diagnostic, and clinical value., (© 2021 S. Karger AG, Basel.)
- Published
- 2022
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48. New mint on the block - Fresh hope for IBS treatment?
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Nakov R and Heinrich H
- Subjects
- Constipation drug therapy, Gastrointestinal Agents therapeutic use, Humans, Irritable Bowel Syndrome drug therapy, Mentha
- Published
- 2021
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49. Meta-analysis of Pharmacokinetic/Pharmacodynamic Results of 3 Phase 1 Studies with Biosimilar Pegfilgrastim.
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Gattu S, Wang J, Bellon A, Schelcher C, Nakov R, and Arani R
- Subjects
- Adolescent, Adult, Cross-Over Studies, Double-Blind Method, Female, Humans, Male, Middle Aged, Young Adult, Biosimilar Pharmaceuticals pharmacokinetics, Clinical Trials, Phase I as Topic methods, Filgrastim pharmacokinetics, Polyethylene Glycols pharmacokinetics, Randomized Controlled Trials as Topic methods
- Abstract
A meta-analysis using data from 3 phase 1 studies evaluated the pharmacokinetics (PK) and pharmacodynamics (PD) of Sandoz biosimilar versus US- and EU-reference pegfilgrastim. The studies included a single-dose, double-blind, 3-arm, parallel-group study (study 1); a single-dose, double-blind, 2-way crossover study (study 2); and a single-dose, double-blind, 3-way, 6-sequence crossover study (study 3). Healthy male and female subjects were randomized to receive the proposed biosimilar (all studies), US-reference biologic (studies 1 and 3), or EU-reference biologic (studies 1, 2, and 3). For PK parameters (area under the serum concentration-time curve from time of dosing and extrapolated to infinity, area under the serum concentration-time curve from the time of dosing to the last measurable concentration, and maximum observed serum concentration) and PD parameters (absolute neutrophil count area under the effect curve from the time of dosing to the last measurable concentration and maximum measured absolute neutrophil count) geometric mean ratios and 90% confidence intervals (CIs) for treatment comparisons were calculated using the meta-analysis approach with a fixed-effects model. PK/PD biosimilarity was concluded if the 90%CIs were within the equivalence margins of 0.80 to 1.25. The 90%CIs for the geometric mean ratios for the PK/PD parameters were all within the equivalence margins. Safety and tolerability were similar between the proposed biosimilar and the US- and EU-reference pegfilgrastim in healthy subjects. This meta-analysis of 3 phase 1 studies supports PK/PD similarity of Sandoz biosimilar pegfilgrastim to US- and EU-reference pegfilgrastim. No clinically meaningful differences in safety or tolerability were observed., (© 2021 Sandoz Biopharmaceuticals. Clinical Pharmacology in Drug Development published by Wiley Periodicals LLC on behalf of American College of Clinical Pharmacology.)
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- 2021
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50. How to identify, encourage, and support suitable candidates for leading roles in scientific societies: The UEG experience.
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Nakov R, Alboraie M, and Tiniakos D
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- Advisory Committees, Committee Membership, Cultural Diversity, Europe, Female, Humans, Male, Gastroenterology, Leadership, Personnel Selection methods, Societies, Scientific
- Published
- 2021
- Full Text
- View/download PDF
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