11 results on '"N. Yu. Ivashkina"'
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2. Practical Recommendations of Scientific Society for the Study of Human Microbiome and the Russian Gastroenterological Association on Use of Probiotics, Prebiotics, Synbiotics and Functional Foods in Treatment and Prevention of Gastroenterological Diseases in Children and Adults
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V. T. Ivashkin, I. V. Maev, D. I. Abdulganieva, S. A. Alekseenko, A. V. Gorelov, I. N. Zakharova, O. Yu. Zolnikova, N. Yu. Ivashkina, N. V. Korochanskaya, S. N. Mammayev, E. A. Poluektova, A. S. Trukhmanov, D. V. Usenko, Yu. P. Uspensky, V. V. Tsukanov, O. S. Shifrin, I. V. Berezhnaya, K. V. Ivashkin, T. L. Lapina, R. V. Maslennikov, S. V. Nikolaeva, N. G. Sugyan, and A. I. Ulyanin
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probiotic ,probiotic strain ,prebiotic ,symbiotic ,functional food ,functional food ingredient ,acute diarrhea ,antibiotic-associated diarrhea ,c. difficile-associated disease ,h. pylori eradication ,inflammatory bowel disease ,ulcerative colitis ,crohn’s disease ,pouchitis ,irritable bowel syndrome ,functional constipation ,functional dyspepsia ,diarrhoea prevention ,hepatic encephalopathy ,gastroenteritis ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
Aim. The practical guidelines are intended for primary care physicians, general practitioners, paediatricians, gastroenterologists and general internists to advance the treatment and prevention of gastroenterological diseases in adults and children in therapies with probiotics, prebiotics, synbiotics and their enriched functional foods.Key points. Probiotics are live microorganisms that sustain health of the host when supplied in adequate amounts. Prebiotics include human-indigestible but accessible to gut microbiota substances expediting specific changes in the composition and/or activity of gastrointestinal microbiota that favour the host health. The mechanism of probiotic action comprises the quorum resistance maintenance, nutrient substrate metabolism and end metabolite recycling, macroorganism-sustaining substrate production, as well as the mediation of local and adaptive immune responses.The Russian Federation regulates market differently for biologically active food additives (BAFA), medicinal products (drugs) and functional food products (FFP). We overview the probiotic strains regulated in Russia as BAFAs, drugs and FFPs and provide recommendations on the use of these strains in treatment and prevention of gastroenterological diseases in children and adults.Conclusion. The clinical efficacy of probiotics, prebiotics, synbiotics and fortified functional foods depends on the prebiotic and strain properties and is verified in appropriate comparative clinical trials. Not all probiotics registered in Russia as BAFAs, drugs and FFPs have a strain identity, which provides no warranty of the clinical effect expected. The FFP legislation demands improved regulation mechanisms and control for therapeutic efficacy.
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- 2021
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3. Evaluation and management of infectious esophagitis in immunocompromised patients and immunocompetent individuals
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A. S. Trukhmanov, A. A. Makushina, O. A. Storonova, and N. Yu. Ivashkina
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infectious esophagitis ,herpes simplex virus ,candidiasis ,cytomegalovirus ,immunodeficiency ,dysphagia ,odynophagia ,esophageal ulcer ,Medicine - Abstract
Among the many causes of the inflammatory process in the esophagus, infectious diseases are becoming increasingly important due to their steady growth. Previously esophageal infections have traditionally been associated with immunodeficiency syndromes, but now in clinical practice, these disorders are becoming increasingly recognized in immunocompetent individuals. Early diagnosis of infectious esophagitis is necessary to develop effective treatment tactics, and, as a result, reduce the risk of complications and adverse outcomes of the disease. This study reviewed the most clinical relevant pathogens of infectious esophagitis, both among patients with immunodeficiency and among healthy individuals. Specific diagnostic, risk factors, clinical presentation and therapeutic features were considered depending on the immune status of patients.
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- 2020
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4. Practical Recommendations of Scientific Society for the Study of Human Microbiome and Russian Gastroenterological Association (RGA) for Probiotics in Treatment and Prevention of Gastroenterological Diseases in Adults
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V. T. Ivashkin, I. V. Mayev, D. I. Abdulganieva, S. A. Alekseenko, N. Yu. Ivashkina, N. V. Korochanskaya, S. N. Mammaev, E. A. Poluektova, A. S. Trukhmanov, Yu. P. Uspensky, V. V. Tsukanov, O. S. Shifrin, O. Yu. Zolnikova, K. V. Ivashkin, T. L. Lapina, R. V. Maslennikov, and A. I. Ulyanin
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probiotic ,probiotic strain ,acute diarrhea ,antibiotic-associated diarrhea ,c. difficile-associated disease ,h. pylori eradication ,inflammatory bowel disease ,ulcerative colitis ,crohn’s disease ,pouchitis ,irritable bowel syndrome ,functional constipation ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
Aim. To provide practical recommendations on the use of probiotics for the treatment and prevention of gastroenterological diseases in adults.General provisions. Probiotics are living microorganisms that benefit the health of the host when administered in adequate amounts. The main functions of probiotics include the support for colonisation resistance, the metabolism of food substrates and utilisation of end metabolites, the production of substrates necessary for the macro-organism, as well as the regulation of local and adaptive immune responses. Probiotics can be registered in the Russian Federation as biologically active food additives (BAFA) or as pharmaceutical products (drugs) in accordance with the microbiological standards and legislative requirements of the Russian Federation. The probiotics registered in the Russian Federation as BAFA for adults include bacteria of the Lactobacillus, Bifidobacterium, Enterococcus, Pediococcus, Lactococcus, Streptococcus, Bacillus, and Escherichia genera, and fungi of the Saccharomyces genus; probiotics registered as drugs — bacteria of Lactobid, Lactobacid, Escherichia and Enterococcus genera and fungi of the Saccharomyces genus. Some probiotics registered in the Russian Federation include probiotic strains that have proved to be effective for the prevention and treatment of antibiotic-associated diarrhea, the prevention of C. difficile-associated disease, the eradication of H. pylori infection, as well as for the treatment of irritable bowel syndrome and functional constipation.Conclusions. The clinical efficacy of probiotics depends on the probiotic strains included in their composition and is confirmed by a comparative analysis of the results of appropriate clinical studies. Not all probiotics registered in the Russian Federation as BAFA or drugs contain bacterial or fungal strains; as a result, the expected clinical effect may not be achieved.
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- 2020
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5. Clinical Guidelines of the Russian Gastroenterological Association on the Diagnostics and Treatment of Eosinophilic Esophagitis
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V. T. Ivashkin, I. V. Maev, A. S. Trukhmanov, T. L. Lapina, D. N. Andreev, E. K. Baranskaya, A. S. Tertychny, S. S. Pirogov, A. A. Sheptulin, D. I. Abdulganieva, D. T. Dicheva, A. V. Zaborovsky, N. Yu. Ivashkina, N. V. Korochanskaya, and A. V. Paraskevova
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eosinophilic esophagitis ,proton pump inhibitor ,topical steroid ,elimination diet ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
Aim. This paper presents guidelines on the diagnostics and treatment of eosinophilic esophagitis, which can be used by practitioners in their everyday practice.Summary. Eosinophilic esophagitis (EoE) is a chronic immune-mediated disease of the esophagus characterized by the symptoms of esophageal dysfunction and a pronounced eosinophilic infiltration of the esophageal mucosa. The EoE diagnostics is based on the clinical manifestations of the disease (dysphagia, food impaction, chest pain regardless of swallowing), as well as on the combination of endoscopic and histological signs. The diagnostic criterion is the eosinophilic infiltration of the esophageal mucosa with an eosinophil density of ≥ 15 per high power field (×400) in at least one of the biopsy specimens (about 60 eosinophils in 1 mm2). Total IgE levels, peripheral blood eosinophilia and skin allergy tests are considered to be additional diagnostic means. Several approaches are used for the treatment of EoE, including proton pump inhibitors (PPIs) and topical glucocorticosteroids (GCS), as well as elimination diets. The choice of therapy should be individualized, with the mandatory assessment of the treatment efficacy after 6–12 weeks using esophagogastroduodenoscopy with biopsy sampling. Endoscopic dilatation should be considered in patients suffering from severe dysphagia due to esophagus stricture.Conclusion. Increased incidence of EoE predominantly among children and young people, as well as its chronic character requiring long-term maintenance therapy, make EoE a significant issue to the practice of gastroenterology.
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- 2019
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6. Pharmacokinetics of dipeptide anxiolytic GB-115 after oral administration in different animals species and humans
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S. Yu. Raskin, G. B. Kolyvanov, A. A. Litvin, P. O. Bochkov, R. V. Shevchenko, V. V. Smirnov, O. G. Grybakina, A. A. Novitskyi, V. P. Zherdev, L. G. Kolik, T. A. Gudasheva, and N. Yu. Ivashkina
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гб-115 ,фармакокинетика ,межвидовые различия ,gb-115 ,pharmacokinetics ,interspecies differences ,Pharmacy and materia medica ,RS1-441 - Abstract
Results of pharmacokinetic study of a new dipeptide anxiolytic GB-115 in rats, rabbits and volunteers were presented. After oral drug administration significant differences were found. For example, a dose-independent parameter - the elimination rate constant was decreased: rat < human < rabbit. By contrast the half-life of GB-115 was increased: rat
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- 2017
7. Clinical pharmacokinetics of а new original dipeptide anxiolytic GB-115
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V. P. Zherdev, G. B. Kolyvanov, A. A. Litvin, V. V. Smirnov, L. G. Kolik, S. Yu. Raskin, N. Yu. Ivashkina, T. A. Gudasheva, and S. B. Seredenin
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таблетки гб-115 ,высокоэффективная жидкостная хроматография-масс-спектрометрия ,клиническая фармакокинетика ,tablets of gb-115 ,high-performance liquid chromatography/mass-spectroscopy ,clinical pharmacokinetics ,Pharmacy and materia medica ,RS1-441 - Abstract
Pharmacokinetic study of а new original anxiolytic drug GB-115, developed on the basis of endogenous tetrapeptide cholecystokinin, in healthy volunteers was performed. Volunteers were received drug as single 1, 3, 7, 11 or 15 mg tablets. The parent drug in the human blood plasma was detected within 2-6 hours after ingestion. Cmax/AUC0-T for doses 3-15 mg were averaged 0,482-0,552 h-1. Cmax were averaged from 7,29±2,83 ng/ml (for dose 1 mg) to 44,02±13,23 ng/ml (for dose 15 mg). Half-life of the drug is changed in the range of 0,6-1,0 h. Vd/F amounted to an average of 2,47 l/kg. Summarizing the obtained results it can be concluded that consistent, linear increase in the dose of GB-115 from 1 to 15 mg there is an increase in dose-dependent pharmacokinetic parameters. In the studied range of doses pharmacokinetics of GB-115 was linear.
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- 2017
8. Options of improvement of efficacy of gastroesophageal reflux disease treatment by dioctaedric smectite
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O. A. Storonova, A. S. Trukhmanov, N. Yu. Ivashkina, and V. T. Ivashkin
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gastroesophageal reflux disease ,рн-impedance recording ,duodenogastroesophageal reflux ,smecta ,Diseases of the digestive system. Gastroenterology ,RC799-869 - Abstract
Aim of investigation. To analyze efficacy of heartburn relief and pathological gastroesophageal reflux (GER) elimination as well as dynamics of endoscopic changes at gastroesophageal reflux disease (GERD) under dioctaedric smectite (Smecta) treatment in standard doze as monotherapy and within complex mode of treatment.Material and methods. Overall 45 case records of GERD patients (25 women and 20 men, mean age 43,06 years) were analyzed. All patients underwent esophagogastroduodenoscopy (EGDS) and 24-hour рН-impedance recording prior to the treatment onset and at the 14-th day of therapy. The first group included patients with erosive esophagitis (EE) of the I–II degree receiving combination of proton pump inhibitors (PPI) and Smecta, the second group included patients with EE, receiving PPI monotherapy, the third group — patients with non-erosive reflux disease (NERD) at Smecta monotherapy.Results. On a background of treatment by PPI + Smecta relief of heartburn was achieved at the 3rd day in 10 (66,7%) patients, at PPI monotherapy — in 4 (26,7%) patients with EE, at monotherapy by Smecta — in 6 (40%) patients. At the 5th day heartburn has been completely relieved in 11 (73,3%), 9 (60%) and 8 (53,3%), and at the 14-th day — in 13 (86,7%), 11 (73,3%) and 12 (80%) patients respectively. In the first group according to upper endoscopy data healing of erosions was confirmed in 13 (86,7%) patients, in the second — in 10 (66,7%). In the third group cessation of catarrhal signs was revealed in 13 (86,7%) patients. According to 24-hour рН-impedance esophageal recording prior at the beginning of therapy pathological acidic, weakly acidic and weakly alkalinic GERs were diagnosed in 34 (75,5%), 18 (40%) and 12 (26,7%) patients in group as a whole respectively. On a background of therapy by PPI + Smecta acidic refluxes have been eliminated in 14 (93%), at PPI monotherapy — in 11 (73%), at Smecta monotherapy — in 100% of patients. In the first group weakly acidic refluxes disappeared in 2 (67%), in the second — in 1 (50%), in the third – in 9 (69%) cases, weakly alkaline refluxes: in 4 (80%), in 2 (40%) and in 100% of cases respectively.Conclusions. Addition of Smecta in treatment mode at erosive form of GERD essentially increases treatment response rate, significantly reducing terms of clinical improvement onset. Dioctaedric smectite appears an effective drug as monotherapy of NERD. The chief advantage in treatment of GERD is ability of the drug to stop all reflux types: acidic, weakly acidic, and weakly alkalinic.
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- 2015
9. Elimination Half-Life of Short Peptide Drugs in Humans Extrapolated From Animal Pharmacokinetic Pharmacokinetic Studies
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L. G. Kolik, G. B. Kolyvanov, O. G. Gribakina, T. A. Gudasheva, A. A. Litvin, V. V. Smirnov, R. V. Shevchenko, P. O. Bochkov, V. P. Zherdev, N. Yu. Ivashkina, and S. Yu. Raskin
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Pharmacology ,chemistry.chemical_classification ,010405 organic chemistry ,Chemistry ,medicine.drug_class ,medicine.medical_treatment ,Pharmacology toxicology ,Peptide ,01 natural sciences ,Anxiolytic ,0104 chemical sciences ,010404 medicinal & biomolecular chemistry ,Pharmacokinetics ,Interspecies scaling ,Drug Discovery ,medicine ,Biological half-life ,Antipsychotic - Abstract
Results from an interspecies scaling study of the elimination half-lives of the anxiolytic GB-115 and the antipsychotic dilept in rats, rabbits, and humans are presented. The elimination half-lives of the studied drugs are calculated in real (chronological) and corrected time (pharmacokinetic). Elimination half-lives in animals and volunteers are compared. Rabbits are found to be a better scaling model for GB-115 although a single preference for dilept was not found.
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- 2019
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10. [Results of a clinical study of a new anxiolytic, a blocker of central cholecystokinin receptors]
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S V Minaev, M. V. Metlina, G G Neznamov, S B Seredenin, Dorofeeva Oa, N Yu Ivashkina, T S Syunyakov, and V A Martyanov
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Adult ,Male ,medicine.medical_specialty ,Generalized anxiety disorder ,Hamilton Anxiety Rating Scale ,medicine.drug_class ,Anxiolytic ,Cholecystokinin receptor ,03 medical and health sciences ,Young Adult ,0302 clinical medicine ,Internal medicine ,medicine ,Humans ,Psychiatric Status Rating Scales ,business.industry ,Middle Aged ,medicine.disease ,Effective dose (pharmacology) ,Anxiety Disorders ,030227 psychiatry ,Psychiatry and Mental health ,Treatment Outcome ,Tolerability ,Anti-Anxiety Agents ,Clinical Global Impression ,Anxiety ,Female ,Receptors, Cholecystokinin ,Neurology (clinical) ,medicine.symptom ,business ,030217 neurology & neurosurgery - Abstract
To evaluate anxiolytic action of GB-115, a low-affinity blocker of central cholecystokinin receptors, used in tablets in a dose of 1 mg for the treatment of patients with anxiety disorders in order to determine effective dose, safety, tolerability and efficacy in clinical settings.The study included 31 patients (22 women, 9 men) diagnosed with generalized anxiety disorder (GAD, F41.1 according to ICD-10), aged from 22 to 53 years. The duration of treatment was 21 days. The Hamilton Anxiety Rating scale, Psychopathologic symptoms severity evaluation scale (PSSES), Spilberger State-Anxiety Inventory, Multidimensional Fatigue Inventory (MFI), Clinical Global Impression scale (CGI), computerized battery for evaluation of cognitive functions ('NS-Psychotest') were used.The effective dose of GB-115 was determined at 6 mg per day. Drug action is characterized by fast onset of anxiolytic effect with stimulating properties and beneficial effect on sleep disturbances and autonomic symptoms. GB-115 treatment was associated with favorable changes in attention parameters, reaction time and overall performance. In contrast to first-line drugs for GAD treatment (SSRIs and SNRIs), GB-115 does not induce initial overactivation, anxiety and sleep disturbances. GB-115 is safe and has a good tolerability.Цель исследования. Клинико-фармакологическая характеристика анксиолитического действия препарата ГБ-115 - низкоаффинного блокатора центральных холецистокининовых рецепторов, в таблетках по 1 мг, в качестве анксиолитического средства у больных с тревожными расстройствами. Основные задачи - определение эффективных терапевтических доз препарата, изучение его переносимости, безопасности и эффективности в клинических условиях. Материал и методы. В исследование включен 31 больной (22 женщины, 9 мужчин), с генерализованным тревожным расстройством (ГТР - F41.1 по МКБ-10), в возрасте от 22 до 53 лет. ГБ-115 применялся в течение 21 дня. Использовались методики оценки действия препарата: шкала тревоги Гамильтона, шкала выраженности симптоматики, тест Спилбергера-Ханина, субъективная шкала оценки астении (МFI), шкала общего клинического впечатления (CGI), компьютеризованная методика психофизиологического исследования НС-Психотест. Результаты и заключение. Установлено, что терапевтически эффективной дозой ГБ-115 является 6 мг в сутки. Особенностями клинико-фармакологического действия препарата является наличие быстро реализующегося анксиолитического эффекта со стимулирующим компонентом и положительным влиянием на нарушения сна и вегетативные функции. Выявлено позитивное влияние ГБ-115 на показатели внимания, скорости реакции, эффективность операторской работоспособности. В отличие от препаратов из группы селективных ингибиторов обратного захвата серотонина (СИОЗС) и норадреналина (СИОЗСН), рекомендуемых в настоящее время в качестве препаратов первой линии для лечения ГТР, ГБ-115 не проявляет гиперстимуляции, усиления тревоги и нарушения засыпания, выявляющихся у антидепрессантов на начальных этапах терапии. Установлены хорошая переносимость и безопасность применения препарата.
- Published
- 2019
11. The clinical significance of disorders of the motor function of the esophagus, stomach and duodenum
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A S Trukhmanov and N Yu Ivashkina
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cardia achalasia ,esophagism ,gastroesophageal reflux disease ,hiatal hernia ,functional dyspepsia ,motor-evacuation function ,peristalsis ,dysphagia ,antroduodenal motility ,duodenogastric reflux ,manometry ,high resolution manometry ,high resolution manometry ph-metry ,Medicine - Abstract
The purpose of the review is to determine the relationship between the clinical symptoms of diseases and disorders of the motor function of the esophagus, stomach and duodenal bulb, to present modern methods of their diagnosis and pathogenetic principles of treatment of diseases. Depending on the pathogenesis, it is possible to distinguish secondary motility disorders resulting from organic lesions, and primary (functional) changes. The emergence of clinical symptoms is associated with impaired motor - evacuation function of the digestive tract, which can be divided into two large groups: changes in the peristaltic activity of the organ wall and the work of the sphincter apparatus. The basis of the regulation of motility of the esophagus, stomach and duodenum is the interaction of nervous and humoral factors, the central processing of impulses is carried out in the cerebral cortex. In case of violation of the coordinated action of inhibitory and excitatory regulation systems, pathological contractile activity occurs, which manifests itself as hypo - or hyper - motor dyskinesia. X-ray, ultrasound, high resolution manometry of the esophagus, pH-meter, scintigraphy, computed tomography, antroduodenal manometry and a number of others are used to diagnose disorders of the motor function of the digestive tract, which can determine the mechanism of the development of symptoms and prescribe pathogenetic treatment to the patient. Thus, the occurrence of clinical symptoms is associated with changes in the motor - evacuation function of the digestive tract due to a violation of the coordinating action of inhibitory and excitatory factors. The use of modern diagnostic methods for the study of motor function makes it possible to determine the mechanism for the development of clinical symptoms, which allows the patient to prescribe an effective pathogenetic treatment.
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- 2019
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