No 2 (2026)
Articles
Evolution of the probiotic paradigm: From general recommendations to the targeted utilization of specific strains. A review
Abstract
The contemporary pharmaceutical market is characterized by a plethora of probiotic formulations with various microorganism combinations, dosages, and claimed indications for usage. Different probiotics show divergent evidence for efficacy and safety, and markedly different spectra of action. This diversity presents a significant challenge for practitioners in selecting the optimal probiotic for individual patients, necessitating consideration of evidence-based medicine principles and unique clinical characteristics. Strain specificity is the most critical attribute of probiotics, as it directly influences their functional potential. Recent advancements have identified a select group of probiotic strains with demonstrated efficacy for several common clinical conditions, particularly in relation to functional gastrointestinal disorders. This development facilitates a paradigm shift for pediatricians, moving from the empirical use of general probiotics to the targeted selection of specific strains or combinations designed to address well-defined clinical issues. Both Russian and international studies underscore the substantial impact of intestinal microbiota composition on the health of young children. In routine clinical practice, pediatricians frequently observe the consequences of imbalances in the qualitative and quantitative composition of the intestinal microbiota. In this context, combinations of Pediococcus pentosaceus CECT 8330/Bifidobacterium longum CECT 7894 (Bifistim® Baby) and Lactobacillus plantarum CECT 7315/ CECT 7316 (Bifistim® Immuno) strains are of particular interest. These strains and their respective combinations exhibit strain-specific effects that are beneficial for infants in their early months and years. This review analyzes the role of these strains in shaping microbiota, preventing and correcting functional gastrointestinal disorders, and supporting immune function.
90-100
The impact of human milk oligosaccharides on the metabolic potential of the microbiota and the prevalence of pathogens in breastfed infants. A prospective longitudinal non-interventional cohort study
Abstract
Background. The gut microbiota of infants experiences substantial alterations during the initial years of life, which are imperative for immune maturation, nutrient absorption, and metabolic programming. Among various microbial metabolites, short-chain fatty acids (SCFAs), particularly acetate produced by gut bacteria during fermentation of dietary fibers, are critical for regulating interactions between the host and the microbiota. A significant factor influencing the composition and functional capacity of the microbiota in the early months of life is the feeding type.
Aim. To assess the influence of breastfeeding on the changes in the intestinal microbiota, specifically the proportion of bacteria capable of synthesizing SCFAs, particularly acetate, during the first four months of life, and to compare these changes with the frequency of pathogen detection.
Materials and methods. The study was conducted as part of a prospective longitudinal non-interventional cohort study with parallel groups. Follow-up assessments occurred during the first 4 months of life, with scheduled visits at approximately 30±2, 60±2, and 120±2 days. Participants were categorized into groups based on their feeding type: breastfed (BF) and formula-fed (FF). The composition of the intestinal microbiota, the proportion of SCFA-synthesizing bacteria, and the frequency of pathogenic organism detection were analyzed.
Results. The findings indicate that feeding type is associated with variations in taxonomic composition and in the estimated metabolic potential of the intestinal microbiota. In breastfed infants, there was a more favorable progression in the proportion of acetate-producing bacteria. In contrast, in the formula-fed group, there was greater variability in microbial profiles and a lower abundance of potentially protective microbial communities. The observed differences were associated with variations in pathogen detection.
Conclusion. The type of feeding during the early months of life significantly impacts the development of the metabolic potential of the intestinal microbiota, representing a crucial factor in early microbial and metabolic adaptation.
101-106
Infant microbiome programming during the introduction of complementary feeding: changes and long-term consequences. A review
Abstract
The introduction of complementary foods is a crucial stage in the development of the intestinal microbiome, shaping the body's metabolic and immune programming. During this period, a transition occurs from the microbial community characteristic of dairy foods, predominantly represented by Bifidobacterium, to a more mature microbiota dominated by Firmicutes and Bacteroidetes. The characteristics of this process have a significant impact on subsequent health, including the risk of metabolic disorders, the development of immune tolerance, and the prevention of allergic diseases. Research shows that dietary fiber and prebiotics (inulin, fructooligosaccharides, and galactooligosaccharides) promote the growth of beneficial microflora and the synthesis of short-chain fatty acids, which play a crucial role in maintaining intestinal barrier function and the immune response. Fermented milk products, particularly yogurt, are also important, containing probiotic and prebiotic microorganisms and promoting microbial diversity. Modern industrial complementary foods are considered an effective tool for nutritional support in young children. Their advantages stem not only from a high level of safety and quality control, but also from the ability to specifically optimize their composition. The use of prebiotics and other functional components improves nutrient absorption while simultaneously maintaining a favorable intestinal microbiota.
107-113
The use of liquid probiotic complexes in children: A review
Abstract
The composition of the intestinal microbiota significantly influences the progression of various pathological processes within the human body. There is now clear evidence supporting the role of dysbiosis in the emergence of functional gastrointestinal disorders in young children. This article examines the current understanding of the treatment of these disorders in children using liquid probiotic complexes—specifically, the Normoflorin synbiotics. These synbiotic complexes comprise live and physiologically active lactobacilli and bifidobacteria (Lactobacillus acidophilus, Bifidobacterium longum, and Bifidobacterium bifidum), along with their metabolic products, including short-chain fatty acids, enzymes, and vitamins. Liquid probiotic formulations can colonize the intestine more rapidly (within 2 hours) than lyophilized formulations. Clinical observations demonstrate the beneficial effects of Normoflorin synbiotics for conditions such as lactase deficiency, atopic dermatitis, and functional gastrointestinal disorders in children, suggesting that these agents may serve as a promising adjunct to therapy; however, further randomized studies are needed to confirm these findings.
114-117
Infant teething syndrome: practical experience of a pediatrician. An observational study
Abstract
Background. Teething in infants during the first year of life is frequently associated with both localized and systemic manifestations that may concern caregivers and complicate clinical evaluation. As a result, continuous observation of symptom changes and treatment approaches in pediatric practice is of significant value. This article presents practical experiences in managing infants aged 6 to 12 months exhibiting teething syndrome, focusing on clinical signs that hinder the differentiation between physiological teething and concurrent illnesses.
Aim. To assess the spectrum of signs and symptoms associated with teething in infants during their first year of life, followed by an analysis of their frequency and progression. Additionally, the study aims to compare the clinical efficacy of multicomponent medications for the treatment of teething-related conditions.
Materials and methods. The observational study included two in-person visits (on days 1 and 6) and a telephone consultation with the child's legal guardians on Day 3, enabling an assessment of the condition's change in the early stages following diagnosis. Diagnosis relied on a combination of local symptoms (such as hyperemia and edema of the gums, assessed using a scoring system; pain upon palpation; itching as reported by caregivers; presence of an eruption hematoma) and systemic manifestations (modifications in appetite, sleep patterns, activity levels, and irritability), recorded by parents on structured scales. To reduce subjectivity, the assessments of hyperemia and swelling by caregivers and the pediatrician were compared. Additionally, stool monitoring was conducted using the Bristol scale. Viburcol®, a multicomponent agent, was administered as a suppository based on fever levels as the basic treatment. Symptomatic therapy, including nasal irrigation with saline and antipyretic usage for fever, was permitted in the presence of respiratory symptoms.
Results. The mean age of participants was 8.6 months, with a relatively uniform distribution by sex: boys constituted 56% (n=10), while girls accounted for 44% (n=8). Data collected during Visit 1 revealed that 33% of the children experienced fever, with two exceeding 38.0°C. At Visit 2, normal body temperature was recorded for all patients. At the baseline visit, the distribution of local symptom severity indicated that 7 patients (38.9%) had mild or moderate hyperemia and swelling, and 4 (22%) had severe hyperemia. At Visit 3, only one patient displayed mild oral mucosal changes. Parent-reported data indicated that the percentage of children experiencing no negative impact on appetite increased from 39% at Visit 1 to 72% by Visit 3. At baseline, most children presented with sleep disturbances; however, by Visit 3, parents characterized sleep as normal or only mildly impaired in 83% of cases.
Conclusion. The observations indicate that the therapy was well-tolerated, with no reported allergic reactions. Clinical improvement was evident, as signified by the resolution of fever by Day 3, improvements in sleep and appetite, and a reduction in the severity of systemic symptoms.
118-127
Parental assessment of the quality of life of preschool children born prematurely
Abstract
Background. Increased survival of extremely preterm infants highlights the importance of assessing their long-term quality of life (QoL). The effectiveness of inpatient rehabilitation should be evaluated not only through clinical data but also through family perception to personalize recovery programs.
Aim. To assess the QoL of children aged 3–6 years who underwent comprehensive inpatient medical rehabilitation for various degrees of prematurity.
Materials and methods. A retrospective analysis was conducted on 47 children (gestational age – 30 [27; 34] weeks). QoL was assessed by parents using the Kiddy-KINDL questionnaire. The Rasch model was applied to analyze the latent developmental potential.
Results. The overall QoL level was high; however, the lowest scores were observed in the "educational process" domain. Extreme prematurity (< 28 weeks) significantly lowered only physical well-being (p=0.02), with no significant impact on other domains. A correlation was found between a history of surgery and higher scores in family relations. Children rehabilitated exclusively at a single specialized center showed better physical and social functioning. The Rasch model confirmed high intrinsic potential: most children are capable of achieving above-average QoL indicators.
Conclusion. Early, comprehensive rehabilitation minimizes the impact of gestational age on QoL. Success depends primarily on the continuity of care and family involvement. A child's individual potential often compensates for the expected risks associated with prematurity.
128-134
Organizing pneumonia in children: A clinical case
Abstract
Respiratory diseases are the most common reason for seeking medical care in pediatric practice. Interstitial lung diseases and other rare pulmonary conditions hold a distinct position within this group. Organizing pneumonia (OP) is a serious condition that can impair lung function and quality of life. Diagnosing OP can be challenging because symptoms may resemble those of other respiratory illnesses, such as bacterial pneumonia. The lack of timely diagnosis of the disease significantly worsens the patient's prognosis. The objective of this paper is to report a new clinical case and to consolidate and summarize the available data on the OP. The article presents the clinical case of a 4-year-old patient with progressive dyspnea and infiltrative changes in the lungs, which were initially interpreted as a manifestation of bilateral pneumonia. Chest computed tomography showed a characteristic pattern for OP. Significant clinical and radiological improvement was achieved with glucocorticosteroid therapy.
135-139
Unification of terminology for lower urinary tract disorders in children and adolescents in Russian practice
Abstract
Lower urinary tract (LUT) dysfunction in pediatric populations is among the most common reasons for consultation with a pediatric urologist. This condition requires a standardized approach to the diagnosis and interpretation of urodynamic data. A significant advancement in establishing a cohesive professional lexicon occurred in 2004 with the publication of a document by the International Children's Continence Society (ICCS) to standardize terminology, which was subsequently revised and updated in 2015–2016. This report analyzes the ICCS consensus document entitled "Standardization of Terminology of Lower Urinary Tract Function in Children and Adolescents" (2015–2016), published in the Neurourology and Urodynamics journal, and compares it with its 2004 predecessor. Furthermore, the current literature was reviewed, and clinical experiences using ICCS terminology in pediatric urology were summarized. The ICCS terminology adopted in international practice defines terms for bladder filling and emptying symptoms, various types of urinary incontinence, and urodynamic study parameters. Currently, the terminology concerning LUT dysfunction in children remains unstandardized within Russian practice. There is a critical need to implement uniform terminology across clinical applications, regardless of the disorder's underlying etiology, to enhance the comparability of clinical data and diagnostic accuracy. The integration of standardized ICCS terminology into Russian practice is essential for the effective diagnosis and management of children with LUT dysfunction, thereby fostering improvements in both clinical and scientific endeavors.
140-151
Rehabilitation of children with neurogenic urination disorders. A case report
Abstract
Neurogenic urinary disorders refer to bladder dysfunction that arises due to neurological and neurosurgical conditions, as well as malformations of the bladder and urethra. The treatment and medical rehabilitation of children with neurogenic urinary disorders are crucial from the point of diagnosis and continue throughout the child’s life until transitioning to public health organizations that provide healthcare services to the adult population. The primary rehabilitation objectives include preserving renal function, preventing and treating urinary tract infections, and addressing the significant concern of socialization and improving the quality of life for both the patient and their family. Pediatricians play a pivotal role in the medical rehabilitation of these children throughout their growth, serving as key coordinators of interdisciplinary collaboration. This paper presents two clinical cases of children diagnosed with neurogenic urinary disorders, highlighting the challenges healthcare providers encounter in diagnosis and treatment. Clinical case 1. A three-year-old girl diagnosed with caudal regression syndrome, neurogenic bladder, and recurrent grade 4 vesicoureteral reflux on the left side (after endoscopic correction) and a recurrent chronic secondary pyelonephritis. Clinical case 2. A two-year-old boy who presented with recurrent urinary tract infections following surgical treatment for a myelocele. The integration of urodynamic test methods into the diagnosis and evaluation of bladder function has enhanced treatment quality and enabled individualized medical rehabilitation strategies for children.
152-158
A contemporary perspective on the use of rectal laxatives in children with functional constipation. Expert Panel Decision November 29, 2025, Moscow
Abstract
Constipation presents a significant challenge in modern pediatrics, with functional constipation (FC) being the predominant cause, accounting for up to 95% of all cases. Despite pediatricians' engagement in tackling this issue, certain aspects of diagnosis and treatment across age groups remain inadequately addressed. On November 29, 2025, a Council of Experts convened in Moscow, where a resolution was passed focusing on the topic, "A Contemporary Perspective on the Use of Rectal Laxatives in Children with Functional Constipation". To effectively manage FC, a holistic approach is necessary, including addressing the patient's psychoemotional well-being, implementing dietary modifications, and, if these initial strategies prove ineffective, considering medication options. Among the preferred initial therapeutic agents are medicinal microclysters containing sodium lauryl sulfoacetate, sodium citrate, and sorbitol, known for their rapid laxative effect when used alone or in combination with oral laxatives. The features of the FC trajectory determine the treatment duration, and each case is addressed individually.
159-164
Helminthiasis in children. A clinical case of helminthic polyinvasion in a child with bronchial asthma
Abstract
Helminthiasis is a significant part of infectious pathology in children. The spread of parasitic diseases is recorded in all regions of the world. In Russia, more than 20 million people fall ill with helminthiasis every year. The article sets out the basic ideas about epidemiology and clinical manifestations, treatment and prevention of the most common helminthiasis in children. The issue of the relationship between allergic diseases and parasitoses is considered, when under the mask of allergic diseases hides helminthprotozoal invasion. The growth of allergopathology and the widespread prevalence of parasitic diseases among children make this problem urgent. A clinical case of helminthiasis is presented in a 7-year-old child with bronchial asthma, in combination with mixed invasion: 2 helminths and protozoosis (ascariasis + toxocarosis + giardiasis).
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