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Children, Volume 12, Issue 11 (November 2025) – 26 articles

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17 pages, 736 KB  
Article
Making Sense of Missense: Assessing and Incorporating the Functional Impact of Constitutional Genetic Testing
by Meaghann Weaver
Children 2025, 12(11), 1449; https://doi.org/10.3390/children12111449 (registering DOI) - 24 Oct 2025
Abstract
Background/Objectives: With the emergence of accessible and affordable next-generation sequencing platforms, pediatric oncologists are now accountable to diligently ascertain genetic causes of cancer, with an amenable opportunity to test for cancer predisposition syndromes. Methods: This study incorporates triangulated interviews of family [...] Read more.
Background/Objectives: With the emergence of accessible and affordable next-generation sequencing platforms, pediatric oncologists are now accountable to diligently ascertain genetic causes of cancer, with an amenable opportunity to test for cancer predisposition syndromes. Methods: This study incorporates triangulated interviews of family members diagnosed with Li–Fraumeni syndrome through clinical TP53 testing. The interview content was coded using NVivo 10.0 software to determine psychosocial themes relevant to genetic testing, diagnosis, and surveillance. Results: Interview content revealed opportunities to apply social themes analogous to TP53 biologic language. Conclusions: This report models the systematic inclusion of patient, parent, and health care provider perspectives when testing individuals for familial cancer predisposition syndromes. Full article
14 pages, 694 KB  
Article
Machine Learning for ADHD Diagnosis: Feature Selection from Parent Reports, Self-Reports and Neuropsychological Measures
by Yun-Wei Dai and Chia-Fen Hsu
Children 2025, 12(11), 1448; https://doi.org/10.3390/children12111448 (registering DOI) - 24 Oct 2025
Abstract
Background: Attention-deficit/hyperactivity disorder (ADHD) is a heterogeneous neurodevelopmental condition that currently relies on subjective clinical judgment for diagnosis, emphasizing the need for objective, clinically applicable tools. Methods: We applied machine learning techniques to parent reports, self-reports, and performance-based measures in a sample of [...] Read more.
Background: Attention-deficit/hyperactivity disorder (ADHD) is a heterogeneous neurodevelopmental condition that currently relies on subjective clinical judgment for diagnosis, emphasizing the need for objective, clinically applicable tools. Methods: We applied machine learning techniques to parent reports, self-reports, and performance-based measures in a sample of 255 Taiwanese children and adolescents (108 ADHD and 147 controls; mean age = 11.85 years). Models were trained under a nested cross-validation framework to avoid performance overestimation. Results: Most models achieved high classification accuracy (AUCs ≈ 0.886–0.906), while convergent feature importance across models highlighted parent-rated social problems, executive dysfunction, and self-regulation traits as robust predictors. Additionally, ex-Gaussian parameters derived from reaction time distributions on the Continuous Performance Test (CPT) proved more informative than raw scores. Conclusions: These findings support the utility of integrating multi-informant ratings and task-based measures in interpretable ML models to enhance ADHD diagnosis in clinical practice. Full article
(This article belongs to the Special Issue Attention Deficit/Hyperactivity Disorder in Children and Adolescents)
10 pages, 262 KB  
Article
The Prevalence of and Factors Associated with Prediabetes Among Adolescents in Central Sudan: A Community-Based Cross-Sectional Study
by Walaa M. Alsafi, Abdullah Al-Nafeesah, Ashwaq AlEed and Ishag Adam
Children 2025, 12(11), 1447; https://doi.org/10.3390/children12111447 (registering DOI) - 24 Oct 2025
Abstract
Background: Prediabetes is a significant precursor to type 2 diabetes mellitus (T2DM) and its well-known complications. In Sudan, data on the epidemiology of prediabetes among adolescents are scarce, especially in the central region. Thus, this study aimed to determine the prevalence of and [...] Read more.
Background: Prediabetes is a significant precursor to type 2 diabetes mellitus (T2DM) and its well-known complications. In Sudan, data on the epidemiology of prediabetes among adolescents are scarce, especially in the central region. Thus, this study aimed to determine the prevalence of and factors associated with prediabetes among adolescents in central Sudan. Methods: This community-based cross-sectional study was carried out in East Gezira, central Sudan, from April to June 2025 and included 379 adolescents. Sociodemographic characteristics, anthropometric data (body mass index and BMI-z-score), and clinical information were gathered. Prediabetes was defined as a glycated hemoglobin (HbA1c) level in the range of 5.7% to 6.4%. Multivariate binary analysis was applied to identify the factors associated with prediabetes. Results: The median (interquartile range, IQR) age and BMI-z-score of the 379 enrolled adolescents were 14 (12–16) years and −1.4 (−2.1–−0.39), respectively. Sixty-four (17.0%) adolescents had prediabetes. Univariate analysis did not reveal any significant associations between the investigated factors and prediabetes. However, multivariate binary analysis showed that being female was independently associated with prediabetes among adolescents (adjusted odds ratio, AOR = 1.80, 95% confidence interval, CI 1.01–3.18). Age, BMI z-score, parent education, and occupation were not associated with prediabetes. Conclusions: The prevalence of prediabetes among adolescents in central Sudan is substantial, highlighting a potential future surge in T2DM. The finding that female adolescents are at a higher risk underscores the need for targeted, gender-sensitive screening and preventive health programs to mitigate the progression from prediabetes to T2DM. Full article
(This article belongs to the Section Pediatric Endocrinology & Diabetes)
15 pages, 540 KB  
Systematic Review
Continuous Antibiotic Prophylaxis for Vesicoureteral Reflux: Impact on the Pediatric Microbiome—A Systematic Review
by Olivia Oana Stanciu, Andreea Moga, Laura Balanescu, Radu Balanescu and Mircea Andriescu
Children 2025, 12(11), 1446; https://doi.org/10.3390/children12111446 (registering DOI) - 24 Oct 2025
Abstract
Background: Continuous antibiotic prophylaxis (CAP) is widely used in infants with vesicoureteral reflux (VUR) to prevent recurrent urinary tract infections and renal scarring. However, this practice entails prolonged low-dose antibiotic exposure during a critical period of microbiome establishment, potentially influencing long-term microbial [...] Read more.
Background: Continuous antibiotic prophylaxis (CAP) is widely used in infants with vesicoureteral reflux (VUR) to prevent recurrent urinary tract infections and renal scarring. However, this practice entails prolonged low-dose antibiotic exposure during a critical period of microbiome establishment, potentially influencing long-term microbial and immune development. Methods: A systematic review was conducted according to PRISMA 2020 guidelines. PubMed, Embase, Scopus, Web of Science, and the Cochrane Library were searched up to September 2025 for studies evaluating gut or urinary microbiome changes in children receiving CAP for VUR. Eligible studies included human participants under 18 years with microbiome outcomes assessed by sequencing or culture-based methods. Results: Twenty-one records were identified, and four studies met inclusion criteria—three observational microbiome studies and one randomized controlled trial. CAP preserved overall microbial alpha diversity but induced compositional changes, notably enrichment of Enterobacteriaceae and reduction in Bifidobacteriaceae. The included RCT confirmed reduced UTI recurrence but increased antimicrobial resistance and non–E. coli infections. Conclusions: CAP in early life maintains microbial diversity but alters microbiota composition and resistance profiles. Identifying these shifts may support individualized prophylaxis strategies and microbiome-preserving interventions to balance infection prevention with ecological safety in infancy. Full article
12 pages, 639 KB  
Article
The Value of HALP Score, SII, and SIRI in Predicting the Need for Intensive Care and Assessing Disease Severity in Pediatric Diabetic Ketoacidosis Cases
by Muhammed Selçuk Sinanoğlu, Turgut Dolanbay, Bilgehan Demir, Süleyman Nogay, Can Celiloğlu and Muhammed Eyyüb Polat
Children 2025, 12(11), 1445; https://doi.org/10.3390/children12111445 (registering DOI) - 24 Oct 2025
Abstract
Objective: The aim of this study was to evaluate whether Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) scores, the Systemic Immune-Inflammation Index (SII), and the Systemic Inflammatory Response Index (SIRI) can predict intensive care unit (ICU) or inpatient admissions in pediatric diabetic ketoacidosis [...] Read more.
Objective: The aim of this study was to evaluate whether Hemoglobin, Albumin, Lymphocyte, and Platelet (HALP) scores, the Systemic Immune-Inflammation Index (SII), and the Systemic Inflammatory Response Index (SIRI) can predict intensive care unit (ICU) or inpatient admissions in pediatric diabetic ketoacidosis (DKA) cases and to determine their sensitivity and specificity. Methods: This retrospective study included 39 pediatric patients (<18 years) diagnosed with DKA (pH < 7.3, HCO3 < 15). HALP, SII, SIRI, and urine ketone values were collected from medical records. Statistical analyses included ROC curve analysis, correlation tests, and appropriate parametric or non-parametric comparisons to evaluate associations with 30-day outcomes. Results: The median age was 13 years (IQR: 8–15), 56.4% were male, and 64.1% required ICU monitoring. ICU patients had significantly lower pH (p = 0.005) and HCO3 (p = 0.012) and significantly higher monocyte, SII, and SIRI values (all p ≤ 0.018). ROC analysis showed SIRI had the highest predictive power for ICU admission (cut-off: 3911; sensitivity: 76%; specificity: 85.7%), followed by SII. HALP scores did not demonstrate any value in assessingdisease severity for predicting ICU admission (AUC = 0.25). Conclusion: SIRI and SII are reliable predictors of ICU admission in pediatric DKA. HALP scores do not predict ICU admission and should not be considered a marker of disease severity. Incorporating SIRI and SII into clinical decision-making may improve early risk stratification. Prospective multicenter studies are warranted to validate these results. Full article
(This article belongs to the Section Pediatric Emergency Medicine & Intensive Care Medicine)
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15 pages, 1239 KB  
Article
Garden on the Go: A Feasibility Study of a Gardening Program to Support Mental Health and Resilience in Youth with Adverse Childhood Experiences
by Glenda E. Hux, Sydney Rice, Amy Wagenfeld and Sarah A. Schoen
Children 2025, 12(11), 1444; https://doi.org/10.3390/children12111444 (registering DOI) - 24 Oct 2025
Abstract
Background/Objectives: The benefits of nature-based interventions to support well-being and mental health are increasingly well-documented in the literature; however, study of an occupational therapy gardening program for adolescents with exposure to adverse childhood experiences (ACEs) is limited. Methods: This study evaluates the feasibility [...] Read more.
Background/Objectives: The benefits of nature-based interventions to support well-being and mental health are increasingly well-documented in the literature; however, study of an occupational therapy gardening program for adolescents with exposure to adverse childhood experiences (ACEs) is limited. Methods: This study evaluates the feasibility of a novel school gardening program for youth with a history of ACEs including the following: (1) recruitment; (2) data collection procedures and outcome measures; (3) acceptability and suitability of the intervention; and (4) evaluation of the response to a gardening intervention as measured by a visual analog scale of emotional state, a heartbeat counting task designed to capture changes in interoceptive awareness, and qualitative data from the teacher and researchers. This feasibility study was designed as an 8- to 10-week program (10 sessions minimum) to accommodate the school’s academic curriculum and support the participants’ academic progression. Three adolescents were recruited, ages 12–17, two of whom completed a shorter version of the program and one who dropped out. Results: Results indicated the gardening intervention recruitment and data collection procedures were feasible. Intervention was acceptable to participants. Outcome measures that produce both quantitative and qualitative changes are needed. Interoceptive measures show promise but require further refinement. Response to intervention seemed to be influenced by the participant’s psychosocial history but suggests possible changes in prosocial behavior. External factors such as absenteeism influenced aspects of participation, including frequency and duration of intervention. Conclusions: These findings suggest gardening interventions in occupational therapy are feasible and suitable for adolescents with a history of adversity. Potential exists for enhanced social connectedness, which supports mental health and well-being. Suggestions are offered for implementation and outcome measurements appropriate for this population. Full article
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15 pages, 2362 KB  
Article
Genetic Pleiotropy and Causal Pathways Linking Glycemic Traits to Asthma: An Integrated Proteogenomic Investigation
by Lin Chen, Juntao Lin, Yan Zhao, Guangli Zhang, Zhenxuan Kong, Chunlan Qiu, Kaicheng Peng, Hui Liu and Zhengxiu Luo
Children 2025, 12(11), 1443; https://doi.org/10.3390/children12111443 (registering DOI) - 24 Oct 2025
Abstract
Background: While diabetes is a recognized risk factor for asthma, the shared genetic components between diabetes/glycemic traits and asthma remain unclear. This study investigates the genetic associations, causal relationships, and underlying mechanisms linking these conditions. Methods: We assessed global genetic correlations using linkage [...] Read more.
Background: While diabetes is a recognized risk factor for asthma, the shared genetic components between diabetes/glycemic traits and asthma remain unclear. This study investigates the genetic associations, causal relationships, and underlying mechanisms linking these conditions. Methods: We assessed global genetic correlations using linkage disequilibrium score regression (LDSC), high-definition likelihood analysis (HDL), and genetic covariance analysis (GNOVA). Trait pairs with significant correlations subsequently underwent genetic overlap analysis (Genetic analysis integrating Pleiotropy and functional Annotation, GPA) and local genetic correlation analysis (Local Genetic Variant Association Analysis, LAVA). Cross-phenotype association (CPASSOC) and multitrait analysis of GWAS (MTAG) identified potential pleiotropic loci, followed by colocalization and functional annotation. Proteome-wide association study (PWAS) revealed proteins and pathways shared between diabetes/glycemic traits and asthma. Generalized summary-data-based Mendelian randomization (GSMR) was used to evaluate causal effects between diabetes/glycemic traits and asthma. Results: Significant genetic correlations were observed between body mass index (BMI) and asthma (rg = 0.280–0.397; FDR < 0.05), type 2 diabetes mellitus (T2DM) and asthma (rg = 0.240–0.289; FDR < 0.05) across all three methods. GPA revealed significant genome-wide genetic overlap, highest for BMI and asthma (pleiotropy association ratio [PAR] = 0.377) and T2DM-asthma (PAR = 0.353). LAVA identified 111 significant local correlation regions, predominantly between T2DM and asthma (70 regions). Colocalization analysis identified 24 shared pleiotropic loci, predominantly on chromosome 8. Local genetic correlation analysis revealed extensive correlations between T2DM and asthma. PWAS identified 46 shared proteins, with IL6R, MAPK3, and CSF2 being key hubs. Protein–protein interaction analysis highlighted enrichment in JAK-STAT signaling, Th1/Th2 differentiation, and IL-17 pathways. GSMR demonstrated causal effects of BMI (OR = 1.47, 95% CI: 1.42–1.53, FDR < 0.05) and T2DM (OR = 1.06, 95% CI: 1.04–1.08, FDR < 0.05) on increased asthma risk, with no evidence of reverse causality. Conclusions: Obesity (BMI) and T2DM exert causal effects on asthma risk via shared genetic loci and inflammatory pathways, particularly involving IL6R, MAPK3, CSF2, and JAK-STAT signaling. Targeting these colocalized proteins may offer potential therapeutic strategies. Full article
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11 pages, 568 KB  
Systematic Review
Furosemide-Induced Nephrocalcinosis in Premature Neonates: A Critical Review of Observational Data
by John Dotis, Alexandra Skarlatou, Maria Fourikou, Athina Papadopoulou and Elpis Chochliourou
Children 2025, 12(11), 1442; https://doi.org/10.3390/children12111442 (registering DOI) - 24 Oct 2025
Abstract
Background/Objectives: Furosemide is frequently used in preterm neonates for respiratory and fluid management but has been linked to nephrocalcinosis (NC), a renal complication with unclear long-term impact. Clarifying this association is crucial for safe diuretic use. Methods: A focused literature review included observational [...] Read more.
Background/Objectives: Furosemide is frequently used in preterm neonates for respiratory and fluid management but has been linked to nephrocalcinosis (NC), a renal complication with unclear long-term impact. Clarifying this association is crucial for safe diuretic use. Methods: A focused literature review included observational studies published between 1982 and 2025 reporting NC incidence by renal ultrasound in preterm infants receiving furosemide. Data on sample size, gestational age, birth weight, NC prevalence, and furosemide dosing/duration were extracted. Results were synthesized descriptively. Results: Twenty-two studies with 1489 infants were included. NC prevalence ranged 6–83%, higher in infants <32 weeks’ gestation or <1500 g. Across studies, incidence clustered at 17–41% between 4 weeks and term-equivalent age. Cumulative furosemide doses were generally three- to fourfold higher in NC groups (10–19 mg/kg cumulative vs. ≤5 mg/kg cumulative, p < 0.001). A dose-dependent risk was noted, with odds ratios increasing above a cumulative dose of 10 mg/kg. Some studies found no significant dose–response, indicating variability and confounding factors. NC was detected during NICU stay or around term-equivalent age; ~60% resolved after discontinuation, while persistent cases were associated with prolonged exposure and renal dysfunction. A recent multicenter, dose-escalation randomized trial showed that carefully dosed furosemide (≤2 mg/kg/day for 28 days) did not increase NC risk, though electrolyte disturbances were more frequent. Conclusions: Evidence supports a dose-related association between furosemide and NC in preterm infants. When administered cautiously within defined limits, risk may be mitigated. Careful dosing, monitoring, and further studies are essential for safe use. Full article
(This article belongs to the Section Pediatric Neonatology)
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15 pages, 380 KB  
Article
The Incidence of Pulmonary Hypertension and the Association with Bronchopulmonary Dysplasia in Preterm Infants of Extremely Low Gestational Age: Single Centre Study at the Maternity Hospital of University Medical Centre Ljubljana, Slovenia
by Tomaž Križnar, Štefan Grosek and Tina Perme
Children 2025, 12(11), 1441; https://doi.org/10.3390/children12111441 (registering DOI) - 24 Oct 2025
Abstract
Background: Pulmonary hypertension (PH) occurs in ~25% of infants with moderate-to-severe bronchopulmonary dysplasia (BPD) and is associated with substantial morbidity and mortality. The American Heart Association and American Thoracic Society recommend routine echocardiographic screening for PH in preterm infants with BPD at [...] Read more.
Background: Pulmonary hypertension (PH) occurs in ~25% of infants with moderate-to-severe bronchopulmonary dysplasia (BPD) and is associated with substantial morbidity and mortality. The American Heart Association and American Thoracic Society recommend routine echocardiographic screening for PH in preterm infants with BPD at 36 weeks’ postmenstrual age (PMA), yet the true incidence remains unclear owing to non-uniform diagnostic criteria. Emerging evidence suggests a potential role for earlier screening. Objectives: (i) to determine the incidence of pulmonary hypertension (PH) and bronchopulmonary dysplasia (BPD) in preterm infants of extremely low gestational age; (ii) to determine the incidence of PH among infants diagnosed with BPD (BPD-PH); and (iii) to evaluate the utility of early screening at 7 days of life and late screening at discharge in relation to subsequent BPD. Methods: We conducted a prospective cohort study of all infants born at 22 + 0 to 28 + 6 weeks’ gestation and admitted to our tertiary NICU between 1 September 2022 and 31 December 2024. Clinical and echocardiographic assessments for PH and BPD were performed by neonatologists trained in neonatal echocardiography. Results: Seventy-eight infants born at 22 + 0–28 + 6 weeks’ gestation were enrolled; 71 underwent early screening and 57 underwent late screening. Early echocardiography at day 7 and late screening at discharge identified no cases of PH. PH was diagnosed clinically and/or echocardiographically in 10 infants before day 7 and in one infant at 38 weeks’ PMA. BPD developed in 42 of 57 infants (73.7%). Conclusions: In this cohort of extremely low-gestational-age infants, echocardiographic screening performed by neonatologists detected no PH at day 7 and only one case at late screening (at 38 weeks’ PMA/before discharge). Most PH was identified prior to day 7 on clinical and/or echocardiographic grounds. Full article
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16 pages, 940 KB  
Review
Non-Classic Cornelia de Lange Syndrome Due to BRD4 Gene Alterations: A Literature Review
by Fortunato Lonardo, Mariateresa Falco, Claudia Costabile and Paolo Fontana
Children 2025, 12(11), 1440; https://doi.org/10.3390/children12111440 - 24 Oct 2025
Abstract
Cornelia de Lange Syndrome (CdLS) is a rare congenital disorder characterised by distinctive facial features, growth retardation, limb abnormalities and developmental delays. It is characterised by genetic heterogeneity and also presents a broad clinical variability, with a spectrum of manifestations ranging from mild [...] Read more.
Cornelia de Lange Syndrome (CdLS) is a rare congenital disorder characterised by distinctive facial features, growth retardation, limb abnormalities and developmental delays. It is characterised by genetic heterogeneity and also presents a broad clinical variability, with a spectrum of manifestations ranging from mild to severe, with milder phenotypes that can be difficult to ascertain based on physical characteristics. Pathogenic variations in the NIPBL gene account for the majority of cases, but variations in several other genes, including BRD4, have been identified as causative factors for non-classic or milder forms of the syndrome. This review aims to analyse the roles that BRD4 plays in the various pathways in which it is involved and to summarise current knowledge on atypical CdLS associated with BRD4 gene alterations, highlighting clinical features, molecular mechanisms, and implications for diagnostic assessment and patient care. Full article
(This article belongs to the Section Translational Pediatrics)
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10 pages, 563 KB  
Article
The Predictive Role of the Triglyceride/High-Density Lipoprotein Ratio and the Triglyceride–Glucose Index, Along with Anthropometric Measurements, in Diagnosing Non-Alcoholic Fatty Liver Disease in Obese Kids and Juveniles, and the Evaluation of Novel Cardiovascular Risk Markers in Pediatric NAFLD
by Emrah Çığrı, Funda Çatan İnan, Sedat Gülten, Mehmet Akif Bildirici, Ayşe Ece Gökkaya, Metin Asıleren, Mustafa Koyun, Bahadır Reis and Merve Esen
Children 2025, 12(11), 1439; https://doi.org/10.3390/children12111439 - 24 Oct 2025
Abstract
Aim: This current research aims to determine the predictive value of the ratio of triglyceride (TG)/high-density lipoprotein cholesterol (HDL-C), index of triglyceride–glucose (TyG), homeostatic model assessment for insulin resistance (HOMA-IR) score, and anthropometric measurements at the onset of non-alcoholic fatty liver disease (NAFLD) [...] Read more.
Aim: This current research aims to determine the predictive value of the ratio of triglyceride (TG)/high-density lipoprotein cholesterol (HDL-C), index of triglyceride–glucose (TyG), homeostatic model assessment for insulin resistance (HOMA-IR) score, and anthropometric measurements at the onset of non-alcoholic fatty liver disease (NAFLD) in obese kids and juveniles. It also sought to assess how novel cardiovascular risk markers are affected in obese pediatric patients with NAFLD. Materials and Methods: Between November 2024 and May 2025, a total of 199 pediatric patients were prospectively evaluated, including 150 children with obesity and 49 entirely healthy controls. Two categories of obese patients were created based on whether or not they had non-alcoholic fatty liver disease. These groups were compared with each other and with the control group in terms of HOMA-IR score, index of TyG, ratio of TG/HDL-C, anthropometric parameters (percentage of body fat [BFP], index of body mass [BMI], body fat mass [BFM], waist circumference [WC]), and cardiovascular risk markers. The cutoff values, sensitivity, and specificity of the HOMA-IR score, ratio of TG/HDL-C, anthropometric measurements, and index of TyG in predicting NAFLD were assessed using Receiver Operating Characteristic (ROC) analysis. Results: Obese kids and juveniles with NAFLD had significantly higher TG/HDL-C ratios, TyG indices, HOMA-IR scores, anthropometric measurements, and cardiovascular risk markers than those without NAFLD (p < 0.001). The TG/HDL-C ratio (AUC: 0.936; 81.8% sensitivity, 95.9% specificity) and the TyG index (AUC: 0.912; 81.8% sensitivity, 91.8% specificity) showed strong predictive value for NAFLD, while HOMA-IR and WC were found to be relatively weaker predictors. Conclusions: The index of TyG and ratio of TG/HDL-C are highly effective parameters in predicting NAFLD development in obese kids and juveniles. Those with increased WC and BFP should be closely monitored for NAFLD development. Pediatric patients with NAFLD should be carefully followed up for potential cardiovascular diseases. Full article
(This article belongs to the Section Pediatric Endocrinology & Diabetes)
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16 pages, 619 KB  
Article
Indications, Trends and Outcomes in Pediatric Lung Resections: A 12-Year Study in a Tertiary Referral Center
by Gloria Mandrile, Giulia Barone, Vittorio Guerriero, Girolamo Mattioli and Michele Torre
Children 2025, 12(11), 1438; https://doi.org/10.3390/children12111438 - 23 Oct 2025
Abstract
Background: Lung resections in children are rare but critical for congenital lung malformations (CLMs) and acquired pathologies; few studies have analyzed the full spectrum of indications. This study evaluated indications, complications, outcomes, and temporal trends in a tertiary pediatric center. Methods: [...] Read more.
Background: Lung resections in children are rare but critical for congenital lung malformations (CLMs) and acquired pathologies; few studies have analyzed the full spectrum of indications. This study evaluated indications, complications, outcomes, and temporal trends in a tertiary pediatric center. Methods: We retrospectively analyzed patients who underwent lung resection (2012–2024), focusing on indications, approaches, complications, and outcomes. Comparisons between pathologies (CLMs vs. acquired pathologies), approaches (thoracoscopy vs. thoracotomy), an temporal trends were evaluated. Results: Among 160 patients (mean age: 7.8 years), acquired lesions (68.6%) were more common than CLMs (31.4%), predominating in children under 8 years. Compared with thoracotomy, thoracoscopy (72.8% of cases, conversion rate: 22.8%) was correlated with shorter operative times (p < 0.001) and hospital stays (p = 0.001). The complication rate was 19.5%, with 71.9% of patients achieving disease-free, asymptomatic status at follow-up. Risk factors for conversion from thoracoscopy to open surgery included intraoperative adhesions (p = 0.003), underlying pathology (p = 0.013), and age < 8 years (p = 0.017). Compared with acquired lesions, CLMs were associated with fewer complications (14.3% vs. 23.1%, p = 0.041) and more favorable outcomes (89.2% vs. 64.7%; p < 0.05). Over time, the use of thoracoscopy increased (p = 0.012), with reduced operative time (p = 0.005); complication and outcome rates remained stable. Conclusions: Pediatric lung resections address diverse pathologies; outcomes are linked to the pathology, and CLMs are associated with lower complication rates in our cohort. Thoracoscopy has progressively become the preferred approach in the last decade, offering advantages particularly in postoperative recovery, though its success depends on careful, pathology-driven patient selection. Full article
(This article belongs to the Special Issue Challenges and Innovations in Pediatric General Surgery)
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9 pages, 325 KB  
Article
Implementation of the Finnish Good Practice “Smart Family” in Poland
by Justyna Nowak, Agata Szymczak, Barbara Kaczmarska, Katarzyna Anna Klonowska, Marta Morawska, Heli Kuusipalo, Emma Koivurinta, Kati Kuisma, Päivi Mäki, Taina Sainio, Nella Savolainen and Katarzyna Brukało
Children 2025, 12(11), 1437; https://doi.org/10.3390/children12111437 - 23 Oct 2025
Abstract
Background: Childhood obesity is a growing public health challenge in Poland and worldwide, associated with serious long-term health consequences. Effective prevention requires family-centered, evidence-based interventions that actively engage both children and their caregivers. This study presents the Finnish Smart Family practice—an evidence-based lifestyle [...] Read more.
Background: Childhood obesity is a growing public health challenge in Poland and worldwide, associated with serious long-term health consequences. Effective prevention requires family-centered, evidence-based interventions that actively engage both children and their caregivers. This study presents the Finnish Smart Family practice—an evidence-based lifestyle counseling method developed by the Finnish Heart Association—and describes its adaptation and implementation in Poland as part of the EU Health4EUkids project. The study emphasizes the method’s practical utility for professionals working with families of children with obesity. Methods: The Smart Family approach is a structured lifestyle counseling method based on findings from the Special Turku Coronary Risk Factor Intervention Project (STRIP) that is grounded in health psychology and strength-based counseling principles. Unlike traditional counseling, which focuses mainly on information transfer, Smart Family promotes motivation, families’ active participation, and recognition of their strengths in areas such as nutrition, physical activity, sleep, and oral hygiene. The method uses practical tools including the Smart Family card, other supporting materials, and dedicated online platforms for both families and healthcare providers. These tools enable families to self-assess their lifestyle, select discussion topics during visits, and set achievable goals while supporting professionals in initiating non-judgmental, collaborative conversations. In Poland, the program was adapted using culturally appropriate materials and professional training, followed by pilot implementation in primary healthcare and educational settings that included pre-implementation planning, practical training sessions, the application of intervention tools, and outcome evaluation. Results: Pilot implementation demonstrated high usability and effectiveness. The approach enabled non-judgmental, supportive engagement with families, facilitated active participation in setting health goals, and promoted sustainable lifestyle changes in nutrition, physical activity, sleep, and other health behaviors. Evaluation highlighted the importance of supporting program objectives at the national level, standardizing child healthcare practices, and engaging media and local authorities to create a supportive ecosystem. Conclusions: The Polish experience confirms that Smart Family is an evidence-based intervention that strengthens professional competence, provides practical tools for family-centered care, and supports the long-term prevention of child-hood obesity and related non-communicable diseases. Its integration into healthcare and educational settings offers a promising strategy for improving public health outcomes. Full article
(This article belongs to the Section Global Pediatric Health)
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12 pages, 261 KB  
Article
Pediatric Inhaled Medication: A Cross-Sectional Analysis on Usage Trends and Parental Perceptions in Romania
by Alina Angelica Ciolpan, Mihai Craiu, Andreea Pușcașu, Mihai Alexandru Borcan and Valentina Daniela Comănici
Children 2025, 12(11), 1436; https://doi.org/10.3390/children12111436 - 23 Oct 2025
Abstract
Background: Inhaled medications are central in managing pediatric respiratory diseases, yet device complexity and nebulizer use often challenge caregivers and affect adherence. This study assessed current usage patterns and parental perceptions of inhaled therapies in Romania, aiming to identify modifiable factors for targeted [...] Read more.
Background: Inhaled medications are central in managing pediatric respiratory diseases, yet device complexity and nebulizer use often challenge caregivers and affect adherence. This study assessed current usage patterns and parental perceptions of inhaled therapies in Romania, aiming to identify modifiable factors for targeted education. Methods: A cross-sectional observational survey was distributed via SVC® (Spitalul Virtual pentru Copii—Virtual Children’s Hospital), a widely accessed social media platform for Romanian parents. Data included demographics, inhaled medication use, prescribing sources, adherence, and treatment perceptions. Results: A total of 1825 parents participated, mostly urban residents (87.6%). Chronic respiratory disease, mainly asthma, was reported in 7.3% of children. Inhaled therapy was used in 71.9% of cases, predominantly saline solutions, bronchodilators, and corticosteroids, marking a decline compared with the past decade. Nebulizers (74.1%) were the main devices used. Prescriptions were largely pediatrician-based, though self-medication occurred, particularly with saline solutions, often influenced by non-medical sources (p = 0.003). Parents of children with chronic disease were less likely to self-medicate (p = 0.042), especially with β2-agonists and corticosteroids (p < 0.001). Additionally, 31.3% reported use of complementary remedies, including homeopathy. Overall, 73.5% perceived inhaled therapy as effective, with adverse events reported by only 8.3%. Conclusions: Inhaled therapy remains prevalent in Romanian children, though self-medication and alternative treatments persist, shaped by cultural factors and limited medical education. Parents of children with chronic disease show better adherence and reliance on prescribed therapy. Enhancing parental education via accessible digital platforms may reduce inappropriate practices and improve outcomes in low-resource settings. Full article
(This article belongs to the Special Issue Lung Function and Respiratory Diseases in Children and Infants)
13 pages, 837 KB  
Article
Real-World Effectiveness of DIMS Spectacle Lenses for Myopia Control in a Turkish Pediatric Population: A Retrospective Study Using Age-Specific Physiological Growth Curves
by Nilay Akagun and Ugur Emrah Altiparmak
Children 2025, 12(11), 1435; https://doi.org/10.3390/children12111435 - 23 Oct 2025
Abstract
Background/Objectives: This study aimed to evaluate the one-year real-world effectiveness of Defocus Incorporated Multiple Segments (DIMS) spectacle lenses in controlling myopia progression in a Turkish pediatric cohort and to identify predictors of treatment response using age-specific physiological growth curves. Methods: This retrospective single-center [...] Read more.
Background/Objectives: This study aimed to evaluate the one-year real-world effectiveness of Defocus Incorporated Multiple Segments (DIMS) spectacle lenses in controlling myopia progression in a Turkish pediatric cohort and to identify predictors of treatment response using age-specific physiological growth curves. Methods: This retrospective single-center study included 54 patients (108 eyes) aged 6–16 years with myopia who wore DIMS spectacle lenses full time for 12 months. The primary outcomes were spherical equivalent refraction (SER) success and axial length (AL)-based treatment response. Treatment success was defined as an SER progression of ≤0.50 dioptres per year and AL elongation within age-specific physiological limits. Subgroup analyses were performed according to age, gender, and the baseline AL group. Results: After 12 months, the mean AL elongation was 0.14 ± 0.31 mm, and the mean SER change was −0.28 ± 0.42 D. SER-based success was achieved in 85.2% of eyes. For AL-based response, 61.1% of eyes showed a good response, 16.7% showed a low–moderate response, and 22.2% had no response. Eyes with moderate baseline AL exhibited significantly less axial elongation than those with high baseline AL (p = 0.001). Children aged ≥ 10 years demonstrated better AL-based responses (p = 0.016). The baseline AL group significantly predicted the AL treatment response, while both the baseline AL group and gender predicted SER success. Gender was associated with SER outcomes but not with AL-based response. Conclusions: DIMS spectacle lenses effectively reduced myopia progression and axial elongation in this real-world Turkish pediatric cohort. Baseline AL and gender were significant predictors of treatment outcomes. Incorporating age-specific physiological growth curves provided an individualized framework for interpreting treatment success. Further prospective studies with larger samples and longer follow-up are warranted to confirm these findings. Full article
(This article belongs to the Section Pediatric Ophthalmology)
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10 pages, 410 KB  
Review
Cystic Fibrosis and CFTR Modulators: The Impact on Bone Density, Muscle Mass and Strength in Children and Young Adolescents
by Katerina Iordanidou, Nikolaos D. Karakousis, Elpis Hatziagorou, Elisavet-Anna Chrysochoou, Maria Galogavrou, Athina Sopiadou and Maria Papagianni
Children 2025, 12(11), 1434; https://doi.org/10.3390/children12111434 - 23 Oct 2025
Abstract
Background/Objectives: Cystic fibrosis (CF) is a multisystemic and genetic disorder. Mutations in the CF transmembrane conductance regulator (CFTR) gene impair the function of the CFTR protein, leading to various complications in multiple organs, mainly the lungs. Methods: In this article, we [...] Read more.
Background/Objectives: Cystic fibrosis (CF) is a multisystemic and genetic disorder. Mutations in the CF transmembrane conductance regulator (CFTR) gene impair the function of the CFTR protein, leading to various complications in multiple organs, mainly the lungs. Methods: In this article, we have tried to investigate the potential impact of CFTR modulators on bone density, muscle mass, and strength in children and young adolescents with CF by using the existing literature and conducting a narrative (non-systematic) review. Results: It has been demonstrated that CFTR modulators may positively influence bone mineral density. On the other hand, the impact of CFTR modulators on muscle mass and strength seems to vary among studies. Conclusions: Besides the current literature, further studies are needed to validate the existing claims. Full article
(This article belongs to the Section Pediatric Pulmonary and Sleep Medicine)
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11 pages, 500 KB  
Article
Early Use of Incisional Negative Pressure Wound Therapy in Pediatric Abdominal and Thoracic Surgery: A Single-Center Retrospective Study on Clinical and Economic Outcomes
by Biagio Nicolosi, Felice Curcio, Marina Maffeo, Marika Di Leva, Mirco Gregorini, Emanuele Buccione and Riccardo Coletta
Children 2025, 12(11), 1433; https://doi.org/10.3390/children12111433 - 23 Oct 2025
Abstract
Aim: To evaluate the effectiveness and economic impact of early Incisional Negative Pressure Wound Therapy (iNPWT) in promoting surgical wound healing in pediatric patients undergoing abdominal and thoracic surgery. Background: Surgical wound complications, such as dehiscence and infection, are frequent in [...] Read more.
Aim: To evaluate the effectiveness and economic impact of early Incisional Negative Pressure Wound Therapy (iNPWT) in promoting surgical wound healing in pediatric patients undergoing abdominal and thoracic surgery. Background: Surgical wound complications, such as dehiscence and infection, are frequent in pediatric patients, especially in high-risk cases. Although iNPWT is increasingly used in surgical care, evidence supporting its efficacy in pediatric populations remains limited. Methods: This single-center, retrospective observational study analyzed 49 pediatric patients who underwent abdominal or thoracic surgery between January and December 2023. Patients received either intraoperative iNPWT (early application) or standard dressings. The outcomes assessed included time to complete wound healing, incidence of complications, pain levels, and healthcare costs. Results: Patients treated with early iNPWT showed significantly faster wound healing and fewer complications—particularly dehiscence and infections—compared to those receiving standard dressing. Pain perception did not significantly differ between groups. Although the initial costs of iNPWT were higher, overall costs were lower due to fewer complications and shorter hospital stays. Conclusions: Early iNPWT is a clinically effective and cost-efficient intervention for pediatric surgical patients at high risk of wound complications. However, limitations related to the retrospective design and small sample size suggest that prospective multicenter studies are needed to confirm these findings and support the development of standardized pediatric protocols. Full article
(This article belongs to the Special Issue Innovations and Evolving Practices in General Paediatric Surgery)
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11 pages, 377 KB  
Systematic Review
Quality of Patient Information on Allergic Rhinitis in Children on the Internet
by Nikolaos Kitsos, Aspasia Michoula and Ioanna Grivea
Children 2025, 12(11), 1432; https://doi.org/10.3390/children12111432 - 23 Oct 2025
Abstract
Background: The vast majority of patients, considering information for allergic conditions, use the Internet as a source of health information. The aim of our study is to assess the quality of patient information on allergic rhinitis available on the internet. Methods: [...] Read more.
Background: The vast majority of patients, considering information for allergic conditions, use the Internet as a source of health information. The aim of our study is to assess the quality of patient information on allergic rhinitis available on the internet. Methods: Three hundred Websites, found through the most recognizable search engines, were evaluated using the modified Ensuring Quality Information for Patients (EQIP) instrument. Results: Eighty-five websites were assessed after the exclusion of duplicates and Websites in languages other than English. Websites that scored higher than 21 (over the 75th percentile) were categorized as high-score sites. Websites that were developed by health professionals tended to have a higher score. The EQIP score of the websites ranged between 5 and 26 out of the total of 34 points, with a median value of 16.5 points. Conclusions: The quality of patient information on allergic rhinitis on the Internet is inferior, and the existing Websites present insufficient information. Full article
(This article belongs to the Section Pediatric Allergy and Immunology)
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14 pages, 286 KB  
Article
Tracing the Cognitive–Motor Connection: Prospective-Longitudinal Associations Between Early Parent–Toddler Literacy Activities and Subsequent Gross Motor Skills in Adolescence
by Nairy Kazandjian, Kianoush Harandian, Marie-Michèle Dufour, Elena A. Chichinina, Michel Desmurget and Linda S. Pagani
Children 2025, 12(11), 1431; https://doi.org/10.3390/children12111431 - 23 Oct 2025
Abstract
Background/objectives: Early literacy is widely promoted, yet its broader developmental benefits remain underexamined regarding key indicators of brain development. This study examines whether early literacy exposure in toddlerhood predicts motor skill development at the end of kindergarten. Methods: Participants comprised 1006 [...] Read more.
Background/objectives: Early literacy is widely promoted, yet its broader developmental benefits remain underexamined regarding key indicators of brain development. This study examines whether early literacy exposure in toddlerhood predicts motor skill development at the end of kindergarten. Methods: Participants comprised 1006 boys and 991 girls from the Quebec Longitudinal Study of Child Development (QLSCD) birth cohort. Early literacy stimulation was measured at age 2 years using parent reports of frequency of shared reading, looking at books or comics, and pre-writing activities such as scribbling and tracing. At age 6 years, child motor development was assessed by trained examiners. Sex-stratified multiple regression models were examined, adjusting for pre-existing and concurrent child and family characteristics. Results: Early literacy stimulation was significantly associated with better motor control skills among girls (β = 0.10, p < 0.05). For boys, a non-significant positive trend was observed for both motor and locomotion skills. Conclusions: Our findings underscore the lasting influence of early literacy stimulation and subsequent motor skills—particularly for girls who may receive less gross motor encouragement than boys. As such, promoting literacy-rich environments in toddlerhood is a family strategy to support healthy, confident, and active youth development. Full article
(This article belongs to the Special Issue Physical and Motor Development in Children)
13 pages, 953 KB  
Article
Early-Life Events and the Prevalence of Gut–Brain Interaction Disorders in Children
by Atchariya Chanpong, Natchayada Ponjorn, Nattaporn Tassanakijpanich, Vanlaya Koosakulchai, Pornruedee Rachatawiriyakul, Sirinthip Kittivisuit, Puttichart Khantee and Kamolwish Laoprasopwattana
Children 2025, 12(11), 1430; https://doi.org/10.3390/children12111430 - 23 Oct 2025
Abstract
Background/Objectives: Disorders of gut–brain interaction (DGBI) include a spectrum of disorders with chronic/recurrent gastrointestinal symptoms, caused by dysregulation of microbiota–gut–brain interaction. Early-life events have been suggested as the main factors influencing the microbiota–gut–brain axis. We aimed to evaluate the prevalence of DGBI [...] Read more.
Background/Objectives: Disorders of gut–brain interaction (DGBI) include a spectrum of disorders with chronic/recurrent gastrointestinal symptoms, caused by dysregulation of microbiota–gut–brain interaction. Early-life events have been suggested as the main factors influencing the microbiota–gut–brain axis. We aimed to evaluate the prevalence of DGBI in 3-year-old children and its relationship with early-life events. Methods: The parents of children aged 3 years, who had been followed up in a well-baby clinic since they were 2 months old, were asked about any GI symptoms their child had experienced during the check-up visits between September 2023 and June 2024. The final diagnosis of DGBI was based on ROME IV criteria. Demographic data, including early-life factors, were collected. Results: Overall, 568 children (48.6% boys) were included, of whom 139 (24.5%) had symptoms consistent with at least one DGBI diagnosis. The most prevalent DGBI was functional constipation (20.4%), followed by colic (4.6%), infant regurgitation (2.8%), and dyschezia (1.6%). Approximately 48% of the children were breastfed for ≥6 months, and 21% were exposed to ≥1 antibiotic/antiviral drugs in the first year of life. DGBI prevalence was significantly higher in girls than in boys (28.1% vs. 20.7%; p = 0.041). Exclusive breastfeeding was the most significant protective factor against DGBI, particularly if performed for ≥3 months. Conclusions: Sex was the most significant factor affecting DGBI prevalence in children aged ≤3 years; breastfeeding offers the most effective protection against DGBI development. Full article
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8 pages, 1978 KB  
Case Report
Neonatal Kaposiform Hemangioendothelioma with Kasabach–Merritt Phenomenon Presenting as Severe Airway Obstruction at Birth: A Case Report
by Soyoung Shin and Yejee Shim
Children 2025, 12(11), 1429; https://doi.org/10.3390/children12111429 - 23 Oct 2025
Abstract
Background/Objectives: Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor of infancy, often complicated by Kasabach–Merritt phenomenon (KMP), a consumptive coagulopathy characterized by severe thrombocytopenia and hypofibrinogenemia. Airway involvement at birth is exceptionally rare and can be life-threatening. This study reports [...] Read more.
Background/Objectives: Kaposiform hemangioendothelioma (KHE) is a rare, locally aggressive vascular tumor of infancy, often complicated by Kasabach–Merritt phenomenon (KMP), a consumptive coagulopathy characterized by severe thrombocytopenia and hypofibrinogenemia. Airway involvement at birth is exceptionally rare and can be life-threatening. This study reports the clinical presentation and treatment course of a full-term male neonate with severe airway obstruction caused by KHE with KMP. Case Presentation: The patient had unremarkable prenatal imaging but presented at birth with severe respiratory distress requiring emergent intubation. Physical examination revealed firm violaceous swelling over the right cervicothoracic region. Laboratory tests showed profound thrombocytopenia (22,000/μL), hypofibrinogenemia (75 mg/dL), and coagulopathy. Imaging findings were consistent with KHE complicated by KMP. Due to bleeding risk, the biopsy was not performed. Initial treatment included platelet and plasma transfusions, intravenous immunoglobulin (IVIG), corticosteroids, and antithrombin III replacement. Vincristine was discontinued owing to gastrointestinal toxicity. Sirolimus therapy was initiated on day 14. Following sirolimus initiation, rapid platelet recovery was observed. At three months, marked tumor regression was documented. After mild recurrence, sirolimus was reintroduced, and the patient remained stable at 16-month follow-up. Conclusions: This case underscores the critical importance of prompt airway stabilization, early recognition of consumptive coagulopathy, and sirolimus-based therapy in managing neonatal KHE with airway involvement. Full article
(This article belongs to the Special Issue Providing Care for Preterm Infants)
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20 pages, 285 KB  
Article
The Polish Version of the Parental Assistance with Child Emotion Regulation (PACER) Questionnaire: Preliminary Psychometric Properties and Links with Parental Burnout, Mental Health Outcomes, and Emotion Beliefs
by Paweł Larionow, Monika Mazur, Natalia Pilarska, Karolina Mudło-Głagolska, Dorota Szczygieł and David A. Preece
Children 2025, 12(11), 1428; https://doi.org/10.3390/children12111428 - 22 Oct 2025
Abstract
Background/Objectives: This study presents a brief report on the preliminary psychometric properties of a first Polish version of the Parental Assistance with Child Emotion Regulation (PACER) Questionnaire. The PACER measures ten emotion regulation (ER) strategies parents use to assist their children in [...] Read more.
Background/Objectives: This study presents a brief report on the preliminary psychometric properties of a first Polish version of the Parental Assistance with Child Emotion Regulation (PACER) Questionnaire. The PACER measures ten emotion regulation (ER) strategies parents use to assist their children in their ER. We aimed to examine PACER’s internal consistency reliability, convergent, divergent and discriminant validity. Methods: The sample included 74 Polish-speaking parents aged from 27 to 50, recruited in 2025. Along with the PACER, we used a robust set of psychometric tools for measuring parental burnout, anxiety and depression symptoms, somatic complaints, well-being, and beliefs about emotions. Results: All PACER subscale scores demonstrated good-to-excellent internal consistency reliability (i.e., Cronbach’s alpha of ≥0.83). Encouraging adaptive strategies (e.g., reappraisal) in one’s children was associated with better outcomes (e.g., lower parental burnout and psychopathology symptoms), whereas maladaptive strategies (e.g., avoidance) were associated with worse outcomes. We also demonstrated that PACER strategy scores were statistically separable from maladaptive beliefs about emotions, indicating good discriminant validity. Conclusions: Overall, the Polish PACER demonstrated promising psychometric properties and strong clinical relevance. These findings can help to inform interventions targeted at improving parents’ capacity to help their children regulate emotions, which in turn may help to prevent parental burnout. Full article
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14 pages, 272 KB  
Review
Beyond Weight Loss: Optimizing GLP-1 Receptor Agonist Use in Children
by Hussein Zaitoon, Aimee D. Wauters, Luisa M. Rodriguez and Jane L. Lynch
Children 2025, 12(11), 1427; https://doi.org/10.3390/children12111427 - 22 Oct 2025
Abstract
Background/Objectives: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have emerged as a transformative therapy for obesity and type 2 diabetes (T2D) in pediatric populations. This review synthesizes current evidence on efficacy, safety, and knowledge gaps in children and adolescents. Methods: A structured review [...] Read more.
Background/Objectives: Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have emerged as a transformative therapy for obesity and type 2 diabetes (T2D) in pediatric populations. This review synthesizes current evidence on efficacy, safety, and knowledge gaps in children and adolescents. Methods: A structured review of randomized controlled trials, extension studies, and mechanistic investigations evaluating GLP-1RAs in pediatric obesity and T2D was conducted. Outcomes of interest included body weight, BMI, body composition, glycemic control, and adverse events. Results: In adolescents, liraglutide and semaglutide consistently produce clinically meaningful reductions in BMI, body weight, and waist circumference, with modest improvements in systolic blood pressure and minimal effects on lipid levels or HbA1c. A newer trial in children 6 to <12 years showed liraglutide reduced BMI compared with placebo, with GI events consistent with prior safety profiles. Weight loss tends to include both fat and lean components; rapid weight loss may impair muscle strength or bone density if resistance exercise and adequate protein intake are not ensured. Risks include micronutrient gaps, misuse, and uncertain long-term effects on growth and puberty. These important considerations remain largely unaddressed in pediatric studies, and adult data can’t be directly extrapolated to children due to developmental, hormonal, and physiological differences. Conclusions: GLP-1 RAs are a promising adjunct to lifestyle therapy for pediatric obesity, but pediatric-specific protocols are needed to safeguard musculoskeletal health, ensure nutritional adequacy, and minimize misuse. Critical gaps remain in pediatric pharmacokinetics, dosing strategies, and long-term developmental safety. Further research is essential to develop evidence-based guidelines for safe and effective pediatric anti-obesity therapy. Full article
(This article belongs to the Section Pediatric Endocrinology & Diabetes)
17 pages, 1436 KB  
Article
Aloe vera Adjunctive Therapy for Pediatric Oral Candidiasis: A Prospective Controlled Study on Microbial Clearance and Treatment Adherence
by Alexandru-Emilian Flondor, Irina-Georgeta Sufaru, Maria-Alexandra Martu, Vasilica Toma, Stefan-Lucian Burlea and Ioana Martu
Children 2025, 12(11), 1426; https://doi.org/10.3390/children12111426 - 22 Oct 2025
Abstract
Background/Objectives: Oral candidiasis is frequently encountered in pediatric populations, particularly in infants and toddlers, where the development of immunity and inconsistent oral hygiene contribute to disease susceptibility. While topical antifungal agents remain the standard of care, treatment challenges persist, especially regarding adherence and [...] Read more.
Background/Objectives: Oral candidiasis is frequently encountered in pediatric populations, particularly in infants and toddlers, where the development of immunity and inconsistent oral hygiene contribute to disease susceptibility. While topical antifungal agents remain the standard of care, treatment challenges persist, especially regarding adherence and recurrence. Aloe vera, recognized for its antimicrobial, anti-inflammatory, and mucosal healing properties, may offer therapeutic benefits when used in conjunction with standard regimens. This study aimed to evaluate the adjunctive effect of topical Aloe vera gel, when added to standard antifungal therapy, on reducing fungal load and improving treatment adherence in children with moderate oral candidiasis. Methods: A prospective controlled study was conducted among 54 children diagnosed with moderate oral candidiasis. Participants were randomly assigned to receive either standard topical nystatin or nystatin in conjunction with Aloe vera gel over a 7 day treatment duration. Fungal load was assessed using colony-forming units (CFU) counts from oral swabs collected at baseline and day 7, analyzed via ANCOVA. Additional parameters included treatment adherence, compared using an independent t-test, and clinical recurrence at a 14-day post-treatment follow-up, assessed through logistic regression. Results: Baseline characteristics were similar across groups. By day 7, children in the Aloe vera group exhibited a greater reduction in fungal load compared to those receiving standard therapy alone. Adherence was significantly higher in the aloe group (92.73% vs. 89.21%; p < 0.0001). Regression analysis identified both baseline fungal burden and adherence as factors associated with an increased risk of recurrence. Conclusions: The addition of Aloe vera gel to standard therapy may support a more effective fungal clearance and improved treatment adherence in children with moderate oral candidiasis, suggesting its potential as a complementary treatment option. Given the single-center design, short follow-up, and underpowered recurrence analysis, these findings should be considered preliminary, pending confirmation in larger studies with symptom-anchored endpoints. Full article
(This article belongs to the Special Issue New Research Progress of Clinical Pediatric Dentistry: 2nd Edition)
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15 pages, 928 KB  
Article
Addressing Access to Child Mental Health Services in Primary Care: Implementation and Feasibility of the Colorado Pediatric Psychiatry Consultation and Access Program
by Kaitlin A. Whelan, J. Kyle Haws, Susan Young, Ryan Asherin, David Keller and Sandra Fritsch
Children 2025, 12(11), 1425; https://doi.org/10.3390/children12111425 - 22 Oct 2025
Viewed by 14
Abstract
Background/Objectives: Pediatric mental health is a major public health concern worldwide and primary care providers struggle to meet the growing demand for mental healthcare. Child Psychiatry Access Programs have emerged to fill gaps in primary care provider (PCP) training, confidence, and workflow support. [...] Read more.
Background/Objectives: Pediatric mental health is a major public health concern worldwide and primary care providers struggle to meet the growing demand for mental healthcare. Child Psychiatry Access Programs have emerged to fill gaps in primary care provider (PCP) training, confidence, and workflow support. This study aimed to describe the iterative development of a Child Psychiatry Access Program and present initial findings on its reach and feasibility in supporting PCPs. Methods: The Practical, Robust Implementation and Sustainability Model (PRISM) implementation framework guided the development and evaluation of the program. Pre-implementation surveys and invested partner interviews informed the creation of a multidisciplinary program comprising three components: (1) consultation services and resource navigation, (2) education and training, and (3) provider care guides. The program was then implemented, and reach was assessed via consultation calls, attendance at education and training series, resource navigation encounters, and care guide usage. Feasibility was evaluated through pre- and post-series self-reported ratings across six learning objectives. Results: Pre-implementation evaluation indicated high provider interest across all educational modalities. The resulting program included consultation services, education and training, resource navigation, and provider care guides. Educational trainings led to significant improvements in self-reported knowledge and confidence across six learning objectives, including assessment, treatment planning, family engagement, and navigating local resources. Resource navigation primarily facilitated ongoing management within the primary care setting, with PCPs retaining care in the majority of cases. Engagement with the Colorado Care Guide demonstrated sustained reach, with over 4600 page views from 1300 active users, reflecting broad and ongoing utilization of program resources. Consultation call data mirrored these trends, highlighting both frequently addressed diagnoses and expanding program reach over time. Conclusions: Child psychiatry access programs help support access to youth mental health care in the primary care space and offer potential solutions to workforce limitations during an era of increasing mental health concerns in youth and teens. Findings from this implementation may inform adaptation of child psychiatry access programs in other regions seeking to expand mental health support for children and adolescents in primary care settings. Full article
(This article belongs to the Special Issue New Insights in Pediatric Mental Healthcare)
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17 pages, 319 KB  
Review
Burns in Early Childhood: Age-Specific Causes, Risks, Management, and Implications—A Narrative Review
by Gloria Pelizzo, Valeria Calcaterra, Carlotta Paola Maria Canonica, Vittoria Carlotta Magenes, Michela Marinaro, Eleonora Durante, Erika Cordaro and Gianvincenzo Zuccotti
Children 2025, 12(11), 1424; https://doi.org/10.3390/children12111424 - 22 Oct 2025
Viewed by 53
Abstract
Burn injuries represent a significant global burden, with children under the age of five among the most vulnerable groups. This narrative review will explore the main causes of burns in early childhood (under 6 years of age), the associated risks, current treatment approaches, [...] Read more.
Burn injuries represent a significant global burden, with children under the age of five among the most vulnerable groups. This narrative review will explore the main causes of burns in early childhood (under 6 years of age), the associated risks, current treatment approaches, and the long-term implications of these injuries. It will also highlight areas where further research is needed to improve prevention and management strategies for burns in this vulnerable population. Results showed that burns in children under six years old represent a significant clinical and preventive challenge, with physical, psychological, and social implications. Research has identified common causes, particularly scalds from hot liquids, while advancing innovative treatments such as bioengineered skin substitutes, virtual reality, and telemedicine. Preventive interventions at the household and community levels have also proven effective. However, major limitations remain: studies often lack age-specific focus, rely on retrospective data, underrepresent low-resource settings, and lack standardized protocols. To improve outcomes, future research must adopt a more targeted, multidisciplinary approach and address long-term physical and psychological effects to ensure comprehensive, age-appropriate care. Full article
(This article belongs to the Section Pediatric Surgery)
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