INDIAN JOURNAL OF PEDIATRICS印度儿科学杂志
INDIAN JOURNAL OF PEDIATRICS(英文缩写 INDIAN J PEDIATR),ISSN 0019-5456,eISSN 0973-7693,中文译名:印度儿科学杂志 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。
发文量统计区间：2025-09-27 至 2026-09-27，按本站收录文献的发表日期统计。
期刊介绍
历年影响因子趋势
| JCR 数据年份 | 影响因子 | JCR 分区 |
|---|---|---|
| 2021 | 5.319 | Q1 |
| 2022 | 4.300 | Q1 |
| 2023 | 2.100 | Q2 |
| 2024 | 2.000 | Q2 |
| 2025 | 2.400 | Q2 |
INDIAN JOURNAL OF PEDIATRICS 最新收录文献
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4. Safety and Tolerability of Early Minimal Enteral Nutrition from Birth in Preterm Neonates with Antenatal Doppler Abnormalities.
PMID:日期:2026-09-21Small-for-gestational-age neonates with absent / reversal of end diastolic flow (AREDF) in umbilical artery doppler are at increased risk of perinatal complications. The authors conducted a retrospective cohort study in SGA neonates (≤34 wk) with AREDF to study the tolerability of early minimal enteral nutrition (MEN) initiated from birth, and compared the outcomes with those without AREDF. Out of 207 SGA neonates, 82 had AREDF. AREDF group had a significantly lower mean birth weight (1185 g vs. 1368 g; p <0.001) and a higher incidence of birth by caesarean section (85.4% vs. 60.8%, p < 0.0001). There was no difference in the primary outcome of feed intolerance [20.7% vs. 12.8%; RR 1.62 (0.87-3.02)]. Mortality, necrotizing enterocolitis (NEC), culture-proven sepsis were also similar between the groups. Multivariable logistic regression analysis revealed that gestational age and not AREDF status was associated with increased odds of feed intolerance.
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5. Optimising Bone Health in Adolescents: Preventing Poor Bone Accrual and Secondary Osteoporosis.
PMID:日期:2026-09-21Bone health during adolescence is influenced by a complex interplay of various factors, disruptions in which may impair bone mineral accrual and predispose to both primary and secondary osteoporosis. Adolescents with chronic medical conditions are at particularly high risk of skeletal deficits. Clinical data from Indian cohorts demonstrate a high burden of low bone mineral density in these populations, with important observations such as the presence of vertebral fractures even in adolescents with BMD Z-scores above -2.0, highlighting the limitations of relying on densitometry alone. Assessment of bone health requires careful interpretation of dual-energy X-ray absorptiometry in the context of growth, with use of size-adjusted measures such as bone mineral apparent density. Vertebral fracture assessment may improve detection of clinically silent skeletal fragility. Optimisation of bone health includes ensuring adequate nutrition, promoting physical activity, and managing underlying disease, with pharmacological therapy considered in selected cases. Early identification and targeted intervention during adolescence provide an opportunity to improve peak bone mass and reduce long-term skeletal morbidity.
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6. Quality Improvement in Kangaroo Mother Care Compliance and Its Duration.
PMID:日期:2026-09-21该文献暂无摘要。
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7. Clinical Effectiveness of High-Flow Nasal Cannula and Bilevel Positive Airway Pressure in Children with Critical Asthma - A Systematic Review and Meta-Analysis.
PMID:日期:2026-09-21The most common reason for admission to the pediatric intensive care unit (PICU) is asthma. The high-flow nasal cannula (HFNC) and bilevel positive airway pressure (BiPAP) are adjunctive therapies in the treatment of critical asthma. The purpose of this systematic review is to evaluate the clinical effectiveness of HFNC and BiPAP in the treatment of Pediatric critical asthma. Following PRISMA 2020 guidelines, a comprehensive search was conducted in PubMed, Scopus, Google Scholar, Embase, Lilacs, and ProQuest till September 2025. Bias assessment was done using the JBI risk of bias tool. In STATA version 16, 2019 software, a meta-analysis was conducted using eligible study data, with a 95% confidence interval. The analysis included five studies evaluating the clinical effectiveness of HFNC and BiPAP. A moderate to low risk of bias was demonstrated by the majority of the studies. A statistically significant difference was not observed between the HFNC and BIPAP groups in terms of the length of stay in the PICU (p = 0.48), the length of stay in the hospital (p = 0.13), the rate of escalation, the duration of respiratory support, the level of sedation, or the amount of adjunctive medication needed. There were insufficient data on intubation rates and mortality. Furthermore, there was considerable heterogeneity in the results, and the certainty of the evidence was low overall. Therefore, current evidence remains inconclusive, and well-designed, adequately powered randomized controlled trials are needed for definitive conclusions.
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9. Genetic Modulation of One-Carbon Metabolism in Autism Spectrum Disorder: An MTHFR-Based Cross-Sectional Study with Neurotypical Controls.
PMID:日期:2026-09-21Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental condition in which disruptions in one-carbon metabolism, regulated by methylenetetrahydrofolate reductase (MTHFR), may contribute to phenotypic variability. This study investigated MTHFR C677T and A1298C polymorphisms and their association with serum vitamin B12, folate, and ASD risk in children. One hundred children with ASD and 100 age-matched neurotypical controls were enrolled. MTHFR genotyping was performed by allele-specific real-time PCR. Serum vitamin B12 and folate by enzyme-linked immunosorbent assay. Associations were assessed using logistic regression under dominant, additive, and recessive genetic models. Discrimination was evaluated by receiver operating characteristic analysis. The C677T TT genotype was overrepresented in ASD cases (57% vs. 43% controls), with significant Hardy-Weinberg deviation (χ² = 21.812, p <0.0001). Mutant A1298C genotypes were observed in 79% of cases. Vitamin B12 declined with increasing C677T T-allele dosage (p <0.001) and folate with A1298C C-allele burden (p = 0.003). Higher vitamin B12 independently associated with reduced ASD odds (OR 0.36, 95% CI 0.17-0.76, p = 0.008). C677T TT homozygosity was significantly associated with increased ASD odds under the recessive model (OR 1.76, 95% CI 1.00-3.08, p = 0.049). A1298C was non-significant across all models, indicating modest discrimination suitable for exploratory purposes only. Children with ASD showed a high burden of functional MTHFR variants with genotype-linked metabolic variation. TT homozygosity was associated with ASD risk under recessive model, supporting a threshold-dependent genetic effect on one-carbon metabolism. These findings warrant prospective validation in larger independent cohorts.
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10. Fatal Hurst Disease-Like Neuroleptospirosis in an Adolescent: A Rare Imaging Phenotype.
PMID:日期:2026-09-19该文献暂无摘要。