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Objectives: The present study examined the clinical profile of COVID-19, related morbidity and mortality in children at a tertiary care hospital in Uttarakhand. Understanding the clinical profile of the disease in this specific population is vital for better preparedness and targeted interventions to safeguard the health of children during future outbreaks. This is the first study from this region in this Methods: The present study was a hospital based observational study carried out on patients aged 1 month-18 years who tested covid-19 positive and were admitted to Department of Pediatrics at a tertiary care center in Garhwal region of Uttarakhand during study period July 2020 to May 2023 after getting ethical clearance from Institutional Review Committee and informed consent from patient or patient relatives. Statistical testing has been conducted using R Studio Software version 4. Results: A total of 51 patients with Covid-19 infection, tested positive by either rapid antigen test (RAT) or reverse transcriptase polymerase chain reaction (RTPCR) were admitted to our hospital during the study period. History of covid contact was positive in 11% patients. Comorbidities were seen in 10% patients. Respiratory system (41%) was most commonly involved followed by central nervous system (febrile seizures). Fever (70%) followed by cough (33%) were the most common symptoms. Raised ESR levels was the most common laboratory finding. Conclusions: The infection in children is usually mild, with low mortality rate (2%). Respiratory system was most commonly involved and fever and cough were the most common symptoms. [ABSTRACT FROM AUTHOR]

Research on vitamin D status in Indian children has been confined to studies conducted on small samples from certain regions and using non-standard techniques to quantify 25(OH)D3. Vitamin D insufficiency was observed in this multicenter research that used a standardized technique to evaluate 25(OH)D3 concentrations from dried blood spots (DBS) in children and adolescents from 5 to 18 years old in India. This school-based cross-sectional observational research used a multi-stage stratified random sampling technique. We picked a city and its surrounding hamlet from six states in India, which span a lot of ground. Data was gathered on demographics, anthropometry, body composition, food intakes, and DBS samples. Liquid chromatography with tandem-mass spectrometry was used to evaluate 25(OH)D3 in DBS. A total of 2450 youngsters had their vitamin D level checked, with a subset (n = 672) having extra data obtained for the purpose of evaluating predictors. In the study, 36.8% of participants had adequate vitamin-D levels (> 50 nmol/L), with greater concentrations seen in rural respondents and boys (p < 0.05). The mean vitamin-D concentration was 45.8 ± 23.9 nmol/L. [ABSTRACT FROM AUTHOR]

Introduction and Objectives: Cystic fibrosis is the most common life-limiting genetic condition in Caucasians, affecting 1 in 2500 births. The study examined the percentage of cystic fibrosis patients in paediatric respiratory clinics with pancreatic insufficiency. To compare the clinical and demographic parameters of pancreatic insufficiency and sufficient cystic fibrosis children. Methods: This study was conducted on children with cystic fibrosis, specifically targeting individuals aged 0 to 15 years. It was an observational study aimed at describing and analyzing the characteristics of the participants. This study was conducted at the, Department of Pediatrics, Ayaan Institute of Medical Sciences, Moinabad, Telangana, India, between the November 2022 to December 2023. Pancreatic insufficiency was established when the faecal elastase level was below 200 micrograms per gramme of stool. The prevalence of pancreatic insufficiency was determined by calculating the percentage along with a 95% confidence interval. Results: Pancreatic insufficiency was observed in 62.4% of a group of 20 children. The faecal elastase test identified an additional 19% of patients with pancreatic insufficiency compared to relying solely on the standard history of steatoorhoea for diagnosis. All patients experienced recurrent respiratory infections and 78.8% had a weight below the 5th centile on the growth chart. Only a small proportion of patients had additional characteristic symptoms of cystic fibrosis, such as meconium ileus, rectal prolapse, and nasal polyposis. The pancreatic insufficient group had a higher prevalence of foul-smelling stool, frequent bowel movements, and lower Cooperman score, in comparison to both the pancreatic sufficient group. This disparity was shown to be statistically significant. Conclusions: From the above study it can be concluded two risk factors identified for calculating a clinical score to predict pancreatic insufficiency were a history of foulsmelling stool and frequent bowel movements. To generate this score, a more extensive investigation with a larger sample size will be necessary. [ABSTRACT FROM AUTHOR]