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Serum Vitamin D Status in Critically Ill Children With Acute Respiratory Infections

Observational Acute Respiratory Infections Critical Illness in Children Vitamin D Deficiency Pediatric Respiratory Infections

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Serum 25-Hydroxyvitamin D Assessment.
Who it may be relevant to
Registry conditions: Acute Respiratory Infections, Critical Illness in Children, Vitamin D Deficiency, Pediatric Respiratory Infections. Basic parameters: 1 months — 16 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Assessment of Serum Vitamin D Status and Its Association With Disease Severity and Mortality Risk Among Critically Ill Children With Acute Respiratory Infections: A Cross-Sectional Study

Overview

Acute respiratory infections (ARIs) are among the leading causes of hospitalization, morbidity, and mortality in children worldwide, particularly among critically ill patients admitted to pediatric intensive care units (PICUs). Vitamin D has an important role not only in bone metabolism but also in regulation of innate and adaptive immune responses, especially within the respiratory tract. Recent evidence suggests that vitamin D deficiency may be associated with increased susceptibility to respiratory infections, greater disease severity, prolonged hospitalization, and higher mortality rates in critically ill children. This observational cross-sectional study aims to assess serum vitamin D status among critically ill children admitted to the PICU with acute respiratory infections and to evaluate the relationship between vitamin D levels, severity of respiratory illness, and risk of mortality. The study will include pediatric patients aged 1 month to 16 years admitted to the Pediatric Intensive Care Unit of Assiut University Children's Hospital. Clinical evaluation and laboratory investigations, including serum 25-hydroxyvitamin D levels, serum calcium, and alkaline phosphatase, will be performed within the first 24 hours of admission. Severity of respiratory distress will be assessed using the Pediatric Respiratory Severity Score (PRESS), while mortality risk will be evaluated using the Pediatric Risk of Mortality Score (PRISM III). The findings of this study may contribute to better understanding of the role of vitamin D in critically ill children with respiratory infections and may support future strategies for early risk assessment and improved clinical management in pediatric intensive care settings.

Detailed description

Acute respiratory infections remain a major global health problem and are a leading cause of morbidity and mortality among pediatric populations, particularly in low- and middle-income countries. Critically ill children admitted to pediatric intensive care units (PICUs) with severe respiratory infections are at increased risk of complications, prolonged hospitalization, and mortality. Identifying modifiable risk factors associated with disease severity and poor outcomes is therefore of significant clinical importance.

Vitamin D is a fat-soluble steroid hormone traditionally recognized for its role in calcium and phosphorus homeostasis and skeletal development. However, increasing evidence has demonstrated that vitamin D also has immunomodulatory functions through its effects on innate and adaptive immunity. Vitamin D receptors are expressed in immune cells, including macrophages and respiratory epithelial cells, supporting its role in host defense against respiratory pathogens.

Recent studies have suggested an association between vitamin D deficiency and increased susceptibility to acute respiratory infections, sepsis, and adverse outcomes in critically ill children. Nevertheless, available evidence remains inconsistent, and data from pediatric intensive care populations in Egypt and similar settings are limited.

This cross-sectional observational study will be conducted at the Pediatric Intensive Care Unit of Assiut University Children's Hospital. The study will include children aged 1 month to 16 years admitted with acute respiratory infections. Patients with chronic illnesses affecting vitamin D metabolism, severe immunodeficiency, congenital heart disease, malnutrition, rickets, or recent vitamin D supplementation will be excluded.

At PICU admission, all eligible participants will undergo detailed history taking, complete clinical examination, and laboratory investigations. Serum 25-hydroxyvitamin D \[25(OH)D\] levels will be measured within the first 24 hours of admission as the standard indicator of vitamin D status. Vitamin D levels will be categorized according to international clinical practice guidelines into deficiency, insufficiency, sufficiency, and toxicity.

Severity of respiratory illness will be evaluated using the Pediatric Respiratory Severity Score (PRESS), a validated clinical scoring system for respiratory distress in children. Mortality risk will be assessed using the Pediatric Risk of Mortality Score (PRISM III), which incorporates physiological and laboratory parameters obtained during the first 24 hours of PICU admission.

The primary outcome of the study is the prevalence of vitamin D deficiency among critically ill children with acute respiratory infections. Secondary outcomes include the association between serum vitamin D levels and both respiratory disease severity and mortality risk.

Data will be statistically analyzed using SPSS software. Appropriate statistical tests will be selected according to the type and distribution of data, and statistical significance will be considered at p \< 0.05.

This study may provide important insights into the clinical significance of vitamin D deficiency in critically ill pediatric patients and may support future preventive and therapeutic strategies aimed at improving outcomes in children with severe respiratory infections.

Interventions

  • Diagnostic test Serum 25-Hydroxyvitamin D Assessment
    Blood samples will be collected within the first 24 hours of admission to the Pediatric Intensive Care Unit (PICU) to measure serum 25-hydroxyvitamin D \[25(OH)D\] levels, which is the standard biomarker used to assess vitamin D status. The measured vitamin D levels will be analyzed in relation to the severity of acute respiratory infections using the Pediatric Respiratory Severity Score (PRESS) and the risk of mortality using the Pediatric Risk of Mortality Score (PRISM III). No therapeutic int

Primary outcome measures

  • Prevalence of Vitamin D Deficiency among critically ill children with acute respiratory infections. [Time frame: Within the first 24 hours of admission to the Pediatric Intensive Care Unit (PICU).]
Secondary outcome measures (2)
  • Association between Vitamin D and Severity of ARI [Time frame: Within the first 24 hours of PICU admission.]
  • Association between Vitamin D and Risk of Mortality [Time frame: Within the first 24 hours of PICU admission.]

Eligibility criteria

Inclusion criteria

  • Children aged between 1 month and 12 years.
  • Admitted to the PICU with a primary diagnosis of acute respiratory infection.
  • Diagnosis confirmed by clinical symptoms and radiological evidence.

Exclusion criteria

  • Children with known chronic bone diseases or metabolic disorders.
  • Patients receiving vitamin D supplementation prior to admission.
  • Patients with chronic renal or hepatic failure.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Assiut university — Asyut

Publications

  • Thokngaen J, Karoonboonyanan W. Pediatric respiratory severity score evaluates disease severity of respiratory tract infection in children. Chulalongkorn Med J. 2019;63(1):Article 7. doi: 10.58837/CHULA.CMJ.63.1.6
  • Kangel D, Kıral A. The effect of vitamin D level on the clinical course of the disease in patients with lower respiratory tract infection. Cam Sakura Med J. 2025;5(1):17-24. doi: 10.58519/csmedj.galenos.2025.2025-3-2
  • Gunes N, Cam H. An observational study of serum vitamin D status in critically ill children admitted to the pediatric intensive care unit. Arch Med Sci. 2022 Oct 6;21(2):471-477. doi: 10.5114/aoms/155137. eCollection 2025. PMID 40395895
  • Chandana HNG, Jyotirmanju CS, Jeniffer NV. Association of vitamin D levels and mortality in critically ill children: a prospective observational study. Lex Localis Journal of Local Self-Government. 2025;23(S6). Available from: https://lexlocalis.org/index.php/LexLocalis/article/view/802821/2956
  • Zhang C, Wang D, Zhu C, Lei X, Meng L, Shen C. Halogen-Engineered Copper-Based Materials with Multicolor Emission for Dual-Functional Anticounterfeiting and LED Applications. ACS Appl Mater Interfaces. 2025 Jul 30;17(30):43298-43306. doi: 10.1021/acsami.5c11245. Epub 2025 Jul 22. PMID 40693518
  • Pollack MM, Patel KM, Ruttimann UE. PRISM III: an updated Pediatric Risk of Mortality score. Crit Care Med. 1996 May;24(5):743-52. doi: 10.1097/00003246-199605000-00004. PMID 8706448
  • Pludowski P, Takacs I, Boyanov M, Belaya Z, Diaconu CC, Mokhort T, Zherdova N, Rasa I, Payer J, Pilz S. Clinical Practice in the Prevention, Diagnosis and Treatment of Vitamin D Deficiency: A Central and Eastern European Expert Consensus Statement. Nutrients. 2022 Apr 2;14(7):1483. doi: 10.3390/nu14071483. PMID 35406098
  • Petkova GS, Mineva EN, Botsova VT. Clinical Study of Vitamin D Levels in Hospitalized Children with Acute Respiratory Infections. Pediatr Rep. 2024 Nov 22;16(4):1034-1041. doi: 10.3390/pediatric16040088. PMID 39585042

Identifiers

NCT: NCT06547749 · VITD01

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗