Related Experiment Videos

Improved vitamin A supplementation regimen for breastfed very low birth weight infants

Anne K Aurvåg1, Christine Henriksen, Christian A Drevon

  • 1Department of Pediatrics, Akershus University Hospital and Akershus Faculty Division, University of Oslo, Norway. anne.aurvaag@ahus.no

Insights

A new vitamin A protocol significantly improved plasma retinol levels in very low birth weight infants at hospital discharge. This modified approach enhances nutritional status for vulnerable preterm infants.

Area of Science:

  • Neonatal nutrition
  • Pediatric endocrinology
  • Vitamin A metabolism

Background:

  • Preterm infants, particularly very low birth weight (VLBW) infants, often present with suboptimal retinol status at birth and hospital discharge.
  • Low vitamin A levels can impact infant development and health outcomes.
  • Existing protocols may not adequately address the vitamin A needs of VLBW infants.

Purpose of the Study:

  • To evaluate a novel protocol for vitamin A supplementation in very low birth weight infants.
  • To determine if the new protocol can improve plasma retinol concentrations at hospital discharge.
  • To compare the efficacy of the modified vitamin A protocol against standard care in Norwegian hospitals.

Main Methods:

  • An open intervention trial involving 60 VLBW infants (birth weight < 1500 g).
  • Vitamin A was administered daily mixed with human milk via a fortifier, with dosage adjusted by body weight.
  • Plasma retinol levels were measured using high-performance liquid chromatography at enrollment and discharge.

Main Results:

  • The modified protocol group showed significantly higher median plasma retinol concentrations at discharge (0.49 microM) compared to the reference group (0.30 microM; p = 0.008).
  • A lower percentage of infants in the modified group had plasma retinol levels below 0.35 microM (44%) compared to the reference group (69%; p = 0.04).
  • These findings suggest improved hepatic stores of vitamin A in infants receiving the modified protocol.

Conclusions:

  • The modified vitamin A supplementation protocol effectively improved plasma retinol levels in VLBW infants by hospital discharge.
  • This new protocol offers a promising strategy to enhance vitamin A status in this vulnerable population.
  • Further research may explore long-term outcomes associated with improved retinol status in VLBW infants.
Abstract

Related Concept Videos

Drug Dosing: Infants and Children01:29

Drug Dosing: Infants and Children

Pediatric patient dosages diverge from adults due to disparities in body surface area, total body water, and extracellular fluid per kilogram of body weight. The dosing regimen considers the variations in pharmacokinetics and pharmacology across distinct age groups, encompassing preterm newborns, infants, young children, older children, and adolescents. Calculation of pediatric patient doses is predicated on determining body surface area, which exhibits a superior correlation with the child's...
Role of Skin in Vitamin D Synthesis01:23

Role of Skin in Vitamin D Synthesis

The skin plays a crucial role in the synthesis of vitamin D, a vital nutrient for various physiological processes in the body. Vitamin D is unique because it can be synthesized in the skin through a series of chemical reactions triggered by exposure to ultraviolet B (UVB) radiation from sunlight.
The solar UV B rays (290-315 nm) are absorbed by the skin, and 7-dehydrocholesterol (provitamin D3) photolyzes it to previtamin D3, which undergoes a rapid transformation to vitamin D3(cholecalciferol).
Dosage Regimen: Individualization01:24

Dosage Regimen: Individualization

Individualization in dosing regimens is the customization of medication doses for individual patients. Its necessity arises from the goal of maximizing therapeutic benefits while minimizing risks. This approach is pivotal because human responses to drugs can vary widely; what is effective for one person may be inadequate or excessive for another. Interpatient (intersubject) variability refers to differences in drug responses between individuals, while intrapatient (intrasubject) variability...
Development of Immunocompetence01:22

Development of Immunocompetence

The initiation of cell-mediated immunity can be observed as early as the third month of fetal growth, with active antibody-mediated immunity following approximately one month later.
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...
Development of Human Microbiota01:30

Development of Human Microbiota

The human microbiota begins developing at birth and undergoes continual change as we age. Infancy marks a critical period of microbial sensitivity, offering a “window of opportunity” during which beneficial microbes help mature the immune system. By age three, children typically develop a more stable and diverse microbial community. Newborns acquire microbes from their immediate environment; vaginal delivery favors maternal vaginal microbes, while cesarean births favor microbes from the skin...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...