Personalized Neonatal Therapy: Application of Magistral Formulas in Therapeutic Orphan Populations
Wenwen Shao1, Angela Gomez2, Alejandra Alejano1
1Facultad de Ciencias de la Salud, Universidad Rey Juan Carlos, 28922 Alcorcón, Spain.
Insights
Magistral formulas (MFs) offer potential solutions for neonates lacking approved therapies. This review highlights challenges in pediatric drug development and the need for better-formulated, evidence-based neonatal medicines.
Area of Science:
- Neonatal pharmacology
- Pediatric drug formulation
- Evidence-based medicine
Background:
- Limited availability of approved therapies for neonates.
- Physiological differences between neonates and adults complicate drug formulation.
- Challenges in pediatric research include few clinical trials and off-label drug use.
Purpose of the Study:
- To explore magistral formulas (MFs) as a therapeutic option for neonates.
- To analyze pharmaceutical forms, indications, and dosage recommendations for neonatal MFs.
- To address the shortage of approved neonatal medications.
Main Methods:
- Review of scientific literature on neonatal medicines.
- Analysis of magistral formulas commonly used in pediatrics, specifically for neonates.
- Classification of medications by therapeutic group (antihypertensives, corticosteroids, antiepileptics).
Main Results:
- Neonates often receive off-label medications in neonatal intensive care units and primary healthcare.
- Magistral formulas are frequently prepared by pharmacists for pediatric use.
- Significant pharmacokinetic differences exist between neonates and adults.
Conclusions:
- There is a critical need to promote research and development of pediatric drug design for neonates.
- Age-appropriate dosage forms and improved drug information are essential.
- Addressing the shortage of approved neonatal medicines requires expanded studies and regulatory support.
Abstract:
This review explores the potential of magistral formulas (MFs) as a viable option to meet the needs of neonates, given the lack of adequate therapies for this vulnerable group. The scientific literature on medicines available for neonates is limited. The physiological differences between neonates and adults make it difficult to formulate these medicines. In addition, there are a variety of difficulties in conducting research on neonates: few clinical trials are performed, and there is frequent use of unauthorized medicines. Pharmacokinetics in neonates was investigated in comparison to adults, and different aspects of the absorption, distribution, metabolism, and excretion were observed. One of the main problems is the different pharmacokinetics between the two populations. It is necessary to promote and allow research related to pediatric drug design, approve a specific authorization for use in age-appropriate dosage forms, and improve the quality and availability of information on drugs. This study focused on the MFs typically used for pediatrics, specifically for neonates, analyzing the pharmaceutical forms currently available and the presence of indications and dosage recommendations of the European Medicines Agency. Medications were classified according to therapeutic group, as antihypertensives, corticosteroids, and antiepileptics. The use of off-label medicines remains high in neonatal intensive care units and in primary healthcare, besides in the preparation of MFs by pharmacists. The shortage of medicines specifically designed and approved for neonates is a serious problem for society. Neonates continue to be treated, on numerous occasions, with off-label medicines. Studies and research should be expanded in this vulnerable population group.
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