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. 2023 Nov 13;10(11):1802. doi: 10.3390/children10111802

Comment on Shaniv et al. Neonatal Drug Formularies—A Global Scope. Children 2023, 10, 848

Elisabeth V Giger 1, Romy Tilen 1,*
Editors: Johannes Van Den Anker1, Elizabeth Asztalos1
PMCID: PMC10670639  PMID: 38002893

We read the article by Shaniv D. et al. entitled “Neonatal Drug Formularies—A Global Scope” [1] with great interest. As mentioned in this study, SwissPedDose, the organization that is harmonizing the Swiss national pediatric drug doses, unfortunately missed the opportunity to participate, which we sincerely regret. We would like to briefly explain our process in providing neonatal dosing recommendations based on the questionnaire sent to the participants of the above-mentioned article (see the Supplementary Materials of the article, Document S1).

The Swiss database for dosing medicinal products in pediatrics is an online database (www.swisspeddose.ch/database (accessed on 26 September 2023)) containing nationally harmonized dosage recommendations for neonates and children. It is intended for health care professionals and is free of charge [2]. Age categories can be chosen to distinguish between children and newborn dosing recommendations that are published in German, French and English. Institutional users can download the complete data set as an XML file and integrate the SwissPedDose dosage recommendations directly into their respective clinical information systems with a free subscription. The development of the formulary is based on a legal basis [3] and is therefore financially supported by the Federal Office of Public Health. Experts from the largest children’s hospitals in Switzerland are actively participating in the development of the formulary.

Drugs are chosen by asking the senior pediatricians involved in the dosage-finding process about the requirements for clinical practice. The cases for the selected substances are prepared using a standardized process and cover the relevant indications and routes of administration. In-house dosage data provided by hospital pharmacists of the participating children’s hospitals, drug labeling in Switzerland and/or from a country with similar standards of drug approval (if available), information found in recognized international and national referenced handbooks and online databases such as the British National Formulary for Children (BNFc), uptodate, kinderformulariumn.nl and NNF8, together with results from a literature search, are all considered for this process. This PubMed search consists of keywords relating to aspects such as substance, indication, route of administration and age filter (“newborn: birth-1 month”). All the literature consulted in the process is listed for each case. Age and weight are specified where needed: current weight, birth weight, gestational age (GA), postmenstrual age (PMA) and postnatal age (PNA).

The neonatal formulary cases are revised and discussed with senior neonatologists from nine Swiss children’s hospitals. Only if a consensus among the experts can be reached is the case published as the national neonatal drug dose. If there are major concerns among the experts about a dosage recommendation, a research question for SwissPedNet, the Swiss Research Network of Clinical Pediatric Hubs, is formulated.

At least every four years, dosage recommendations are revised in a defined re-evaluation process taking the most recent literature into consideration. Feedback from users provided directly via the feedback button or new evidence found by anyone involved in the process can lead to immediate changes. Subscribers are informed via an automatic email about updates, while all users can find updates on the changelog page. At the time of writing, 157 dosage recommendations for 88 substances are available in the Swiss neonatal formulary. More information about the formulary is available upon request from the authors.

We would like to thank the authors of “Neonatal Drug Formularies—A Global Scope” for their important work and for their invitation to describe our process in this comment.

Acknowledgments

We thank Jane McDougall for critically reading and improving this comment.

Author Contributions

Writing—original draft preparation, E.V.G.; writing—review and editing, R.T. All authors have read and agreed to the published version of the manuscript.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

SwissPedDose is funded by the Federal Office of Public Health, Switzerland.

Footnotes

Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

References

  • 1.Shaniv D., Bolisetty S., Young T.E., Mangum B., Ainsworth S., Elbers L., Schultz P., Cucchi M., de Wildt S.N., van der Zanden T.M., et al. Neonatal Drug Formularies—A Global Scope. Children. 2023;10:848. doi: 10.3390/children10050848. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Tilen R., Panis D., Aeschbacher S., Sabine T., Meyer Zu Schwabedissen H.E., Berger C. Development of the Swiss Database for dosing medicinal products in pediatrics. Eur. J. Pediatr. 2022;181:1221–1231. doi: 10.1007/s00431-021-04304-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Federal Act of 15 December 2000 on Medicinal Products and Medical Devices (Therapeutic Products Act, TPA) [(accessed on 26 September 2023)]. Available online: https://www.fedlex.admin.ch.

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