Literature DB >> 34145575

Benefit-Risk Assessment of Off-Label Drug Use in Children: The Bravo Framework.

Tjitske M van der Zanden1,2,3, Miriam G Mooij4, Nienke J Vet5, Antje Neubert6, Wolfgang Rascher6, Florian B Lagler7, Christoph Male8, Helene Grytli9, Thomas Halvorsen10, Matthijs de Hoog1, Saskia N de Wildt2,3,11.   

Abstract

A drug is granted a license for use after a thorough assessment of risks and benefits based on high-quality scientific proof of its efficacy and safety. Many drugs that are relevant to children are not licensed for use in this population implying that a thorough assessment of risks and benefits in the pediatric population has not been made at all, implying a negative risk-benefit balance in children, or implying insufficient information to establish the risk-benefit balance. Use of drugs without positive assessment of risks and benefits exposes children to potential lack of efficacy, unknown toxicity, and harm. To aid guideline committees and individual prescribers, we here present a tutorial of the Benefit and Risk Assessment for Off-label use (BRAvO) decision framework. This pragmatic framework offers a structured assessment of benefits and risks of off-label drug use, including a clinical pharmacological based approach to age-appropriate dose selection. As proof of concept and to illustrate the practical use, we have applied the framework to assess benefits and risks of off-label use of ondansetron for gastroenteritis-induced nausea and vomiting. The framework could also guide decisions on off-label use in other special populations (e.g., pregnant women, elderly, obese, or critically ill patients) where off-label drug use is frequent, thereby contributing to effective and safe pharmacotherapy.
© 2021 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

Entities:  

Year:  2021        PMID: 34145575     DOI: 10.1002/cpt.2336

Source DB:  PubMed          Journal:  Clin Pharmacol Ther        ISSN: 0009-9236            Impact factor:   6.875


  4 in total

1.  Development and evaluation of an assessment of the age-appropriateness/inappropriateness of formulations used in children.

Authors:  Jennifer C Duncan; Louise E Bracken; Anthony J Nunn; Matthew Peak; Mark A Turner
Journal:  Int J Clin Pharm       Date:  2022-10-08

2.  Development of the Swiss Database for dosing medicinal products in pediatrics.

Authors:  Romy Tilen; Dalibor Panis; Samuel Aeschbacher; Thomas Sabine; Henriette E Meyer Zu Schwabedissen; Christoph Berger
Journal:  Eur J Pediatr       Date:  2021-11-05       Impact factor: 3.860

3.  Best Evidence-Based Dosing Recommendations for Dexmedetomidine for Premedication and Procedural Sedation in Pediatrics: Outcome of a Risk-Benefit Analysis By the Dutch Pediatric Formulary.

Authors:  Jolien J M Freriksen; Tjitske M van der Zanden; Inge G A Holsappel; Bouwe Molenbuur; Saskia N de Wildt
Journal:  Paediatr Drugs       Date:  2022-03-28       Impact factor: 3.930

4.  Guideline for the management of pediatric off-label use of drugs in China (2021).

Authors:  Min Meng; Enmei Liu; Bo Zhang; Quan Lu; Xiaobo Zhang; Bin Ge; Ye Wu; Li Wang; Mo Wang; Zhengxiu Luo; Ziyu Hua; Xiaoling Wang; Wei Zhao; Yi Zheng; Xinan Wu; Ruiling Zhao; Wenbo Meng; Li Xiang; Gang Wang; Yuntao Jia; Yongchuan Chen; Xiaoyan Dong; Lina Hao; Chengjun Liu; Meng Lv; Xufei Luo; Yunlan Liu; Quan Shen; Wenjuan Lei; Ping Wang; Yajia Sun; Juanjuan Zhang; Ling Wang; Ruobing Lei; Tianchun Hou; Bo Yang; Qiu Li; Yaolong Chen
Journal:  BMC Pediatr       Date:  2022-07-23       Impact factor: 2.567

  4 in total

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