» Articles » PMID: 33672395

Acceptability of a Sublingual Drug Formulation for Respiratory Tract Infections in Children Aged 3 to 5 Years

Overview
Journal Pharmaceutics
Publisher MDPI
Date 2021 Mar 6
PMID 33672395
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

In pediatrics, acceptability has emerged as a key factor for compliance, and consequently for treatment safety and efficacy. Polyvalent mechanical bacterial lysate (PMBL) in 50-mg sublingual tablets is indicated in children and adults for the prophylaxis of recurrent respiratory tract infections. This medication may be prescribed in children over 3 years of age; the appropriateness of this sublingual formulation should thus be demonstrated amongst young children. Using a multivariate approach integrating the many aspects of acceptability, standardized observer reports were collected for medication intake over the course of treatment (days 1, 2, and 10) in 37 patients aged 3 to 5 years, and then analyzed in an intelligible model: the acceptability reference framework. According to this multidimensional model, 50-mg PMBL sublingual tablets were classified as "positively accepted" in children aged 3 to 5 years on all three days of evaluation. As the acceptability evaluation should be relative, we demonstrated that there was no significant difference between the acceptability of these sublingual tablets and a score reflecting the average acceptability of oral/buccal medicines in preschoolers. These results highlight that sublingual formulations could be appropriate for use in preschoolers.

Citing Articles

Sublingually administered bacterial lysates: rationale, mechanisms of action and clinical outcomes.

Braido F, Melioli G, Nicolini G, Ferraris M, Di Girolamo S, Di Gioacchino M Drugs Context. 2024; 13.

PMID: 39165613 PMC: 11335356. DOI: 10.7573/dic.2024-1-5.


A Guide to Best Practice in Sensory Analysis of Pharmaceutical Formulations.

Clapham D, Belissa E, Inghelbrecht S, Pense-Lheritier A, Ruiz F, Sheehan L Pharmaceutics. 2023; 15(9).

PMID: 37765288 PMC: 10535428. DOI: 10.3390/pharmaceutics15092319.


Effect of immunostimulation with bacterial lysate on the clinical course of allergic rhinitis and the level of γδT, iNKT and cytotoxic T cells in children sensitized to grass pollen allergens: A randomized controlled trial.

Janeczek K, Kowalska W, Zarobkiewicz M, Suszczyk D, Mikolajczyk M, Markut-Miotla E Front Immunol. 2023; 14:1073788.

PMID: 36733480 PMC: 9887322. DOI: 10.3389/fimmu.2023.1073788.


Dosage Forms Suitability in Pediatrics: Acceptability of Analgesics and Antipyretics in a German Hospital.

Klingmann V, Vallet T, Munch J, Stegemann R, Wolters L, Bosse H Pharmaceutics. 2022; 14(2).

PMID: 35214070 PMC: 8879646. DOI: 10.3390/pharmaceutics14020337.


Acceptability of Mebendazole Chewable Tablet in Children Aged 2 to 4 Years in Peru.

Perez F, Vallet T, Bravo Z, Callahan K, Ruiz F Pharmaceutics. 2022; 14(1).

PMID: 35056923 PMC: 8780656. DOI: 10.3390/pharmaceutics14010027.


References
1.
Cazzola M, Anapurapu S, Page C . Polyvalent mechanical bacterial lysate for the prevention of recurrent respiratory infections: a meta-analysis. Pulm Pharmacol Ther. 2011; 25(1):62-8. DOI: 10.1016/j.pupt.2011.11.002. View

2.
Clement C, Evans S, Evans C, Hawke D, Kobayashi R, Reynolds P . Stimulation of lung innate immunity protects against lethal pneumococcal pneumonia in mice. Am J Respir Crit Care Med. 2008; 177(12):1322-30. PMC: 2427056. DOI: 10.1164/rccm.200607-1038OC. View

3.
Esposito S, Principi N . Guidelines for the diagnosis and treatment of acute and subacute rhinosinusitis in children. J Chemother. 2008; 20(2):147-57. DOI: 10.1179/joc.2008.20.2.147. View

4.
Vallet T, Ruiz F, Lavarde M, Pense-Lheritier A, Aoussat A . Standardised evaluation of medicine acceptability in paediatric population: reliability of a model. J Pharm Pharmacol. 2017; 70(1):42-50. PMC: 5765461. DOI: 10.1111/jphp.12829. View

5.
Ruiz F, Vallet T, Pense-Lheritier A, Aoussat A . Standardized method to assess medicines' acceptability: focus on paediatric population. J Pharm Pharmacol. 2016; 69(4):406-416. PMC: 5396311. DOI: 10.1111/jphp.12547. View