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      Paediatric medicine issues and gaps from healthcare workers point of view: survey results and a narrative review from the global accelerator for paediatric formulations project

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          Abstract

          The WHO Model List of Essential Medicines for Children (EMLc) has not been systematically revised in the last few years. We conducted a survey addressed to healthcare professionals prescribing, preparing, or administering medicines to children and a narrative review to identify problematic paediatric formulations or missing medicines in all therapeutic fields to inform the review of the EMLc in 2023. A total of 285 physicians (63%), 28 nurses (6%) and 142 pharmacists (31%), mostly working in the hospital setting, reported at least one problematic medicine. 290 medicines were reported as missing (completely or the child-appropriate formulation). The top three most mentioned were ciprofloxacin together with phenobarbital and omeprazole. 387 medicines were reported as problematic (34% were oral liquid formulations, 34% tablets, 18% parenteral preparations. Mostly of the products were antibacterials (27%), cardiovascular medicines (11%) and antivirals (11%). The obtained responses show the perspective of healthcare workers working around the world, particularly in the European region (25%), in the African region (24%), and in the Region of the Americas (19%), with limited representation from Northern Africa and the Middle East. Our results need to be analysed with the outputs of other ongoing works before specific products can enter the WHO-hosted Global Accelerator for Paediatric formulations network prioritisation process. Efforts to develop appropriate formulations for children should be accelerated so that the uncertainties associated with off-label drug preparation and use are minimised, and therapeutic benefits are optimised.

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          Holding chambers (spacers) versus nebulisers for beta-agonist treatment of acute asthma

          In acute asthma inhaled beta(2)-agonists are often administered by nebuliser to relieve bronchospasm, but some have argued that metered-dose inhalers with a holding chamber (spacer) can be equally effective. Nebulisers require a power source and need regular maintenance, and are more expensive in the community setting.
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            Adherence and health-related quality of life in adolescent liver transplant recipients.

            Adolescence is a particularly high-risk period for non-adherence with post-transplant medical regimens. There remains a lack of research investigating factors related to non-adherence in adolescent LT recipients. The present study empirically assessed the relationship between adherence and HRQOL in adolescent LT recipients. Participants included 25 adolescents (mean = 15.1 yr, range 12-17.9) and their parent/guardian(s). Adherence was assessed using multiple indices including clinician-conducted interviews, rate of clinic attendance, and s.d. of consecutive tacrolimus blood levels. HRQOL was examined using self-report and parent-proxy report on well-validated assessment measures. Results indicated that 76% of participants were non-adherent on at least one measure of adherence, and HRQOL was significantly lower than normative data for healthy children. Tacrolimus s.d. were significant related to poor HRQOL across domains of physical, school, and social functioning. Non-adherent adolescents reported poorer health perceptions, self-esteem, mental health, family cohesion, and more limitations in social and school activities related to physical, emotional, and behavioral problems. These results suggest that empirically based assessment of HRQOL may help identify those at highest risk for behavior, emotional and school difficulties, as well as non-adherence. The examination of tacrolimus s.d. may also help identify patients who may benefit from intervention to promote adherence and HRQOL. Prospective investigations are necessary to further identify the impact of HRQOL on adherence and long-term health outcomes to further guide clinical intervention.
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              Hydroxyurea for Children with Sickle Cell Disease

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                Author and article information

                Contributors
                Journal
                Front Pharmacol
                Front Pharmacol
                Front. Pharmacol.
                Frontiers in Pharmacology
                Frontiers Media S.A.
                1663-9812
                17 July 2023
                2023
                : 14
                : 1200848
                Affiliations
                [1] 1 Division of Pediatric Infectious Diseases , Department of Women’s and Children’s Health , University of Padova , Padova, Italy
                [2] 2 Penta—Child Health Research , Padova, Italy
                [3] 3 Department of Health Products Policy and Standards , World Health Organization , Geneva, Switzerland
                [4] 4 WHO Research for Health Department , World Health Organization , Geneva, Switzerland
                [5] 5 Faculty of Associated Medical Sciences , Chiang Mai University , Chiang Mai, Thailand
                Author notes

                Edited by: Elke Smits, Antwerp University Hospital, Belgium

                Reviewed by: Marc De Broe, University of Antwerp, Belgium

                Mathangi Gopalakrishnan, University of Maryland, United States

                *Correspondence: Elisa Barbieri, elisa.barbieri@ 123456unipd.it
                Article
                1200848
                10.3389/fphar.2023.1200848
                10390094
                a49bbe12-a1ad-4387-b35b-7384aee228b4
                Copyright © 2023 Barbieri, Minotti, Cavagnis, Giaquinto, Cappello, Penazzato and Lallemant.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 05 April 2023
                : 29 June 2023
                Funding
                Funded by: Bill and Melinda Gates Foundation , doi 10.13039/100000865;
                Award ID: INV-006317
                This publication is based on research funded by the Bill and Melinda Gates Foundation (grant number INV-006317). The findings and conclusions contained within are those of the authors and do not necessarily reflect positions or policies of the Bill and Melinda Gates Foundation.
                Categories
                Pharmacology
                Original Research
                Custom metadata
                Obstetric and Pediatric Pharmacology

                Pharmacology & Pharmaceutical medicine
                medicine access,essential medicines,children,paediatric formulation,survey

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