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Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial

BACKGROUND: Young children with sickle cell anaemia (SCA) often have slowed processing speed associated with reduced brain white matter integrity, low oxygen saturation, and sleep-disordered breathing (SDB), related in part to enlarged adenoids and tonsils. Common treatments for SDB include adenoton...

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Autores principales: Hood, Anna M., Stotesbury, Hanne, Kölbel, Melanie, DeHaan, Michelle, Downes, Michelle, Kawadler, Jamie M., Sahota, Satwinder, Dimitriou, Dagmara, Inusa, Baba, Wilkey, Olu, Pelidis, Maria, Trompeter, Sara, Leigh, Andrea, Younis, Janine, Drasar, Emma, Chakravorty, Subarna, Rees, David C., Height, Sue, Lawson, Sarah, Gavlak, Johanna, Gupta, Atul, Ridout, Deborah, Clark, Christopher A., Kirkham, Fenella J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502503/
https://www.ncbi.nlm.nih.gov/pubmed/34629091
http://dx.doi.org/10.1186/s13063-021-05626-6
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author Hood, Anna M.
Stotesbury, Hanne
Kölbel, Melanie
DeHaan, Michelle
Downes, Michelle
Kawadler, Jamie M.
Sahota, Satwinder
Dimitriou, Dagmara
Inusa, Baba
Wilkey, Olu
Pelidis, Maria
Trompeter, Sara
Leigh, Andrea
Younis, Janine
Drasar, Emma
Chakravorty, Subarna
Rees, David C.
Height, Sue
Lawson, Sarah
Gavlak, Johanna
Gupta, Atul
Ridout, Deborah
Clark, Christopher A.
Kirkham, Fenella J.
author_facet Hood, Anna M.
Stotesbury, Hanne
Kölbel, Melanie
DeHaan, Michelle
Downes, Michelle
Kawadler, Jamie M.
Sahota, Satwinder
Dimitriou, Dagmara
Inusa, Baba
Wilkey, Olu
Pelidis, Maria
Trompeter, Sara
Leigh, Andrea
Younis, Janine
Drasar, Emma
Chakravorty, Subarna
Rees, David C.
Height, Sue
Lawson, Sarah
Gavlak, Johanna
Gupta, Atul
Ridout, Deborah
Clark, Christopher A.
Kirkham, Fenella J.
author_sort Hood, Anna M.
collection PubMed
description BACKGROUND: Young children with sickle cell anaemia (SCA) often have slowed processing speed associated with reduced brain white matter integrity, low oxygen saturation, and sleep-disordered breathing (SDB), related in part to enlarged adenoids and tonsils. Common treatments for SDB include adenotonsillectomy and nocturnal continuous positive airway pressure (CPAP), but adenotonsillectomy is an invasive surgical procedure, and CPAP is rarely well-tolerated. Further, there is no current consensus on the ability of these treatments to improve cognitive function. Several double-blind, randomised controlled trials (RCTs) have demonstrated the efficacy of montelukast, a safe, well-tolerated anti-inflammatory agent, as a treatment for airway obstruction and reducing adenoid size for children who do not have SCA. However, we do not yet know whether montelukast reduces adenoid size and improves cognition function in young children with SCA. METHODS: The Study of Montelukast In Children with Sickle Cell Disease (SMILES) is a 12-week multicentre, double-blind, RCT. SMILES aims to recruit 200 paediatric patients with SCA and SDB aged 3–7.99 years to assess the extent to which montelukast can improve cognitive function (i.e. processing speed) and sleep and reduce adenoidal size and white matter damage compared to placebo. Patients will be randomised to either montelukast or placebo for 12 weeks. The primary objective of the SMILES trial is to assess the effect of montelukast on processing speed in young children with SCA. At baseline and post-treatment, we will administer a cognitive evaluation; caregivers will complete questionnaires (e.g. sleep, pain) and measures of demographics. Laboratory values will be obtained from medical records collected as part of standard care. If a family agrees, patients will undergo brain MRIs for adenoid size and other structural and haemodynamic quantitative measures at baseline and post-treatment, and we will obtain overnight oximetry. DISCUSSION: Findings from this study will increase our understanding of whether montelukast is an effective treatment for young children with SCA. Using cognitive testing and MRI, the SMILES trial hopes to gain critical knowledge to help develop targeted interventions to improve the outcomes of young children with SCA. TRIAL REGISTRATION: ClinicalTrials.govNCT04351698. Registered on April 17, 2020. European Clinical Trials Database (EudraCT No. 2017-004539-36). Registered on May 19, 2020
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spelling pubmed-85025032021-10-12 Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial Hood, Anna M. Stotesbury, Hanne Kölbel, Melanie DeHaan, Michelle Downes, Michelle Kawadler, Jamie M. Sahota, Satwinder Dimitriou, Dagmara Inusa, Baba Wilkey, Olu Pelidis, Maria Trompeter, Sara Leigh, Andrea Younis, Janine Drasar, Emma Chakravorty, Subarna Rees, David C. Height, Sue Lawson, Sarah Gavlak, Johanna Gupta, Atul Ridout, Deborah Clark, Christopher A. Kirkham, Fenella J. Trials Study Protocol BACKGROUND: Young children with sickle cell anaemia (SCA) often have slowed processing speed associated with reduced brain white matter integrity, low oxygen saturation, and sleep-disordered breathing (SDB), related in part to enlarged adenoids and tonsils. Common treatments for SDB include adenotonsillectomy and nocturnal continuous positive airway pressure (CPAP), but adenotonsillectomy is an invasive surgical procedure, and CPAP is rarely well-tolerated. Further, there is no current consensus on the ability of these treatments to improve cognitive function. Several double-blind, randomised controlled trials (RCTs) have demonstrated the efficacy of montelukast, a safe, well-tolerated anti-inflammatory agent, as a treatment for airway obstruction and reducing adenoid size for children who do not have SCA. However, we do not yet know whether montelukast reduces adenoid size and improves cognition function in young children with SCA. METHODS: The Study of Montelukast In Children with Sickle Cell Disease (SMILES) is a 12-week multicentre, double-blind, RCT. SMILES aims to recruit 200 paediatric patients with SCA and SDB aged 3–7.99 years to assess the extent to which montelukast can improve cognitive function (i.e. processing speed) and sleep and reduce adenoidal size and white matter damage compared to placebo. Patients will be randomised to either montelukast or placebo for 12 weeks. The primary objective of the SMILES trial is to assess the effect of montelukast on processing speed in young children with SCA. At baseline and post-treatment, we will administer a cognitive evaluation; caregivers will complete questionnaires (e.g. sleep, pain) and measures of demographics. Laboratory values will be obtained from medical records collected as part of standard care. If a family agrees, patients will undergo brain MRIs for adenoid size and other structural and haemodynamic quantitative measures at baseline and post-treatment, and we will obtain overnight oximetry. DISCUSSION: Findings from this study will increase our understanding of whether montelukast is an effective treatment for young children with SCA. Using cognitive testing and MRI, the SMILES trial hopes to gain critical knowledge to help develop targeted interventions to improve the outcomes of young children with SCA. TRIAL REGISTRATION: ClinicalTrials.govNCT04351698. Registered on April 17, 2020. European Clinical Trials Database (EudraCT No. 2017-004539-36). Registered on May 19, 2020 BioMed Central 2021-10-10 /pmc/articles/PMC8502503/ /pubmed/34629091 http://dx.doi.org/10.1186/s13063-021-05626-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Study Protocol
Hood, Anna M.
Stotesbury, Hanne
Kölbel, Melanie
DeHaan, Michelle
Downes, Michelle
Kawadler, Jamie M.
Sahota, Satwinder
Dimitriou, Dagmara
Inusa, Baba
Wilkey, Olu
Pelidis, Maria
Trompeter, Sara
Leigh, Andrea
Younis, Janine
Drasar, Emma
Chakravorty, Subarna
Rees, David C.
Height, Sue
Lawson, Sarah
Gavlak, Johanna
Gupta, Atul
Ridout, Deborah
Clark, Christopher A.
Kirkham, Fenella J.
Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title_full Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title_fullStr Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title_full_unstemmed Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title_short Study of montelukast in children with sickle cell disease (SMILES): a study protocol for a randomised controlled trial
title_sort study of montelukast in children with sickle cell disease (smiles): a study protocol for a randomised controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8502503/
https://www.ncbi.nlm.nih.gov/pubmed/34629091
http://dx.doi.org/10.1186/s13063-021-05626-6
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