It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine
Advances in therapies and management of conditions encountered by paediatric respiratory specialists have led to improved outcomes and improved survival rates dramatically in chronic diseases such as cystic fibrosis. However, this has also meant an increase in treatment burden. A variety of inhaled...
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European Respiratory Society
2021-03-01
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doaj-cee057f3e7fb4224acf364ef7d2b64d02021-06-14T06:57:41ZengEuropean Respiratory SocietyBreathe1810-68382073-47352021-03-0117110.1183/20734735.0005-20210005-2021It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicineAnneka Sareen0Manisha Ramphul1Jayesh Mahendra Bhatt2 Pharmacy Dept, Nottingham Children's Hospital, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK Paediatric Respiratory Medicine, Nottingham Children's Hospital, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK Paediatric Respiratory Medicine, Nottingham Children's Hospital, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK Advances in therapies and management of conditions encountered by paediatric respiratory specialists have led to improved outcomes and improved survival rates dramatically in chronic diseases such as cystic fibrosis. However, this has also meant an increase in treatment burden. A variety of inhaled treatments are crucial in managing paediatric respiratory diseases, but these patients also have to take many oral medications. It is widely recognised that developing oral formulations appropriate for the paediatric population can affect how well a product is received by patients and their families. Consideration should be given to palatability and the number of medicines to be administered as these can all contribute to treatment adherence. Polypharmacy specifically in the context of management of patients with cystic fibrosis is not a new concept, but the recently introduced cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies and their potential for interactions and adverse reactions create novel challenges. There are some strategies that families and healthcare professionals can implement to reduce treatment burden. This review will also provide some insight into the life of a teenager with cystic fibrosis and the relative complexities of her treatment and the impacts on daily life. Educational aims To describe the difficulties faced by children with long-term respiratory conditions having to take oral medication. To discuss oral drug interactions that may exist within paediatric respiratory medicine and to consider issues with polypharmacy. To highlight strategies that may be used to reduce the burden of care for children on oral medication.http://breathe.ersjournals.com/content/17/1/210005.full |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Anneka Sareen Manisha Ramphul Jayesh Mahendra Bhatt |
spellingShingle |
Anneka Sareen Manisha Ramphul Jayesh Mahendra Bhatt It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine Breathe |
author_facet |
Anneka Sareen Manisha Ramphul Jayesh Mahendra Bhatt |
author_sort |
Anneka Sareen |
title |
It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
title_short |
It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
title_full |
It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
title_fullStr |
It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
title_full_unstemmed |
It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
title_sort |
it's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine |
publisher |
European Respiratory Society |
series |
Breathe |
issn |
1810-6838 2073-4735 |
publishDate |
2021-03-01 |
description |
Advances in therapies and management of conditions encountered by paediatric respiratory specialists have led to improved outcomes and improved survival rates dramatically in chronic diseases such as cystic fibrosis. However, this has also meant an increase in treatment burden. A variety of inhaled treatments are crucial in managing paediatric respiratory diseases, but these patients also have to take many oral medications. It is widely recognised that developing oral formulations appropriate for the paediatric population can affect how well a product is received by patients and their families. Consideration should be given to palatability and the number of medicines to be administered as these can all contribute to treatment adherence. Polypharmacy specifically in the context of management of patients with cystic fibrosis is not a new concept, but the recently introduced cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies and their potential for interactions and adverse reactions create novel challenges. There are some strategies that families and healthcare professionals can implement to reduce treatment burden. This review will also provide some insight into the life of a teenager with cystic fibrosis and the relative complexities of her treatment and the impacts on daily life.
Educational aims
To describe the difficulties faced by children with long-term respiratory conditions having to take oral medication. To discuss oral drug interactions that may exist within paediatric respiratory medicine and to consider issues with polypharmacy. To highlight strategies that may be used to reduce the burden of care for children on oral medication. |
url |
http://breathe.ersjournals.com/content/17/1/210005.full |
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