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It's not all about inhaled treatment: challenges with oral therapy in paediatric respiratory medicine
Anneka Sareen1, Manisha Ramphul2, Jayesh Mahendra Bhatt2
1Pharmacy Dept, Nottingham Children's Hospital, Nottingham University Hospitals NHS Trust, Queen's Medical Centre, Nottingham, UK.
Insights
Managing cystic fibrosis in children involves significant treatment burdens from multiple oral medications. New therapies present challenges, but strategies exist to ease care for young patients with chronic respiratory conditions.
Area of Science:
- Pediatric Respiratory Medicine
- Pharmacology
- Chronic Disease Management
Background:
- Advances in pediatric respiratory care improve survival in chronic diseases like cystic fibrosis.
- Increased survival leads to a higher treatment burden, including numerous inhaled and oral medications.
- Paediatric oral formulations require consideration of palatability and administration to enhance adherence.
Purpose of the Study:
- To describe challenges children with chronic respiratory conditions face with oral medications.
- To discuss potential oral drug interactions and polypharmacy issues in paediatric respiratory medicine.
- To highlight strategies for reducing the treatment burden in children on oral medication.
Main Methods:
- Literature review focusing on paediatric respiratory conditions, oral medications, and treatment burden.
- Analysis of challenges related to polypharmacy and drug interactions in cystic fibrosis management.
- Exploration of strategies for improving adherence and reducing care burden for children and families.
Main Results:
- Children with chronic respiratory conditions experience significant difficulties with oral medication regimens.
- New cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapies introduce complex interactions and adverse reactions.
- Strategies for reducing treatment burden and improving adherence are crucial for patient well-being.
Conclusions:
- Optimizing oral formulations and managing polypharmacy are essential in paediatric respiratory care.
- Addressing treatment burden is key to improving quality of life for children with chronic respiratory diseases.
- Further research into effective strategies for managing complex medication regimens in paediatric patients is warranted.
Abstract:
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.
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