Related Experiment Video
Updated: Oct 25, 2026

Implementation of Non-invasive Point of Care Transient Elastography for Evaluation of Liver Disease in Pediatric Populations with Cystic Fibrosis
Published on: August 29, 2025
Paediatric palliative care in advanced cystic fibrosis: from prognosis-based to needs-based care across the disease
Beatriz Rodrigues-Tiago1, Cristiana Rolão-Carvalho2, Paulo Reis-Pina2
1Centre for Palliative Medicine, Faculty of Medicine, University of Lisbon, Avenida Prof. Egas Moniz, 1649-028 Lisbon, Portugal.
Abstract:
Advances in cystic fibrosis care, particularly highly effective cystic fibrosis transmembrane conductance regulator modulator therapies, have transformed disease trajectories for many children and adolescents, improving health and survival. However, advanced disease, symptom and treatment burden, psychosocial distress, and uncertainty persist, requiring continued attention to palliative care needs. This narrative review examines palliative care in children and adolescents with advanced cystic fibrosis, focusing on multidimensional symptom burden, communication, shared decision-making, advance care planning, lung transplantation, and integration within multidisciplinary care. Building on the established longitudinal, needs-based framework for palliative care in cystic fibrosis, we examine its application specifically to paediatric care in the era of highly effective modulator therapies. Palliative care can complement disease-directed therapies throughout the disease trajectory rather than being reserved for end-of-life care. In children and adolescents, needs are shaped not only by disease severity but also by developmental stage, evolving autonomy, family circumstances, education and social participation, transplantation, and transition to adulthood. Multidisciplinary cystic fibrosis teams can provide primary palliative care within their expertise, with specialist paediatric palliative care added when needs become complex or refractory. In the era of highly effective modulator therapies, the challenge is therefore to operationalise longitudinal, needs-based palliative care for children and families across increasingly heterogeneous disease trajectories. Future research should define approaches to needs assessment, escalation of palliative support, specialist referral, and implementation within multidisciplinary cystic fibrosis services, with the aim of improving quality of life alongside longer survival.
Related Concept Videos
Cystic Fibrosis: Management
Sinus disease and chronic sinusitis...
Continuing Care
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
Cancer Survival Analysis
Chronic Pancreatitis II: Collaborative Care
Assessment:
COPD: Pathogenesis and Clinical Features
The primary cause for the onset of COPD is cigarette smoking and exposure to air pollution. These hazardous factors initiate a chain reaction within the lungs, resulting in chronic inflammation, damage to the airways, and a...