‘It gives me more freedom’: Family perspectives on travelling with children on nocturnal ventilation

Author:

Riley Mollie1ORCID,Brotherston Stephanie1,Samuels Martin12,Pike Katharine C.3,Kelly Paula4ORCID

Affiliation:

1. Lung Function Laboratory Great Ormond Street Hospital for Children NHS Foundation Trust London UK

2. Respiratory Medicine Great Ormond Street Hospital for Children NHS Foundation Trust London UK

3. Bristol Royal Hospital for Children Bristol UK

4. Centre for Outcomes and Experience Research in Children's Health Illness and Disability Great Ormond Street Hospital for Children NHS Foundation Trust London UK

Abstract

AbstractBackgroundChildren with neuromuscular weakness or central hypoventilation often require nocturnal ventilation. Children with these conditions are living longer and the numbers of children affected are increasing. The challenges associated with managing ventilation at home have been documented; however, there has been limited investigation into accessing wider experiences such as travel. Air travel, in particular, may be considered challenging for children with these conditions because oxygen levels are lower in airplane cabins than at sea levels.ObjectiveWe sought to understand experiences of and attitudes towards travel amongst families of children using nocturnal ventilation for neuromuscular weakness or central hypoventilation.MethodsTwo semi‐structured interviews were conducted amongst participants enrolled in a trial of a new pre‐flight assessment of their tolerance of reduced oxygen levels during flight (known as a hypoxic challenge test). Children participating in the trial were aged 19 months to 18 years. Parents were interviewed and provided proxy views for younger children, and older children were encouraged to present their own views during these interviews. One interview was conducted immediately after the assessment, and a second 3 months later. Data were analysed utilising the framework approach to thematic analysis.ResultsSeventeen families participated in the first interview with 14 of these families completing the follow‐up interview. Three further families participated in the follow‐up interview only. Here, we report three themes relating to participant experience of travel and how this is impacted by their condition. The three themes and their sub‐themes were (1) insight into children's lives: hospital attendances, gaining knowledge and confidence, and child as a person; (2) travelling with your child: planes, trains and automobiles, rules of air travel, and uncertainty; and (3) the meaning of travel: normalisation, connection to extended family, expanded experiences, and freedom and equality.ConclusionsThis population of children and their families aspire to travel but face challenges from clinical and social barriers. It is essential that we further our understanding of the physiological, social and cultural aspects of their experience to facilitate their access to broadened life experiences.

Publisher

Wiley

Subject

Public Health, Environmental and Occupational Health,Developmental and Educational Psychology,Pediatrics, Perinatology and Child Health

Reference38 articles.

1. Changes in UK paediatric long-term ventilation practice over 10 years

2. Bayes H. K. Barnham S. W. &Davidson S.(2012).Commercial air travel: A handbook for people with neuromuscular weakness. West of Scotland Long Term Ventilation Unit Department of Respiratory Medicine Southern General University Hospitals Glasgow.

3. Long-term ventilation in children

4. Daily Living With Distress and Enrichment: The Moral Experience of Families With Ventilator-Assisted Children at Home

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