The Impact on Parents of Diagnosing PCD in Young Children

Author:

Driessens Corine,Carr Siobhan,Clough Edel,Copeland Fiona,Dell Sharon,Dixon Lucy,Harris Amanda,Knibb RebeccaORCID,Leigh Margaret,Narayanan Manjith,Redfern Beatrice,Robson EvieORCID,Sawras Michael,Schofield Lynne,Sullivan Kelli,Tipping Myra,Tran Nhu,Walker Woolf,Lucas Jane S.ORCID,Behan LauraORCID

Abstract

Primary ciliary dyskinesia (PCD) is an incurable, rare, inherited, chronic condition. Treatment includes the regular clearing of airway mucus, aggressive treatment of infections and management of hearing loss. Caregiver burden has not been explored, hence we interviewed 18 mothers and 6 fathers of children under 6 years to understand the impact of diagnostic testing and implications of a positive diagnosis. Interviews were transcribed and thematically analysed and five key themes were identified. These included the parents’ experiences following child’s diagnosis, impact of child’s treatment regimen on parent, impact of child’s health status on parent, parent’s coping strategies, and parental concerns for the future. Parents described their diagnostic journey, with the findings revealing how a lack of awareness among clinicians of the PCD symptom pattern can lead to a delayed diagnosis. Parents discussed the emotional and practical impact of a PCD diagnosis and the coping strategies employed to deal with challenges arising following a diagnosis. Parents use a variety of different lifestyle changes to accommodate their child’s treatment regimen and to cope with disruptive life events such as the COVID-19 pandemic. This study provides valuable insights into parental adjustment and adaptation to a PCD diagnosis and management regimen. Going forward, this research highlights the need for integrated social care for PCD patients and their families.

Funder

National Institute for Health Research

Publisher

MDPI AG

Subject

General Medicine

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