The patient's experience of primary ciliary dyskinesia: a systematic review

dc.contributor.authorBehan, Laura
dc.contributor.authorRubbo, Bruna
dc.contributor.authorLucas, Jane S.
dc.contributor.authorDunn Galvin, Audrey
dc.contributor.funderNational Health Service, United Kingdom
dc.contributor.funderAAIR Charity
dc.contributor.funderWellcome Trust
dc.contributor.funderNational Institute for Health Research
dc.description.abstractPrimary ciliary dyskinesia (PCD) is a rare genetic disorder characterised by progressive sinopulmonary disease, with symptoms starting soon after birth. The aim of this study is to critically review, analyse, and synthesise the literature in order to understand the experiences of patients with primary ciliary dyskinesia (PCD) and the impact on health-related quality of life. MEDLINE, EBSCO, Cumulative Index to Nursing and Allied Health Literature (CINAHL), PsycINFO and EMBASE were searched according to the inclusion criteria. A qualitative analysis of 14 studies was conducted. Fourteen studies were included in the review, five with qualitative methodologies. Studies originated from the UK, USA, Italy, Denmark and Belgium, one study included a survey distributed internationally. Significant relationships were found between age and worsening of respiratory symptoms, physical, and mental domains of health-related quality of life, with a greater decline compared with reference populations. Variations between the UK and Italy were found for health-related quality of life and its correlation with time since diagnosis. PCD was found to have a physical impact in all age groups: patients found it difficult to keep up with others, and found energy levels were easily depleted compared to family or peers. In terms of social impact, symptoms lead to embarrassment and a sense of isolation, with patients concealing symptoms and/or their diagnosis. In turn, isolation was also linked with the lack of public and medical knowledge. In relation to emotional impact, anxiety was reported in a number of qualitative studies; patients were anxious about getting sick or when thinking about their future health. The burden of treatment and factors influencing adherence were also discussed in depth. Health-related quality of life decreases with age in patients with PCD. For all age groups, PCD was found to greatly impact physical, emotional, social functioning, and treatment burden. More research is needed on the psychosocial impact of the illness, disease burden and its effect on quality of life.en
dc.description.sponsorshipNHS England; National Institute for Health Research (Southampton Respiratory Biomedical Research Unit); National Institute for Health Research/ Wellcome Trust (Clinical Research Facility); AAIR Charity (1129698)en
dc.description.statusPeer revieweden
dc.description.versionPublished Versionen
dc.identifier.citationBehan, L., Rubbo, B., Lucas, J. S. and Dunn Galvin, A. (2017) 'The patient’s experience of primary ciliary dyskinesia: a systematic review', Quality of Life Research, 26(9), pp. 2265-2285. 10.1007/s11136-017-1564-yen
dc.identifier.journaltitleQuality of Life Researchen
dc.publisherSpringer International Publishing AGen
dc.rights© 2017, the Authors. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.en
dc.subjectPrimary ciliary dyskinesiaen
dc.subjectPatient perspectiveen
dc.subjectHealth-related quality of lifeen
dc.subjectPatient experienceen
dc.titleThe patient's experience of primary ciliary dyskinesia: a systematic reviewen
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