Can 129Xe ventilation MRI guide personalisation of airway clearance regimens in children with Primary Ciliary Dyskinesia?
Children with Primary Ciliary Dyskinesia (PCD) use airway clearance techniques (ACT), but clinicians lack sensitive outcome methods to guide ACT personalisation. We explored if providing data from highly sensitive <sup>129</sup>Xe Ventilation MRI (<sup>129</sup>Xe-MRI) influenced physiotherapists’ decision making. During cognitive task analysis interviews, physiotherapists were asked to “think aloud” their clinical decisions whilst reviewing the data of children with PCD under their care: routine clinical information; baseline structural MRI; <sup>129</sup>Xe-MRI data acquired pre, post-ACT and 4-hours post-ACT. 5 experienced physiotherapists from four NHS trusts reviewed data from a total of 19 children with PCD (age 5-17years). <sup>129</sup>Xe-MRI data aligned with the physiotherapists’ existing clinical impression for nine cases. In these reviews, the <sup>129</sup>Xe-MRI either confirmed the physiotherapists’ ACT regimen decision or led them to propose modifications. In ten cases <sup>129</sup>Xe-MRI either challenged the current clinical impression or <sup>129</sup>Xe-MRI findings differed from structural MRI findings. For these cases, the physiotherapist either: re-evaluated their clinical decisions and proposed ACT regimen modifications or; felt unsure what regimen changes to propose during the review, so planned to reassess the patient in light of the <sup>129</sup>Xe-MRI findings. Clinical review of <sup>129</sup>Xe-MRI led physiotherapists to propose ACT regimen changes in some children with PCD. In some cases, clinical re-assessment was warranted prior to making regimen modifications. <sup>129</sup>Xe-MRI provides an intuitive 3D lung ventilation image, which is sensitive to airways obstruction and can inform ACT regimen personalisation.
Authors
- Jim M. Wild (ORCID: https://orcid.org/0000-0002-7246-8660)
- Laurie Smith (ORCID: https://orcid.org/0000-0002-5769-423X)
- Lynne Schofield (ORCID: https://orcid.org/0000-0002-5124-430X)
- Anna Shawcross (ORCID: https://orcid.org/0000-0003-1788-5493)
- Eduardo Moya (ORCID: https://orcid.org/0000-0001-9356-9009)
- Sally J. Singh (ORCID: https://orcid.org/0000-0002-9834-0366)
- Daniel Hind (ORCID: https://orcid.org/0000-0002-6409-4793)
- David Hughes (ORCID: https://orcid.org/0000-0003-0994-1977)
- N. West (ORCID: https://orcid.org/0000-0002-8927-8839)
- Evie Robson (ORCID: https://orcid.org/0000-0003-1247-7431)
- Alberto Biancardi (ORCID: https://orcid.org/0009-0000-2765-0773)
- Helen Marshall (ORCID: https://orcid.org/0000-0002-7425-1449)
- David Capener (ORCID: https://orcid.org/0000-0003-2394-8729)
- Susi Shanks
Institutions
- University of Leicester (GB)
- Leeds Teaching Hospitals NHS Trust (GB)
- House of Representatives (NL)
- Sheffield Teaching Hospitals NHS Foundation Trust (GB)
- Royal Manchester Children's Hospital (GB)
- Sheffield Children's Hospital (GB)
- Bradford Teaching Hospitals NHS Foundation Trust (GB)
- University of Sheffield (GB)
Publication Details
- Published
- 2024-09-14
- DOI
- https://doi.org/10.1183/13993003.congress-2024.pa1430
- Primary Topic
- Congenital Diaphragmatic Hernia Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00