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Comparative sensitivity of early cystic fibrosis lung disease detection tools in school aged children.
Bayfield, Katie J; Weinheimer, Oliver; Middleton, Anna; Boyton, Christie; Fitzpatrick, Rachel; Kennedy, Brendan; Blaxland, Anneliese; Jayasuriya, Geshani; Caplain, Neil; Wielpütz, Mark O; Yu, Lifeng; Galban, Craig J; Robinson, Terry E; Bartholmai, Brian; Gustafsson, Per; Fitzgerald, Dominic; Selvadurai, Hiran; Robinson, Paul D.
Afiliação
  • Bayfield KJ; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Weinheimer O; Department of Diagnostic and Interventional Radiology, University Hospital of Heidelberg, Heidelberg, Germany; Translational Lung Research Center Heidelberg, German Center for Lung Research DZL, Heidelberg, Germany.
  • Middleton A; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Boyton C; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Fitzpatrick R; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Kennedy B; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Blaxland A; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Jayasuriya G; The Children's Hospital at Westmead, Westmead, New South Wales, Australia; Woolcock Institute of Medical Research, Sydney, New South Wales, Australia.
  • Caplain N; The Children's Hospital at Westmead, Westmead, New South Wales, Australia.
  • Wielpütz MO; Department of Diagnostic and Interventional Radiology, University Hospital of Heidelberg, Heidelberg, Germany; Translational Lung Research Center Heidelberg, German Center for Lung Research DZL, Heidelberg, Germany.
  • Yu L; Division of Radiology, Mayo Clinic Rochester, Rochester, MN, USA.
  • Galban CJ; Department of Radiology, Michigan Medicine, Ann Arbor, MI, USA.
  • Robinson TE; Department of Pediatrics, Center of Excellence in Pulmonary Biology, Stanford University School of Medicine, Stanford, CA, USA.
  • Bartholmai B; Division of Radiology, Mayo Clinic Rochester, Rochester, MN, USA.
  • Gustafsson P; Department of Paediatrics, Central Hospital, Skövde, Sweden.
  • Fitzgerald D; The Children's Hospital at Westmead, Westmead, New South Wales, Australia; The University of Sydney, Sydney, New South Wales, Australia.
  • Selvadurai H; The Children's Hospital at Westmead, Westmead, New South Wales, Australia; The University of Sydney, Sydney, New South Wales, Australia.
  • Robinson PD; The Children's Hospital at Westmead, Westmead, New South Wales, Australia; Woolcock Institute of Medical Research, Sydney, New South Wales, Australia; The University of Sydney, Sydney, New South Wales, Australia; Children's Health and Environment Program, Child Health Research Centre, University of
J Cyst Fibros ; 23(5): 918-925, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38969602
ABSTRACT

BACKGROUND:

Effective detection of early lung disease in cystic fibrosis (CF) is critical to understanding early pathogenesis and evaluating early intervention strategies. We aimed to compare ability of several proposed sensitive functional tools to detect early CF lung disease as defined by CT structural disease in school aged children.

METHODS:

50 CF subjects (mean±SD 11.2 ± 3.5y, range 5-18y) with early lung disease (FEV1≥70 % predicted 95.7 ± 11.8 %) performed spirometry, Multiple breath washout (MBW, including trapped gas assessment), oscillometry, cardiopulmonary exercise testing (CPET) and simultaneous spirometer-directed low-dose CT imaging. CT data were analysed using well-evaluated fully quantitative software for bronchiectasis and air trapping (AT).

RESULTS:

CT bronchiectasis and AT occurred in 24 % and 58 % of patients, respectively. Of the functional tools, MBW detected the highest rates of abnormality Scond 82 %, MBWTG RV 78 %, LCI 74 %, MBWTG IC 68 % and Sacin 51 %. CPET VO2peak detected slightly higher rates of abnormality (9 %) than spirometry-based FEV1 (2 %). For oscillometry AX (14 %) performed better than Rrs (2 %) whereas Xrs and R5-19 failed to detect any abnormality. LCI and Scond correlated with bronchiectasis (r = 0.55-0.64, p < 0.001) and AT (r = 0.73-0.74, p < 0.001). MBW-assessed trapped gas was detectable in 92 % of subjects and concordant with CT-assessed AT in 74 %.

CONCLUSIONS:

Significant structural and functional deficits occur in early CF lung disease, as detected by CT and MBW. For MBW, additional utility, beyond that offered by LCI, was suggested for Scond and MBW-assessed gas trapping. Our study reinforces the complementary nature of these tools and the limited utility of conventional oscillometry and CPET in this setting.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes de Função Respiratória / Espirometria / Tomografia Computadorizada por Raios X / Fibrose Cística Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Testes de Função Respiratória / Espirometria / Tomografia Computadorizada por Raios X / Fibrose Cística Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Cyst Fibros Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Austrália