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Development of CT-based methods for longitudinal analyses of paranasal sinus osteitis in granulomatosis with polyangiitis.
Holme, Sigrun Skaar; Moen, Jon Magnus; Kilian, Karin; Haukeland, Hilde; Molberg, Øyvind; Eggesbø, Heidi B.
  • Holme SS; Division of Radiology and Nuclear Medicine, Oslo University Hospital, PB 4950 Nydalen, Oslo, 0424, Norway. sigrun.skaar.holme@gmail.com.
  • Moen JM; Institute of Clinical Medicine, University of Oslo, PB 1072 Blindern, Oslo, 0316, Norway. sigrun.skaar.holme@gmail.com.
  • Kilian K; Division of Radiology and Nuclear Medicine, Oslo University Hospital, PB 4950 Nydalen, Oslo, 0424, Norway.
  • Haukeland H; Institute of Clinical Medicine, University of Oslo, PB 1072 Blindern, Oslo, 0316, Norway.
  • Molberg Ø; Department of Rheumatology, Dermatology and Infectious Diseases, PB 4950 Nydalen, Oslo, 0424, Norway.
  • Eggesbø HB; Department of Rheumatology, Martina Hansen Hospital, Dønskiveien 8, Gjettum, 1346, Norway.
BMC Med Imaging ; 19(1): 13, 2019 02 04.
Article en En | MEDLINE | ID: mdl-30717680
ABSTRACT

BACKGROUND:

Even though progressive rhinosinusitis with osteitis is a major clinical problem in granulomatosis with polyangiitis (GPA), there are no studies on how GPA-related osteitis develops over time, and no quantitative methods for longitudinal assessment. Here, we aimed to identify simple and robust CT-based methods for capture and quantification of time-dependent changes in GPA-related paranasal sinus osteitis and compare performance of the methods under study in a largely unselected GPA cohort.

METHODS:

GPA patients (n = 121) with ≥3 paranasal CT scans obtained ≥12 months apart and control patients not having GPA or rhinosinusitis (n = 15) were analysed by (i) Global osteitis scoring scale (GOSS), originally developed for chronic rhinosinusitis; (ii) Paranasal sinus volume by manual segmentation; (iii) Mean maxillary and sphenoid diameter normalised to landmark distances (i.e. diameter ratio measurement, DRM).

RESULTS:

Time-dependent changes in GPA-related osteitis were equally well measured by the simple DRM and the labour-intensive volume method while GOSS missed ongoing changes in cases with extensive osteitis. GOSS at last CT combined with DRM identified three distinct patient groups (i) The no osteitis group, who had no osteitis and no change in DRM from baseline CT to last CT (45/121 GPA patients and 15/15 disease controls); (ii) Stable osteitis group, with presence of osteitis, but no change in DRM across time (31 GPA); (iii) Progressive osteitis, defined by declining DRM (45 GPA).

CONCLUSIONS:

We suggest DRM and GOSS as complementary methods for capturing, classifying and quantifying time-dependent changes in GPA-related osteitis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteítis / Senos Paranasales / Sinusitis / Tomografía Computarizada por Rayos X / Granulomatosis con Poliangitis Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Osteítis / Senos Paranasales / Sinusitis / Tomografía Computarizada por Rayos X / Granulomatosis con Poliangitis Tipo de estudio: Diagnostic_studies / Etiology_studies / Guideline / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Child / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article