Rofo 2014; 186(1): 54-60
DOI: 10.1055/s-0033-1350297
Thorax
© Georg Thieme Verlag KG Stuttgart · New York

Cystic Fibrosis in Adults: Short-Term and Long-Term Reproducibility of the Brody Score for Lung Morphology in Low-Dose MDCT Scans

Cystische Fibrose (CF) bei Erwachsenen: Kurz- und Langzeit-Reproduzierbarkeit des Brody-Scores bei Niedrig-Dosis-MDCT-Aufnahmen
K. Weber
1   Department of Radiology, University of Munich, Muenich
,
M. Paolini
1   Department of Radiology, University of Munich, Muenich
,
M. Schmitz
1   Department of Radiology, University of Munich, Muenich
,
R. Fischer
2   Medical Hospital V, University of Munich, Munich
,
E. Coppenrath
1   Department of Radiology, University of Munich, Muenich
,
R. Huber
2   Medical Hospital V, University of Munich, Munich
,
M. Reiser
1   Department of Radiology, University of Munich, Muenich
,
U. G. Mueller-Lisse
1   Department of Radiology, University of Munich, Muenich
› Author Affiliations
Further Information

Publication History

25 February 2013

25 June 2013

Publication Date:
30 August 2013 (online)

Abstract

Purpose: The semi-quantitative Brody score measures the severity of cystic fibrosis (CF)-related lung disease. We investigated the short-term (28 – 60 days) and long-term (2 – 7 years) intra- and inter-observer reproducibility of the Brody score in low-dose multidetector row computed tomography examinations performed in inspiration (LDCTs) of adult CF patients.

Materials and Methods: Composite Brody scores and respective underlying bronchiectasis, mucus plugging, peribronchial thickening, parenchymal opacity, and hyperinflation subscores were evaluated twice (time interval, 1 – 84 months) by each of 3 independent radiologists (1 – 20 years of professional diagnostic radiology experience) in LDCTs (4 – 64 rows, 120 KVp, 10 – 15 mAs/slice, CTDIw approx. 1.0 mGy, effective dose approx. 0.5 mSv) of 15 adult patients with CF-related lung disease (8 female, 7 male, age, 18 – 50 years, mean, 33 years).

Results: The average reproducibility of the Brody score was within +/–7 % (range, 2 – 30 %) between radiologists, and +/–6 % (3 – 12 %) within radiologists (short-term, 28 – 60 days, 4 %, 0 – 12 %, long-term, 2 – 7 years, 12 %, 1 – 36 %). For the different subscores, the reproducibility was within +/–25 % (15 – 41 %) between radiologists and +/–23 % (12 – 46 %) within radiologists.

Conclusion: The Brody score shows high average inter-observer reproducibility in LDCTs of adult CF patients. The Brody score also demonstrates high average intra-observer reproducibility if subsequent assessments are made within 28 – 61 days. With time intervals of 2 – 7 years between subsequent evaluations, however, intra-observer reproducibility decreases. Respective subscores each demonstrate lower intra- and inter-observer reproducibility than does the composite Brody score.

Citation Format:

  • Weber K, Paolini M, Schmitz M et al. Cystic Fibrosis in Adults: Short-Term and Long-Term Reproducibility of the Brody Score for Lung Morphology in Low-Dose MDCT Scans. Fortschr Röntgenstr 2014; 186: 54 – 60

Zusammenfassung

Ziel: Auswertungen des semiquantitativen Brody- Score quantifizieren das Ausmaß CF-bedingter Lungenschädigung. Die Studie untersuchte die Kurz- (KZI, 28 – 60 Tage) und Langzeit- (LZI, 2 – 7 Jahre), Intra- und Inter-Betrachter-Reproduzierbarkeit des Brody-Scores und seiner Subscores (Bronchiektasen, peribronchiale Zeichnungsvermehrung, Mucusplugging, Gewebekonsolidierung und Überblähung) anhand von Niedrig-Dosis-Multidetektor-CT-Aufnahmen in Inspiration (LDCT) von 15 erwachsenen CF-Patienten.

Material und Methoden: Die Niedrig-Dosis-Multidetektor-CT-Aufnahmen (Schichtdicke 1,5 und 3 mm, 120 kV, mAS/Schicht 10 – 15, effektive Dosis 0,5 mSv, CDTi 1,0 Gy/Patient) von 15 Patienten (8 weiblich, 7 männlich, Altersspanne 18 – 50 Jahre, durchschnittliches Alter 33 J.) mit pulmonaler Manifestation bei CF wurden bzgl. des Brody-Score und seiner Subscores (Bronchiektasen, peribronchiale Zeichnungsvermehrung, Schleimverlegung, Gewebekonsolidierung, Überblähung) von 3 unabhängigen Radiologen (1 – 20 Jahre Berufserfahrung) jeweils zweimal ausgewertet (Zeitintervall zwischen den Auswertungen, 1 – 84 Monate).

Ergebnisse: Die durchschnittliche Inter-Betrachter-Reproduzierbarkeit des Brody-Score betrug +/– 7 % (2 – 30 %). Die Intra-Betrachter-Reproduzierbarkeit lag bei +/–6 % (3 – 12 %) (KZI, 4 %, 0 – 12 %, LZI, 12 %, 1 – 36 %). Für die Subscores betrug die Inter-Betrachter-Reproduzierbarkeit durchschnittlich +/–25 % (15 – 41 %), die Intra-Betrachter-Reproduzierbarkeit +/–23 % (12 – 46 %).

Schlussfolgerung: Der Brody-Score zeigt eine hohe Inter-Betrachter-Reproduzierbarkeit bei LDCTs erwachsener CF-Patienten sowie eine gute Intra-Betrachter-Reproduzierbarkeit im KZI erfolgen, welche jedoch im LZI sinkt. Im Vergleich zum Gesamtscore zeigen die Subscores durchschnittlich eine geringere Inter- und Intra-Betrachter-Reproduzierbarkeit.

 
  • References

  • 1 Radivojevic D, Guc-Scekic M, Djurisic M et al. Povezanost izmedju genskih mutacija i egzokrine funkcije pankreasa kod osoba obolelih od cisticne fibroze. Srp Arh Celo Lek 2001; 129: 6-9
  • 2 Judge EP, Dodd JD, Masterson JB et al. Pulmonary abnormalities on high-resolution CT demonstrate more rapid decline than FEV1 in adults with cystic fibrosis. Chest 2006; 130: 1424-1432
  • 3 Estivill X, Bancells C, Ramos C et al. Geographic Distribution and Regional Origin of 272 Cystic Fibrosis Mutations in European Populations. Hum Mutat 1997; 10: 135-154
  • 4 Merlo CA, Boyle MP. Modifier genes in cystic fibrosis lung disease. J Lab Clin Med 2003; 141: 237-241
  • 5 Files/research/ClinicalResearch/2008-Patient-Registry-Report.pdf. www.cff.org/Uploaded CFF patient registry report 2008
  • 6 Dodd JD, Barry SC, Barry RB et al. Thin-section CT in patients with cystic fibrosis: correlation with peak exercise capacity and body mass index. Radiology 2006; 240: 236-245
  • 7 Tiddens HA. Chest Computed Tomography Scans Should Be Considered as a Routine in Investigation in Cystic Fibrosis. Paediatr Respir Rev 2006; 7: 202-208
  • 8 Söderberg M, Gunnarsson M. Automatic exposure control in computed tomography – an evaluation of systems from different manufacturers. Acta Radiol 2010; 51: 625-634
  • 9 Mueck FG, Körner M, Scherr MK et al. Upgrade to iterative image reconstruction (IR) in abdominal MDCT imaging: a clinical study for detailed parameter optimization beyond vendor recommendiations using the adaptive statistical iterative reconstruction environment (ASIR). Fortschr Röntgenstr 2012; 184: 229-238
  • 10 Coppenrath E, Mueller-Lisse UG, Lechel U et al. Niedrigdosis-Spiral-CT des Thorax in der Verlaufskontrolle nichtmaligner Lungenerkrankungen. Fortschr Röntgenstr 2004; 176: 522-528
  • 11 Robinson TE. Imaging of the chest in cystic fibrosis. Clin Chest Med 2007; 28: 405-421
  • 12 de Jong PA, Tiddens HA. Cystic-fibrosis-specific computed tomography scoring. Proc Am Soc Thorac Soc 2007; 4: 338-342
  • 13 Brody AS, Klein JS, Molina PL et al. High-resolution computed tomography in young patients with cystic fibrosis: distribution of abnormalities and with pulmonary function tests. J Pediatr 2004; 145: 32-38
  • 14 Brody AS, Kosorok MR, Li Z et al. Reproducibility of a scoring system for computed correlation tomography scanning in cystic fibrosis. J Thorac Imaging 2006; 21: 14-21
  • 15 Wiedemann B, Steinkamp G, Sens B et al. The German Cystic Fibrosis Quality Assurance Project: Clinical Features in Children and Adults. Eur Respir J 2001; 17: 1187-1194
  • 16 Glantz SA. Primer of Biostatistics. 6th edn. New York: McGraw-Hill Medical Publishing Division; 2005
  • 17 Bhalla M, Turcios N, Aponte V et al. Cystic Fibrosis: Scoring System with Thin Section CT. Radiology 1991; 179: 783-788