Abstract

A fully automated, unsupervised lobe segmentation algorithm is presented based on a probabilistic segmentation of the fissures and the simultaneous construction of a populationmodel of the fissures. A two-class probabilistic segmentation segments the lung into candidate fissure voxels and the surrounding parenchyma. This was combined with anatomical information and a groupwise fissure prior to drive non-parametric surface fitting to obtain the final segmentation. The performance of our fissure segmentation was validated on 30 patients from the chronic obstructive pulmonary disease COPDGene cohort, achieving a high median F1 -score of 0.90 and showed general insensitivity to filter parameters. We evaluated our lobe segmentation algorithm on the Lobe and Lung Analysis 2011 dataset, which contains 55 cases at varying levels of pathology. We achieved the highest score of 0.884 of the automated algorithms. Our method was further tested quantitatively and qualitatively on 80 patients from the COPDgene study at varying levels of functional impairment. Accurate segmentation of the lobes is shown at various degrees of fissure incompleteness for 96% of all cases. We also show the utility of including a groupwise prior in segmenting the lobes in regions of grossly incomplete fissures.

Highlights

  • S EGMENTATION of the pulmonary lobes can facilitate the localisation and quantification of respiratory diseasesManuscript received January 16, 2017; revised March 17, 2017; accepted March 21, 2017

  • We did not define a volume of interest (VoI) using a 40mm width band around each reference as this ignores potential false positives in the validation

  • Voxels of S are classified as true positive (T P1) if they fall within the 3mm band and false positive (F P) if otherwise

Read more

Summary

Introduction

S EGMENTATION of the pulmonary lobes can facilitate the localisation and quantification of respiratory diseases. Manuscript received January 16, 2017; revised March 17, 2017; accepted March 21, 2017. Date of publication April 18, 2017; date of current version July 30, 2017. It used data (phs000179.v5.p2) generated by the COPDGene study, supported by NIH Grant U01HL089856 and Grant U01HL0899897.

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call