QUANTITATIVE SONOGRAPHIC FEATURE ANALYSIS OF CLINICAL INFANT HYPOXIA - A PILOT-STUDY

Citation
Ll. Barr et al., QUANTITATIVE SONOGRAPHIC FEATURE ANALYSIS OF CLINICAL INFANT HYPOXIA - A PILOT-STUDY, American journal of neuroradiology, 17(6), 1996, pp. 1025-1031
Citations number
12
Categorie Soggetti
Clinical Neurology","Radiology,Nuclear Medicine & Medical Imaging
ISSN journal
01956108
Volume
17
Issue
6
Year of publication
1996
Pages
1025 - 1031
Database
ISI
SICI code
0195-6108(1996)17:6<1025:QSFAOC>2.0.ZU;2-G
Abstract
PURPOSE: To determine whether textural features derived from sonograph ic pixel intensities differ significantly between healthy infants and infants who have had acute clinical hypoxic episodes, METHODS: Neuroso nographic and calibration phantom-processed image data were evaluated prospectively from 9 infants (age range, 1 to 163 days) with at least 1 episode of hypoxia and compared with image data from a control popul ation of 16 healthy infants (age range, 1 to 191 days). Custom softwar e was used to make 45 textural feature measurements on 40 x 40-pixel r egions of interest within brain parenchyma in the distribution of each major cerebral artery, the thalami, and the cerebellum and in a tissu e-mimicking calibration phantom, Means comparison testing was followed by logistic regression to assess statistical variation between the pa tients and the control group. RESULTS: Nine of 45 textural features sh owed statistically significant differences between mean values compari ng the two groups. Mean gray level was the most sensitive predictor of differences between the two populations (mean gray level for healthy subjects was 46.8; mean gray level for patients was 56.3). An average of mean gray values in areas supplied by the posterior cerebral arteri es and the cerebellum was even more sensitive for differentiating heal thy subjects from patients. CONCLUSIONS: Quantitative sonographic text ural feature analysis showed differences between the brains of healthy infants and those of infants with clinical hypoxia.