Application of Statistical Shape Modeling to Predict Clinical Metric of Femoral Head Coverage in Patients with Developmental Dysplasia

Developmental dysplasia of the hip (DDH) is described as under-coverage of the femoral head by the acetabulum, resulting in mechanical instability. Though DDH is often diagnosed using plain film radiographs, these images cannot adequately capture 3D joint coverage. Herein, we applied a 3D statistical shape model (SSM) to the femur and hemi-pelvis of patients with DDH to objectively measure shape variation and evaluated whether SSM outputs could predict measurements of joint coverage. The femur and hemi-pelvis were semi-automatically segmented from CT images (83 hips from 47 females with DDH). Surfaces of each hip were reconstructed from segmentations, aligned, and input into a multi-domain SSM (shapeworks.sci.utah.edu). Correspondence particles were automatically placed over the bone surfaces and a subset on the femoral head and acetabulum were isolated for a joint-specific model. Modes of shape variation were determined with principal component analysis (PCA). A sparse model of PCA modes predicting coverage was determined using linear regression with Lasso regularization. Coverage measurements ranged from 27.3% to 39.4%. Eight and 13 modes were selected for the full bone and joint-specific models, respectively. These modes represented 6.1% and 39.6% of the overall shape variation for full bone and joint-specific models with mean prediction errors of 0.9% and 0.6% coverage, respectively (Figure 1). Selected modes represented the depth of the acetabulum and oblateness of the femoral head, aligning well with the clinical description of DDH. In addition, the full bone model captured morphological and pose-related differences potentially related to altered muscle paths or differences in femoral torsion

Prenatal sonographic evaluation of Arnold Chiari II Malformation

Arnold Chiari malformations are a broad group of malformations with distinctive imaging findings. They are named after an Austrian pathologist Hans Chiari who first identified types I-III in 1891. It is a spectrum of congenital abnormalities of CNS, characterized by downward displacement of the parts of the cerebellum, fourth ventricle, pons and medulla oblongata into the spinal canal. Type II is the most common subtype and is invariably associated with open neural tube defects like myelomeningocele. They constitute an important cause of neonatal morbidity and mortality and hence the need for prenatal evaluation with ultrasound to detect the anomalies. In this article we describe the features of Arnold chiari malformation, illustrate type II cases with sonological parameters for assessment, discuss the findings for diagnosis and conclude with prognosis and management