Osteonecrosis secondary to the treatment of developmental dysplasia of the hip is a relatively benign condition in children and teenagers. While it was associated with limited hip function, it was not associated with physical disability. However, we speculate that this function will decline with increasing age. With regard to clinical outcome, Bucholz-Ogden grade-I hips are similar to grade-II hips and grade-III hips are similar to grade-IV hips.
This study assessed the reliability of bone age determination in normal central European children using the Greulich and Pyle method and determined the effects of readers' experience on the measured bone ages. Plain hand radiographs of 47 children (aged 2 months to 18.8 years) with normal growth were analysed by four radiologists (two experienced paediatric radiologists and two radiology residents). The readers were blinded to the age of the children. The images were re-read by the same readers 2 months later. The mean intraobserver and interobserver variations were lower for experienced readers than for radiology residents. However, these differences were not statistically significant at the 5% level. The difference between the chronological age and the measured bone age was -1.5 +/- 7.6 months (p = 0.20) for the experienced readers and 2.7 +/- 10.3 months (p = 0.09) for the radiology residents. The differences between the measured bone age and chronological age were statistically significant (p = 0.04) for only one of the two radiology residents. Although the measurements by all four readers underestimated the chronological age, the differences between chronological age and bone age were within the normal variations of skeletal maturation as reported by Greulich and Pyle. Our data suggest that the reliability of bone age measurements increases with experience and that the Greulich and Pyle method may be used for central European children.
Background Clinicians use various criteria to diagnose developmental dysplasia of the hip (DDH) in early infancy, but the importance of these various criteria for a definite diagnosis is controversial. The lack of uniform, widely agreed-on diagnostic criteria for DDH in patients in this age group may result in a delay in diagnosis of some patients. Questions/Purposes Our purpose was to establish a consensus among pediatric orthopaedic surgeons worldwide regarding the most relevant criteria for diagnosis of DDH in infants younger than 9 weeks. Material and Methods We identified 212 potential criteria relevant for diagnosing DDH in infants by surveying 467 professionals. We used the Delphi technique to reach a consensus regarding the most important criteria. We then sent the survey to 261 orthopaedic surgeons from 34 countries. Results The response rate was 75%. Thirty-seven items were identified by surgeons as most relevant to diagnose DDH in patients in this age group. Of these, 10 of 37 (27%) related to patient characteristics and history, 13 of 37 (35%) to clinical examination, 11 of 37 (30%) to ultrasound, and three of 37 (8%) to radiography. A Cronbach alpha of 0.9 for both iterations suggested consensus among the panelists. Conclusion We established a consensus regarding the most relevant criteria for the diagnosis of DDH in early infancy and established their relative importance on an international basis. The highest ranked clinical criteria included the Ortolani/Barlow test, asymmetry in abduction
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.