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Closed Reduction for Developmental Dysplasia of the Hip: Early-term Results From a Prospective, Multicenter Cohort
Wudbhav N Sankar1, Alex L Gornitzky1, Nicholas M P Clarke2
1Division of Orthopaedics, Children's Hospital of Philadelphia, Philadelphia, PA.
Insights
Closed reduction for infantile hip dysplasia shows a 9% failure rate and 25% avascular necrosis risk. Early outcomes are not influenced by reducibility, age, or prior bracing.
Area of Science:
- Orthopedics
- Pediatric Orthopedics
- Hip Dysplasia Treatment
Background:
- Infantile developmental dysplasia of the hip (DDH) is commonly treated with closed reduction (CR).
- Early outcomes of CR for DDH require further investigation.
Purpose of the Study:
- To determine the early outcomes following closed reduction for infantile developmental dysplasia of the hip.
- To assess the incidence of failure, avascular necrosis (AVN), and residual dysplasia after CR.
Main Methods:
- Prospective, international, multicenter observational study of 78 patients (87 hips) treated from 2010-2014.
- Minimum 1-year follow-up, defining failure as IHDI grade 3/4 hip or need for open reduction.
- Assessed AVN, residual dysplasia, need for further surgery, and factors influencing outcomes.
Main Results:
- 91% of initially successful CRs remained stable at median 22-month follow-up.
- 25% of successfully reduced hips developed AVN; 11% required osteotomy for residual dysplasia.
- No significant correlation found between CR success/AVN and initial reducibility, age at CR, or prior bracing.
Conclusions:
- Closed reduction for infantile DDH has an early-term failure rate of 9% and AVN rate of 25%.
- Factors like femoral head reducibility, prior bracing, and age at CR did not impact success or AVN risk.
- Longer follow-up is needed to establish definitive success and complication rates for CR in infantile DDH.
Background:
Closed reduction (CR) is a common treatment for infantile developmental dysplasia of the hip. The purpose of this observational, prospective, multicenter study was to determine the early outcomes following CR.
Methods:
Prospectively collected data from an international multicenter study group was analyzed for patients treated from 2010 to 2014. Baseline demographics, clinical exam, radiographic/ultrasonographic data, and history of previous orthotic treatment were assessed. At minimum 1-year follow-up, failure was defined as an IHDI grade 3 or 4 hip and/or need for open reduction. The incidence of avascular necrosis (AVN), residual dysplasia, and need for further surgery was assessed.
Results:
A total of 78 patients undergoing CR for 87 hips were evaluated with a median age at initial reduction of 8 months (range, 1 to 20 mo). Of these, 8 hips (9%) were unable to be closed reduced initially. At most recent follow-up (median 22 mo; range, 12 to 36 mo), 72/79 initially successful CRs (91%) remained stable. The likelihood of failure was unaffected by initial clinical reducibility of the hip (P=0.434), age at initial CR (P=0.897), or previous treatment in brace (P=0.222). Excluding those hips that failed initial CR, 18/72 hips (25%) developed AVN, and the risk of osteonecrosis was unaffected by prereduction reducibility of the hip (P=0.586), age at CR (P=0.745), presence of an ossific nucleus (P=0.496), or previous treatment in brace (P=0.662). Mean acetabular index on most recent radiographs was 25 degrees (±6 degrees), and was also unaffected by any of the above variables. During the follow-up period, 8/72 successfully closed reduced hips (11%) underwent acetabular and/or femoral osteotomy for residual dysplasia.
Conclusions:
Following an initially successful CR, 9% of hips failed reduction and 25% developed radiographic AVN at early-term follow-up. History of femoral head reducibility, previous orthotic bracing, and age at CR did not correlate with success or chances of developing AVN. Further follow-up of this prospective, multicenter cohort will be necessary to establish definitive success and complication rates following CR for infantile developmental dysplasia of the hip.
Level Of Evidence:
Level II-prospective observational cohort.
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