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Selective sonographic screening for developmental dysplasia of the hip - increasing trends in late diagnosis
Insights
Selective screening for developmental dysplasia of the hip (DDH) appears ineffective, with a concerning trend towards late diagnosis and increased surgical intervention in the UK. Early diagnosis is linked to risk factors like breech presentation.
Area of Science:
- Paediatric Orthopaedics
- Developmental Dysplasia of the Hip (DDH)
- Medical Screening Effectiveness
Background:
- Selective sonographic screening for DDH is a common practice.
- Concerns exist regarding the suboptimal effectiveness of current screening protocols.
- Identifying trends in DDH presentation and surgical treatment is crucial.
Purpose of the Study:
- To evaluate the effectiveness of selective sonographic screening for DDH.
- To identify trends in the diagnosis and surgical management of DDH.
- To assess the impact of risk factors on DDH diagnosis timing.
Main Methods:
- Retrospective review of 103 children surgically treated for DDH (1997-2018).
- Analysis of demographic data, risk factors, age at diagnosis, and surgical treatments.
- Statistical analysis to identify trends in diagnosis and referral rates.
Main Results:
- 60.2% of patients were diagnosed late (after 4 months), with a median diagnosis age of 18.5 months in this group.
- A statistically significant increasing trend towards late diagnosis was observed over the study period.
- Late diagnosis necessitated more aggressive surgical management, particularly for irreducible hip dislocations.
Conclusions:
- The current selective sonographic screening program for DDH in the UK shows a deterioration in effectiveness.
- Late diagnosis of DDH is prevalent, particularly for irreducible hip dislocations.
- Risk factors such as breech presentation or family history are associated with earlier diagnosis.
Abstract:
There are concerns that selective sonographic screening for developmental dysplasia of the hip (DDH) may be suboptimal. Our aim was to test this hypothesis by identifying trends in presentation and surgical treatment in patients with DDH. This is a retrospective review of children born between 1997-2018 who were treated surgically for DDH at our sub- regional paediatric orthopaedic unit. Demographic data, risk factors, age of diagnosis and surgical treatments were analysed. Late diagnosis was defined as greater than 4 months. 103 children (14 male, 89 female) underwent surgery. 93 hips were operated for dislocation and 21 for dysplasia. 13 patients presented with bilateral hip dislocations. The median age at diagnosis was 10 months (95% CI: 4-15). 62/103 (60.2%) were diagnosed late (after 4 months) and the median age for diagnosis in this group was 18.5 months (95% CI: 16-20.5). Significantly more patients were referred late (p=0.0077). The presence of risk factors (breech presentation or family history) was associated with early diagnosis. Over the duration of our study the operation rate per 1000 live births gradually increased, and on Poisson regression analysis there was a statistically significant increasing trend towards late diagnosis in recent years (p=0.0237), which necessitated more aggressive surgical management. In the UK, the current selective sonographic screening programme for DDH has shown a deterioration over the years of this study and this questions its current effectiveness. It appears that the majority of irreducible hip dislocations are diagnosed late, with an increased need for surgical management.
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