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DOI 10.1136/archdischild-2013-303647

Медицинская библиотека · Archives of disease in childhood · 2013

Screening of selected risk factors in developmental dysplasia of the hip: an observational study.

Talbot Christopher L, Paton Robin W

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Аннотация

BACKGROUND

Developmental dysplasia of the hip (DDH) is the most common neonatal musculoskeletal condition. In 2008, the NHS Newborn and Infant Physical Examination committee added selective 'at risk' screening to the existing universal neonatal and general practitioner clinical hip screening guidelines.

OBJECTIVE

Assessment of breech and family history risk factors in DDH.

DESIGN

A 15 year prospective, observational, longitudinal cohort study.

METHOD: Breech presentation and evidence of a strong family history for DDH were the 'risk factors' studied. All infants referred were clinically and sonographically screened by one consultant paediatric orthopaedic surgeon.

RESULTS

From a cohort of 64 670 live births, 2984 neonates/infants, 46.1 (95% CI 44.6 to 47.8) per 1000 live births, were referred and sonographically screened with these risk factors alone. 1360 were male, of which four were identified as having 'pathological' DDH (an incidence of 0.003 (95% CI 0.001 to 0.008)). 1624 were female, of which 45 were identified as having 'pathological' DDH (an incidence of 0.028 (95% CI 0.021 to 0.037)). This difference in incidence of 0.025 (95% CI 0.016 to 0.033) was statistically significant (p<0.001). From those who were clinically stable and screened with either or both of the two risk factors, four individuals were diagnosed with irreducible hip dislocation (0.06 (95% CI 0.024 to 0.159) per 1000 live births). All were females.

CONCLUSIONS

This study questions the current UK screening policy for DDH in clinically stable males referred with risk factors, and may influence future DDH screening programme policy.

Для цитирования: Talbot Christopher L, Paton Robin W. Screening of selected risk factors in developmental dysplasia of the hip: an observational study.. Archives of disease in childhood. 2013. DOI: 10.1136/archdischild-2013-303647.

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