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[Developmental dysplasia of the hip in children with a psychomotor disorder. A risk factor for a poor outcome?]
Iván Pipa-Muñiz1, María de Los Llanos Rodríguez-Rodríguez2, M Blanca Felgueroso-Juliana3
1Servicio de COT, Hospital de Cabueñes, Gijón, Asturias, España.
Insights
Cerebral impairment significantly worsens outcomes for developmental dysplasia of the hip (DDH) treatment, increasing poor outcome risk by 7.2 times. Delayed walking in DDH patients warrants neurological assessment.
Area of Science:
- Orthopaedics
- Paediatric Neurology
- Developmental Paediatrics
Background:
- Early diagnosis of developmental dysplasia of the hip (DDH) typically leads to successful orthopaedic treatment.
- Outcomes for DDH patients with co-occurring cerebral impairment are not well-established.
- Cerebral impairment may impact the success of DDH treatment.
Purpose of the Study:
- To investigate the outcomes of developmental dysplasia of the hip (DDH) treatment in patients with cerebral impairment.
- To determine the impact of neurological disorders on DDH treatment success.
Main Methods:
- Retrospective observational study of 325 DDH cases (293 patients).
- Inclusion of patients with poor orthopaedic treatment outcomes and unknown psychomotor status.
- Clinical, radiological, and neurological assessments by a Child Neurology Unit.
Main Results:
- 10 patients (3%) with DDH also had cerebral impairment.
- Orthopaedic treatment success was only 25% (4/16 hips); 12 hips required surgery.
- Surgical treatment improved Acetabular Index (p=0.005) and Reimers Extrusion Index (p=0.042).
- Cerebral impairment diagnosed at 2.5 years; delayed walking noted at 2.4 years.
Conclusions:
- Cerebral impairment is associated with a 7.2 times higher relative risk of poor DDH treatment outcomes.
- Unfavourable DDH outcomes should prompt suspicion of neurological disorders, especially with delayed walking.
- Early identification of neurological issues is crucial for managing DDH patients.
Introduction:
Orthopaedic treatment of developmental dysplasia of the hip (DDH) has a high success rate in cases that are diagnosed early. However, the outcomes of these patients are not really known when they are subsequently diagnosed with some type of cerebral impairment.
Materials And Methods:
A retrospective observational study was conducted on cases of DDH with a poor outcome after orthopaedic treatment, being unknown if they had any type of psychomotor disorder. The patients were clinically and radiologically assessed, and afterwards received neurological valuation by the Child Neurology Unit.
Results:
Of the 325 cases of DDH diagnosed in 293 patients, 10 patients (3%) with 16 hips with DDH were diagnosed of any cerebral impairment. All them were initially treated orthopedically. Clinical and radiologically evolution was succesful only in 4 cases (25%) being necessary any surgical procedure in the remaining 12 cases. After surgical treatment we got an improvement in the Acetabular Index (p=0.005) and Reimers Extrusion Index (p=0.042). Neck-shaft angle and Wiberg CE angle also improved but this difference was not statically significant. Cerebral impairment was diagnosed at 2,5 years of age and the begining of walking was delayed at 2.4 years of age.
Conclusions:
Cerebral impairment can lead to an unfavourable outcome in the treatment of DDH, with the relative risk of a poor outcome being 7.2 times higher in these patients. An unfavourable outcome with conventional treatment of DDH must make us suspect the presence of some type of neurological disorder, particularly if there is a delay in walking.
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