Progression to musculoskeletal deformity in childhood dystonia. (May 2016)

• Record Type: Journal Article
• Authors: Lumsden, Daniel E.; Gimeno, Hortensia; Elze, Markus; Tustin, Kylee; Kaminska, Margaret; Lin, Jean-Pierre
• Is Part Of: European journal of paediatric neurology. Volume 20:Number 3(2016:May)
• Page Start: 339
• Page End: 345
• Publication Date: 2016-05
• Subjects: Dystonia -- Contracture -- Spasticity -- Childhood -- Deformity; Pediatric neurology -- Periodicals; Nervous System Diseases -- Periodicals; Child -- Periodicals; Infant -- Periodicals; Neurologie pédiatrique -- Périodiques; Pediatric neurology; Electronic journals; Periodicals; Electronic journals; 618.928
• DOI: 10.1016/j.ejpn.2016.02.006
• Languages: English
• ISSNs: 1090-3798

Abstract

Abstract: Aim: Dystonia is a movement disorder characterized by involuntary muscle contractions, resulting in abnormalities of posture and movement. Children with dystonia are at risk of developing fixed musculoskeletal deformities (FMDs). FMDs cause pain, limit function and participation and interfere with care. We aimed to explore factors relating to the development of FMD in a large cohort of children with dystonia. Method: The case notes of all children referred to our Complex Motor Disorder service between July 2005 and December 2011 were reviewed. Data from 279 children (median age 9 years 10 months, Standard Deviation 4 years 2 months) with motor disorders including a prominent dystonic element were analyzed. Parametric accelerated failure time regression was used to identify the factors related to development of contractures. Results: FMDs were present at referral in more than half (n = 163, 58%) of cases. Three quarters (n = 120, 74%) of children with FMD had deformities around the hip, and 42% had spinal deformity (n = 68). Compared to pure primary dystonia, FMD onset was earlier with a diagnosis of secondary or heredodegenerative dystonia, and a mixed spastic–dystonic phenotype (all p < 0.001). FMD onset was also earlier with increasing Gross Motor Function Classification System (GMFCS) level (p < 0.001). The effect of aetiological classification was lost when controlling for GMFCS level and motor phenotype. Interpretation: Children with secondary or heredodegenerative dystonia are at greater risk of progression to FMD compared to primary dystonia, likely due to more severe dystonia within these groups. Children with additional spasticity are at particular risk, requiring close monitoring. Highlights: Fixed Musculoskeletal Deformity (FMD) are common in children with dystonia at the time of referral. Progression to FMD is faster with worsening GMFCS level. Progression to FMD is faster in children with both dystonia and spasticity.