Viruses (Nov 2022)

Acquired Hip Dysplasia in Children with Congenital Zika Virus Infection in the First Four Years of Life

  • Marcos Vinicius da Silva Pone,
  • Tallita Oliveira Gomes da Silva,
  • Carla Trevisan Martins Ribeiro,
  • Elisa Barroso de Aguiar,
  • Pedro Henrique Barros Mendes,
  • Saint Clair dos Santos Gomes Junior,
  • Tatiana Hamanaka,
  • Andrea Araujo Zin,
  • José Paulo Pereira Junior,
  • Maria Elisabeth Lopes Moreira,
  • Karin Nielsen-Saines,
  • Sheila Moura Pone

DOI
https://doi.org/10.3390/v14122643
Journal volume & issue
Vol. 14, no. 12
p. 2643

Abstract

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Acquired hip dysplasia has been described in children with cerebral palsy (CP); periodic surveillance is recommended in this population to prevent hip displacement and dislocation. Children with congenital zika syndrome (CZS) may present a spectrum of neurological impairments with changes in tonus, posture, and movement similar to children with CP. However, the relationship between CZS and hip dysplasia has not been characterized. In this prospective cohort study, we aimed to describe the occurrence of hip dysplasia in patients with CZS. Sixty-four children with CZS from 6 to 48 months of age were included and followed at a tertiary referral center in Rio de Janeiro, Brazil, with periodic radiologic and clinical hip assessments. Twenty-six (41%) patients were diagnosed with hip dysplasia during follow-up; mean age at diagnosis was 23 months. According to the Gross Motor Function Classification System (GMFCS), 58 (91%) patients had severe impairment (GMFCS IV and V) at the first evaluation. All patients with progression to hip dysplasia had microcephaly and were classified as GMFCS IV or V. Pain and functional limitation were reported by 22 (84%) caregivers of children with hip dysplasia. All patients were referred to specialized orthopedic care; eight (31%) underwent surgical treatment during follow-up. Our findings highlight the importance of implementing a hip surveillance program and improving access to orthopedic treatment for children with CZS in order to decrease the chances of dysplasia-related complications and improve quality of life.

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