Your browser doesn't support javascript.
loading
Severity of cerebral palsy and likelihood of adverse events after botulinum toxin A injections.
Swinney, Caitlyn M; Bau, Karen; Burton, Karen L Oakley; O'Flaherty, Stephen J; Bear, Natasha L; Paget, Simon P.
Afiliação
  • Swinney CM; University of Sydney, Sydney, NSW, Australia.
  • Bau K; The Children's Hospital at Westmead, Westmead, NSW, Australia.
  • Burton KLO; The Children's Hospital at Westmead, Westmead, NSW, Australia.
  • O'Flaherty SJ; Sydney Children's Hospital, Randwick, NSW, Australia.
  • Bear NL; Child and Adolescent Health Services, Perth, WA, Australia.
  • Paget SP; The Children's Hospital at Westmead, Westmead, NSW, Australia.
Dev Med Child Neurol ; 60(5): 498-504, 2018 05.
Article em En | MEDLINE | ID: mdl-29451702
ABSTRACT

AIM:

To determine the incidence of common adverse events after botulinum toxin A (BoNT-A) injections in children with cerebral palsy (CP) and to identify whether the severity of CP influences the incidence of adverse events.

METHOD:

This was an observational study of patients attending a BoNT-A clinic at a tertiary paediatric hospital (2010-2014). Data examined included procedural adverse events at the time of injection and at follow-up. Systemic adverse events were defined as lower respiratory tract illnesses, generalized weakness, dysphagia, and death. Severity of CP was categorized by the Gross Motor Function Classification System (GMFCS). The relationships between GMFCS and adverse events were analysed using negative binomial regression models.

RESULTS:

In total, 591 children underwent 2219 injection episodes. Adverse events were reported during the procedure (130 [6%] injection episodes) and at follow-up (492 [22%] injection episodes). There were significantly increased rates of systemic adverse events in injection episodes involving children in GMFCS level IV (incidence rate ratio [IRR] 3.92 [95% confidence interval] 1.45-10.57]) and GMFCS level V (IRR 7.37 [95% confidence interval 2.90-18.73]; p<0.001).

INTERPRETATION:

Adverse events after BoNT-A injections are common but mostly mild and self-limiting. Children in GMFCS levels IV and V are at increased risk of systemic adverse events. The relationship between CP severity and BoNT-A adverse events is complex and further research is required to better understand this relationship. WHAT THIS PAPER ADDS Adverse events reported at the time of botulinum toxin A injection occurred in 6% of injection episodes. Adverse events were reported at follow-up in 22% of injection episodes. Children in Gross Motor Function Classification System (GMFCS) levels IV and V have increased rates of systemic adverse events. Children in GMFCS levels IV and V report less local weakness and pain.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Toxinas Botulínicas Tipo A / Fármacos Neuromusculares Tipo de estudo: Observational_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Cerebral / Toxinas Botulínicas Tipo A / Fármacos Neuromusculares Tipo de estudo: Observational_studies Limite: Child / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article