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Clinical characteristics of children with severe neurologic impairment: A scoping review.
Nelson, Katherine E; Finlay, Melissa; Huang, Emma; Chakravarti, Vishakha; Feinstein, James A; Diskin, Catherine; Thomson, Joanna; Mahant, Sanjay; Widger, Kimberley; Feudtner, Chris; Cohen, Eyal.
Afiliação
  • Nelson KE; Pediatric Advanced Care Team, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Finlay M; Department of Paediatrics, Division of Paediatric Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Huang E; Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.
  • Chakravarti V; Institute for Clinical Evaluative Sciences, Toronto, Ontario, Canada.
  • Feinstein JA; Institute for Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
  • Diskin C; Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.
  • Thomson J; Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.
  • Mahant S; Pediatric Advanced Care Team, Hospital for Sick Children, Toronto, Ontario, Canada.
  • Widger K; Child Health Evaluative Sciences, SickKids Research Institute, Toronto, Ontario, Canada.
  • Feudtner C; Adult and Child Consortium for Health Outcomes Research and Delivery Science, University of Colorado and Children's Hospital Colorado, Aurora, Colorado, USA.
  • Cohen E; Department of Paediatrics, Division of Paediatric Medicine, Hospital for Sick Children, Toronto, Ontario, Canada.
J Hosp Med ; 18(1): 65-77, 2023 01.
Article em En | MEDLINE | ID: mdl-36484088
ABSTRACT

OBJECTIVE:

The aim of this study is to extrapolate the clinical features of children with severe neurologic impairment (SNI) based on the functional characteristics and comorbidities described in published studies.

METHODS:

Four databases were searched. We included studies that describe clinical features of a group of children with SNI (≥20 subjects <19 years of age with >1 neurologic diagnosis and severe functional limitation) using data from caregivers, medical charts, or prospective collection. Studies that were not written in English were excluded. We extracted data about functional characteristics, comorbidities, and study topics.

RESULTS:

We included 102 studies, spanning 5 continents over 43 years, using 41 distinct terms for SNI. The terms SNI and neurologic impairment (NI) were used in 59 studies (58%). Most studies (n = 81, 79%) described ≥3 types of functional characteristics, such as technology assistance and motor impairment. Studies noted 59 comorbidities and surgeries across 10 categories. The most common comorbidities were related to feeding, nutrition, and the gastrointestinal system, which were described in 79 studies (77%). Most comorbidities (76%) were noted in <10 studies. Studies investigated seven clinical topics, with "Gastrointestinal reflux and feeding tubes" as the most common research focus (n = 57, 56%). The next most common topic, "Aspiration and respiratory issues," included 13 studies (13%). Most studies (n = 54, 53%) were retrospective cohorts or case series; there were no clinical trials.

CONCLUSIONS:

Despite the breadth of described comorbidities, studies focused on a narrow set of clinical topics. Further research is required to understand the prevalence, clinical impact, and interaction of the multiple comorbidities that are common in children with SNI.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cuidadores / Doenças do Sistema Nervoso Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cuidadores / Doenças do Sistema Nervoso Tipo de estudo: Diagnostic_studies / Observational_studies / Risk_factors_studies / Systematic_reviews Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article