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Strategies to improve communication about neurocognitive impacts in pediatric oncology: Quality improvement findings.
Ruble, Kathy; Paré-Blagoev, Juliana; Carey, Lisa B; Milla, Kimberly; Thornton, Clifton P; Henegan, Sydney; Jacobson, Lisa A.
Afiliação
  • Ruble K; Division of Pediatric Oncology, Johns Hopkins University School of Medicine, Baltimore, MD, United States.
  • Paré-Blagoev J; Division of Advanced Studies in Education, Johns Hopkins University School of Education, Baltimore, MD, United States.
  • Carey LB; Division of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, United States.
  • Milla K; Division of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, United States.
  • Thornton CP; Center for Pediatric Nursing Research and Evidence-Based Practice, Children's Hospital of Phildelphia, Philadelphia, United States.
  • Henegan S; Department of Nursing, Children's Hospital of Philadelphia, Philadelphia, MD, United States.
  • Jacobson LA; Division of Neuropsychology, Kennedy Krieger Institute, Baltimore, MD, United States.
Pediatr Blood Cancer ; 70(1): e30072, 2023 01.
Article em En | MEDLINE | ID: mdl-36326122
BACKGROUND: Neurocognitive deficits are common among children who receive central nervous system (CNS)-directed therapy for childhood cancer. Parents report that they lack information from and communication with oncology providers about neurocognitive impacts of therapy. Furthermore, oncology providers report they lack training and institutional support to appropriately address the neurocognitive needs of these patients/families. METHODS: A parent/provider stakeholder informed, quality improvement (QI) project was conducted to educate providers about neurocognitive impacts, increase parent/provider communication, and improve adherence to supportive care guidelines for neuropsychological assessment for children receiving CNS-directed therapy. A 1-h Continuing Medical Education (CME) course was developed to educate providers about neurocognitive impacts and their relation to schooling. A provider-focused electronic medical record (EMR) strategy was used to deliver parent stakeholder-informed return-to-school "roadmaps," with prompts to scaffold parent/provider communication and enhance documentation of findings. RESULTS: Hospital-based CME sessions were attended by 76% (41 out of 54) of providers from our institution. Among the 34 who completed both pretest and posttest, the mean knowledge score improved from 56% at pretest to 74% at posttest. Compliance with the EMR strategy was 80% and there was a 42% increase in neuropsychological assessment referrals. CONCLUSIONS: We conclude that this QI project is an example of a successful parent/provider stakeholder collaboration that achieved demonstrable positive change in the areas of provider knowledge, patient/provider communication, and alignment of neuropsychological assessment referrals with existing guidelines. Our results confirm that improving knowledge, communication, and compliance with neuropsychological standards of care is possible with this evidence-based approach.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Melhoria de Qualidade / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Melhoria de Qualidade / Neoplasias Tipo de estudo: Diagnostic_studies / Guideline Limite: Child / Humans Idioma: En Ano de publicação: 2023 Tipo de documento: Article