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The burden of a brain tumor: guiding patient centric care in neuro-oncology.
Loughan, Ashlee R; Reid, Morgan; Willis, Kelcie D; Davies, Alexandria; Boutté, Rachel L; Barrett, Sarah; Lo, Karen.
Afiliação
  • Loughan AR; Division of Neuro-Oncology, Department of Neurology, VCU Massey Cancer Center, Virginia Commonwealth University, School of Medicine, 1201 East Marshall St, Richmond, VA, 23298-0037, USA. ashlee.loughan@vcuhealth.org.
  • Reid M; VCU Massey Cancer Center, Richmond, VA, USA. ashlee.loughan@vcuhealth.org.
  • Willis KD; Virginia Commonwealth University, School of Medicine, Richmond, VA, USA. ashlee.loughan@vcuhealth.org.
  • Davies A; Department of Psychology, Virginia Commonwealth University, Richmond, VA, USA.
  • Boutté RL; Department of Psychology, Virginia Commonwealth University, Richmond, VA, USA.
  • Barrett S; Department of Psychology, Virginia Commonwealth University, Richmond, VA, USA.
  • Lo K; Department of Psychiatry and Behavioral Medicine, Rush University Medical Center, Chicago, IL, USA.
J Neurooncol ; 157(3): 487-498, 2022 May.
Article em En | MEDLINE | ID: mdl-35394618
ABSTRACT

PURPOSE:

Brain tumor patients report an overwhelming sense of uncertainty when navigating the course of their terminal disease. Historically, organizational experts and/or treating physicians have established neuro-oncology programs. However, given the disease burden and incurable nature of current medical treatments, patient-centric care should be prioritized alongside institutional and academic objectives. Integrating patient perspectives into interdisciplinary programmatic development can improve comprehensive care and empower patients to advocate for their own quality healthcare needs.

METHODS:

Data was derived from four focus groups with adult brain tumor patients (N = 15; Mage = 46 years, 53% female). A trained moderator led each 90-min group and posed semi-structured questions regarding patients' care needs throughout their neuro-oncological disease trajectory. Emphasis was placed on quality of life and psychological distress reduction for both patients and their loved ones. Common themes were identified via thematic content analysis using NVivo software. A high inter-rater reliability (Mkappa = 0.92, range= 0.85-0.93) was achieved.

RESULTS:

Six distinct themes emerged, where the frequency of each theme ranged from 12.5 to 23.3%. Specifically, patients discussed relational concerns, navigation of interdisciplinary care, neurobehavioral impacts, emotional responses to stressors, existential concerns, and caregiver support. A discussion of themes follows.

CONCLUSIONS:

It is imperative that we include the patient perspective in the development of neuro-oncology programs; considering the quality of survival in addition to quantity. Neuro-oncology quality care themes identified were relational concerns, navigating interdisciplinary care, neurobehavioral impact, emotional response to stressors, existential concerns, and caregiver support. A paramount concentration for comprehensive neuro-oncology programs must include patients' quality needs.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Neoplasias Encefálicas Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Qualidade de Vida / Neoplasias Encefálicas Tipo de estudo: Prognostic_studies / Qualitative_research Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2022 Tipo de documento: Article