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Critical Issues for Patients and Caregivers in Neuro-Oncology during the COVID-19 Pandemic: What We Have Learnt from an Observational Study.
Anghileri, Elena; Tramacere, Irene; Morlino, Sara; Leuzzi, Catia; Gutierrez, Lorena Pareja; Motta, Saba; Silvani, Antonio; Amato, Anna; Berrini, Francesca Romana.
Affiliation
  • Anghileri E; Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.
  • Tramacere I; Department of Research and Clinical Development, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Morlino S; Radiotherapy Unit, Neurosurgery Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Leuzzi C; Clinical Neuro-Science Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Gutierrez LP; Clinical Neuro-Science Department, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Motta S; Scientific and Patients Library, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy.
  • Silvani A; Neuro-Oncology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, Via Celoria 11, 20133 Milan, Italy.
  • Amato A; Department of Medicine and Surgery, University of Milano-Bicocca, 20126 Milan, Italy.
  • Berrini FR; AITC-Associazione Italiana Tumori Cerebrali (Italian Brain Tumor Association), 20133 Milan, Italy.
Curr Oncol ; 31(7): 3895-3907, 2024 Jul 04.
Article in En | MEDLINE | ID: mdl-39057160
ABSTRACT

OBJECTIVE:

The COVID-19 pandemic affected neuro-oncological patients and their caregivers regarding tumor care and emotional functioning, including Quality of Life (QoL). This study aimed to understand how COVID-19 affected their psychological state and the relations between patients and health personnel in neuro-oncology.

METHODS:

A cross-sectional study was conducted on neuro-oncological patients and their caregivers.

RESULTS:

A total of 162 patients and 66 caregivers completed the questionnaire. Altogether, 37.5% of patients perceived a greater risk of contracting COVID-19 compared to the general population. On a 0-10 scale, the patients' tumor-related anxiety score was 5.8, and their COVID-19-related score was 4.6. The caregivers reported 7.7 and 5.5, respectively. QoL was described as at least good in 75% of both patients and caregivers; the caregivers' care burden increased in 22.7% of cases during the pandemic, with no correlation with QoL. Future perception often changed, both in patients and caregivers. In 18% of cases, the cancer treatment schedule was changed, either by patient decision or by medical decision. However, 93.5% of patients were satisfied with their overall care.

CONCLUSIONS:

A considerable proportion of patients and caregivers still perceived the tumor disease as more burdensome than the pandemic, and their future as more uncertain. Such data suggest the need to build a productive alliance between patients and health professionals.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Caregivers / COVID-19 Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Curr Oncol Year: 2024 Document type: Article Affiliation country: Italy Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Caregivers / COVID-19 Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: Curr Oncol Year: 2024 Document type: Article Affiliation country: Italy Country of publication: Switzerland