The benefits and consequences of the COVID‐19 pandemic for patients diagnosed with cancer and their family caregivers. Issue 6 (1st February 2022)

• Record Type: Journal Article
• Authors: Steel, Jennifer L.; Amin, Aarshati; Peyser, Tristen; Olejniczak, Donna; Antoni, Michael; Carney, Maureen; Tillman, Emily; Hecht, Carol Lynn; Pandya, Niva; Miceli, Jessica; Reyes, Vincent; Nilsen, Marci; Johnson, Jonas; Kiefer, Gauri; Pappu, Bhanu; Zandberg, Dan P.; Geller, David A.
• Is Part Of: Psycho-oncology. Volume 31:Issue 6(2022)
• Page Start: 1003
• Page End: 1012
• Publication Date: 2022-02-01
• Subjects: cancer -- cancer care -- COVID‐19 pandemic -- oncology -- patient‐reported outcomes; Cancer -- Psychological aspects -- Periodicals; Cancer -- Social aspects -- Periodicals; Neoplasms -- psychology -- Periodicals; 616.9940019
• DOI: 10.1002/pon.5891
• Languages: English
• ISSNs: 1057-9249

Abstract

Abstract: Background: The objectives of this study were to examine benefits and consequences of the COVID‐19 pandemic for patients diagnosed with cancer and their family caregivers. Methods: A 23‐item questionnaire assessing COVID‐19‐related issues, the Patient Health Questionnaire‐2, Generalized Anxiety Disorder‐2, Pittsburgh Sleep Quality Index, and the Perceived Stress Scale (PSS)‐4 were administered to patients diagnosed with cancer and their family caregivers. Results: Of the 161 patients and 78 caregivers who participated, 38.1% and 32.8 were male, 95% and 84.6% Caucasian, and the mean age was 66 and 64.6 years, respectively. A total of 16.5% and 15.2% reported depressive symptoms, 18.4% and 19% reported anxiety; 35.5% and 26.6% reported poor sleep quality, and 66% and 63.3% scored one standard deviation above the norms for the PSS, respectively. Predictors of poorer patient‐ and caregiver‐reported outcomes included greater loneliness, worry about self or family being infected by the COVID‐19, and worsening relationships with family. The fear of COVID‐19 led to 20.8% of patients and 24.4% of family caregivers cancelling medical appointments, procedures, and treatments. A total of 52.5% of patients and 53.2% caregivers reported that the pandemic led to benefit finding but these changes were not associated with any of the measured patient‐ or caregiver‐related outcomes. Conclusions: Psychological functioning for patients and caregivers was similar to that of pre‐pandemic levels, however the decrease in health care utilization secondary to fear of COVID‐19 was notable. While there were many negative effects of the pandemic, the majority of patients and caregivers reported some benefit to the pandemic.