Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster Display session

380P - Understanding the burden and mental health of informal caregivers for stomach and pancreatic cancer patients

Date

27 Jun 2024

Session

Poster Display session

Presenters

Mohit Pandey

Citation

Annals of Oncology (2024) 35 (suppl_1): S119-S161. 10.1016/annonc/annonc1481

Authors

M.K. Pandey

Author affiliations

  • International Institute for Population Science, Mumbai/IN

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 380P

Background

The current study examines psychological health of informal caregivers and estimate the time costs association with informal caregiving for cancer survivors.

Methods

We intend to select a sample of 350 patients, which represents approximately 18 percent of the overall gastro-intestinal cancer patient of Tata Memorial Hospital (TMH), India’s one of the largest cancer hospitals in Mumbai. However, among them we select 200 patients and we collect the data three point of times. This study got Ethical clearance from Tata Memorial Hospital and International Institute for Population Sciences. We used The Zarit Burden questionnaire, Anxiety Symptoms Questionnaire, Composite International Diagnostic Interview (CIDI) for accessing the burden, anxiety, and depression of caregiver. The median wage rate was used to value caregiver time, and other methods to value time were evaluated with sensitivity analyses.

Results

The data underscores the burden experienced by caregivers, who often grapple with emotional and financial distress. Notably, 37% of caregivers report greater financial distress than emotional strain, emphasizing the dire need for support in both domains. Caregiver characteristics, such as marital status, education, and family type, significantly influence the burden experienced. In addition, the patient's employment status and treatment facility type also play pivotal roles in caregiver dynamics. Spouses constituted the highest percentage of caregiving, accounting for 64% of caregivers, followed by sons and daughters at 15%.

Conclusions

The prevalence of depression and anxiety among caregivers highlights the urgency of providing accessible support services. Moreover, the economic implications of caregiving emphasize the need for comprehensive assistance programs. Addressing these challenges is vital to ensure the well-being of both caregivers and patients in the cancer care journey.

Legal entity responsible for the study

Mohit Kumar Pandey.

Funding

Has not received any funding.

Disclosure

The author has declared no conflicts of interest.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.