|LETTER TO THE EDITOR
|Year : 2015 | Volume
| Issue : 4 | Page : 590-591
Exploring the psychosocial and financial impact of cancer on caretakers
Saurabh RamBihariLal Shrivastava, Prateek Saurabh Shrivastava, Jegadeesh Ramasamy
Department of Community Medicine, Shri Sathya Sai Medical College and Research Institute, Kancheepuram, Tamil Nadu, India
|Date of Web Publication||2-Jul-2015|
Saurabh RamBihariLal Shrivastava
Department of Community Medicine, Shri Sathya Sai Medical College and Research Institute, 3rd Floor, Ammapettai Village, Thiruporur, Guduvancherry Main Road, Sembakkam Post, Kancheepuram -email@example.com 603 108, Tamil Nadu
Source of Support: None, Conflict of Interest: None
|How to cite this article:|
Shrivastava SR, Shrivastava PS, Ramasamy J. Exploring the psychosocial and financial impact of cancer on caretakers. Clin Cancer Investig J 2015;4:590-1
|How to cite this URL:|
Shrivastava SR, Shrivastava PS, Ramasamy J. Exploring the psychosocial and financial impact of cancer on caretakers. Clin Cancer Investig J [serial online] 2015 [cited 2020 Apr 4];4:590-1. Available from: http://www.ccij-online.org/text.asp?2015/4/4/590/159846
In the year 2012 alone, 14 million new cases and 8.2 million cancer-related deaths have been reported worldwide.  In fact, the current trends suggest that the incidence of cancer can augment up to 70% in the next couple of decades.  Establishment of a diagnosis of any form of cancer in an individual is a major event not only for the person, but even for their family members and caretakers.  In fact, the findings of some of the studies have even shown that family members are the one, who are more severely affected, than the patient themselves. ,
Although, in most of the settings, partners and other family members remain the key supports and cope well with their responsibilities, nevertheless, families do respond in a variable manner to the illness.  These responses include distress among the family members; lack of awareness, understanding, or ability to respond on a positive note to the expressed thoughts or feelings of other family members; attempts to counter the tension and stress associated with the cancer; and they can even struggle to maintain their core functions. , Owing to the stress attributed to the diagnosis of a cancer among one of the family members, some of the caretakers do suffer from physical ailments, depression, anxiety, stress reactions, post-traumatic stress disorder, and even mood disorders. , Also, caretakers are often exposed to disruption in their social connectivity network and loneliness and having no time to pursue their personal interests or hobbies. , Moreover, the families have to counter the financial burden as well, as the cancer treatment and care is quite expensive. 
Acknowledging the impact of diagnosis of cancer on the quality of life of the patient and their caretakers, it is high time that appropriate strategies should be developed in order to avert any untoward consequences among the family members. , Although, multiple measures can be implemented, based on the case-to-case scenario, the key stakeholder is the treating physician. , Thus, measures like organizing training for improving the communication skills of the physicians to conduct effectively counseling sessions.  In addition, interventions such as sensitizing outreach workers to have a high index of suspicion while interacting with cancer caretakers; strengthening the cancer surveillance mechanism; taking steps to monitor follow-up of cancer victims at periodic intervals; interviewing patients to detect any signs of distress among the caretakers; and involving nongovernmental organizations to impart counseling to the patients and family members, can also be implemented to improve the quality of life of cancer patients and their caretakers. ,,
To conclude, the public health menace of cancer not only affects the lives of cancer survivors, but even cast a huge physical, mental, social, and financial impact on the lives of millions of caretakers. As, the problem of cancer is going to further increase in coming decades, it is the need of the hour to strengthen the general health system and improve the area of palliative care in cancer.
| References|| |
Girgis A, Lambert S, Johnson C, Waller A, Currow D. Physical, psychosocial, relationship, and economic burden of caring for people with cancer: A review. J Oncol Pract 2013;9:197-202.
Couper JW, Bloch S, Love A, Duchesne G, Macvean M, Kissane DW. The psychosocial impact of prostate cancer on patients and their partners. Med J Aust 2006;185:428-32.
Pitceathly C, Maguire P. The psychological impact of cancer on patients′ partners and other key relatives: A review. Eur J Cancer 2003;39:1517-24.
Edwards B, Clarke V. The psychological impact of a cancer diagnosis on families: The influence of family functioning and patients′ illness characteristics on depression and anxiety. Psychooncology 2004;13:562-76.
Clerc L, Jooste V, Lejeune C, Schmitt B, Arveux P, Quantin C, et al.
Cost of care of colorectal cancers according to health care patterns and stage at diagnosis in France. Eur J Health Econ 2008;9:361-7.
Stenberg U, Ruland CM, Miaskowski C. Review of the literature on the effects of caring for a patient with cancer. Psychooncology 2010;19:1013-25.
Lienard A, Merckaert I, Libert Y, Delvaux N, Marchal S, Boniver J, et al.
Factors that influence cancer patients′ and relatives′ anxiety following a three-person medical consultation: Impact of a communication skills training program for physicians. Psychooncology 2008;17:488-96.