Assessment of caregivers' strain during radiation therapy of head-and-neck cancer patients: An institutional report using modified caregivers' strain index scale
Correspondence Address: Source of Support: None, Conflict of Interest: None DOI: 10.4103/IJPC.IJPC_159_18
Source of Support: None, Conflict of Interest: None
Aims: Very little works have been reported on the issues of burden perceived by the caregivers of head-and-neck cancer (HNC) patients. Job of the caregiver is complex, and it limits their social, psychological, and economical well-being. Our study aims at assessing caregivers' strain during radiation therapy (RT) of HNC patients using the Modified Caregivers' Strain Index (MCSI) Scale. Materials and Methods: In this single-institutional cross-sectional study, we interviewed caregivers of HNC patients undergoing curative RT. Along with MCSI, a 13-point questionnaire, which was self-administered in local languages; we collected baseline data of patients and their caregivers. Scores were evaluated. For each question, score varies 0–2. Higher the Median Hazard Score (H Score), more was the level of the strain. Results: We interviewed 24 participants. Response rate was 100%. About 45.8% of patients were in Stage III. The median age of caregivers was 40 years; 58.3% were male, 79.2% were employed, and 58.3% were belonging to the upper-lower class. Nearly 66.6% were spouse of the patients and 70.8% belong to joint family. In MCSI score analysis, H Score was 22 (range 14) with a minimum score of 14 and maximum score of 26. The most common score was 20. About 65.1% of participants responded Score 2 in all aspects of strain indices. Travel time had a significant positive association with total H Scores (Pearson's r = 0.663, P < 0.05). Conclusion: Majority of the caregivers was suffering from severe physical, personal, emotional, and social/financial strain. This issue must be addressed in holistic cancer care.
Keywords: Caregiver, head-and-neck cancer, strain
Head-and-neck cancer (HNC) is a major health problem in India with 77,000 new cases being diagnosed every year, accounting for 3% of all neoplasms. There are enormous challenges associated with it due to the disease itself, and intense and prolonged treatment that demands efficacious and persistent caregiving. Nightingale et al. in their work showed different challenges in formal caregivers and family members of HNC patients face in day-to-day life that impedes their social, personal, and psychological health. Despite best efforts by health-care professionals, a lot of patients end up in palliative care suffering from increased pain and anxiety as majority of patients in Southeast Asia present as Stages III and IV. Bond et al. demonstrated that facial disfigurement, speech, swallowing dysfunction, poor feeding, pain, and depression are the different problems that make the task of the informal caregiver difficult in such patients.
Certainly, little have been focused on the issues of the caregivers' burden of HNC patients.
Although there have been quite a few published literature addressing the caregiver strain using different scales (caregiver strain inventory and caregiver reaction assessment) in the Western world, data from India are lacking to a large extent to plan a proper follow-up and intervention to reduce the burden of caregivers.
With this background, we decided to study on this topic to see the status of caregivers of patients of head-and-neck malignancies attending our clinic using Modified Caregiver's Strain Index (MCSI).
MCSI is a 13-item questionnaire tool that is easy to use, self-administered, and broadly encompasses physical, personal, emotional, and social/financial health of the caregivers. Caregiver's Strain Index, originally developed in 1983, has been updated and MCSI showed a little more internal consistency (Cronbach's alpha=0.90). The advantage being it included equivocal responses perceived by the caregivers. The validity of this tool has been tested in multiple studies to assess the strain of the informal caregivers both in oncology and chronic medical conditions such as stroke and dementia patients.
Materials and Methods
Between September 2015 and April 2016, a cross-sectional survey was carried out among informal caregivers of 27 HNC patients who are undergoing radical and curative radiation therapy (RT) at our institute using convenience sampling. Caregiver in our study was defined as the person who principally took care of the patient and accompanied him to our center with whom we interacted as doctors. Informed consent was obtained, and the study was approved by the Institutional Ethical Committee. Out of 27 caregivers, 1 was not ready to give consent and 2 others were lost to follow-up after giving consent. It was a single-time, single-institutional study having a sample size of 24 caregivers. Each of the participants was given the MCSI questionnaire explained in their own language (Hindi/Bengali/English). While most of them ticked the options after self-understanding, for some options were read aloud and explained after which they could comfortably answer. Along with MCSI questionnaire, we also collected baseline data of the patients (age, sex, and Eastern Cooperative Oncology Group Performance Status), stage of the disease (American Joint Committee of Cancer staging, 7th edition), and location of residence (rural/urban) and caregivers (age, sex, socioeconomic status, employment status [employed/unemployed], relation with the patient, and family status [joint/nuclear]). For socioeconomic status, we used modified Kuppuswamy's Socioeconomic Scale update 2015.
This process was carried out in a single room, besides outpatient department where there was no interference. We interviewed the caregivers on the 5th week of their patients' RT. At the end of survey, each participant was told about their score out of maximum 26. For each question, if the answer was yes 2 points given, for sometimes answer was 1 and for no zero mark awarded. Higher the score more was the level of strain, though there was no definite cutoff. In cases, where the caregivers were found to be suffering from depression, they were referred for psychological counseling.
We interviewed 24 caregivers and analyzed the results. Response rate was 100%. All of the 24 caregivers answered all topics of the questionnaire.
Baseline characteristics of patient and respective caregivers
Baseline parameters of the patient and his/her caregivers are detailed in [Table 1] and [Table 2].
Travel time and mode
We stratified travel time (residence to RT unit) into three groups. About 33.3% (8) of patients reside <2 h distance and 58.3% (14) and 8.3% (2) of patients reside 2–5 h and >5 h distance, respectively. About 70.8% (17) of patients availed public transport and 29.2% (7) had availed private transport.
Modified Caregiver's Strain Index score
MCSI score distribution (question wise) is detailed in [Table 3]. On average, 65.1% of participants responded “Yes-on Regular Basis” (Score 2) in all aspects of strain indices, 33.3% of participants responded as “Yes-sometimes” (Score 1) in all indices, and 1.6% of participants responded as “No” (Score 0) in all indices. Median Hazard Score (H Score) was 22 (range 14) with a minimum score of 14 and maximum score of 26. The most common score was 20.
Correlation between scores and baseline parameters
We tried to find correlation between different parameters and H Score and question-wise subscore also. We used Pearson's Correlation coefficient, Spearman's correlation coefficient, and nonparametric tests to analyze the association between different parameters (continuous and categorical variables) and scores. Majority of the parameters do not have correlation which is statistically significant. Only travel time has a significant positive association with total H Scores (Pearson's r = 0.663, P < 0.05).
Ours was a cross-sectional descriptive study with an aim to assess the burden of caregivers of patients of HNC in a tertiary oncology clinic. It showed that males of fifth decade of life are the most common hit (median age was 47.5 years and male: female ratio = 1.18) by the disease with majority presenting as Stage III disease (45.8%), which was roughly in tune with the patient profile data of other Indian and overseas literature.
As discussed above caregiving in any cancer is a unique job that is often overlooked in therapeutic arena with a negative impact of personal/social/financial life of caregiver. In an Indian study by Sivakumar, majority of the caregivers were females (75%) which is in contrast to our studies where majority were male caregivers (58.3%) though the most common age group of caregivers in both the studies was third-to-fourth decades (the median age was 40 years in our study).
Ross et al. and Geriani et al. in their study demonstrated that spouse turned out to be the most common caregiver for chronically ill/terminal cancer patient, which was compatible with the results of our study where majority of the primary caregivers were spouse of the patient.
Nayak et al. conducted a study on 768 caregivers of cancer patients from South India, and 85.1% of the study population had financial problems for caregiving and 70.3% could not continue their functional daily activities. In our study, 95.8% of the caregivers had financial difficulties and majority (91.7%) had to do work adjustment during their patients' treatment.
In another Indian study, Varma et al. reported that 91% of the caregivers of cancer patients were employed but had an annual income of <40,000 Indian rupees. In our study, 79.2% of the caregivers were breadwinners for their family, and majority of them belonged to upper-lower class (58.3%) according to economic scale. A significant number of caregivers had to play dual roles and had drop in their educational activities and social disruptions to look after their patients as evidenced in literature.
Maheswari and Mahal in their study showed that belonging to a rural area and distance from the treatment centers are important variables that affect the family burden. Similarly, in our study also, the duration of travel time was on the only stressor found to be statistically significant. It ascribed to a significant number of patients belonging to rural belt and availing public transport during busy office hours.
Although there is a paucity of worldwide as well as Indian data on this ill-explored topic, our attempt to find the shortfalls in our patients and their family just could provide a small glimpse as limited by small sample size, single institutional, based on a specific subsite and lack of interventional or active support. We understand and suggest similar studies on larger population to validate this utmost issue.
In this single-institutional cross-sectional study, we tried to estimate the different aspects of strain of caregivers of the HNC patients undergoing curative RT. Majority of the caregivers was suffering from severe physical, personal, emotional, and social/financial strain as evident by the score responses. Distance from home to hospital is also a pivotal factor here. This unaddressed issue is very crucial for holistic cancer care, especially in low resourceful country such as India, where paucity of cancer care facilities and poor socioeconomic conditions of majority of patients also make the task of the caregiver more challenging.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
[Table 1], [Table 2], [Table 3]