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 Table of Contents  
ORIGINAL ARTICLE
Year : 2020  |  Volume : 7  |  Issue : 4  |  Page : 375-381

Assessment of Information Needs of Patients with Breast Cancer: A Hospital-Based Study in Sri Lanka


1 Medical Library, Faculty of Medicine, University of Colombo, Maharagama, Sri Lanka
2 Department of Obstetrics and Gynecology, Faculty of Medicine, University of Colombo, Maharagama, Sri Lanka
3 World Health Organization Country Office, Maharagama, Sri Lanka
4 National Cancer Institute, Maharagama, Sri Lanka

Date of Submission07-Jan-2020
Date of Acceptance30-Mar-2020
Date of Web Publication14-Sep-2020

Correspondence Address:
PhD, MSc, MPhil, BSc Daya Chandrani Kuruppu
Medical Library, Faculty of Medicine, University of Colombo, Colombo 08
Sri Lanka
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/apjon.apjon_23_20

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  Abstract 


Objective: This study assessed the information needs of breast cancer (BC) patients who presented themselves to the outpatient clinics or wards of the National Cancer Institute, Maharagama, Sri Lanka. Methods: Information needs were measured using the validated questionnaire in the vernacular (Sri Lankan Information Needs Assessment Questionnaire – BC). Results: All affected women indicated a strong need for information related to the disease, treatment, and psychosocial service while the need for information on procedures for diagnosis and physical care was not strong. Younger women (age ≤37) (P < 0.0001) and women with higher education (P < 0.0001) had significantly higher information needs. Conclusions: The results indicated that information needs to be addressed in educational packages require that younger women and those with higher education have specific needs.

Keywords: Breast cancer, information needs, Sri Lankan Information Needs Assessment Questionnaire – Breast Cancer


How to cite this article:
Kuruppu DC, Wijeyaratne CN, Gunawardane N, Amarasinghe I. Assessment of Information Needs of Patients with Breast Cancer: A Hospital-Based Study in Sri Lanka. Asia Pac J Oncol Nurs 2020;7:375-81

How to cite this URL:
Kuruppu DC, Wijeyaratne CN, Gunawardane N, Amarasinghe I. Assessment of Information Needs of Patients with Breast Cancer: A Hospital-Based Study in Sri Lanka. Asia Pac J Oncol Nurs [serial online] 2020 [cited 2020 Oct 23];7:375-81. Available from: https://www.apjon.org/text.asp?2020/7/4/375/295057




  Introduction Top


Breast cancer (BC), as a common life-threatening disease, is a significant health problem worldwide. It is a treatable illness when diagnosed early. In the early 20th century, it was also shown that detecting and intervening early with the latest advances in the treatment is the most effective way to increase the cure rate or prolong survival of afflicted patients.[1] In Sri Lanka, BC has remained one of the most common cancers affecting the lives of women.[2] Despite effective screening programs for BC being in place, the existing evidence suggests that the majority of the women in Sri Lanka do not use these services effectively and regularly. The reasons suggested are the lack of knowledge of the services that are offered and disinterest in seeking accurate information.[3]

Adopting strategies to reduce the risk behaviors for BC and regular screening for early signs of BC are the key to reducing BC morbidity and mortality. The essential ingredient for achieving an effective behavioral change is the provision of correct information. Knowledge plays a vital role in the improvement of health-seeking behavior.[4] In addition, ensuring the acquisition of the appropriate knowledge among patients with BC has shown to facilitate better psychological health outcomes.[5],[6],[7] Nevertheless, a detailed review of the literature found no recorded initiative that targeted at improving the awareness of BC, which was designed based on an needs assessment among patients with BC and their families. This study was aimed to assessing the informational needs of Sri Lankan women with BC.


  Methods Top


Study design

The study was a hospital-based BC patient survey using a cross-sectional study design.

Study setting

The study was conducted at National Cancer Institute, Maharagama (NCIM), more recently named Apeksha Hospital. The hospital serves as the apex tertiary referral center, and it is state funded for the provision of a free health service in managing malignancies. The provisions made are for outpatients and inpatients services that face a very high throughput among many challenges of resource limitation.

Study participants

The study population consisted of histologically confirmed female BC patients who presented themselves to the outpatient clinics or wards of NCIM. Patients who had major mental health problems affecting their ability to respond to an interviewer-administered questionnaire and who were unable to comprehend and respond to the local language (Sinhala) questionnaire were excluded.

Sample size and sampling technique

The sample size of the cross-sectional descriptive study was estimated on the following formula:[8]



Where, N = the required sample size.

Z1-α/2= taken as 1.96 corresponding to a confidence interval CI of 95% (α = 0.05).

d = the degree of accuracy (precision) desired for the margin of error taken as 0.05.

P = 0.50 Literature review did not reveal any publication on informational needs of BC patients have not been studied in Sri Lanka nor in any countries in the South-east Asia region. Therefore, this was considered 50% to obtain the highest sample size needed. The sample size calculated was 384. The final sample size was rounded off to 400.

Nonprobability sampling technique of consecutive sampling was used as the most feasible and appropriate technique to recruit study units from the NCIM. The required number was selected consecutively from among those eligible. Data collection was done on all five working days of the week. The data collection was scheduled from 9.00 a.m. to 12.00 noon in each clinic and from 1.00 p.m. to 4.00 p.m. at the wards. In selecting the study units, those who visited outpatient clinics and those who admitted to wards for in-house treatment were invited to participate.

Study instrument

The main study instrument was the Sri Lankan Information Needs Assessment Questionnaire – BC (SINAQ-BC). The questionnaire was an interviewer-administered tool developed and validated to assess the information needs among patients with BC in the Sri Lankan settings.[9] It contained 58 items to assess information needs in five domains, namely disease, diagnosis, treatment, physical care, and psychosocial services. SINAQ-BC assessed the information needs by inquiring the study units to rate the importance of each item on a five-point scale of 1 (not important), 2 (slightly important), 3 (moderetly important), 4 (very important), and 5 (extremly important). Further sections were included to obtain the information related to socio-demographic and other basic characteristics in parallel with details of treatment.

Data collection

Three bio-science graduates were recruited as research assistants and were trained as data collectors. Interviews were carried out at a time and place convenient to the participants, without disturbing other patients and the staff either in the clinic or in the ward. The Principal Investigator supervised the selection of study units, data collection, and administering the questionnaire.

Statistical analysis

Assessment of information needs on breast cancer

In the analysis, frequency distributions of responses to each domain of SINAQ-BC were estimated.

The rates were considered as a score and the mean values for each domain were calculated. As different domains of SINAQ-BC contained a different number of items, in an attempt to compare the information needs across the domains, scores for each domain were convereted to be out of a total of 100 marks. Finally, the scores were summarized using the descriptive statistics (mean, standard deviation [SD], minimum and maximum).

The association between age of the respondent and the mean score obtained for SINAQ-BC was evaluated using the regression analysis. Respondents were divided into different age categories, and the relationship between age and the scores were assesssed for each age category.

The mean scores obtained by those in different education categories were assessed using the one-way between group analysis of variance. P < 0.05 was considered statistically significant.

Ethical approval

The project was approved by the Ethics Committee in the Faculty of Medicine, University of Colombo, Sri Lanka (Approved No. EC-10-035).


  Results Top


Background information on the study sample

A total of 405 eligible study units were invited. Out of the invitation, 400 consented and participated in the study giving a response rate of 98.8% (400/405). These 400 women were aged 27–76 years (Mean = 56.35; SD = 11.81; 95% CI = 55.16–57.53). Their basic sociodemographic characteristics of the study population are shown in [Table 1].
Table 1: Distribution of the study population by their basic sociodemographic characteristics (n=400)

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Most of the women were married (69.8%, n = 279) had completed either GCE (O/L) or GCE (A/L) (59.0%, n = 236). A minority were university degree/postgraduate degree holders (17.3%, n = 69). Approximately half had an average household income of Rs. 20,000–Rs. 30,000 (49.5%, n = 198).

Information needs on breast cancer using the validated Sri Lankan Information Needs Assessment Questionnaire – Breast Cancer

The frequency distribution and mean ratings of the responses for the five domains of the questionnaire are shown in [Table 2], [Table 3], [Table 4], [Table 5], [Table 6].
Table 2: Frequency distribution and mean rating of responses on disease domain (n=400)

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Table 3: Frequency distribution and mean rating of responses on diagnosis domain (n=400)

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Table 4: Frequency distribution and mean rating of responses of treatment domain (n=400)

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Table 5: Frequency distribution and mean rating of responses on physical care domain (n=400)

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Table 6: Frequency distribution and mean rating of responses on psychosocial service domain (n=400)

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Out of the different items in the domain of “disease,” nearly 50% responded that “the age at which the women should get screened for cancer” (n = 176, 44.0%) and “how to detect whether I have any other cancer” (n = 184, 46.0%) are extremely important information needs.

In the domain of diagnosis, the study units responded “the investigations that confirm the diagnosis of BC” (n = 24, 6.0%), “whether there are different stages of BC and what do they mean” (n = 38, 9.5%), “whether the test can identify the stage of it” (n = 38, 9.5%), “the reasons why doctors suggest certain additional tests” (n = 35, 8.8%), “whether the tests can identify the stage of it” (n = 38, 9.5%) and “how my illness could affects my life in future” (n = 47, 11.8%) are as extremely important information needs. Two third of the study units stated that these items as very important.

In the domain of “treatment,” all the items other than “how to decide a particular treatment plan” (n = 170, 42.5%) were classified as either very important or extremely important.

In the domain of “physical care,” “How to care for my wound or incision” (n = 207, 51.8%) and “When should the breast be examined after surgery” (n = 186, 46.5%) were responded by more than half as extremely important information needs.

In the domain of “psychosocial service,” the items “How to tell if the cancer has come back” (n = 215, 53.8%), “What are the symptoms to get admitted” (n = 203, 50.8%) and “What are the symptoms to come to the clinic immediately” (n = 203, 50.8%) were responded as extremely important by approximately half of the respondents.

Descriptive statistics of the score for each domain and all items of SINAQ-BC were calculated and shown in [Table 7].
Table 7: Descriptive statistics for each domain and all items of Sri Lankan Information Needs Assessment Questionnaire - Breast Cancer

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The domains of disease, treatment, and psychosocial service scored the highest depicting that they are the aspects of high needs of information by the BC patients.

Information needs of breast cancer patients by age and educational level

Mean of the total score for SINAQ-BC by the age category of the respondent are shown in [Table 8].
Table 8: Mean of the total score for Sri Lankan Information Needs Assessment Questionnaire - breast cancer by the age category of the respondent

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The results revealed that information needs of BC and the respondent's age below 37 years has a moderate (negative) linear relationship and a weak (negative) linear relationship with over 38 years age of the respondents.

The association of the level of education of BC patient on informational needs is shown in [Table 9].
Table 9: Association of the level of education of the breast cancer patient on informational needs

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The level of education of the respondent was statistically significantly associated with the SINAQ-BC scores (P < 0.05). Post hoc comparisons using the Turkey HSD test indicated that the means score for No schooling/Passed Grade 5 or 9 (Mean = 216.6, SD = 26.0) was significantly different from mean score of those in the GCE (O/L) or GCE (A/L) category (Mean = 229.7, SD = 24.4) and mean scores of those in the Degree or Postgraduate qualification category (Mean = 228.7, SD = 31.6). Those in the Degree or Postgraduate qualification category group did not differ significantly from those in the GCE (O/L) or GCE (A/L) category.

Analysis of the scores by the categories based on educational level revealed that women with higher education had greater information needs regarding BC.


  Discussion Top


This study used the validated SINAQ-BC data collection tool to reliably assess the information needs of BC patients. Evidence-based practice depends on establishing partnership between scientific evidence, clinical expertise, individual needs, and the choice of patients.[10],[11],[12] Utilizing a validated tool to assess the information needs can be considered the first step toward an evidence-based approach.

Information needs of breast cancer patients

All patients indicated a strong need for information.

The most striking findings of this study were that patients with BC gave the highest importance to the domains of disease, treatment, and psychosocial services. This finding is consistent with the existing European countries' literature, where information about disease, treatment, and psychosocial service were rated greater than diagnosis and physical care.

The findings of this study are in parallel with former research. Graydon et al.[13] have identified that information on recurrence was the greatest concern among women with BC. Patient's information needs are at their highest during radiotherapy, especially, at the first appointment with the radiation oncologist and when their planning this appointment.[14] Providing information during this time increases patient satisfaction.[15] It is very important to provide reassurance that the therapy is acceptable and safe. Patients require information on other treatment modes that would aid in their preferences for treatment choices in their decision-making. Women with BC undergoing chemotherapy have significant information needs.[16] Other studies have indicated that patients require information on chemotherapy, particularly on cancer and its spread, the side effects of chemotherapy and management of the side effects. Consistent with the previous studies, all items in the treatment scale were highly rated by the participants of our study as the important information needs.

Information-seeking preferences of patients may be influenced by the several factors such as the time from diagnosis, sociodemographic variables (age, gender, and education) and disease variables (a type of cancer, treatment, and stage of disease).[15],[17] In addition to time since diagnosis,[17],[18],[19],[20] age is the only significant influencing factor in information-seeking behavior.[13],[21] Concerning age, younger women require more information than older patients.[5] At the initial stage of the instrument development, the need for information on contraception, sexual activity among premenopausal women with BC was assessed; and the participants did not rate these as important information needs, probably due to socio-cultural influences. However, other researchers have highlighted that participants were willing to receive counseling on issues related to infertility, fertility preservation, contraception, and menopause.[7] It is most likely that during this stage of coping with the diagnosis of BC, knowledge plays an important role in improving health-seeking behavior specific to sexual and reproduction health. Previous studies showed that lack of knowledge is a significant factor for delayed health-seeking behavior.[4]

Previous researchers revealed that many of the information needs noted for various other contexts of cancer, especially in palliative care did vary.[22] Each patient expressed very different information needs – the younger patients desired factual information on disease, prognosis, and life expectancy while elderly patients had a dormant information need. Our results indicated that younger patients (age <37) and patients who had received higher education have significantly higher information needs (P < 0.0001). The two groups need to be specifically targeted to fulfill their information requirements.

In line with our findings, previous research had also shown the importance of age and education level when catering for information needs of BC patients. Vivar and McQueen[5] had shown that age is a meaningful variable that should be kept in mind when caring for BC survivors. Furthermore, women with higher education level show a greater demand for information than the less educated.[5] Given the fact the younger generations of women in South Asia are being more empowered through education, our health-care systems need to respond appropriately and adapt services to suit the needs of patients and ensure optimal receiver satisfaction irrespective of their disease status.


  Conclusion Top


Younger women and educated women of South Asia origin have a greater demand for information on BC. It is recommended that a sociocultural appropriate educational package on BC is developed to target the differing patient needs.

Acknowledgments

The authors are thankful to the Director of NCIM and all health professionals in the hospitals for the immense support rendered.

Financial suppor and sponsorship

This study was financially supported by the Acknowledge University of Colombo for funding of the study (Grant No. AP/3/2012/PG/05).

Conflicts of interest

There are no conflicts of interest.



 
  References Top

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Ries LA, Eisner MP, Kosary CL, Hankey BF, Miller BA, Clegg L, et al., editors. SEER Cancer Statistics Review, 1975-2000. Bethesda, MD: Narional Cancer Institute; 2003. Available from: http://seer.cancer.gov/csr/1975_2000/. [Last accessed on 2019 May 25].  Back to cited text no. 1
    
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National Policy & Strategic Framework on Cancer Prevention & Control - Sri Lanka 2015, Ministry of Health, Nutrition & Indigenous Medicine Sri Lanka; 2016. Available from: http://www.nccp.health.gov.lk/images/PDF_PUBLICATIONS/National_Cancer_Control_Policy.pdf. [Last accessed on 2019 May 15].  Back to cited text no. 2
    
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Vithana PVSC, Ariyaratne M, Jayawardana P. Quality of breast cancer early detection services conducted by well woman clinics in the district of Gampaha, Sri Lanka. Asian Pac J Cancer Prev 2013;14:75-80.   Back to cited text no. 3
    
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Vivar CG, McQueen A. Informational and emotional needs of long-term survivors of breast cancer. J Adv Nurs 2005;51:520.  Back to cited text no. 5
    
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Karaöz B, Aksu H, Küçük M. A qualitative study of the information needs of premenopausal women with breast cancer in terms of contraception, sexuality, early menopause, and fertility. Int J Gynaecol Obstet 2010;109:118-120.   Back to cited text no. 7
    
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Kuruppu DC, Wijeyaratne CN, Gunawardane N, Amarasinghe I. Development and validation of an instrument to measure informational needs of breast cancer patients in Sri Lanka. Ceylon J Med Sci 2007;54:9-17.  Back to cited text no. 9
    
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Rycroft-Malone J, Seers K, Titchen A, Harvey G, Kitson A, McCormack B. What counts as evidence in evidence-based practice? J Adv Nurs 2004;47:81-90.  Back to cited text no. 11
    
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Graydon J, Galloway S, Palmer-Wickham S, Harrison D, Rich-van der BI, West L, et al. Information needs of women during early treatment for breast Cancer. J Adv Nurs 1997;26:59-64.  Back to cited text no. 13
    
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Halkett GK, Kristjanson LJ. Validity and reliability testing of two instruments to measure breast cancer patients' concerns and information needs relating to radiation therapy. Radiat Oncol 2007;2:43.  Back to cited text no. 14
    
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D' haese S, Vinh-Hung V, Bijdekerke P, Spinnoy M, De Beukeleer M, Lochie N,et al. The effect of timing of the provision of information on anxiety and satisfaction of cancer patients receiving radiotherapy. J Cancer Educ 2000;15:223-7.   Back to cited text no. 15
    
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Lee YM, Francis K, Walker J, Lee SM. What are the information needs of Chinese breast cancer patients receiving chemotherapy? Eur J Oncol Nurs 2004;8:224-33.   Back to cited text no. 16
    
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Eheman CR, Berkowitz Z, Lee J, Mohile S, Purnell J, Rodriguez EM,et al. Information-seeking styles among cancer patients before and after treatment by demographics and use of information sources. J Health Commun 2009;14:487-502.   Back to cited text no. 17
    
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Northouse LL. The impact of breast cancer on patients and husbands. Cancer Nurs 1989;12:276-84.  Back to cited text no. 19
    
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Adams M. Information and education across the phases of cancer care. Semin Oncol Nurs 1991;7(2):105-11.   Back to cited text no. 20
    
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Galloway S, Graydon J, Harrison D, Evans-Boyden B, Palmer-Wickham S, Burlein-Hall S, et al. Informational needs of women with a recent diagnosis of breast cancer: development and initial testing of a tool. J Adv Nurs 1997;25:1175-83.  Back to cited text no. 21
    
22.
Docherty A, Owens A, Asadi-Lari M, Petchey R, Williams J, Carter YH. Knowledge and information needs of informal caregivers in palliative care: A qualitative systematic review. Palliat Med 2008;22:153-171.  Back to cited text no. 22
    



 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7], [Table 8], [Table 9]



 

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