Supportive Care in Cancer

, Volume 21, Issue 11, pp 2999–3007 | Cite as

Satisfaction with information and its association with illness perception and quality of life in Indonesian breast cancer patients

  • Aulia Iskandarsyah
  • Cora de Klerk
  • Dradjat R.  Suardi
  • Monty P.  Soemitro
  • Sawitri S.  Sadarjoen
  • Jan Passchier
Original Article

Abstract

Purpose

The aims of this study were to assess the level of satisfaction with the information on illness and treatment among breast cancer patients, to explore its association with patients’ illness perceptions and quality of life, and to provide recommendations for improvement of the information provided.

Methods

Seventy breast cancer patients at the Outpatient Surgical Oncology Clinic in Hasan Sadikin Hospital in Indonesia were recruited consecutively in a cross-sectional study design. They completed a demographic form, the Satisfaction with Cancer Information Profile, the Brief Illness Perception Questionnaire, and the World Health Organization Quality of Life.

Results

A considerable number of breast cancer patients (41–86 %) were dissatisfied with the amount and content of the information they received, particularly on the information about access to patient support groups and the impact of their treatment on long-term quality of life. The majority of patients were dissatisfied with the amount of written information provided. Patients who were satisfied with the type and timing of information received had stronger beliefs in personal control (β = −0.30, p < 0.05), lesser concerns about their health condition (β = −0.47, p < 0.01), and better understanding of their illness (β = −0.27, p < 0.05), and were less emotionally affected by their illness (β = −0.27, p < 0.05). In addition, the satisfied patients had a more positive perception of their general health (β = 0.31, p < 0.05) and better psychological health condition (β = 0.33, p < 0.05).

Conclusions

Satisfaction with the information provided is associated with better health outcomes, including more positive illness perceptions. This study appears to highlight the importance of providing adequate and sufficient information that meets the needs of patients.

Keywords

Satisfaction with information Illness perceptions Quality of life Breast cancer Indonesia 

References

  1. 1.
    Al-Azri M, Al-Awisi H, Al-Moundhri M (2009) Coping with a diagnosis of breast cancer-literature review and implications for developing countries. Breast J 15:615–622PubMedCrossRefGoogle Scholar
  2. 2.
    Arraras JI, Greimel E, Chie WC, Sezer O, Bergenmar M, Costantini A, Young T, Vlasic KK, Velikova G, on behalf of the European Organisation for R, Treatment of Cancer Quality of Life G (2013) Cross-cultural differences in information disclosure evaluated through the EORTC questionnaires. Psychooncology 22:268–275PubMedGoogle Scholar
  3. 3.
    Au A, Lam W, Tsang J, Yau TK, Soong I, Yeo W, Suen J, Ho WM, Wong KY, Kwong A, Suen D, Sze WK, Ng A, Girgis A, Fielding R (2013) Supportive care needs in Hong Kong Chinese women confronting advanced breast cancer. Psychooncology 22:1144–1151PubMedCrossRefGoogle Scholar
  4. 4.
    Broadbent E, Petrie KJ, Main J, Weinman J (2006) The brief illness perception questionnaire. J Psychosom Res 60:631–637PubMedCrossRefGoogle Scholar
  5. 5.
    Claramita M, Utarini A, Soebono H, Van Dalen J, Van der Vleuten C (2011) Doctor-patient communication in a Southeast Asian setting: the conflict between ideal and reality. Adv Health Sci Educ Theory Pract 16:69–80PubMedCrossRefGoogle Scholar
  6. 6.
    Davies NJ, Kinman G, Thomas RJ, Bailey T (2008) Information satisfaction in breast and prostate cancer patients: implications for quality of life. Psychooncology 17:1048–1052PubMedCrossRefGoogle Scholar
  7. 7.
    Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM (2010) GLOBOCAN 2008 v1.2, Cancer incidence and mortality worldwide: IARC Cancer Base No. 10.International Agency for Research on Cancer. Available via http://globocan.iarc.fr. Accessed 2 December 2010
  8. 8.
    Ferlay J, Shin HR, Bray F, Forman D, Mathers C, Parkin DM (2010) Estimates of worldwide burden of cancer in 2008: GLOBOCAN 2008. Int J Cancer 127:2893–2917PubMedCrossRefGoogle Scholar
  9. 9.
    Frostholm L, Fink P, Oernboel E, Christensen KS, Toft T, Olesen F, Weinman J (2005) The uncertain consultation and patient satisfaction: the impact of patients' illness perceptions and a randomized controlled trial on the training of physicians' communication skills. Psychosom Med 67:897–905PubMedCrossRefGoogle Scholar
  10. 10.
    Hagger MS, Orbell S (2003) A meta-analytic review of the common-sense model of illness representations. Psychol Heal 18:141–184CrossRefGoogle Scholar
  11. 11.
    Harrison JD, Young JM, Price MA, Butow PN, Solomon MJ (2009) What are the unmet supportive care needs of people with cancer? A systematic review. Support Care Cancer 17:1117–1128PubMedCrossRefGoogle Scholar
  12. 12.
    Helgeson VS, Cohen S (1996) Social support and adjustment to cancer: reconciling descriptive, correlational, and intervention research. Health Psychol 15:135–148PubMedCrossRefGoogle Scholar
  13. 13.
    Hu WY, Chiu TY, Chuang RB, Chen CY (2002) Solving family-related barriers to truthfulness in cases of terminal cancer in Taiwan. A professional perspective. Cancer Nurs 25:486–492PubMedCrossRefGoogle Scholar
  14. 14.
    Husson O, Mols F, van de Poll-Franse LV (2011) The relation between information provision and health-related quality of life, anxiety and depression among cancer survivors: a systematic review. Ann Oncol 22:761–772PubMedCrossRefGoogle Scholar
  15. 15.
    Husson O, Thong MS, Mols F, Oerlemans S, Kaptein AA, van de Poll-Franse LV (2013) Illness perceptions in cancer survivors: what is the role of information provision? Psychooncology 22:490–498PubMedCrossRefGoogle Scholar
  16. 16.
    Iskandarsyah A, de Klerk C, Suardi DR, Soemitro MP, Sadarjoen S, Passchier J (2013) Psychosocial and cultural reasons for delay in seeking help and non-adherence to treatment in Indonesian women with breast cancer: a qualitative study. Health Psychol. doi:10.1037/a0031060 PubMedGoogle Scholar
  17. 17.
    Jemal A, Clegg LX, Ward E, Ries LA, Wu X, Jamison PM, Wingo PA, Howe HL, Anderson RN, Edwards BK (2004) Annual report to the nation on the status of cancer, 1975-2001, with a special feature regarding survival. Cancer 101:3–27PubMedCrossRefGoogle Scholar
  18. 18.
    Leventhal H, Meyer D, Nerenz DR (1980) The common sense representation of illness danger. In: Rachmand S (ed) Contributions to medical psychology. Pergamon, New York, pp 17–30Google Scholar
  19. 19.
    Leydon GM, Boulton M, Moynihan C, Jones A, Mossman J, Boudioni M, McPherson K (2000) Cancer patients' information needs and information seeking behaviour: in depth interview study. BMJ 320:909–913PubMedCrossRefGoogle Scholar
  20. 20.
    Lin CC, Tsay HF (2005) Relationships among perceived diagnostic disclosure, health locus of control, and levels of hope in Taiwanese cancer patients. Psychooncology 14:376–385PubMedCrossRefGoogle Scholar
  21. 21.
    Lithner M, Johansson J, Andersson E, Jakobsson U, Palmquist I, Klefsgard R (2012) Perceived information after surgery for colorectal cancer—an explorative study. Colorectal Dis 14:1340–1350PubMedCrossRefGoogle Scholar
  22. 22.
    Llewellyn CD, Horne R, McGurk M, Weinman J (2006) Development and preliminary validation of a new measure to assess satisfaction with information among head and neck cancer patients: the satisfaction with cancer information profile (SCIP). Head Neck 28:540–548PubMedCrossRefGoogle Scholar
  23. 23.
    Llewellyn CD, McGurk M, Weinman J (2006) How satisfied are head and neck cancer (HNC) patients with the information they receive pre-treatment? Results from the satisfaction with cancer information profile (SCIP). Oral Oncol 42:726–734PubMedCrossRefGoogle Scholar
  24. 24.
    Montazeri A, Milroy R, Hole D, McEwen J, Gillis CR (2003) How quality of life data contribute to our understanding of cancer patients' experiences? A study of patients with lung cancer. Qual Life Res 12:157–166PubMedCrossRefGoogle Scholar
  25. 25.
    Moore MA, Manan AA, Chow KY, Cornain SF, Devi CR, Triningsih FX, Laudico A, Mapua CA, Mirasol-Lumague MR, Noorwati S, Nyunt K, Othman NH, Shah SA, Sinuraya ES, Yip CH, Sobue T (2010) Cancer epidemiology and control in peninsular and island South-East Asia—past, present and future. Asian Pac J Cancer Prev 11(Suppl 2):81–98PubMedGoogle Scholar
  26. 26.
    Nicolaije KA, Husson O, Ezendam NP, Vos MC, Kruitwagen RF, Lybeert ML, van de Poll-Franse LV (2012) Endometrial cancer survivors are unsatisfied with received information about diagnosis, treatment and follow-up: a study from the population-based PROFILES registry. Patient Educ Couns 88:427–435PubMedCrossRefGoogle Scholar
  27. 27.
    Park BW, Hwang SY (2012) Unmet needs of breast cancer patients relative to survival duration. Yonsei Med J 53:118–125PubMedCrossRefGoogle Scholar
  28. 28.
    Rehnberg G, Absetz P, Aro AR (2001) Women's satisfaction with information at breast biopsy in breast cancer screening. Patient Educ Couns 42:1–8PubMedCrossRefGoogle Scholar
  29. 29.
    Salim OC, Sudharma NI, Rina K, Kusumaratna RK, Hidayat A (2007) Validity and reliability of World Health Organization Quality of Life-BREF to assess the quality of life in the elderly. Univ Med 26:27–38Google Scholar
  30. 30.
    Salonen P, Tarkka MT, Kellokumpu-Lehtinen PL, Koivisto AM, Aalto P, Kaunonen M (2013) Effect of social support on changes in quality of life in early breast cancer patients: a longitudinal study. Scand J Caring Sci 27:396–405PubMedCrossRefGoogle Scholar
  31. 31.
    Scharloo M, Baatenburg de Jong RJ, Langeveld TP, van Velzen-Verkaik E, Doorn-op den Akker MM, Kaptein AA (2005) Quality of life and illness perceptions in patients with recently diagnosed head and neck cancer. Head Neck 27:857–863PubMedCrossRefGoogle Scholar
  32. 32.
    Skevington SM, Lotfy M, O'Connell KA, Group W (2004) The World Health Organization's WHOQOL-BREF quality of life assessment: psychometric properties and results of the international field trial. A report from the WHOQOL group. Qual Life Res 13:299–310CrossRefGoogle Scholar
  33. 33.
    Tomlinson K, Barker S, Soden K (2012) What are cancer patients' experiences and preferences for the provision of written information in the palliative care setting? A focus group study. Palliat Med 26:760–765PubMedCrossRefGoogle Scholar
  34. 34.
    World Health Organization (1997) WHOQOL Measuring Quality of Life, Division of Mental Health and Prevention of Substance Abuse. WHO, GenevaGoogle Scholar

Copyright information

© Springer-Verlag Berlin Heidelberg 2013

Authors and Affiliations

  • Aulia Iskandarsyah
    • 1
    • 2
    • 3
  • Cora de Klerk
    • 1
  • Dradjat R.  Suardi
    • 4
  • Monty P.  Soemitro
    • 4
  • Sawitri S.  Sadarjoen
    • 3
  • Jan Passchier
    • 1
    • 2
  1. 1.Department of Psychiatry, Section Medical Psychology and PsychotherapyErasmus MC University Medical CenterRotterdamThe Netherlands
  2. 2.Department of Clinical PsychologyVU UniversityAmsterdamThe Netherlands
  3. 3.Department of Clinical PsychologyPadjadjaran UniversityBandungIndonesia
  4. 4.Department of Surgical OncologyHasan Sadikin HospitalBandungIndonesia

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