Colorectal Cancer Screening: The Role of Psychological, Social and Background Factors in Decision-making Process

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REVIEW ARTICLE

Colorectal Cancer Screening: The Role of Psychological, Social and Background Factors in Decision-making Process

Clinical Practice & Epidemiology in Mental Health 21 Mar 2018 REVIEW ARTICLE DOI: 10.2174/1745017901814010063

Abstract

Since ColoRectal Cancer (CRC) remains the third cause of cancer death in the world, a better understanding of the reasons underlying poor adherence to and delay in undergoing CRC screening programs is important.

CRC screening decision-making process can be conceptualized as the relationship between intention and behavior and needs to be investigated including the impact on patients’ decision of a broad range of psychological factors and personal predisposition as fear of a positive screening test, poor understanding of the procedure, psychological distress, anxiety, anticipation of pain, feelings of embarrassment and vulnerability. Also socioeconomic, ethnic and sociological influences, and organizational barriers have been identified as factors influencing CRC screening adherence. Decision-making process can finally be influenced by the healthcare background in which the intervention is promoted and screening programs are carried out.

However, there is still a gap on the scientific knowledge about the influences of diverse elements on screening adherence and this deserves further investigations in order to carry out more focused and effective prevention programs.

Keywords: Cancer screening, Compliance, Barriers, Cancer fear, Cancer worry, Health anxiety, Embarrassment, Risk perception, Colorectal cancer.

1. COLORECTAL CANCER SCREENING TESTS

Although its incidence and mortality have decreased over the past 20 years, ColoRectal Cancer (CRC) remains one of the leading causes of mortality and morbidity in the world [1, 2]. According to guidelines, CRC screening tests are strongly recommended starting from 50 years of age for average risk individuals [3-5] and should continue up to age 75 [6].

The options currently offered for CRC screening include Fecal Occult Blood Test (FOBT), Flexible Sigmoidoscopy (FS), Optical Colonoscopy (OC) and the recently proposed CT Colonography (CTC). FOBT is probably the least expensive screening test and is also well accepted with participation rates of 48% to 63%. However, it has some limitations, such as the need to repeat the test every one/two years and the low sensitivity for large adenomas (≥10 mm) [7]. In spite of being the most complete diagnostic test for CRC and colorectal adenomas, OC shows low acceptance as a screening test. CTC is a highly sensitive and minimally invasive procedure for the detection of cancer (96%) and large adenomas (90%) and has a low risk of complications [7]. The relationship between cost and effectiveness of CTC has been recently debated in order to assess whether and how to include it in the screening programmes [8-13]. CTC is expensive and requires the patient’s ability to complete a successful preparation similar to colonoscopy. However, its main drawback is the radiation dose delivered to the patient [14]. In particular, exposure to ionizing radiations has emerged as a general obstacle to participation in radiological screening of cancers, that is associated with practical and emotional barriers related to the fear of radiation [15, 16]. We carried out a computerized search on Google and PubMed database combining the search terms “cancer screening”, “compliance barriers” and “colorectal cancer” to assess studies that have tried to identify the main adherence barriers to CRC screening programs.

2. REASONS FOR NON-ADHERENCE TO COLORECTAL CANCER SCREENING

Despite evidence suggesting that 90% of CRC incidence and 60% of deaths can be prevented through screenings [17, 18], 38% of adults aged 50 years and older have never had a sigmoidoscopy/colonoscopy and 79% have never had a FOBT [19]. Better understanding of the reasons for poor adherence and delay in undergoing screening programs is important in the context of the significant challenge represented by the reduction of CRC incidence and morality [3, 18]. Usually, the CRC screening strategies include FOBT as first exam and OC as further work-up procedure. As it has been underlined, colonoscopy participation rates can be significantly lower than FOBT, and even when FOBT is positive, some patients can refuse to continue the screening process declining OC [20, 21].

Reasons underlying non-adherence to CRC screening are diverse and include socioeconomic, ethnic and sociological influences [22], organizational barriers [23, 24] and General Practitioner (GP) endorsement bent [25]. Also a male gender, long waiting time for appointment and psychiatric illnesses have been reported as factors that are implicated in colonoscopy non-adherence [26-28].

However, a lower educational level has been found to be associated with low colonoscopy compliance. Finally, obese patients have been shown to be more likely to be non-compliant than non-obese patients [29]. Therefore, it is necessary that promotional CRC screening activities take into greater account these factors that predispose some types of patients to poor adherence.

However, there seems to be a gap in the scientific literature especially on the psychosocial factors that might influence patient’s decision to undergo or refuse CRC screening. In particular, knowledge of the psychological effects on participating in CRC screening is limited and there are few studies, with mixed and contradictory results, that have tried to aassess which psychological aspects such as fear can affect the probability that patients undergo specific screening and how much participants may experience psychological stress from participation even after a long time [30].

3. PSYCHOLOGICAL FACTORS

In general, fear of a positive test, poor understanding of the procedure, psychological distress, anxiety, anticipation of pain, feelings of embarrassment and vulnerability can determine a poor adherence to cancer screening [23, 31, 32].

However, according to some studies, cancer fear itself can act both as a facilitator and a deterrent to screening participation for breast [33, 34], prostate [34] and ovarian cancer [35] cancers. According to some Authors, cancer fear could promote adherence to screening since the latter can be viewed as a means for seeking reassurance, while for other Authors, cancer fear would be associated with elusive or fatalistic views that are deterrent to screening [36-38]

Regarding CRC screening, fear before undergoing screening was associated with higher adherence, while fear during screening was associated with lower adherence in a sample of elderly adults in Singapore [39] and in a sample of Hispanic Americans [40]. However, this ambivalent relationship between cancer fear and adherence to CRC and other cancer screening was not found in other studies [41, 42]. The main factor that would require greater insight seems to be how fear can lead to a specific behavioral response facilitating, hindering or delaying people from undergoing the screening test.

One possible explanation for the above inconsistencies could be the low uniformity and accuracy of tools used to measure and examine “cancer fear” in its different aspects. Usually, history of psychiatric illness, defined as mood, anxiety, and/or psychotic [28] or panic [43-45] disorder, has shown a potential correlation with low adherence to screening and has been assessed using standard instruments.

However fear of undergoing medical examinations and of being affected by specific pathologies may include other psychological features as worry of receiving a positive screening test result, discomfort associated with the invasiveness of the screening tests, some cognitive and affective factors and anxiety predisposition. Accordingly, it is reasonable to assume that specific tools need to be developed considering all the diverse psychological elements that can be involved. In general, the fear of receiving a CRC diagnosis needs to be better understood as a multi-dimensional construct with its cognitive, biological, affective and behavioural components [46, 47]. A review that took into account inhomogeneous definitions and measurement strategies has pointed out that ‘worry about cancer’, ‘cancer-related distress’, ‘intrusive and avoidant thoughts about cancer’, and ‘effects of cancer-related thoughts on mood and daily activities’ are some of the main elements with which the fear of cancer has been operationalised [38]. Three aspects of cancer fear: cognitive, affective and psychobiological aspects and their association with different behavioural effects [47]. It has also been observed that cognitive/affective aspects of cancer fear (cancer as greatest health fear, worry about cancer) may exert their effects at different stages in the decisional process. They were significant facilitators of screening intention because of the desire of being reassured, while to think about cancer can lead to a more visceral negative response that can be a deterrent at the action stage. As outlined by other Authors, the relationship between intention and behaviour needs to be better understood as well as the role of factors that can influence intention and action [48].

4. HEALTHCARE BACKGROUND FACTORS

Decision-making process can also be influenced by the healthcare background in which the intervention is promoted and how preventive measurements are presented and screening actions are performed. Full knowledge of the different CRC screening examinations available and their different invasiveness level can also be a relevant factor for adherence. However, research results are not yet exhaustive on these aspects and further studies are required.

Since the CRC screenings remain an elective and voluntary medical procedure and the rate of deaths attributable to low rate of compliance to CRC screening are not negligible, some studies have been carried out with the aim to evaluate efficacy of some preventive health measures. For instance, patient navigation and community health liaisons were developed and trained to guide candidates through screening colonoscopy using a direct endoscopy referral system [49]. They proved to be effective in helping patients to overcome barriers to CRC screening, but with an effect of small size [50, 51].

For this reason, both decision aids and patient navigation have been tested as complementary interventions for promoting CRC screening adherence by influencing the decision process both on a practical/behavioral and cognitive level including patients awareness, knowledge and preferences [52]. Increasing the patient’s knowledge using advanced visual media through local campaigns was found to be associated with higher acceptance rates for screening colonoscopies [53]. Moreover, a community-focused education program has been evaluated as a potential prevention action to reduce poor adherence and make the patient an active participant in their care [54]. The program has provided instruction on CRC prevention and screening through flyer distribution, newspaper advertisements, radio advertisements, and publicly displayed poster to allow patients to keep information and make an appointment showing increasing compliance [54]. Culturally, targeted educational programs about CRC for Blacks and Latinos including education about screening, peer testimony given by a colonoscopy-adherent person, and pre- and post-knowledge assessment have also been realized [55].

Colonoscopy is one of the main CRC screening tests that requires compliance to the procedure, as well as the ability to complete a successful colonoscopy preparation. For this reason, some authors have assessed the role that communication and understanding of basic health information during the process can have for patients adherence. The use of an educational pamphlet has been found to reduce the anxiety levels before colonoscopy, to determine a better colon preparation and to have effect on the quality and the amount of medications used during the procedure [56]. A web-based multimedia program illustrates to patients information material before colonoscopy can increase knowledge, decrease anxiety, procedure time and medication requirements [57].

Since colonoscopy is usually done with sedation to reduce anxiety and discomfort in patients during the examination, some studies have evaluated the capability of listening to music, as an alternative method to reduce pain during the procedure [58-60]. Other alternative methods, such as showing a relaxing video, have been tested in order to evaluate their effects on patient anxiety, pain and experience during colonoscopy with an improved satisfaction especially among patients with a high pre-procedural anxiety score [61]. Finally, in order to evaluate possible benefits of hypnosis during colonoscopy, some authors performed a pilot study selecting the time for procedure, number of vasovagal events, and recovery time as outcomes [62]. The results have suggested that hypnosis can be an effective method to manage anxiety and pain associated with colonoscopy and can reduce the need for sedation, recovery time and vasovagal events.

CONCLUSION

The CRC screening decision-making process conceptualized as the relationship between intention and behaviour needs to be better understood by examining the impact of a broad range of factors on screening adherence and future prevention programs. In particular, since there is a gap on the scientific knowledge about psychological factors and personal predisposition elements underlying patients’ decision, further studies of these elements are necessary.

It is also necessary that studies take also into consideration the environmental factors that can interfere or facilitate the decision-making process and their specific peculiarities including healthcare background and the characteristics of families, communities, cities and neighborhoods where the interventions are promoted and screening programs are carried out.

CONSENT FOR PUBLICATION

Not applicable.

CONFLICT OF INTEREST

The authors declare no conflict of interest, financial or otherwise.

ACKNOWLEDGEMENTS

Declared none.

REFERENCES

1
Torre LA, Bray F, Siegel RL, Ferlay J, Lortet-Tieulent J, Jemal A. Global cancer statistics, 2012. CA Cancer J Clin 2015; 65(2): 87-108.
2
Gandomani HS, Aghajani M, Mohammadian-Hafshejani A, Tarazoj AA, Pouyesh V, Salehiniya H. Colorectal cancer in the world: Incidence, mortality and risk factors. Biomed Res Ther 2017; 4(10): 1656-75.
3
Smith RA, Cokkinides V, Brawley OW. Cancer screening in the United States, 2009: A review of current American Cancer Society guidelines and issues in cancer screening. CA Cancer J Clin 2009; 59(1): 27-41.
4
Lieberman DA, Rex DK, Winawer SJ, Giardiello FM, Johnson DA, Levin TR. Guidelines for colonoscopy surveillance after screening and polypectomy: A consensus update by the US multi-society task force on colorectal cancer. Gastroenterology 2012; 143(3): 844-57.
5
Ruco A, Stock D, Hilsden RJ, et al. Evaluation of a risk index for advanced proximal neoplasia of the colon. Gastrointest Endosc 2015; 81(6): 1427-32.
6
Bibbins-Domingo K, Grossman DC, Curry SJ, et al. Screening for colorectal cancer: US preventive services task force recommendation statement, us preventive services task force. JAMA 2016; 315(23): 2564-75.
7
Sali L, Mascalchi M, Falchini M, et al. Reduced and full-preparation ct colonography, fecal immunochemical test, and colonoscopy for population screening of colorectal cancer: A randomized trial. J Natl Cancer Inst 2015; 108(2): djv319.
8
Sali L, Grazzini G, Mascalchi M. CT colonography: role in FOBT-based screening programs for colorectal cancer. Clin J Gastroenterol 2017; 10(4): 312-9.
9
Zorzi M, Fedato C, Grazzini G, et al. [Screening for colorectal cancer in Italy, 2010 survey]. Epidemiol Prev 2012; 36(6)(Suppl. 1): 55-77.
10
Kapidzic A, Grobbee EJ, Hol L, et al. Attendance and yield over three rounds of population-based fecal immunochemical test screening. Am J Gastroenterol 2014; 109(8): 1257-64.
11
Sali L, Falchini M, Della Monica P, et al. CT colonography before colonoscopy in subjects with positive faecal occult blood test. Preliminary experience. Radiol Med (Torino) 2010; 115(8): 1267-78.
12
Sali L, Regge D. CT colonography for population screening of colorectal cancer: Hints from European trials. Br J Radiol 2016; 89(1068): 20160517.
13
Mantellini P, Lippi G, Sali L, et al. Cost analysis of colorectal cancer screening with CT colonography in Italy. Eur J Health Econ 2017.
14
Prokop M. Cancer screening with CT: Dose controversy. Eur Radiol 2005; 15(Suppl. 4): D55-61.
15
Khayyat YM, Ibrahim EM. Public awareness of colon cancer screening among the general population: A study from the Western Region of Saudi Arabia. Qatar Med J 2014; 2014(1): 17-24.
16
Ali N, Lifford KJ, Carter B, et al. Barriers to uptake among high-risk individuals declining participation in lung cancer screening: A mixed methods analysis of the UK Lung Cancer Screening (UKLS) trial. BMJ Open 2015; 5(7): e008254.
17
Smith RA, Cokkinides V, Eyre HJ. Cancer screening in the United States, 2007: A review of current guidelines, practices, and prospects. CA Cancer J Clin 2007; 57(2): 90-104.
18
Levin B, Lieberman DA, McFarland B, et al. Screening and surveillance for the early detection of colorectal cancer and adenomatous polyps, 2008: A joint guideline from the American Cancer Society, the US Multi-Society Task Force on Colorectal Cancer, and the American College of Radiology. CA Cancer J Clin 2008; 58(3): 130-60.
19
Bynum SA, Davis JL, Green BL, Katz RV. Unwillingness to participate in colorectal cancer screening: Examining fears, attitudes, and medical mistrust in an ethnically diverse sample of adults 50 years and older. Am J Health Promot 2012; 26(5): 295-300.
20
Sali L, Grazzini G, Ventura L, et al. Computed tomographic colonography in subjects with positive faecal occult blood test refusing optical colonoscopy. Dig Liver Dis 2013; 45(4): 285-9.
21
Szczepura A, Johnson M, Orbell S, et al. 2003.
22
von Wagner C, Baio G, Raine R, et al. Inequalities in participation in an organized national colorectal cancer screening programme: Results from the first 2.6 million invitations in England. Int J Epidemiol 2011; 40(3): 712-8.
23
Murdock A, Rodgers C, Lindsay H, Tham TC. Why do patients not keep their appointments? Prospective study in a gastroenterology outpatient clinic. J R Soc Med 2002; 95(6): 284-6.
24
Sanasi-Bhola K, Williams CD, Burnside C, et al. Age, sex, marital status and adherence to scheduled out-patient endoscopy. Gastroenterology 2011; 140(5)
25
Raine R, Duffy SW, Wardle J, et al. Impact of general practice endorsement on the social gradient in uptake in bowel cancer screening. Br J Cancer 2016; 114(3): 321-6.
26
Beydoun HA, Beydoun MA. Predictors of colorectal cancer screening behaviors among average-risk older adults in the United States. Cancer Causes Control 2008; 19(4): 339-59.
27
Holden DJ, Jonas DE, Porterfield DS, Reuland D, Harris R. Systematic review: Enhancing the use and quality of colorectal cancer screening. Ann Intern Med 2010; 152(10): 668-76.
28
Blumenthal DM, Singal G, Mangla SS, Macklin EA, Chung DC. Predicting non-adherence with outpatient colonoscopy using a novel electronic tool that measures prior non-adherence. J Gen Intern Med 2015; 30(6): 724-31.
29
Anderson JC, Fortinsky RH, Kleppinger A, Merz-Beyus AB, Huntington CG III, Lagarde S. Predictors of compliance with free endoscopic colorectal cancer screening in uninsured adults. J Gen Intern Med 2011; 26(8): 875-80.
30
Kirkøen B, Berstad P, Botteri E, et al. Psychological effects of colorectal cancer screening: Participants vs individuals not invited. World J Gastroenterol 2016; 22(43): 9631-41.
31
Mladen DM, Dragoslav MP, Sanja Z, Bozidar B, Snezana D. Problems in screening colorectal cancer in the elderly. World J Gastroenterol 2003; 9(10): 2335-7.
32
McLachlan SA, Clements A, Austoker J. Patients’ experiences and reported barriers to colonoscopy in the screening context: A systematic review of the literature. Patient Educ Couns 2012; 86(2): 137-46.
33
Sutton S, Bickler G, Sancho-Aldridge J, Saidi G. Prospective study of predictors of attendance for breast screening in inner London. J Epidemiol Community Health 1994; 48(1): 65-73.
34
Consedine NS, Morgenstern AH, Kudadjie-Gyamfi E, Magai C, Neugut AI. Prostate cancer screening behavior in men from seven ethnic groups: the fear factor. Cancer Epidemiol Biomarkers Prev 2006; 15(2): 228-37.
35
Drescher C, Holt SK, Andersen MR, Anderson G, Urban N. Reported ovarian cancer screening among a population-based sample in Washington state. Obstet Gynecol 2000; 96(1): 70-4.
36
Champion VL, Skinner CS, Menon U, et al. A breast cancer fear scale: Psychometric development. J Health Psychol 2004; 9(6): 753-62.
37
Consedine NS, Magai C, Krivoshekova YS, Ryzewicz L, Neugut AI. Fear, anxiety, worry, and breast cancer screening behavior: A critical review. Cancer Epidemiol Biomarkers Prev 2004; 13(4): 501-10.
38
Hay JL, Buckley TR, Ostroff JS. The role of cancer worry in cancer screening: A theoretical and empirical review of the literature. Psychooncology 2005; 14(7): 517-34.
39
Wong RK, Wong ML, Chan YH, Feng Z, Wai CT, Yeoh KG. Gender differences in predictors of colorectal cancer screening uptake: A national cross sectional study based on the health belief model. BMC Public Health 2013; 13: 677.
40
Jandorf L, Ellison J, Villagra C, et al. Understanding the barriers and facilitators of colorectal cancer screening among low income immigrant hispanics. J Immigr Minor Health 2010; 12(4): 462-9.
41
Moser RP, McCaul K, Peters E, Nelson W, Marcus SE. Associations of perceived risk and worry with cancer health-protective actions: Data from the Health Information National Trends Survey (HINTS). J Health Psychol 2007; 12(1): 53-65.
42
Llanos AA, Pennell ML, Young GS, Tatum CM, Katz ML, Paskett ED. No association between colorectal cancer worry and screening uptake in Appalachian Ohio. J Public Health (Oxf) 2015; 37(2): 322-7.
43
Chung YW, Han DS, Yoo KS, Park CK. Patient factors predictive of pain and difficulty during sedation-free colonoscopy: A prospective study in Korea. Dig Liver Dis 2007; 39(9): 872-6.
44
Hu PH, Peng YC, Lin YT, Chang CS, Ou MC. Aromatherapy for reducing colonoscopy related procedural anxiety and physiological parameters: A randomized controlled study. Hepatogastroenterology 2010; 57(102-103): 1082-6.
45
Sly JR, Edwards T, Shelton RC, Jandorf L. Identifying barriers to colonoscopy screening for nonadherent African American participants in a patient navigation intervention. Health Educ Behav 2013; 40(4): 449-57.
46
Arne Ö. Fear and Anxiety: Overlaps and Dissociations Handbook of emotions 3rd ed. 2008.
47
Vrinten C, Waller J, von Wagner C, Wardle J. Cancer fear: Facilitator and deterrent to participation in colorectal cancer screening. Cancer Epidemiol Biomarkers Prev 2015; 24(2): 400-5.
48
Sheeran P. Intention-behavior relations: A conceptual and empirical review. Eur Rev Soc Psychol 2002; 12: 1-36.
49
Lebwohl B, Neugut AI, Stavsky E, et al. Effect of a patient navigator program on the volume and quality of colonoscopy. J Clin Gastroenterol 2011; 45(5): e47-53.
50
Leone LA, Reuland DS, Lewis CL, et al. Reach, usage, and effectiveness of a Medicaid patient navigator intervention to increase colorectal cancer screening, Cape Fear, North Carolina, 2011. Prev Chronic Dis 2013; 10: E82.
51
Ali-Faisal SF, Colella TJ, Medina-Jaudes N, Benz Scott L. The effectiveness of patient navigation to improve healthcare utilization outcomes: A meta-analysis of randomized controlled trials. Patient Educ Couns 2017; 100(3): 436-48.
52
Reuland DS, Brenner AT, Hoffman R, et al. Effect of combined patient decision aid and patient navigation vs. usual care for colorectal cancer screening in a vulnerable patient population: A randomized clinical trial. JAMA Intern Med 2017; 177(7): 967-74.
53
Albrecht H, Gallitz J, Hable R, et al. The offer of advanced imaging techniques leads to higher acceptance rates for screening colonoscopy: A Prospective Study. Asian Pac J Cancer Prev 2016; 17(8): 3871-5.
54
Tucker A, Tucker SP. Increasing colorectal cancer screening compliance through community education. Gastroenterol Nurs 2012; 35(6): 416-9.
55
Crookes DM, Njoku O, Rodriguez MC, Mendez EI, Jandorf L. Promoting colorectal cancer screening through group education in community-based settings. J Cancer Educ 2014; 29(2): 296-303.
56
Shaikh AA, Hussain SM, Rahn S, Desilets DJ. Effect of an educational pamphlet on colon cancer screening: A randomized, prospective trial. Eur J Gastroenterol Hepatol 2010; 22(4): 444-9.
57
Parker S, Zipursky J, Ma H, Baumblatt GL, Siegel CA. A web-based multimedia program before colonoscopy increased knowledge and decreased anxiety, sedation requirement, and procedure time. J Clin Gastroenterol 2017.
58
Andrada JM, Vidal AA, Aguilar-Tablada TC, et al. Anxiety during the performance of colonoscopies: Modification using music therapy 2004.
59
Bechtold ML, Perez RA, Puli SR, Marshall JB. Effect of music on patients undergoing outpatient colonoscopy 2006.
60
Ko CH, Chen YY, Wu KT, et al. Effect of music on level of anxiety in patients undergoing colonoscopy without sedation. J Chin Med Assoc 2017; 80(3): 154-60.
61
Umezawa S, Higurashi T, Uchiyama S, et al. Visual distraction alone for the improvement of colonoscopy-related pain and satisfaction. World J Gastroenterol 2015; 21(15): 4707-14.
62
Elkins G, White J, Patel P, Marcus J, Perfect MM, Montgomery GH. Hypnosis to manage anxiety and pain associated with colonoscopy for colorectal cancer screening: Case studies and possible benefits. Int J Clin Exp Hypn 2006; 54(4): 416-31.