- Research article
- Open Access
Individual- and provider-level factors associated with colorectal cancer screening in accordance with guideline recommendation: a community-level perspective across varying levels of risk
BMC Public Health volume 13, Article number: 248 (2013)
Participation rates in colorectal cancer screening (CRC) are low. Relatively little is known about screening uptake across varying levels of risk and across population groups. The purpose of the current study was to identify factors associated with (i) ever receiving colorectal cancer (CRC) testing; (ii) risk-appropriate CRC screening in accordance with guidelines; and (iii) recent colonoscopy screening.
1592 at-risk persons (aged 56–88 years) were randomly selected from the Hunter Community Study (HCS), Australia. Participants self-reported family history of CRC was used to quantify risk in accordance with national screening guidelines.
1117 participants returned a questionnaire; 760 respondents were eligible for screening and analysis. Ever receiving CRC testing was significantly more likely for persons: aged 65–74 years; who had discussed with a doctor their family history of CRC or had ever received screening advice. For respondents “at or slightly above average risk”, guideline-appropriate screening was significantly more likely for persons: aged 65–74 years; with higher household income; and who had ever received screening advice. For respondents at “moderately or potentially high risk”, guideline-appropriate screening was significantly more likely for persons: with private health insurance and who had discussed their family history of CRC with a doctor. Colonoscopy screening was significantly more likely for persons: who had ever smoked; discussed their family history of CRC with a doctor; or had ever received screening advice.
The level of risk-appropriate screening varied across populations groups. Interventions that target population groups less likely to engage in CRC screening are pivotal for decreasing screening inequalities.
Worldwide, colorectal cancer (CRC) is a significant health burden with over one million persons diagnosed annually . The five-year survival rate for localised disease is high, yet few CRCs (less than 40%) are detected at this stage . Many CRC deaths are preventable as screening can reduce incidence through the identification and removal of precancerous polyps [3, 4] and increase early detection of disease [5, 6]. Australian National Health and Medical Research Council (NHMRC) screening guidelines  recommend that asymptomatic persons “at or slightly above average risk” receive either FOBT screening biennially or sigmoidoscopy (preferably flexible) every five years commencing at age 50 years . For persons at “moderately increased risk”, colonoscopy is endorsed every five years starting at age 50 or at an age ten years younger than the age of first diagnosis of bowel cancer in the family, whichever comes first . Endoscopy screening for persons at “potentially high risk” is recommended at least on a five-yearly basis in the NHMRC screening guidelines. However, age at screening commencement, test type and repeat testing interval are dependent on the type of family-specific mutation identified .
Australia’s National Bowel Cancer Screening Program
In Australia, Medicare administers the National Bowel Cancer Screening Program (NBCSP) Register . Medicare selects eligible participants from either the Medicare enrolment records or the Department of Veterans’ Affairs . The NBCSP Register is responsible for mailing of screening invitations and FOBT kits, the recording of participants’ details and the issuing of reminder letters . As part of the NBCSP, participants are encouraged to nominate their usual primary care provider on their participants details form; however, this is not compulsory . The recently re-funded NBCSP offers persons turning 50, 55 and 65 years of age via mail a one-off immunochemical Faecal Occult Blood Test (FOBT) screening invitation . It is important to note that the limited format of the NBCSP (restriction of screening to persons in selected age brackets across the at-risk population),  is not consistent with the NHMRC recommendation of biennial FOBT screening of all Australians in the at-risk population . A recent study examining the costs and outcomes from full (rather than limited) implementation of a biennial FOBT screening for adults in the at-risk population (50–74 years) identified a likely mortality reduction of 25% and saving of 500 deaths per year .
Screening participation in Australia
Participation rates in Australia’s NBCSP appear to have reached a plateau since the pilot program’s introduction [9, 11–13]. The pilot program received a response rate of 45%, with the roll-out of the NBCSP (with screening offered to persons 50 and 65 years of age) in 2006 receiving a slightly lower rate of 41% . The rate of participation only marginally increased in 2008 to 42.9% when the program widened to offer screening to persons aged 55 years of age . Most recent estimates suggest a similar rate of low participation (40.1%) . The experience in other countries with national screening programs offering repeated FOBT screening to a wider section of the at-risk population suggests that much higher screening rates are achievable. For example, FOBT screening rates in the United Kingdom and Finnish screening programs are currently 52% and 71% respectively [14, 15]. In Australia, previous community- based evaluations have also indicated low rates of CRC screening, with 5 to 20% of individuals ever undertaking FOBT [16–18]. The most recent assessment in New South Wales (NSW) indicated that 18% of persons aged over 50 years had undertaken FOBT in the previous five years . In relation to colonoscopy screening in Australia, two population-based assessments in NSW have suggested under screening among persons at elevated levels of risk [16, 19].
Given low rates of CRC screening, it is important to identify factors which may influence screening uptake. Previous studies have indicated that the following factors influence CRC screening behaviour: socio-demographic characteristics (e.g. older age, higher education, higher income); lifestyle factors (e.g. smoking history, chronic disease); family history (e.g. personal or family history of CRC); awareness (e.g. knowledge of CRC and perceived risk of developing CRC) and health care utilisation (e.g. usual source of care, number of GP visits, and health care coverage) [20–26]. In the Australian context, a small number of studies have explored determinants of CRC screening uptake [17–19, 27, 28] with little known about predictors of screening behaviour for persons at varying levels of risk . Since the introduction of the NBCSP in 2006, no community- or population-based assessments in Australia have been conducted. Recent evidence pertaining to FOBT screening uptake and inequalities in participation have been confined to annual NBCSP monitoring reports, which report screening rates among a limited section of the at-risk population (persons 50, 55 and 65 years of age) [9, 11–13]. Further, since the NHMRC guidelines’ implementation in 1999, only one study has assessed the predictors of risk-appropriate screening for persons at each level of risk in accordance with guideline-recommendation . The identification of factors associated with risk-appropriate screening is of critical importance for future planning and implementation of tailored CRC screening programs.
This study aimed to assess among a large community-based cohort of at-risk persons (aged 56–88 years), the factors associated with: (1) ever receiving any CRC testing; (2) receiving screening in accordance with screening guidelines; and (3) recent use of colonoscopy screening.
The University of Newcastle and Hunter New England Population Health Human Research Ethics Committees granted ethical approval.
The Hunter Community Study (HCS) is a longitudinal community cohort aged 55–85 years at baseline in the Hunter Region, New South Wales (NSW), Australia. The sampled population, Hunter Community Study participants are at-risk of developing CRC with clinical practice guidelines recommending all persons commence CRC screening from the age of 50 years . HCS participants were randomly selected from the NSW State electoral roll between December 2004 and December 2007. A modified Dillman recruiting strategy  was used for this study, whereby two letters of introduction and an invitation to participate were posted to selected persons. Persons not speaking English and living in a residential aged-care facility were deemed ineligible. Following consent to participate, individuals were asked to complete two self-reported questionnaires and were asked to return these when they attended the HCS data collection centre, at which time a series of clinical measures were obtained. For further details on the HCS cohort and an exhaustive list of measures obtained from HCS participants, see the cohort profile . The HCS cohort profile reflects state and national profiles for gender and marital status but is slightly younger in age . For the current study, a randomly selected sub-sample of the HCS (n = 1592) aged 56–88 years (reflective of age since HCS data collection point) were mailed a questionnaire during November, 2009. The sample size of 1592 was chosen to investigate delay in seeking medical advice for primary symptoms of CRC in additional studies using the HCS cohort [31, 32] in order to achieve a power of 80%, so that the proportion of individuals who delay seeking medical advice for symptoms or treatment for CRC will be estimated with 95% confidence intervals.
Questions and responses options are presented in the study questionnaire (see Additional file 1). Respondents were asked whether they had ever undertaken FOBT, colonoscopy or sigmoidoscopy. Those ever undertaking each test were asked to specify timing of most recent testing and “Did you have your last X test because you had a symptom” (Yes/ No). All respondents were asked about their family history of CRC (see Additional file 1) to allocate each respondent to a level of risk (see Table 1) in accordance with screening guidelines .
Predictors of CRC screening behaviour
Based on existing literature, the following items selected from the HCS databank, assessed at HCS baseline were investigated: Socio-demographic characteristics: age, gender, education, marital status, country of birth, household income, retirement, private health insurance status, tobacco or alcohol use; Clinical characteristics: number of general practice visits over the past 12 months, previous cancer diagnosis (excluding CRC), body mass index, and presence of a chronic health-condition; and Psychosocial characteristics: physical health (SF-36) and mental health (K-10 Kessler Scale). Predictors ascertained at survey completion included: risk category, discussion of family history of CRC with doctor and notification of any “increased risk” (Never discussed/ discussed and informed of possible “increased risk”/ discussed and not informed of any possible “increased risk”), and ever received screening advice from doctor (Yes/No).
Descriptive statistics including frequencies, percentages, means, and standard deviations were used to describe the characteristics of participants. Chi-squared testing was used to assess any responder bias in relation to age, gender, and level of education. “Ever received CRC testing” was calculated by combining the proportion of respondents indicating “Yes” to undertaking any of the following CRC tests (i.e. FOBT, sigmoidoscopy or colonoscopy) divided by the total number of respondents. Respondents who had not provided any information on any of these CRC tests were excluded from analysis. The proportion of respondents screened in accordance with screening guidelines (Yes/ No) was assessed by risk category  as follows: “at or slightly above average risk” (FOBT within two years or sigmoidoscopy preferably flexible within five years) and “moderately increased risk/ potentially high risk” (colonoscopy within 5 years). Self reported family history of CRC was used to allocate respondents to a risk category in accordance with screening guidelines. Respondents with missing values relating to type or number of relative(s) diagnosed or age at their diagnosis were excluded from analysis. Multiple logistic regression modelling was used to assess the association between socio-demographic, clinical and psychosocial characteristics and each study outcome: ever received CRC test, screened in accordance with guidelines for level of risk (“at or slightly above average risk” and “moderately/ potentially increased risk”), and recent colonoscopy screening (within previous five years). Variables with a p value <.25 following simple logistic regression analysis (see Additional file 2) were entered into a stepwise multiple logistic regression analysis. Forward and Backward stepwise regression was used on complete cases so that the likelihood ratio test could be used to determine the best fit from one iteration to the next. Both the forward selection and backward elimination regression analysis produced equivalent results. Results from the backward stepwise elimination model were reported. Variables that met the significance cut point (p value < .05) were included in the final model. Data were analysed using STATA 11 (STATA, Texas, USA).
Characteristics of the sample
Of the 1592 mailed surveys, 1117 respondents completed and returned a survey (response rate = 70%). Respondents previously diagnosed with CRC (n = 24) or reporting they had undergone major abdominal surgery (n = 8) were excluded from analysis, leaving a total sample of 1085 participants with data. Responder bias was assessed on the following key characteristics: gender, age (56–64, 65–74, 75–88), and education (secondary schooling completed, secondary schooling not competed, trade qualification or TAFE, university or other tertiary education and other). Pearson’s χ2 test found no significant differences relating to gender (χ2 = .09; df =1 ; p = .76 ) or education (χ2 = 8.75; df = 4; p = .07). However, for age, respondents were significantly more likely to be of a younger age compared to non-respondents (χ2 = 11.12; df = 2; p < .01).
Inclusion and exclusion for CRC screening
Respondents were classified as asymptomatic and eligible for screening if they had not reported the following: undertaking FOBT, sigmoidoscopy or colonoscopy due to a symptom episode in the previous five years; any bowel related condition; previous history of CRC; or consulting a doctor for their first primary symptom episode of CRC (rectal bleeding or change in bowel habit) in the previous five years. Following exclusion of such persons, a total sample of 777 asymptomatic persons were identified. 17 asymptomatic persons were excluded from analysis due to insufficient family history information available to derive a level of risk in accordance with CRC screening guidelines. Table 2 describes the characteristics of respondents allocated to a level of risk in accordance with screening guidelines (n = 760) and eligible for analysis.
Ever received CRC testing
Overall, 63% (475/ 760) of respondents allocated to a level of risk had ever received any CRC testing (FOBT/ sigmoidoscopy or colonoscopy). The proportion ever undertaking CRC testing by risk category were: “at or slightly above average risk” 61% (431/ 707), “moderately increased risk” 82% (28/34) and “potentially high risk” 84% (16/19). Simple logistic regression analyses identified items with a p value < .25 which were entered into multiple logistic regression modelling. Table 3 presents the results of this analysis. Persons significantly more likely to have ever been tested for CRC were aged between 65–74 years of age and had ever received screening advice from a doctor. Persons who had discussed their family history of CRC with a doctor, irrespective of whether they were informed of any possible “increased risk”, were significantly more likely to be tested than those never having discussed their family history with a doctor.
CRC screening in accordance with national screening guidelines
Of the 707 respondents “at or slightly above average risk”, 697 provided information on either FOBT or sigmoidoscopy screening, with 21% (145/697) of respondents screened in accordance with national screening recommendation (see Table 4). Screening in accordance with guideline recommendation was significantly more likely to occur for “at or slightly above average risk” persons: aged 65–74 years of age; with a higher household income (> $70, 000 compared to <= $39, 999); and who had ever received screening advice from a doctor.
Of the 53 respondents at “moderately increased risk/ potentially high risk” and providing colonoscopy screening information, 45% (24/53) were screened in accordance with screening recommendation. Screening in accordance with guideline recommendation (colonoscopy within 5 years) was significantly more likely to occur for persons who had private health insurance and who had discussed their family history of CRC with a doctor (see Table 5).
Recent colonoscopy screening irrespective of level of risk
Of the 760 respondents allocated to a level of risk, 752 respondents provided colonoscopy screening information, with 16% (124/752) of respondents receiving a colonoscopy within the previous five years. Table 6 presents the multiple logistic regression model for recent colonoscopy screening (within 5 years) irrespective of level of risk. Recent colonoscopy screening was significantly more likely for persons: that had ever smoked; discussed their family history of CRC with a doctor regardless of whether informed of “increased risk”; and who had ever received screening advice from a doctor.
The behaviour of health care providers including discussing family history of CRC and making a CRC screening recommendation were predictors of CRC screening uptake, screening in accordance with guideline recommendation and recent colonoscopy screening. Individual and lifestyle characteristics associated with some but not all of the above CRC screening outcomes included: higher household income, age, private health insurance and smoking.
Factors associated with CRC screening behaviour
Health care provider recommendation for CRC screening
The variable most strongly associated with CRC testing and screening was receiving screening advice from a health care provider. This finding is consistent with previous literature which identified physician encouragement as an important predictor of CRC screening [20, 22, 24]. Strategies such as general practitioner screening invitations sent to patients [33, 34] and provider reminder/ prompt systems are effective in increasing the likelihood of screening participation . Relatively little is known about how well CRC screening is included within practice-based reminder systems [36, 37]. Improvement in the systematic delivery of CRC screening advice and implementation of effective primary-care based interventions are likely to be beneficial.
Discussion of family history of CRC with doctor
Persons who had discussed their family history of CRC regardless of whether they were informed of possible “increased risk” were more likely to be ever tested, screened in accordance with guideline recommendation (“moderately/ potentially high risk” persons) and screened recently using colonoscopy. Such findings highlight the importance of family history of CRC assessment in the primary care setting. Studies of cancer risk assessment tools suggest that such an approach is feasible and effective for collection of family history of cancer information, automation of familial risk stratification and risk-appropriate screening advice [38, 39].
Among persons who were “at or slightly above average risk”, those who were older were more likely to ever be tested and screened in accordance with CRC screening guidelines, as per previous studies [19, 24, 40, 41]. The literature suggests that an inverted U-relationship is observed, with the lowest rates of CRC screening participation found among persons 50–55 years and 70–80 years of age [24, 42]. Further, it has also been demonstrated that non-adherence to repeat FOBT screening is evident for persons aged less than 65 years . Given the rapid increase in CRC risk after age 50, the targeting of those aged 50–65 years is of particular importance if optimal screening rates are to be achieved.
A gradient in CRC screening participation has been identified worldwide related to socio-economic status [20, 24, 42]. Patient screening preference is sensitive to out of pocket expenses  with lower participation among disadvantaged persons [21, 24]. In the current study, persons “at or slightly above average risk” with household incomes above >$70,000 were more likely to be screened in accordance with guideline recommendation, suggesting a need for interventions facilitating CRC screening among low income households. In Australia, annual NBCSP monitoring reports and cross-sectional analysis of participation in this program have also indicated significantly lower levels of CRC screening participation among persons from the most deprived socio-economic quintiles in the population [9, 11–13, 45]. It is important to consider that this disparity in participation among differing socio-economic groups in Australia and the United Kingdom (UK) occurs in the presence of universal programs offering FOBT screening at no cost . A similar socio-economic gradient in screening participation has also been identified for cervical and breast cancer screening programs . These findings, lend support to the suggestion that direct economic barriers alone do not explain the socio-economic differential in participation . Previous studies have indicated that the provision of universal healthcare or re-imbursement for the cost of screening has little appreciable effect on eliminating equality in screening participation [46–49]. It appears that some health service access hurdles appear to dominate among disadvantaged persons [42, 50]. Additionally, it is argued that there are distinct differences in healthcare-seeking behaviour and beliefs among persons from lower socio-economic groups, compared with those from higher socio-economic groups [42, 50]. Taken together, this suggests that strategies to improve equality in screening must recognise factors other than financial coverage . It is paramount that future formative research examines the beliefs and barriers to CRC screening participation among lower socio-economic persons, to assist in the development of effective interventions [51, 52]. When considering future decisions about Australia’s NBCSP, it is critical that policy makers consider the reasons for non-screening compliance among persons from lower socio-economic status if increased equality in participation is to eventuate.
Private health insurance
Persons with private health insurance were marginally more likely to have recent colonoscopy screening. Previous literature indicates that private health insurance is a strong predictor of CRC screening [19, 24, 53]. Importantly, the current finding that private health insurance is a predictor for all colonoscopies but not for colonoscopies in accordance with guidelines casts some doubt on the process by which colonoscopies are decided. There is a pressing need to identify ways to improve guideline-appropriate use of colonoscopies.
Previous studies have indicated that smokers tend to be less compliant with CRC screening [19, 24]. The increased likelihood of recent colonoscopy screening among persons who had ever smoked in the current study may be due to health providers’ identification of this risk factor and provision of colonoscopy screening. Alternatively, ex-smokers who have already made a health behaviour change in their lives may have an increased motivation for health screening compared to persons who had never smoked.
It should be acknowledged that responder bias place some limitations on the interpretation of findings and their generalisability. For the most part, the HCS is a representative sample of the Hunter Region and NSW in comparison to Census data on a number of demographic characteristics, with the exception of age . Analysis of responders’ bias identified that responders were more likely to be younger than non-responders from the HCS cohort. In addition, persons living in residential care facilities and those from non-English speaking background were excluded in this study. Previous literature has indicated that non-English speaking persons are significantly less likely to undertake CRC screening [11–13, 19]. Future population based CRC screening programmes could benefit from strategies to improve CRC screening in non-English speaking persons and migrant groups . For respondents undertaking FOBT, type of test undertaken (guaiac or immunochemical) and the outcome of testing (negative/ positive) was not assessed, and this should be considered when interpreting the rate of colonoscopy screening (previous five years), as it may be an independent predictor for seeking a colonoscopy.
While it must be acknowledged that self-reported screening behaviour may have some recall bias, it has been shown to have reasonable agreement with physician report and relatively high levels of sensitivity and specificity [54, 55]. Although two new studies and a recent meta-analysis have indicated high levels of sensitivity and specificity for self-reported screening behaviour, [56–58] it is important to recognise that accuracy of self-reported screening varies across patient characteristics and test modalities . A meta-analysis of validation studies on self-reported CRC cancer screening use in the United States found that self-report versus documented history of screening had a high level of specificity (endoscopy .90 and FOBT .78) and sensitivity (endoscopy .82 and FOBT .79) .
To enhance recall, the current study adopted descriptions of CRC tests to increase the accurate recall of CRC testing. Self-reported family history of CRC was used to assign level of risk. Previous studies have indicated self-reported family history of CRC has relatively high levels of sensitivity and specificity for reporting of affected first-degree relatives [59–61]. However, the level of accuracy is substantially reduced for affected second-degree relatives [59–61]. The accuracy of reporting of age at diagnosis in CRC- affected relatives has not been identified in the literature. Further, the extent to which misleading family history information reorients risk classification for relatives following verification is largely unknown . Therefore, it is possible that the classification of risk may be inaccurate for a small proportion of study respondents given the limitation of no objective verification of self reported family history. For respondents at “moderately increased/ potentially high risk”, level of risk may have been overestimated for a small minority of respondents. For respondents indicating that both a first-degree relative and second-degree relative were diagnosed with CRC, an assumption was made that both relatives were diagnosed on the same side of the family. This assumption may have over-estimated the level of risk for some respondents.
Finally, the current study is subject to limitations associated with stepwise regression analysis including: parameter estimation, error rate estimation and reliance on a single best model [62–65]. Conducting stepwise regression models with a large number of independent variables and a small sample size, may over-estimate model fit [63, 64]. However, this limitation is difficult to overcome when applying statistical modelling techniques to identify predictors associated with rare occurrences in the population i.e. persons at increased familial risk of disease. It is conceivable that future large scale population-based studies examining CRC screening behaviour across varying levels of familial risk will assist in further defining the predictors of risk-appropriate CRC screening.
Empirical randomised controlled trial evidence suggests that the offering of repeated (annual or biennial) FOBT screening to the at-risk population is effective in reducing mortality and incidence associated with CRC [3, 6, 66, 67]. In Australia, there is a pressing need for expansion of the NBCSP and offering of repeated screening to the at-risk population, if the CRC-related disease burden and economic cost is to be reduced . Multiple strategies and messages targeting specific demographic groups as well as healthcare provider factors are needed if increases in overall screening participation are to be achieved. A pressing issue is the reduction of inequalities in CRC screening participation to reduce inequality in health outcomes. High quality research is required to unravel the barriers to CRC screening, as well as the mechanisms by which screening inequalities are maintained.
World Health Organisation: International Agency for Research on Cancer. GLOBOCAN. Cancer incidence and mortality worldwide in. 2008, http://globocan.iarc.fr/,
National Cancer Institute Surveillance Epidemiology and End Results: SEER Stats Facts Sheets. Colon and rectum cancer survival and stage. http://seer.cancer.gov/statfacts/html/colorect.html,
Mandel JS, Church TR, Bond JH, Ederer F, Geisser MS, Mongin SJ, Snover DC, Schuman LM: The effect of fecal occult-blood screening on the incidence of colorectal cancer. N Engl J Med. 2000, 343: 1603-1607. 10.1056/NEJM200011303432203.
Winawer SJ, Zauber AG, Ho MN, O'Brien MJ, Gottlieb LS, Sternberg SS, Waye JD, Schapiro M, Bond JH, Panish JF: Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med. 1993, 329: 1977-1981. 10.1056/NEJM199312303292701.
Ananda SS, McLaughlin SJ, Chen F, Hayes IP, Hunter AA, Skinner IJ, Steel MCA, Jones IT, Hastie IA, Rieger NA, Shedda S, Compston DJ, Gibbs P: Initial impact of Australia's National Bowel Cancer Screening Program. Med J Aust. 2009, 191: 378-381.
Hardcastle JD, Chamberlain JO, Robinson MH, Moss SM, Amar SS, Balfour TW, James PD, Mangham CM: Randomised controlled trial of fecal occult blood screening for colorectal cancer. Lancet. 1996, 348: 1472-1477. 10.1016/S0140-6736(96)03386-7.
Australian Cancer Network Colorectal Cancer Guidelines Revision Committee: Clinical Practice Guidelines for the Prevention, Early Detection and Management of Colorectal Cancer. http://www.nhmrc.gov.au/_files_nhmrc/publications/attachments/cp106_0.pdf,
National Bowel Cancer Screening Program - information for the public. http://www.medicareaustralia.gov.au/public/services/nbcsp/index.jsp,
Australian Institute of Health & Welfare & Australian Government Department of Health Ageing: National Bowel Cancer Screening Program: annual monitoring report 2009 data and data supplement 2010. 2010, Canberra: AIHW, Cancer Series no.57. Cat. No. CAN 53
Pignone M, Flitcroft KL, Howard K, Trevana LJ, Salkeld GP, St John J: Costs and cost-effectiveness of full implementation of a biennial faecal occult blood test screening program for bowel cancer in Australia. Med J Aust. 2010, 194: 180-185.
Australian Institute of Health & Welfare & Australian Government Department of Health Ageing: National Bowel Cancer Screening Program: annual monitoring report 2009. 2009, Canberra: AIHW, Cancer series no. 49. Cat. no. CAN 45
Australian Institute of Health & Welfare & Australian Government Department of Health Ageing: National Bowel Cancer Screening Program monitoring report 2007. 2008, Canberra: AIHW, Cancer series no. 40. Cat. no. CAN 35
Australian Institute of Health & Welfare & Australian Government Department of Health Ageing: National Bowel Cancer Screening Program monitoring report 2008. 2008, Canberra: AIHW, Cancer series 44. Cat. no. 40
Weller D, Coleman D, Robertson R, Butler P, Melia J, Campbell C, Parker R, Patnick J, Moss S: The UK colorectal cancer screening pilot: results of the second round of screening in England. Br J Cancer. 2007, 97: 1601-1605. 10.1038/sj.bjc.6604089.
Malila N, Oivanen T, Malminiemi O, Hakama M: Test, episode, and programme sensitivities of screening for colorectal cancer as a public health policy in Finland: experimental design. BMJ. 2008, 337: 3371-3375.
Cockburn J, Paul C, Tzelepis F, McElduff P, Byles J: Screening for bowel cancer among NSW adults with varying levels of risk: a community survey. Aust N Z J Public Health. 2002, 26: 236-241. 10.1111/j.1467-842X.2002.tb00680.x.
Thomas RJ, Clarke VA: Colorectal cancer: a survey of community beliefs and behaviours in Victoria. Med J Aust. 1998, 169: 37-40.
Weller DP, Owen N, Hiller JE, Willson K, Wilson D: Colorectal cancer and its prevention: prevalence of beliefs, attitudes, intentions and behaviour. Aust J Public Health. 1995, 19: 19-23.
Weber MF, Banks E, Ward R, Sitas F: Population characteristics related to colorectal cancer testing in New South Wales, Australia: results from the 45 and Up Study cohort. J Med Screen. 2008, 15: 137-142. 10.1258/jms.2008.008050.
Guessous I, Dash C, Lapin P, Doroshenk M, Smith RA, Klabunde CN: Colorectal cancer screening barriers and facilitators in older persons. Prev Med. 2010, 50: 3-10. 10.1016/j.ypmed.2009.12.005.
McCaffery K, Wardle J, Nadel M, Atkin W: Socioeconomic variation in participation in colorectal cancer screening. J Med Screen. 2002, 9: 104-108. 10.1136/jms.9.3.104.
Rees G, Martin PR, Macrae FA: Screening particpation in individuals with a family history of colorectal cancer: a review. Eur J Cancer Care. 2007, 17: 221-232.
Seeff LC, Nadel MR, Klabunde CN, Thompson T, Shapiro JA, Vernon SW, Coates RJ: Patterns and predictors of colorectal cancer test use in the adult U.S. population. Cancer. 2004, 100: 2093-2103. 10.1002/cncr.20276.
Subramanian S, Klosterman BA, Amonkar MM, Hunt TL: Adherence with colorectal cancer guidelines: a review. Prev Med. 2004, 38: 536-540. 10.1016/j.ypmed.2003.12.011.
Wardle J, Miles A, Atkin W: Gender difference in utilization of colorectal cancer screening. J Med Screen. 2005, 12: 20-27. 10.1258/0969141053279158.
Zapka JG, Puleo E, Vickers-Lahti M, Luckmann R: Healthcare system factors and colorectal cancer screening. Am J Prev Med. 2002, 23: 28-35. 10.1016/S0749-3797(02)00444-0.
Duncan A, Wilson C, Cole SR, Mikocka-Walus A, Turnbull D, Young GP: Demographic associations with stage of readiness to screen for colorectal cancer. Health Promotion Journal of Australia. 2009, 20: 7-12.
Koo JH, Arasaratnam MM, Liu K, Redmond DM, Connor SJ, Sung JJY, Leong RWL: Knowledge, perception and practices of colorectal cancer screening in an ethnically diverse population. Cancer Epidemiol. 2010, 34: 604-610. 10.1016/j.canep.2010.05.013.
Dillman DA: Mail and Telephone Surveys: The Total Design Method. 1978, New York: John Wiley & Sons
McEvoy M, Smith W, D'Este C, Duke J, Peel R, Schofield P, Scott R, Byles J, Henry D, Ewald B, Hancock S, Smith D, Attia J: Cohort profile: The Hunter Community Study. Int J Epidemiol. 2010, 39: 1452-1463. 10.1093/ije/dyp343.
Courtney RJ, Paul CL, Sanson-Fisher RW, Macrae F, Attia J, McEvoy M: Current state of medical-advice-seeking behaviour for symptoms of colorectal cancer: determinants of failure and delay in medical consultation. Col Dis. 2012, 14: 222-229. 10.1111/j.1463-1318.2012.02881.x.
Courtney RJ, Paul CL, Sanson-Fisher RW, Macrae FA, Attia J, McEvoy M: Factors associated with consultation behaviour for primary symptoms potentially indicating colorectal cancer: A cross-sectional study on response to symptoms. BMC Gastroenterol. 2012, 12: 100-10.1186/1471-230X-12-100.
Cole SR, Young GP, Byrne D, Guy JR, Morcom J: Participation in screening for colorectal cancer based on a faecal occult blood test is improved by endorsement by the primary care practitioner. J Med Screen. 2002, 9: 147-152. 10.1136/jms.9.4.147.
Zajac IT, Whibley AH, Cole SR, Byrne D, Guy J, Morcom J, Young GP: Endorsement by the primary care practitioner consistently improves participation in screening for colorectal cancer: a longitudinal analysis. J Med Screen. 2010, 17: 19-24. 10.1258/jms.2010.009101.
Stone EG, Morton SC, Hulscher ME, Maglione MA, Roth EA, Grimshaw JM, Mittman BS, Rubenstein LV, Shekelle PG: Interventions that increase the use of adult immunization and cancer screening services: a meta-analysis. Ann Intern Med. 2002, 136: 641-651.
Ellerbeck EF, Engelman KK, Gladden J, Mosier MC, Raju GS, Ahluwalia JS: Direct observation of counselling on colorectal cancer in rural primary care practices. J Gen Intern Med. 2001, 16: 697-700. 10.1111/j.1525-1497.2001.01224.x.
Klabunde CN, Riley GF, Mandelson MT, Frame PS, Brown ML: Health plan policies and programs for colorectal cancer screening: a national profile. Am J Manag Care. 2004, 10: 273-279.
Kelly KM, Sweet K: In search of a familial cancer risk assessment tool. Clin Genet. 2007, 71: 76-83.
Westman J, Hampel H, Bradley T: Efficacy of touchscreen computer based family cancer history questionnaire and subsequent cancer risk assessment. J Med Genet. 2000, 37: 354-360. 10.1136/jmg.37.5.354.
Ioannou GN, Chapko MK, Dominitz JA: Predictors of colorectal cancer screening participation in the United States. Am J Gastroenterol. 2003, 98: 2082-2091. 10.1111/j.1572-0241.2003.07574.x.
Sewitch MJ, Fournier C, Ciampi A, Dyachenko A: Colorectal cancer screening in Canada: Results of a national survey. Chronic Dis Can. 2008, 29: 9-21.
Javanparast S, Ward P, Young G, Wilson C, Carter S, Misan G, Cole S, Jiwa M, Tsourtos G, Martini A, Gill T, Baratiny G, Matt MA: How equitable are colorectal cancer screening programs which include FOBTs? A review of the qualitative and quantitiative studies. Prev Med. 2010, 50: 165-172. 10.1016/j.ypmed.2010.02.003.
Myers RE, Balshem AM, Wolf TA, Ross EA, Millner L: Adherence to continuous screening for colorectal neoplasia. Med Care. 1993, 31: 508-519. 10.1097/00005650-199306000-00004.
Pignone M, Bucholtz D, Harris R: Patient preferences for colon cancer screening. J Gen Intern Med. 1999, 14: 432-437. 10.1046/j.1525-1497.1999.00018.x.
Ward PR, Javanparast S, Ah Matt M, Martini A, Tsourtos G: Equity of colorectal cancer screening: a cross-sectional anlaysis of National Bowel Cancer Screening Program data for South Australia. Aust N Z J Public Health. 2010, 35: 61-65.
von Wagner C, Good A, Wright D, Rachet B, Obichere A, Bloom S, Wardle J: Inequalities in colorectal cancer screening participation in the first round of the national screening programme in England. Br J Cancer. 2009, 101: 60-63.
Singh SM, Paszat LF, Li C, He J, Vinden C, Rabeneck L: Association of socioeconomic status and receipt of colorectal cancer investigations: a population-based retrospective cohort study. CMAJ. 2004, 171: 461-465. 10.1503/cmaj.1031921.
Schenck AP, Peacock SC, Klabunde CN, Lapin P, Coan JF, Brown ML: Trends in colorectal cancer test use in the medicare population, 1998–2005. Am J Prev Med. 2009, 37: 1-7. 10.1016/j.amepre.2009.03.009.
O'Malley AS, Forrest CB, Feng S, Mandelblatt J: Disparities despite coverage. Gaps in colorectal cancer screening among medicare beneficiaries. Arch Intern Med. 2005, 165: 2129-2135. 10.1001/archinte.165.18.2129.
Dixon A, Legrand J, Henderson J, Murray R, Poteliakhoff E: Is the NHS equitable? A review of evidence. http://www.erpho.org.uk/viewResource.aspx?id=8772,
Ulin PR, Robinson ET, Tolley EE: Qualititative methods in public health. 2005, San Francisco, CA: Jossey-Boss
Fishbein M: Developing effective behavior change interventions: some lessons learned from behavioral research. 1995, Rockville, MD: National Institutes of Health
Matthews BA, Anderson RC, Nattinger AB: Colorectal cancer screening behavior and health insurance status. Cancer Cause Control. 2005, 16: 735-742. 10.1007/s10552-005-1228-z.
Baier M, Calonge N, Cutter G, McClatchey M, Schoentgen S, Hines S, Marcus A, Ahnen D: Validity of self-reported colorectal cancer screening behavior. Cancer Epidemiol Biomarkers Prev. 2000, 9: 229-232.
Khoja S, McGregor ES, Hilsden RJ: Validation of self-reported history of colorectal cancer screening. Can Fam Physician. 2007, 53: 1192-1197.
Rauscher GH, Johnson TP, Cho YL, Walk JA: Accuracy of self-reported cancer-screening histories: a meta-analysis. Cancer Epidemiol Biomarkers Prev. 2008, 17: 748-757. 10.1158/1055-9965.EPI-07-2629.
Partin MR, Grill J, Noorbaloochi S, Powell A, Burgess DJ, Vernon SW, Halek K, Griffin JM, van Ryn M, Fisher DA: Validation of self-reported colorectal cancer screening behaviour from a mixed-mode survey of veterans. Cancer Epidemiol Biomarkers Prev. 2008, 17: 768-776. 10.1158/1055-9965.EPI-07-0759.
Jones RM, Mongin SJ, Lazovich D, Church TR, Yeazel MW: Validity of four self-reported colorectal cancer screening modalities in a general population: differences over time and by intervention assignment. Cancer Epidemiol Biomarkers Prev. 2008, 17: 777-784. 10.1158/1055-9965.EPI-07-0441.
Ziogas A, Anton-Culver H: Validation of family history data in cancer family registries. Am J Prev Med. 2003, 24: 190-198. 10.1016/S0749-3797(02)00593-7.
Murff HJ, Spigel DR, Syngal S: Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history. JAMA. 2004, 292: 1480-1489. 10.1001/jama.292.12.1480.
Mitchell RJ, Brewster D, Campbell H, Porteous MEM, Wyllie AH, Bird CC, Dunlop G: Accuracy of family history of colorectal cancer. Gut. 2008, 53: 291-295.
Whittingham MJ, Stephens PA, Bradbury RB, Freckelton RP: Why do we still use stepwise modelling in ecology and behaviour?. J Anim Ecol. 2006, 75: 1182-1189. 10.1111/j.1365-2656.2006.01141.x.
Soledad Cepeda M, Boston R, Farrar JT, Strom BL: Comparison of logistic regression versus propensity score when the number of events is low and there a multiple confounders. Am Epidemiol. 2003, 158: 280-287. 10.1093/aje/kwg115.
Rutter C, Virgina F, Lachenbruch P: Bias in error rate estimates in discriminant analysis when stepwise variable selection is employed. Commun Stat Simulat. 1991, 20: 1-22. 10.1080/03610919108812935.
Derksen S, Keselman HJ: Backward, forward and stepwise automated subset selection algoritms: Frequency of obtaining authentic and noise variables. Brit J Math Stat Psy. 1992, 45: 265-282. 10.1111/j.2044-8317.1992.tb00992.x.
Mandel JS, Bond JH, Church TR, Snover DC, Bradley GM, Schuman LM, Ederer F: Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota colon cancer control study. N Engl J Med. 1993, 328: 1365-1371. 10.1056/NEJM199305133281901.
Kronborg O, Fenger C, Olsen J, Jorgensen OD, Sondergaard O: Randomised study of screening for colorectal cancer with faecal occult blood test. Lancet. 1996, 348: 1467-1471. 10.1016/S0140-6736(96)03430-7.
Cancer Council Australia: Cancer Council Australia pre-budget submission. 2011, http://www.cancer.org.au/policy/submissionstogovernment/Cancer_Council_Australia_pre-budget_submission_2011-2012.htm, –12. Bowel cancer screening: program expansion would reduce Medicare and PBS costs - and save lives,
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2458/13/248/prepub
The research on which this paper is based was conducted as part of the Hunter Community Study, The University of Newcastle. We are grateful to The University of Newcastle, the Hunter Medical Research Institute & Lions Club of Adamstown for funding and to the men and women of the Hunter region who provided the information recorded. We thank Roseanne Peel for her contribution to the development of the studied cohort; Stephen Hancock for design of the current study’s database; Tracey Watt for her assistance with data entry and the mail out/ reminder call process; and Daniel Barker and Michael Fitzgerald for their statistical support. Recognition and thanks to Australian Rotary Health Research Fund and the Rotary District 9650 Bowelscan Committee for their funding of PhD scholar - RJC.
The authors declare that there are no conflicts of interest.
RJC, CLP, RSF were responsible for study design, data collection, analysis and drafting. All authors contributed to the interpretation of results and writing of this manuscript. All authors read and approved the final manuscript.
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Additional file 2: Simple logistic regression analysis for socio-demographic, lifestyle, clinical and psychosocial characteristics associated with CRC testing/ screening outcomes.(DOC 120 KB)
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Courtney, R.J., Paul, C.L., Sanson-Fisher, R.W. et al. Individual- and provider-level factors associated with colorectal cancer screening in accordance with guideline recommendation: a community-level perspective across varying levels of risk. BMC Public Health 13, 248 (2013). https://doi.org/10.1186/1471-2458-13-248
- Faecal Occult Blood Test
- Private Health Insurance
- Colonoscopy Screening
- Faecal Occult Blood Test Screening
- National Bowel Cancer Screen Program