Variations in Screening Quality in a Federal Colorectal Cancer Screening Program for the Uninsured

Marion R. Nadel, PhD, MPH¹; Janet Royalty, MS¹; Djenaba Joseph, MD, MPH¹; Tanner Rockwell, BA²; William Helsel, MS²; William Kammerer, BS²; Simone C. Gray, PhD¹; Jean A. Shapiro, PhD¹ (View author affiliations)

Suggested citation for this article: Nadel MR, Royalty J, Joseph D, Rockwell T, Helsel W, Kammerer W, et al. Variations in Screening Quality in a Federal Colorectal Cancer Screening Program for the Uninsured. Prev Chronic Dis 2019;16:180452. DOI: http://dx.doi.org/10.5888/pcd16.180452.

PEER REVIEWED

Abstract

Introduction

Screening can decrease colorectal cancer incidence and mortality and is recommended in clinical practice guidelines. Poor quality of colorectal cancer screening can negate the benefit of screening. The objective of this study was to assess the quality of screening services provided by the Centers for Disease Control and Prevention’s Colorectal Cancer Control Program from July 2009 through June 2015.

Methods

We collected data from the program’s 29 grantees, funded to provide colorectal cancer screening and diagnostic services to asymptomatic, low-income, and underinsured or uninsured adults aged 50 to 64. We collected data on the dates and results of all screening and diagnostic tests and, for colonoscopies, on whether the cecum was reached, whether bowel preparation was adequate, and endoscopists’ recommendations for the next test.

Results

Overall, 82.9% (range among grantees, 50.0%–97.2%) of positive FOBTs/FITs were followed up by colonoscopy; 95.2% of colonoscopies occurred within 180 days of the positive stool test. Cecal intubation rates ranged among grantees from 94.2% to 100%. Adenoma detection rates met recommended threshold levels for almost all grantees. Recommendations for rescreening and surveillance intervals deviated from guidelines in both directions. Of clients with normal colonoscopies, 85.3% (range, 37.7%–99.7%) were told to return in 10 years, as recommended in national guidelines. Of clients with advanced adenomas, 55.2% (range, 20.0%–84.6%) were told to return in 3 years as recommended, 25.4% (range, 3.8%–56.6%) in 5 or more years, and 18.6% (range, 0%–47.2%) in less than 3 years.

Conclusion

Although overall screening quality was good, it varied considerably. Ongoing monitoring to identify performance problems is essential for all colorectal cancer screening activities, so that efforts designed to improve performance can be targeted to individual clinicians.

Top

Introduction

Screening can decrease colorectal cancer (CRC) incidence and mortality and is recommended in clinical practice guidelines (1). However, only two-thirds of adults aged 50 to 75 were up-to-date with CRC screening in 2016, well below the target set by the National Colorectal Cancer Roundtable’s initiative,“80% by 2018” (2,3). Screening can be of little value, however, if performed poorly. Because of well-documented variability in the quality of screening implementation (4–7), efforts to assess and improve screening quality need to accompany efforts to increase screening uptake. Common implementation problems include failure to follow up positive stool tests with colonoscopy, wide variation in the ability of endoscopists to detect adenomas, and recommended rescreening or surveillance intervals that do not comply with national guidelines. Improved colonoscopy quality has become a priority of professional societies. Quality indicators were defined for routine monitoring in clinical practice, and colonoscopy registries were developed to facilitate the process (5,8). Payment to providers increasingly incorporates quality assessment (9). Monitoring quality can lead to targeted improvement activities.

In 2005, the Centers for Disease Control and Prevention (CDC) launched the Colorectal Cancer Screening Demonstration Program (CRCSDP) at 5 sites to assess the feasibility of providing CRC screening, diagnostic, and surveillance services to low-income persons (10). An assessment of screening quality in the CRCSDP showed the need for improvement in several areas, such as the follow-up of positive stool tests and recommendations for rescreening and surveillance intervals (11).

After the CRCSDP, CDC established the Colorectal Cancer Control Program (CRCCP) at 29 sites in the United States (12). The objective of this study was to assess the quality of services provided in this expanded program from July 2009 through June 2015.

Top

Methods

From 2009 to 2015, CDC provided CRCCP funding to grantees in 25 states and 4 tribal organizations for CRC screening, surveillance, and diagnostic services to asymptomatic, low-income, and underinsured or uninsured adults aged 50 to 64 (Figure 1). Details on the CRCCP are provided elsewhere (12). Our analyses consisted of data collected from 28 grantees, identified herein by randomly assigned numbers; we excluded 1 grantee from our analyses because a high percentage of its client records had missing information.

Figure 1.
Twenty-nine grantees in the Centers for Disease Control and Prevention’s Colorectal Cancer Control Program, 2009–2015. Shading indicates a grantee state. An asterisk indicates a tribal grantee. [A text version of this figure is also available.]

As part of the program, grantees were permitted to use any screening tests recommended by the US Preventive Services Task Force in 2008: colonoscopy, guaiac fecal occult blood tests (FOBT), fecal immunochemical tests (FIT), or flexible sigmoidoscopy (13). For each CRCCP client, grantees collected a standardized set of CRC clinical data elements (CCDEs): age, sex, personal history of colorectal polyps or cancer, self-report of any prior CRC screening before CRCCP enrollment (but not information on which tests they had), and family history of CRC. Each grantee defined its own criteria for increased risk based on available guidelines (14).

For each test, grantees recorded the date of the test, the reason for test (screening, surveillance, or diagnostic), and the results of the test. For each colonoscopy, the CCDEs specified whether the cecum was reached (the cecum marks the beginning of the large intestine and a complete examination is one in which the scope progresses all the way to the cecum), whether the endoscopist considered the bowel preparation adequate, whether a polypectomy was performed, the number of polyps found, the worst histology among all polyps removed, and the clinician’s recommendation for which test the client should have next and when. Because endoscopy reporting was not standardized, grantee staff members occasionally converted the terms found in reports to fit the categories specified in the CCDEs.

Data quality was monitored at multiple steps. Before biannual submission of data to CDC, grantees checked their data with editing software provided by CDC to identify invalid values, missing fields, and cross-field inconsistencies. The data were then checked by CDC, and standard quality reports were produced. Calls were held with grantees to resolve identified discrepancies and discuss problem areas.

We tabulated data from the CCDEs for the period July 2009 through June 2015 on tests received by clients who did not report having CRC symptoms. We considered clients to be at average risk of CRC if they did not report any personal history of CRC or adenomas and were not at increased risk because of reported family history. We classified a colonoscopy as complete if the cecum was reached, bowel preparation was adequate, polyps were completely removed, and the procedure was not terminated early. All other colonoscopies were classified as incomplete. Only complete colonoscopies were included in our analyses of rescreening and surveillance recommendations and of adenoma detection rates (ADRs).

Statistical analysis

We computed several quality indicators related to stool testing (completeness and timeliness of follow-up of positive tests) and to colonoscopy (cecal intubation rate, adequacy of bowel preparation quality, appropriateness of recommendations for rescreening and surveillance intervals after colonoscopy, and ADR). We compared our findings to targets established by CDC for the CRCCP and to targets established by various professional organizations (4,5,14–19).

We computed the ADR as the percentage of colonoscopies in which at least 1 adenoma was reported. An adenoma is a type of polyp that may be a precursor lesion to colorectal cancer. Because adenoma prevalence varies by age and sex, we computed sex-specific ADRs for clients aged 50 years or older to allow comparison with published rates. For ADRs and the clinician’s recommendation after colonoscopy, we limited our analysis to data on the first screening colonoscopy received by each client in the CRCCP. We limited our analysis of clinicians’ follow-up recommendations to average-risk clients. We computed the cecal intubation rate as the percentage of colonoscopies in which the cecum was reached.

We tabulated combined data on all 28 grantees. In addition, we tabulated data for each grantee separately; for these data, we tabulated data only for grantees with at least 30 data points. We computed ADRs only for grantees that had at least 30 clients in the categories sex and reason for test. Although the reliability of rates based on small numbers may be low and may not accurately measure performance, we chose to calculate grantee-specific data based on a low cutoff so that we could present data from as many grantees as possible. Rates based on small numbers should be interpreted cautiously.

For all analyses, we used SAS version 9.4 (TS1M5) (SAS Institute Inc).

Top

Results

Some grantees provided colonoscopy as the primary screening test, some provided stool tests (FOBT or FIT), and others used both types of test (Table 1). For tests used for screening, the ratio of stool tests to endoscopy was approximately 3:2.

Stool tests

Positivity rate

Of the 24,983 FITs completed by clients at 21 grantees, 8.7% were positive. Among the 18 grantees with at least 30 tests, positivity rates ranged from 0% to 25.1% (Figure 2A). Of the 13,157 FOBTs completed by clients at 12 grantees, 7.4% were positive. Among the 7 grantees with at least 30 tests, positivity rates ranged from 0.7% to 13.0% (Figure 2B).

Figure 2.
Positivity rates for FITs and FOBTs among clients aged ≥50, by grantee, Colorectal Cancer Control Program, 2009–2015. N’s indicate number of tests. A, FIT positivity rates. Only the 18 grantees that recorded ≥30 FITs are shown individually. “All grantees” refers to all grantees, including grantees that had <30 tests. B, FOBT positivity rates. Only the 7 grantees that recorded ≥30 FOBTs are shown individually. “All grantees” refers to all grantees, including the grantees that had <30 tests. Tests for which results were not known were excluded from these analyses. Abbreviations: FIT, fecal immunochemical test; FOBT, fecal occult blood test. [A tabular version of this figure is also available.]

The low positivity rate at grantee no. 3 for FIT and grantee no. 16 for FOBT cannot be explained by frequent rescreening of the same clients. These low rates persisted when we included only first stool tests in the CRCCP and excluded clients who reported screening before the program. The high FIT positivity rate at grantee no. 27 cannot be explained by a high proportion of clients with positive family or personal history of CRC. When these clients were excluded, the FIT positivity rate was nearly unchanged.

Completeness and timeliness of follow-up of positive tests

Overall, 82.9% (range by grantee, 50.0%–97.2%) of the 3,197 positive FOBT/FITs were followed up by diagnostic colonoscopy in the CRCCP; 1 in 6 (17.1%) were not followed up (range, 2.8%–50.0%) (Table 2). Of the 2,649 tests with follow-up, 79.8% had colonoscopy within 90 days of the positive stool test, just below the 80% quality indicator established for the CRCCP, and 15.4% had colonoscopy between 91 and 180 days; 95.2% of colonoscopies occurred within 180 days of the positive stool test. Our 80% quality indicator was not met at 5 of the 16 grantees with ≥30 positive tests.

Only grantee no. 7 provided sigmoidoscopy as the primary screening test to more than 10 clients. Of 492 sigmoidoscopies at this grantee, 96 (19.5%) were positive; of these, 76 (79.2%) were followed by colonoscopy, 63 (82.9%) of them within 90 days.

Colonoscopy

Of the 27,612 colonoscopies performed in asymptomatic clients, the cecum was reached in 98.2%. The grantee-specific cecal intubation rate ranged from 94.2% to 100%, and was above 95% at all but 1 grantee. Bowel preparation quality was adequate in 97.9% of exams. The percentage of adequate preparation ranged from 93.0% to 99.6%.

Rescreening and surveillance recommendations after colonoscopy

A total of 20,928 average-risk clients had complete first colonoscopies in the CRCCP, either for primary screening or to follow up positive FOBTs or FITs. We excluded 853 of 20,928 (4.1%) clients because data on their screening outcome or recommended interval to the next test were incomplete.

Clients with a normal examination. Of 20,075 average-risk clients, 11,192 (55.8%) had a normal outcome (ie, no polyps were found). Of these, 9,542 (85.3%) were told to return in 10 years for another colonoscopy (range among grantees, 37.7%–99.7%) as recommended in national guidelines (15), and another 9.2% (range among grantees, 0.3%–50.4%) were told to return in 5 years (Table 3, Appendix, Table A). A total of 242 (2.2%) of clients with a normal outcome were told to return for a test other than colonoscopy, usually an FOBT or FIT. At the 2 grantees with at least 30 clients who were told to have a stool test, 83% or more were told to have the test in 1 year, earlier than recommended.

Clients with hyperplastic or other nonadenomatous polyps. Of the 3,019 clients whose colonoscopies found only hyperplastic or other nonadenomatous polyps, 65.0% (range among grantees, 18.8%–96.0%) were told to return in 10 years for colonoscopy as recommended in national guidelines (15), 22.4% (range among grantees, 3.4%–51.9%) were told to return in 5 years, and 7.1% (range among grantees, 0%–29.0%) in 3 years or less (Table 3, Appendix, Table B). At the 1 grantee with at least 30 clients who were told to return for a stool test, all were told to have the stool test in 1 year.

Clients with 1 or 2 small tubular adenomas. Of the 2,989 clients who had only 1 or 2 small tubular adenomas, 4.3% (range among grantees, 0%–49.4%) were told to return in 10 years, and 74.1% (range among grantees, 32.1%–100%) in 5 years, both consistent with national guidelines that patients return in 5 to 10 years (15). A total of 20.4% (range among grantees, 0%–66.0%) were told to return in 3 years or less (Table 3, Appendix, Table C).

Clients with advanced adenomas. Of the 2,516 clients with advanced adenomas (3–10 adenomas, ≥1 adenoma ≥1 cm, or ≥1 adenoma with villous histology or high-grade dysplasia), 55.2% (range among grantees, 20.0%–84.6%) were told to return in 3 years as recommended in national guidelines (15), 24.8% (range among grantees, 3.8%–53.3%) in 5 years, and 15.3% (range among grantees, 0%–34.7%) within a year (Table 3, Appendix, Table D).

Adenoma detection rate

Overall, the ADR for average-risk clients who had colonoscopy as their primary screening test was 36.0% (range among grantees, 19.3%–54.5%) for men and 25.7% (range among grantees, 11.7%–43.3%) for women (Table 4). The ADR results were similar after excluding clients who reported prior screening.

The numbers of clients with positive family history who had screening colonoscopy and the numbers who had diagnostic colonoscopy after positive stool tests were small at most grantees, especially for men. Overall, the ADRs for screening colonoscopy for clients with family history of CRC were 42.2% for men and 30.1% for women. The ADRs for clients with diagnostic colonoscopy after positive stool tests or sigmoidoscopy were 47.9% for men and 35.6% for women.

Top

Discussion

Most of the quality indicators examined in our study were met at most grantees. Follow-up of positive stool tests took place within a reasonable amount of time for most grantees. Cecal intubation rates and bowel preparation quality were high at all grantees. Almost all grantees met recommended thresholds for ADRs (18). However, we found considerable variation in quality indicators, and some grantees fell short of desired levels for certain indicators.

Stool test positivity rates were higher or lower than expected at a few grantees. Positivity rates depend on population characteristics, including screening history, and test characteristics, including threshold values for positivity. Although only extra-sensitive FOBTs were used in the CRCCP, various FITs were used. Positivity rates should be monitored, and unusually high or low rates and changes in rates over time should be investigated to rule out problems with test kits or processing and to identify any need to improve client instructions.

Stool tests are effective only when patients with positive findings are followed up with colonoscopy. In the CRCCP, 82.9% of positive results were followed up with colonoscopy, below the 90% quality indicator originally set for the CRCCP but exceeding the 80% target recently set as a quality metric by the US Multi-Society Task Force (USMSTF) (19) and exceeding rates reported in many settings (20–22). Some of the apparent lack of follow-up might be due to follow-up outside the CRCCP.

Follow-up of positive stool tests with colonoscopy is known to be challenging. A recent systematic review of interventions to improve follow-up found that patient navigators and provider reminders or performance data may help improve follow-up rates (22).

Follow-up of positive stool tests occurred within a reasonable amount of time for most grantees. Of those with follow-up in the CRCCP, 79.8% had colonoscopy within 90 days of the positive stool test (just below the 80% quality indicator established for the CRCCP) and 15.4% had colonoscopy 91 to 180 days after a positive stool test. The United States has no consensus guidelines for the time interval between a positive stool test and follow-up colonoscopy. A recent large study of a community-based setting found no significant increase in risk of CRC or advanced-stage disease associated with colonoscopy follow-up within 10 months of a positive FIT compared with 8 to 30 days (23). Although disease progression may be slow in most people, a short target interval may heighten patients’ sense of urgency to follow up positive screening tests and reduce loss-to-follow-up due to patients moving or changing providers.

For colonoscopy, the specialty societies have proposed quality indicators for use in continuous quality improvement programs (4,5,18). To guide these efforts, the American Society for Gastrointestinal Endoscopy/American College of Gastroenterology Task Force on Quality in Endoscopy recommended a subset of 3 high-priority indicators: 1) ADR in asymptomatic average-risk persons (screening), 2) frequency of colonoscopies following recommended surveillance and rescreening intervals, and 3) cecal intubation rate with photodocumentation (5).

The cecal intubation rate was high for all grantees. The recommended performance target is 90% or more cecal intubation with photodocumentation for all examinations and 95% or more for screening examinations (5). In the CRCCP, the cecal intubation rate was more than 95% for all but 1 grantee, where the rate was 94.2%. We did not collect information on photodocumentation.

The ADR is generally considered the most important quality measure for colonoscopy. Its validity as a quality indicator was first demonstrated in a study of the Polish national colonoscopy screening program, in which ADRs were inversely related to the risk of interval CRC after screening colonoscopy (24). A larger study at Kaiser Permanente showed a dose-dependent inverse association between ADR and the risks of all-stage, advanced-stage, and fatal interval CRC (25). Recently, a prospective study of Poland’s national program found that improvement in ADR, achieved by a comprehensive quality assurance program, translated into reduced risks of interval cancer and CRC death after screening colonoscopy (26).

In 2006, the USMSTF recommended that ADRs in first-time screening examinations for people aged 50 or older should be at least 25% for men and 15% for women (18). In the CRCCP, these thresholds were met at all but 1 grantee for men and all but 2 grantees for women. In 2014, the USMSTF raised these targets to 30% for men and 20% for women (5). Five grantees had ADRs below the new target of 30% for men, and 2 grantees had ADRs below the new target of 20% for women.

Efforts to increase ADRs have met with mixed success (27). Some factors that may improve ADR include split-dose preparation, and provider education on flat and depressed lesions and on withdrawal technique and public reporting of ADR (5,28). Several studies have demonstrated improvement in ADR through regular feedback and monitoring (29).

We found deviations from recommended rescreening and surveillance intervals in both directions, as has been documented in other settings (11,30). For example, for clients with a normal colonoscopy, 1 in 10 were recommended to receive the next colonoscopy in 5 years or less. For clients with advanced adenomas, 1 in 4 were told to return in 5 or more years. Surveillance that occurs too frequently provides little or no benefit while exposing patients to the risk of complications, increasing costs, and wasting resources that could instead be used for primary screening. Waiting too long increases risk of disease progression to a point where treatment may be less effective.

Some clients were told to have a test other than colonoscopy, usually a stool test, as their next test. At a few grantees, most of these clients were told to return in 1 year for the stool test. Clients who have a negative colonoscopy may have a stool test as their next screening test, but it should be after a 10-year interval. Because the risk of advanced adenomas within a few years after negative findings is low, interval testing is discouraged (15).

In the CRCCP, endoscopists used their usual report formats and terminology, and site staff had to assign bowel preparation quality (adequate vs inadequate) based on the descriptors in the endoscopy report. Some of the recommendations to return sooner than indicated in the guidelines might reflect endoscopists’ concern that bowel preparation was suboptimal although classified as adequate in our database.

For hyperplastic polyps, the 10-year recommendation is for polyps 1 cm or less in the rectum or sigmoid colon. Hyperplastic polyps proximal to the sigmoid may warrant earlier return (17). Because we did not collect information about polyp location, we could not determine whether some of the recommendations for 5-year intervals were appropriate.

The quality measures discussed here were intended to measure the performance of individual endoscopists. However, we were able to look only at aggregated measures of performance at the grantee level. Poor performance by a clinician can be masked when data from large numbers of clinicians are combined. Variability among endoscopists is undoubtedly greater than variability among grantees. Screening programs and endoscopy practices should monitor performance at the level of the endoscopist so that improvement activities can be targeted to poor performers.

Under the Medicare Access and CHIP Reauthorization Act of 2015 (31), the Centers for Medicare & Medicaid Services (CMS) is required to implement a quality payment incentive program to reward value and outcomes (9). Clinicians, including those performing colonoscopy, may receive an increase or decrease in payments based on whether or not they participate in quality assessment. CMS is also moving toward public reporting of performance information to help consumers make informed choices about the health care they receive through Medicare.

Colonoscopy registries have been developed to facilitate monitoring. The GI Quality Improvement Consortium, a collaboration of the American Society for Gastrointestinal Endoscopy and American College of Gastroenterology, is a quality benchmarking registry for gastroenterology practices; it has more than 7.5 million colonoscopy cases as of January 2019 (8). Members submit data and receive reports that include the measures discussed here.

Even with the availability of funding, support services, and oversight provided by the federal screening program, CRCCP, we identified gaps in performance. Our findings reinforce the need for quality monitoring and improvement. Efforts to improve uptake that also monitor screening performance could achieve better patient outcomes. Enhanced education and feedback to providers on rescreening and surveillance guidelines may be needed in addition to expanded enrollment protocols to ensure that clients understand follow-up procedures.

Top

Acknowledgments

No financial support was received for this work. No copyrighted material was used. The findings and conclusions in this report are those of the authors and do not necessarily represent the official position of the Centers for Disease Control and Prevention.

Top

Author Information

Corresponding Author: Marion Nadel, PhD, MPH, Division of Cancer Prevention and Control, Centers for Disease Control and Prevention, 4770 Buford Hwy, Mailstop S107-4, Chamblee, GA 30341. Telephone: 770-488-4772. Email: mrn1@cdc.gov.

Author Affiliations: ¹Division of Cancer Prevention and Control, Centers for Disease Control and Prevention, Atlanta, Georgia. ²Information Management Services Inc, Calverton, Maryland.

Top

References

1. Bibbins-Domingo K, Grossman DC, Curry SJ, Davidson KW, Epling JW Jr, García FAR, et al. Screening for colorectal cancer: US Preventive Services Task Force recommendation statement. JAMA 2016;315(23):2564–75. CrossRef PubMed
2. Centers for Disease Control and Prevention, National Center for Chronic Disease Prevention and Health Promotion, Division of Population Health. BRFSS prevalence & trends data. 2015. https://www.cdc.gov/brfss/brfssprevalence. Accessed on April 10, 2019.
3. National Colorectal Cancer Roundtable. Working toward the shared goal of 80% screened for colorectal cancer by 2018. http://nccrt.org/tools/80-percent-by-2018/. Accessed on April 10, 2019.
4. Rex DK, Bond JH, Winawer S, Levin TR, Burt RW, Johnson DA, et al. Quality in the technical performance of colonoscopy and the continuous quality improvement process for colonoscopy: recommendations of the U.S. Multi-Society Task Force on Colorectal Cancer. Am J Gastroenterol 2002;97(6):1296–308. CrossRef PubMed
5. Rex DK, Schoenfeld PS, Cohen J, Pike IM, Adler DG, Fennerty MB, et al. Quality indicators for colonoscopy. Gastrointest Endosc 2015;81(1):31–53. CrossRef PubMed
6. Nadel MR, Berkowitz Z, Klabunde CN, Smith RA, Coughlin SS, White MC. Fecal occult blood testing beliefs and practices of U.S. primary care physicians: serious deviations from evidence-based recommendations. J Gen Intern Med 2010;25(8):833–9. CrossRef PubMed
7. Klabunde CN, Lanier D, Nadel MR, McLeod C, Yuan G, Vernon SW. Colorectal cancer screening by primary care physicians: recommendations and practices, 2006–2007. Am J Prev Med 2009;37(1):8–16. CrossRef PubMed
8. GI Quality Improvement Consortium. http://giquic.gi.org. Accessed March 25, 2019.
9. Centers for Medicare & Medicaid Services. CMS quality payment program. https://www.cms.gov/Medicare/Quality-Payment-Program/Quality-Payment-Program.html. Accessed August 14, 2018.
10. Seeff LC, Royalty J, Helsel WE, Kammerer WG, Boehm JE, Dwyer DM, et al. Clinical outcomes from the CDC’s Colorectal Cancer Screening Demonstration Program. Cancer 2013;119(Suppl 15):2820–33. CrossRef PubMed
11. Nadel MR, Royalty J, Shapiro JA, Joseph D, Seeff LC, Lane DS et al. Assessing screening quality in the CDC’s Colorectal Cancer Screening Demonstration Program. Cancer 2013;119(Suppl 15):2834–41.
12. Joseph DA, DeGroff AS, Hayes NS, Wong FL, Plescia M. The Colorectal Cancer Control Program: partnering to increase population level screening. Gastrointest Endosc 2011;73(3):429–34. CrossRef PubMed
13. US Preventive Services Task Force. Screening for colorectal cancer: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med 2008;149(9):627–37. CrossRef PubMed
14. Levin B, Lieberman DA, McFarland B, Smith RA, Brooks D, Andrews KS, 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. CrossRef PubMed
15. 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. CrossRef PubMed
16. Kahi CJ, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, Kaltenbach T, et al. Colonoscopy surveillance after colorectal cancer resection: recommendations of the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2016;150(3):758–768.e11. CrossRef PubMed
17. Rex DK, Ahnen DJ, Baron JA, Batts KP, Burke CA, Burt RW, et al. Serrated lesions of the colorectum: review and recommendations from an expert panel. Am J Gastroenterol 2012;107(9):1315–29, quiz 1314, 1330. CrossRef PubMed
18. Rex DK, Petrini JL, Baron TH, Chak A, Cohen J, Deal SE, et al. Quality indicators for colonoscopy. Am J Gastroenterol 2006;101(4):873–85. CrossRef PubMed
19. Robertson DJ, Lee JK, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, et al. Recommendations on fecal immunochemical testing to screen for colorectal neoplasia: a consensus statement by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2017;152(5):1217–37. PubMed
20. Chubak J, Garcia MP, Burnett-Hartman AN, Zheng Y, Corley DA, Halm EA, et al. Time to colonoscopy after positive fecal blood test in four U.S. health care systems. Cancer Epidemiol Biomarkers Prev 2016;25(2):344–50. CrossRef PubMed
21. Jimbo M, Myers RE, Meyer B, Hyslop T, Cocroft J, Turner BJ, et al. Reasons patients with a positive fecal occult blood test result do not undergo complete diagnostic evaluation. Ann Fam Med 2009;7(1):11–6. CrossRef PubMed
22. Selby K, Baumgartner C, Levin TR, Doubeni CA, Zauber AG, Schottinger J, et al. Interventions to improve follow-up of positive results on fecal blood tests: a systematic review. Ann Intern Med 2017;167(8):565–75. CrossRef PubMed
23. Corley DA, Jensen CD, Quinn VP, Doubeni CA, Zauber AG, Lee JK, et al. Association between time to colonoscopy after a positive fecal test result and risk of colorectal cancer and cancer stage at diagnosis. JAMA 2017;317(16):1631–41. CrossRef PubMed
24. Kaminski MF, Regula J, Kraszewska E, Polkowski M, Wojciechowska U, Didkowska J, et al. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med 2010;362(19):1795–803. CrossRef PubMed
25. Corley DA, Jensen CD, Marks AR, Zhao WK, Lee JK, Doubeni CA, et al. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med 2014;370(14):1298–306. CrossRef PubMed
26. Kaminski MF, Wieszczy P, Rupinski M, Wojciechowska U, Didkowska J, Kraszewska E, et al. Increased rate of adenoma detection associates with reduced risk of colorectal cancer and death. Gastroenterology 2017;153(1):98–105. CrossRef PubMed
27. Corley DA, Jensen CD, Marks AR. Can we improve adenoma detection rates? A systematic review of intervention studies. Gastrointest Endosc 2011;74(3):656–65. CrossRef PubMed
28. Abdul-Baki H, Schoen RE, Dean K, Rose S, Leffler DA, Kuganeswaran E, et al. Public reporting of colonoscopy quality is associated with an increase in endoscopist adenoma detection rate. Gastrointest Endosc 2015;82(4):676–82. CrossRef PubMed
29. Umar SB, Ramirez FC. The proof is in the pudding: improving adenoma detection rates reduces interval colon cancer development. Transl Gastroenterol Hepatol 2017;2(12):99. CrossRef PubMed
30. Schoen RE, Pinsky PF, Weissfeld JL, Yokochi LA, Reding DJ, Hayes RB, et al. Utilization of surveillance colonoscopy in community practice. Gastroenterology 2010;138(1):73–81. CrossRef PubMed
31. Medicare Access and CHIP Reauthorization Act of 2015. HR 2, Pub L. No. 114–10.

Top

Tables

Abbreviations: FIT, fecal immunochemical test; FOBT, guaiac fecal occult blood test.
^a The Centers for Disease Control and Prevention provided Colorectal Cancer Control Program funding to grantees in 25 states and 4 tribal organizations for colorectal cancer screening, surveillance, and diagnostic services for underinsured or uninsured asymptomatic, low-income adults aged 50–64. One grantee was excluded from analysis because of missing data.
^b Grantees identified by randomly assigned numbers.

^a The Centers for Disease Control and Prevention provided Colorectal Cancer Control Program funding to grantees in 25 states and 4 tribal organizations for colorectal cancer screening, surveillance, and diagnostic services for underinsured or uninsured asymptomatic, low-income adults aged 50–64. One grantee was excluded from analysis because of missing data. Table shows data only for grantees (16 of 28) that had a total number of at least 30 positive tests (fecal occult blood tests or fecal immunochemical tests) during the program.
^b Grantees identified by randomly assigned numbers.
^c Percentages based on total N in row.
^d Percentages based on the number of clients that had colonoscopy follow-up. Percentages may not sum to 100% because of rounding.
^e Includes grantees that had fewer than 30 positive fecal occult blood tests or fecal immunochemical tests during the program.

^a The Centers for Disease Control and Prevention provided Colorectal Cancer Control Program funding to grantees in 25 states and 4 tribal organizations for colorectal cancer screening, diagnostic, and surveillance services for underinsured or uninsured asymptomatic, low-income adults aged 50–64. One grantee was excluded from analysis because of missing data. Includes clients at average risk who underwent an initial complete colonoscopy as a primary screening test or to follow up a positive stool test. A total of 853 clients were excluded because of incomplete data on screening outcome or recommended interval to the next test.
^b Intervals that adhere to national guidelines (15,16).
^c Recommended surveillance interval for small (<1 cm) hyperplastic polyps in the rectum or sigmoid. Hyperplastic polyps proximal to the sigmoid may require earlier follow up (17).
^d Recommended follow-up interval for serrated polyps depends on the location, size, number and histology of polyps (15,17).
^e Advanced adenoma category includes findings of 3–10 adenomas of any size, ≥1 adenoma ≥1 cm, or ≥1 adenoma with villous histology or high-grade dysplasia.

Abbreviations: —, grantee had fewer than 30 clients in category; ADR, adenoma detection rate; CRC, colorectal cancer; FOBT, fecal occult blood test; FIT, fecal immunochemical test.
^a Defined as the percentage of clients with ≥1 adenoma detected.
^b The Centers for Disease Control and Prevention provided Colorectal Cancer Control Program funding to grantees in 25 states and 4 tribal organizations for colorectal cancer screening, surveillance, and diagnostic services for underinsured or uninsured asymptomatic, low-income adults aged 50–64. One grantee was excluded from analysis because of missing data. Data are shown only for grantees that had at least 30 clients in the categories for sex and reason for test. Includes data on only the first colonoscopy obtained by each client in the program.
^c Grantees identified by randomly assigned numbers.

Top

Top

Appendix: Supplemental Tables A–D

^a Grantee-specific data are displayed only for those grantees with at least 30 clients with this screening outcome. For some grantees, percentages do not add to 100% because recommendations for >3 year to <5 year intervals are not displayed because there were so few.

^a Grantee-specific data are displayed only for those grantees with ≥30 clients with this screening outcome. For some grantees, percentages do not add to 100% because recommendations for >3 year to <5 year intervals are not displayed because there were so few.

^a Grantee-specific data are displayed only for those grantees with ≥30 clients with this screening outcome. For some grantees, percentages do not add to 100% because recommendations for >3 year to <5 year intervals, >5 year to <10 year intervals, and other test recommended are not displayed because there were so few.

^a Advanced adenoma includes findings of 3–10 adenomas of any size, ≥1 adenoma ≥1 cm, or ≥1 adenoma with villous features or high grade dysplasia.
^b Grantee-specific data are displayed for those grantees with ≥30 clients with this screening outcome. For some grantees, percentages do not add to 100% because recommendations for >3 year to <5 year intervals, >5 year intervals, and other test recommended are not displayed because there were so few.

Top