Open Access
CC BY-NC-ND 4.0 · Endosc Int Open 2025; 13: a24094916
DOI: 10.1055/a-2409-4916
Original article

Patient adherence to surveillance colonoscopy after endoscopic resection of colorectal polyps and factors associated with loss to follow-up

Authors

  • Aimen Farooq

    1   Gastroenterology, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • BahaAldeen Bani Fawwaz

    1   Gastroenterology, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • Arooj Mian

    2   Internal Medicine, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • Gurdeep Singh

    2   Internal Medicine, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • Yiyang Zhang

    3   Statistics, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • Peter Gerges

    2   Internal Medicine, AdventHealth Central Florida, Orlando, United States (Ringgold ID: RIN558924)
  • Kambiz Kadkhodayan

    4   Center for Interventional Endoscopy, AdventHealth Orlando, Orlando, United States (Ringgold ID: RIN440172)
  • Deepanshu Jain

    4   Center for Interventional Endoscopy, AdventHealth Orlando, Orlando, United States (Ringgold ID: RIN440172)
  • Natalie Cosgrove

    4   Center for Interventional Endoscopy, AdventHealth Orlando, Orlando, United States (Ringgold ID: RIN440172)
  • Mustafa A Arain

    4   Center for Interventional Endoscopy, AdventHealth Orlando, Orlando, United States (Ringgold ID: RIN440172)
  • Muhammad Khalid Hasan

    5   Center for Interventional Endoscopy, Florida Hospital Orlando, Orlando, United States (Ringgold ID: RIN6244)
  • Dennis Yang

    4   Center for Interventional Endoscopy, AdventHealth Orlando, Orlando, United States (Ringgold ID: RIN440172)
 

Abstract

Background and study aims

Post-polypectomy surveillance colonoscopy (SC) plays an integral role in efforts to reduce colorectal cancer risk, but its effectiveness is invariably dependent on patient compliance. This study aimed to evaluate patient adherence to SC after endoscopic resection (ER) of polyps ≥ 20 mm and identify potential barriers associated with loss to follow-up.

Patients and methods

This was a single-center retrospective study evaluating adherence to SC after ER of polyps ≥ 20 mm between April 2018 to December 2021. Adherence to SC was defined as the proportion of patients who underwent follow-up colonoscopy. Multivariate logistic regression was performed to identify factors associated with loss to follow-up.

Results

A total of 959 patients (mean age 67 years; 47.9% women) underwent endoscopic resection of colorectal polyps ≥ 20 mm (mean size 33.2 ± 13.7 mm). Nearly half of the patients (n = 478; 49.8%) were lost to follow-up. On multivariate analysis, factors associated with a higher likelihood of SC non-adherence were: lack of a primary care physician (odds ratio [OR] 1.7;95% confidence interval [CI] 1.3- 2.3; P < 0.05), American Society of Anesthesiologists grade 3 or 4 (OR 1.4; 95% CI 1.1–1.9; P < 0.05), residence > 60 miles from the endoscopy suite (OR 1.6; 95% CI 1.2–2.3; P = 0.02), being referred by a physician outside of our healthcare system (OR 1.4; 95% CI 1.1–1.8; P = 0.01), and lack of written follow-up recommendations on the colonoscopy report (OR 3.6; 95% CI 1.4–10.2; P = 0.01).

Conclusions

Nearly half of patients undergoing ER of colorectal polyps ≥ 20 mm are lost to follow-up. We identified several patient- and healthcare-related factors as barriers to SC adherence. Strategies to address these issues and targeting of high-risk populations are urgently needed to enhance SC programs.


10.1055/a-2401-0777

Introduction

10.1055/a-2401-0777

Colorectal cancer (CRC) is the third most common cancer in the United States [1]. Colonoscopy reduces CRC incidence and mortality by detection and resection of neoplastic polyps [2] [3]. Patients with polyps are at higher risk for metachronous advanced neoplasia as compared with those with no neoplasia detected on prior colonoscopy [4]. Given the increased risk for advanced neoplasia and CRC in these patients on follow-up, post-polypectomy surveillance colonoscopy (SC) plays an integral part in the effort to reduce CRC risk [4]. However, the effectiveness of SC as a tool is invariably dependent on patient compliance [5].

Patient non-adherence to screening colonoscopy has been well-documented, with rates ranging from 20% to 43% [6] [7]. Several studies document barriers to initial colonoscopy [8] [9], but even after the initial colonoscopy is performed, appropriate surveillance is often neglected with potential serious consequences [6] [10]. There is a paucity of data on patient adherence to SC [11] [12], specifically after endoscopic resection of large polyps ≥ 20 mm in size (about 0.79 in). This study aimed to evaluate patient adherence to SC and to identify potential barriers associated with loss to follow-up.


Patients and methods

Study population and data collection

The study was approved by the institutional review board (IRB) at AdventHealth, Orlando, Florida, United States. To be eligible for inclusion in this study, the prospectively maintained electronic endoscopy database (Provation, Minneapolis, Minnesota, United States) was retrospectively searched for all patients who had undergone colonoscopy between April 1, 2018 and April 22, 2022 at the Center for Interventional Endoscopy (CIE) at AdventHealth, Orlando, Florida, United States. Patients are scheduled for colonoscopy either by open access or following a consultation. Each colonoscopy report was then reviewed to identify those in which polyp resection had been performed as an index procedure at the CIE. Patients were excluded if they were undergoing colonoscopy for an indication other than CRC screening or polyp resection. Patients were also excluded from final analysis if their polyp histopathology showed invasive cancer because the follow-up interval and treatment plan in these patients differed from those with benign polyps or if they were instructed to undergo additional SC based on age/comorbidities. Baseline data included patient demographics, marital status, type of medical insurance, assignment of a primary care physician, distance of residence from the endoscopy unit, and whether the referring physician was part of our health care system (affiliated to AdventHealth Hospitals). Procedure data extracted from the colonoscopy and pathology reports included quality of bowel preparation, type of endoscopic resection, and polyp characteristics (number, location, size, histopathology).


Outcomes and definitions

The primary outcome was to evaluate patient non-adherence, defined as failure to attend SC appointment at the CIE at any point after their index procedure. Patients were considered adherent if they arrived at their scheduled appointment, regardless of whether the SC was then cancelled or incomplete. Factors associated with non-adherence (loss to follow-up) to SC were examined as a secondary outcome.


Statistical analysis

Continuous variables were compared using the Wilcoxon rank sum test. Categorical variables were compared using the Chi-square or Fisher’s exact test. Univariate logistic regression was used with respect to each covariate to identify variables significantly associated with the outcome, defined as those with P < 0.20. These variables were then included in a stepwise selection, multiple logistic regression analysis to identify those factors most significantly associated with the outcome, based on P < 0.05.



Results

The patient flow chart is shown in [Fig. 1]. A total of 4344 colonoscopies were performed at the CIE during the study period. Of these, 1327 patients underwent colonoscopy with endoscopic resection, of which 959 patients (mean age 67.0 years; 47.9% women) had polyps ≥ 20 mm in size and were included in the final analysis. Patient characteristics are summarized in [Table 1]. Most patients were of White race (796; 83.0%), American Society of Anesthesiologists (ASA) class I or II (665; 69.3%), married (633; 66%), and on either private insurance (427; 44.5%) or Medicare/Medicaid (439; 45.8%). Nearly two-thirds of the patients had an assigned primary care physician (PCP) (573; 59.7%) and approximately half were referred by a physician affiliated with our health care system (427; 44.5%). Most patient residences were located in a < 60-mile radius from the endoscopy unit (806; 84%).

Zoom
Fig. 1 Patient flow chart.

Table 1 Baseline characteristics.

Entire cohort
(n = 959)

ASA, American Society of Anesthesiologists; BMI, body mass index; IQR, interquartile range; PCP, primary care physician; SD, standard deviation.

Age; median (IQR), years

68 (61–74)

Female; n (%)

459 (47.9)

BMI, mean (SD); kg/m2

29.2 (10.8)

ASA grade; n (%)

  • I/II

665 (69.3)

  • III/IV

294 (30.7)

Race; n (%)

  • White

796 (83.0)

  • African American

58 (6.0)

  • Asian

12 (1.3)

  • Native American

3 (0.3)

  • Other

90 (9.4)

Marital status; n (%)

  • Single

127 (13.2)

  • Married

633 (66.0)

  • Divorced/widowed

199 (20.8)

Health insurance; n (%)

  • Non-insured

93 (9.7)

  • Commercial

427 (44.5)

  • Government

439 (45.8)

Primary care physician; n (%)

  • No PCP

386 (40.3)

  • Have PCP

573 (59.7)

Referring physician; n (%)

  • PCP

16 (1.7)

  • Gastroenterologist

891 (92.9)

  • Colorectal surgeon

34 (3.5)

  • Other

18 (1.9)

Distance of residence from endoscopy unit

  • ≤ 60-mile radius

806 (84.0)

  • > 60-mile radius

153 (16.0)

Procedure characteristics are shown in [Table 2]. Median polyp size and number of polyps removed were 30 mm (IQR: 25–50 mm) and 1.0 polyp (IQR: 1.0–3.0), respectively. In all, most polyps were in the right colon (proximal to the splenic flexure) (784; 81.8%) and more than two-thirds were categorized as either lateral spreading granular (406; 42.3%) or non-granular lesions (270; 28.8%). Most lesions were adenomas (774; 80.7%), followed by serrated adenomas (156; 16.3%) and hyperplastic polyps (29; 3.0%). Post-procedure bleeding or perforation were reported in 2.6% and 0.1% of the cases, respectively. All adverse events were managed endoscopically and/or with medical therapy.

Table 2 Procedure and polyp characteristics.

Entire cohort
(n = 959)

EMR, endoscopic mucosal resection; ESD, endoscopic submucosal dissection; HF, hepatic flexure; IQR, interquartile range; SD, standard deviation.

Procedure characteristics

Quality of bowel prep, n (%)

  • Poor/fair

442 (46.1)

  • Good/excellent

482 (50.3)

  • Not available

35 (3.6)

Technique; n (%)

  • EMR

946 (98.6)

  • ESD

13 (1.4)

Adverse event; n (%)

  • Bleeding

25 (78.1)

  • Perforation

1 (3.1)

  • Respiratory failure

2 (6.3)

  • Abdominal pain

3 (9.4)

  • Not available

1 (3.1)

Polyp characteristics

Polyps removed during colonoscopy, median (IQR)

1 (1–3)

Polyp size; median (IQR), mm

30 (25–40)

Polyp location, n (%)

  • Ileocecal valve

43 (4.5)

  • Cecum

209 (21.8)

  • Ascending colon

326 (33.9)

  • Transverse colon/HF

206 (21.5)

  • Descending colon

62 (6.5)

  • Sigmoid colon

74 (7.7)

  • Rectum

39 (4.1)

Morphology; n (%)

  • Sessile

381 (39.7)

  • Pedunculated

41 (4.3)

  • Flat

68 (7.1)

  • N/A

469 (48.9)

Lateral spreading; n (%)

  • Granular

406 (42.3)

  • Non-granular

270 (28.2)

  • Mixed

77 (8.0)

  • N/A

206 (21.5)

Histopathology, n (%)

  • Hyperplastic polyp

29 (3.0)

  • Tubular adenoma

411 (42.9)

  • Villous adenoma

22 (2.3)

  • Tubulovillous adenoma

341 (35.5)

  • Serrated adenoma

156 (16.3)

Surveillance colonoscopy and loss to follow-up

Of the 959 patients in this study, 481 (50.2%) underwent SC at a median of 6 months (IQR: 5–7 months); whereas 478 (49.8%) were lost to follow-up (did not have SC at CIE). Baseline and procedure characteristics between the two groups are available in the supplementary material. Factors associated with loss to follow-up are summarized in [Table 3].

Table 3 Univariate and multivariate analysis of factors associated with loss to follow-up colonoscopy after endoscopic resection of colorectal polyps.

Baseline characteristics

Univariate OR (95% CI)

Univariate P value

Multivariate OR (95% CI) for all P < 0.05

Multivariate P value

ASA, American Society of Anesthesiologists; CI, confidence interval; OR, odds ratio.

Age

1.01 (0.99–1.02)

0.12

1.01(0.99 – 1.02)

0.31

Female

1.26 (0.98–1.62)

0.07

1.21 (0.91- 1.60)

0.18

ASA class (III/IV vs I/II)

1.42 (1.07–1.87)

< 0.05

1.41 (1.045 – 1.90)

< 0.05

Marital Status (not married vs married)

1.27 (0.87–1.86)

0.22

1.24 (0.82 – 1.85)

0.31

Residence distance from endoscopy unit (> 60 miles vs ≤ 60 miles)

1.83 (1.27–2.66)

0.001

1.56 (1.05 – 2.32)

0.02

Lack of primary care physician (yes vs no)

1.88 (1.44–2.44)

< 0.0001

1.74 (1.31 – 2.31)

0.0001

Referring physician outside of our hospital system (yes vs no)

1.58 (1.22–2.04)

< 0.001

1.40 (1.06 – 1.84)

0.01

Lack of written surveillance recommendations on index colonoscopy report

4.34 (1.61–11.66)

0.003

3.64 (1.36 – 10.18)

0.01

The following variables were associated with a higher likelihood for loss to SC follow-up on univariate analysis: patient ASA grade 3 or 4 (odds ratio [OR] 1.41; 95% CI 1.05–1.90; P < 0.05), patients living > 60-mile radius away from the endoscopy suite (OR 1.6; 95% CI 1.05–2.32; P = 0.02), lack of PCP (OR 1.74; 95% CI 1.31–2.31; P = 0.0001), being referred by a physician outside of the health care system (OR 1.40; 95% CI 1.06–1.84; P < 0.0001), and those in whom written follow-up recommendations for SC interval were not available on index colonoscopy report (OR 3.64; 95% CI 1.36–10.18; P = 0.01). All these variables remained as independent factors associated with a higher likelihood of loss to follow-up to SC on multivariate analysis.



Discussion

Compared with the general population, patients who undergo endoscopic resection of neoplastic polyps are at an increased risk of metachronous neoplasia [1] [2]. Hence, surveillance colonoscopy (SC) is recommended to reduce risk of developing CRC [4]. In this study, we demonstrate that only half of patients (50.2%) who undergo endoscopic resection of polyps ≥ 20 mm in size were adherent to SC. We identified several factors independently associated with a higher likelihood for loss to follow-up.

Data on patient compliance with SC after polypectomy remain scarce. In this study, nearly half the patients (49.8%) did not undergo SC after endoscopic resection of colorectal polyps ≥ 20 mm in size. This is somewhat slightly higher than the non-adherence rate to colonoscopy reported in prior studies, ranging between 20% and 43% [13] [14] [15] [16]. Patients undergoing endoscopic resection of ≥ 20 mm colorectal polyps are recommended to have repeat colonoscopy at 6 months [4]. We speculate that the shorter interval between index procedure and SC may, in part, contribute to the high patient nonadherence rate. Many patients lack understanding of the purpose of screening colonoscopy and the need for follow-up, and often underestimate risk of colon cancer in the asymptomatic stage [17]. These issues may be further compounded by an open access setting, such as in our unit, in which patients can be scheduled without a prior clinic visit [14]. Potential strategies to improve adherence may include raising awareness and emphasizing the importance of SC at the time of the index procedure and preemptively scheduling repeat colonoscopy prior to discharge from the endoscopy unit. Furthermore, recent data suggest that extending the interval surveillance following piecemeal resection of large polyps may be safe and effective [18], which may also help ameliorate the lower compliance associated with shorter interval procedures [16]. Future studies aimed to enhance patient adherence are urgently needed because effectiveness of SC is foremost dependent on patient receptiveness.

This study identified several factors associated with nonadherence to SC. Insight into these factors is of paramount importance, because directed interventions may further help decrease the nonattendance rate. We classified factors affecting loss to follow-up into two main categories: patient-related factors and health care system-related factors.

Our results demonstrated that patients with more comorbidities (ASA grade 3 or higher) and those living farther away from the endoscopy unit were more likely to be lost to follow-up. Patients with higher ASA grade may have more restricted mobility and possibly more difficulty/intolerability of large-volume (polyethylene glycol) preparations, which may contribute to nonattendance [16]. Implementing a telephone call reminder at least 7 days prior to the procedure may help troubleshoot attendance issues and potentially identify patients who may not be able to attend due to either recent or present illness/hospitalization. Discussing barriers to bowel preparation at their index procedure may help identify potentially more acceptable bowel preparation alternatives for their repeat colonoscopy. Prior studies have that demonstrated long travel distance is a recurrent barrier to medical care, given the additional burden (time and cost of transportation) associated with these appointments [19] [20]. Alternatively, patients could be directed to their local health care providers for the SC. Nonetheless, it is imperative to implement a checking system in which completion of follow-up procedures can be confirmed. Developing and providing a transportation resource guide tailored to local settings has also been proposed as another strategy to assist those in under-resourced regions [19].

Healthcare-related factors may be more modifiable than patient-related factors [14] [16]. In this study, we identified lack of a PCP and of written instructions for follow-up on the colonoscopy report as two barriers to patient adherence to SC. It should be noted that these factors are not an indication of patient non-compliance, but rather, potentially modifiable factors that may contribute to non-adherence, simply due to lack of guidance for patients. Indeed, PCP engagement and support of patient care has been shown to be essential for effective health care delivery [21]. Several studies have demonstrated that PCP-led follow-up results in a significant increase in patient compliance [22] [23], irrespective of insurance status [24]. PCP recommendation has been shown to be one of the most common factors motivating patient decisions to proceed with testing, further underscoring the importance of the PCP [25]. In addition, our study also highlights that ensuring clear written instructions on the index colonoscopy report with regard to timing and need for SC is imperative. The report provides guidance to the PCP, referring physician, and patient regarding the recommendations and can also serve as a reminder on subsequent clinic visits. Furthermore, we also noted that patients who were referred by gastroenterologists within our healthcare system (AdventHealth) were more likely to undergo SC. Patients and referring physicians integrated into our center share the same electronic medical record (EMR) system, which facilitates reviewing reports, ordering, scheduling procedures, and communication between the different parties.

There are several strengths to this study. For one, there are many studies focused on physician adherence to post-polypectomy surveillance guidelines, but there are limited data on patient compliance with such recommendations. Furthermore, we included nearly 1000 patients in the final analysis, thereby providing one of the largest studies on this issue. We also specifically evaluated patient adherence after endoscopic resection of polyps ≥ 20 mm in size, thus excluding other patients with smaller polyps that may have introduced heterogeneity in the follow-up recommendations and data interpretation. Lastly, comprehensive review and acquisition of multiple data points was performed to identify patient- and systems-related barriers to patient nonadherence.

We also recognize the limitations of this study, including its retrospective design. Second, CIE is an open-access, tertiary care endoscopy unit. Although we routinely recommend that patients complete their first SC at CIE, it is possible that many patients may have elected to perform their repeat colonoscopy with their local provider. As such, we recognize that the definition for non-adherence in this context included all patients who did not follow-up at CIE, and may not necessarily equate with lack of compliance because many of them may have elected to follow up locally. Patients who may have completed these tests locally may not have been captured, leading to overestimation of the loss to follow-up rate. With this in mind, we performed a subgroup analysis (available in the supplementary material) including only patients whose referring gastroenterologists were within our health care system, to ensure that all colonoscopies after their index procedure at CIE would be available for review in the EMR. Among these 385 patients, the nonadherence rate was still high at 42.6%, which further validates the results for our entire cohort. Furthermore, multivariate analysis of factors associated with non-compliance with SC within this cohort showed that lack of a PCP remained a significant independent factor. This subgroup analysis further supports our overall findings and mitigates the possibility that our overall results were simply due to lack of follow-up data. Third, several patient-level factors were unavailable that would have been of interest because of their potential impact on adherence to surveillance recommendations (i.e., socioeconomic status and education). Fourth, the study period of 2018 to 2022 overlapped with the COVID-19 pandemic, which may have led to reduced healthcare utilization [26]. Nonetheless, our nonadherence rate was, to some extent, similar to those previously reported [27], thereby mitigating the potential impact of COVID-19 on our findings.


Conclusions

In summary, our study suggests high nonadherence to SC in patients undergoing endoscopic resection of polyps ≥ 20 mm in size. Several patient- and healthcare-related factors were identified as potential barriers to adherence to SC recommendations. Nonadherence negatively impacts health care resource utilization and patient-related outcomes. Strategies to address these issues and targeting high-risk vulnerable populations are urgently needed to enhance adherence to SC.



Conflict of Interest

D. Yang is a consultant for Olympus, Fujifilm, Apollo Endosurgery, Medtronic, and Microtech. D. Yang receives research support from Microtech and 3D-Matrix. M.K. Hasan is a consultant for Boston Scientific, Microtech, and Olympus. M. Arain is a consultant for Boston Scientific and Olympus. N. Cosgrove is a consultant for Boston Scientific and Olympus. All other authors have nothing to disclose.

Supplementary Material

  • References

  • 1 Siegel RL, Miller KD, Goding Sauer A. et al. Colorectal cancer statistics, 2020. CA Cancer J Clin 2020; 70: 145-164
  • 2 Zauber AG, Winawer SJ, O’Brien MJ. et al. Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med 2012; 366: 687-696
  • 3 Winawer SJ, Zauber AG, Ho MN. et al. Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med 1993; 329: 1977-1981
  • 4 Gupta S, Lieberman D, Anderson JC. et al. Recommendations for follow-up after colonoscopy and polypectomy: A consensus update by the US Multi-Society Task Force on Colorectal Cancer. Am J Gastroenterol 2020; 115: 415-434
  • 5 Saini SD, Schoenfeld P, Vijan S. et al. Surveillance colonoscopy is cost-effective for patients with adenomas who are at high risk of colorectal cancer. Gastroenterology 2010; 138: 2292-2299
  • 6 Greenspan M, Chehl N, Shawron K. et al. Patient Non-adherence and cancellations are higher for screening colonoscopy compared with surveillance colonoscopy. Dig Dis Sci 2015; 60: 2930-2936
  • 7 Rogers MC, Keswani RN. Adherence to screening colonoscopy: Can we get our recommendations to stick?. Dig Dis Sci 2015; 60: 2855-2856
  • 8 Stenwachs D, Allen JD, Barlow WE. et al. National Institutes of Health state-of-the science conference statement: enhancing use and quality of colorectal cancer screening. Ann Intern Med 2010; 152: 663-667
  • 9 Klabunde CN, Cronin KA, Breen N. et al. Trends in colorectal cancer test use among vulnerable populations in the United States. Cancer Epidemiol Biomarkers Prev 2011; 20: 1611-1621
  • 10 Leffler DA, Neeman N, Rabb JM. et al. An alerting system improves adherence to follow-up recommendations from colonoscopy examinations. Gastroenterology 2011; 140: 1166-1173
  • 11 Colquhoun P, Chen HC, Kim JI. et al. High compliance rates observed for follow-up colonoscopy post-polypectomy are achievable outside of clinical trials: efficacy of polypectomy is not reduced by low compliance for follow-up. Colorectal Dis 2004; 6: 158-161
  • 12 Siddiqui AA, Patel A, Huerta S. Determinants of compliance with colonoscopy in patients with adenomatous colon polyps in a veteran population. Aliment Pharmacol Ther 2006; 24: 1623-1630
  • 13 Turner BJ, Weiner M, Yang C. et al. Predicting adherence to colonoscopy or flexible sigmoidoscopy on the basis of physician appointment-keeping behavior. Ann Intern Med 2004; 140: 528-532
  • 14 Badurdeen DS, Umar NA, Begum R. et al. Timing of procedure and compliance with outpatient endoscopy among an underserved population in an inner-city tertiary institution. Ann Epidemiol 2012; 22: 531-535
  • 15 Kazarian ES, Carreira FS, Torbara NW. et al. Colonoscopy completion in large safety net health care system. Clin Gastroenterol Hepatol 2008; 6: 438-442
  • 16 Gurudu SR, Fry LC, Fleischer DE. et al. Factors contributing to patient nonadherence at open-access endoscopy. Dig Dis Sci 2006; 51: 1942-1945
  • 17 Honein-AbouHaidar GN, Kastner M, Vuong V. et al. Systematic review and meta-study synthesis of qualitative studies evaluating facilitators and barriers to participation in colorectal cancer screening. Cancer Epidemiol Biomarkers Prev 2016; 25: 907-917
  • 18 Perry N, Bhatte S, Ginsberg G. et al. Extended interval surveillance colonoscopy following piecemeal EMR is safe and effective. Gastrointest Endosc 2023; 97: AB460-AB461
  • 19 Lee KM, Hunleth J, Rolf L. et al. Distance and transportation barriers to colorectal cancer screening in a rural community. J Prim Care Community Health 2023; 14
  • 20 Josey MJ, Odahowski CL, Zahnd WE. et al. Disparities in utilization of medical specialists for colonoscopy. Health Equity 2019; 3: 464-471
  • 21 Triantafillidis JK, Vagianos C, Gikas A. et al. Screening for colorectal cancer: the role of the primary care physician. Eur J Gastroenterol Hepatol 2018; 29: e1-e7
  • 22 Cole SR, Young GP, Byrne D. et al. Participation in screening for colorectal cancer based on fecal occult blood test is improved by endorsement by the primary care practitioner. J Med Screen 2002; 9: 147-152
  • 23 Le V, Syed S, Vega KJ. et al. Patient prompting of their physician resulted in increased colon cancer screening referrals. World J Gastrointest Oncol 2014; 6: 257-262
  • 24 Emery JD, Shaw K, Williams B. et al. The role of primary care in early detection and follow-up cancer. Nat Rev Clin Oncol 2014; 11: 38-48
  • 25 Feeley TH, Cooper J, Foels T. et al. Efficacy expectations for colorectal cancer screening in primary care: identifying barriers and facilitators for patients and clinicians. Health Commun 2009; 24: 304-315
  • 26 Mason MC, Vedhanayagam K, Jernigan JA. Evaluating patient adherence to routine and symptom indicated colonoscopies during the COVID-19 pandemic. Cureus 2021; 13: e16711
  • 27 Stock C, Holleczek B, Hoffmeister M. et al. Adherence to physician recommendations for surveillance in opportunistic colorectal cancer screening: The necessity of organized surveillance. PLoS One 2013; 8: e82676

Correspondence

Dr. Dennis Yang
Center for Interventional Endoscopy, AdventHealth Orlando
601 East Rollins Street
32803 Orlando
United States   

Publication History

Received: 11 March 2024

Accepted after revision: 12 June 2024

Article published online:
29 January 2025

© 2025. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial-License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).

Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany

Bibliographical Record
Aimen Farooq, BahaAldeen Bani Fawwaz, Arooj Mian, Gurdeep Singh, Yiyang Zhang, Peter Gerges, Kambiz Kadkhodayan, Deepanshu Jain, Natalie Cosgrove, Mustafa A Arain, Muhammad Khalid Hasan, Dennis Yang. Patient adherence to surveillance colonoscopy after endoscopic resection of colorectal polyps and factors associated with loss to follow-up. Endosc Int Open 2025; 13: a24094916.
DOI: 10.1055/a-2409-4916
  • References

  • 1 Siegel RL, Miller KD, Goding Sauer A. et al. Colorectal cancer statistics, 2020. CA Cancer J Clin 2020; 70: 145-164
  • 2 Zauber AG, Winawer SJ, O’Brien MJ. et al. Colonoscopic polypectomy and long-term prevention of colorectal-cancer deaths. N Engl J Med 2012; 366: 687-696
  • 3 Winawer SJ, Zauber AG, Ho MN. et al. Prevention of colorectal cancer by colonoscopic polypectomy. The National Polyp Study Workgroup. N Engl J Med 1993; 329: 1977-1981
  • 4 Gupta S, Lieberman D, Anderson JC. et al. Recommendations for follow-up after colonoscopy and polypectomy: A consensus update by the US Multi-Society Task Force on Colorectal Cancer. Am J Gastroenterol 2020; 115: 415-434
  • 5 Saini SD, Schoenfeld P, Vijan S. et al. Surveillance colonoscopy is cost-effective for patients with adenomas who are at high risk of colorectal cancer. Gastroenterology 2010; 138: 2292-2299
  • 6 Greenspan M, Chehl N, Shawron K. et al. Patient Non-adherence and cancellations are higher for screening colonoscopy compared with surveillance colonoscopy. Dig Dis Sci 2015; 60: 2930-2936
  • 7 Rogers MC, Keswani RN. Adherence to screening colonoscopy: Can we get our recommendations to stick?. Dig Dis Sci 2015; 60: 2855-2856
  • 8 Stenwachs D, Allen JD, Barlow WE. et al. National Institutes of Health state-of-the science conference statement: enhancing use and quality of colorectal cancer screening. Ann Intern Med 2010; 152: 663-667
  • 9 Klabunde CN, Cronin KA, Breen N. et al. Trends in colorectal cancer test use among vulnerable populations in the United States. Cancer Epidemiol Biomarkers Prev 2011; 20: 1611-1621
  • 10 Leffler DA, Neeman N, Rabb JM. et al. An alerting system improves adherence to follow-up recommendations from colonoscopy examinations. Gastroenterology 2011; 140: 1166-1173
  • 11 Colquhoun P, Chen HC, Kim JI. et al. High compliance rates observed for follow-up colonoscopy post-polypectomy are achievable outside of clinical trials: efficacy of polypectomy is not reduced by low compliance for follow-up. Colorectal Dis 2004; 6: 158-161
  • 12 Siddiqui AA, Patel A, Huerta S. Determinants of compliance with colonoscopy in patients with adenomatous colon polyps in a veteran population. Aliment Pharmacol Ther 2006; 24: 1623-1630
  • 13 Turner BJ, Weiner M, Yang C. et al. Predicting adherence to colonoscopy or flexible sigmoidoscopy on the basis of physician appointment-keeping behavior. Ann Intern Med 2004; 140: 528-532
  • 14 Badurdeen DS, Umar NA, Begum R. et al. Timing of procedure and compliance with outpatient endoscopy among an underserved population in an inner-city tertiary institution. Ann Epidemiol 2012; 22: 531-535
  • 15 Kazarian ES, Carreira FS, Torbara NW. et al. Colonoscopy completion in large safety net health care system. Clin Gastroenterol Hepatol 2008; 6: 438-442
  • 16 Gurudu SR, Fry LC, Fleischer DE. et al. Factors contributing to patient nonadherence at open-access endoscopy. Dig Dis Sci 2006; 51: 1942-1945
  • 17 Honein-AbouHaidar GN, Kastner M, Vuong V. et al. Systematic review and meta-study synthesis of qualitative studies evaluating facilitators and barriers to participation in colorectal cancer screening. Cancer Epidemiol Biomarkers Prev 2016; 25: 907-917
  • 18 Perry N, Bhatte S, Ginsberg G. et al. Extended interval surveillance colonoscopy following piecemeal EMR is safe and effective. Gastrointest Endosc 2023; 97: AB460-AB461
  • 19 Lee KM, Hunleth J, Rolf L. et al. Distance and transportation barriers to colorectal cancer screening in a rural community. J Prim Care Community Health 2023; 14
  • 20 Josey MJ, Odahowski CL, Zahnd WE. et al. Disparities in utilization of medical specialists for colonoscopy. Health Equity 2019; 3: 464-471
  • 21 Triantafillidis JK, Vagianos C, Gikas A. et al. Screening for colorectal cancer: the role of the primary care physician. Eur J Gastroenterol Hepatol 2018; 29: e1-e7
  • 22 Cole SR, Young GP, Byrne D. et al. Participation in screening for colorectal cancer based on fecal occult blood test is improved by endorsement by the primary care practitioner. J Med Screen 2002; 9: 147-152
  • 23 Le V, Syed S, Vega KJ. et al. Patient prompting of their physician resulted in increased colon cancer screening referrals. World J Gastrointest Oncol 2014; 6: 257-262
  • 24 Emery JD, Shaw K, Williams B. et al. The role of primary care in early detection and follow-up cancer. Nat Rev Clin Oncol 2014; 11: 38-48
  • 25 Feeley TH, Cooper J, Foels T. et al. Efficacy expectations for colorectal cancer screening in primary care: identifying barriers and facilitators for patients and clinicians. Health Commun 2009; 24: 304-315
  • 26 Mason MC, Vedhanayagam K, Jernigan JA. Evaluating patient adherence to routine and symptom indicated colonoscopies during the COVID-19 pandemic. Cureus 2021; 13: e16711
  • 27 Stock C, Holleczek B, Hoffmeister M. et al. Adherence to physician recommendations for surveillance in opportunistic colorectal cancer screening: The necessity of organized surveillance. PLoS One 2013; 8: e82676

Zoom
Fig. 1 Patient flow chart.