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. 2017 Dec 18;2017:6710931. doi: 10.1155/2017/6710931

Proximal Sessile Serrated Adenomas Are More Prevalent in Caucasians, and Gastroenterologists Are Better Than Nongastroenterologists at Their Detection

Malav P Parikh 1, Sujit Muthukuru 1, Yash Jobanputra 1, Kushal Naha 2, Niyati M Gupta 1, Vaibhav Wadhwa 1, Rocio Lopez 3, Prashanthi N Thota 1, Madhusudhan R Sanaka 1,
PMCID: PMC5748307  PMID: 29403530

Abstract

Background and Aim

Proximal sessile serrated adenomas (PSSA) leading to colorectal cancer (CRC) represent an alternate pathway for CRC development. In this study, we aim to determine the prevalence of PSSAs and the impact of patient, colonoscopy, and endoscopist-related factors on PSSA detection.

Methods

Patients ≥ 50 years of age undergoing a screening colonoscopy between 2012 and 2014 were included. Detection rates based on patient gender, race, colonoscopy timing, fellow participation, bowel preparation quality, and specialty of the endoscopist were calculated. t-tests were used to compare detection rates and a multivariate-adjusted analysis was performed.

Results

140 PSSAs were detected from 4151 colonoscopies, with a prevalence of 3.4%. Detection rate was higher in Caucasians compared to African-Americans (AA) (3.7 ± 4.1 versus 0.96 ± 3.5; p < 0.001). Gastroenterologists detected more PSSAs compared to nongastroenterologists (3.9 ± 3.5 versus 2.2 ± 3.0; p = 0.028). These findings were still significant after adjusted multivariate analysis. The rest of the factors did not make significant difference in PSSA detection rate.

Conclusions

PSSAs are more prevalent in Caucasians compared to AAs. Racial difference in prevalence of PSSAs is intriguing and warrants further investigation. Gastroenterologists have a significantly higher PSSADR compared to nongastroenterologists. Educational measures should be implemented in nongastroenterologists to improve their PSSA detection rates.

1. Introduction

In recent times, the serrated adenoma-neoplasia pathway has emerged as an alternative mechanism to the conventional adenoma-carcinoma pathway for the development of colorectal cancer (CRC) [16]. This alternate pathway can account for almost 15–20% of the incident CRCs and majority of the interval cancers after a screening colonoscopy [7, 8]. These tumors have a high frequency of BRAF mutations, microsatellite instability, and hypermethylation of genes [911]. Serrated lesions are often difficult to detect during a screening colonoscopy as they are flat or sessile, have an indiscriminate edge, may be covered by a mucous cap, and are located mostly in the proximal colon [12, 13].

Originally, all the serrated lesions were believed to be hyperplastic polyps (HP) with no malignant potential; however, now, it has been identified that few subtypes of serrated lesions do harbor malignant potential [36, 14]. According to the world health organization (WHO), serrated lesions are classified into (1) hyperplastic polyps; (2) sessile serrated adenomas (SSA) with or without dysplasia; and (3) traditional serrated adenomas (TSA) [15]. HPs are essentially benign. TSAs have malignant potential; however, they are uncommon. Hence, SSAs, which are located mostly in the proximal colon, appear to be the principal precursor lesions leading to CRC via the alternate pathway. It has been shown that serrated polyp detection rate is dependent on the endoscopist, experience of the pathologist, and colonoscopy withdrawal times [13, 16, 17]. However, there is only limited data on the impact of patient-related factors such as gender and race or endoscopy-related factors such as quality of bowel preparation, timing of the procedure, fellow participation, or specialty of the endoscopist, on the proximal sessile serrated adenoma detection rate (PSSADR) [18, 19]. The aim of this study was to determine the prevalence of proximal SSAs (PSSA) in an average risk screening population and the effect of various patient and endoscopy-related factors on PSSADR.

2. Materials and Methods

This is a retrospective chart review study performed at the Cleveland Clinic Foundation, Cleveland, OH, USA. Patients aged 50 years and older with average risk factors for CRC who underwent a complete screening colonoscopy between January 1, 2012 and December 31, 2014 were included in the study. Institutional review board at the Cleveland Clinic Foundation approved the study. Demographic details including patient age, gender, and race were collected. Endoscopy and pathology reports from all included colonoscopies were reviewed. A screening examination was defined, as a colonoscopy for which there was no surveillance or diagnostic indication. The proximal colon was defined as inclusive of the cecum, ascending colon, transverse colon, and splenic flexure. Distal to this was defined as distal colon. Adenoma detection rate (ADR) was defined as the proportion of screening colonoscopies in which at least one histologically confirmed colorectal adenoma was detected. Proximal serrated polyp detection rate (PSPDR) was defined as the proportion of colonoscopies in which at least one proximal serrated polyp (inclusive of HP, SSA, and TSA) was detected. PSSADR was defined as the proportion of screening colonoscopies in which at least one PSSA was detected. Overall (proximal + distal) sessile serrated adenoma detection rate (SSADR) was defined as the proportion of screening colonoscopies in which at least one SSA was detected. PSSADR according to patient gender and race, timing of colonoscopy, quality of bowel preparation, fellow participation, and endoscopist specialty were calculated. Overall ADR, SSADR, and PSPDR were also calculated.

Timing of the procedure was defined as morning (before 12 : 00 pm) or afternoon (after 12 : 00 pm) based on the procedure start time. Quality of bowel preparation was determined as per the Aronchick scale (excellent, good, adequate, inadequate, or poor). Patients with inadequate and poor bowel preparation were excluded from the analysis. Participation of a trainee fellow along with the attending physician during the procedure was noted. Colonoscopy was performed by gastroenterologists, general surgeons (GS), colorectal surgeons (CS), and one primary care physician (PCP). GS and CS were grouped together as nongastroenterologists. Colonoscopy performed by the PCP was not included in the study due to a very small number (n = 1). Individual endoscopists with less than 10 procedures each were also excluded. All the cases were reviewed by one of the 15 subspecialty gastroenterology pathologists. Educational interventions are regularly implemented to improve serrated polyp detection and standardize classification to minimize any variation in PSSADR due to pathology interpretation. All the screening colonoscopies were performed in an academic medical setting.

2.1. Statistical Analysis

Data are presented as mean ± standard deviation, median (25th, 75th percentiles) or frequency (percent). All endoscopist-level data was calculated from patient-level data. Paired t-tests were used to compare PSSADR by patient gender, race, presence of fellow, and timing of the procedure. Linear mixed models were used to compare detection rates among patients with excellent, good, and adequate preparation; a random effect was modeled to account for endoscopist. Also, detection rates were compared between physician specialty using t-tests.

A multinomial regression analysis was performed to check for the association between dependent and independent variables. All analyses were done using SAS (version 9.4, The SAS Institute, Cary, NC), and a p < 0.05 was considered statistically significant.

3. Results

A total of 4151 patients underwent screening colonoscopy over the study period. Average patient age was 60.0 ± 7.7 years, 53.2% (n = 2207) patients were females and Caucasians comprised 80.3% (n = 3334) of the entire cohort (Table 1). A total of 84 endoscopists performed the colonoscopies, with an average of 49.41 (22–65) procedures per endoscopist. 54 endoscopists (63.5%) were gastroenterologists, and 30 (36.5%) were nongastroenterologists. Fellows participated in 8.8% (n = 367) of the procedures. Majority of the colonoscopies were performed in the morning (70.3%). As per the Aronchick bowel preparation scale, majority of the colonoscopies were classified as having good quality bowel preparation (64.4%; n = 2675) (Table 2). A total of 140 PSSA were detected among the 4151 screening colonoscopies with a prevalence of 3.4% and a mean PSSADR of 0.04 ± 0.25 per patient. Overall and gender-specific ADR, PSPDR, PSSADR, and SSADR are shown in Table 3.

Table 1.

Patient characteristics.

Factor Overall
Number of patients 4151
Patient age (years) 60.0 ± 7.7
Patient gender
Female 2207(53.2)
Male 1944(46.8)
Race
Caucasian 3334(80.3)
African-American 631(15.2)
Other 186(4.5)

Table 2.

Colonoscopy details.

Factor Overall
Number of endoscopists 84
Number of procedures/endoscopist 49.41 (22.0, 65.0)
Specialty of the endoscopist
Gastroenterology 54(63.5)
General surgery 9(10.6)
Colorectal surgery 21(24.7)
Fellow participation 367(8.8)
Timing of colonoscopy
Morning 2920(70.3)
Afternoon 1231(29.7)
Bowel preparation quality
Excellent 652(15.7)
Good 2675(64.4)
Adequate 824 (19.9)

Table 3.

Overall and gender-specific ADR, PSPDR, PSSADR, and SSADR.

Factor Overall Males Females
ADR 26.4 ± 11.0 32.7 ± 14.7 22.0 ± 12.7
PSPDR 6.1 ± 5.5 7.0 ± 7.8 5.5 ± 6.6
PSSADR 3.3 ± 3.4 3.9 ± 5.4 2.8 ± 4.1
SSADR (proximal + distal) 4.3 ± 3.9 5.2 ± 6.8 3.7 ± 4.7

ADR: adenoma detection rate; PSPDR: proximal serrated polyp detection rate; PSSADR: proximal sessile serrated adenoma detection rate; SSADR: sessile serrated adenoma detection rate.

Overall PSSADR was significantly higher in Caucasians as compared to African-Americans (AA) (3.7 ± 4.1 versus 0.96 ± 3.5; p < 0.001). This was seen in both males (4.2 ± 6.3 versus 1.10 ± 5.0; p = 0.003) and females (3.4 ± 5.1 versus 0.88 ± 3.3; p < 0.001). Patient gender, timing of the procedure, quality of the bowel preparation, and fellow participation had no effect on PSSADR. Gastroenterologists were more likely to detect PSSA compared to nongastroenterologists (3.9 ± 3.5 versus 2.2 ± 3.0; p = 0.028) (Table 4). ADR was also significantly higher for gastroenterologist as compared to the surgeons (28.8 ± 10.5 versus 22.1 ± 10.8; p = 0.007) (Table 5). When assessing the detection rates for general surgeons versus colorectal surgeons, a trend towards higher ADR, PSPDR, PSSADR, and SSADR was noted for colorectal surgeons as compared to general surgeons; however, this was statistically not significant (Table 6). Data should be interpreted carefully as there were fewer general surgeons (n = 9) in the study as compared to colorectal surgeons (n = 21). A multinomial regression analysis was performed to check for the association between dependent and independent variables. Caucasian race and gastroenterologists performing the colonoscopy were associated with increased PSSADR even after adjusting for all the independent variables, and this was statically significant (Caucasians versus AAs: p = 0.003 and gastroenterologist versus nongastroenterologists: p = 0.001).

Table 4.

Proximal sessile serrated adenoma detection rate (PSSADR) based on patient gender, timing of the procedure, quality of the bowel preparation, and fellow participation.

Factor PSSADR p value
Race
Caucasians (overall) (n = 3334) 3.7 ± 4.1 <0.001
African-Americans (overall) (n = 631) 0.96 ± 3.5
Caucasian males 4.2 ± 6.3 0.003
African-American males 1.10 ± 5.0
Caucasian females 3.4 ± 5.1 <0.001
African-American females 0.88 ± 3.3
Gender
Males (n = 1944) 3.9 ± 5.4 0.12
Females (n = 2207) 2.8 ± 4.1
Procedure time
Morning (n = 2920) 3.2 ± 4.8 0.71
Afternoon (n = 1231) 3.0 ± 5.5
Quality of bowel preparation
Excellent (n = 652) 3.2 ± 13.8 0.92
Good (n = 2675) 3.7 ± 5.4
Adequate (n = 824) 3.1 ± 10.1
Fellow participation
Fellow present (n = 367) 2.4 ± 13.4 0.49
Fellow absent (n = 3784) 3.5 ± 3.8
Endoscopist specialty
Gastroenterologist (n = 64) 3.9 ± 3.5 0.028
Nongastroenterologist (n = 30) 2.2 ± 3.0

Table 5.

Adenoma detection rate for gastroenterologists and surgeons.

Factor Gastroenterologist (n = 54) Surgeon (n = 30) p value
Overall 28.8 ± 10.5 22.1 ± 10.8 0.007
Males 35.2 ± 14.7 28.2 ± 14.2 0.037
Females 24.2 ± 12.4 17.8 ± 12.7 0.027

Table 6.

Detection rates for general surgeons and colorectal surgeons.

Factor General surgeon (n = 9) Colorectal surgeon (n = 21) p value
ADR 19.8 ± 8.7 23.1 ± 11.7 0.46
PSPDR 2.1 ± 2.2 5.8 ± 5.5 0.060
PSSADR 1.2 ± 2.1 2.6 ± 3.3 0.23
SSADR 1.2 ± 2.1 3.8 ± 4.0 0.072

ADR: Adenoma detection rate; PSPDR: proximal serrated polyp detection rate; PSSADR: proximal sessile serrated adenoma detection rate; SSADR: sessile serrated adenoma detection rate.

4. Discussion

CRC is the second leading cause of cancer-related deaths in the US and the third most common cancer in both men and women. A total of 51,651 deaths were reported due to CRC in 2014 in the US [20]. Traditionally linked only to the adenoma-carcinoma sequence, it is now well known that CRC can also arise from an “alternate,” serrated neoplasia pathway, SSA being the chief precursor lesion [16]. We specifically studied a cohort of 4151 average risk patient population undergoing screening colonoscopy that is representative of the general US population, enabling us to identify important patient- and endoscopy-related factors that affect PSSADR.

In average risk screening patients, the reported SSA prevalence ranges from 2% to 7% [1, 21]. Other investigators have studied PSPDR, and it is reported to range from 1% to 22% [13, 16, 22]. In our study, the prevalence for PSSA was 3.4% and PSPDR was 6.2% (inclusive of HPs, SSAs, and TSAs). Patient gender was not associated with significant differences in the PSSADR. These findings are similar to prior studies [1].

4.1. Race and PSSADR

According to the 2015 US census bureau [23], racial composition of the US population was 77.1% Caucasians and 13.3% AAs. Our study population was similar and largely reflective of this racial distribution, where Caucasians were 80.3% and AAs were 15.2%. In our study, after adjusting for all the independent variables, PSSADR was significantly higher in Caucasians compared to AAs (p = 0.003). This was true for both Caucasian males and females. PSPDR (inclusive of HPs, SSAs, and TSAs) was also higher in Caucasians compared to AA, similar to prior studies [24]. Wallace et al., in a study of uninsured and low-income population showed similar results, where Caucasians were noted to have a higher prevalence of SSAs and any serrated polyps compared to AAs [25]. A study comparing the prevalence of SSAs in Caucasian and Chinese populations also found that SSAs were more common in Caucasians than Chinese (7% versus 2%; p = 0.001) [21]. This would imply that “serrated pathway” might be largely responsible for incident and interval CRC in Caucasians compared to other race or ethnic groups [21, 25, 26].

Adenomas developing within different carcinogenic pathways (e.g., conventional or serrated) may evolve into invasive carcinomas with differing prognostic features. MSI-H sporadic cancers evolve from the precursor lesions of the serrated pathway [15], which is observed to be more common in whites than blacks. In accordance with this, a population-based study comparing MSI-H cancer by race has shown whites to have a higher prevalence of MSI-H cancers as compared to blacks [27].

On the contrary, studies have reported a more proximal distribution of adenomas in AAs than whites [2730]. Also, AAs are at a higher risk (OR 1.15; 1.03–1.29) for detection of large proximal polyps as compared to whites [31]. Further, a large study evaluated the relationship of race and the location of CRC and found that AAs were significantly more likely than Whites to develop proximal CRC [32]. Given the rarity of serrated polyps in AAs, serrated pathway does not seem to contribute significantly towards the occurrence of proximal CRC in AAs and it is possibly related to adenoma-carcinoma pathway.

4.2. Timing of Colonoscopy and PSSADR

A study by Sanaka et al. showed that adenoma detection (ADR) rates were significantly higher for colonoscopies performed in the morning as compared to in the afternoon [33]. Similarly, in a study by Chan et al, more polyps were detected in patients receiving colonoscopies early in the morning and adenoma detection rate reduced as the day progressed [33, 34]. Operator fatigue is proposed as a probable reason for reduced colonoscopy efficiency in the afternoon. On the contrary, a study, which included more than 100,000 screening colonoscopies in fact, found that afternoon procedures were 1.14 times more likely to detect advanced lesions as compared to the morning colonoscopies [35]. There is paucity of studies that assessed the impact of colonoscopy timing on detection of serrated lesions. In our study, PSSADR did not differ significantly between morning and afternoon procedures [36]. Hetzel et al. noted similar results in a study, where SSA detection was not associated with the hour of the endoscopy [1].

4.3. Quality of Bowel Preparation and PSSADR

Detection of conventional adenomas seems clearly linked to better quality bowel preparation.

A meta-analysis showed that ADR did not decrease between high and intermediate quality bowel preparation; however, it was significantly reduced with low-quality bowel preparation [37]. PSSAs are more difficult to detect during a colonoscopy, as they are sessile, mostly proximal in location, and have subtle endoscopic features [15, 16, 37]. Hence, it can be reasonably hypothesized that better quality of bowel preparation should yield higher PSSADR.

Interestingly, our study shows that PSSADR, in fact, did not change significantly with excellent, good, or adequate bowel preparation. SSAs have not just one but several characteristic endoscopic features that aid in their detection. On high resolution while “light endoscopy,” “mucous cap,” “indistinct borders,” and a “cloud-like surface” are the features, which have been validated to assist the endoscopists in the detection of SSAs [38, 39] it can be postulated that some of these features are probably more prominent when the quality of bowel preparation is excellent allowing detection of PSSAs. On the contrary, less than optimal bowel preparation may leave a rim of stool around these flat lesions or the mucous cap accompanying the lesions may appear thicker and endoscopically more prominent permitting identification of SSAs. Our results are consistent with two prior studies, in which quality of the bowel preparation had no impact on serrated polyp detection rate [13, 40]. A limitation of these studies was the documentation of PSPDR and not PSSADR specifically.

A recent study by Clark et al. showed results, which are contrasting from our findings. It showed that any quality of bowel preparation less than high quality (excellent/good quality) was associated with a significant decrease in PSSADR. However, it has limited generalizability as the study population consisted of male veterans and colonoscopies were performed by endoscopists with relatively high ADRs than in general clinical practice. That study included both screening and surveillance colonoscopies, in contrast to our study which included only average risk screening colonoscopies. It also did not permit differentiation between good and excellent quality preparations as both these groups were studied together as a high-quality group.

4.4. Fellow Participation

It has been shown in previous studies that fellow participation is associated with improved ADR [41] and small adenoma (<5 mm) detection rates [42]. A stepwise increase in ADR was also noted across the years of gastroenterology fellowship training [43, 44]. As compared to adenomas, sessile serrated polyps are particularly challenging to detect due to their subtle features and proximal location [12, 13]. Currently, there are no reported studies, which have assessed the effect of fellow participation on the PSSADR. Our study showed that overall PSSADR was not significantly different with or without fellow participation.

4.5. Endoscopist Specialty and PSSADR

There is a definitive gap in the literature about PSSADR when nongastroenterologists perform colonoscopies [19]. Our study shows that gastroenterologists have a significantly higher PSSADR as compared to nongastroenterologists. Development of CRC by serrated pathway is a relatively newer concept and it is likely that surgeons may not be up to date with the current SSA literature, its identifying features, clinical implications of its detection, complete retrieval, and appropriate surveillance measures. Literature review shows conflicting results when comparing the quality of a colonoscopy between a gastroenterologists and surgeons [4549]. However, none of these studies have systematically compared PSSADR between these two groups of endoscopists. We recommend that educational measures should be implemented to improve the PSSADR in surgeons, which might help in reducing the occurrence of CRC via serrated pathway.

5. Limitations

Some limitations of our study are due to its retrospective nature with potential for incomplete data entry and unmeasured bias. It is known that serrated polyp detection rate varies significantly among endoscopists [1]; however, our study included eighty-four endoscopists from different specialties and we did not calculate PSSADR individually for each endoscopist. Also, we did not take colonoscopy withdrawal time into account, as these were not available. Studies have documented higher PSPDR with longer withdrawal time; however, there are no reported studies showing an association between withdrawal time and PSSADR specifically. Split dose bowel preparation was associated with increased sessile serrated polyp detection rates as compared to single-dose preparation [50]. We could not account for these findings in our study, as information about the method and agents used for bowel preparation was not available. Fellow participation and level of fellowship training are shown to be associated with improved ADRs [41, 44]. In terms of serrated lesions, we showed that fellow participation did not make a significant difference in PSSADR; however, current level of fellowship training was not taken into consideration. This association has not been studied before, and future research should be directed to address this important question.

6. Conclusion

According to our study results, PSSADR is significantly higher in Caucasians compared to AAs. Hence, it can be reasonably concluded that serrated pathway leading to CRC might play a far greater role in Caucasians than in AAs. Future research should be directed at identifying risk factors associated with this finding. Gastroenterologist outperformed surgeons in terms of PSSADR. Detection of serrated adenomas might be associated with a significant learning curve, and educational measures should be implemented in surgeons to improve their detection rates.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this article.

References

  • 1.Hetzel J. T., Huang C. S., Coukos J. A., et al. Variation in the detection of serrated polyps in an average risk colorectal cancer screening cohort. The American Journal of Gastroenterology. 2010;105(12):2656–2664. doi: 10.1038/ajg.2010.315. [DOI] [PubMed] [Google Scholar]
  • 2.Fearon E. R., Vogelstein B. A genetic model for colorectal tumorigenesis. Cell. 1990;61(5):759–767. doi: 10.1016/0092-8674(90)90186-I. [DOI] [PubMed] [Google Scholar]
  • 3.Leggett B., Whitehall V. Role of the serrated pathway in colorectal cancer pathogenesis. Gastroenterology. 2010;138(6):2088–2100. doi: 10.1053/j.gastro.2009.12.066. [DOI] [PubMed] [Google Scholar]
  • 4.O'Brien M. J. Hyperplastic and serrated polyps of the colorectum. Gastroenterology Clinics of North America. 2007;36(4):947–968. doi: 10.1016/j.gtc.2007.08.007. [DOI] [PubMed] [Google Scholar]
  • 5.Torlakovic E., Snover D. C. Serrated adenomatous polyposis in humans. Gastroenterology. 1996;110(3):748–755. doi: 10.1053/gast.1996.v110.pm8608884. [DOI] [PubMed] [Google Scholar]
  • 6.Huang C. S., O'Brien M. J., Yang S., Farraye F. A. Hyperplastic polyps, serrated adenomas, and the serrated polyp neoplasia pathway. The American Journal of Gastroenterology. 2004;99(11):2242–2255. doi: 10.1111/j.1572-0241.2004.40131.x. [DOI] [PubMed] [Google Scholar]
  • 7.Goldstein N. S. Serrated pathway and APC (conventional)-type colorectal polyps: molecular-morphologic correlations, genetic pathways, and implications for classification. American Journal of Clinical Pathology. 2006;125(1):146–153. doi: 10.1309/87BD0C6UCGUG236J. [DOI] [PubMed] [Google Scholar]
  • 8.Arain M. A., Sawhney M., Sheikh S., et al. CIMP status of interval colon cancers: another piece to the puzzle. The American Journal of Gastroenterology. 2009;105(5):1189–1195. doi: 10.1038/ajg.2009.699. [DOI] [PubMed] [Google Scholar]
  • 9.Spring K. J., Zhao Z. Z., Karamatic R., et al. High prevalence of sessile serrated adenomas with BRAF mutations: a prospective study of patients undergoing colonoscopy. Gastroenterology. 2006;131(5):1400–1407. doi: 10.1053/j.gastro.2006.08.038. [DOI] [PubMed] [Google Scholar]
  • 10.Weisenberger D. J., Siegmund K. D., Campan M., et al. CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer. Nature Genetics. 2006;38(7):787–793. doi: 10.1038/ng1834. [DOI] [PubMed] [Google Scholar]
  • 11.Kambara T., Simms L. A., Whitehall V. L., et al. BRAF mutation is associated with DNA methylation in serrated polyps and cancers of the colorectum. Gut. 2004;53(8):1137–1144. doi: 10.1136/gut.2003.037671. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Snover D. C., Jass J. R., Fenoglio-Preiser C., Batts K. P. Serrated polyps of the large intestine: a morphologic and molecular review of an evolving concept. American Journal of Clinical Pathology. 2005;124(3):380–391. doi: 10.1309/V2EPTPLJRB3FGHJL. [DOI] [PubMed] [Google Scholar]
  • 13.de Wijkerslooth T. R., Stoop E. M., Bossuyt P. M., et al. Differences in proximal serrated polyp detection among endoscopists are associated with variability in withdrawal time. Gastrointestinal Endoscopy. 2013;77(4):617–623. doi: 10.1016/j.gie.2012.10.018. [DOI] [PubMed] [Google Scholar]
  • 14.Rex D. K., Ahnen D. J., Baron J. A., et al. Serrated lesions of the colorectum: review and recommendations from an expert panel. The American Journal of Gastroenterology. 2012;107(9):1315–1329. doi: 10.1038/ajg.2012.161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Snover D., Ahnen D. J., Burt R. W., Odze R. D. Serrated polyps of the colon and rectum and serrated (“hyperplastic”) polyposis. In: Bozman F. T., Carneiro F., Hruban R. H., et al., editors. WHO Classification of Tumours Pathology and Genetics Tumours of the digestive system. 4th. Berlin: Springer-Verlag; 2010. [Google Scholar]
  • 16.Kahi C. J., Hewett D. G., Norton D. L., Eckert G. J., Rex D. K. Prevalence and variable detection of proximal colon serrated polyps during screening colonoscopy. Clinical Gastroenterology and Hepatology. 2011;9(1):42–46. doi: 10.1016/j.cgh.2010.09.013. [DOI] [PubMed] [Google Scholar]
  • 17.Abdeljawad K., Vemulapalli K. C., Kahi C. J., Cummings O. W., Snover D. C., Rex D. K. Sessile serrated polyp prevalence determined by a colonoscopist with a high lesion detection rate and an experienced pathologist. Gastrointestinal Endoscopy. 2015;81(3):517–524. doi: 10.1016/j.gie.2014.04.064. [DOI] [PubMed] [Google Scholar]
  • 18.Gurudu S. R., Heigh R. I., de Petris G., et al. Sessile serrated adenomas: demographic, endoscopic and pathological characteristics. World Journal of Gastroenterology. 2010;16(27):3402–3405. doi: 10.3748/wjg.v16.i27.3402. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Sanaka M. R., Gohel T., Podugu A., et al. Adenoma and sessile serrated polyp detection rates: variation by patient sex and colonic segment but not specialty of the endoscopist. Diseases of the Colon & Rectum. 2014;57(9):1113–1119. doi: 10.1097/DCR.0000000000000183. [DOI] [PubMed] [Google Scholar]
  • 20.U.S. Cancer Statistics Working Group. United States Cancer Statistics: 1999–2014 Incidence and Mortality Web-based Report. Atlanta (GA): Department of Health and Human Services, Centers for Disease Control and Prevention, and National Cancer Institute; 2017. http://www.cdc.gov/uscs. [Google Scholar]
  • 21.Kumbhari V., Behary J., Hui J. M. Prevalence of adenomas and sessile serrated adenomas in Chinese compared with Caucasians. Journal of Gastroenterology and Hepatology. 2013;28(4):608–612. doi: 10.1111/jgh.12100. [DOI] [PubMed] [Google Scholar]
  • 22.Kahi C. J., Li X., Eckert G. J., Rex D. K. High colonoscopic prevalence of proximal colon serrated polyps in average-risk men and women. Gastrointestinal Endoscopy. 2012;75(3):515–520. doi: 10.1016/j.gie.2011.08.021. [DOI] [PubMed] [Google Scholar]
  • 23.US Census Bureau. 2015. May 2017, https://www.census.gov/quickfacts/fact/table/US/PST045216.
  • 24.Parikh M. P., Wadhwa V., Jobanputra Y., Naha K., Thota P. N., Sanaka M. R. Tu1024 high-risk adenoma detection rate: varies by race and fellow participation but not by timing of colonoscopy. Gastrointestinal Endoscopy. 2017;85(5, article AB538) doi: 10.1016/j.gie.2017.03.1254. [DOI] [Google Scholar]
  • 25.Wallace K., Brandt H. M., Bearden J. D., et al. Race and prevalence of large bowel polyps among the low-income and uninsured in South Carolina. Digestive Diseases and Sciences. 2016;61(1):265–272. doi: 10.1007/s10620-015-3862-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Pietrak S. J., Kang M., Patel D., Colangelo T., Ahmad A. S. Su1668 risk factors for the development of sessile serrated adenomas in a predominantly African-American, female, obese inner city population. Gastrointestinal Endoscopy. 2017;85(5, article AB388) doi: 10.1016/j.gie.2017.03.897. [DOI] [Google Scholar]
  • 27.Carethers J. M., Murali B., Yang B., et al. Influence of race on microsatellite instability and CD8+ T cell infiltration in colon cancer. PLoS One. 2014;9(6, article e100461) doi: 10.1371/journal.pone.0100461. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Corley D. A., Jensen C. D., Marks A. R., et al. Variation of adenoma prevalence by age, sex, race, and colon location in a large population: implications for screening and quality programs. Clinical Gastroenterology and Hepatology. 2013;11(2):172–180. doi: 10.1016/j.cgh.2012.09.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Cordice J. W., Jr., Johnson H., Jr. Anatomic distribution of colonic cancers in middle-class black Americans. Journal of the National Medical Association. 1991;83(8):730–732. [PMC free article] [PubMed] [Google Scholar]
  • 30.Chu K. C., Tarone R. E., Chow W. H., Alexander G. A. Colorectal cancer trends by race and anatomic subsites, 1975–1991. Archives of Family Medicine. 1995;4(10):849–856. doi: 10.1001/archfami.4.10.849. [DOI] [PubMed] [Google Scholar]
  • 31.Lieberman D. A., Williams J. L., Holub J. L., et al. Race, ethnicity, and sex affect risk for polyps greater than 9 mm in average-risk individuals. Gastroenterology. 2014;147(2):351–358. doi: 10.1053/j.gastro.2014.04.037. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Rex D. K., Khan A. M., Shah P., Newton J., Cummings O. W. Screening colonoscopy in asymptomatic average-risk African Americans. Gastrointestinal Endoscopy. 2000;51(5):524–527. doi: 10.1016/S0016-5107(00)70283-5. [DOI] [PubMed] [Google Scholar]
  • 33.Sanaka M. R., Deepinder F., Thota P. N., Lopez R., Burke C. A. Adenomas are detected more often in morning than in afternoon colonoscopy. The American Journal of Gastroenterology. 2009;104(7):1659–1664. doi: 10.1038/ajg.2009.249. [DOI] [PubMed] [Google Scholar]
  • 34.Chan M. Y., Cohen H., Spiegel B. M. R. Fewer polyps detected by colonoscopy as the day progresses at a veteran’s administration teaching hospital. Clinical Gastroenterology and Hepatology. 2009;7(11):1217–1223. doi: 10.1016/j.cgh.2009.07.013. [DOI] [PubMed] [Google Scholar]
  • 35.Diamond S., Hoda K. M., Holub J. L., Lieberman D. A., Eisen G. M. 392 does the time of day predict the yield for significant neoplasia on screening colonoscopy? Gastroenterology. 2010;138(5):S-57–S-58. doi: 10.1016/S0016-5085(10)60260-0. [DOI] [Google Scholar]
  • 36.Parikh M. P., Jobanputra Y., Naha K., Wadhwa V., Thota P. N., Sanaka M. R. Mo1130 impact of race, timing of colonoscopy and fellow participation on sessile serrated adenoma detection rate (SSADR) Gastrointestinal Endoscopy. 2017;85(5, article AB440) doi: 10.1016/j.gie.2017.03.1022. [DOI] [Google Scholar]
  • 37.Clark B. T., Rustagi T., Laine L. What level of bowel prep quality requires early repeat colonoscopy: systematic review and meta-analysis of the impact of preparation quality on adenoma detection rate. The American Journal of Gastroenterology. 2014;109(11):1714–1723. doi: 10.1038/ajg.2014.232. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38.Yark H., López-Cerón M., East J. E., et al. Endoscopic features of sessile serrated adenomas: validation by international experts using high-resolution white-light endoscopy and narrow-band imaging. Gastrointestinal Endoscopy. 2013;77(6):916–924. doi: 10.1016/j.gie.2012.12.018. [DOI] [PubMed] [Google Scholar]
  • 39.Yang H.-J., Lee J. I., Park S.-K., et al. External validation of the endoscopic features of sessile serrated adenomas in expert and trainee colonoscopists. Clinical Endoscopy. 2017;50(3):279–286. doi: 10.5946/ce.2016.107. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Anderson J. C., Butterly L. F., Robinson C. M., Goodrich M., Weiss J. E. Impact of fair bowel preparation quality on adenoma and serrated polyp detection: data from the New Hampshire colonoscopy registry by using a standardized preparation-quality rating. Gastrointestinal Endoscopy. 2014;80(3):463–470. doi: 10.1016/j.gie.2014.03.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Rogart J. N., Siddiqui U. D., Jamidar P. A., Aslanian H. R. Fellow involvement may increase adenoma detection rates during colonoscopy. The American Journal of Gastroenterology. 2008;103(11):2841–2846. doi: 10.1111/j.1572-0241.2008.02085.x. [DOI] [PubMed] [Google Scholar]
  • 42.Buchner A. M., Shahid M. W., Heckman M. G., et al. Trainee participation is associated with increased small adenoma detection. Gastrointestinal Endoscopy. 2011;73(6):1223–1231. doi: 10.1016/j.gie.2011.01.060. [DOI] [PubMed] [Google Scholar]
  • 43.Qayed E., Shea L., Goebel S., Bostick R. M. Association of trainee participation with adenoma and polyp detection rates. World Journal of Gastrointestinal Endoscopy. 2017;9(5):204–210. doi: 10.4253/wjge.v9.i5.204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Peters S. L., Hasan A. G., Jacobson N. B., Austin G. L. Level of fellowship training increases adenoma detection rates. Clinical Gastroenterology and Hepatology. 2010;8(5):439–442. doi: 10.1016/j.cgh.2010.01.013. [DOI] [PubMed] [Google Scholar]
  • 45.Ko C. W., Dominitz J. A., Green P., Kreuter W., Baldwin L. M. Specialty differences in polyp detection, removal, and biopsy during colonoscopy. The American Journal of Medicine. 2010;123(6):528–535. doi: 10.1016/j.amjmed.2010.01.016. [DOI] [PubMed] [Google Scholar]
  • 46.Wexner S. D., Forde K. A., Sellers G., et al. How well can surgeons perform colonoscopy? Surgical Endoscopy. 1998;12(12):1410–1414. doi: 10.1007/s004649900870. [DOI] [PubMed] [Google Scholar]
  • 47.Bhangu A., Bowley D. M., Horner R., Baranowski E., Raman S., Karandikar S. Volume and accreditation, but not specialty, affect quality standards in colonoscopy. The British Journal of Surgery. 2012;99(10):1436–1444. doi: 10.1002/bjs.8866. [DOI] [PubMed] [Google Scholar]
  • 48.Charbel J. M., Bastawrous A. L., Froese D., et al. Colon and rectal surgeons: raising the endoscopy bar. Journal of the American College of Surgeons. 2015;221(4, article e57) doi: 10.1016/j.jamcollsurg.2015.08.047. [DOI] [Google Scholar]
  • 49.Pace D., Borgaonkar M., Evans B., et al. Annual colonoscopy volume and maintenance of competency for surgeons. Surgical Endoscopy. 2017;31(6):2630–2635. doi: 10.1007/s00464-016-5275-1. [DOI] [PubMed] [Google Scholar]
  • 50.Horton N., Garber A., Hasson H., Lopez R., Burke C. A. Impact of single- vs. split-dose low-volume bowel preparations on bowel movement kinetics, patient inconvenience, and polyp detection: a prospective trial. The American Journal of Gastroenterology. 2016;111(9):1330–1337. doi: 10.1038/ajg.2016.273. [DOI] [PubMed] [Google Scholar]

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