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. 2020 Oct 16;99(42):e22738. doi: 10.1097/MD.0000000000022738

Will purposely seeking detect more colorectal polyps than routine performing during colonoscopy?

Yanliu Chu a,b, Juan Zhang b, Ping Wang b, Tian Li b, Shuyi Jiang b, Qinfu Zhao b, Feng Liu b, Xiaozhong Gao b, Xiuli Qiao b, Xiaofeng Wang b, Zhenhe Song b, Heye Liang b, Jing Yue b, Enqiang Linghu a,
Editor: Muhammad Tarek Abdel Ghafar
PMCID: PMC7572006  PMID: 33080734

Abstract

Background & Goals:

We observed that the number of colorectal polyps found intraoperatively was often higher than that encountered preoperatively during elective colonoscopic polypectomy. To evaluate whether more polyps can be detected when they are purposely sought than when they are routinely examined during colonoscopy.

Materials and methods:

Patients undergoing colonoscopy were randomized into groups A and B. Before colonoscopy was performed, endoscopists were instructed to seek polyps for group A purposely but not for group B. Polypectomy was electively completed. In groups A and B, the cases of elective polypectomy were named groups AR and BR, including groups AR-1 and BR-1, during the first colonoscopy and groups AR-2 and BR-2 during the second colonoscopy for polypectomy, respectively. The following data were calculated: the number of polyps detected (NPD) and the polyp detection rate (PDR) in all cases and the number of polyps missed (NPM) and partial polyp miss rate (PPMR) in the cases of colorectal polyps.

Results:

A total of 419 cases were included in group A, 421 in group B, 43 in group AR, and 35 in group BR. No significant differences in PDR were found between groups A and B and in PPMR between groups AR-1 and BR-1 (P > .05), although PPMR in group AR-1 was higher than in group AR-2 (P < .05), similar results were found in PPMR between groups BR-1 and BR-2 (P < .05).

Conclusion:

Purposely seeking for colorectal polyps did not result in more polyps detected compared with routine colonoscopy.

Keywords: colonoscopy, partial polyp miss rate, polyp detection rate, screening colonoscopy

1. Introduction

Colorectal cancer usually originates from a small neoplastic polyp, which gradually increases in size and is accompanied by dysplasia and malignancy.[1,2] Moreover, missed colorectal polyps in colonoscopy have been progressively recognized as a significant cause of interval colorectal cancer (ICC).[3,4] Therefore, colorectal polyp detection rate (PDR) or adenoma detection rate (ADR) has gradually become an important parameter for evaluating the quality of colonoscopy.[59] In the endoscopic clinical practice, obtaining the corresponding pathological data of all polyps is difficult; thus, PDR is a more practical approach compared with ADR.[6,8,1012] Therefore, improving PDR and decreasing polyp miss rate (PMR) have become our aims during colonoscopy. During elective colonoscopic polypectomy, we observed an interesting phenomenon: the number of colorectal polyps found intraoperatively was often higher than that encountered preoperatively. As such, we conducted the present study to determine whether more colorectal polyps can be detected by purposely seeking them compared with routine colonoscopy.

2. Materials and methods

2.1. Grouping and design

From August 9, 2016 to January 5, 2018, patients undergoing colonoscopy were randomized into groups A and B. In group A, the endoscopists were instructed to seek colorectal polyps purposely before performing colonoscopy. In group B, colonoscopy was performed without the above implications. In group A, patients with colorectal polyps for elective endoscopic removal were named as group AR, which was named as group AR-1 during the first colonoscopy. They were named as group AR-2 during the second colonoscopy for polypectomy. In accordance with the above rules, groups BR, BR -1, and BR-2 were named. This study was conducted with the approval of the Weihai Municipal Hospital Ethics Committee. Before the endoscopic procedures were initiated, every patient signed informed consent.

2.2. Inclusion and exclusion criteria

Cases involving emergency colonoscopy, inflammatory bowel disease, history of colorectal surgery, history of colorectal polyp resection, and less than 18 years of age were not enrolled. Colonoscopy cases that did not reach the ileocecal were also excluded.

2.3. Anesthesia

All explorations were performed under intravenous anesthesia with sufentanil followed by propofol. Loss of eyelash reflex indicated successful induction of anesthesia, thereby prompting the endoscopists to commence with the procedures. Colonoscopy and colonoscopic polypectomies were performed by 16 endoscopists.

2.4. Bowel preparation score

Boston bowel preparation scale (BBPS) was used to evaluate bowel preparation.[1315]

2.5. Parameter acquisition

The following data were prospectively collected: sex, age, weight, height, single/double operating colonoscopy, BBPS, intubation time, withdrawal time, and the number and size of polyps. The characteristics of endoscopists included colonoscopy operation period, average annual colonoscopy cases, and total colonoscopy cases. The number of polyps detected (NPD) and the polyp detection rate (PDR) in all cases and the number of polyps missed (NPM) and partial polyp miss rate (PPMR) in the cases of colorectal polyp were calculated. PDR is defined as the number of cases of colorectal polyps found in every 100 cases of colonoscopy. PPMR is defined as the number of cases of partial polyps missed in every 100 cases of colorectal polyps. PPMR was obviously different from PMR. PMR is defined as the number of cases of colorectal polyps missed in every 100 colonoscopies. The actual total number of polyps in patients involves the number of polyps found pre-polypectomy and polypectomy intraoperatively.

2.6. Statistical analysis

Quantitative variables were expressed as mean ± standard deviation. The t-test was used for testing the significance between quantitative variables, and χ2-test was used to detect the significant differences between qualitative variables. Kolgomorov–Smirnoff test was used to verify the normal distribution of quantitative data. Wilcoxon rank sum test was used for non-normally distributed data. P-value less than .05 was considered significant.

3. Results

3.1. General information

A total of 1390 patients met the inclusion criteria, and 550 patients were not included in the study. A total of 419 patients were enrolled in group A, 421 in group B, 43 in group AR, and 35 in group BR.

3.2. Patient features

No differences in terms of sex, age, weight, and height were found between groups A and B, groups AR-1 and BR-1, and groups AR-2 and BR-2 (P > .05). The above data are shown in Tables 1 and 4.

Table 1.

The general characteristics of patients and endoscopists in the studied groups.

3.2.

Table 4.

Main statistical results of each group.

3.2.

3.3. Endoscopists’ characteristics

In terms of endoscopist's colonoscopy operation period, average annual colonoscopy cases, and total colonoscopy cases, no differences were found between groups A and B, AR-1 and BR-1, AR-2 and BR-2, AR-1 and AR-2, and BR-1 and BR-2 (P > .05, Tables 1 and 4).

3.4. Colonoscopy operation-related parameters

In terms of single/double operating colonoscopy, withdrawal time, and intubation time, no differences were observed between groups A and B, AR-1 and BR-1, AR-2 and BR-2, AR-1 and AR-2, and BR-1 and BR-2 (P > .05). No significant differences were found in BBPS between groups A and B, AR-1 and BR-1, and AR-2 and BR-2 (P > .05). However, significant differences were observed between AR-1 and AR-2 and BR-1 and BR-2 (P < .05, Tables 2 and 4).

Table 2.

The colonoscopy operation-related parameters in the studied groups.

3.4.

3.5. PDR, NPD, SPD, PPMR, NPM, and SPM

No significant differences were observed in terms of PDR, NPD, and SPD between groups A and B; PPMR, NPM, and SPM between groups AR-1 and BR-1; and PPMR, NPM, and SPM between groups AR-2 and BR-2 (P > .05). PPMR in group AR-1 was higher than that in group AR-2 (P < .05), and similar results were found in PPMR between group BR-1 and BR-2 (P < .05). The differences in NPD, SPD, NPM, and SPM in AR-1 and AR-2 (P > .05) were not significant. However, significant differences were observed in NPD, NPM, and SPM in BR-1 and BR-2 (P < .05). However, no significant differences were found in SPD between groups BR-1 and BR-2 (P > .05). The above data are shown in Tables 3 and 4. Besides, whether the diameter of the polyp was less or greater than 0.5 cm did not lead to significant differences in PDR between groups A and B in NPD and PPMR, NPM, and SPM between groups AR-1 and BR-1 (P > .05, Table 5).

Table 3.

The polypectomy-related parameters in the studied groups.

3.5.

Table 5.

The impact of polyp size on polypectomy-related parameters in the studied groups.

3.5.

4. Discussion

Colorectal polyps are rarely accompanied by symptoms before canceration other than occasional stool abnormalities. Therefore, current research focuses on increasing PDR and decreasing PMR during colonoscopy, thereby reducing the incidence of colorectal cancer and even ICC.[3,79,16]

Many studies have been conducted on colorectal polyps. Similarly, many instruments and technological innovations, such as the advent of endocuff,[17,18] third eye retroscope,[1921] high definition endoscopy,[2225] full-spectrum endoscopy,[26,27] and a variety of chromoendoscopy,[2830] have been developed. To improve PDR, some endoscopists add a transparent cap in front of the colonoscope[31] or use water-aided colonoscopy.[3234] In addition, a few reports have focused on the effects of bowel preparation on improving PDR.[3539] Several studies have explored the correlation between the features of colonoscopy operators, including endoscopists and nurses, and PDR.[4042] Besides, much research has been devoted to the control of withdrawal time.[4350]

The above studies explored the objective factors related to colonoscopy. The results showed that several elements, such as adequate bowel preparation and withdrawal time of more than 6 minutes, have contributed to improving PDR.[40]

However, whether endoscopists subjectively affect PDR during colonoscopy and the different levels of focus of the operators that may cause different PDR are factors that must be considered. We often detect new polyps by chance in the second colonoscopy for polypectomy. As such, questions, such as “Was the first colonoscopy conducted carelessly?”, “Did the focus of the second colonoscopy lead to such result?”, and “Will purposely seeking colorectal polyps increase detection rate compared with routine colonoscopy?”, may arise.

Our study showed that partial data were almost consistent with our expectations. First, the interesting phenomena found in our previous clinical practices were statistically confirmed by our study. The number of polyps removed in the second colonoscopy was significantly higher than that found in the first colonoscopy. This finding was supported by the significantly higher number of NPD in BR-2 compared with BR-1. However, the differences in NPD between AR-1 and AR-2 were not significant. Unfortunately, our findings indicated that the differences in NPD between groups A and B were not significant. Purposely seeking colorectal polyps did not decrease PPMR compared with routine performance during colonoscopy. No significant differences in PPMR and NPM were found between AR-1 and BR-1. In other words, purposely seeking colorectal polyps did not increase PDR and reduce PPMR compared with routine colonoscopy. This result is not consistent with those of other studies showing that focusing on detecting polyps may help doctors improve ADR. Madhoun et al reported that video recording may help endoscopists increase ADR.[51]

The differences in NPD and SPM between AR-1 and AR-2 were not significant. Although no significant differences were found in SPD between BR-1 and BR-2, significant differences were observed in SPM in the two groups. However, this finding does not suggest that additional focus may result in a significant difference in sensitivity to polyps of different sizes. Further analysis indicated that a polyp diameter less than or greater than 0.5 cm had no significant effect on PDR between groups A and B in NPD, PPMR, NPM, and SPM between groups AR-1 and BR-1 (Table 5). Several polyps, which had been found in groups AR-1 and BR-1, were missed in groups AR-2 and BR-2. In other words, the polyps found in the first colonoscopy were not found in the second colonoscopy for removal. This result suggests that omission is unavoidable because “change blindness” and “inattention blindness” are common phenomena in science.[40]

In our single-center study, PDR and reduction of the rate of polyp missed diagnosis in colonoscopy were not improved by purposely seeking polyps. The current trend in colonoscopy research is artificial intelligence (AI), and its application may serve as a promising direction. We are also conducting research on this topic. We hope that AI can help us observe more colorectal polyps and nip more cases of colorectal cancer in the bud.

Author contributions

Conceptualization: Yanliu Chu, Juan Zhang, Enqiang Linghu.

Data curation: Ping Wang, Shuyi Jiang.

Formal analysis: Ping Wang.

Funding acquisition: Yanliu Chu, Xiaozhong Gao.

Investigation: Tian Li, Shuyi Jiang, Xiaozhong Gao, Xiaofeng Wang, Zhenhe Song.

Methodology: Yanliu Chu, Juan Zhang, Shuyi Jiang, Qinfu Zhao, Feng Liu, Xiaozhong Gao, Xiuli Qiao, Xiaofeng Wang, Zhenhe Song, Heye Liang, Jing Yue.

Project administration: Yanliu Chu, Juan Zhang, Tian Li, Shuyi Jiang, Qinfu Zhao, Feng Liu, Xiaozhong Gao, Xiuli Qiao, Xiaofeng Wang, Zhenhe Song, Heye Liang, Jing Yue.

Resources: Shuyi Jiang, Feng Liu, Xiaozhong Gao, Xiuli Qiao, Heye Liang.

Software: Shuyi Jiang, Feng Liu.

Supervision: Yanliu Chu, Feng Liu, Xiaozhong Gao, Xiuli Qiao, Xiaofeng Wang, Zhenhe Song, Heye Liang, Jing Yue, Enqiang Linghu.

Validation: Yanliu Chu, Feng Liu, Xiaozhong Gao, Xiuli Qiao, Xiaofeng Wang, Zhenhe Song, Heye Liang, Enqiang Linghu.

Visualization: Feng Liu.

Writing – original draft: Yanliu Chu, Tian Li, Qinfu Zhao.

Writing – review & editing: Yanliu Chu, Tian Li, Qinfu Zhao.

Footnotes

Abbreviations: ADR = adenoma detection rate, AI = artificial intelligence, BBPS = Boston bowel preparation scale, ICC = interval colorectal cancer, NPD = the number of polyps detection, NPM = the number of polyps missed, PDR = polyp detection rate, defined as the number of cases of colorectal polyps found in every 100 colonoscopies, PMR = polyp miss rate, defined as the number of cases of colorectal polyps missed in every 100 colonoscopies, PPMR = partial polyp miss rate, defined as the number of cases of partial polyps missed in every 100 cases of colorectal polyps, SPD = the size of polyps detection, SPM = the size of polyps missed.

How to cite this article: Chu Y, Zhang J, Wang P, Li T, Jiang S, Zhao Q, Liu F, Gao X, Qiao X, Wang X, Song Z, Liang H, Yue J, Linghu E. Will purposely seeking detect more colorectal polyps than routine performing during colonoscopy? Medicine. 2020;99:42(e22738).

The authors have no conflicts of interest to disclose.

The datasets generated during and/or analyzed during the current study are not publicly available, but are available from the corresponding author on reasonable request.

Project Number 2016WS0637, Study and application of potential factors to improve the detection rate of adenoma in colonoscopy, Medical and health science and Technology Development Plan of Shandong Province

References

  • [1].Hill MJ, Morson BC, Bussey HJ. Aetiology of adenoma--carcinoma sequence in large bowel. Lancet 1978;1:245–7. [DOI] [PubMed] [Google Scholar]
  • [2].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;329:1977–81. [DOI] [PubMed] [Google Scholar]
  • [3].Cai B, Liu Z, Xu Y, et al. Adenoma detection rate in 41,010 patients from Southwest China. Oncol Lett 2015;9:2073–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [4].Kaminski MF, Regula J, Kraszewska E, et al. Quality indicators for colonoscopy and the risk of interval cancer. N Engl J Med 2010;362:1795–803. [DOI] [PubMed] [Google Scholar]
  • [5].Boroff ES, Gurudu SR, Hentz JG, et al. Polyp and adenoma detection rates in the proximal and distal colon. Am J Gastroenterol 2013;108:993–9. [DOI] [PubMed] [Google Scholar]
  • [6].Elhanafi S, Ortiz AM, Yarlagadda A, et al. Estimation of the adenoma detection rate from the polyp detection rate by using a conversion factor in a predominantly hispanic population. J Clin Gastroenterol 2015;49:589–93. [DOI] [PubMed] [Google Scholar]
  • [7].Schramm C, Scheller I, Franklin J, et al. Predicting ADR from PDR and individual adenoma-to-polyp-detection-rate ratio for screening and surveillance colonoscopies: a new approach to quality assessment. United European Gastroenterol J 2017;5:742–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [8].Murchie B, Tandon K, Zackria S, et al. Can polyp detection rate be used prospectively as a marker of adenoma detection rate? Surg Endosc 2018;32:1141–8. [DOI] [PubMed] [Google Scholar]
  • [9].Atia MA, Patel NC, Ratuapli SK, et al. Nonneoplastic polypectomy during screening colonoscopy: the impact on polyp detection rate, adenoma detection rate, and overall cost. Gastrointest Endosc 2015;82:370–5. [DOI] [PubMed] [Google Scholar]
  • [10].Delavari A, Salimzadeh H, Bishehsari F, et al. Mean polyp per patient is an accurate and readily obtainable surrogate for adenoma detection rate: results from an opportunistic screening colonoscopy program. Middle East J Dig Dis 2015;7:214–9. [PMC free article] [PubMed] [Google Scholar]
  • [11].Francis DL, Rodriguez-Correa DT, Buchner A, et al. Application of a conversion factor to estimate the adenoma detection rate from the polyp detection rate. Gastrointest Endosc 2011;73:493–7. [DOI] [PubMed] [Google Scholar]
  • [12].Williams JE, Holub JL, Faigel DO. Polypectomy rate is a valid quality measure for colonoscopy: results from a national endoscopy database. Gastrointest Endosc 2012;75:576–82. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [13].Calderwood AH, Schroy PC, Lieberman DA, et al. Boston Bowel Preparation Scale scores provide a standardized definition of adequate for describing bowel cleanliness. Gastrointest Endosc 2014;80:269–76. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [14].Lai EJ, Calderwood AH, Doros G, et al. The Boston bowel preparation scale: a valid and reliable instrument for colonoscopy-oriented research. Gastrointest Endosc 2009;69(3 Pt 2):620–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [15].Calderwood AH, Jacobson BC. Comprehensive validation of the Boston Bowel Preparation Scale. Gastrointest Endosc 2010;72:686–92. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [16].Citarda F, Tomaselli G, Capocaccia R, et al. Efficacy in standard clinical practice of colonoscopic polypectomy in reducing colorectal cancer incidence. Gut 2001;48:812–5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [17].Baek MD, Jackson CS, Lunn J, et al. Endocuff assisted colonoscopy significantly increases sessile serrated adenoma detection in veterans. J Gastrointest Oncol 2017;8:636–42. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [18].Zippi M, Hong W, Crispino P, et al. New device to implement the adenoma detection rate. World J Clin Cases 2017;5:258–63. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [19].DeMarco DC, Odstrcil E, Lara LF, et al. Impact of experience with a retrograde-viewing device on adenoma detection rates and withdrawal times during colonoscopy: the Third Eye Retroscope study group. Gastrointest Endosc 2010;71:542–50. [DOI] [PubMed] [Google Scholar]
  • [20].Gralnek IM. Emerging technological advancements in colonoscopy: Third Eye( Retroscope( and Third Eye( Panoramic(TM), Fuse( Full Spectrum Endoscopy( colonoscopy platform, Extra-Wide-Angle-View colonoscope, and NaviAid(TM) G-EYE(TM) balloon colonoscope. Dig Endosc 2015;27:223–31. [DOI] [PubMed] [Google Scholar]
  • [21].Rex DK. Third Eye Retroscope: rationale, efficacy, challenges. Rev Gastroenterol Disord 2009;9:1–6. [PubMed] [Google Scholar]
  • [22].Longcroft-Wheaton G, Brown J, Cowlishaw D, et al. High-definition vs. standard-definition colonoscopy in the characterization of small colonic polyps: results from a randomized trial. Endoscopy 2012;44:905–10. [DOI] [PubMed] [Google Scholar]
  • [23].Basford PJ, Longcroft-Wheaton G, Higgins B, et al. High-definition endoscopy with i-Scan for evaluation of small colon polyps: the HiSCOPE study. Gastrointest Endosc 2014;79:111–8. [DOI] [PubMed] [Google Scholar]
  • [24].Rath T, Tontini GE, Nägel A, et al. High-definition endoscopy with digital chromoendoscopy for histologic prediction of distal colorectal polyps. BMC Gastroenterol 2015;15:145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [25].Pigò F, Bertani H, Manno M, et al. i-Scan high-definition white light endoscopy and colorectal polyps: prediction of histology, interobserver and intraobserver agreement. Int J Colorectal Dis 2013;28:399–406. [DOI] [PubMed] [Google Scholar]
  • [26].Roepstorff S, Hadi SA, Rasmussen M. Full spectrum endoscopy (FUSE) versus standard forward-viewing endoscope (SFV) in a high-risk population. Scand J Gastroenterol 2017;52:1298–303. [DOI] [PubMed] [Google Scholar]
  • [27].Gralnek IM, Segol O, Suissa A, et al. A prospective cohort study evaluating a novel colonoscopy platform featuring full-spectrum endoscopy. Endoscopy 2013;45:697–702. [DOI] [PubMed] [Google Scholar]
  • [28].Matsuda T, Ono A, Sekiguchi M, et al. Advances in image enhancement in colonoscopy for detection of adenomas. Nat Rev Gastroenterol Hepatol 2017;14:305–14. [DOI] [PubMed] [Google Scholar]
  • [29].Hashimoto K, Higaki S, Nishiahi M, et al. Does chromoendoscopy improve the colonoscopic adenoma detection rate? Hepatogastroenterology 2010;57:1399–404. [PubMed] [Google Scholar]
  • [30].Manfredi MA, Abu Dayyeh BK, Bhat YM, et al. Electronic chromoendoscopy. Gastrointest Endosc 2015;81:249–61. [DOI] [PubMed] [Google Scholar]
  • [31].Pohl H, Bensen SP, Toor A, et al. Cap-assisted colonoscopy and detection of Adenomatous Polyps (CAP) study: a randomized trial. Endoscopy 2015;47:891–7. [DOI] [PubMed] [Google Scholar]
  • [32].Yen AW, Leung JW, Leung FW. A novel method with significant impact on adenoma detection: combined water-exchange and cap-assisted colonoscopy. Gastrointest Endosc 2013;77:944–8. [DOI] [PubMed] [Google Scholar]
  • [33].Leung FW. PDR or ADR as a quality indicator for colonoscopy. Am J Gastroenterol 2013;108:1000–2. [DOI] [PubMed] [Google Scholar]
  • [34].Hsieh YH, Koo M, Leung FW. A patient-blinded randomized, controlled trial comparing air insufflation, water immersion, and water exchange during minimally sedated colonoscopy. Am J Gastroenterol 2014;109:1390–400. [DOI] [PubMed] [Google Scholar]
  • [35].Calderwood AH, Thompson KD, Schroy PC, 3rd, et al. Good is better than excellent: bowel preparation quality and adenoma detection rates. Gastrointest Endosc 2015;81:691–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [36].Gurudu SR, Ramirez FC, Harrison ME, et al. Increased adenoma detection rate with system-wide implementation of a split-dose preparation for colonoscopy. Gastrointest Endosc 2012;76:603–8. e601. [DOI] [PubMed] [Google Scholar]
  • [37].Clark BT, 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. Am J Gastroenterol 2014;109:1714–23. quiz 1724. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [38].Anderson JC, Butterly LF, Robinson CM, et al. 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. Gastrointest Endosc 2014;80:463–70. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [39].Tholey DM, Shelton CE, Francis G, et al. Adenoma detection in excellent versus good bowel preparation for colonoscopy. J Clin Gastroenterol 2015;49:313–9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [40].Aranda-Hernández J, Hwang J, Kandel G. Seeing better--Evidence based recommendations on optimizing colonoscopy adenoma detection rate. World J Gastroenterol 2016;22:1767–78. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [41].Jung DK, Kim TO, Kang MS, et al. The colonoscopist's expertise affects the characteristics of detected polyps. Clin Endosc 2016;49:61–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [42].Jover R, Zapater P, Bujanda L, et al. Endoscopist characteristics that influence the quality of colonoscopy. Endoscopy 2016;48:241–7. [DOI] [PubMed] [Google Scholar]
  • [43].Kashiwagi K, Inoue N, Yoshida T, et al. Polyp detection rate in transverse and sigmoid colon significantly increases with longer withdrawal time during screening colonoscopy. PLoS One 2017;12:e0174155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [44].Baker SL, Miller RA, Creighton A, et al. Effect of 6-minute colonoscopy withdrawal time policy on polyp detection rate in a community hospital. Gastroenterol Nurs 2015;38:96–9. [DOI] [PubMed] [Google Scholar]
  • [45].Butterly L, Robinson CM, Anderson JC, et al. Serrated and adenomatous polyp detection increases with longer withdrawal time: results from the New Hampshire Colonoscopy Registry. Am J Gastroenterol 2014;109:417–26. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [46].Moritz V, Bretthauer M, Ruud HK, et al. Withdrawal time as a quality indicator for colonoscopy - a nationwide analysis. Endoscopy 2012;44:476–81. [DOI] [PubMed] [Google Scholar]
  • [47].Shaukat A, Rector TS, Church TR, et al. Longer withdrawal time is associated with a reduced incidence of interval cancer after screening colonoscopy. Gastroenterology 2015;149:952–7. [DOI] [PubMed] [Google Scholar]
  • [48].Vavricka SR, Sulz MC, Degen L, et al. Monitoring colonoscopy withdrawal time significantly improves the adenoma detection rate and the performance of endoscopists. Endoscopy 2016;48:256–62. [DOI] [PubMed] [Google Scholar]
  • [49].Singh S. Colonoscopy withdrawal time and adenoma detection rates for trainees. Surg Endosc 2013;27:2243–4. [DOI] [PubMed] [Google Scholar]
  • [50].Lee TJ, Blanks RG, Rees CJ, et al. Longer mean colonoscopy withdrawal time is associated with increased adenoma detection: evidence from the Bowel Cancer Screening Programme in England. Endoscopy 2013;45:20–6. [DOI] [PubMed] [Google Scholar]
  • [51].Madhoun MF, Tierney WM. The impact of video recording colonoscopy on adenoma detection rates. Gastrointest Endosc 2012;75:127–33. [DOI] [PubMed] [Google Scholar]

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