Subscribe to RSS

DOI: 10.1055/a-2788-3397
Adenoma detection rates and complications of colonoscopy in patients aged 75 to 79 vs 70 to 74 years: Propensity score-matching study
Authors
Abstract
Background and study aims
Several guidelines recommend discontinuation of routine surveillance colonoscopy after age 75 years. Because Japan has one of the longest life expectancies, we considered ceasing at age 80 years. We compared patients aged 75 to 79 years with those aged 70 to 74 years, regarding adenoma detection rate (ADR), mean number of adenomas per colonoscopy, and adverse events.
Patients and methods
This propensity score-matching (PSM) study included patients aged 70 to 79 years with a performance status of 0 to 1 who underwent colonoscopies at Toyoshima Endoscopy Clinic between 2017 and 2024. Patients aged 75 to 79 years were matched with those aged 70 to 74 years for baseline characteristics using the propensity score. ADR, mean number of adenomas per colonoscopy, frequency of respiratory depression, hypotension, and delayed post-polypectomy bleeding were compared between the two groups.
Results
During the study period, 3415 patients were included. The ADR in patients aged 75 to 79 years was higher than that in patients aged 70 to 74 years (66.5% vs 62.2%, P = 0.021). Mean number of adenomas per colonoscopy in patients aged 75 to 79 years was higher than that in patients aged 70 to 74 years (1.54 vs 1.38, P = 0.014). The two groups did not show significant differences in respiratory depression (2.6% vs 2.3%), hypotension (0.8% vs 1.0%) or delayed post-polypectomy bleeding (0.2% vs 0.4%).
Conclusions
Colonoscopies for patients aged 75 to 79 are safe and effective in Japan.
Keywords
Endoscopy Lower GI Tract - Polyps / adenomas / ... - CRC screening - Endoscopic resection (polypectomy, ESD, EMRc, ...)Introduction
Colorectal cancer (CRC) is a fatal disease that occurs worldwide. Because CRCs mainly develop from conventional adenomas or serrated polyps, their removal prevents CRC [1] [2]. Surveillance colonoscopy has proven beneficial through decreased incidence and mortality of CRC [3]. Endoscopists with high adenoma detection rates (ADRs) could enhance these benefits [4] [5]. In addition, there is a controversy regarding when to discontinue surveillance, especially in an aging population. United States guidelines recommend discontinuing routine surveillance colonoscopy after age 75 years [6], whereas European guidelines suggest stopping endoscopic surveillance at age 80 years [7]. Although the life expectancy is 78.8 years in the United States, Japan has one of the longest at 84.4 years [8]. In Japan, life expectancy is approximately 5 years longer; therefore, we considered ceasing at age 80 years. With advances in endoscopic techniques and equipment, colonoscopies may become safe and effective, even in patients aged 75 to 79 years. In this study, we compared patients aged 75 to 79 years with those aged 70 to 74 years regarding ADR,% mean number of adenomas per colonoscopy (APC), and adverse events (AEs).
Patients and methods
Study overview
This retrospective, single-center, propensity score-matching (PSM) study was conducted at the Toyoshima Endoscopy Clinic, a representative outpatient clinic specializing in endoscopy in Japan. Patients aged 70 to 79 years who underwent colonoscopy at our clinic between April 2017 and April 2024 were eligible for the study. Indications for colonoscopy included symptom examination, screening, and surveillance of colorectal polyps. Symptoms included hematochezia, abnormal bowel habits, and abdominal pain. Patients with poor bowel preparation, prior colorectal surgical resection, incomplete cecal intubation, or treatment purpose were excluded. Treatments included planned polypectomy and emergency hematemesis. Colonoscopy was scheduled for patients with a performance status (PS) of 0 or 1 [9] [10] and American Society of Anesthesiologists (ASA) physical status classification of I or II [11]. PS was divided into five levels ranging from 0 to 4. PS 0, normal activity; PS 1, some symptoms, but still nearly fully ambulatory; PS 2, less than 50%; PS 3, more than 50% of daytime in bed; and PS 4, completely bedridden. ASA physical status classification was divided into six levels ranging from 1 to 6. ASA I, healthy patients; ASA II, mild systemic disease; ASA III, severe systemic disease; ASA IV, constant threat to life; ASA V, moribund patients; and ASA VI, brain-dead patients.
This retrospective study was approved by the Certified Institutional Review Board of the Yoyogi Mental Clinic on July 16, 2021 (approval no. RKK227). We published the study protocol on our clinic website (www.ichou.com); thus, patients could opt out if desired. Written informed consent was obtained from all participants. All the clinical investigations were conducted in accordance with the ethical guidelines of the Declaration of Helsinki.
Colonoscopy
The endoscopy system used was either Olympus EVIS LUSERA ELITE (CV-290) or EVIS X1 (CV-1500). CF-EZ1500D, CF-XZ1200, CF-HQ290, CF-HQ290Z, CF-H290EC, PCF-H290Z, or PCF-PQ260 (Olympus Corp., Japan) were used. Sedation was performed based on patient willingness. Midazolam, pethidine, and/or propofol were used [12]. Pan-colonic chromoendoscopy with indigo carmine was used routinely [13]. Moreover, endoscopic observation was performed using texture and color enhancement imaging, as well as white-light imaging, to increase polyp detection [14] [15]. Endoscopic resection techniques included endoscopic mucosal resection and hot or cold polypectomy using snares or forceps [16] [17]. Bowel preparations were classified into four groups. We used the Harefield Cleansing Scale because it is the standard scoring method in our institution and is integrated into our reporting system. Grade A was defined as cleanliness or a minor amount of fluid in all colonic segments (good). Grade B was defined as residual semi-solid stool that could be easily removed (average). Grade C was defined as partially removable stool that prevented complete visualization of the mucosa (marginal). Grade D was defined as remaining solid stool that prevented examination (poor) [18] [19]. Grade D patients were excluded because of poor patient preparation. Withdrawal time included time required for polypectomy. A withdrawal time of less than 6 minutes was excluded as an inappropriate examination [20].
Respiratory depression was defined as reduction in oxygen saturation < 90% for > 20 seconds or implementation of oxygen inhalation based on the judgment of the on-site endoscopist [21]. Hypotension was defined as reduction in systolic blood pressure < 80 mm Hg [22]. Delayed post-polypectomy bleeding (DPPB) was defined as bleeding within 14 days of polypectomy that required emergent endoscopy [23].
Data collection and outcome parameters
Our electronic endoscopy reporting system was the T-File System (STS Medic, Japan) integrated into the electronic medical record system, the Qualis (BML, Japan). The endoscopy reporting system outputted the information for this study in Microsoft Excel file format [24] [25].
Background information included patient age, sex, indications for colonoscopy, endoscopist, endoscopy system, colonoscope, bowel preparation, withdrawal time, and doses of midazolam, pethidine, and propofol. The indications were divided into three groups: A, evaluation of symptoms; B, screening; and C, surveillance [26]. Endoscopists were classified into two groups: experts and standard [27]. Expert endoscopists were defined as those with > 20,000 colonoscopies. Endoscopy systems were classified into two groups: X1 and ELITE. Colonoscopes were classified into three groups: A, CF-EZ1500D and CF-XZ1200; B, CF-HQ290, CF-HQ290Z, CF-H290EC, and PCF-H290Z; and C, PCF-PQ260 [28].
Outcome parameters were ADR; APC; advanced ADR; mean number of advanced APCs; adenocarcinoma detection rate; sessile serrated lesion detection rate (SSLDR); mean number of sessile serrated lesions per colonoscopy (SSLPC); and frequency of respiratory depression, hypotension, and DPPB. Advanced adenomas included adenomas ≥ 10 mm in size, villous adenomas, and adenomas with high-grade dysplasia.
Statistical analysis
PSM was used to adjust patient characteristics to reduce effects of selection bias and potential confounding factors. The adjustment items included all baseline patient characteristics such as sex, indication, endoscopist, endoscopy system, colonoscope, bowel preparation, withdrawal time, and doses of midazolam, pethidine, and propofol. Patients aged 75 to 79 years were identified and the propensity score was matched with those aged 70 to 74 years. Matching was performed with a 1:1 matching protocol using nearest-neighbor matching without replacement and a caliper width of 0.1 of the pooled standard deviation of the logit of the propensity score [29].
After PSM, we analyzed differences in ADR, APC, advanced ADR, advanced APC, adenocarcinoma detection rate, SSLDR, and SSLPC, as well as frequency of respiratory depression, hypotension, and DPPB between the two groups. We performed additional subanalyses by indications for colonoscopy. P values for baseline characteristics were calculated using Brunner-Munzel and Wilcoxon signed-rank sum tests for before and after matching, respectively. We assessed P values for outcomes using the Wald test with logistic regression. Statistical significance was set at P < 0.05. To assess quality of matching, we evaluated covariate balance using standardized mean differences (SMDs), with an SMD < 0.10 considered indicative of adequate balance. In addition, Love plots were generated to visually compare covariate balance before and after matching. Calculations were performed using Bell Curve for Excel version 4.07 (Social Survey Research Information Co., Ltd., Japan).
Results
During the study period, 3545 consecutive patients aged 70 to 79 years who underwent colonoscopy were enrolled. We excluded 105 patients for therapeutic purposes, 17 patients for poor bowel preparation, 13 patients for prior colorectal resection, seven patients for incomplete cecal intubation, and one patient for an inappropriate withdrawal time. Of the 17 patients with poor bowel preparation, 13 were aged 70 to 74 years and four were aged 75 to 79 years. Of the seven patients with incomplete cecal intubation, four were aged 70 to 74 years and three were aged 75 to 79 years. Finally, 3402 patients were included in the study. There were 2079 patients aged 70 to 74 years and 1323 aged 75 to 79 years. The two age groups were paired and 1,291 pairs were matched and extracted ([Fig. 1]). [Fig. 2] shows the Love plot of the SMD before and after PSM. Of these, 46.9% were male and average withdrawal time was 14.9 minutes. The two groups did not show significant differences in sex, purpose, endoscopist, endoscopy system, colonoscopy, bowel preparation, withdrawal time, or doses of midazolam, pethidine, or propofol after PSM ([Table 1]). As shown in [Table 2], ADR in patients aged 75 to 79 years was significantly higher than that in patients aged 70 to 74 years (66.5% vs 62.2%, P = 0.021). APC in patients aged 75 to 79 years was larger than that in patients aged 70 to 74 years (1.54 vs 1.38, P = 0.014). There were no significant differences between the two groups in terms of SSLDR (4.5% vs 5.6%) or SSLPC (0.05 vs 0.07). The two groups did not show significant differences in respiratory depression (2.6% vs 2.3%), hypotension (0.8% vs 1.0%), or DPPB (0.2% vs 0.4%). One patient aged 70 to 74 years was hospitalized because of arrhythmia after colonoscopy. There were no cases with perforation or uncontrollable immediate bleeding.




[Table 3] shows the subanalysis in which indications for colonoscopy were limited to surveillance of colorectal polyps and the results remained unchanged.
[Table 4] shows the subanalysis in which indications for colonoscopy were limited to screening and the results remained unchanged.
[Table 5] shows the subanalysis in which indications for colonoscopy were limited to symptoms. There were no significant differences between the two groups.
Discussion
In this study, patients aged 75 to 79 years showed a higher ADR and APC than those aged 70 to 74 years. In addition, there were no differences in frequencies of respiratory depression and DPPB. Because the ADR and APC were high, it might have been effective in preventing colorectal cancer in patients aged 75 to 79 years as well. If patients aged 75 to 79 years have good activities of daily living (ADL) and are classified as ASA I–II, they would be able to complete colonoscopies safely, similar to those aged 70 to 74 years.
Our clinic has previously reported ADRs of 50.8% in 2021 [26] and 55.0% in 2024 in all age groups [29]. In this study, ADRs were 62.0% and 66.4% in patients aged 70 to 74 and 75 to 79 years, respectively. ADRs have been reported to increase with age [30], and this study indicated that ADRs increased in patients aged 75 to 79 years. Considering the ceiling effect of ADR [31], further improvement may be difficult.
Considerable evidence suggests that risk associated with colonoscopy increases with age. A population-based cohort study reported adverse gastrointestinal events within 30 days after colonoscopy [32]. Risks were 0.5% for patients aged 66 to 69 years, 0.58% for patients aged 70 to 74 years, 0.72% for patients aged 75 to 79 years, 0.88% for patients aged 80 to 84 years, and 1.21% for patients aged 85 or older years, respectively. Compared with patients aged 66 to 69 years, risk was significantly higher in patients aged 80 years or older. A multicenter study reported complications directly related to colonoscopy within 30 days [33]. Risks were 0.11% for patients aged 40 to 59 years, 0.18% for patients aged 60 to 69 years, 0.35% for patients aged 70 to 79 years, and 0.44% for patients aged 80 or older years, respectively. Incidence of AEs after colonoscopy increases with age.
The United States Preventive Services Task Force determined that screening should not be continued after age 85 years because the risk could exceed the potential benefit [6]. For patients aged 75 to 85 years, the United States guidelines recommend continued routine screening but argue for individualization based on an assessment of benefit, risk, and comorbidities. Assessment of benefits included prior colonoscopy findings and life expectancy. Patients with high-risk adenomas are at higher risk of developing advanced neoplasia than average-risk individuals. Therefore, the potential benefit of surveillance may be higher for average-risk individuals. Although elderly patients with high-risk adenomas may benefit from surveillance, this depends on their life expectancy. Patients aged 75 to 85 years require individualized decisions to continue surveillance.
Life expectancy in Japan is approximately 5 years longer than in the United States. There may also be coordination at the national level. In Japan, screening colonoscopies may target individuals younger than age 80 years. However, comorbidities should be considered. This coordination may be similar in countries with a long life expectancy, such as Japan.
This study had some limitations. First, this is a retrospective single-center study. However, the medical data recordings are well-controlled. Second, timeframes and patient cohorts were limited. Third, cost analysis was not performed. A detailed cost-effectiveness analysis is a topic for future research. Fourth, AEs related to bowel preparation were not analyzed. Fifth, withdrawal time included time required for polypectomy in this study. Both American and European guidelines define appropriate withdrawal time as the duration of mucosal observation, explicitly excluding time spent on polypectomy. Sixth, patients with poor PS were excluded from undergoing colonoscopy based on clinical judgment, and none of these patients were tested after being ruled out during the interview stage.
Conclusions
In conclusion, colonoscopy in patients aged 75 to 79 years in Japan may be considered safe and effective in carefully selected individuals with good ADL. However, due to the lack of evaluation of certain AEs—especially those related to bowel preparation—these findings should be interpreted with caution. Further studies are warranted to comprehensively assess risks associated with the procedure in this age group.
Contributorsʼ Statement
Osamu Toyoshima: Formal analysis, Investigation, Writing - original draft. Toshihiro Nishizawa: Formal analysis, Investigation, Writing - original draft, Writing - review & editing. Shuntaro Yoshida: Investigation. Tomoharu Yamada: Investigation. Keisuke Mabuchi: Investigation. Takuma Kaneko: Investigation. Mari Mizutani: Investigation. Hirotoshi Ebinuma: Resources. Mitsuhiro Fujishiro: Supervision. Keisuke Hata: Project administration.
Conflict of Interest
The authors declare that they have no conflict of interest.
-
References
- 1 He X, Hang D, Wu K. et al. Long-term risk of colorectal cancer after removal of conventional adenomas and serrated polyps. Gastroenterology 2020; 158: 852-861 e4
- 2 Saito Y, Oka S, Kawamura T. et al. Colonoscopy screening and surveillance guidelines. Dig Endosc 2021; 33: 486-519
- 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 Kaminski MF, Regula J, Kraszewska E. et al. Quality indicators for colonoscopy and the risk of interval cancer. New Engl J Med 2010; 362: 1795-1803
- 5 Corley DA, Levin TR, Doubeni CA. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med 2014; 370: 2541
- 6 Lieberman DA, Rex DK, Winawer SJ. et al. Guidelines for colonoscopy surveillance after screening and polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2012; 143: 844-857
- 7 Hassan C, Antonelli G, Dumonceau JM. et al. Post-polypectomy colonoscopy surveillance: European Society of Gastrointestinal Endoscopy (ESGE) Guideline - Update 2020. Endoscopy 2020; 52: 687-700
- 8 Pichon-Riviere A, Drummond M, Palacios A. et al. Determining the efficiency path to universal health coverage: cost-effectiveness thresholds for 174 countries based on growth in life expectancy and health expenditures. Lancet Glob Health 2023; 11: e833-e842
- 9 Oken MM, Creech RH, Tormey DC. et al. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 1982; 5: 649-655
- 10 Isohata N, Shimojima R, Utano K. et al. Colonoscopy in patients aged 85 years or older: An observational study. J Anus Rectum Colon 2018; 2: 155-161
- 11 Mayhew D, Mendonca V, Murthy BVS. A review of ASA physical status - historical perspectives and modern developments. Anaesthesia 2019; 74: 373-379
- 12 Nishizawa T, Suzuki H, Arita M. et al. Pethidine dose and female sex as risk factors for nausea after esophagogastroduodenoscopy. J Clin Biochem Nutr 2018; 63: 230-232
- 13 Nishizawa T, Watanabe H, Yoshida S. et al. Association between colonic adenoma size and proliferative zone in the crypt. Scand J Gastroenterol 2024; 59: 875-879
- 14 Hiramatsu T, Nishizawa T, Kataoka Y. et al. Improved visibility of colorectal tumor by texture and color enhancement imaging with indigo carmine. World J Gastrointest Endosc 2023; 15: 690-698
- 15 Mitev S, Saeed H, Rasheed CF. et al. Texture and color enhancement imaging versus white light imaging for the detection of colorectal adenomas: Systematic review and meta-analysis. Endosc Int Open 2025; 13: a24749676
- 16 Toyoshima O, Nishizawa T, Watanabe H. et al. Endoscopic characteristics to differentiate SSLs and microvesicular hyperplastic polyps from goblet cell-rich hyperplastic polyps. Endosc Int Open 2024; 12: E1251-E1259
- 17 Toyoshima O, Nishizawa T, Yoshida S. et al. Hemorrhoids as a risk factor for colorectal adenomas on colonoscopy. Endosc Int Open 2023; 11: E497-E503
- 18 Ell C, Fischbach W, Bronisch HJ. et al. Randomized trial of low-volume PEG solution versus standard PEG + electrolytes for bowel cleansing before colonoscopy. Am J Gastroenterol 2008; 103: 883-893
- 19 Halphen M, Heresbach D, Gruss HJ. et al. Validation of the Harefield Cleansing Scale: a tool for the evaluation of bowel cleansing quality in both research and clinical practice. Gastrointest Endosc 2013; 78: 121-131
- 20 Barclay RL, Vicari JJ, Doughty AS. et al. Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006; 355: 2533-2541
- 21 Nishizawa T, Sakitani K, Suzuki H. et al. Adverse events associated with bidirectional endoscopy with midazolam and pethidine. J Clin Biochem Nutr 2020; 66: 78-81
- 22 Nishizawa T, Suzuki H, Sagara S. et al. Dexmedetomidine versus midazolam for gastrointestinal endoscopy: a meta-analysis. Dig Endosc 2015; 27: 8-15
- 23 Oh CK, Cho YW, Jung J. et al. Comparison of cold snare endoscopic mucosal resection and hot snare endoscopic mucosal resection for small colorectal polyps: a randomized controlled trial. Sci Rep 2024; 14: 20335
- 24 Bretthauer M, Aabakken L, Dekker E. et al. Requirements and standards facilitating quality improvement for reporting systems in gastrointestinal endoscopy: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement. Endoscopy 2016; 48: 291-294
- 25 Nishizawa T, Sakitani K, Suzuki H. et al. Small-caliber endoscopes are more fragile than conventional endoscopes. Endosc Int Open 2019; 7: E1729-E1732
- 26 Toyoshima O, Yoshida S, Nishizawa T. et al. Simple feedback of colonoscopy performance improved the number of adenomas per colonoscopy and serrated polyp detection rate. Endosc Int Open 2021; 9: E1032-E1038
- 27 Toyoshima O, Nishizawa T, Yoshida S. et al. Expert endoscopists with high adenoma detection rates frequently detect diminutive adenomas in proximal colon. Endosc Int Open 2020; 8: E775-E782
- 28 Toyoshima O, Yoshida S, Nishizawa T. et al. CF290 for pancolonic chromoendoscopy improved sessile serrated polyp detection and procedure time: a propensity score-matching study. Endosc Int Open 2019; 7: E987-e993
- 29 Toyoshima O, Nishizawa T, Hiramatsu T. et al. Colorectal adenoma detection rate using texture and color enhancement imaging versus white light imaging with chromoendoscopy: a propensity score matching study. J Gastroenter Hepatol 2024; 39: 2105-2111
- 30 Karsenti D, Tharsis G, Burtin P. et al. Adenoma and advanced neoplasia detection rates increase from 45 years of age. World J Gastroenterol 2019; 25: 447-456
- 31 Yun GY, Eun HS, Kim JS. et al. Colonoscopic withdrawal time and adenoma detection in the right colon. Medicine (Baltimore) 2018; 97: e12113
- 32 Warren JL, Klabunde CN, Mariotto AB. et al. Adverse events after outpatient colonoscopy in the Medicare population. Ann Intern Med 2009; 150: 849-857
- 33 Ko CW, Riffle S, Michaels L. et al. Serious complications within 30 days of screening and surveillance colonoscopy are uncommon. Clin Gastroenterol Hepatol 2010; 8: 166-173
Correspondence
Publication History
Received: 07 March 2025
Accepted after revision: 14 January 2026
Accepted Manuscript online:
14 January 2026
Article published online:
03 February 2026
© 2026. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/).
Georg Thieme Verlag KG
Oswald-Hesse-Straße 50, 70469 Stuttgart, Germany
Osamu Toyoshima, Toshihiro Nishizawa, Shuntaro Yoshida, Tomoharu Yamada, Keisuke Mabuchi, Takuma Kaneko, Mari Mizutani, Hirotoshi Ebinuma, Mitsuhiro Fujishiro, Keisuke Hata. Adenoma detection rates and complications of colonoscopy in patients aged 75 to 79 vs 70 to 74 years: Propensity score-matching study. Endosc Int Open 2026; 14: a27883397.
DOI: 10.1055/a-2788-3397
-
References
- 1 He X, Hang D, Wu K. et al. Long-term risk of colorectal cancer after removal of conventional adenomas and serrated polyps. Gastroenterology 2020; 158: 852-861 e4
- 2 Saito Y, Oka S, Kawamura T. et al. Colonoscopy screening and surveillance guidelines. Dig Endosc 2021; 33: 486-519
- 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 Kaminski MF, Regula J, Kraszewska E. et al. Quality indicators for colonoscopy and the risk of interval cancer. New Engl J Med 2010; 362: 1795-1803
- 5 Corley DA, Levin TR, Doubeni CA. Adenoma detection rate and risk of colorectal cancer and death. N Engl J Med 2014; 370: 2541
- 6 Lieberman DA, Rex DK, Winawer SJ. et al. Guidelines for colonoscopy surveillance after screening and polypectomy: a consensus update by the US Multi-Society Task Force on Colorectal Cancer. Gastroenterology 2012; 143: 844-857
- 7 Hassan C, Antonelli G, Dumonceau JM. et al. Post-polypectomy colonoscopy surveillance: European Society of Gastrointestinal Endoscopy (ESGE) Guideline - Update 2020. Endoscopy 2020; 52: 687-700
- 8 Pichon-Riviere A, Drummond M, Palacios A. et al. Determining the efficiency path to universal health coverage: cost-effectiveness thresholds for 174 countries based on growth in life expectancy and health expenditures. Lancet Glob Health 2023; 11: e833-e842
- 9 Oken MM, Creech RH, Tormey DC. et al. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 1982; 5: 649-655
- 10 Isohata N, Shimojima R, Utano K. et al. Colonoscopy in patients aged 85 years or older: An observational study. J Anus Rectum Colon 2018; 2: 155-161
- 11 Mayhew D, Mendonca V, Murthy BVS. A review of ASA physical status - historical perspectives and modern developments. Anaesthesia 2019; 74: 373-379
- 12 Nishizawa T, Suzuki H, Arita M. et al. Pethidine dose and female sex as risk factors for nausea after esophagogastroduodenoscopy. J Clin Biochem Nutr 2018; 63: 230-232
- 13 Nishizawa T, Watanabe H, Yoshida S. et al. Association between colonic adenoma size and proliferative zone in the crypt. Scand J Gastroenterol 2024; 59: 875-879
- 14 Hiramatsu T, Nishizawa T, Kataoka Y. et al. Improved visibility of colorectal tumor by texture and color enhancement imaging with indigo carmine. World J Gastrointest Endosc 2023; 15: 690-698
- 15 Mitev S, Saeed H, Rasheed CF. et al. Texture and color enhancement imaging versus white light imaging for the detection of colorectal adenomas: Systematic review and meta-analysis. Endosc Int Open 2025; 13: a24749676
- 16 Toyoshima O, Nishizawa T, Watanabe H. et al. Endoscopic characteristics to differentiate SSLs and microvesicular hyperplastic polyps from goblet cell-rich hyperplastic polyps. Endosc Int Open 2024; 12: E1251-E1259
- 17 Toyoshima O, Nishizawa T, Yoshida S. et al. Hemorrhoids as a risk factor for colorectal adenomas on colonoscopy. Endosc Int Open 2023; 11: E497-E503
- 18 Ell C, Fischbach W, Bronisch HJ. et al. Randomized trial of low-volume PEG solution versus standard PEG + electrolytes for bowel cleansing before colonoscopy. Am J Gastroenterol 2008; 103: 883-893
- 19 Halphen M, Heresbach D, Gruss HJ. et al. Validation of the Harefield Cleansing Scale: a tool for the evaluation of bowel cleansing quality in both research and clinical practice. Gastrointest Endosc 2013; 78: 121-131
- 20 Barclay RL, Vicari JJ, Doughty AS. et al. Colonoscopic withdrawal times and adenoma detection during screening colonoscopy. N Engl J Med 2006; 355: 2533-2541
- 21 Nishizawa T, Sakitani K, Suzuki H. et al. Adverse events associated with bidirectional endoscopy with midazolam and pethidine. J Clin Biochem Nutr 2020; 66: 78-81
- 22 Nishizawa T, Suzuki H, Sagara S. et al. Dexmedetomidine versus midazolam for gastrointestinal endoscopy: a meta-analysis. Dig Endosc 2015; 27: 8-15
- 23 Oh CK, Cho YW, Jung J. et al. Comparison of cold snare endoscopic mucosal resection and hot snare endoscopic mucosal resection for small colorectal polyps: a randomized controlled trial. Sci Rep 2024; 14: 20335
- 24 Bretthauer M, Aabakken L, Dekker E. et al. Requirements and standards facilitating quality improvement for reporting systems in gastrointestinal endoscopy: European Society of Gastrointestinal Endoscopy (ESGE) Position Statement. Endoscopy 2016; 48: 291-294
- 25 Nishizawa T, Sakitani K, Suzuki H. et al. Small-caliber endoscopes are more fragile than conventional endoscopes. Endosc Int Open 2019; 7: E1729-E1732
- 26 Toyoshima O, Yoshida S, Nishizawa T. et al. Simple feedback of colonoscopy performance improved the number of adenomas per colonoscopy and serrated polyp detection rate. Endosc Int Open 2021; 9: E1032-E1038
- 27 Toyoshima O, Nishizawa T, Yoshida S. et al. Expert endoscopists with high adenoma detection rates frequently detect diminutive adenomas in proximal colon. Endosc Int Open 2020; 8: E775-E782
- 28 Toyoshima O, Yoshida S, Nishizawa T. et al. CF290 for pancolonic chromoendoscopy improved sessile serrated polyp detection and procedure time: a propensity score-matching study. Endosc Int Open 2019; 7: E987-e993
- 29 Toyoshima O, Nishizawa T, Hiramatsu T. et al. Colorectal adenoma detection rate using texture and color enhancement imaging versus white light imaging with chromoendoscopy: a propensity score matching study. J Gastroenter Hepatol 2024; 39: 2105-2111
- 30 Karsenti D, Tharsis G, Burtin P. et al. Adenoma and advanced neoplasia detection rates increase from 45 years of age. World J Gastroenterol 2019; 25: 447-456
- 31 Yun GY, Eun HS, Kim JS. et al. Colonoscopic withdrawal time and adenoma detection in the right colon. Medicine (Baltimore) 2018; 97: e12113
- 32 Warren JL, Klabunde CN, Mariotto AB. et al. Adverse events after outpatient colonoscopy in the Medicare population. Ann Intern Med 2009; 150: 849-857
- 33 Ko CW, Riffle S, Michaels L. et al. Serious complications within 30 days of screening and surveillance colonoscopy are uncommon. Clin Gastroenterol Hepatol 2010; 8: 166-173




