| Literature DB >> 33269319 |
Venkat Nutalapati1, Madhav Desai2, Vivek Sandeep Thoguluva-Chandrasekar1, Mojtaba Olyaee1, Amit Rastogi1.
Abstract
Background and study aims The adenoma detection rate (ADR) is an important quality metric of colonoscopy. Higher ADR correlates with lower incidence of interval colorectal cancer. ADR is variable between endoscopists and depends upon the withdrawal technique amongst other factors. Dynamic position change (lateral rotation of patients with a view to keep the portion of the colon being inspected at a higher level) helps with luminal distension during the withdrawal phase. However, impact of this on ADR is not known in a pooled sample. We performed a systematic review and meta-analysis to study the impact of dynamic position changes during withdrawal phase of colonoscopy on ADR Methods A comprehensive search of MEDLINE, EMBASE, Google Scholar, and the Cochrane Database was conducted from each database's inception to search for studies comparing dynamic position changes during colonoscope withdrawal with static left lateral position (control). The primary outcome of interest was ADR. Other studied outcomes were polyp detection rate (PDR) and withdrawal time. Outcomes were reported as pooled odds ratio (OR) with 95 % confidence intervals (CI) with statistical significance ( P < 0.05). RevMan 5.3 software was used for statistical analysis. Results Six studies were included in our analysis with 2860 patients. Of these, dynamic position change was implemented in 1177 patients while 1183 patients served as the controls. ADR was significantly higher in the dynamic position change group with pooled OR 1.36 (95 % CI, 1.15-1.61; P < 0.01). There was low heterogeneity in inclusion studies (I 2 = 0 %). PDR was numerically higher in position change group (53.4 % vs 49.6 %) but not statistically significant ( P = 0.16). Mean withdrawal time did not significantly change with dynamic position change (12.43 min vs 11.46 min, P = 0.27). Conclusion Position change during the withdrawal phase of colonoscopy can increase the ADR compared to static left lateral position. This is an easy and practical technique that can be implemented to improve ADR. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commecial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/).Entities:
Year: 2020 PMID: 33269319 PMCID: PMC7671762 DOI: 10.1055/a-1265-6634
Source DB: PubMed Journal: Endosc Int Open ISSN: 2196-9736
PRISMA checklist.
| Section/topic | # | Checklist item | Reported on page # |
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| Title | 1 | Identify the report as a systematic review, meta-analysis, or both. | 1 |
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| Structured summary | 2 | Provide a structured summary including, as applicable: background; objectives; data sources; study eligibility criteria, participants, and interventions; study appraisal and synthesis methods; results; limitations; conclusions and implications of key findings; systematic review registration number. | 1 |
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| Rationale | 3 | Describe the rationale for the review in the context of what is already known. | 2 |
| Objectives | 4 | Provide an explicit statement of questions being addressed with reference to participants, interventions, comparisons, outcomes, and study design (PICOS). | 2 |
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| Protocol and registration | 5 | Indicate if a review protocol exists, if and where it can be accessed (e. g., Web address), and, if available, provide registration information including registration number. | 3 |
| Eligibility criteria | 6 | Specify study characteristics (e. g., PICOS, length of follow-up) and report characteristics (e. g., years considered, language, publication status) used as criteria for eligibility, giving rationale. | 3 |
| Information sources | 7 | Describe all information sources (e. g., databases with dates of coverage, contact with study authors to identify additional studies) in the search and date last searched. | 3 |
| Search | 8 | Present full electronic search strategy for at least one database, including any limits used, such that it could be repeated. | 3 |
| Study selection | 9 | State the process for selecting studies (i. e., screening, eligibility, included in systematic review, and, if applicable, included in the meta-analysis). | 3 |
| Data collection process | 10 | Describe method of data extraction from reports (e. g., piloted forms, independently, in duplicate) and any processes for obtaining and confirming data from investigators. | 3 |
| Data items | 11 | List and define all variables for which data were sought (e. g., PICOS, funding sources) and any assumptions and simplifications made. | 3 |
| Risk of bias in individual studies | 12 | Describe methods used for assessing risk of bias of individual studies (including specification of whether this was done at the study or outcome level), and how this information is to be used in any data synthesis. | 5 |
| Summary measures | 13 | State the principal summary measures (e. g., risk ratio, difference in means). | 5 |
| Synthesis of results | 14 | Describe the methods of handling data and combining results of studies, if done, including measures of consistency (e. g., I 2 ) for each meta-analysis. | 5 |
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| Risk of bias across studies | 15 | Specify any assessment of risk of bias that may affect the cumulative evidence (e. g., publication bias, selective reporting within studies). | 5 |
| Additional analyses | 16 | Describe methods of additional analyses (e. g., sensitivity or subgroup analyses, meta-regression), if done, indicating which were pre-specified. | 5 |
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| Study selection | 17 | Give numbers of studies screened, assessed for eligibility, and included in the review, with reasons for exclusions at each stage, ideally with a flow diagram. | 5 |
| Study characteristics | 18 | For each study, present characteristics for which data were extracted (e. g., study size, PICOS, follow-up period) and provide the citations. | 5 |
| Risk of bias within studies | 19 | Present data on risk of bias of each study and, if available, any outcome level assessment (see item 12). | 5 |
| Results of individual studies | 20 | For all outcomes considered (benefits or harms), present, for each study: (a) simple summary data for each intervention group (b) effect estimates and confidence intervals, ideally with a forest plot. | 5 |
| Synthesis of results | 21 | Present results of each meta-analysis done, including confidence intervals and measures of consistency. | 5 |
| Risk of bias across studies | 22 | Present results of any assessment of risk of bias across studies (see Item 15). | 5 |
| Additional analysis | 23 | Give results of additional analyses, if done (e. g., sensitivity or subgroup analyses, meta-regression [see Item 16]). | 5 |
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| Summary of evidence | 24 | Summarize the main findings including the strength of evidence for each main outcome; consider their relevance to key groups (e. g., healthcare providers, users, and policy makers). | 5 |
| Limitations | 25 | Discuss limitations at study and outcome level (e. g., risk of bias), and at review-level (e. g., incomplete retrieval of identified research, reporting bias). | 6 |
| Conclusions | 26 | Provide a general interpretation of the results in the context of other evidence, and implications for future research. | 6 |
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| Funding | 27 | Describe sources of funding for the systematic review and other support (e. g., supply of data); role of funders for the systematic review. | None (1) |
Fig. 1Flowchart.
Study characteristics, patient demographics.
| Study | Study design | Jadad score | Bowel preparation | Patients (male) | Regions of examination | Country | Position changes |
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East et al
| Randomized cross‐over study | 3 | Good, Adequate | 70 | Cecum to descending colon | UK | Cecum, ascending colon, and hepatic flexure: left lateral position; transverse colon: supine position; splenic flexure and descending colon: right lateral position |
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Köksal et al
| Randomized cross‐over study | 2 | NA | 50 | Cecum to sigmoid colon | Turkey | Cecum, ascending colon and hepatic flexure; transverse colon; and splenic flexure, descending colon and sigmoid colon. The first region was examined in the left lateral position twice. The second region was examined in the left lateral and supine positions. The third region was examined in the left lateral, right lateral and supine positions |
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Yamaguchi et al
| Randomized parallel‐group study | 2 | NA | 98 | Cecum to rectum | Japan | Examination in the supine position was followed by either the following dynamic position changes (cecum to transverse colon, supine; splenic flexure and descending colon, right lateral; sigmoid colon, supine; and rectum, left lateral) or minimal position changes (cecum to sigmoid colon, supine; and rectum, left lateral) |
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Ball et al
| Randomized cross‐over study | 1 | NA | 130 | Cecum to descending colon | UK | The position change was left lateral position for examination of the right side of the colon(cecum, ascending colon, and hepatic flexure) and right lateral position for examination of the left side of the colon(splenic flexure and descending colon but not including the sigmoid colon). |
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Ou et al
| Randomized parallel‐group study | 3 | Fair, good and excellent | 355 | Ascending colon to rectum | Canada | Ascending colon/hepatic flexure examined in left lateral decubitus position, transverse colon in supine position, and splenic flexure/descending colon/sigmoid colon/rectum in right lateral decubitus position |
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Lee et al
| Randomized multicenter parallel-group study | 3 | Excellent, Good and Fair | 506 | Cecum to rectum | Korea | Cecum, ascending colon, and hepatic flexure: left lateral position; transverse colon: supine position; splenic flexure, descending colon, sigmoid colon, and rectum: right lateral position |
NA, not available.
Fig. 2Forest plot of ADR.
Fig. 3Forest plot of PDR.
Fig. 4Publication bias funnel plot.