| Literature DB >> 27484810 |
Abstract
In Korea, gastric cancer screening, either esophagogastroduodenoscopy or upper gastrointestinal series (UGIS), is performed biennially for adults aged 40 years or older. Screening endoscopy has been shown to be associated with localized cancer detection and better than UGIS. However, the diagnostic sensitivity of detecting cancer is not satisfactory. The National Endoscopy Quality Improvement (QI) program was initiated in 2009 to enhance the quality of medical institutions and improve the effectiveness of the National Cancer Screening Program (NCSP). The Korean Society of Gastrointestinal Endoscopy developed quality standards through a broad systematic review of other endoscopic quality guidelines and discussions with experts. The standards comprise five domains: qualifications of endoscopists, endoscopic unit facilities and equipment, endoscopic procedure, endoscopy outcomes, and endoscopic reprocessing. After 5 years of the QI program, feedback surveys showed that the perception of QI and endoscopic practice improved substantially in all domains of quality, but the quality standards need to be revised. How to avoid missing cancer in endoscopic procedures in daily practice was reviewed, which can be applied to the mass screening endoscopy. To improve the quality and effectiveness of NCSP, key performance indicators, acceptable quality standards, regular audit, and appropriate reimbursement are necessary.Entities:
Keywords: Endoscopy; Mass screening; Quality; Stomach neoplasms
Year: 2016 PMID: 27484810 PMCID: PMC4977749 DOI: 10.5946/ce.2016.084
Source DB: PubMed Journal: Clin Endosc ISSN: 2234-2400
Sensitivity to Detect Gastric Cancer by Endoscopy in the National Cancer Screening Program of Korea and Japan
| Country | Time period | Population | <3 Years miss rate, n (%) | Positive predictive value, % (95% CI) | Sensitivity, % (95% CI) | Specificity, % (95% CI) | Study design |
|---|---|---|---|---|---|---|---|
| Korea [ | 2002–2005 | 765,813 | 1,093/3,498 (40) | 6.2 (6.0–6.4) | 69.0 (66.3–71.8) | 96.0 (95.8–96.2) | Screening |
| Japan [ | 1990–1995 | 51,411 | 188/730 (25.8) | 88.6 (69.8–97.6)[ | Retrospective |
CI, confidence interval.
It was calculated be incidence method in prevalence screening.
Quality Criteria of EGD in the National Quality Improvement Program of Screening Endoscopy [3]
| Criteria for ‘qualification of endoscopist’ |
| 1. Qualification of endoscopists performing EGD |
| 1) Is the endoscopist a specialist who is able to perform EGD? |
| 2) Did the endoscopist receive endoscopy training for more than 1 year after becoming a medical specialist? |
| 2. Continuous medical education for EGD (one point per 1 hour education) |
| Criteria for ‘process’ |
| 1. Are fasting state, general health status, and past medical and medication history of the patients checked before the EGD? |
| 2. Has the patient received explanations for the necessity, notabilia, and any complications of EGD? |
| Or have they been asked to sign informed consent? |
| 3. Is the patient’s status monitored and recorded during the EGD? |
| 4. Is endoscopic biopsy performed in order to verify any suspicious lesions? |
| 5. Are retroflexed or close observations of the EGD made in order to have more precise observation for the suspicious lesion? |
| 6. Is the EGD inserted thoroughly into the duodenum and photo documentation of the second part of the duodenum obtained at all times? |
| 7. Are the instruments for emergency resuscitation or therapeutic endoscopy available in case of any complications? |
| 8. Does the EGD report include information about the location, shape, and size of sighted polyps/cancerous lesions? |
| 9. Are the results of the EGD preserved as digital files or photo documents? |
| 10. Is informed consent for conscious sedative endoscopy obtained? |
| 11. Are SaO2 and heart rate monitored during conscious sedative endoscopy? |
| 12. Is the patient managed based on discharge criteria when leaving the endoscopy unit after conscious sedative endoscopy? |
| Criteria for ‘facility and equipment’ |
| 13. Are the cardia and fundus observed clearly with the retroflexed vision of the EGD from the gastric angle? |
| 14. Are there endoscopy examination rooms for EGDs separate from those at the outpatient clinic? |
| 15. Do you maintain a specimen reception registry for EGD? |
| 16. Do you maintain a medication administration registry for EGD? |
| Criteria for ‘outcome’ |
| 17. Is the date of examination precisely recorded in the EGD report? |
| 18. Is the registration number precisely recorded in the EGD report? |
| 19. Is the name of the endoscopist precisely recorded in the EGD report? |
| 20. Is the presence of medication usage (e.g., anesthetics, analgesics, and sedatives) precisely recorded in the EGD report? |
| 21. Is the presence of biopsy tests precisely recorded in the EGD report? |
| 22. Are the EGD findings precisely recorded in the EGD report? |
| 23. Is the endoscopic diagnosis precisely recorded in the EGD report? |
| 24. Is the Helicobacter pylori infection test performed in cases of gastric or duodenal ulcer? |
| 25. Do endoscopists attend endoscopy quality education or does your hospital have such a program? |
| Criteria for ‘reprocessing’ |
| Is the reprocessing process followed by the ‘endoscopy cleansing and disinfection guidelines of Korean Society of Gastrointestinal Endoscopy’? |
| 26. Is the precleaning and cleaning process completely performed? |
| 27. Is the endoscopy channel brushed repeatedly during the reprocessing process? |
| 28. Are all detachable parts including valves and rubber cap separated from the endoscope and exchanged for every examination? |
| 29. Are the disinfectant solutions changed optimally according to recommended cycles of the disinfectant solution manufacturer? |
| 30. Is the soaking time obeyed according to the guidelines of the disinfectant solution manufacturer? |
| 31. Are the reusable components and accessories disinfected? |
| 32. Do the clinicians, nurses, and cleansing staff attend the endoscopy cleansing and disinfection education of the ‘Korean Society of |
| Gastrointestinal endoscopy’? |
| 33. Is the reprocessing room and equipment available? |
| 34. Optimal keeping of the endoscope after the reprocessing process |
| 1) Is the endoscope hung vertically after the reprocessing process? |
| 2) Is the endoscope reprocessed just before the first examination of the next day? |
EGD, esophagogastroduodenoscopy.
Improvement in the Current Endoscopic Quality Standards
| Performance target is focusing to meet minimum standard requirement, rather than high quality endoscopic service |
| The priority outcomes measurement is not defined |
| e.g., Whether prophylactic antibiotics are administered for appropriate indication[ |
| Evidence based studies are required to support the use of indicators |
| The indicators measuring patient’s satisfaction are necessary |
| The after-procedure outcome measurement is necessary |
| e.g., Documentation of adverse events[ |
| Communication with referring physicians[ |
| Documentation of follow-up |
Examples of American Society of Gastrointestinal Endoscopy quality measurement.
Limiting Factors and Suggestions to Minimize Missing Cancer in Screening Endoscopy in Daily Practice
| Limiting factor | Suggestion |
|---|---|
| Technical limitations in endoscopy technique and lesion recognition | |
| To reduce endoscopists’ errors | Specially trained endoscopists. |
| Continuous medical education | |
| Adequate supervision of trainees | |
| To reduce sampling errors | Multiple biopsies |
| Proper sampling | |
| More meticulous endoscopy | Increase patient tolerance (e.g., adequate sedation) |
| To increase lesion recognition | Mucolytics to improve mucosal visibility |
| Longer procedure time | |
| Extensive photographic documentation | |
| After-procedure errors | Appropriate follow-up schedule |
| Notification to patients | |
| Pathologists’ errors |