Colon Capsule Endoscopy (CCE)

LCD Information Document Information Source LCD ID N/A LCD ID L38755 Original ICD-9 LCD ID Not Applicable LCD Title Colon Capsule Endoscopy (CCE) Proposed LCD in Comment Period N/A Source Proposed LCD DL38755 Opens in a new window Original Effective Date For services performed on or after 04/12/2021 Revision Effective Date N/A Revision Ending Date N/A Retirement Date N/A Notice Period Start Date 02/25/2021 Notice Period End Date 04/11/2021 CPT codes, descriptions, and other data only are copyright 2025 American Medical Association. All Rights Reserved. Fee schedules, relative value units, conversion factors and/or related components are not assigned by the AMA, are not part of CPT, and the AMA is not recommending their use. The AMA does not directly or indirectly practice medicine or dispense medical services. The AMA assumes no liability for data contained or not contained herein. CPT is a registered trademark of the American Medical Association. 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Issue Issue Description Issue - Explanation of Change Between Proposed LCD and Final LCD CMS National Coverage Policy This Local Coverage Determination (LCD) supplements but does not replace, modify or supersede existing Medicare applicable National Coverage Determinations (NCDs) or payment policy rules and regulations for colon capsule endoscopy (CCE). Federal statute and subsequent Medicare regulations regarding provision and payment for medical services are lengthy. They are not repeated in this LCD. Neither Medicare payment policy rules nor this LCD replace, modify or supersede applicable state statutes regarding medical practice or other health practice professions acts, definitions and/or scopes of practice. All providers who report services for Medicare payment must fully understand and follow all existing laws, regulations and rules for Medicare payment for CCE and must properly submit only valid claims for them. Please review and understand them and apply the medical necessity provisions in the policy within the context of the manual rules. Relevant Centers for Medicare and Medicaid Services (CMS) manual instructions and policies may be found in the following Internet-Only Manuals (IOMs) published on the CMS website. Title XVIII of the Social Security Act, §1862(a)(1)(A) states that no Medicare payment shall be made for items or services which are not reasonable and necessary for the diagnosis or treatment of illness or injury Title XVIII of the Social Security Act, §1862(a)(7) excludes routine physical examinations 42 CFR §410.32 Diagnostic x-ray tests, diagnostic laboratory tests, and other diagnostic tests: Conditions 42 CFR §410.33 Independent diagnostic testing facility 42 CFR §414.510 Laboratory date of service for clinical laboratory and pathology specimens CMS Internet-Only Manual, Pub. 100-03, Medicare National Coverage Determinations (NCD) Manual, Chapter 1, Part 4, §210.3 Colorectal Cancer Screening Tests CMS Internet-Only Manual, Pub. 100-08, Medicare Program Integrity Manual, Chapter 13, §13.5.4 Reasonable and Necessary Provision in an LCD Coverage Indications, Limitations, and/or Medical Necessity Compliance with the provisions in this policy may be monitored and addressed through post payment data analysis and subsequent medical review audits. History/Background and/or General Information Colon capsule endoscopy (CCE) is a noninvasive procedure that does not require air inflation or sedation and allows for minimally invasive and painless colonic evaluation. CCE utilizes a tiny wireless camera that takes pictures of the gastrointestinal tract. The wireless camera is housed inside a vitamin-sized capsule that is swallowed with water. As the capsule travels through the digestive tract, the camera system takes pictures. The images are then transmitted to a computer with special software where the images are strung together to create a video. The provider reviews the video to look for any abnormalities within the gastrointestinal tract. Covered Indications Diagnostic/surveillance, when performed for signs and symptoms of disease CCE, is medically necessary when EITHER of the following criteria are met: 1. Primary procedure in patients with major risks for Optical Colonoscopy (OC) or moderate sedation as indicated from an evaluation of the patient by a board certified or board eligible gastroenterologist, a surgeon trained in endoscopy, or a physician with equivalent endoscopic training when EITHER of the following criteria are met3: Fecal Occult Blood Test (FOBT) positive (guaiac or immunochemical); OR Multitarget Stool DNA (sDNA) Test positive; OR Other evidence of lower GI bleeding in hemodynamically stable patients 2. Secondary procedure: For the detection or surveillance of colon polyp(s) if the diagnostic OC was incomplete OR When an incomplete diagnostic OC was performed for either: Fecal Occult Blood Test (FOBT) positive (guaiac or immunochemical) OR Multitarget Stool DNA (sDNA) Test positive OR Other evidence of lower GI bleeding in hemodynamically stable patients Limitations The following are considered not medically reasonable and necessary: Patients with known or suspected gastrointestinal obstruction, stricture, or fistula Patients with a cardiac pacemaker or another implanted electro-medical device that emits a radiofrequency or other interfering signal Patients with swallowing disorder(s) Patients with a known contraindication or allergy to any medication or preparation agent used before or during the procedure CCE performed in conjunction with Computed Tomographic Colonography (CTC) CCE performed for screening, regardless of family history or other risk factors for the development of colonic disease Notice: Services performed for any given diagnosis must meet all of the indications and limitations stated in this policy, the general requirements for medical necessity as stated in CMS payment policy manuals, any and all existing CMS NCDs, and all Medicare payment rules. The redetermination process may be utilized for consideration of services performed outside of the reasonable and necessary requirements in this LCD. Summary of Evidence Clinical Literature PillCam™ COLON 2 is a capsule endoscopy device. The first-generation device had low sensitivity and specificity for polyps in the colon, however, a second-generation device received United States (U.S.) Food and Drug Administration (FDA) clearance in January 2014 and expanded use in January 2016.1,2 The improved design is slightly bigger with 2 cameras and an increased angle of view, allowing nearly 360-degree coverage of the colon. The capsule battery lasts 10 hours with a slower frame rate. Improvements in software allow estimation of polyp size and improved mucosal surface evaluation. Unless indicated, a reference to CCE is specific to the second-generation device. Both FDA indications are specific to colon polyp detection, but whereas the original was restricted to use as a secondary procedure after failed OC, the expanded indication included use as a primary procedure in patients at major risk for colonoscopy or moderate sedation, and with evidence of lower GI bleeding. The pivotal trial that led to FDA clearance was a prospective blinded study of 884 asymptomatic patients classified as average colorectal cancer (CRC) risk.4 Technical failures (short transit time plus poor preparation) occurred in 9% of patients. The authors conclude based on polyp detection sensitivity and specificity data that: “capsule performance seems adequate for patients who cannot undergo colonoscopy or who had incomplete colonoscopies.” Two studies comparing CCE to CTC demonstrated at least non-inferiority in terms of sensitivity and specificity.5,6 One found improved sensitivity and specificity for CCE, but both studies had methodological flaws with low-quality evidence. The advantages of CTC include the ability to use when obstruction or stricture is a concern and to obtain visualization of other abdominal structures. Advantages to CCE are the lack of radiation exposure and direct visualization of colorectal mucosa. Patient preference and availability of the technology also may play a role in test selection. Several studies have shown that CCE sensitivity and specificity remain high in the detection of polyps in positive FOBT patients.5,7,8 FOBT sensitivity for small adenomas is reported to be 7% , so the majority in these cases will not need a referral to OC if the CCE is adequate and negative.9 The authors generally conclude that in patients at high risk for OC or who have incomplete OC, CCE may be a reasonable alternative. Several studies included FOBT positive patients, among other indications (e.g., melena), but did not stratify results.10-12 Rex, et al.4 2015, is a prospective blinded study of 884 patients classified as average risk. There were 695 of the 884 patients that underwent CCE followed by screening OC. According to the findings, “Capsule colonography identified subjects with 1 or more polyps 6 mm or larger with 81% sensitivity (95% confidence interval [CI], 77%-84%) and 93% specificity (95% CI, 91%-95%), and polyps 10 mm or larger with 80% sensitivity (95% CI, 74%-86%) and 97% specificity (95% CI, 96%-98%). Capsule colonoscopy identified subjects with 1 or more conventional adenomas 6 mm or larger with 88% sensitivity (95% CI, 82%-93) and 82% specificity (95% CI, 80%-83%), and 10 mm or larger with 92% sensitivity (95% CI, 82%-97%) and 95% specificity (95% CI, 94%-95%). Sessile serrated polyps and hyperplastic polyps accounted for 26% and 37% respectively, of false negative findings from capsule analyses” and resulted in 1 missed malignancy. In per segment analysis, right colon sensitivity was lower than left colon (72% compared to 88% respectively). The study is strengthened by blinding, large sample size, and screening population. Study results may be impacted by allocation bias due to non-consecutive enrollment. Sessile serrated and hyperplastic polyps showed reduced sensitivity with CCE and this technology may not be reliable for detection. These types of polyps are also more difficult to detect on OC and CTC. There were no serious adverse events. Rondonotti, et al.5 2014, is a pilot study of 50 patients with a positive immunochemical fecal occult blood tests (iFOBTs-positive) who underwent CCE, CTC and OC. According to the findings “CTC identified the polyps with 88.2% sensitivity, 84.8% specificity, a 3.0 positive likelihood ratio, and a 0.07 negative likelihood ratio. PillCam™ COLON 2 identified the polyps with 88.2% sensitivity, 87.8% specificity, a 3.75 positive likelihood ration, and a 0.06 negative likelihood ratio.” The study demonstrates performance of CCE in a population with fecal occult positive results. The study results may be impacted by the small sample size and high risk of bias. There were no serious adverse events. Spada, et al.6 2015, is a prospective single-blinded study of 100 patients with a previous incomplete colonoscopy. There were 97 of 100 patients enrolled consecutively that underwent CCE and CTC on the same day. According to the findings, “CCE and CTC were able to achieve complete colonic evaluation in 98% of cases. In a per-patient analysis for polyps ≥6 mm, CCE detected 24 patients (24.5%) and CTC 12 patients (12.2%). The relative sensitivity of CCE compared to CTC was 2.0 (95% CI, 1.34 to 2.98), indicating a significant increase in sensitivity for lesions ≥6 mm. Of larger polyps (≥10 mm), these values were 5.1% for CCE and 3.1% for CTC (relative sensitivity: 1.67 (95% CI, 0.69 to 4.00)). Positive predictive values for polyps ≥6 mm and ≥10 mm were 96% and 85.7%, and 83.3% and 100% for CCE and CTC, respectively. No missed cancer occurred at clinical follow-up of a mean of 20 months.” The study demonstrates utility of the test in a population of patients with incomplete colonoscopies. Analysis demonstrates non-inferiority between CCE and CTC. The study is strengthened by a blinded cohort and consecutive enrollment. Patients received both studies for comparison purposes; however, if the results were negative, OC was not performed so false negatives could not be excluded. There were no serious adverse events. Holleran, et al.7 2014, is a comparative cohort study of 62 screening patients who had positive iFOBTs. All the patients had complete studies with both CCE and OC. According to the findings, “OC detected at least 1 polyp in 36 participants (58%), significant lesions in 18 (29%), and cancer in 1 (2%). There was good correlation between CCE and OC for any lesion and for significant lesions (r=0.62 and 0.84, respectively). The negative predictive value of CCE was high both for any polyp (90%) and for significant lesions (96%).” Kobaek-Larsen, et al.8 2018, is a comparative cohort study of 253 patients who had positive iFOBTs. There were 126 out of 253 patients that had complete studies with both CCE and OC. According to the findings “The polyp detection rate was significantly higher in CCE compared with colonoscopy (P=0.02) in the complete study group. The per-patient sensitivity for the entire population for >9 mm polyps for CCE and colonoscopy was 87% (95% CI: 83-91%) and 88% (95% CI: 84-92%) respectively. One malignancy was missed in the incomplete study group and was found on colonoscopy.” The study demonstrates performance of CCE in a population with fecal occult positive test results. The high rate of incomplete studies was attributed to the lack of booster in bowel prep. The study result may be impacted by small sample size and high risk of bias. There were 2 bowel perforations in the colonoscopy group. Multiple international papers reported similar findings for sensitivity and specificity.13-16 The completion rate was found to be lower than OC, and incomplete studies (range from 0-46%) were more likely to miss malignancies.8 CCE performance was less accurate than OC, confirming that OC remains the preferred testing modality. A 2015 Health Quality Ontario meta-analysis on CCE for the detection of colorectal polyps included 5 studies that evaluated CCE with a pooled total of 357 subjects.17 It found an 87% sensitivity and 76% specificity for 6 mm polyps and 89% sensitivity and 91% specificity for 10 mm polyps, which was described as good sensitivity and specificity. The analysis did not include papers published after 2014. A 2016 meta-analysis with 2,420 subjects reported the following: for polyps > 6 mm: 86% (82%-89%) sensitivity and 88% (74%-95%) specificity. For polyps > 10 mm: 87% (81%-91%) sensitivity and 95% (92%-98%) specificity.18 The consistency in the findings among the studies over an 8-year period, and improved sample size and design in the more recent studies, improve the overall quality of the data from the earlier assessments. Limitations of the technology include poor sensitivity for sessile polyps and a high rate of incomplete studies. Systematic Reviews A 2018 ECRI Technology assessment rates evidence as “somewhat favorable” and concludes: “Evidence from 2 systematic reviews indicates CCE can detect polyps in patients unable or unwilling to undergo colonoscopy or who had an incomplete colonoscopy”.20 Studies also indicate CCE related adverse events (AEs) are rare. The ECRI report also reviewed FDA Manufacturer and User Facility Device Experience (MAUDE) reports, which was consistent with the literature in terms of adverse events and safety profile; the most common complication is capsule retention. A 2019 Hayes technology assessment assigns CCE a “C” rating for use in diagnosis and surveillance of adults with signs or symptoms of colorectal cancer and risk factors for the disease.21 It concludes: “CCE may be a suitable alternative for patients who cannot tolerate or refuse to undergo conventional colonoscopy (CC) and for patients with an incomplete CC.” The rating was downgraded due to paucity of evidence regarding the clinical utility of CCE for this indication. The report calls for further studies to determine the accuracy of CCE versus CTC. The American Society for Gastrointestinal Endoscopy (ASGE) U.S. Multi-Society Task Force (MSTF) on CRC recommends CCE as “an appropriate screening test when patients decline colonoscopy, fecal immunochemical test (FIT), FIT-fecal DNA, CTC, and flexible sigmoidoscopy” (weak recommendation, low-quality evidence).22 Analysis of Evidence (Rationale for Determination) Based on the clinical literature and systematic review results, combined with the consistent positive safety profile, sensitivity and specificity of CCE in detecting polyps ≥6 mm, the evidence supports the recommendation that CCE is an alternative to OC or CTC as a primary procedure in patients with major risks for OC or moderate sedation or as a secondary procedure for surveillance of colon polyp(s) in previously diagnosed patients where diagnostic OC was incomplete or was contraindicated. In addition, CCE may be useful as a secondary procedure when an incomplete diagnostic OC was performed for either fecal occult blood test (FOBT) positive (guaiac or immunochemical), for multi-target stool DNA (sDNA) test positive, or other evidence of lower GI bleeding in hemodynamically stable patients.

Compliance with the provisions in this policy may be monitored and addressed through post payment data analysis and subsequent medical review audits. History/Background and/or General Information Colon capsule endoscopy (CCE) is a noninvasive procedure that does not require air inflation or sedation and allows for minimally invasive and painless colonic evaluation. CCE utilizes a tiny wireless camera that takes pictures of the gastrointestinal tract. The wireless camera is housed inside a vitamin-sized capsule that is swallowed with water. As the capsule travels through the digestive tract, the camera system takes pictures. The images are then transmitted to a computer with special software where the images are strung together to create a video. The provider reviews the video to look for any abnormalities within the gastrointestinal tract. Covered Indications Diagnostic/surveillance, when performed for signs and symptoms of disease CCE, is medically necessary when EITHER of the following criteria are met: 1. P rimary procedure in patients with major risks for Optical Colonoscopy (OC) or moderate sedation as indicated from an evaluation of the patient by a board certified or board eligible gastroenterologist, a surgeon trained in endoscopy, or a physician with equivalent endoscopic training when EITHER of the following criteria are met 3 : Fecal Occult Blood Test (FOBT) positive (guaiac or immunochemical); OR M ultitarget Stool DNA (sDNA) Test positive; OR Other evidence of lower GI bleeding in hemodynamically stable patients 2. S econdary procedure: For the detection or surveillance of colon polyp(s) if the diagnostic OC was incomplete OR When an incomplete diagnostic OC was performed for either: Fecal Occult Blood Test (FOBT) positive (guaiac or immunochemical) OR Multitarget Stool DNA (sDNA) Test positive OR Other evidence of lower GI bleeding in hemodynamically stable patients Limitations The following are considered not medically reasonable and necessary: Patients with known or suspected gastrointestinal obstruction, stricture, or fistula Patients with a cardiac pacemaker or another implanted electro-medical device that emits a radiofrequency or other interfering signal Patients with swallowing disorder(s) Patients with a known contraindication or allergy to any medication or preparation agent used before or during the procedure CCE performed in conjunction with Computed Tomographic Colonography (CTC) CCE performed for screening, regardless of family history or other risk factors for the development of colonic disease Notice: Services performed for any given diagnosis must meet all of the indications and limitations stated in this policy, the general requirements for medical necessity as stated in CMS payment policy manuals, any and all existing CMS NCDs, and all Medicare payment rules. The redetermination process may be utilized for consideration of services performed outside of the reasonable and necessary requirements in this LCD.