Copyright
©2013 Baishideng Publishing Group Co.
World J Gastroenterol. Jun 28, 2013; 19(24): 3726-3746
Published online Jun 28, 2013. doi: 10.3748/wjg.v19.i24.3726
Published online Jun 28, 2013. doi: 10.3748/wjg.v19.i24.3726
Capsule device | Company | Country | Field of view (°) | Lens | LEDs | Image sensor | Transmission | Frames per second (fps) | Dimensions (mm) | Weight (g) | Battery life (h) | Real-time imager | FDA approval | Reviewing software | Optical enhancements |
PillCam®SB2 | Given®Imaging, Yokneam | Israel | 156 | Multi-element | 4 | CMOS | Radiofrequency | 2-41 | 11 × 26 | 3.45 | 9->11.52 | Yes | Yes | Rapid®v7 | Blue-mode FICE 1,2,3 |
MiroCam®v2 | IntroMedic® Co., Seoul | South Korea | 170 | N/A | 4 | CMOS | EFP | 3 | ø11 × 24 | 3.2 | 12 | Yes | Yes | MiroView®v2 | ALICE colour-mode |
EndoCapsule® | Olympus© Co., Tokyo | Japan | 145 | N/A | 4 | CCD | Radiofrequency | 2 | ø11 × 26 | 3.45 | 10 | Yes | Yes | OLYMPUS®WS-1 | Contrast imaging |
OMOM® (SmartCapsule) | Chongding Jinshan Science and Technology Co., Beijing | China | 140 | N/A | 4 | CCD | Radiofrequency | 2 (variable) | 13 × 27.9 | 6 | 8 | Yes | No | OMOM® workstation | N/A |
CapsoCam®SV1 | CapsoVision® Inc., Saratoga | United States | 360 | N/A | 16 | N/A | On-board EPROM flash memory (USB) | 16 (4 per camera) | 11 × 31 | N/A | 15 | No | No | CapsoView® | N/A |
Ref. | Country | Centre | Objective(s) | Study type | Design | CE type | Outcome(s) | Conclusion |
Hart-mann et al[7] | Germany | Single centre | Head-to-head evaluation of technical performance and DY of two CE systems (PillCam®SB vs EndoCapsule®) | Prospective | ►OGIB pts; | ►PillCam®SB (Given®Imaging, Yoqneam, Israel); | ►Pts enrolled: 40; | ►Statistically non-significant trend for EndoCapsule® to detect more bleeding sources in pts with suspected small-bowel bleeding than PillCam®SB; |
►Pts randomized to undergo 2 CEs using different CE in random order | ►CR: PillCam®SB 33/40 (82%); EndoCapsule® 40/40 (100%); P = NS; | |||||||
►Overall DY: PillCam®SB 26/50 (52%); EndoCapsule® 29/50 (58%); P = NS; | ||||||||
►Pts randomized to undergo 2 CEs using different CE in random order | ►DY (SB P2): PillCam®SB 22/50 (44%), EndoCapsule® 25/50 (50%), P = NS; | |||||||
►In all discordant SB P2findings (not detected by the PillCam®SB but detected by EndoCapsule®), PillCam®SB examinations were incomplete | ►This is (likely) due to the longer recording time with EndoCapsule® | |||||||
Cave et al[8] | United States | Multi-centre (4 centres) | Comparison of performance (DY in pts with OGIB): EndoCapsule®vs PillCam®SB | Prospective | ►OGIB pts; | ►EndoCapsule® (Olympus© America, Allentown, PA); | ►Pts with OGIB (transfused or with haematocrit < 31%) (males) or < 28% (females): 63; | ►Both devices are safe and have comparable DY within the previously reported range; |
►EndoCapsule® and PillCam®SB swallowed by each participant 40 min apart; | ►Available data 51/63; 9 pts excluded for technical reasons + 3 pts for protocol violation; | |||||||
►24 videos read as normal, 14 as abnormal (from both CEs). Disagreement occurred in 13; | ►Subjective difference in image quality favouring the EndoCapsule®; | |||||||
►Ingestion of CEs in randomized order; | ►PillCam®SB (Given®Imaging, Yoqneam, Israel) | ►No adverse events reported for either CE. Overall agreement: 38/51 (74.5%), κ = 0.48, P = 0.008; | ||||||
►Head-to-head comparison of CEs | Limitations: Although ingestion randomized, videos reading not blind (different shape of the image margin) | ►Lack of electromechanical interference between 2 different CE | ||||||
Kim et al[9] | South Korea | Single centre | Head-to-head evaluation of technical performance DY and of two capsule systems (PillCam®SB vs MiroCam®) | Prospective | ►Pts referred to CE for various indications; | ►MiroCam® (IntroMedic Co. Ltd., Seoul, South Korea); | ►Pts enrolled: 24; | ►MiroCam shows a longer operating time and a higher CR; |
►Each pt was randomly assigned to swallow 1 of 2 CEs, the second CE was swallowed once fluoroscopy indicated that first CE had reached the SB | ►Mean operating time: MiroCam® 702 min; PillCam®SB 446 min, P < 0.001; | |||||||
►CR: MiroCam® 20/24 (83%); PillCam®SB 14/24 (59%), P = 0.031; | ►Nevertheless, the 2 capsule systems showed comparable efficiency; | |||||||
►PillCam®SB (Given®Imaging, Yoqneam, Israel) | ►DY: MiroCam® 11/24 (45.8%); PillCam®SB 10/24 (41.7%), P = 1.0; | |||||||
►DY (additive of both capsules): 12/24 (50%); | ►Sequential capsule endoscopy with the MiroCam and PillCam SB produced slight (but NS) increase in DY | |||||||
►Concordance of findings among the two capsule systems 87.5%, κ = 0.74 | ||||||||
Pioche et al[10] | France | Multi-centre | Head-to-head evaluation of the diagnostic concordance (κ value): PillCam®SB SB2 vs MiroCam® | Prospective | ►OGIB pts; | ►MiroCam®; (IntroMedic Co. Ltd., Seoul, South Korea); | ►83 pts; drop-outs explained (10 technical issues), 73 pts/videos analysed; | ►MiroCam® showed a slightly higher DY, difference not statistically significant; |
►Each pt ingested 2 CEs at a 1 h interval in a random order; | ►31 concordant (-) ve cases (42.4%) and 30 concordant (+) ve cases (41.1%); | |||||||
►Satisfactory diagnostic concordance between the 2 systems (κ = 0.66); | ►The 2 CE systems showed comparable efficiency for the diagnosis of OGIB | |||||||
►Videos read in a random order by 2 experienced (> 200 CEs) readers; | ►PillCamSB2 (Given®Imaging, Yoqneam, Israel) | ►DY similar among the 2 CE systems(PillCam®SB 2 vs MiroCam®: 46.6% vs 56.2%, respectively; P = 0.02); | ||||||
►Image-by-image review of cases of disagreement between the readers was performed by 3 expert readers | ►SBTT longer with MiroCam®vs PillCam®SB (mean SBTT: 268 vs 234 min, < 0.05); | |||||||
►Reading time longer with MiroCam®vs PillCam®SB (mean reading time 40 vs 23 min, P < 0.05); | ||||||||
►(+) ve diagnosis obtained in 46.6% vs 56.2% of pts with PillCam®SB2 vs MiroCam®, respectively; | ||||||||
►PillCam®SB2 vs MiroCam®CEs identified 78.6% vs 95.2% of (+) ve cases, respectively, P = 0.02 | ||||||||
Dolak et al[11] | Austria | Single centre | Head-to-head comparison (MiroCam®vs EndoCapsule®) of: CR of SB examinations, DY in SB disease | Prospective | ►Pts referred to CE for various indications; | ►MiroCam® (IntroMedic Co. Ltd., Seoul, South Korea); | ►Pts enrolled: 50; | ►The two capsule endoscopy systems were not statistically different with regards to CR and DY; |
►Each pt was randomly assigned to swallow either MiroCam® first, followed by the EndoCapsule® 2 h later, or vice versa; | ►CR: MiroCam® 48/50 (96%) vs EndoCapsule® 45/50 (90%); P = 0.38; | |||||||
►DY in SB: MiroCam® 25/50 (50%) vs EndoCapsule® 24/50 (48%); P > 0.99; | ||||||||
►EndoCapsule® (Olympus America, Allentown, PA) | ►Concordance of findings among the two CE systems: 68%; κ = 0.50 | ►Moderate concordance, mainly caused by missed pathological findings (which affected both devices), needs consideration in clinical practice | ||||||
►All videos analysed by two investigators independently |
Ref. | Title | Search (start - end date) | Type | Subject | Data extractors | Total titles found | Titles entered meta-analysis | Individuals included | Outcome/conclusion |
Liao et al[13] | Indications, detection, completion, and retention rates of SBCE: A systematic review | 2000 - Jan 2009 | Systematic review of evidence base | Indications, DR, CR and RR of SBCE | 2 | 227 | 227 | 22753 Pts; 22840 CE | ►Most common indications: OGIB (66.0%); investigation of clinical symptoms (10.6%); definite/suspected CD (10.4%); |
►Pooled DRs for overall, OGIB, CD, neoplasia: 59.4%, 60.5%, 55.3%, 55.9%, respectively; | |||||||||
►Commonest cause for OGIB: angiodysplasia (50.0%); | |||||||||
►Pooled CRs (overall): 83.5%; breakdown 83.6% (OGIB), 85.4% (clinical symptoms), 84.2% (CD); | |||||||||
►Pooled RRs (overall): 1.4%; breakdown 1.2% (OGIB), 2.6% (clinical symptoms), 2.1% (CD); | |||||||||
►Hence, most common indication for SBCE is OGIB, with high DR and low RR; | |||||||||
►A relatively high RR is associated with definite/suspected CD and neoplasms | |||||||||
Marmo et al[17] | Meta-analysis: Capsule enteroscopy vs conventional modalities in diagnosis of SB diseases | Jan 1966 - Mar 2005 | Meta-analysis of diagnostic test accuracy | DY/safety of SBCE vs alternative modalities (PE, SBBaR or enteroclysis) in SB disease | 2 | 187 | 17 | 526 pts (289 OGIB and 237 CD) | ►17 studies (526 patients) met inclusion criteria; |
►Overall, the rate difference for SB disease (i.e., the absolute pooled difference in the rate of positive findings) of SBCE vs alternative modalities was 41% (95%CI: 35.6-45.9); | |||||||||
►For OGIB, 37% (95%CI: 29.6-44.1) for Crohn's disease 45% (95%CI: 30.9-58.0); | |||||||||
►Incomplete SBCE occurred in 13%, more often in OGIB (17%) than in pts with CD (8%) (P < 0.006); | |||||||||
►Adverse events: 29 pts (6%); | |||||||||
►Capsule retention more frequent in pts with CD (3% vs 1%, OR 4.37) | |||||||||
Triester et al[18] | A meta-analysis of the yield of CE compared to other diagnostic modalities in patients with OGIB | N/A - April 2005 | Meta-analysis of diagnostic test accuracy | IY (yield of CE-yield of comparative modality) and 95%CI of CE over comparative modalities | 2 | 80 | 14 | 396 CE-PE; 88 CE-SBBaR | ►14 studies (n = 396) compared DY CE vs PE in OGIB, 63% vs 28%, respectively (IY = 35%, P < 0.00001, 95%CI: 26%-43%); |
►For clinically significant findings (n = 376) DY was 56% (CE) vs 26% (PE), IY = 30%, P < 0.00001, 95%CI: 21%-38%; | |||||||||
►3 studies (n = 88) compared DY of CE vs SBBaR, 67% vs 8%, respectively (IY = 59%, P < 0.00001, 95%CI: 48%-70%); | |||||||||
►For clinically significant findings DY was 42% (CE) vs 6% (SBBaR); IY = 36%, P < 0.00001, 95%CI: 25%-48%; | |||||||||
►NNT to yield one additional clinically significant finding with CE over either modality: 3 (95%CI: 2-4); | |||||||||
►1 study compared DY (significant findings) of CE vs intraoperative enteroscopy (n = 42, IY = 0%, P = 1.0, 95%CI: -16%-16%); | |||||||||
►1 study compared DY (significant findings) of CE vs CT enteroclysis (n = 8, IY = 38%, P = 0.08, 95%CI: -4%-79%); | |||||||||
►1 study compared DY (significant findings) of CE vs mesenteric angiogram (n = 17, IY = -6%, P = 0.73, 95%CI: -39%-28%); | |||||||||
►1 study compared DY (significant findings) of CE vs SB MRI (n = 14, IY = 36%, P = 0.007, 95%CI: 10%-62%); | |||||||||
►CE-DY vs PE (vascular lesions): 36% vs 20% (IY = 16%, P < 0.00001, 95%CI: 9%-23%); | |||||||||
►CE-DY vs PE (inflammatory lesions): 11% vs 2% (IY = 9%, P = 0.0001, 95%CI: 5%-13%); | |||||||||
►CE-DY vs PE (tumours or "other" findings): no difference | |||||||||
Leighton et al[19] | Capsule endoscopy: A meta-analysis for use with OGIB and CD | N/A - April 2005 | Meta-analysis of diagnostic test accuracy | DY and safety of SBCE vs alternative modalities (PE, SBBaR or enteroclysis) in SB disease | 2 | 80 | 20 | 537 pts | ►CE superior to PE/SB radiography for diagnosing SB pathology in pts with OGIB (yield comparable to intraoperative endoscopy); |
►Incremental yield of CE over PE/SB radiography is > 30% for clinically significant findings, due to visualization of additional vascular, inflammatory lesions by CE; | |||||||||
►CE was also superior to SB radiography, C + IL, CT enterography, PE for diagnosing non-stricturing SBCD; | |||||||||
►Marked improvement in yield with the use of CE over all other methods in pts who had established CD and were evaluated for SB recurrence; | |||||||||
►Unknown whether these results will translate into improved pt outcomes with the use of CE vs alternate methods | |||||||||
Leighton et al[19] | Capsule endoscopy: A meta-analysis for use with OGIB and CD | N/A - April 2005 | Meta-analysis of diagnostic test accuracy | DY and safety of SBCE vs alternative modalities (PE, SBBaR or enteroclysis) in SB disease | 2 | 80 | 20 | 537 pts | ►CE superior to PE/SB radiography for diagnosing SB pathology in pts with OGIB (yield comparable to intraoperative endoscopy); |
►Incremental yield of CE over PE/SB radiography is > 30% for clinically significant findings, due to visualization of additional vascular, inflammatory lesions by CE; | |||||||||
►CE was also superior to SB radiography, C + IL, CT enterography, PE for diagnosing non-stricturing SBCD; | |||||||||
►Marked improvement in yield with the use of CE over all other methods in pts who had established CD and were evaluated for SB recurrence; | |||||||||
►Unknown whether these results will translate into improved pt outcomes with the use of CE vs alternate methods | |||||||||
Triester et al[20] | A meta-analysis of the yield of CE compared to other diagnostic modalities in patients with non-stricturing SB Crohn’s disease | N/A - Aug 2005 | Meta-analysis of diagnostic test accuracy | 2 | 82 | 9 | 250 pts | ►9 studies (n = 250) compared DY CE vs SBBaR in CD: 63% vs 23%, respectively (IY = 40%, P < 0.001, 95%CI: 28%-51%); | |
►4 studies (n = 114) compared DY CE vs C + IL in CD: 61% vs 46%, respectively (IY = 15%, P = 0.02, 95%CI: 2%-27%); | |||||||||
►3 studies (n = 93) compared DY CE vs CT enterography/enteroclysis: 69% vs 30%, respectively (IY = 38%, P = 0.001, 95%CI: 15%-60%); | |||||||||
►2 studies compared DY CE vs PE: (IY = 38%, P < 0.001, 95%CI: 26%-50%); | |||||||||
►1 study compared DY CE vs SBMRI (IY = 22%, P = 0.16, 95%CI: -9%-53%); | |||||||||
Sub-analysis (pts with suspected CD): no difference in DY CE vs SBBaR (P = 0.09), C + IL (P = 0.48), CT enterography (P = 0.07) or PE (P = 0.51); | |||||||||
Sub-analysis (pts with established CD): difference in DY CE vs SBBaR (P < 0.001 C + IL (P = 0.002), CT enterography (P < 0.001) and PE (P < 0.001) | |||||||||
Pasha et al[21] | DBE and CE have comparable DY in SB disease: A meta-analysis | N/A - Dec 2006 | Meta-analysis of diagnostic test accuracy | Comparison of DY of CE vs DBE | 2 | 113 | 11 | 397 pts | ►Pooled DY CE vs DBE: 60% vs 57% (IYW = 3%, 95%CI: -4%-10%, P = 0.42, FEM); |
►Pooled DY CE vs DBE (vascular findings, 10 studies): 24% vs 24% (IYW = 0%, 95%CI: -5%-6%, P = 0.88, REM); | |||||||||
►Pooled DY CE vs DBE (inflammatory findings, 9 studies): 18% vs 16% (IYW = 0%, 95%CI: -5%-6%, P = 0.89, FEM); | |||||||||
►Pooled DY CE vs DBE (polyps/tumours, 9 studies): 11% vs 11% (IYW = -1%, 95%CI: -5%-4%, P = 0.76, FEM); | |||||||||
►SB disease: CE vs DBE have comparable DY, including OGIB, CE should be the initial diagnostic test for determining the insertion route of DBE | |||||||||
Niv[22] | Efficiency of bowel preparation for capsule endoscopy examination: A meta-analysis | N/A - July 2007 | Meta-analysis of RCTs and cohort studies | Purgative use vs fasting alone for SBCE | 1 | 6 | 8 | 130 bowel prep; 107 fasting | ►237 pts, 130 with and 107 without preparation; |
►Seven out of 8 studies included a comparison of GTT, SBTT and CR; | |||||||||
►SBCE CR: 76% in pts with preparation vs 68% without prep (difference did not reach statistical significance); | |||||||||
►No statistically significant difference between CEs performed with or without preparation in GTT (pooled effect size, -0.054; 95%CI: -0.418-0.308) or SBTT (pooled effect size, -0.327; 95%CI: -1.419 - -0.765) | |||||||||
El-Matary et al[23] | Diagnostic characteristics of given video capsule endoscopy in diagnosis of celiac disease: A meta-analysis | Meta-analysis of diagnostic test accuracy | Coeliac and CE | 2 | N/A | 3 | 107 pts | ►3 studies (n = 107, 63 pts with CD/44 without) met inclusion criteria; | |
►Pooled SBCE (overall) Sens and Spec: 83% (95%CI: 71%-90%) and 98% (95%CI: 88%-99.6%), respectively; | |||||||||
►No major complications reported; | |||||||||
►Costs mentioned only in 1 study. Overall, diagnostic characteristics of SBCE, could not justify the routine use of SBCE as alternative to biopsy | |||||||||
Chen et al[24] | A meta-analysis of the yield of CE compared to DBE in pts with SB diseases | N/A - Feb 2007 | Meta-analysis of diagnostic test accuracy | Comparison of DY of CE vs DBE | 2 | 163 | 8 | 277 pts | ►8 studies (n = 277 pts) prospectively compared the yield of CE and DBE were included; |
►No difference between the yield of CE and DBE (170/277 vs 156/277, OR 1.21, 95%CI: 0.64-2.29); | |||||||||
►Sub analysis: yield of CE significantly higher than that of DBE without combination of oral+anal insertion approaches (137/219 vs 110/219, OR 1.67, 95%CI: 1.14-2.44, P < 0.01), but not superior to the yield of DBE with combination of the two insertion approaches (26/48 vs 37/48, OR 0.33, 95%CI: 0.05-2.21, P < 0.05); | |||||||||
►Focused meta-analysis of the fully published articles concerning OGIB showed similar results wherein the yield of CE was significantly higher than that of DBE without combination of oral + anal insertion approaches (118/191 vs 96/191, fixed model: OR 1.61, 95%CI: 1.07-2.43, P < 0.05) and the yield of CE was significantly lower than that of DBE by oral+ anal combinatory approaches (11/24 vs 21/24, fixed model: OR 0.12, 95%CI: 0.03-0.52, P < 0.01) | |||||||||
Rokkas et al[25] | Does purgative preparation influence the diagnostic yield of small bowel video capsule endoscopy? A meta-analysis | N/A - Feb 2008 | Meta-analysis of RCTs and cohort studies | Purgative use vs fasting alone for SBCE | 2 | 194 | 12 | 718 pts purgative; 444 controls | ►12 eligible studies (6 prospective/6 retrospective), including 16 sets of data; |
►Significant difference in DY between pts prepared with purgatives (n = 263) vs pts prepared with clear liquids (n = 213): OR = 1.813 (95%CI: 1.251-2.628, P = 0.002); | |||||||||
►Significant difference in SBVQ between pts prepared with purgatives (n = 404) vs pts prepared with clear liquids (n = 249): OR = 2.113 (95%CI: 1.252-3.566, P = 0.005); There was no statistically significant difference regarding CR rate. Purgatives did not affect VCE GTT or VCE SBTT | |||||||||
Dionisio et al[26] | CE has a significantly higher DY in patients with suspected and established small-bowel CD: A meta-analysis | 2000 - May 2009 | Meta-analysis of diagnostic test accuracy | DY of CE vs modalities in patients with suspected/ established CD | 2 | 291 | 12 | 428 pts | ►8 studies (n = 236 pts) compared CE vs C + IL, 4 (n = 119 pts) CE vs CTE, 2 (n = 102 pts) vs PE, 4 (n = 123 pts) vs MRE; |
►For suspected CD, several comparisons met statistical significance; Yields in this subgroup were: CE vs SBR: 52% vs 16% (IYw = 32%, P < 0.0001, 95%CI: 16%-48%), CE vs CTE: 68% vs 21% (IYw = 47%, P < 0.00001, 95%CI: 31%-63%), CE vs C + IL: 47% vs 25% (IYw = 22%, P = 0.009, 95%CI: 5%-39%); | |||||||||
►For established CD, statistically significant yields for CE vs an alternate diagnostic modality in patients were seen: CE vs PE: 66 vs 9% (IYw = 57%, P < 0.00001, 95%CI: 43-71%), CE vs SBR: 71 vs 36% (IYw = 38%, P < 0.00001, 95%CI: 22%-54%), CE vs CTE: 71 vs 39% (IYw = 32%, P ≤ 0.0001, 95%CI: 16%-47%) | |||||||||
Wu et al[27] | Systematic review and meta-analysis of RCTs of Simethicone for GI endoscopic visibility | N/A- Nov 2009 | Meta-analysis of RCTs | Simethicone and CE | 2 | 128 | 4 | 121 pts | ►Adequate or excellent/good SB mucosa visualization in pts receiving Simethicone vs those who did not (66.1% vs 37.2%); |
►Pooled OR = 2.84 (95%CI: 1.74-4.65, P = 0.00); no significant heterogeneity (P = 0.16, I2 = 38.8%) or publication bias (P = 0.251); | |||||||||
►Sens analysis: studies stratified by factors such as bowel preparation (purgative vs fasting): Significant results for bowel preparation + fasting (OR = 4.43, 95%CI: 1.82-10.76, P = 0.00) with P = 0.78, I2 = 0.0%, No significant results for bowel preparation + purgative (OR = 1.59, 95%CI: 0.78-3.27, P = 0.203) with P = 0.20, I2 = 38.9% | |||||||||
Rokkas et al[25] | Does purgative preparation influence the diagnostic yield of small bowel video capsule endoscopy? A meta-analysis | N/A - Feb 2008 | Meta-analysis of RCTs and cohort studies | Purgative use vs fasting alone for SBCE | 2 | 194 | 12 | 718 pts purgative; 444 controls | ►12 eligible studies (6 prospective/6 retrospective), including 16 sets of data; |
►Significant difference in DY between pts prepared with purgatives (n = 263) vs pts prepared with clear liquids (n = 213): OR = 1.813 (95%CI: 1.251-2.628, P = 0.002); | |||||||||
►Significant difference in SBVQ between pts prepared with purgatives (n = 404) vs pts prepared with clear liquids (n = 249): OR = 2.113 (95%CI: 1.252-3.566, P = 0.005); There was no statistically significant difference regarding CR rate. Purgatives did not affect VCE GTT or VCE SBTT | |||||||||
Dionisio et al[26] | CE has a significantly higher DY in patients with suspected and established small-bowel CD: A meta-analysis | 2000 - May 2009 | Meta-analysis of diagnostic test accuracy | DY of CE vs modalities in patients with suspected/ established CD | 2 | 291 | 12 | 428 pts | ►8 studies (n = 236 pts) compared CE vs C + IL, 4 (n = 119 pts) CE vs CTE, 2 (n = 102 pts) vs PE, 4 (n = 123 pts) vs MRE; |
►For suspected CD, several comparisons met statistical significance; Yields in this subgroup were: CE vs SBR: 52% vs 16% (IYw = 32%, P < 0.0001, 95%CI: 16%-48%), CE vs CTE: 68% vs 21% (IYw = 47%, P < 0.00001, 95%CI: 31%-63%), CE vs C + IL: 47% vs 25% (IYw = 22%, P = 0.009, 95%CI: 5%-39%); | |||||||||
►For established CD, statistically significant yields for CE vs an alternate diagnostic modality in patients were seen: CE vs PE: 66 vs 9% (IYw = 57%, P < 0.00001, 95%CI: 43-71%), CE vs SBR: 71 vs 36% (IYw = 38%, P < 0.00001, 95%CI: 22%-54%), CE vs CTE: 71 vs 39% (IYw = 32%, P ≤ 0.0001, 95%CI: 16%-47%) | |||||||||
Wu et al[27] | Systematic review and meta-analysis of RCTs of Simethicone for GI endoscopic visibility | N/A - Nov 2009 | Meta-analysis of RCTs | Simethicone and CE | 2 | 128 | 4 | 121 pts | ►Adequate or excellent/good SB mucosa visualization in pts receiving Simethicone vs those who did not (66.1% vs 37.2%); |
►Pooled OR = 2.84 (95%CI: 1.74-4.65, P = 0.00); no significant heterogeneity (P = 0.16, I2 = 38.8%) or publication bias (P = 0.251); | |||||||||
►Sens analysis: studies stratified by factors such as bowel preparation (purgative vs fasting): Significant results for bowel preparation + fasting (OR = 4.43, 95%CI: 1.82-10.76, P = 0.00) with P = 0.78, I2 = 0.0%, No significant results for bowel preparation + purgative (OR = 1.59, 95%CI: 0.78-3.27, P = 0.203) with P = 0.20, I2 = 38.9% | |||||||||
Cohen et al[28] | Use of CE in diagnosis and management of pediatric patients, based on meta-analysis | Jan 2001 - May 2010 | Systematic review of evidence base | Systematic compilation of data on indications and outcomes of CE in paediatric patients | 2 | N/A | 15 | 740 examinations; 723 pts | ►Most common indication for CE (in pts < 18 yr): suspicion or evaluation of IBD (overall 54%), Breakdown: suspected CD (34%), known CD (16%), UC (1%), indeterminate colitis (3%) |
►CR and RR: 86.2% (95%CI: 81.5-90.3%) and 2.6% (95%CI: 1.5-4.0%), respectively; | |||||||||
►CE RR (gastric and SB): 0.5% and 1.9%, respectively, similar to those of adults, by indication; | |||||||||
►CE with positive findings: 65.4% (95%CI: 54.8%-75.2%); | |||||||||
►CE resulting in new diagnosis: 69.4% (95%CI: 46.9%-87.9%); CE leading to change in therapy: 68.3% (95%CI: 43.6%-88.5%) | |||||||||
Teshima et al[29] | DBE and CE for OGIB: An updated meta-analysis | N/A - June 2010 | Meta-analysis of diagnostic test accuracy | OGIB; CE or DBE | 2 | 147 | 10 | 651 CE; 642 DBE | ►Pooled DY for CE: 62% (95%CI: 47.3%-76.1%) |
►Pooled DY for DBE 56% (95%CI: 48.9%-62.1%); OR for CE vs DBE of 1.39 (95%CI: 0.88-2.20; P = 0.16); | |||||||||
Subgroup analyses | |||||||||
►DBE-DY after (+)ve CE: 75.0% (95%CI: 60.1%-90.0%) | |||||||||
►DBE-DY after (-)ve CE: 27.5% (95%CI: 16.7%-37.8%) | |||||||||
►DBE-OR (for successful diagnosis after (+)ve CE) compared with DBE: 1.79 (95%CI: 1.09-2.96, P = 0.02) | |||||||||
►In OGIB CE and DBE have similar DY, DBE-DY significantly higher when performed in pts with prior positive CE | |||||||||
Belsey et al[30] | Meta-analysis: efficacy of SB preparation for SBCE | Jan 2000 - Dec 2010 | Meta-analysis of RCTs | Purgative use vs fasting alone for SBCE | 2 | 33 | 8 | 291 PEG; 133 NaP; 322 fasting | ►8 studies, using PEG or NaP-based bowel cleansing regimens; |
►Any form of purgative significantly better visibility than fasting alone (OR = 2.31; 95%CI: 1.46-3.63, P < 0.0001); | |||||||||
►Similar results on DY (OR = 1.88; 95%CI: 1.24-2.84; P = 0.023); | |||||||||
Subgroup analyses (per cleansing regimen used): | |||||||||
►PEG-based regimens showed benefit (OR = 3.11; 95%CI: 1.96-4.94, P < 0.0001); | |||||||||
►NaP-based regimens no significant difference from fasting alone (OR = 1.32; 95%CI: 0.59-2.96, P < 0.0001); | |||||||||
►Use of purgatives (alongside fasting) is recommended in SBCE; PEG-based regimens offer a clear advantage over NaP; | |||||||||
►Lower volume PEG regimens as efficacious as higher volumes traditionally used for colonoscopy preparation | |||||||||
Rokkas et al[31] | The role of video CE in the diagnosis of coeliac disease: A meta-analysis | N/A - April 2011 | Meta-analysis of diagnostic test accuracy | Coeliac and CE | 2 | 461 | 6 | 166 pts | ►Pooled CE Sens: 89% (95%CI: 82%-94%) and Spec: 95% (95%CI: 89%-98%), AuROC: 0.9584; |
►Although not as accurate as pathology, CE a reasonable alternative method of diagnosing coeliac disease | |||||||||
Koulaouzidis et al[32] | Diagnostic yield of SBCE in patients with IDA: A systematic review | Jan 2001 - Nov 2011 | Systematic review of evidence base | IDA and CE | 2 | 1225 | 24 | 1960 pts | ►Pooled SBCE-DY in IDA: 47% (95%CI: 42%-52%), with significant heterogeneity among included studies (I2 = 78.8%, P < 0.0001); |
Ref. | Country | Centre | Study type | Design | Participants | FC | CE | Objective(s) | Outcome(s) |
Goldstein et al[41] | United States | Multi-centre | Prospective | Double-blind, triple-dummy, placebo controlled | 334 healthy subjects | N/A | M2A®; Given®Imaging, Yokneam, Israel | Evaluate incidence of SB injury and correlation with FC in healthy subjects on celecoxib or ibuprofen + omeprazole | ►Mean increase in FC higher in subjects on ibuprofen+omeprazole compared with celecoxib alone (P < 0.001); |
►No correlation between FC and SB mucosal breaks | |||||||||
Hawkey et al[42] | Germany, United Kingdom | Multi-centre | Prospective | Double-blind, double-dummy, placebo controlled | 139 healthy subjects | Phical Calprotectin Test Kit NovaTec Immunodiagnostica, GmbH Dietzenbac, Germany | M2A®; Given®Imaging, Yokneam, Israel | Investigate SB injury lumiracoxib reduces vs naproxen + omeprazole | ►More SB mucosal breaks on naproxen+omeprazole (77.8% vs 40.4%, P < 0.001); |
►Furthermore, higher FC vs placebo (96.8 vs 14.5 μg/g, P < 0.001); | |||||||||
►27.7% on lumiracoxib had SB mucosal breaks (vs placebo, P = 0.196; vs naproxen, P < 0.001) | |||||||||
►No increase in FC (-5.7 μg/g; vs placebo, P = 0.377; vs naproxen, P < 0.001) | |||||||||
Smecuol et al[43] | Argentina, Spain, Canada | Multi-centre | Prospective | Non-blinded study | 20 healthy subjects | Calprest® Eurospital SpA, Trieste, Italy | M2A®; Given®Imaging, Yokneam, Israel | Determine SB damage by low-dose ASA (on a short-term basis) | ►Short-term administration of low-dose ASA associated with mucosal abnormalities of the SB mucosa; |
►Median baseline FC (6.05 μg/g; range: 1.9-79.2 μg/g) increased significantly after ASA use | |||||||||
Werlin et al[44] | United States, Israel, United Kingdom | Multi-centre | Prospective | N/A | 42 pts with CF* (aged 10-36 yr); 29 had pancreatic insufficiency | Calprest® Eurospital SpA, Trieste, Italy | PillCam®SB; Given®Imaging, Yokneam, Israel | Examine the SB of pts with CF without overt evidence of GI disease using CE | ►Varying degrees of diffuse areas of inflammatory findings in the SB: oedema, erythema, mucosal breaks and frank ulcerations; |
►No adverse events recorded; | |||||||||
FC markedly high in pts with pancreatic insufficiency, 258 μg/g (normal < 50) | |||||||||
Koulaouzidis et al[45] | United Kingdom | Single centre | Retrospective | Chart review | 70 pts with suspected CD and (-) ve bi-directional endoscopy | CALPRO NovaTec Immunodiagnostica GmbH, Dietzenbac, Germany | (1) PillCam®SB; Given®Imaging, Yokneam, Israel; (2) MiroCam®; IntroMedic Co., Seoul, South Korea | Value of FC as selection tool for further investigation of the SB with SBCE, in a cohort of pts with suspected CD | ►FC = 50-100 μg/g: normal SBCE, despite symptoms suggestive of IBD; |
►FC > 100 μg/g: good predictor of positive SBCE; | |||||||||
►FC > 200 μg/g: associated with higher SBCE DY (65%); confirmed CD in 50%; | |||||||||
►Measurement of FC prior SBCE: useful tool to select patients for referral. If FC < 100 μg/g: SBCE is not indicated (NPV 1.0) | |||||||||
Jensen et al[46] | Denmark | Single centre | Prospective | Blinded study | 83 pts from GI OPD clinics with suspected CD | Calprotectin ELISA, BÜHLMANN Laboratories AG, Basel, Switzerland | PillCam®SB; Given®Imaging, Yokneam, Israel | Determine FC levels in CD restricted to SB compared to colonic CD, in pts on first diagnostic work-up; Assess the Sens and Spec of FC in suspected CD | ►In pts with SB or colonic CD FC is equal: median 890 μg/g vs 830 mg/kg, respectively (P = 1.0); |
►FC cut-off = 50 μg/g: 92% and 94% Sens for SB and colonic CD, respectively; | |||||||||
►Overall, Sens and Spec for FC: 95% and 56%; | |||||||||
►CD was ruled out with NPV of 92%; | |||||||||
►In suspected CD, FC is effective marker to r/o CD and select patients for endoscopy | |||||||||
Koulaouzidis et al[47] | United Kingdom | Single centre | Retrospective | Chart review | 49 pts; known or suspected CD | CALPRO NovaTec Immunodiagnostica GmbH, Dietzenbac, Germany | PillCam®; Given®Imaging, Yokneam, Israel; MiroCam®; IntroMedic Co., Seoul, South Korea | Assess performance of 2 SBCE inflammation scoring systems (LS and CECDAI) correlating them with FC; Define threshold levels for CECDAI | ►LS performs better than CECDAI in describing SB inflammation, especially at FC < 100 μg/g |
►CECDAI levels of 3.8 and 5.8 correspond to LS thresholds of 135 and 790, respectively | |||||||||
Sipponen et al[48] | Finland | Single centre | Prospective | Blinded study | 84 pts; known or suspected CD | Calprest® Eurospital SpA, Trieste, Italy | PillCam®; Given®Imaging, Yokneam, Israel; MiroCam®; IntroMedic Co., Seoul, South Korea | Study the role of FC and S100A12 in predicting SB inflammatory lesions | ►CE abnormal in 35/84 (42%) pts: 14 CD, 8 NSAID-enteropathy, 8 angioectasias, 4 polyps/tumours, 1 ischemic stricture |
►Median FC/S100A12: 22 μg/g (range: 2-342 μg/g)/0.048 μg/g (range: 0.003-1.215 μg/g) | |||||||||
►FC significantly higher in CD pts (median 91, range: 2-312) compared with pts with normal CE or other abnormalities (P = 0.008) | |||||||||
►Faecal S100A12 (0.087 μg/g, range: 0.008-0.896 μg/g): no difference between the groups (P = 0.166) | |||||||||
►Sens, Spec, PPV, NPV in detecting SB inflammation; FC (cut-off 50 μg/g): 59%, 71%, 42%, 83%; S100A12 (cut-off 0.06 μg/g): 59%, 66%, 38%, 82%, respectively |
Ref. | CE | Type of CE model; Company | AoV seen, n (%) | Reviewers | Reviewing speed (fps) | Frames AoV visible2 | Comments |
Wijeratne et al[53]1 | 138 | NS | 9 (6.0) | 1 | NS | NS | 4 FAP patients (AoV not seen) |
Kong et al[54] | 110 | M2A®; Given®Imaging Ltd. | 48 (43.6) | 2 | 15 | 3.5 ± 2.5 | |
Clarke et al[55] | 125 | M2A®; Given®Imaging Ltd. | 13 (10.4) | 2 | 5 | NS | |
Iaquinto et al[56] | 23 | PillCam®SB; Given®Imaging Ltd. | 0 (0.0) | 2 | NS | N/A | FAP patients (11/23 had duodenal polyps) |
Metzger et al[57] | 20 | PillCam®SB1; Given®Imaging Ltd. | 1 (5.0) | NS | NS | NS | Repeat examinations |
PillCam®SB2; Given®Imaging Ltd. | 5 (25.0) | NS | NS | NS | |||
Katsinelos et al[58] | 14 | NS | 0 (0.0) | 1 | NS | N/A | FAP patients |
Nakamura et al[59] | 96 | PillCam®SB1; Given®Imaging Ltd. | 18 (18.0) | 2 | 10 | NS | |
Karagiannis et al[60] | 10 | PillCam®Colon; Given®Imaging Ltd. | 6 (60.0) | NS | NS | NS | Two-headed PillCam® |
Lee et al[61]1 | 30 | PillCam®SB; Given®Imaging Ltd. | 13 (43.3) | NS | NS | NS | |
30 | PillCam®SB2; Given®Imaging Ltd. | 15 (50.0) | NS | NS | NS | ||
50 | PillCam®SB1; Given®Imaging Ltd. | 0 (0.0) | 2 | NS | N/A | ||
Selby et al[62] | 50 | PillCam®SB2; Given®Imaging Ltd. | 9 (18.0) | 2 | NS | NS | |
8 | PillCam®ESO1; Given®Imaging Ltd. | 0 (0.0) | 2 | NS | N/A | Two-headed PillCam® | |
12 | PillCam®ESO2; Given®Imaging Ltd. | 1 (8.0) | 2 | NS | NS | Two-headed PillCam® | |
Koulaouzidis et al[63] | 11 | PillCam®ESO1; Given®Imaging Ltd. | 4 (36.4) | 1 | 7 | NS | Two-headed PillCam® |
7 | PillCam®ESO2; Given®Imaging Ltd. | 1 (14.3) | 1 | 9 | NS | Two-headed PillCam® | |
Park et al[64] | 30 | PillCam®SB; Given®Imaging Ltd. | 13 (43.3) | 6 | 7 | 3.1 ± 1.1 | |
30 | PillCam®SB2; Given®Imaging Ltd. | 15 (50.0) | 6 | 9 | 3.1 ± 1.5 | ||
262 | PillCam®SB1; Given®Imaging Ltd. | 28 (10.7) | 1 | 6 | 36.35 ± 73.24 | ||
Koulaouzidis et al[65] | 148 | PillCam®SB2; Given®Imaging Ltd. | 13 (8.8) | 1 | 6 | 42.46 ± 69.3 | |
209 | MiroCam®; IntroMedic Ltd. | 18 (8.6) | 1 | 6 | 87.20 ± 248.4 | ||
Friedrich et al[66] | 25 | CapsoCam®SV1; Capsovision Ltd. | 22 (71) | 3 | NS | 3.1 ± 1.8 |
Ref. | Case (age/gender) | Comorbidities | CE model/company | Swallowing difficulties | No. of attempts to swallow CE/gagging or coughing | Aspiration time/where in bronchial tree CE seen | Capsule removal (if employed) | Final diagnosis |
Schneider et al[72] | 64/male | Mechanical MV on phenprocoumon, BMI 15.5 | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | 4/gagging and spitting capsule - last attempt recurrent coughing (aspiration presumed) | 2 min/trachea-bronchi | Spontaneous resolution | NS |
Fleischer et al[73] | 76/male | HHT | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | 1/lodged in his throat - no respiratory difficulty, could talk, vital signs normal | 60 min/cricopharyngeus | Endoscopy-Roth net; 6 d post-dilation, patient ingested capsule with no problem | Spasticity, prominence of cricopharyngeus; endoscopy and oesophageal dilation 1 wk later |
Sinn et al[74] | 69/female | On phenprocoumon | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | 1/coughed several times | 50 s/bifurcation of the trachea | Spontaneous resolution | NS |
Tabib et al[75] | 87/female | Recent onset IDA, CHF, IHD, AF, bladder cancer, CRF | M2A®; Given®Imaging Ltd. | No Hx of dysphagia, pre-CE barium meal | 2/choking, dyspnoea, CE felt lodged in the throat | NS/right main-stem bronchus - bronchus intermedius | Rigid bronchoscopy | NS |
Buchkremer et al[76] | 74/male | Recent diagnosis of coeliac disease; past Hx of ankylosing spondylitis | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | NS/dyspnoea started after CE ingestion | NS/right main-stem bronchus | Flexible bronchoscopy | NS |
Rondonotti et al[77] | NS | NS | M2A®; Given®Imaging Ltd. | NS | NS/coughed several times | NS/NS | Spontaneous resolution | NS |
Nathan et al[78] | 93/male | No significant past medical Hx | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | 1/coughed hours post-ingestion | Approximately 8 h/bronchial tree | Spontaneous resolution | NS |
Shiff et al[79] | 75/male | NS | M2A®; Given®Imaging Ltd. | No Hx of dysphagia | 2/some coughing | NS/bronchi | Spontaneous resolution | NS |
Eventually, CE endoscopic placement | ||||||||
Sepehr et al[80] | 67/male | HTN, DM, CVA | NS | Hx of dysphagia (intermittent) | 1/coughing, tachypnoea, and tachycardia | NS/trachea | Endoscopy-Roth net | NS |
Koulaouzidis et al[81] | 76/male | NS | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | 1/coughed weakly | 15 s/trachea | Spontaneous resolution | NS |
Guy et al[82] | 90/male | Ischaemic CVA | NS | No Hx of dysphagia | NS/no symptoms | NS/bronchial tree | Rigid bronchoscopy - stone retrieval basket | NS |
Leeds et al[83] | 85/male | NS | NS | No Hx of dysphagia | NS/difficulty swallowing CE, slightly painful | 8 h/lobar bronchus | Spontaneous resolution | NS |
Bredenoord et al[84] | 65/male | Sigmoid colectomy for diverticulae; Ileal carcinoid resected | NS | Hx of dysphagia | Lengthy swallowing attempt/coughing noted | NS/right main bronchus | Spontaneous resolution, eventually, CE was swallowed on same session | Normal small-bowel |
Choi et al[85] | 75/male | Prior CVA | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | NS/coughed several times | 2 h/left main bronchus | Flexible Bronchoscopy-Roth net and bronchial wall irrigation to induce cough | NS, patient declined further investigations |
Depriest et al[86] | 90/male | IHD, AF, PVD (warfarin + clopidogrel) | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | NS/some cough | NS/left main bronchus, then right main bronchus | Chest percussive therapy + postural drainage; Flexible bronchoscopy + extraction basket + Roth net | NS |
Depriest et al[86] | 90/male | IHD, AF, PVD (warfarin + clopidogrel) | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | NS/some cough | NS/left main bronchus, then right main bronchus | Chest percussive therapy + postural drainage; flexible bronchoscopy + extraction basket + Roth net | NS |
Kurtz et al[87] | 73/male | Renal cell cancer, MV (bovine), hyperlipidaemia, melaena | NS | No Hx of dysphagia | Sips of water, 1st attempt, 2 min later non-productive cough (20 s) | Level of carina; then right main stem bronchus | Bronchoscopy-retrieval basket (multiple spontaneous ejections from trachea prior bronchoscopy) | NS |
Lucendo et al[88] | 80/male | Advanced PD, DM, walking + speech difficulties | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | Several attempts/persistent coughing and some dyspnoea | 20 s/tracheobronchial tree | Spontaneous resolution | Oesophageal ulcer + ileal ulcer |
Pezzoli et al[89] | 82/male | Unexplained anemia, HTN | NS | No Hx of dysphagia | NS/asymptomatic (minimal cough) | 3 d/in the right bronchus | Spontaneous resolution | NS |
Parker et al[90] | 77/female | Hysterectomy | NS | No Hx of dysphagia | Initial attempt unsuccessful/chocking episode, CE coughed-up | NS/NS | Spontaneous resolution, endoscopic placement with AdvanCE® device | Patient suffered intracranial bleed, eventually succumbed |
Despott et al[91] | 65/male | COPD, cirrhosis, pancreatitis | NS | No Hx of dysphagia | NS/asymptomatic | NS/right main bronchus | Rigid bronchoscopy-Roth net | Endoscopic placement with AdvanCE® device |
73/male | COPD | NS | NS | NS/brief coughing | NS/left main bronchus | Bronchoscopy-snare + Roth net | Endoscopic placement with AdvanCE® device | |
81/male | NS | NS | NS | NS/fleeting choking sensation | NS/right main bronchus | Rigid bronchoscopy-crocodile grasping forceps | NS | |
Girdhar et al[92] | 83/male | COPD, GORD | PillCam®SB; Given®Imaging Ltd. | No Hx of dysphagia | Difficult, requiring multiple sips of water/some cough, after 1 h mild shortness of breath | NS/left main bronchus | Flexible bronchoscopy + rat-tooth alligator forceps + stiff-wire basket with a pin-vise handle | NS |
Poudel et al[93] | 80/male | AF, IHD, CVA on anti-coagulants, anaemia + melaena | M2A®; Given®Imaging Ltd. | NS | NS | 24 h/left main stem bronchus; then right bronchus | Flexible bronchoscopy + net + snare forceps + tripod; eventually, grasped with basket | NS |
Ref. | Country | Centre | Objective(s) | Study type | Design | CE type | Outcome(s) | Conclusions |
Gross et al[96] | United States | Single centre | Accuracy of SBI to number of blood transfusions | Retrospective | ►Gold standard for lesions detected by experienced CE reviewer | M2A; Given® Imaging Ltd. | ►Gold standard: 72 pts; | Pts receiving blood transfusions are more likely to have a positive SBI correlating with the localization of active bleeding |
►pts received blood transfusions ranging between 0-16 units; | ||||||||
►Overall: A total of 17 pts had positive SBI. Active bleeding in 16 pts, who were transfused an average of 8 units before the study; | ||||||||
►55 pts had a negative SBI and no active bleeding was seen on their capsule studies. In this group, the average number of PRBC transfused was 1 unit. There was one patient who had a false positive SBI with no active bleeding seen in the capsule study review | ||||||||
Liangpunsakul et al[97] | United States | Single centre | Assess accuracy of SBI | Retrospective | ►Gold standard for lesions detected by experienced CE reviewer; | M2A; Given® Imaging Ltd. | ►Gold standard: 109 lesions; | SBI has good Sens and PPV for actively bleeding SB lesions |
►SBI: 31 potential areas of blood; correctly identified lesions: 28; | ||||||||
►Significant lesions considered AVMs, ulcers, erosions, active bleeding; | ►Overall: SBI (Sens, PPV, accuracy): 25.7%, 90%, 34.8%, respectively; | |||||||
►For actively bleeding SB lesions only: SBI (Sens, PPV, accuracy): 81.2%, 81.3%, 83.3%, respectively | ||||||||
►Reviewing speed: 15fps | ||||||||
D'Halluin et al[98] | France | Multi-centre (7 centres) | Assess Sens/Spec of SBI (in OGIB) | Retrospective | ►Gold standard for lesions detected by experienced CE reviewer, SBI tags marked by another investigator; | M2A; Given® Imaging Ltd. | ►156 SBCE recordings evaluated: In 83 (normal): either no lesion (n = 71) or P0 lesion (n = 12); in 73 abnormal: P2 (n = 114) and P1 (n = 92) lesions; | ►SBI-based detection of SB lesions (with bleeding potential) is of limited clinical value |
►Significant lesions considered Bleeding or having a bleeding potential: high (P2), low (P1), or absent (P0); | ►154 red tags analysed: SBI (Sens, Spec, PPV, NPV) for P2 or P1: 37%, 59%, 50%, 46%, respectively | |||||||
►Concordance: same time code in frames selected by expert reader and those tagged by SBI; | ||||||||
►Reviewing speed: NS | ||||||||
Singnorelli et al[99] | Italy | Single centre | Assess Sens/Spec of SBI per lesion, overall, according to red findings (identified by the reader), and per patient | Retrospective | ►Gold standard for lesions detected by four experienced CE reviewers; | M2A; Given® Imaging Ltd. | ►95 patients; 209 red findings; | ►SBI has low Sens/Spec in per-lesion and per-patient SBCE evaluation; |
►Overall Sens: 28%; | ||||||||
►Outcomes: Sens, Spec and accuracy calculated both per lesion/patient; | ►Sens higher for identification of blood (61%) than for nonbleeding “red” findings, e.g., AVMs (26%); | |||||||
►Reviewing speed: NS | ►Per-patient Sens, Spec: 41%, 70%, respectively | ►Complementary/rapid screening tool; | ||||||
►Complete review of the recordings is still necessary | ||||||||
Ponferrada et al[100] | Spain | Single centre | Assess accuracy/performance of SBI | Prospective | ►Gold standard for lesions detected by experienced CE reviewers | M2A; Given® Imaging Ltd. | ►57 consecutive patients; | |
►Indications: OGIB (64.9%), CD (14%), malabsorption (14%), suspicion of SB tumour (7.1%); | ||||||||
►SBI Sens, Spec, PPV, NPV: 58.3%, 75.5%, 38.8%, 87.2%, respectively | ||||||||
Buscaglia et al[101] | United States | Single centre | Assess accuracy/performance of SBI according to CE indications | Retrospective | ►Gold standard for lesions detected by experienced CE reviewer; | M2A; Given® Imaging Ltd. | ►CE indications: OGIB (n = 112), suspected CD (n = 122), anaemia of unknown origin (n = 53), other (n = 4); | ►SBI performance characteristics suboptimal/insufficient to screen for SB lesions with bleeding potential; |
►Significant lesions:AVMs, varices, venous ectasias, red spots, ulcers, erosions, blood, blood clots | ►221 lesions with bleeding potential; | |||||||
►Overall: SBI (Sens, Spec, PPV, NPV): 56.4%, 33.5%, 24.0%, 67.3%, respectively; | ||||||||
►Concordant and discordant findings between CE reviewer and SBI; | ||||||||
►For actively bleeding lesions: SBI (Sens, PPV): 58.3%, 70%, respectively; | ►Even in pts with active intestinal bleeding, SBI Sens was only < 60% | |||||||
►Reviewing speed: 8-15 fps | ►For suspected CD: SBI (Sens, NPV): 64%, 80.4%, respectively; | |||||||
►For OGIB: SBI Sens 58.3%; | ||||||||
►For anaemia: SBI Sens 41.3%; | ||||||||
Park et al[102] | South Korea | Single centre | Investigate whether SBI is affected by background colour and CE velocity | Experimental | ►Paper-made phantom SB models in a variety of colours to simulate the background colours observed in CE; | M2A; Given® Imaging Ltd. | ►SBI red spots detection rate differed significantly per background colour of SB model, P < 0.001; | ►SBI Sens affected by background colour and capsule passage velocity in the models |
►SBI red spots detection rate highest for very pale magenta, burnt sienna, yellow background; | ||||||||
►Red spots were attached inside them; | ||||||||
►CE manually passed through models; | ||||||||
►SBI red spots detection rate was evaluated based on colours of SB models and CE velocities (0.5, 1, 2 cm/s) | ►SBI red spots detection rate lowest for dark brown, very pale yellow background |
Ref. | QuickView sampling rate | QuickView reading frame mode/reading speed (fps) | Average reading time (mean) | Comparison with/reading frame mode/reading speed used (fps) | Rapid®Reader version | Reviewers | Cases | QuickView | Lesions missed | |||||
Total | OGIB | CD | Polyposis | Other | Sensitivity (%) | Specificity (%) | ||||||||
Ponferrada et al[100] | NS | 25, 15, 5 | NS | Conventional/NS/15, 15, 5 | 2 | 57 | 37 | 8 | N/A | 12 | 96.5 (5 fps) | NS | NS | |
Schmelkin[104] | NS | NS | NS | NS | 4.0 | 1 | 47 | 47 | N/A | N/A | N/A | 100 | 100 | N/A |
Appalaneni et al[105] | NS | Single frame, 25 | 3 min | NS | NS | 2 | 50 | NS | NS | NS | NS | NS | NS | 2 |
Westerhof et al[106] | High (17) | NS | 4.4 min (median) | Conventional/dual view/18 | 4.0 | 2 | 100 | 56 | 30 | 2 | 12 | NS | NS | 13 |
Shiotani et al[107] | High (17) | Single, 6 | 17.9 min | NS | 5.0 | 3 | 44 | NS | NS | NS | 14 | NS | NS | 10 |
Hosoe et al[108] | Normal | NS | NS | NS | 5.0 | 3 | 45 | NS | NS | NS | 14 | NS | NS | NS |
Saurin et al[109] | NS | NS | 11.6 min | Conventional/NS/NS | 5.0 | 12 | 106 | 106 | N/A | N/A | N/A | 89.2 | Jul-84 | 8 |
Shiotani et al[110] | 5, 15, 25, 35 | Single, NS | NS | NS | 6.5 | 4 | 87 | NS | NS | NS | NS | NS | NS | NS |
Koulaouzidis et al[111] | 35 | Dual view (WL + BM) | 475 s (QuickView WL) | Conventional/single or dual view/12-20 | 7.0 | 1 | 200 | 106 | 81 | 4 | 9 | 92.3 (QVWL P1 + P2) | 96.3 (QVWL P1 + P2) | |
18 | 450 s (QuickView BM) | 91 (QVBM P1+P2) | 96 (QVBM P1 + P2) | |||||||||||
Kyriakos et al[112] | NS | NS, 3 | 16.3 min (6.7) | Conventional/NS/NS | 5.0 | 2 | 100 | 55 | 22 | 3 | 20 | NS | NS | 12 |
Ref. | Country | Centre | Study type | Objective(s) | Design | Images | FICE | CE | Outcome(s) |
Imagawa et al[114] | Japan | Single centre | Retrospective | Assess whether visualization of SB lesions improves with FICE | ►5 experienced readers compared CE-WL images to their FICE counterparts | ►Angiectasis (n = 23); | FICE 1,2,3 | PillCam®SB1; Given®Imaging Ltd. | ►FICE 1: AVMs: improvement in 87% (20/23) cases; erosion/ulceration: improvement 53.3% (26/47) cases; tumour images: improvement 25.3% (19/75) cases; |
►Erosion/ulcers (n = 47); | |||||||||
►FICE 2: AVMs: improvement in 87% (20/23) cases; erosion/ulceration: improvement in 25.5% (12/47) cases; tumour images: improvement in 20.0% (15/75) cases; | |||||||||
►Tumour (n = 75) | |||||||||
►FICE 3: All images groups: only equivalence achieved in all cases; intra-observer agreement: good to satisfactory (5.4 or higher) | |||||||||
Imagawa et al[115] | Japan | Single centre | Prospective | Assess whether FICE improves detection rate of SB lesions in CE | ►A CE reader reviewed CE-WL videos; | 50 pts | FICE 1,2,3 | PillCam®SB1; Given®Imaging Ltd. | ►Angioectasias detection: CE-WL: 17 AVMs; CE-FICE 1: 48 AVMs; CE-FICE 2: 45 AVMs; CE-FICE 3: 24 AVMs; significant CE-FICE 1 and 2 (P = 0.0003 and P < 0.0001, respectively) |
►Another reader, reviewed CE-FICE videos with FICE 1,2,3 | |||||||||
►Detection rate for erosion, ulceration and tumour did not differ statistically between CE-WL and CE-FICE 1,2,3; | |||||||||
Gupta et al[116] | Belgium | Single centre | Retrospective | Assess potential benefit of FICE for SB lesion detection in patients with OGIB | CE videos analysed by 2 GI fellows with and without FICE 1,2,3; | 60 pts with OGIB | FICE 1,2,3 | PillCam®SB1; Given®Imaging Ltd. | ►Overall, 157 lesions diagnosed with CE-FICE vs 114 with CE-WL (P = 0.15); |
►For P2 lesions; CE-FICE Sens/Spec: 94%/95% vs CE-WL Sens/Spec: 97%/96%, respectively; 5/55 AVMs better characterized with CE-FICE than CE-WL | |||||||||
Reference standard: Senior consultant described findings as P0, P1 and P2 lesions | |||||||||
►More P0 diagnosed by CE-FICE than CE-WL (39 vs 8, P < 0.001); | |||||||||
►Intra-class kappa correlations between fellows and reference: CE-FICE vs CE-WL for P2 lesions: 0.88 vs 0.92; CE-FICE vs CE-WL for P1 lesions: 0.61 vs 0.79 | |||||||||
Krystallis et al[117] | United Kingdom | Single centre | Retrospective | Assess FICE and Blue mode visualisation of SB lesions in CE | ►2 experienced reviewers CE-WL images to FICE/Blue mode counterparts | ►Angioectasias (n = 18); | Blue mode; FICE 1,2,3 | Pillcam®SB1/SB2; Given®Imaging Ltd. | ►Total of 167 images, for all lesion categories: |
►Erosion/ulcers (n = 60); | ►Blue mode vs WL: image improvement in 83%; κ = 0.786 | ||||||||
►Villi oedema (n = 17); | ►FICE 1 vs WL: image improvement in 34%; κ = 0.646 | ||||||||
►Cobblestone (n = 11); | ►FICE 2 vs WL: image improvement in 8.6%; κ = 0.617 | ||||||||
►Blood lumen (n = 15); | ►FICE 3 vs WL: image improvement in 7.7%; κ = 0.669 | ||||||||
►LICS/other (n = 46) | |||||||||
Duque et al[118] | Portugal | Single centre | Prospective | Assess reproducibility and diagnostic accuracy of CE-FICE | ►4 physicians reviewed 150 FICE images; | 20 patients with OGIB | Blue mode; FICE 1,2,3 | PillCam®SB2; Given®Imaging Ltd. | ►Concordance between the 4 gastroenterologists: 0.650; |
►CE-WL identified 75 findings and the CE-FICE 95; | |||||||||
►2 experienced physicians analysed 20 CE; 1 interpreted CE-WL; the other, CE-FICE videos | ►CE-FICE did not miss any lesions identified by CE-WL and allowed the identification of a higher number of AVMs (35 vs 32) and erosions (41 vs 24) | ||||||||
Nakamura et al[119] | Japan | Single centre | Prospective | Assess preview of angioectasias by CE-FICE preview (compared to CE-WL) | ►One experienced physician analysed CEs in QuickView mode; | 50 pts with angiodysplasia were randomly assigned to 2 equally sized groups of CE-WL reading and CE-FICE reading | SBI; Blue mode; FICE 1,2,3 | PillCam®SB2; Given®Imaging Ltd. | ►Mean reading time: 14min for both CE-WL and CE-FICE reading; |
►The two previews for angiodysplasia were significantly superior to the function of SBI (P < 0.01); | |||||||||
►Mean reading time, sensitivity and specificity for angiodysplasia detection were evaluated including SBI | |||||||||
►Sens and Spec of CE-WL: 80% and 100%, respectively; | |||||||||
►Sens and Spec of CE-FICE: 91% and 86%, respectively; | |||||||||
►FICE reading was superior in Sens, while it resulted in more false (+) ve lesion findings and lower Spec | |||||||||
Sakai et al[120] | Japan | Single centre | Prospective | ►Assess whether CE-FICE improves detectability of SB lesions by CE trainees and if it contributes to reducing the bile-pigment effect; | ►4 gastroenterology trainees interpreted 12 CE videos with WL and FICE 1,2,3; | ►60 AVMs; ►82 erosions/ulcers | FICE 1,2,3 | PillCam®SB2; Given®Imaging Ltd. | ►60 angioectasias; CE trainees identified: 26 by CE-WL, 40 by CE-FICE1, 38 by CE-FICE2, 31 by CE-FICE3; |
►82 erosions/ulcerations, CE trainees identified: 38 by CE-WL, 62 by CE-FICE1, 60 CE- FICE2, 20 by CE-FICE3; | |||||||||
►Lesion detection rate under each of the three FICE settings was compared with that by conventional CE-WL | |||||||||
►CE-FICE 1 and 2 significantly improved detectability of angioectasias (P = 0.0017 and P = 0.014, respectively) and erosions/ulcers (P = 0.0012 and P = 0.0094, respectively); | |||||||||
►Evaluate whether poor bowel preparing affects the accuracy of lesion recognition by FICE | ►Detectability of SB lesions by CE-FICE1 was not affected (P = 0.59) by the presence of bile-pigments; | ||||||||
►Detectability of SB lesions by CE-WL (P = 0.020) and CE-FICE2 (P = 0.0023) was reduced by the presence of bile-pigments; | |||||||||
►In poor bowel visibility conditions, CE-FICE yielded a high rate of false-positive findings |
Ref. | Project | Status | Active actuation | Magnetic propulsion | Therapeutic capabilities |
Johannessen et al[124] | IDEAS: A miniature lab-in-a-pill multi-Sens or microsystem | Prototype | No | Yes | Yes |
Karagozler et al[125] | Miniature endoscopy capsule robot using biomimetic micro-patterned adhesives | Prototype | Yes | No | No |
Quirini et al[126] | An approach to capsular endoscopy with active motion | Prototype | Yes | No | No |
Valdastri et al[127] | Wireless therapeutic endoscopic capsule: in vivo experiment | Prototype | No | Yes | Yes |
Glass et al[128] | A legged anchoring mechanism for capsule endoscopes using micro-patterned adhesives | Prototype | Yes | No | No |
Valdastri et al[129] | An endoscopic capsule robot: a meso-scale engineering case study | Concept | Yes | No | No |
Tortora et al[130] | Propeller-based wireless device for active capsular endoscopy in the gastric district | Prototype | Yes | No | No |
Valdastri et al[131] | A magnetic internal mechanism for precise orientation of the camera in wireless endoluminal applications | Prototype | No | Yes | No |
Ciuti et al[132] | Robotic magnetic steering and locomotion of capsule endoscope for diagnostic and surgical endoluminal procedures | Prototype | No | Yes | Yes |
Bourbakis et al[133] | Design of new-generation robotic capsules for therapeutic and diagnostic endoscopy | Concept | Yes | No | Yes |
Gao et al[134] | Design and fabrication of a magnetic propulsion system for self-propelled capsule endoscope | Concept | No | Yes | No |
Simi et al[135] | Design, fabrication, and testing of a capsule with hybrid locomotion for gastrointestinal tract exploration | Concept | No | Yes | No |
Morita et al[136] | A further step beyond wireless capsule endoscopy | Concept | No | Yes | No |
Yang et al[137] | Autonomous locomotion of capsule endoscope in gastrointestinal | Concept | Yes | No | No |
Filip et al[138] | Electronic stool (e-Stool): A novel self-stabilizing video capsule endoscope for reliable non-invasive colonic imaging | Prototype | Yes | No | No |
Yim et al[139] | Design and rolling locomotion of a magnetically actuated soft capsule endoscope | Prototype | Yes | No | No |
Kong et al[140] | A robotic biopsy device for capsule endoscopy | Prototype | Yes | No | Yes |
Woods et al[141] | Wireless capsule endoscope for targeted drug delivery: Mechanics and design considerations | Prototype | Yes | No | Yes |
- Citation: Koulaouzidis A, Rondonotti E, Karargyris A. Small-bowel capsule endoscopy: A ten-point contemporary review. World J Gastroenterol 2013; 19(24): 3726-3746
- URL: https://www.wjgnet.com/1007-9327/full/v19/i24/3726.htm
- DOI: https://dx.doi.org/10.3748/wjg.v19.i24.3726