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Longitudinal and Circumferential Distributions of Dysplasia and Early Neoplasia in Barrett's Esophagus: A Pooled Analysis of Three Prospective Studies
Raphael, Kara L; Inamdar, Sumant; McKinley, Matthew J; Martinez, Nichol; Cavaliere, Kimberly; Kahn, Allon; Leggett, Cadman L; Iyer, Prasad; Wang, Kenneth K; Trindade, Arvind J
INTRODUCTION/BACKGROUND:Studies have shown that dysplasia in Barrett's esophagus (BE) has a predilection for the right hemisphere. There is limited information on the longitudinal distribution. The aim was to determine both the longitudinal and circumferential distributions of dysplasia and early neoplasia from 3 prospective studies. METHODS:This is a pooled analysis from 3 prospective studies of patients with treatment-naive BE. Both circumferential and longitudinal locations (for BE segments greater than 1 cm) of dysplastic and early neoplastic lesions were recorded. RESULTS:A total of 177 dysplastic and early neoplastic lesions from 91 patients were included in the pooled analysis; of which 59.3% (n = 105) were seen on high-definition white light endoscopy, 29.4% (n = 52) on advanced imaging, and 11.2% (n = 20) with random biopsies. The average Prague score was C3M5. Of 157 lesions within BE segments greater than 1 cm, 49 (34.8%) lesions were in the proximal half, whereas 92 lesions (65.2%) were in the distal half (P < 0.001). The right hemisphere of the esophagus contained 55% (86/157) of the total lesions compared with 45% (71/157) for the left hemisphere (P = 0.02). This was because of the presence of high-grade dysplasia being concentrated in the right hemisphere compared with the left hemisphere (60% vs 40%, P = 0.002). DISCUSSION/CONCLUSIONS:In this pooled analysis of prospective studies, both low-grade dysplasia and high-grade dysplasia are more frequently found in the distal half of the Barrett's segment. This study confirms that the right hemisphere is a hot spot for high-grade dysplasia. Careful attention to these locations is important during surveillance endoscopy.
PMCID:7901801
PMID: 33617190
ISSN: 2155-384x
CID: 4794262
Use of a Novel Portable Non-powered Suction Device in Patients With Oropharyngeal Dysphagia During a Choking Emergency
McKinley, Matthew J; Deede, Jennifer; Markowitz, Brian
Choking remains a leading cause of accidental death and morbidity worldwide. Currently, there is no device to assist in the resuscitation of a choking victim when standard maneuvers fail. A novel portable non-powered suction device (LifeVac; LifeVac LLC, Nesconset, NY) has been developed and may have potential use in patients with oropharyngeal dysphagia who are at increased risk of choking. The device is FDA registered and distributed worldwide. This case series provides a summary of self-reported data regarding the use of the suction device in adult patients with oropharyngeal dysphagia during real-world choking emergencies recorded between January 2014 and July 2020. Over a 6-year monitoring period the device has been reported to be successful in the resuscitation of 38 out of 39 patients with oropharyngeal dysphagia during choking emergencies. Although the obstruction was removed with the device from the 39th patient, resuscitation was not successful and he succumbed to his injuries. This portable, non-powered suction device may be useful in resuscitating patients with oropharyngeal dysphagia who are choking. The reported cases describe successful use of the device in real-world settings with minimal risk. Resuscitating patients with oropharyngeal dysphagia using this device may be a viable option when abdominal thrusts or back blows fail to resolve a choking emergency.
PMCID:8847721
PMID: 35186960
ISSN: 2296-858x
CID: 5164952
Successful treatment of refractory Barrett's neoplasia with hybrid argon plasma coagulation: a case series
Trindade, Arvind J; Wee, Diana; Wander, Praneet; Stewart, Molly; Lee, Calvin; Benias, Petros C; McKinley, Matthew J
PMID: 32106320
ISSN: 1438-8812
CID: 4323602
Volumetric laser endomicroscopy and its application to Barrett's esophagus: results from a 1,000 patient registry
Smith, M S; Cash, B; Konda, V; Trindade, A J; Gordon, S; DeMeester, S; Joshi, V; Diehl, D; Ganguly, E; Mashimo, H; Singh, S; Jobe, B; McKinley, M; Wallace, M; Komatsu, Y; Thakkar, S; Schnoll-Sussman, F; Sharaiha, R; Kahaleh, M; Tarnasky, P; Wolfsen, H; Hawes, R; Lipham, J; Khara, H; Pleskow, D; Navaneethan, U; Kedia, P; Hasan, M; Sethi, A; Samarasena, J; Siddiqui, U D; Gress, F; Rodriguez, R; Lee, C; Gonda, T; Waxman, I; Hyder, S; Poneros, J; Sharzehi, K; Di Palma, J A; Sejpal, D V; Oh, D; Hagen, J; Rothstein, R; Sawhney, M; Berzin, T; Malik, Z; Chang, K
Volumetric laser endomicroscopy (VLE) uses optical coherence tomography (OCT) for real-time, microscopic cross-sectional imaging. A US-based multi-center registry was constructed to prospectively collect data on patients undergoing upper endoscopy during which a VLE scan was performed. The objective of this registry was to determine usage patterns of VLE in clinical practice and to estimate quantitative and qualitative performance metrics as they are applied to Barrett's esophagus (BE) management. All procedures utilized the NvisionVLE Imaging System (NinePoint Medical, Bedford, MA) which was used by investigators to identify the tissue types present, along with focal areas of concern. Following the VLE procedure, investigators were asked to answer six key questions regarding how VLE impacted each case. Statistical analyses including neoplasia diagnostic yield improvement using VLE was performed. One thousand patients were enrolled across 18 US trial sites from August 2014 through April 2016. In patients with previously diagnosed or suspected BE (894/1000), investigators used VLE and identified areas of concern not seen on white light endoscopy (WLE) in 59% of the procedures. VLE imaging also guided tissue acquisition and treatment in 71% and 54% of procedures, respectively. VLE as an adjunct modality improved the neoplasia diagnostic yield by 55% beyond the standard of care practice. In patients with no prior history of therapy, and without visual findings from other technologies, VLE-guided tissue acquisition increased neoplasia detection over random biopsies by 700%. Registry investigators reported that VLE improved the BE management process when used as an adjunct tissue acquisition and treatment guidance tool. The ability of VLE to image large segments of the esophagus with microscopic cross-sectional detail may provide additional benefits including higher yield biopsies and more efficient tissue acquisition. Clinicaltrials.gov NCT02215291.
PMCID:6853704
PMID: 31037293
ISSN: 1442-2050
CID: 4268322
Volumetric laser endomicroscopy feature discovery and diagnostic performance optimization for barrett's esophagus dysplasia using laser-targeted biopsies with histopathologic correlation [Meeting Abstract]
Leggett, C; Trindade, A; McKinley, M; Chang, K J; Samarasena, J; Singh, S; Mashimo, H; Smith, M S; Bechard, V; Vieth, M; Odze, R; Tearney, G J; Wang, K K
INTRODUCTION: Volumetric laser endomicroscopy (VLE) is a high-resolution imaging modality used in Barrett's esophagus (BE) surveillance. Established VLE scoring systems use a combination of features to guide BE dysplasia diagnosis but it remains unclear whether these features are sufficient to reach optimal VLE diagnostic performance. This study explores an exhaustive list of VLE features using one-to-one imaging to pathology correlation to develop optimal VLE diagnostic models for BE dysplasia.
METHOD(S): In this prospective, multi-center (5 sites) study, patients with dysplastic BE underwent VLE with laser targeted regions of interest (ROIs), followed by standard surveillance endoscopy and biopsy directed to laser-marked sites. Histology was reviewed by two GI pathologists (MV, RO) who achieved a consensus diagnosis (gold-standard). ROIs were dysplastic if low-grade dysplasia (LGD), high-grade dysplasia (HGD) or intramucosal adenocarcinoma (IMC) was present. Two VLE experts (CLL, GJT) reviewed ROIs and corresponding endoscopic images to identify and define a set of VLE features associated with BE dysplasia. A multi-variable logistic regression model based on least absolute shrinkage and selection operator (LASSO) method was developed to determine the optimal diagnostic performance of these features. A decision tree model with high clinical usability also was developed to evaluate VLE diagnostic performance for real-time image interpretation.
RESULT(S): A total of 461 VLE ROIs with matching histology were obtained from 150 patients (Table 1). A final dataset of 55 neoplastic (LGD, 12; HGD, 24; IMC, 19) and 56 randomly selected non-dysplastic ROIs were reviewed. Twenty-eight VLE features were identified describing layering, signal intensity, surface topography, and glandular characteristics. LASSO logistic regression modeling identified 5 VLE features which when utilized optimized diagnostic performance with an area under the curve (AUC) for BE dysplasia of 0.95 (Figure 1). To improve clinical usability, a decision tree model was optimized to three levels with an AUC of 0.90 (Figure 2).
CONCLUSION(S): This study represents the most comprehensive review of VLE features associated with BE dysplasia to date. The proposed high-performing diagnostic models suggest that VLE can be used efficiently and effectively to enhance BE surveillance by identifying ROIs for targeted biopsy. Further validation of the proposed VLE models will determine their clinical utility
EMBASE:630836552
ISSN: 1572-0241
CID: 4316452
Endoscopic Surveillance of Barrett's Esophagus Using Volumetric Laser Endomicroscopy With Artificial Intelligence Image Enhancement
Trindade, Arvind J; McKinley, Matthew J; Fan, Cathy; Leggett, Cadman L; Kahn, Allon; Pleskow, Douglas K
PMID: 31078625
ISSN: 1528-0012
CID: 4097332
Mutational load may predict risk of progression in patients with Barrett's oesophagus and indefinite for dysplasia: a pilot study
Trindade, Arvind J; McKinley, Matthew J; Alshelleh, Mohammad; Levi, Gabriel; Stewart, Molly; Quinn, Kathy J; Thomas, Rebecca M
Background and aims/UNASSIGNED:Mutational load (ML) has been shown to help risk-stratify those that may progress from non-dysplastic Barrett's oesophagus (BE) to dysplastic disease. Management of patients with BE and indefinite for dysplasia (BE-IND) is challenging and risk stratification tools are lacking. The aim of this pilot study is to evaluate the utility of ML for risk stratification in patients with BE-IND. Methods/UNASSIGNED:This is a single-centre, retrospective pilot study evaluating ML quantification in patients with BE-IND. Histology at follow-up endoscopy at least 1 year after the baseline endoscopy was used to determine if a patient progressed to low or high dysplasia. The ML levels were then compared among patients who progressed to dysplasia versus those who did not. Results/UNASSIGNED:Thirty-five patients who met the inclusion criteria were identified, and seven met the exclusion criteria. Twenty-eight patients were analysed, of whom eight progressed to low-grade dysplasia (6) and high-grade dysplasia (2). Seven of these eight patients had some level of genomic instability detected in their IND biopsy (ML ≥0.5). Ten of the 20 (50%) who did not progress had no ML level. At an ML cut-off above 1.5, the risk of progression to high-grade dysplasia was 33% vs 0% (p=0.005), with a sensitivity of 100% and a specificity of 85%. Conclusion/UNASSIGNED:These results indicate that ML may be able to risk-stratify progression to high-grade dysplasia in BE-IND. Larger studies are needed to confirm these findings.
PMCID:6361327
PMID: 30815274
ISSN: 2054-4774
CID: 3722092
Volumetric laser endomicroscopy features of dysplasia at the gastric cardia in Barrett's oesophagus: results from an observational cohort study
Trindade, Arvind J; Raphael, Kara L; Inamdar, Sumant; Stewart, Molly; Berkowitz, Joshua; Vegesna, Anil; McKinley, Matthew J; Benias, Petros C; Kahn, Allon; Leggett, Cadman L; Lee, Calvin; Sejpal, Divyesh V; Rishi, Arvind
Objective/UNASSIGNED:Volumetric laser endomicroscopy (VLE) is an advanced imaging modality used in Barrett's oesophagus (BE) to help identify dysplasia in the oesophagus. VLE criteria exist for oesophageal dysplasia but not for dysplasia in the gastric cardia. The aim of this study was to determine if there are in vivo VLE features that can predict gastric cardia dysplasia in BE. Design/UNASSIGNED:This was a single-centre observational cohort study from August 2016 to August 2018. Patients were included if they had BE, were undergoing a VLE exam as standard of care, and had a suspicious target laser marked at the gastric cardia. The following VLE features were correlated to histology to determine if an association existed between histology subtype and VLE feature: wide crypts, irregular surface, one large isolated gland, multiple glands, and complex glands. Results/UNASSIGNED:A total of 110 in vivo gastric cardia targets in 77 patients with BE were analysed. The following abnormalities were identified: 61 wide crypts, 34 isolated glands, 16 irregular surfaces, 15 multiple glands, and 11 complex glands. Complex glands were the only VLE feature that correlated to any histology subtype. They were present in 71% of targets with high-grade dysplasia (HGD), T1a cancer or T1b cancer and had a sensitivity, specificity, and accuracy of 71%, 99%, and 85%, respectively. Of the 10 patients with complex glands on VLE and HGD/cancer on histology, 4 had a normal-appearing mucosa (40%) on endoscopy. Conclusion/UNASSIGNED:Identification of complex glands on VLE may aid in detection of HGD or early cancer in the gastric cardia in BE. This is particularly important, as dysplasia at the gastric cardia can be difficult to see endoscopically.
PMCID:6827805
PMID: 31749979
ISSN: 2054-4774
CID: 4209172
Incremental yield of dysplasia detection in Barrett's esophagus using volumetric laser endomicroscopy with and without laser marking compared with a standardized random biopsy protocol
Alshelleh, Mohammad; Inamdar, Sumant; McKinley, Matthew; Stewart, Molly; Novak, Jeffrey S; Greenberg, Ronald E; Sultan, Keith; Devito, Bethany; Cheung, Mary; Cerulli, Maurice A; Miller, Larry S; Sejpal, Divyesh V; Vegesna, Anil K; Trindade, Arvind J
BACKGROUND AND AIMS/OBJECTIVE:Volumetric laser endomicroscopy (VLE) is a new wide field advanced imaging technology for Barrett's esophagus (BE). No data exist on incremental yield of dysplasia detection. Our aim is to report the incremental yield of dysplasia detection in BE using VLE. METHODS:This is a retrospective study from a prospectively maintained database from 2011-2017 comparing the dysplasia yield of 4 different surveillance strategies in an academic BE tertiary care referral center. The groups were (1) random biopsies (RB), (2) Seattle protocol random biopsies (SP), (3) VLE without laser marking (VLE) and (4) VLE with laser marking (VLEL). RESULTS:A total of 448 consecutive patients (79 RB, 95 SP, 168 VLE, and 106 VLEL) met inclusion criteria. After adjusting for visible lesions, the total dysplasia yield was 5.7%, 19.6%, 24.8%, and 33.7%, respectively. When compared with just the SP group, VLEL group had statistically higher rates of overall dysplasia yield (19.6 % vs 33.7%, p=0.03; OR 2.1, p=0.03). The RB and VLE groups did not have statistically significant differences in dysplasia detection compared with the SP group. Both VLEL and VLE groups have statistically significant differences in neoplasia (high-grade dysplasia and intramucosal cancer) detection compared with the SP group (14% vs 1%, p=0.001 and 11% vs 1%, p=0.003). CONCLUSION/CONCLUSIONS:A surveillance strategy involving VLEL lead to statistically significant higher yield of dysplasia and neoplasia detection compared with a standard random biopsy protocol. These results support the use of VLEL for surveillance in BE in academic centers.
PMID: 29410080
ISSN: 1097-6779
CID: 2989682
LIQUID NITROGEN SPRAY CRYOTHERAPY FOR PALLIATION OF INVASIVE ESOPHAGEAL CARCINOMA: RESULTS FROM A MULTICENTER US REGISTRY [Meeting Abstract]
Ramay, Fariha H.; Shaheen, Nicholas J.; Kaul, Vivek; Nieto, Jose; Joshi, Virendra; Litle, Virginia; Fernando, Hiran C.; Fukami, Norio; Hoffman, Brenda J.; Bizekis, Costas; McKinley, Matthew; Habr, Fadlallah; Nishioka, Norman S.; Tsai, Franklin; Coyle, Walter J.; Pleskow, Douglas K.; Greenwald, Bruce D.
ISI:000435509900430
ISSN: 0016-5107
CID: 3646462