Patrick W. Cleveland
Mayo Clinic
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Featured researches published by Patrick W. Cleveland.
Clinical Gastroenterology and Hepatology | 2010
Anna M. Buchner; Muhammad W. Shahid; Michael G. Heckman; Rebecca B. McNeil; Patrick W. Cleveland; Kanwar R. Gill; Anthony Schore; Marwan Ghabril; Massimo Raimondo; Seth A. Gross; Michael B. Wallace
BACKGROUND & AIMS Adenoma detection rates might be improved through use of high-definition colonoscopy, which can detect subtle mucosal changes. We investigated whether the use of high-definition white-light (HDWL) colonoscopy resulted in a higher rate of adenoma detection than standard-definition white-light (SDWL) colonoscopy in a clinical practice setting. METHODS This retrospective study included 2430 patients who underwent colonoscopies from September 2006 to December 2007; 1226 received SDWL colonoscopy and 1204 received HDWL colonoscopy. We analyzed data from consecutive screening, surveillance, and diagnostic colonoscopies, comparing adenoma and overall polyp detection between procedures. Potentially confounding variables were controlled using multivariable logistic regression analysis. RESULTS The adenoma detection rate was higher among patients who underwent HDWL compared with SDWL colonoscopies (28.8% vs 24.3%; P = .012), as was the polyp detection rate (42.2% vs 37.8%; P = .026). These findings remained after adjustments for potentially confounding variables (P = .018 and .022, respectively). CONCLUSIONS In a general clinical practice setting, HDWL colonoscopy resulted in a higher adenoma detection rate compared with SDWL colonoscopy. The use of SDWL colonoscopy could reduce the number of missed adenomas and the subsequent risk for colorectal cancer.
Gastrointestinal Endoscopy | 2011
Anna M. Buchner; Muhammad W. Shahid; Michael G. Heckman; Nancy N. Diehl; Rebecca B. McNeil; Patrick W. Cleveland; Kanwar R. Gill; Anthony Schore; Marwan Ghabril; Massimo Raimondo; Seth A. Gross; Michael B. Wallace
BACKGROUND Previous studies examining the effect of fellow participation on adenoma detection rate in colonoscopy have yielded conflicting results, and factors such as adenoma size and location have not been rigorously evaluated. OBJECTIVE To examine whether fellow participation during screening, surveillance, or diagnostic colonoscopy affects overall, size-specific, or location-specific adenoma or polyp detection rate. METHODS This was a retrospective study of 2430 colonoscopies performed in our ambulatory surgical center between September 2006 and December 2007, comparing adenoma and polyp detection rates of colonoscopies performed by fellows with supervising staff endoscopists (n = 318) with colonoscopies performed by staff endoscopists without fellow participation (n = 2112). Study participants included patients who underwent screening, surveillance, or diagnostic colonoscopies in our GI suite. Logistic regression analysis was used to evaluate the association of fellow participation with adenoma and polyp detection. RESULTS There was evidence of a higher rate of small (<5 mm) adenoma detection in colonoscopies with a fellow present (25% vs 17%, P = .001). This remained significant after multiple-testing adjustment (P ≤ .003 considered significant). Findings were similar, although not significant for small polyps (36% vs 29%, P = .007). There was a trend toward increased adenoma detection in colonoscopies with a fellow present compared with those without (30% vs 26%, P = .11). Multivariable adjustment for potentially confounding variables did not alter these associations. LIMITATIONS The study had a retrospective design, and information regarding bowel preparation was not available for 37% of patients. CONCLUSION Fellow involvement was associated with increased detection rates of small adenomas, providing evidence that the presence of a fellow during colonoscopy plays a role in enhancing the effectiveness of the examination.
Gastrointestinal Endoscopy | 2010
Patrick W. Cleveland; Kanwar R. Gill; Susan G. Coe; Timothy A. Woodward; Massimo Raimondo; Laith H. Jamil; Seth A. Gross; Michael G. Heckman; Julia E. Crook; Michael B. Wallace
BACKGROUND The factors associated with maximizing the cytological adequacy of EUS-guided FNA (EUS-FNA) in pancreatic tumor evaluation are not well-known. OBJECTIVE To examine associations of physician and procedural factors with the endpoint: the presence of an adequate cytological specimen found by using EUS-FNA in patients with pancreatic tumors and lymph nodes. DESIGN Retrospective cohort study. SETTING A U.S. tertiary care center. PATIENTS Patients undergoing EUS-FNA of pancreatic masses and lymph nodes. INTERVENTIONS Analysis of EUS-FNA procedures performed in our institution from 1997 to 2007. MAIN OUTCOME MEASUREMENTS Associations were evaluated between the primary endpoint of cytological adequacy and factors including the endoscopist, needle gauge, the number of needle passes attempted, the pathologist, and the presence of an onsite cytotechnologist to confirm an adequate specimen. EUS-FNA adequacy was determined by a pathologist based on the presence of definite benign or malignant tissue. RESULTS EUS-FNA was performed in 247 pancreatic masses and 276 lymph nodes. An adequate cytological sample was obtained in 240 (97%) pancreatic tumors (95% CI, 94%-99%) and 252 (91%) lymph nodes (95% CI, 87%-94%). For pancreatic tumors, there was no evidence of any associations between factors and cytological adequacy. For lymph nodes, cytological adequacy was improved when an onsite cytotechnologist was present (96% vs 84%, P = .002); no other factors showed statistically significant associations with cytological adequacy. LIMITATIONS Retrospective study, low power to detect associations. CONCLUSIONS The presence of an onsite cytotechnologist is an important factor in achieving successful EUS-FNA of suspicious lymph nodes in patients with pancreatic masses.
Gastrointestinal Endoscopy | 2008
Anna M. Buchner; Marwan Ghabril; Seth A. Gross; Patrick W. Cleveland; Kanwar R. Gill; Anthony Schore; Michael F. Picco; David S. Loeb; John R. Cangemi; Massimo Raimondo; Herbert C. Wolfsen; Timothy A. Woodward; Kenneth R. DeVault; Michael B. Wallace
Gastrointestinal Endoscopy | 2010
Timothy A. Woodward; Patrick W. Cleveland; Silvio W. De Melo; Massimo Raimondo; Michael G. Heckman; Nancy N. Diehl; Michael B. Wallace
Gastrointestinal Endoscopy | 2010
Patrick W. Cleveland; Timothy A. Woodward; Silvio W. De Melo; Massimo Raimondo; Chakri Panjala; Michael G. Heckman; Michael B. Wallace
Gastrointestinal Endoscopy | 2010
Timothy A. Woodward; Patrick W. Cleveland; Silvio W. De Melo; Massimo Raimondo; Sergio M. Crespo; Michael G. Heckman; Michael B. Wallace
Gastrointestinal Endoscopy | 2009
Timothy A. Woodward; Courtney Duran; Patrick W. Cleveland; Kanwar R. Gill; Michael B. Wallace; Massimo Raimondo; Michael G. Heckman
Gastrointestinal Endoscopy | 2008
Patrick W. Cleveland; Susan G. Coe; Timothy A. Woodward; Massimo Raimondo; Laith H. Jamil; Kanwar R. Gill; Seth A. Gross; Michael G. Heckman; Julia E. Crook; Michael B. Wallace
Gastrointestinal Endoscopy | 2010
Muhammad K. Hasan; Muhammad W. Shahid; Silvio W. De Melo; Timothy A. Woodward; Massimo Raimondo; Patrick W. Cleveland; Michael B. Wallace