Russell D. Cohen, MD, FACG, AGAF
Professor of Medicine, Pritzker School of Medicine
Co-Director, Inflammatory Bowel Disease Center
The University of Chicago Medical Center
Department of Medicine, Section of Gastroenterology
Chicago, Illinois

Russell D. Cohen, MD. FACG, AGAF is a Professor of Medicine in the Department of Medicine, Section of Gastroenterology at the University of Chicago in Illinois. In addition, he is Co-Director of the Inflammatory Bowel Disease Center at the University of Chicago.

Dr. Cohen earned his BS in biological sciences at Cornell University in Ithaca, New York, and his MD with honors at Mount Sinai School of Medicine in New York City. He completed his residency in internal medicine at Beth Israel Hospital/Harvard Medical School in Boston. His fellowship in gastroenterology and nutrition and his senior fellowship in inflammatory bowel diseases were conducted at the University of Chicago. Following his fellowships, Dr. Cohen was a Health Studies Scholar at the University of Chicago.

Research interests of Dr. Cohen includes investigations of both standard and experimental pharmacological therapies, such as novel immunomodulatory agents, as well as studies analyzing quality of life and the economics involved in the diagnosis and treatment of inflammatory bowel disease. He has been Principal Investigator and Co-investigator for more than 50 research projects in his field.

Dr. Cohen is an editor of two medical text books, and has authored or coauthored more than 100 articles, abstracts, reviews, books, book chapters, and audiotapes primarily devoted to Crohn’s disease and ulcerative colitis. His articles on these and related topics are published in prestigious scientific journals such as Gastroenterology, American Journal of Gastroenterology, and Inflammatory Bowel Diseases. He also is a reviewer for multiple journals, including New England Journal of Medicine, Gastroenterology, Gut, and American Journal of Gastroenterology, and is an Associate Section Editor of the journal Inflammatory Bowel Diseases, He is a member of the American Medical Association, the American College of Gastroenterology, the American College of Physicians, and the American Gastroenterological Association. Dr. Cohen is the recipient of multiple honors and awards, and he is named in Best Doctors in America, America’s Top Gastroenterologists, and Top Doctors in the Chicago Metro Area.

University of Chicago Medical Center

The University of Chicago Medical Center has been at the forefront of digestive disease care since 1927, when our doctors created the nation’s first hospital-based gastroenterology department. Today, we provide care for all types of gastrointestinal conditions, from inflammatory bowel disease and liver disorders, to esophageal, pancreatic, and bile duct diseases and all forms of gastrointestinal cancers. U.S.News & World Report ranks our digestive disorders program the highest in Illinois and the ninth in the country. We have patient-centered programs for many common and rare Gi Disorders.

 Study to Determine Risk Factors for Post-operative Infection in Inflammatory Bowel Disease (PUCCINI)

Understanding of how best to treat inflammatory bowel disease (IBD) has evolved over the last ten years. Evidence now suggests that the most effective therapy early in the course of Crohn's disease (CD) and ulcerative colitis (UC) involves the use of immune suppressing medications such as the anti-Tumor Necrosis Factor (anti-TNF) agents infliximab, adalimumab, and certolizumab. However, many CD and UC patients still ultimately require surgery despite the use of these medications. Side effects of the anti-TNF agents include increased risk of infections due to their effect on the immune system. Little is known about how use of these medications near the time of surgery may affect patients' risks of infection or other post-operative complications. The only available studies on this topic have given conflicting results. These studies have been limited by the fact that they have been small in size and retrospective. Retrospective studies primarily involve chart review as the method of identifying potential risk factors for infections and other complications after they have already occurred. This method limits both the type and quality of information/data that can be collected. The conflicting results have led to variance in practice patterns with regards to management of anti-TNF agents, the timing of surgery, and even the types of surgery.

By enrolling patients at the time of their surgery, collecting extensive information may be possible than previously studied on potential risk factors for both infectious and non-infectious complications following surgery. Risk factors to be studied will include individual patient characteristics, disease characteristics, surgical methods, novel characteristics of CT scans and MRIs and extensive medication exposures. The primary objective is to determine if exposure to anti-TNF agents prior to surgery increases the risk of infection post-operatively. And evaluate exposure to anti-TNF agents by both patient history of use and measurement of anti-TNF drug levels at the time of surgery. Monitoring of drug levels at the time of surgery has never been utilized in this way to evaluate the risk of anti-TNF agents in IBD. However, this has been done to assess the risk of other medications in different diseases.

If anti-TNF agents are found to pose a risk for infectious or non-infectious outcomes in IBD patients undergoing surgery, change maybe needed in the way these medications are used around the time of surgery. Additionally, by collecting comprehensive information on other potential risk factors besides medication use patients at greatest risk for bad outcomes can be identified and take protective measures when possible. The aims of this study address the CCFA challenge to better define the risks of medical and surgical therapies to improve the quality of care of IBD patients undergoing surgery.

Estimated Enrollment: 1000
Study Start Date: February 2014
Estimated Study Completion Date: January 2017
Estimated Primary Completion Date: January 2017 (Final data collection date for primary outcome measure)

Ages Eligible for Study: 18 Years and older
Genders Eligible for Study: Both
Accepts Healthy Volunteers: No
Sampling Method: Non-Probability Sample

 Efficacy and Safety of Anti-MAP Therapy in Adult Crohn's Disease (MAPUS)

The investigators hypothesize that RHB-104 will have greater efficacy than placebo in Crohn's disease.

Estimated Enrollment: 240
Study Start Date: September 2013
Estimated Study Completion Date: November 2016
Estimated Primary Completion Date: July 2016 (Final data collection date for primary outcome measure)

Ages Eligible for Study: 18 Years to 75 Years
Genders Eligible for Study: Both
Accepts Healthy Volunteers: No