Jane E. Onken
Duke University
Network
Latest external collaboration on country level. Dive into details by clicking on the dots.
Publication
Featured researches published by Jane E. Onken.
Inflammatory Bowel Diseases | 2004
Bruce E. Sands; Carmen Cuffari; Jeffry A. Katz; Subra Kugathasan; Jane E. Onken; Charles Vitek; Walter A. Orenstein
During the past 2 decades, medical therapy for Crohns disease (CD) and ulcerative colitis (UC) has grown to incorporate a variety of immunesuppressing agents. At the same time, basic insights into the aberrant mucosal immune response underlying inflammatory bowel disease (IBD) have expanded dramatically. The interplay of host susceptibility to infection and the safety and efficacy of immunization for vaccine-preventable diseases has been explored in other immune-mediated disease states but only rarely in IBD. The purpose of this review is to formulate best-practice recommendations for immunization in children and adults with IBD by considering the effects of the IBD disease state and its treatments on both the safety and efficacy of immunization. To do so, we first considered the routine recommendations for immunization of children, adults and distinct populations at increased risk for vaccine-preventable disease. Because it was rarely possible to examine direct data on safety and efficacy of immunization in IBD populations, we relied to a large extent upon extrapolation from similar populations and from knowledge of basic mechanisms. The literature suggests that efficacy of immunization may be diminished in some patients whose immune status is compromised by immune suppression. However, except for live agent vaccines, most immunizations may be safely administered to patients with IBD even when immune compromised. Conversely, protection against vaccine-preventable illness may be of even greater benefit to those at risk for morbid or lethal complications of infections because of an immune compromised state. We conclude that for most patients with IBD, recommendations for immunization do not deviate from recommended schedules for the general population.
Cancer Epidemiology, Biomarkers & Prevention | 2005
Karen M. Emmons; Colleen M. McBride; Elaine Puleo; Kathryn I. Pollak; Elizabeth C. Clipp; Karen M. Kuntz; Bess H. Marcus; Melissa A. Napolitano; Jane E. Onken; Frank Farraye; Robert H. Fletcher
Background: This report examines the outcome data for Project PREVENT, a two-site randomized control trial designed to reduce behavioral risk factors for colorectal cancer among individuals who have been diagnosed with adenomatous colon polyps. Methods: The study sample included 1,247 patients with recent diagnosis of adenomatous colorectal polyps. Within 4 weeks following the polypectomy, participants completed a baseline survey by telephone, and were randomized to either Usual Care (UC) or the PREVENT intervention, which was designed to target multiple risk factors. The intervention consisted of a telephone-delivered intervention plus tailored materials, and focused on the six primary behavioral risk factors for colorectal cancer, including red meat consumption, fruit and vegetable intake, multivitamin intake, alcohol, smoking, and physical inactivity. Results: Participation in the PREVENT intervention was associated with a significantly greater reduction in prevalence of multiple risk factors for colorectal cancer compared with UC. Only about one third of UC participants dropped any risk factors during the study period, compared with almost half of the PREVENT participants. PREVENT participants were also significantly more likely to change more than one behavior than UC participants. Conclusions: The PREVENT intervention was effective in helping patients change multiple risk factors. These results provide further support that more comprehensive interventions that move beyond emphasis on a single risk factor are acceptable to patient populations, can result in improvements, and are cost effective.
The American Journal of Gastroenterology | 1998
Dawn Provenzale; John Wong; Jane E. Onken; Joseph Lipscomb
Abstract Objective: To illustrate the principles of cost-effectiveness analysis, this third article in the “Primer on Economic Analysis for the Gastroenterologist” applies published criteria for appraising an economic analysis to a study of the cost-effectiveness of surveillance of patients with ulcerative colitis. Methods: We review and apply the 10 standard criteria for critical appraisal and evaluation of cost-effectiveness analyses. Summary: We outlined the development and critique of a decision analytic model that examines the cost-effectiveness of surveillance of patients with ulcerative colitis, and we compared the cost-effectiveness of surveillance of patients with ulcerative colitis to other well-accepted medical practices.
Journal of Clinical Gastroenterology | 2001
Dawn Provenzale; Jane E. Onken
This review article on the surveillance of patients with ulcerative colitis provides an overview of the criteria for evaluating screening and surveillance programs and applies the criteria to the available evidence to determine the effectiveness of the surveillance of patients with ulcerative colitis. We examine the clinical outcomes associated with surveillance, the additional clinical time required to confirm the diagnosis of dysplasia and cancer, compliance with surveillance and follow-up, and the effectiveness of the individual components of a surveillance program, including colonoscopy and pathologists interpretation. The disability associated with colectomy is considered, as are the cost and acceptability of surveillance programs. Patients with long-standing ulcerative colitis are at risk for developing colorectal cancer. Recommended surveillance colonoscopy should be supported. New endoscopic and histopathologic techniques to improve the identification of high-risk patients may enhance the effectiveness and cost-effectiveness of surveillance practices.
Transfusion | 2013
Jane E. Onken; David B. Bregman; Robert A. Harrington; David Morris; Peter Acs; Bruce Akright; Charles Barish; Birbal S. Bhaskar; Gioi N. Smith-Nguyen; Angelia Butcher; Todd A. Koch; Lawrence T. Goodnough
Many patients receiving oral iron for iron deficiency anemia (IDA) cannot tolerate or fail to respond to therapy, and existing intravenous (IV) iron formulations often require repeated administrations. Ferric carboxymaltose (FCM), a nondextran IV formulation, permits larger single doses.
Clinical Immunology | 2008
Daniel D. Hampton; Martin H. Poleski; Jane E. Onken
Inflammatory bowel disease (IBD) is a T cell driven inflammatory condition of the gut. Following solid organ transplantation (SOT), de novo IBD has been reported despite anti-T cell therapy for the prevention of organ rejection. This paradox is illustrated with a case report, highlighting the difficult diagnostic criteria, the potential role of Damage or Pathogen Associated Molecular Pattern Molecules [DAMPs and PAMPs] that drives aspects of ongoing inflammation within the transplanted organ as well as the intestine, and the therapeutic strategies applied. Recurrent IBD is more common than de novo IBD following transplantation, with cumulative risks ten years after orthotopic liver transplantation of 70% and 30%, respectively. Furthermore, the annual incidence of de novo IBD following solid organ transplantation has been estimated to be 206 cases/100,000 or ten times the expected incidence of IBD in the general population (approximately 20 cases/100,000). The association of IBD with other autoimmune conditions such as primary sclerosing cholangitis and autoimmune hepatitis, both common indications for liver transplantation, may play a contributory role, particularly in view of the observation that IBD is more common following liver transplant than other solid organ transplants. Recurrent IBD following transplant appears to run a more aggressive course than de novo IBD, with a higher proportion requiring colectomy for medically refractory disease. Risk factors that have been associated with development of post-transplant IBD include acute CMV infection and the use of tacrolimus.
Alimentary Pharmacology & Therapeutics | 2003
Richard S. Bloomfeld; Jane E. Onken
Background : Azathioprine (AZA) and its active metabolite mercaptopurine (MP) are frequently used in the management of inflammatory bowel disease. Measurement of the AZA/MP metabolites, thioguanine (TG) and methylmercaptopurine (MMP), has been suggested as a means to optimize therapy with AZA/MP in inflammatory bowel disease.
The American Journal of Gastroenterology | 2002
Jane E. Onken; Joëlle Y. Friedman; Sujha Subramanian; Kevin P. Weinfurt; Shelby D. Reed; Joshua H Malenbaum; Troy Schmidt; Kevin A. Schulman
OBJECTIVE:Because of the paucity of existing literature on treatment and costs associated with sessile lesions, the objectives of this study were to perform a retrospective analysis on patients with sessile polyps to identify patient and polyp characteristics, to determine treatment patterns, and to estimate the cost of treating these patients.METHODS:We conducted a retrospective, observational cohort study of 280 patients who presented to a large teaching hospital between 1997 and 2000 with at least one sessile or broad-based pedunculated colorectal polyp of any size or histology, not including adenocarcinoma greater than stage T1.RESULTS:Mean polyp size was 1.3 cm, and two thirds of polyps were removed in a single procedure. The number of repeat procedures increased with polyp size (Kendall τ-b = 0.47; 95% CI = 0.39–0.55). Patients with polyps ≥2 cm were 5.88 times more likely than patients with smaller polyps to undergo a surgical procedure. Surgical procedures required 88.01 min longer than nonsurgical procedures (95% CI = 74.43–102.42). Mean total cost of treatment was
Nephrology Dialysis Transplantation | 2014
Jane E. Onken; David B. Bregman; Robert A. Harrington; David Morris; John Buerkert; Douglas Hamerski; Hussain Iftikhar; Roberto Mangoo-Karim; Edouard R. Martin; Carlos O. Martinez; George Edward Newman; Wajeh Y. Qunibi; Dennis L. Ross; Bhupinder Singh; Mark T. Smith; Angelia Butcher; Todd A. Koch; Lawrence T. Goodnough
2,038 (range
Alimentary Pharmacology & Therapeutics | 2016
William J. Sandborn; Bal R. Bhandari; Ronald Fogel; Jane E. Onken; E. Yen; X. Zhao; Z. Jiang; D. Ge; Yan Xin; Z. Ye; D. French; J. A. Silverman; B. Kanwar; G. M. Subramanian; John G. McHutchison; Scott D. Lee; Lisa M. Shackelton; Rish K. Pai; Barrett G. Levesque; Brian G. Feagan
153 to