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Dive into the research topics where Eileen Dimond is active.

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Featured researches published by Eileen Dimond.


Journal of Clinical Oncology | 2004

Colon Cancer Screening Practices After Genetic Counseling and Testing for Hereditary Nonpolyposis Colorectal Cancer

Donald W. Hadley; Jean Jenkins; Eileen Dimond; Maria de Carvalho; Ilan R. Kirsch; Christina G.S. Palmer

PURPOSE Hereditary nonpolyposis colorectal cancer (HNPCC) is the most common hereditary form of colon cancer. Cancer screening recommendations differ between individuals identified to carry an HNPCC mutation and those who do not carry a known family mutation. We assessed the impact of genetic counseling and testing (GCT) on the use of endoscopic screening procedures and adherence to recommended endoscopic screening guidelines in 56 asymptomatic at-risk individuals from families known to carry an HNPCC mutation. PATIENTS AND METHODS We analyzed data on colonoscopy and flexible sigmoidoscopy screenings collected before GCT and 6 months and 12 months post-GCT on 17 mutation-positive and 39 true mutation-negative individuals. Main outcome measures were use of endoscopic screening and adherence to recommended guidelines for the relevant mutation status. Mutation status, age, sex, employment, and income were analyzed as predictor variables. RESULTS Among mutation-negative individuals, use of colonoscopy and flexible sigmoidoscopy decreased significantly between pre- and post-GCT (P <.00001 and P <.0003, respectively). Among mutation-positive individuals, a nonsignificant increase (P =.24) in use was noted. Age was also associated with use of endoscopic screening after GCT (P =.03). Mutation status (odds ratio [OR], 7.5; P =.02) and employment (OR, 8.6; P =.025) were associated with nonadherence to endoscopic screening guidelines. More mutation-negative individuals strictly adhered to guidelines than did mutation-positive individuals (87% v 65%). CONCLUSION Genetic counseling and testing for HNPCC significantly influences the use of colonic endoscopy and adherence to recommendations for colon cancer screening.


Genetics in Medicine | 2007

Randomized comparison of phone versus in-person BRCA1/2 predisposition genetic test result disclosure counseling

Jean Jenkins; Kathleen A. Calzone; Eileen Dimond; David J. Liewehr; Seth M. Steinberg; Oxana Jourkiv; Pam Klein; Peter W. Soballe; Sheila A. Prindiville; Ilan R. Kirsch

Purpose: This study evaluated whether phone results were equivalent to in-person result disclosure for individuals undergoing BRCA1/2 predisposition genetic testing.Methods: A total of 111 of 136 subjects undergoing education and counseling for BRCA1/2 predisposition genetic testing agreed to randomization to phone or in-person result disclosure. Content and format for both sessions were standardized. Data from the State-Trait Anxiety Inventory and the Psychological General Well-Being index were collected at baseline and then again at 1 week and 3 months after disclosure of test results. Baseline measures were administered after the following had occurred: counseling/education session had been conducted, informed consent had been obtained, and decision to be tested had been made. Satisfaction and cost assessments were administered after the result session. At 1 week, participants were asked their preferred method of result disclosure.Results: There were no differences in anxiety and general well-being measures between 50 phone and 52 in-person results disclosure. Both groups reported similar rates of satisfaction with services. Among those with a preference, 77% preferred the notification method assigned. There was a statistically significant preference for phone results among the 23% who did not prefer the method assigned. Greater costs were associated with in-person result disclosure.Conclusions: These data suggest that phone results are a reasonable alternative to traditional in-person BRCA1/2 genetic test disclosure without any negative psychologic outcomes or compromise in knowledge. However, further study is needed in a more clinically representative population to confirm these findings.


Cancer Nursing | 1998

THE ROLE OF THE NURSE IN CANCER GENETICS

Lindsay Middelton; Eileen Dimond; Kathleen A. Calzone; Joie Davis; Jean Jenkins

Knowledge gained from the Human Genome Project and related genetic research is already impacting clinical oncology nursing practice. Because cancer is now understood to be a genetic disease, changes in the traditional approaches to prevention, diagnosis, and therapeutic management of cancer are becoming increasingly genetically based. Therefore, to ensure competency in oncology nursing practice at all levels, nurses must incorporate an understanding of the underlying biology of carcinogenesis and the molecular rationale underlying strategies to prevent, diagnose, and treat cancer.


Cancer Nursing | 2001

Cancer genetics fundamentals.

June A. Peters; Jennifer T. Loud; Eileen Dimond; Jeanne Jenkins

It is often said that cancer is genetic. What exactly does that mean? This article is our answer to that question at the turn of the millennium. We present models of carcinogenesis, review basic cancer genetics terminology, and explain some of the fundamental genetic changes common to all types of cancer. These are organized into 6 sections of (1) self-sufficiency in growth signals, (2) insensitivity to growth-inhibitory signals, (3) evasion of programmed cell death, (4) limitless replicative potential, (5) sustained angiogenesis, and (6) tissue invasion and metastases. Underlying all of these changes are the even more fundamental enabling factors of genetic instability on both the chromosomal and the gene level. Finally, we look toward the future in a field where the future is now!


Cancer Nursing | 2002

CE TEST: The Role of the Nurse in Cancer Genetics

Lindsay Middelton; Eileen Dimond; Kathleen A. Calzone; Joie Davis; Jean Jenkins

Knowledge gained from the Human Genome Project and related genetic research is already impacting clinical oncology nursing practice. Because cancer is now understood to be a genetic disease, changes in the traditional approaches to prevention, diagnosis, and therapeutic management of cancer are becoming increasingly genetically based. Therefore, to ensure competency in oncology nursing practice at all levels, nurses must incorporate an understanding of the underlying biology of carcinogenesis and the molecular rationale underlying strategies to prevent, diagnose, and treat cancer.


Cancer Research | 1997

Mutations in β-Catenin Are Uncommon in Colorectal Cancer Occurring in Occasional Replication Error-positive Tumors

Maria N. Kitaeva; Liam Grogan; John P. Williams; Eileen Dimond; Kenneth Nakahara; Petr Hausner; John Denobile; Peter W. Soballe; Ilan R. Kirsch


Journal of Professional Nursing | 2001

Recommendations for educating nurses in genetics

Jean Jenkins; Cynthia A. Prows; Eileen Dimond; Rita Black Monsen; Janet K. Williams


Journal of Nursing Scholarship | 2001

Preparing for the future through genetics nursing education.

Jean Jenkins; Eileen Dimond; Seth M. Steinberg


Cancer Nursing | 1997

Clinical applications of genetic technologies to cancer care.

June Peters; Eileen Dimond; Jean Jenkins


Cancer Nursing | 2001

CE TEST: Cancer Genetics Fundamentals

June A. Peters; Jennifer T. Loud; Eileen Dimond; Jeanne Jenkins

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Jean Jenkins

National Institutes of Health

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Ilan R. Kirsch

National Institutes of Health

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Jennifer T. Loud

National Institutes of Health

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June A. Peters

National Institutes of Health

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Peter W. Soballe

Uniformed Services University of the Health Sciences

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Seth M. Steinberg

National Institutes of Health

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Cynthia A. Prows

Cincinnati Children's Hospital Medical Center

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David J. Liewehr

National Institutes of Health

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