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Dive into the research topics where Debrah Wirtzfeld is active.

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Featured researches published by Debrah Wirtzfeld.


Cancer | 2008

Hereditary diffuse gastric cancer: diagnosis, genetic counseling, and prophylactic total gastrectomy

Henry T. Lynch; Pardeep Kaurah; Debrah Wirtzfeld; Wendy S. Rubinstein; Scott M. Weissman; Jane F. Lynch; William M. Grady; Sara Wiyrick; Janine Senz; David Huntsman

A subset of patients with diffuse gastric cancer harbor deleterious cancer‐causing germline mutations in the type 1 E‐cadherin (epithelial) gene (CDH1), which predisposes to the autosomal dominantly inherited hereditary diffuse gastric cancer (HDGC) syndrome. These mutations are associated with a 70% life‐time risk for diffuse gastric cancer (DGC) and an additional 40% risk for lobular breast cancer in women. Management options for unaffected mutation carriers include prophylactic total gastrectomy.


American Journal of Surgery | 2009

Practice patterns and career satisfaction of Canadian female general surgeons

Pamela Hebbard; Debrah Wirtzfeld

BACKGROUND We wanted to study how female general surgeons in Canada manage lifestyle and career demands. METHODS All female Canadian general surgeons registered with the Royal College of Physicians and Surgeons of Canada were asked to complete a survey evaluating their practice patterns, personal lives, and levels of satisfaction related to these factors. RESULTS Eighty-five surveys (66%) were returned. Most respondents work in full-time clinical practices. While it was rare to find women in part-time or shared practices, 35% of women reported interest in these alternative models. Respondents described the necessary factors for a transition into alternative models. Job satisfaction was high (3.8 out of 5), with personal and parenting satisfaction being less highly rated (3.3 and 3.2, respectively). CONCLUSIONS Canadian female general surgeons have active and satisfying careers, although many would like to work in alternative practice models that better conform to their lifestyle demands. This pressure will have a significant impact on the future surgical workforce.


Radiotherapy and Oncology | 2016

133: Predictors of Nodal Response after Neoadjuvant Chemoradiotherapy for Rectal Adenocarcinoma; A Retrospective Study

Maged Nashed; Zachary Raizman; Gokulan Sivananthan; Daniel Kroeker; Pascal Lambert; Debrah Wirtzfeld; Robert Wightman

Purpose: Pathological response to neoadjuvant therapy has been linked to long-term outcome in rectal cancer (RC). Predicting nodal response is important especially in cases where watch and wait strategy is being considered. This study was carried out to identify potential predictors of pathological nodal response after long course chemoradiotherapy (CRT). Methods and Materials: A retrospective review of all patients with clinically node positive RC who received neoadjuvant CRT in Manitoba between January 2007 and December 2012 was conducted. Pre CRT tumour staging, treatment-related hematologic toxicities and pathologic nodal response data were recorded. Univariable and Multivariable analyses were performed using Bayesian logistic regression models. Results: Two hundred and six patients with clinically node positive RC were included in this study. The mean number of excised nodes was 16.35. One hundred and seventeen patients (56.8%) achieved a pathologic complete nodal response. Higher pre-treatment carcinoembryonic antigen (CEA) level (p = 0.0072) and presence of lymphovascular space invasion (LVI) in the surgical specimen (p = 0.0002) were independent predictors of lack of nodal response. In the univariable analysis, there was a tendency to a better response in patients who developed less treatment-induced lymphocytopenia. Conclusions: Pre-treatment CEA and presence of LVI predicted less pathological nodal response post CRT for rectal cancer. LVI is a pathological finding, however, signs of vascular invasion can be detected on the pre-treatment MRI. These results could potentially be used to identify favourable responders to CRT and guide management strategies of rectal cancer especially when organ and function preservation are pursued.


Journal of Clinical Oncology | 2012

A RAND/UCLA appropriateness study of the management of familial gastric cancer.

Matthew L. Dixon; Rajini Seevaratnam; Debrah Wirtzfeld; Robin S. McLeod; Lucy Helyer; Calvin Law; Carol J. Swallow; Lawrence Paszat; Jill Tinmouth; Roberta Cardoso; Alyson L. Mahar; Natalie G. Coburn

16 Background: Hereditary diffuse gastric cancer (HDGC) makes up 0.1-0.3% of all gastric cancers. Management of patients with HDGC is inconsistent and there is disagreement regarding management. METHODS A multi-disciplinary expert panel of 16 physicians from 6 countries scored 47 scenarios using the RAND/UCLA Appropriateness Methodology. Appropriateness was scored from 1 (highly inappropriate) to 9 (highly appropriate). Median appropriateness scores (AS) from 1-3 were considered inappropriate, 4-6 uncertain, and 7-9, appropriate. Agreement was reached when 11 of 16 panelists scored the statement similarly. If a statement was agreed to be appropriate, it was given a necessity score (NS) in the same manner. AS and NS are reported if agreement was met. RESULTS Gastric cancer (GC) patients with a family history of diffuse gastric cancer (DGC), lobular breast cancer or multiple family members with GC should be referred for genetics assessment and multidisciplinary decision-making (AS 8.0). It is appropriate for patients with DGC to have CDH1 mutation testing in a family with: (1) two or more cases of GC, with at least one case of DGC diagnosed before the age of 50 (AS 8.0); (2) three or more cases of GC diagnosed at any age, one or more of which is DGC (AS 8.0); (3) a patient diagnosed with DGC and lobular breast cancer (AS 8.0); or (4) a patient diagnosed with DGC under the age of 35 (AS 7.0, NS 5.0). A prophylactic total gastrectomy should be offered to CDH1 mutation carriers 20 years or older (AS 7.0). CONCLUSIONS The Gastric Cancer Processes of Care panelists have outlined high risk patients in whom CDH1 mutation status should be determined, and cases in which a prophylactic gastrectomy is appropriate.


JAMA | 2007

Founder and Recurrent CDH1 Mutations in Families With Hereditary Diffuse Gastric Cancer

Pardeep Kaurah; Andree MacMillan; Niki Boyd; Janine Senz; Alessandro De Luca; Nicki Chun; Gianpaolo Suriano; Sonya Zaor; Lori Van Manen; Cathy Gilpin; Sarah Nikkel; Mary Connolly-Wilson; Scott M. Weissman; Wendy S. Rubinstein; Courtney Sebold; Robert M. Greenstein; Jennifer Stroop; Dwight Yim; Benoît Panzini; Wendy McKinnon; Marc S. Greenblatt; Debrah Wirtzfeld; Daniel Fontaine; Daniel G. Coit; Sam S. Yoon; Daniel C. Chung; Gregory Y. Lauwers; Antonio Pizzuti; Carlos Vaccaro; Maria Ana Redal


Surgical Clinics of North America | 2008

Hereditary Diffuse Gastric Cancer: Prophylactic Surgical Oncology Implications

Henry T. Lynch; Edibaldo Silva; Debrah Wirtzfeld; Pamela Hebbard; Jane F. Lynch; David Huntsman


Canadian Journal of Surgery | 2009

Concordance with clinical practice guidelines for adjuvant chemotherapy in patients with stage I-III colon cancer: experience in 2 Canadian provinces.

Debrah Wirtzfeld; Lynn Mikula; Robert Gryfe; Pietro Ravani; Elizabeth Dicks; Pat Parfrey; Steve Gallinger; William G. Pollett


Canadian Journal of Surgery | 2009

The history of women in surgery

Debrah Wirtzfeld


Annals of Surgical Oncology | 2008

Predictors of Multivisceral Resection in Patients with Locally Advanced Colorectal Cancer

Anand Govindarajan; Novlette Fraser; Vanessa Cranford; Debrah Wirtzfeld; Steve Gallinger; Calvin Law; Andrew J. Smith; Anna R. Gagliardi


Canadian Journal of Surgery | 2007

Aggressive angiomyxoma of the pelvis: a case report.

Alex Mathieson; Soorna Chandrakanth; George Yousef; Patricia Wadden; Eric Sala; Debrah Wirtzfeld

Collaboration


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Pamela Hebbard

Memorial University of Newfoundland

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Pardeep Kaurah

University of British Columbia

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Henry T. Lynch

Case Western Reserve University

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Wendy S. Rubinstein

National Institutes of Health

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David Huntsman

University of British Columbia

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Janine Senz

University of British Columbia

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