Literature DB >> 30349099

A framework to build capacity for a reflex-testing program for Lynch syndrome.

Vanessa N Palter1, Natalie A Baker2,3, Linda Rabeneck4, Jill Tinmouth3,5, Anna R Gagliardi6, Erin D Kennedy3,7, June C Carroll3,7, Steven Gallinger3,8, Nancy N Baxter2,3.   

Abstract

PURPOSE: Lynch syndrome (LS) is the most common inherited cause of colorectal cancer. Although testing all colorectal tumors for LS is recommended, the uptake of reflex-testing programs within health systems has been limited. This multipronged study describes the design of a provincial program for reflex testing in Ontario, Canada.
METHODS: We recruited key stakeholders to participate in qualitative interviews to explore the barriers and facilitators to the implementation of a reflex-testing program. Data were analyzed in an iterative manner, key themes identified, and a framework for a proposed program developed.
RESULTS: Twenty-six key informants participated in our interviews, and several themes were identified. These included providing education for stakeholders (patients, primary care providers, surgeons); challenges with sustaining various resources (laboratory costs, increased workload for pathologists); ensuring consistency of reporting test results; and developing a plan to measure program success. Using these themes, a framework for the reflex-testing program was developed. At a subsequent stakeholder meeting, the framework was refined, and recommendations were identified.
CONCLUSIONS: This study identifies factors to ensure the effective implementation of a population-level program for reflex LS testing. The final product is a prototype that can be utilized in other jurisdictions, taking into account local environmental considerations.

Entities:  

Keywords:  Lynch syndrome; cancer prevention; reflex testing; screening

Mesh:

Year:  2018        PMID: 30349099     DOI: 10.1038/s41436-018-0342-8

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  6 in total

1.  Impact of the Knowledge Translation Research Network's grants program in cancer knowledge translation.

Authors:  M A O'Brien; E Grunfeld
Journal:  Curr Oncol       Date:  2019-08-01       Impact factor: 3.677

2.  When guidelines face reality - Lynch syndrome screening in the setting of public health system in a developing country.

Authors:  Vanessa Nascimento Kozak; Enilze Maria de Souza Fonseca Ribeiro; Milena Massumi Kozonoe; Sergio Ossamu Ioshii; Jose Claudio Casali da Rocha
Journal:  J Community Genet       Date:  2021-10-08

3.  Cost-effectiveness of Active Identification and Subsequent Colonoscopy Surveillance of Lynch Syndrome Cases.

Authors:  Elisabeth F P Peterse; Steffie K Naber; Corinne Daly; Aaron Pollett; Lawrence F Paszat; Manon C W Spaander; Melyssa Aronson; Robert Gryfe; Linda Rabeneck; Iris Lansdorp-Vogelaar; Nancy N Baxter
Journal:  Clin Gastroenterol Hepatol       Date:  2019-10-17       Impact factor: 11.382

4.  Universal tumor screening for Lynch syndrome: Perceptions of Canadian pathologists and genetic counselors of barriers and facilitators.

Authors:  Elizabeth Dicks; Daryl Pullman; Ken Kao; Andrée MacMillan; Gabrielle S Logan; Charlene Simmonds; Holly Etchegary
Journal:  Cancer Med       Date:  2019-05-17       Impact factor: 4.452

5.  Cytoplasmic MSH2 Related to Genomic Deletions in the MSH2/EPCAM Genes in Colorectal Cancer Patients With Suspected Lynch Syndrome.

Authors:  Lin Dong; Shuangmei Zou; Xianglan Jin; Haizhen Lu; Ye Zhang; Lei Guo; Jianqiang Cai; Jianming Ying
Journal:  Front Oncol       Date:  2021-05-14       Impact factor: 6.244

6.  Organizational readiness to implement population-based screening and genetic service delivery for hereditary cancer prevention and control.

Authors:  Sarah Knerr; Kathleen M West; Frank A Angelo
Journal:  J Genet Couns       Date:  2020-01-22       Impact factor: 2.717

  6 in total

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