Evidence map›Paper›PMID 21629123›Full record

ArticleGenetics in medicine : official journal of the American College of Medical Genetics2011

Personalized cancer genetics training for personalized medicine: improving community-based healthcare through a genetically literate workforce.

Kathleen R Blazer, Deborah J Macdonald, Julie O Culver, Carin R Huizenga, Robert J Morgan, Gwen C Uman, Jeffrey N Weitzel

Abstract read
In one paragraph

Article in Genetics in medicine : official journal of the American College of Medical Genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Systematic evidence review and meta-analysis of outcomes associated with cancer genetic counseling.Genetics in medicine : official journal of the American College of Medical Genetics · 2024
    Pooled it
  2. Pooled it
  3. Genetics/genomics education for nongenetic health professionals: a systematic literature review.Genetics in medicine : official journal of the American College of Medical Genetics · 2017
    Pooled it
  4. Review
  5. Mainstreaming genetic testing in community oncology settings.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Article
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  10. Developing Policy Infrastructure to Guide Genomics-Informed Oncology Nursing in Canada: An Interpretive Descriptive Study.The Canadian journal of nursing research = Revue canadienne de recherche en sciences infirmieres · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Kathleen R BlazerDivision of Clinical Cancer Genetics, City of Hope Comprehensive Cancer Center, Duarte, California 91010, USA.
Deborah J Macdonald
Julie O Culver
Carin R Huizenga
Robert J Morgan
Gwen C Uman
Jeffrey N Weitzel

Funding

CLINICAL CANCER GENETICS FELLOWSHIP PROGRAMR25CA085771 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI WEITZEL, JEFFREY N · 2001 to 2010
$3.8M
Community Cancer Genetics and Research Training (Revision)R25CA112486 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI WEITZEL, JEFFREY N · 2005 to 2009
$1.0M
Clinical Cancer Genetics Community Network: A Sustainable Research PartnershipRC4CA153828 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WEITZEL, JEFFREY N · 2010 to 2010
$1.0M
CLINICAL CANCER GENETICS EDUCATIONR25CA075131 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI WEITZEL, JEFFREY N · 1997 to 2005
$848k
NCI NIH HHS 3R25 CA112486-05S1NCI NIH HHS R25 CA075131NCI NIH HHS R25 CA085771NCI NIH HHS R25 CA112486NCI NIH HHS R25 CA75131NCI NIH HHS R25 CA85771NCI NIH HHS RC4 CA153828NCI NIH HHS RC4CA153828
6 · The paper itself

Abstract

purposeTo assess the impact of a multimodal interdisciplinary course on genetic cancer risk assessment and research collaboration for community-based clinicians. Clinicians are increasingly requested to conduct genetic cancer risk assessment, but many are inadequately prepared to provide these services.

methodsA prospective analysis of 131 participants (48 physicians, 41 advanced-practice nurses, and 42 genetic counselors) from community settings across the United States. The course was delivered in three phases: distance didactic learning, face-to-face training, and 12 months of web-based professional development activities to support integration of skills into practice. Cancer genetics knowledge, skills, professional self-efficacy, and practice changes were measured at baseline, immediate, and 14 months postcourse.

resultsKnowledge, skills, and self-efficacy scores were significantly different between practice disciplines; however, postscores increased significantly overall and for each discipline (P < 0.001). Fourteen-month practice outcomes reflect significant increases in provision of genetic cancer risk assessment services (P = 0.018), dissemination of cancer prevention information (P = 0.005) and high-risk screening recommendations (P = 0.004) to patients, patient enrollment in research (P = 0.013), and educational outreach about genetic cancer risk assessment (P = 0.003).

conclusionsResults support the efficacy of the multimodal course as a tool to develop a genetically literate workforce. Sustained alumni participation in web-based professional development activities has evolved into a distance-mediated community of practice in clinical cancer genetics, modeling the lifelong learning goals envisioned by leading continuing medical education stakeholders.

Indexed as

Education, Medical, ContinuingGenetic CounselingGenetic TestingHealth Care SurveysHumansNeoplasmsPrecision MedicineProspective StudiesRisk AssessmentRisk Factors

Identifiers

PMID21629123
PMCPMC3337331

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.