Outcomes of the "BRCA Quality Improvement Dissemination Program": An initiative to improve patient receipt of cancer genetics services at five health systems

Erica M. Bednar, Minxing Chen, Michael T. Walsh, Amanda L. Eppolito, Molly H. Klein, Kelly Teed, Brittany Hodge, Jordan Hunter, Han Gill Chao, Dillon Davis, Wilshauna Serchion, Cara Yobbi, Rebekah Krukenberg, Sandra B. Jenkinson, Jennifer J. Moore, Cassandra Garcia, Fatimaeliza Gonzalez, Towanna Murray, Linda D. Nielsen, Brenda HoMegan Haas, Sarah B. Greenzweig, Abby Anderson, Christina Johnson, Nichole A. Morman, Elizabeth Bowdish, Emaline Wise, Julia N. Cooper, Pauline Kefalas Russ, Katelyn Tondo-Steele, Buonarotti F. de Gracia, Brooke Levin, Kristin Mattie, Kathryn Zarnawski, Molly Kalasinski, Jennifer Stone, Caitlin O'Brien, Alexa Bream, Aidan M. Kennedy, Rachel A. Paul, Michelle Bilbao, Maureen Romero, Rebecca L. Carr, Jennifer M. Siettmann, Anna K. Vercruyssen, Kaycee Leon, Banu K. Arun, Andrew V. Grainger, David P. Warshal, Erin Bowman, Timothy A. Goedde, Deepa Halaharvi, Kellie Rath, Generosa Grana, Lida Mina, Karen H. Lu

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Objective: A quality improvement initiative (QII) was conducted with five community-based health systems' oncology care centers (sites A–E). The QII aimed to increase referrals, genetic counseling (GC), and germline genetic testing (GT) for patients with ovarian cancer (OC) and triple-negative breast cancer (TNBC). Methods: QII activities occurred at sites over several years, all concluding by December 2020. Medical records of patients with OC and TNBC were reviewed, and rates of referral, GC, and GT of patients diagnosed during the 2 years before the QII were compared to those diagnosed during the QII. Outcomes were analyzed using descriptive statistics, two-sample t-test, chi-squared/Fisher's exact test, and logistic regression. Results: For patients with OC, improvement was observed in the rate of referral (from 70% to 79%), GC (from 44% to 61%), GT (from 54% to 62%) and decreased time from diagnosis to GC and GT. For patients with TNBC, increased rates of referral (from 90% to 92%), GC (from 68% to 72%) and GT (81% to 86%) were observed. Effective interventions streamlined GC scheduling and standardized referral processes. Conclusion: A multi-year QII increased patient referral and uptake of recommended genetics services across five unique community-based oncology care settings.

Original languageEnglish (US)
Pages (from-to)106-114
Number of pages9
JournalGynecologic oncology
Volume172
DOIs
StatePublished - May 2023

Keywords

  • Breast cancer
  • Genetic counseling
  • Genetic testing
  • Hereditary cancer
  • Ovarian cancer
  • Quality improvement

ASJC Scopus subject areas

  • Oncology
  • Obstetrics and Gynecology

MD Anderson CCSG core facilities

  • Biostatistics Resource Group

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