Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis

Casey L. Swanson, Amanika Kumar, Joy M. Maharaj, Jennifer L. Kemppainen, Brittany C. Thomas, Megan R. Weinhold, Kristine M. Slaby, Kristin C. Mara, Myra J Wick, Jamie N Bakkum-Gamez

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Objective: To increase genetic counseling referrals for patients with newly diagnosed epithelial ovarian cancer (EOC). Methods: A practice-gap analysis was performed after measuring baseline genetic counseling referral rates to identify barriers to referral from the multidisciplinary single institution EOC care group. A Genetics Referral Toolkit consisting of a referral template, a genetic risk checklist, family history worksheet and provider and patient awareness was developed to address identified gaps with the goal of increasing referral rates. Clinical characteristics, referral placement, completion of genetic counseling/testing were abstracted for a historic cohort and intervention cohort. Data for the two cohorts were compared using chi-square, Fisher's exact test, or t-test. Association with referral was determined by univariate logistic regression. Results: Eighty one patients from July through December 2013 (historic cohort) and 62 patients from July through December 2015 (intervention cohort) were identified as having a new diagnosis of EOC. Among these women, genetic counseling referral rates increased from 48.1% (39/81) in 2013 to 74.2% (46/62) in 2015 (p = 0.002) after implementation of the toolkit. In a subset of patients without a previous genetic counseling referral, 87.9% (29/33) completed counseling and 79.3% (23/29) pursued testing from the historic cohort. In the intervention cohort, 60% (24/40) were seen for counseling and 100% (24/24) had testing. Conclusion: Application of a quality improvement process to create a Genetics Referral Toolkit increased the genetic counseling referral rate in patients with a new diagnosis of EOC. The majority of patients who were referred completed genetics consultation and elected genetic testing.

Original languageEnglish (US)
JournalGynecologic Oncology
DOIs
StateAccepted/In press - Jan 1 2018

Fingerprint

Genetic Counseling
Ovarian Neoplasms
Referral and Consultation
Genetic Testing
Genetic Templates
Counseling
Quality Improvement
Checklist
Logistic Models

Keywords

  • Genetic counseling
  • Genetic testing
  • Ovarian cancer
  • Referral

ASJC Scopus subject areas

  • Oncology
  • Obstetrics and Gynecology

Cite this

Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis. / Swanson, Casey L.; Kumar, Amanika; Maharaj, Joy M.; Kemppainen, Jennifer L.; Thomas, Brittany C.; Weinhold, Megan R.; Slaby, Kristine M.; Mara, Kristin C.; Wick, Myra J; Bakkum-Gamez, Jamie N.

In: Gynecologic Oncology, 01.01.2018.

Research output: Contribution to journalArticle

Swanson, Casey L. ; Kumar, Amanika ; Maharaj, Joy M. ; Kemppainen, Jennifer L. ; Thomas, Brittany C. ; Weinhold, Megan R. ; Slaby, Kristine M. ; Mara, Kristin C. ; Wick, Myra J ; Bakkum-Gamez, Jamie N. / Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis. In: Gynecologic Oncology. 2018.
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abstract = "Objective: To increase genetic counseling referrals for patients with newly diagnosed epithelial ovarian cancer (EOC). Methods: A practice-gap analysis was performed after measuring baseline genetic counseling referral rates to identify barriers to referral from the multidisciplinary single institution EOC care group. A Genetics Referral Toolkit consisting of a referral template, a genetic risk checklist, family history worksheet and provider and patient awareness was developed to address identified gaps with the goal of increasing referral rates. Clinical characteristics, referral placement, completion of genetic counseling/testing were abstracted for a historic cohort and intervention cohort. Data for the two cohorts were compared using chi-square, Fisher's exact test, or t-test. Association with referral was determined by univariate logistic regression. Results: Eighty one patients from July through December 2013 (historic cohort) and 62 patients from July through December 2015 (intervention cohort) were identified as having a new diagnosis of EOC. Among these women, genetic counseling referral rates increased from 48.1{\%} (39/81) in 2013 to 74.2{\%} (46/62) in 2015 (p = 0.002) after implementation of the toolkit. In a subset of patients without a previous genetic counseling referral, 87.9{\%} (29/33) completed counseling and 79.3{\%} (23/29) pursued testing from the historic cohort. In the intervention cohort, 60{\%} (24/40) were seen for counseling and 100{\%} (24/24) had testing. Conclusion: Application of a quality improvement process to create a Genetics Referral Toolkit increased the genetic counseling referral rate in patients with a new diagnosis of EOC. The majority of patients who were referred completed genetics consultation and elected genetic testing.",
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AU - Thomas, Brittany C.

AU - Weinhold, Megan R.

AU - Slaby, Kristine M.

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AU - Wick, Myra J

AU - Bakkum-Gamez, Jamie N

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N2 - Objective: To increase genetic counseling referrals for patients with newly diagnosed epithelial ovarian cancer (EOC). Methods: A practice-gap analysis was performed after measuring baseline genetic counseling referral rates to identify barriers to referral from the multidisciplinary single institution EOC care group. A Genetics Referral Toolkit consisting of a referral template, a genetic risk checklist, family history worksheet and provider and patient awareness was developed to address identified gaps with the goal of increasing referral rates. Clinical characteristics, referral placement, completion of genetic counseling/testing were abstracted for a historic cohort and intervention cohort. Data for the two cohorts were compared using chi-square, Fisher's exact test, or t-test. Association with referral was determined by univariate logistic regression. Results: Eighty one patients from July through December 2013 (historic cohort) and 62 patients from July through December 2015 (intervention cohort) were identified as having a new diagnosis of EOC. Among these women, genetic counseling referral rates increased from 48.1% (39/81) in 2013 to 74.2% (46/62) in 2015 (p = 0.002) after implementation of the toolkit. In a subset of patients without a previous genetic counseling referral, 87.9% (29/33) completed counseling and 79.3% (23/29) pursued testing from the historic cohort. In the intervention cohort, 60% (24/40) were seen for counseling and 100% (24/24) had testing. Conclusion: Application of a quality improvement process to create a Genetics Referral Toolkit increased the genetic counseling referral rate in patients with a new diagnosis of EOC. The majority of patients who were referred completed genetics consultation and elected genetic testing.

AB - Objective: To increase genetic counseling referrals for patients with newly diagnosed epithelial ovarian cancer (EOC). Methods: A practice-gap analysis was performed after measuring baseline genetic counseling referral rates to identify barriers to referral from the multidisciplinary single institution EOC care group. A Genetics Referral Toolkit consisting of a referral template, a genetic risk checklist, family history worksheet and provider and patient awareness was developed to address identified gaps with the goal of increasing referral rates. Clinical characteristics, referral placement, completion of genetic counseling/testing were abstracted for a historic cohort and intervention cohort. Data for the two cohorts were compared using chi-square, Fisher's exact test, or t-test. Association with referral was determined by univariate logistic regression. Results: Eighty one patients from July through December 2013 (historic cohort) and 62 patients from July through December 2015 (intervention cohort) were identified as having a new diagnosis of EOC. Among these women, genetic counseling referral rates increased from 48.1% (39/81) in 2013 to 74.2% (46/62) in 2015 (p = 0.002) after implementation of the toolkit. In a subset of patients without a previous genetic counseling referral, 87.9% (29/33) completed counseling and 79.3% (23/29) pursued testing from the historic cohort. In the intervention cohort, 60% (24/40) were seen for counseling and 100% (24/24) had testing. Conclusion: Application of a quality improvement process to create a Genetics Referral Toolkit increased the genetic counseling referral rate in patients with a new diagnosis of EOC. The majority of patients who were referred completed genetics consultation and elected genetic testing.

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KW - Referral

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