Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program
Population genomic screening has been demonstrated to detect at-risk individuals who would not be clinically identified otherwise. However, there are concerns about the increased utilization of unnecessary services and the associated increase in costs. The objectives of this study are twofold: (1) d...
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doaj-a95de0c9255b468aa4b56c492efa92632020-11-25T01:40:00ZengMDPI AGJournal of Personalized Medicine2075-44262020-02-01101710.3390/jpm10010007jpm10010007Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening ProgramJing Hao0Dina Hassen1Kandamurugu Manickam2Michael F. Murray3Dustin N. Hartzel4Yirui Hu5Kunpeng Liu6Alanna Kulchak Rahm7Marc S. Williams8Amanda Lazzeri9Adam Buchanan10Amy Sturm11Susan R. Snyder12Department of Population Health Sciences, Geisinger, Danville, PA 17822, USADepartment of Population Health Sciences, Geisinger, Danville, PA 17822, USADivision of Genetic and Genomic Medicine, Nationwide Children’s Hospital, Columbus, OH 43205, USADepartment of Genetics, Yale School of Medicine, New Haven, CT 06510, USAPhenomic Analytics and Clinical Data Core, Geisinger, Danville, PA 17822, USADepartment of Population Health Sciences, Geisinger, Danville, PA 17822, USADepartment of Computer Science, University of Central Florida, Orlando, FL 32816, USAGenomic Medicine Institute, Geisinger, Danville, PA 17822, USAGenomic Medicine Institute, Geisinger, Danville, PA 17822, USAGenomic Medicine Institute, Geisinger, Danville, PA 17822, USAGenomic Medicine Institute, Geisinger, Danville, PA 17822, USAGenomic Medicine Institute, Geisinger, Danville, PA 17822, USADepartment of Health Policy and Behavioral Science, School of Public Health, Georgia State University, Atlanta, GA 30302, USAPopulation genomic screening has been demonstrated to detect at-risk individuals who would not be clinically identified otherwise. However, there are concerns about the increased utilization of unnecessary services and the associated increase in costs. The objectives of this study are twofold: (1) determine whether there is a difference in healthcare utilization and costs following disclosure of a pathogenic/likely pathogenic (P/LP) <i>BRCA1/2</i> variant via a genomic screening program, and (2) measure the post-disclosure uptake of National Comprehensive Cancer Network (NCCN) guideline-recommended risk management. We retrospectively reviewed electronic health record (EHR) and billing data from a female population of <i>BRCA1/2</i> P/LP variant carriers without a personal history of breast or ovarian cancer enrolled in Geisinger’s MyCode genomic screening program with at least a one-year post-disclosure observation period. We identified 59 women for the study cohort out of 50,726 MyCode participants. We found no statistically significant differences in inpatient and outpatient utilization and average total costs between one-year pre- and one-year post-disclosure periods ($18,821 vs. $19,359, <i>p</i> = 0.76). During the first year post-disclosure, 49.2% of women had a genetic counseling visit, 45.8% had a mammography and 32.2% had an MRI. The uptake of mastectomy and oophorectomy was 3.5% and 11.8%, respectively, and 5% of patients received chemoprevention.https://www.mdpi.com/2075-4426/10/1/7genomic screening<i>brca1/2</i>healthcare utilizationhealthcare costsuptake of risk management |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jing Hao Dina Hassen Kandamurugu Manickam Michael F. Murray Dustin N. Hartzel Yirui Hu Kunpeng Liu Alanna Kulchak Rahm Marc S. Williams Amanda Lazzeri Adam Buchanan Amy Sturm Susan R. Snyder |
spellingShingle |
Jing Hao Dina Hassen Kandamurugu Manickam Michael F. Murray Dustin N. Hartzel Yirui Hu Kunpeng Liu Alanna Kulchak Rahm Marc S. Williams Amanda Lazzeri Adam Buchanan Amy Sturm Susan R. Snyder Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program Journal of Personalized Medicine genomic screening <i>brca1/2</i> healthcare utilization healthcare costs uptake of risk management |
author_facet |
Jing Hao Dina Hassen Kandamurugu Manickam Michael F. Murray Dustin N. Hartzel Yirui Hu Kunpeng Liu Alanna Kulchak Rahm Marc S. Williams Amanda Lazzeri Adam Buchanan Amy Sturm Susan R. Snyder |
author_sort |
Jing Hao |
title |
Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program |
title_short |
Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program |
title_full |
Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program |
title_fullStr |
Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program |
title_full_unstemmed |
Healthcare Utilization and Costs after Receiving a Positive <i>BRCA1/2</i> Result from a Genomic Screening Program |
title_sort |
healthcare utilization and costs after receiving a positive <i>brca1/2</i> result from a genomic screening program |
publisher |
MDPI AG |
series |
Journal of Personalized Medicine |
issn |
2075-4426 |
publishDate |
2020-02-01 |
description |
Population genomic screening has been demonstrated to detect at-risk individuals who would not be clinically identified otherwise. However, there are concerns about the increased utilization of unnecessary services and the associated increase in costs. The objectives of this study are twofold: (1) determine whether there is a difference in healthcare utilization and costs following disclosure of a pathogenic/likely pathogenic (P/LP) <i>BRCA1/2</i> variant via a genomic screening program, and (2) measure the post-disclosure uptake of National Comprehensive Cancer Network (NCCN) guideline-recommended risk management. We retrospectively reviewed electronic health record (EHR) and billing data from a female population of <i>BRCA1/2</i> P/LP variant carriers without a personal history of breast or ovarian cancer enrolled in Geisinger’s MyCode genomic screening program with at least a one-year post-disclosure observation period. We identified 59 women for the study cohort out of 50,726 MyCode participants. We found no statistically significant differences in inpatient and outpatient utilization and average total costs between one-year pre- and one-year post-disclosure periods ($18,821 vs. $19,359, <i>p</i> = 0.76). During the first year post-disclosure, 49.2% of women had a genetic counseling visit, 45.8% had a mammography and 32.2% had an MRI. The uptake of mastectomy and oophorectomy was 3.5% and 11.8%, respectively, and 5% of patients received chemoprevention. |
topic |
genomic screening <i>brca1/2</i> healthcare utilization healthcare costs uptake of risk management |
url |
https://www.mdpi.com/2075-4426/10/1/7 |
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