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Genetic counselors' experience with reimbursement and patient out-of-pocket cost for multi-cancer gene panel testing for hereditary cancer syndromes.
Weldon, Christine B; Trosman, Julia R; Liang, Su-Ying; Douglas, Michael P; Scheuner, Maren T; Kurian, Allison; Schaa, Kendra L; Roscow, Breanna; Erwin, Deanna; Phillips, Kathryn A.
Afiliação
  • Weldon CB; Center for Business Models in Healthcare, Glencoe, Illinois, USA.
  • Trosman JR; Center for Business Models in Healthcare, Glencoe, Illinois, USA.
  • Liang SY; Department of Clinical Pharmacy, Center for Translational and Policy Research on Personalized Medicine (TRANSPERS), University of California-San Francisco, San Francisco, California, USA.
  • Douglas MP; Sutter Health-Palo Alto Medical Foundation Research Institute, Palo Alto, California, USA.
  • Scheuner MT; Department of Clinical Pharmacy, Center for Translational and Policy Research on Personalized Medicine (TRANSPERS), University of California-San Francisco, San Francisco, California, USA.
  • Kurian A; Departments of Medicine and Pediatrics, School of Medicine, University of California, San Francisco, California, USA.
  • Schaa KL; San Francisco VA Health Care System, San Francisco, California, USA.
  • Roscow B; Departments of Medicine and of Epidemiology and Population Health, Stanford University, Stanford, California, USA.
  • Erwin D; Department of Obstetrics and Gynecology, University of Iowa Hospitals and Clinics, Iowa City, Iowa, USA.
  • Phillips KA; Oncology Regional Medical Specialists Department, Myriad Genetics, Inc, Salt Lake City, Utah, USA.
J Genet Couns ; 31(6): 1394-1403, 2022 12.
Article em En | MEDLINE | ID: mdl-35900261
ABSTRACT
Multi-cancer gene panels for hereditary cancer syndromes (hereditary cancer panels, HCPs) are widely available, and some laboratories have programs that limit patients' out-of-pocket (OOP) cost share. However, little is known about practices by cancer genetic counselors for discussing and ordering an HCP and how insurance reimbursement and patient out-of-pocket share impact these practices. We conducted a survey of cancer genetic counselors based in the United States through the National Society of Genetic Counselors to assess the impact of reimbursement and patient OOP share on ordering of an HCP and hereditary cancer genetic counseling. Data analyses were conducted using chi-square and t tests. We received 135 responses (16% response rate). We found that the vast majority of respondents (94%, 127/135) ordered an HCP for patients rather than single-gene tests to assess hereditary cancer predisposition. Two-thirds of respondents reported that their institution had no protocol related to discussing HCPs with patients. Most respondents (84%, 114/135) indicated clinical indications and patients' requests as important in selecting and ordering HCPs, while 42%, 57/135, considered reimbursement and patient OOP share factors important. We found statistically significant differences in reporting of insurance as a frequently used payment method for HCPs and in-person genetic counseling (84% versus 59%, respectively, p < 0.0001). Perceived patient willingness to pay more than $100 was significantly higher for HCPs than for genetic counseling(41% versus 22%, respectively, p < 0.01). In sum, genetic counselors' widespread selection and ordering of HCPs is driven more by clinical indications and patient preferences than payment considerations. Respondents perceived that testing is more often reimbursed by insurance than genetic counseling, and patients are more willing to pay for an HCP than for genetic counseling. Policy efforts should address this incongruence in reimbursement and patient OOP share. Patient-centered communication should educate patients on the benefit of genetic counseling.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Conselheiros Tipo de estudo: Guideline / Health_economic_evaluation / Prognostic_studies Limite: Humans País como assunto: America do norte Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Neoplásicas Hereditárias / Conselheiros Tipo de estudo: Guideline / Health_economic_evaluation / Prognostic_studies Limite: Humans País como assunto: America do norte Idioma: En Ano de publicação: 2022 Tipo de documento: Article