Literature DB >> 34080181

Out-of-pocket and private pay in clinical genetic testing: A scoping review.

Peter Grant1, Sylvie Langlois1, Larry D Lynd2, Jehannine C Austin1,3,4, Alison M Elliott1,5,6.   

Abstract

Full coverage of the cost of clinical genetic testing is not always available through public or private insurance programs, or a public healthcare system. Consequently, some patients may be faced with the decision of whether to finance testing out-of-pocket (OOP), meet OOP expenses required by their insurer, or not proceed with testing. A scoping review was conducted to identify literature associated with patient OOP and private pay in clinical genetic testing. Seven databases (EMBASE, MEDLINE, CINAHL, PsychINFO, PAIS, the Cochrane Database of Systematic Reviews, and the JBI Evidence-Based Practice database) were searched, resulting in 83 unique publications included in the review. The presented evidence includes a descriptive analysis, followed by a narrative account of the extracted data. Results were divided into four groups according to clinical indication: (1) hereditary breast and ovarian cancer, (2) other hereditary cancers, (3) prenatal testing, (4) other clinical indications. The majority of studies focused on hereditary cancer and prenatal genetic testing. Overall trends indicated that OOP costs have fallen and payer coverage has improved, but OOP expenses continue to present a barrier to patients who do not qualify for full coverage.
© 2021 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  genetic counseling; genomic testing; insurance; out-of-pocket; private pay

Mesh:

Year:  2021        PMID: 34080181     DOI: 10.1111/cge.14006

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  3 in total

Review 1.  Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases.

Authors:  Bryce A Schuler; Erica T Nelson; Mary Koziura; Joy D Cogan; Rizwan Hamid; John A Phillips
Journal:  J Clin Invest       Date:  2022-04-01       Impact factor: 14.808

Review 2.  Gynecologic Cancer Risk and Genetics: Informing an Ideal Model of Gynecologic Cancer Prevention.

Authors:  Lauren C Tindale; Almira Zhantuyakova; Stephanie Lam; Michelle Woo; Janice S Kwon; Gillian E Hanley; Bartha Knoppers; Kasmintan A Schrader; Stuart J Peacock; Aline Talhouk; Trevor Dummer; Kelly Metcalfe; Nora Pashayan; William D Foulkes; Ranjit Manchanda; David Huntsman; Gavin Stuart; Jacques Simard; Lesa Dawson
Journal:  Curr Oncol       Date:  2022-06-30       Impact factor: 3.109

3.  A single center experience with publicly funded clinical exome sequencing for neurodevelopmental disorders or multiple congenital anomalies.

Authors:  Ben Pode-Shakked; Ortal Barel; Amihood Singer; Miriam Regev; Hana Poran; Aviva Eliyahu; Yael Finezilber; Meirav Segev; Michal Berkenstadt; Hagith Yonath; Haike Reznik-Wolf; Yael Gazit; Odelia Chorin; Gali Heimer; Lidia V Gabis; Michal Tzadok; Andreea Nissenkorn; Omer Bar-Yosef; Efrat Zohar-Dayan; Bruria Ben-Zeev; Nofar Mor; Nitzan Kol; Omri Nayshool; Noam Shimshoviz; Ifat Bar-Joseph; Dina Marek-Yagel; Elisheva Javasky; Reviva Einy; Moran Gal; Julia Grinshpun-Cohen; Mordechai Shohat; Dan Dominissini; Annick Raas-Rothschild; Gideon Rechavi; Elon Pras; Lior Greenbaum
Journal:  Sci Rep       Date:  2021-09-27       Impact factor: 4.379

  3 in total

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