| Literature DB >> 34907101 |
Namhee Kim1, Sun-Young Kong2,3, Jongha Yoo4, Do-Hoon Kim5, Soo Hyun Seo6, Jieun Kim7.
Abstract
Genetic testing has become increasingly integrated into all areas of healthcare, and complex genetic testing usage continues to grow; thus, the demand for genetic counseling (GC) is likely to increase. However, it is unclear whether the current clinical GC capacity is sufficient for meeting the existing demand. This review describes the current issues, challenges, and future perspectives of GC in Korea based on a professional survey conducted among laboratory physicians. In view of the growing GC demand in the clinical setting, participants expressed a concern about the lack of support from the national healthcare insurance policy and legal requirements, such as certification, for GC practice. The implementation of genetic testing in the overall healthcare system in Korea is in an early phase. Proper implementation can be achieved through education and training of specialists, collaboration among healthcare personnel, proper regulatory oversight, genomic policies, and public awareness. Understanding the current GC capacity, issues, and challenges is a prerequisite for effective strategic planning by healthcare systems considering the expected growth in the demand for clinical genetic services over the next few decades.Entities:
Keywords: Genetic counseling; Genetic services; Healthcare system; Policy; Specialists
Mesh:
Year: 2022 PMID: 34907101 PMCID: PMC8677483 DOI: 10.3343/alm.2022.42.3.314
Source DB: PubMed Journal: Ann Lab Med ISSN: 2234-3806 Impact factor: 3.464
Fig. 1Growing trend in genetic testing. (A) Number of patients who underwent germline genetic testing in Korea between 2016 and 2019. (B) KNHIS reimbursement for genetic testing for inherited disorders between 2016 and 2019. The karyotyping and microarray were categorized as chromosome tests, whereas special chromosome analysis for fragile X and chromosome breakage were categorized as other chromosome tests. The data were retrieved using the Electronical Data Interchange code from http://opendata.hira.or.kr/.
Abbreviations: KNHIS, Korean National Health Insurance System; NGS, next-generation sequencing; CMA, chromosomal microarray analysis.
Data from a 2020 professional survey of the GC status in Korea conducted by the Genetic Counseling Committee of the Korean Society for Genetic Diagnostics
| Variables | Participants, N (%) |
|---|---|
| GC status (N = 54) | |
| Providing GC | 44 (81.5) |
| Not providing GC | 10 (18.5) |
| Service type (N = 44) | |
| Outpatient clinic | 19 (43.2) |
| Consultation | 18 (40.9) |
| Support online or by phone | 33 (75.0) |
| Multidisciplinary team | 9 (20.5) |
| GC cases per month (N = 44) | |
| ≤ 10 | 32 (72.7) |
| 11–20 | 5 (11.4) |
| ≥ 21 | 7 (15.9) |
| GC sessions per week (N = 44) | |
| Irregular | 26 (59.1) |
| 1 | 4 (9.1) |
| 2 | 3 (6.8) |
| ≥3 | 11 (25.0) |
| Time spent on pre-GC activities (N = 44) | |
| New patients | |
| < 30 min | 9 (20.5) |
| 30–59 min | 15 (34.1) |
| 60–119 min | 10 (22.7) |
| > 120 min | 5 (11.4) |
| Not applicable | 5 (11.4) |
| Follow-up patients | |
| < 30 min | 12 (27.3) |
| 30–59 min | 18 (40.9) |
| Not applicable | 14 (31.8) |
| Time spent on GC (N = 44) | |
| New patients | |
| < 15 min | 9 (20.5) |
| 15–30 min | 18 (40.9) |
| 31–60 min | 9 (20.5) |
| Not applicable | 8 (18.2) |
| Follow-up patients | |
| < 15 min | 13 (29.5) |
| 15–30 min | 15 (34.1) |
| Not applicable | 16 (36.4) |
| Scope of GC (N = 44) | |
| Mendelian disorders | 28 (63.6) |
| Cancer genetics | 28 (63.6) |
| Family test | 26 (59.1) |
| Genetic predisposition (genetic susceptibility) | 19 (43.2) |
| Prenatal genetics | 17 (38.6) |
| Other genetic disorders | 12 (27.3) |
| GC practitioner qualification (N = 54) | |
| Genetics and disease-related profession | 35 (64.8) |
| Interpretation of genetic testing results | 35 (64.8) |
| Psychological and emotional support provision | 28 (51.9) |
| Disease management | 22 (40.7) |
| Challenges and concerns regarding GC (N = 54) | |
| Lack of financial support | 30 (55.6) |
| Collaboration with other specialists for disease management | 9 (16.7) |
| Effort load for acquiring latest medical scientific knowledge | 3 (5.6) |
| Lack of consensus about standard GC | 3 (5.6) |
| Lack of specialized training program | 1 (1.9) |
Abbreviation: GC, genetic counseling.
Regulation states of GC in the US, Canada, UK, EU, and Australia/ New Zealand
| Country | National or state regulation | Type of professional regulation | Accredited training programs | Requirements | Professional GC organizations for licensure and regulation |
|---|---|---|---|---|---|
| US | Yes (22 states with regulation) | Certification | Yes | Accredited training program; case log record | American Board of Genetic Counseling |
| Canada | None | Certification | Yes | Accredited training program; case log record; references | Canadian Association of Genetic Counseling |
| UK | Yes | Registration | Yes | Accredited training program; post-graduate work experience; case log record; references | Genetic Counsellor Registration Board |
| EU | Yes | Registration | Yes | Accredited training program; post-graduate work; case log record; references | European Board of Medical Genetics |
| Australia/New Zealand | In progress | Certification | Yes | Accredited training program; post-graduate work experience; case log record; academic publication | Human Genetics Society of Australasia |
Abbreviations: GC, genetic counseling; US, United States; UK, United Kingdom; EU, European Union.