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European Journal of Human Genetics logoLink to European Journal of Human Genetics
. 2022 Mar 7;30(7):865. doi: 10.1038/s41431-022-01063-4

Correction to: The stepwise process of integrating a genetic counsellor into primary care

Caitlin Slomp 1, Emily Morris 1; GenCOUNSEL Study, Morgan Price 2, Alison M Elliott 3, Jehannine Austin 1,3,
PMCID: PMC9259581  PMID: 35250031

Erratum to: European Journal of Human Genetics 10.1038/s41431-022-01040-x, published online 31 January 2022

In the original publication of the article, Table 2 was incorrect. The correct Table 2 appears as below.

Table 2.

Needs, barriers and facilitators of participants’ progression between stages of collaboration.

Needs required to transition to the next stage Barriers to needs being met Facilitators of needs being met
Disinterest to pre-collaboration Perceived alignment of genetic counselling profession with personal and/or clinic values

Fear of genetic counselling

Negative perceptions of genetic counselling

Higher degree of paternalism

Education and reiteration of the GC’s training or credentials, and purpose of genetic counselling

Strong value for interdisciplinarity and inherent trust in other HCPs

Positive past experiences with genetic counselling/a GC

Pre-collaboration to initial collaboration

To confirm patient safety with the GC

To confirm basic trust in the individual GC; the GC demonstrates alignment with clinic values

Basic understanding of the genetic counselling role and goals

Unfamiliarity with the genetic counselling role

Education on genetic counselling

Positive attributes of the GC (professionalism, approachability, warmth)

Seeing that the GC is knowledgeable and competent

Evidence that the GC practices in a values-aligned way (specific to clinical context)

Seeing safe and comfortable interactions between the GC and patients

Initial collaboration to effective collaboration

Initial development of deeper trust and the beginning of a relationship with the individual GC

Deeper/more practical understanding of genetic counselling

Shared clinical goals and priorities with the GC (“complementing each other’s practice”)

Evidence of genetic counselling utility for these patients

Identification of who should be referred

Regular, effective communication and feedback

Confirmation that genetic counselling is of interest and is acceptable to patients

Disconnect between theoretical and real-life understanding of genetic counselling

Discomfort with referring

Other/acute needs taking priority

Lack of communication or feedback regarding patients

Negative clinician perceptions of genetic counselling

Lack of investment/support from leadership

Time, shared experiences

Casual interactions with the GC

Clinician-observed patient outcomes

Positive patient report/experience

GC identifying and seeking out possible referrals

Clear, informative documentation

Hands-on education RE genetic counselling (observing an appointment, case examples)

Seeing another HCP “model” collaboration with the GC

Contracting with individual clinicians; identifying the needs of patients and clinicians and how the GC can fit into and help meet those needs

GC genetic counsellor, HCP healthcare professional.

Footnotes

The original article can be found online at 10.1038/s41431-022-01040-x.

A list of authors and their affiliations appears online.

Contributor Information

Jehannine Austin, Email: jehannine.austin@ubc.ca.

GenCOUNSEL Study:

Bartha Maria Knoppers, Larry D. Lynd, Alivia Dey, Shelin Adam, Nick Bansback, Patricia Birch, Lorne Clarke, Nick Dragojlovic, Jan Friedman, Deborah Lambert, Daryl Pullman, Alice Virani, Wyeth Wasserman, and Ma’n H. Zawati


Articles from European Journal of Human Genetics are provided here courtesy of Nature Publishing Group

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