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. 2025 Apr 17;62(5):317-325.
doi: 10.1136/jmg-2024-110428.

Uptake, utility and resource requirements of a genetic counselling telephone helpline within the BRCA-DIRECT digital pathway for mainstreamed BRCA testing in patients with breast cancer

Affiliations

Uptake, utility and resource requirements of a genetic counselling telephone helpline within the BRCA-DIRECT digital pathway for mainstreamed BRCA testing in patients with breast cancer

Bethany Torr et al. J Med Genet. .

Abstract

Background: We trialled the first digital pathway (BRCA-DIRECT) aiming to improve capacity for mainstreamed BRCA testing within UK breast oncology services. Patients received standardised digital pretest information, with saliva sampling and consent to testing completed at home. For individualised support, we offered access to a clinical genetics professional via a telephone helpline (TH).

Methods: To evaluate the utilisation, uptake and resource requirements for provision of the TH, we analysed data from structured call logs recorded in the BRCA-DIRECT Study. Mixed-methods analysis included combining quantitative data from call logs and patient demographics with thematic analysis of free-text notes establishing reasons for calls. Additional data were analysed from structured telephone interviews.

Results: Calls were received from 201/1140 (17.6%) patients. We identified that 84.6% of calls (274 calls, 1097 min) pertained to 'administrative' support needs only. The remaining 15.4% required a clinical genetics professional (50 calls, 344 min). Of the clinical calls received: 26.0% were placed prior to test consent, 36.0% while awaiting results and 38.0% post results, with median (interquartile) call lengths of 8 (4-10) min; 5.5 (4-10) min; and 5 (3-7) min, respectively. Across all 1140 patients, a mean of 0.3 min of clinical time was required per patient.

Conclusions: Our findings demonstrate that the 'BRCA-DIRECT' model of standardised information provision served most patients, with a minority using the helpline for supplementary clinical information or support. The modest per-patient requirement for clinical time supports the scalability of this model for expanding mainstream genetic testing within UK oncology services.

Keywords: Genetic Counselling; Genetic Testing; Germline Mutation; Health Services Administration; Medical Oncology.

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Conflict of interest statement

Competing interests: AGe, ZK and CT declare honoraria for educational resources and advisory boards (AstraZeneca; Pfizer). No further conflicts of interest are reported by the authors.

Figures

Figure 1
Figure 1. (a) Proportion of clinical or administrative calls and (b) Total minutes of clinical or administrative calls, received at different time points within the patient pathway: (1) Before the participant consented to genetic testing, (2) While awaiting the results from the testing and (3) After receiving the result from testing.
Figure 2
Figure 2. Patient-reported importance of having the telephone helpline (grey) and likelihood of use (black) for (a) Administrative support or (b) Clinical genetics support. Questions were scored on a 5-point Likert Scale: 1—very unimportant/likely; 2—somewhat unimportant/likely; 3—don’t know/depends; 4—somewhat important/likely; 5—very important/likely, based on structured interviews with 21 patients randomised to receive digital pretest information (fully digital arm), of whom 2/21 (9.5%) reported using the telephone helpline.

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