TY - JOUR
T1 - Use of the BOADICEA Web Application in clinical practice
T2 - appraisals by clinicians from various countries
AU - Brédart, Anne
AU - Kop, Jean Luc
AU - Antoniou, Antonis C.
AU - Cunningham, Alex P.
AU - de Pauw, Antoine
AU - Tischkowitz, Marc
AU - Ehrencrona, Hans
AU - Dolbeault, Sylvie
AU - Robieux, Léonore
AU - Rhiem, Kerstin
AU - Easton, Douglas F.
AU - Devilee, Peter
AU - Stoppa-Lyonnet, Dominique
AU - Schmutlzer, Rita
PY - 2018
Y1 - 2018
N2 - The ‘BOADICEA’ Web Application (BWA) used to assess breast cancer risk, is currently being further developed, to integrate additional genetic and non-genetic factors. We surveyed clinicians’ perceived acceptability of the existing BWA v3. An online survey was conducted through the BOADICEA website, and the British, Dutch, French and Swedish genetics societies. Cross-sectional data from 443 participants who provided at least 50% responses were analysed. Respondents varied in age and, clinical seniority, but mainly comprised women (77%) and genetics professionals (82%). Some expressed negative opinions about the scientific validity of BOADICEA (9%) and BWA v3 risk presentations (7–9%). Data entry time (62%), clinical utility (22%) and ease of communicating BWA v3 risks (13–17%) received additional negative appraisals. In multivariate analyses, controlling for gender and country, data entry time was perceived as longer by genetic counsellors than clinical geneticists (p < 0.05). Respondents who (1) considered hormonal BC risk factors as more important (p < 0.01), and (2) communicated numerical risk estimates more frequently (p < 0.001), judged BWA v3 of lower clinical utility. Respondents who carried out less frequent clinical activity (p < 0.01) and respondents with ‘11 to 15 years’ seniority (p < 0.01) had less favourable opinions of BWA v3 risk presentations. Seniority of ‘6 to 10 years’ (p < 0.05) and more frequent numerical risk communication (p < 0.05) were associated with higher fear of communicating the BWA v3 risks to patients. The level of genetics training did not affect opinions. Further development of BWA should consider technological, genetics service delivery and training initiatives.
AB - The ‘BOADICEA’ Web Application (BWA) used to assess breast cancer risk, is currently being further developed, to integrate additional genetic and non-genetic factors. We surveyed clinicians’ perceived acceptability of the existing BWA v3. An online survey was conducted through the BOADICEA website, and the British, Dutch, French and Swedish genetics societies. Cross-sectional data from 443 participants who provided at least 50% responses were analysed. Respondents varied in age and, clinical seniority, but mainly comprised women (77%) and genetics professionals (82%). Some expressed negative opinions about the scientific validity of BOADICEA (9%) and BWA v3 risk presentations (7–9%). Data entry time (62%), clinical utility (22%) and ease of communicating BWA v3 risks (13–17%) received additional negative appraisals. In multivariate analyses, controlling for gender and country, data entry time was perceived as longer by genetic counsellors than clinical geneticists (p < 0.05). Respondents who (1) considered hormonal BC risk factors as more important (p < 0.01), and (2) communicated numerical risk estimates more frequently (p < 0.001), judged BWA v3 of lower clinical utility. Respondents who carried out less frequent clinical activity (p < 0.01) and respondents with ‘11 to 15 years’ seniority (p < 0.01) had less favourable opinions of BWA v3 risk presentations. Seniority of ‘6 to 10 years’ (p < 0.05) and more frequent numerical risk communication (p < 0.05) were associated with higher fear of communicating the BWA v3 risks to patients. The level of genetics training did not affect opinions. Further development of BWA should consider technological, genetics service delivery and training initiatives.
KW - Appraisal
KW - Breast cancer
KW - Clinical practice
KW - Risk prediction model
KW - Survey
KW - Tool
UR - http://www.scopus.com/inward/record.url?scp=85020540592&partnerID=8YFLogxK
UR - https://doi.org/10.1007/s10689-017-0051-5
U2 - 10.1007/s10689-017-0014-x
DO - 10.1007/s10689-017-0014-x
M3 - Article
C2 - 28623477
AN - SCOPUS:85020540592
SN - 1389-9600
VL - 17
SP - 31
EP - 41
JO - Familial Cancer
JF - Familial Cancer
IS - 1
ER -