- Research article
- Open Access
Development of decision aids for female BRCA1 and BRCA2 mutation carriers in Germany to support preference-sensitive decision-making
BMC Medical Informatics and Decision Making volume 21, Article number: 180 (2021)
Women with pathogenic BRCA1 and BRCA2 mutations possess a high risk of developing breast and ovarian cancer. They face difficult choices when considering preventive options. This study presents the development process of the first decision aids to support this complex decision-making process in the German healthcare system.
A six-step development process based on the International Patient Decision Aid Standards was used, including a systematic literature review of existing decision aids, a topical medical literature review, preparation of the decision aids, focus group discussions with women with BRCA1/2 mutations, internal and external reviews by clinical and self-help experts, and user tests. All reviews were followed by iterative revisions.
No existing decision aids were transferable to the German setting. The medical research revealed a need to develop separate decision aids for women with BRCA1/2 mutations (A) without a history of cancer (previvors) and (B) with a history of unilateral breast cancer (survivors). The focus group discussions confirmed a high level of approval for the decision aids from both target groups. Additionally, previvors requested more information on risk-reducing breast surgery, risk-reducing removal of both ovaries and Fallopian tubes, and psychological aspects; survivors especially wanted more information on breast cancer on the affected side (e.g. biological parameters, treatment, and risk of recurrence).
In a structured process, two target-group-specific DAs for previvors/survivors with BRCA1/2 mutations were developed to support decision-making on risk-adapted preventive options. These patient-oriented tools offer an important addition to existing specialist medical care in Germany.
Women who carry inherited pathogenic mutations in the BRCA1 or BRCA2 genes possess an increased risk of developing breast cancer (BC) and ovarian cancer (OC) compared to women of the general population without these mutations. Up to the age of 80, their average cumulative risk to develop BC is approximately 70% (BRCA1 or BRCA2 mutation) and the average lifetime risk to develop OC is approximately 44% (BRCA1 mutation) or 17% (BRCA2 mutation) . As a rule of thumb, women with BRCA1/2 mutations who have no personal history of cancer (previvors)  develop BC or OC around 20 years earlier compared to women who develop sporadic BC or OC. For women with BRCA1/2 mutations who have a personal history of unilateral BC (survivors) , the average cumulative risk to develop BC on the healthy side (contralateral BC) within 20 years of initial diagnosis is approximately 40% (BRCA1 mutation) or 26% (BRCA2 mutation) .
Women who receive a positive genetic test result confirming a pathogenic mutation in a risk gene face difficult and far-reaching decisions . They need to decide which preventive measures to take and when. In the following, the generic term ‘preventive option or measure’ applies to all measures that can be offered to women with BRCA1/2 mutations either to reduce the risk of breast or ovarian cancer or for breast cancer screening. The preventive options available are an intensified breast cancer screening programme for previvors, an intensified breast cancer screening and aftercare programme for survivors, and risk-reducing surgeries for both groups. Internationally, the use of anti-oestrogenic drugs such as tamoxifen or aromatase inhibitors for primary prevention is also discussed. So far, there is no conclusive evidence of a clear benefit as primary prevention in previvors and recommendations vary internationally [5,6,7,8,9].
Intensified breast cancer screening detects BC at an early, potentially curable stage in almost 85% of cases, but does not reduce the risk of BC . Risk-reducing removal of healthy mammary glands (risk-reducing bilateral mastectomy) significantly reduces the risk of BC and gives women with BRCA1 mutations a survival benefit [11, 12]; however, it also results in permanent loss of the breast and requires additional decisions regarding operations and breast reconstruction processes. For survivors, risk-reducing removal of the healthy breast (contralateral mastectomy) can reduce the risk of contralateral BC and improve overall survival . However, the process of deciding whether to choose this option is made especially complicated by potential competing risks, such as the risk of BC relapse on the affected breast side. Survivors then face the decision of weighing the risk of relapse on the affected side against the benefits of risk-reducing contralateral mastectomy of the healthy side. As there is no effective screening method for OC [14,15,16,17], the only available preventive measure is risk-reducing removal of both ovaries and Fallopian tubes (risk-reducing bilateral salpingo-oophorectomy). This surgical procedure significantly reduces the risk of OC and provides a survival benefit , but results in loss of fertility and may induce premature menopause.
Each preventive measure comes with different benefits and risks, which each woman rates differently. The same applies to breast reconstruction following mastectomy, family planning, and steps for handling side effects . As such, women with BRCA1/2 mutations are faced with preference-sensitive decisions that can lead to decisional conflict, hesitation, dissatisfaction, regret, and assigning blame to therapists [19,20,21,22,23]. A decision is deemed preference-sensitive if the subject has a choice of two or more medical options of nearly equal value that offer no clear advantage in terms of clinical outcome, or that are perceived differently depending on the subject’s own preferences and values [24, 25]. To foster high quality decision-making in such situations, it is important, to provide women with sufficient evidence-based medical information that enables them to get a realistic picture of their risk constellations and their options . On the other hand, it is also important to take into account personal factors such as their individual life situation, family and psychological stressors, as well as their individual values and preferences [19, 25,26,27].
In order to support decision-making on preventive measures for women with BRCA1/2 mutations and improve patient information and decision quality, an increasing number of supporting tools are being implemented worldwide; particularly decision aids (DAs). Evidence-based DAs can effectively support decision-making with regard to therapeutic or screening options. This has been demonstrated in a Cochrane Review covering 105 studies with a total of 31,043 participants  indicating that DAs improve understanding of the available options and the accuracy of risk assessments. They can also improve decision-related criteria. Decisional conflicts resulting from a feeling of not being sufficiently informed are reduced, as is indecision about patients’ values. Fewer patients remain passive during their decision-making process. A systematic review focusing on the effectiveness of DAs for women with BRCA1/2 mutations reported that decision-making is primarily supported by improving decision-related effects . In principle, DAs seem suitable for improving health literacy among target groups.
In Germany, around 70,000 women develop BC and around 7400 women develop OC every year [30, 31]. Approximately 30% of these women have a family history of BC and/or OC . In around 24% of these patients, genetic testing will identify a pathogenic mutation in the BRCA1 or BRCA2 genes . Healthy women with a strong family history of BC/OC are also offered genetic testing . A clear positive genetic test result allows women both with and without a history of BC, to consider whether, and if so, how to address their increased risk of BC, BC in the healthy breast and OC.
Genetic testing at the German Consortium for Hereditary Breast and Ovarian Cancer’s (GC‐HBOC) centres is embedded in a specialised counselling and care concept that ranges from individual risk prediction to discussion of risk-adapted preventive measures and their respective consequences [8, 9, 14, 34]. The counselling takes the form of a personal doctor/patient consultation. Women are also provided with some written information. However, to date, no structured tools such as DAs are available in Germany to help these women make informed decisions based on their individual values.
The aim of this project is to support the decision-making process for women carrying BRCA1/2 mutations and to enable them to make quality decisions. To support these women we developed evidence-based DAs that are compatible with the German healthcare context and the German guidelines in a structured process based on the criteria of the International Patient Decision Aid Standards (IPDAS).
The development was conducted by a multidisciplinary team of experts from healthcare research, medicine, psychology and nursing science, and specialists in obstetrics and gynaecology in the field of hereditary BC and OC. The latter have extensive experience in specialist medical care for the target group and are leading members of the GC-HBOC.
Development process and task distribution
The development followed a six-step work process (Fig. 1) based on the approach described by the IPDAS Collaboration [35,36,37]. The Ottawa Decision Support Framework [38, 39] served as the basis for the theoretical framework. The quality requirements were based on the IPDAS criteria and the Ottawa Health Research Institute’s (OHRI) Workbook on Developing and Evaluating Patient Decision Aids [35, 36, 38, 40, 41].
The development team formulated basic requirements for the DA with regard to targets, format, structure, content, and quality and conducted literature reviews (Steps 1, 2), conceptualisation, preparation and revisions of prototypes, alpha, beta and final versions of the DAs (Steps 3, 5, 6), focus group discussions and user tests (Steps 4a, 6). The clinical experts of the development team assisted the entire development process, paying particular attention to the clinicians needs, and performed the internal medical plausibility reviews (Step 4b).
Independent external women with BRCA1/2 mutations (layperson-patients) were involved in Steps 4a and 6. The external validation (Step 5) used to check that the DAs were medically sound and up-to-date was carried out by independent external medical specialists. Self-help experts from the BRCA-NetzwerkFootnote 1 were brought on board as “professionalised laypersons” (expert patients) with extensive experience in the situations of women with BRCA1/2 mutations and the basic medical and practical skills required for handling them. None of the persons brought in for the external reviews were involved in the development process.
Initially, the requirements for the DA content were defined as shown in Table 1.
Step 1: Survey on existing decision aids
To gather information on international DAs for women with BRCA1/2 mutations, a systematic literature review was conducted. The aim of the review was to assess the compatibility of the available DAs and their structure and/or content with the current German healthcare system.
Altogether, six databases were searched (MEDLINE, Embase, PsycINFO, CINAHL, ERIC, Cochrane Database of Systematic Reviews). Manual search for relevant DAs was performed on the websites of the Institute for Quality and Efficiency in Health Care (IQWiG, www.iqwig.de) and the OHRI Decision Aid Research Group (www.ohri.ca/decisionaid). The review covered DAs in German and English. There were no restrictions on the date or type of publication.
The review included DAs for women with BRCA1/2 mutations aged between 18 and 70 and studies on development, structuring, implementation and evaluation of these DAs. The term “decision aid” was defined in accordance with IPDAS . Screening was conducted by two independent reviewers based on the PRISMA statement . Discrepancies were discussed and resolved with a third reviewer.
The identified DAs were assessed based on formal, structural, medical-content, and quality criteria and rated in terms of their suitability as a basis for adapting/developing a DA for the German healthcare system. A search for incorporated decision-supporting worksheets (guidance) that focussed on comparing the preventive options, clarifying personal values, and doctor/patient consultation aids was also conducted .
The medical-content assessment was based on procedures and evidence-based recommendations for Germany [8, 9, 14] in coordination with the medical specialists of the development team. The quality assessment was conducted using the IPDAS instrument short form (IPDASi-SF) which consists of 16 criteria .
Step 2: Determination of the medical content for the decision aids
The medical content was determined in topical literature searches. It was based on the latest available evidence on the risks of developing BC, contralateral BC and OC and on preventive options including benefits and risks with regard to the following outcomes: Incidence reduction, reduction of BC/OC-specific morbidity and mortality, overall mortality, quality of life, and side effects. References for the German health care context were data from the Centre for Cancer Registry Data of the Robert Koch Institute (RKI) [30, 31], German S3 and S2 guidelines [8, 9, 14] and information from the GC-HBOC . In general, the search followed a top-down approach. The German S3 guidelines were used as the basis, as these represent the evidence-based consensus in Germany at the highest quality level of methodological development. Consistencies, discrepancies or additional information of possible relevance were searched for in the S2 guidelines. Data that may not yet have found their way into the available guidelines were searched via MEDLINE and google scholar, with preference given to studies with an expected evidence level of IIb and higher, if available. The resulting medical content was reviewed and approved by the medical experts of the development team for clinical and patient relevance.
Step 3: Prototype development
The results from Steps 1 and 2 were used to define the structure, content breakdown, medical and decision-supporting contents, overall scope, and format and draw up a prototype, based on established tools for the development and evaluation of evidence-based patient information [40, 44,45,46,47]. With the assistance of the medical specialists of the development team, the medical contents that emerged from the literature search in Step 2 were assessed in terms of clinical and patient relevance in specialist counselling and accepted and converted into information comprehensible to laypersons. Since the medical data obtained in Step 2 suggested that it is reasonable to target previvors and survivors separately due to their different baseline situations and risk constellations, two DA prototypes were designed for each target group.
Step 4: Participation of target groups and internal clinical experts
In Step 4a, each of the DA prototypes was discussed in two guideline-based focus group discussions with previvors and survivors respectively, and their attitudes, expectations and experiences were explored openly in relation to the prototypes [48,49,50]. The aims of this process were to have both DA prototypes discussed and evaluated from a target group-specific retrospective user perspective in terms of their contents and needs. This served to improve and add/remove parts of the prototypes and determine the needs of the specific target groups.
Voluntary participants were recruited by a clinical psychologist of the Centre for Familial Breast and Ovarian Cancer at the University Hospital of Cologne via phone call. The sample was selected using the theoretical guided sampling variant of the purposive sampling approach . The participation requirements were: Clearly pathogenic BRCA1/2 mutation, experience with the decision-making process for choosing a prevention strategy, no personal history of cancer (for participation in the focus groups discussing DA A), a personal history of BC (for participation in the focus groups discussing DA B), receipt of genetic test result at least 3 months prior to the focus group date to ensure a minimum distance from news of a mutation, emotional stability as rated by the psychologist during the phone call, and written informed consent. One week before the focus group discussions, the participants received the DA prototype to review.
The focus group discussions were audio-taped, transcribed verbatim  and evaluated according to Mayring’s qualitative content analysis  by two independent assessors. MAXQDA software was used for analysis. A silent observer for each focus group generated a postscript to record situational and non-verbal aspects such as the mood, and the behaviour of the groups and moderators .
The results were used to comprehensively revise and add to the DA prototypes before they were presented to the clinical experts of the development team in Step 4b for a professional assessment. Following further revisions, these were used to create the alpha versions in manuscript form.
Step 5: Validation by external experts
The alpha versions were checked by independent, external medical specialists in the fields of breast surgery (n = 2), oncological and senological radiology (n = 1), radiotherapy (n = 1), and hereditary BC/OC (n = 2) and self-help experts (n = 3) to ensure that they were medically correct, up to date and patient-oriented. All the review results were discussed and accepted by the development team.
Step 6: User testing
The revised alpha versions were used to create graphical beta versions. These were tested by independent, external test readers from the respective target groups to determine their comprehensibility, usefulness, and the acceptance of their contents [55, 56]. The advertisement for volunteer readers was posted by the BRCA-Netzwerk. Each reader received one test copy. Two weeks later, a guideline-based, semi-structured telephone interview was conducted with each reader. The questions covered their general impressions and assessments on length, amount of information, comprehensibility, balance, usefulness, satisfactory nature, and specific content of the DA. The responses were documented in pseudonymised form. The results were used for the final revision. The final DA versions were printed as A5, profile, paper brochures.
Further details on the methodology of Steps 1 to 6 can be found in Additional file 1.
Step 1: Survey of existing decision aids
A total of 845 studies were retrieved (Fig. 2). Following exclusion of duplicates and screening of title, abstract and full text, eleven studies that deal with a DA remained. Two of the DAs described were obtainable through the developer/study author. Eight DAs were identified using manual searches. Five of these were included. Thus, at the time of the review, seven DAs published between 2006 and 2016 were available for further analysis. A list of the identified DAs is provided in Additional file 2.
Table 2 provides an overview of the basic structural elements found in the identified DAs.
Table 3 summarises the basic medical contents of the identified DAs. None of the DAs met all the predefined requirements and target definitions, and only parts of the German guideline recommendations [8, 9, 14] were reflected. For instance, only two of the DAs explicitly addressed women with BRCA1/2 mutations [57, 58], only one addressed both BC and OC risks . Two DAs did not specify any risks [59, 60], four mentioned lifetime risks of BC [57, 58, 61] or OC [62, 63], and none of them provided adequate information on age or time-related risks, specifically addressed survivors, discussed the risk of contralateral BC, or explained competing risks. Only one DA included breast ultrasound as a part of the breast cancer screening regimen and information on surgical methods used for risk-reducing mastectomy and breast reconstruction . Four DAs mentioned preventive medication with anti-oestrogenic drugs (such as tamoxifen) as a preventive option for BC in previvors [57, 59, 61, 64], which is not compatible with the German S3 guidelines . Two DAs mentioned screening methods for OC [60, 62, 63], which is not compliant to the German S3 guidelines . Due to the limitations, new DAs were developed that discuss risk-adapted prevention options for both BC and OC and are compatible with the current German guidelines.
The analysis of the DAs in terms of the given target definitions is provided in Additional file 2.
The quality assessment revealed considerable differences between the seven DAs: one met all 16 of the IPDASi-SF criteria; one met 13 and five fulfilled seven to nine of them. In most cases information on the development and evaluation of the DA was lacking.
Step 2: Determination of the medical content for the decision aids
The guidelines applicable in Germany are the S3 guidelines on (1) screening, diagnosis, therapy and aftercare for breast carcinomas ; (2) diagnosis, therapy and aftercare for malign ovarian tumours  and (3) of the Gynaecological Oncology Research Group (AGO) on diagnosis and therapy for early-stage and advanced breast carcinomas . The versions valid at the time of DA development were used. The reference risk data for the general population was taken from the RKI [30, 31]. The data derived from the guidelines and the literature review indicated that previvors and survivors require different information due to the differences in risk data and health situations. Thus, two target-group-specific DA prototypes were designed.
Step 3: Prototype development
The results of Steps 1 and 2 led to structure definitions for the form and content of the two DA prototypes, and to definition of the breakdown and the medical content required in each section. Both prototypes were generated as manuscripts with sketch illustrations. These were used as the basis for the focus group discussions and the internal clinical review process in Step 4.
Step 4: Participation of target groups and internal clinical experts
In the focus group discussions with previvors (n = 9), the DA received a highly positive evaluation overall . Participants considered it beneficial that all the information was presented in detail, compiled in one medium and met an adequate language and knowledge level. However, the group recommended that more psychological aspects be taken into account, the mutation be acknowledged as a stress factor, and certain aspects be repeated for emphasis. More information on the consequences of risk-reducing bilateral salpingo-oophorectomy and the procedures following the various breast surgeries was requested. Personal testimonies were also requested; yet, these were not included due to the lack of evidence for their benefits and their potential to cloud a person’s judgement .
The survivors (n = 10) also responded positively to the DA . The volume and detail of the presented information were praised. Some participants also felt that certain sections should be more precise and comprehensible. More information was particularly requested on the following topics: BC on the affected side, BC treatment, risk of recurrence, and biological parameters. More detailed information was also requested on the procedures following risk-reducing breast surgery, breast reconstruction, symmetry following risk-reducing contralateral mastectomy, the consequences of risk-reducing bilateral salpingo-oophorectomy, and the intensified breast cancer screening and aftercare programme.
Both target groups assessed the integrated worksheets positively, but recommended replacing parts of the box-ticking sections with blank space to formulate and clarify their own thoughts and values. Both groups also expressed a wish for photos of genuine breast surgery results; these could not be provided for liability reasons. However, in the DAs the women are encouraged to seek advice from their surgeon about their individually planned surgery and ask for visual material of surgery results. In addition, they are encouraged to contact the self-help organisation BRCA-Netzwerk, which has many testimonials on this topic. For more details of the results of the focus group discussions with previvors and survivors, see Additional file 3.
The internal clinical expert reviews of the revised prototypes led to additional adjustments regarding language, updates, and explanations, particularly with regard to preventive options and their consequences. The results of the updated structure and content layout of the two DAs are listed in Table 4 for previvors and Table 5 for survivors.
Step 5: Validation by external experts
The external expert validation process led to revisions and expansion of the topics, particularly relating to risk-reducing breast surgery, including practical information such as surgery time, length of stay in hospital, and need for follow-up surgery. The self-help experts’ reviews revealed a need for more information and assistance, e.g. on dealing with the mutation, preventive options and their consequences, the decision-making process, and practical information, e.g. for women who decide against reconstruction.
Step 6: User tests
The DAs for previvors (n = 6) and survivors (n = 5) were both rated positively, in particular in terms of length, balanced presentation of options, usefulness for decision-making, sufficient information to make decisions, satisfaction, and likelihood of recommendation to others. Minor content adjustments were required. For more details on the results of the user tests including the underlying interview guideline, see Additional file 4.
In this study, two structured, evidence-based DAs were developed for previvors and survivors with BRCA1/2 mutations to support their decision-making on risk-adapted preventive options for BC and OC. The DAs were developed by a multidisciplinary team that included experts with extensive experience in specialised counselling for the target groups. The six-stage development process was based on the IPDAS criteria. It included literature reviews of available DAs and current medical evidence, internal validation by clinical experts, participation from external previvors/survivors, and validation by external medical specialists and self-help experts. None of the external persons were involved in the development process.
With its multi-level validation and the involvement of independent members of the target groups and external experts, this comprehensive development process is a high-quality procedure based on established approaches [35, 40, 46]. In a deviation from the IPDAS requirements, no separate needs analysis was conducted for the target doctors, as the specialists’ needs were taken into account and reflected throughout the development process due to the direct involvement of specialised medical consultants in the development team.
In principle, the development of DAs should be seen as an innovative approach in Germany, where only a modest number of DAs have been created and are in use [68, 69]. Experience in this country is therefore limited. There are several DAs for women with BRCA1/2 mutations on the international stage . However, the literature review within the presented development process showed that these would need to be adapted to suit the German healthcare setting and sociocultural and socio-economic parameters. The finding that available international DAs for women with BRCA1/2 mutations partly deviate considerably from the recommendations of the German guidelines and are therefore not transferable to the German context could be verified by a recently updated and widely expanded literature review on this topic .
During the development process, it became clear that the medical information required by the two target groups differed in some ways, and that they seemed to require different levels of information on certain aspects. For instance, the risks of first BC and contralateral BC [1, 71], and the respective surgery options have different effects. Furthermore, mutation carriers with prior BC face different considerations than those without a history of cancer. Information needs may also differ in the two target groups . This was supported by the focus group discussions. Survivors requested a lot of information on BC on the affected side, its treatment and the risk of recurrence, while previvors were more interested in information on risk-reducing surgeries and their consequences.
These DAs provide differentiated risk information for women with BRCA1 and BRCA2 mutations and address questions relating to dealing with both the BC risk and the OC risk. This represents an advantage compared to international DAs, which do not differentiate between BRCA1 and BRCA2 mutation carriers with and without a history of BC [72, 73], which address a broader target group of women with an increased risk of BC and/or OC [59,60,61, 64, 74, 75], and which primarily tackle either the risks of BC [59, 64] or OC [60, 63, 74,75,76]. There are very few DAs specifically designed for women with BRCA1/2 mutations with a history of BC . This could be due to the complexity of the information regarding decisional options, the personal situation of these women, and the number of individual factors involved.
This project resulted in two structured, evidence-based DAs for women with BRCA1/2 mutations, each of which is aimed at a clearly defined target group (previvors/survivors) and the content of which is tailored to the respective needs of each target group. After evaluation of their effectiveness and acceptability in clinical use in a randomised controlled trial, both DAs will be available as printed paper brochures to be used in post-test genetic counselling and given to women to take home. Both DAs will also be available as electronic versions that can be downloaded in PDF format. A full revision and update is scheduled for 2 years after completion of the final versions of the DAs.
The strengths of this study include the systematic DA development based on IPDAS criteria and evidence-based medicine following clearly defined and sequential development steps. These ensured that the development and its documentation remained transparent and the DAs developed meet high-quality standards. The literature reviews in Steps 1 and 2 provided a broad basis for defining the basic structural elements, the content structure and the contents of the DAs. For the actual creation of the two DAs, starting with step 3, independent target group persons were included for each development step in order to discuss and evaluate the respective versions from their perspective and thus support patient orientation. It has proven effective and is increasingly recommended to involve the target groups for decision-making-support and shared decision-making tools in the development process [40, 46, 68, 78]. A conscious effort was made to involve expert patients who play an active role in self-help and have an insight into the different perspectives of women with BRCA1/2 mutations, as well as layperson-patients with no active role, who contribute their very own perspective. Involving this range of women with BRCA1/2 mutations could increase the acceptance, relevance and practical applicability of the DAs in daily clinical work. Another strength is the way the DAs clearly address and are aimed at specific target groups, and the level of detail they provide. Each DA version offers its target group the information they need and want on the context, risks, preventive options and questions to consider. Both DAs also provide detailed responses to questions regarding preventive measures for BC and OC.
As the systematic literature review of existing DAs in Step 1 was conducted at the start of the project, there is a limit to how up-to-date the identified DAs may be. However, the basic findings of this review have recently been confirmed . Another limitation is the lack of a systematic evidence review in all parts of the development process in Step 2. On the other hand, it makes sense to use the evidence-based S3 and S2 guidelines that apply to the German healthcare setting as a basis for developing German DAs and include further evidence-based content to make up for missing information. Another limitation is a selection bias resulting from the purposive selection of volunteer target group participants for the focus groups, the external reviews by expert patients and the user tests. Any distortions that may occur due to the expert patients’ advanced knowledge  were counteracted by also involving layperson-patients. A limitation that may arise from the restricted number of target group persons in the final user tests may be mitigated by the fact that both DAs will be tested in an evaluation study. The evaluation for effectiveness and acceptability in clinical use is part of the final quality assurance [35, 40] and a randomised controlled study of both DAs is currently under way (DRKS00015823).
A comprehensive work process based on high-quality standards was used to develop the first evidence-based, structured DAs for previvors and survivors with BRCA1/2 mutations for Germany. They are designed to support these women in coming to an informed, high-quality decision on what preventive measures they wish to take at what time, taking into account their own values and preferences. As patient-oriented tools, these DAs represent an innovative addition to the range of specialised consulting services offered by the GC-HBOC’s 24 centres and the affiliated breast centres. Their implementation in specialised care will be an important step in increasing the autonomy of women with BRCA1/2 mutations.
Availability of data and materials
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
BRCA-Netzwerk: German self-help organisation (registered association) to support persons with familial cancers, in particular familial breast and ovarian cancer, e.g. due to BRCA1/2 mutations (high-risk or affected persons).
Arbeitsgemeinschaft Gynäkologische Onkologie (Working Group for Gynaecological Oncology)
- BRCA1/2 :
BReast CAncer gene 1 and/or 2
German Consortium of Hereditary Breast and Ovarian Cancer
International Patient Decision Aid Standards
IPDAS instrument short form
lobular in situ carcinoma
magnetic resonance imaging
Ottawa Hospital Research Institute
portable data format
Robert Koch Institute
Kuchenbaecker KB, Hopper JL, Barnes DR, Phillips KA, Mooij TM, Roos-Blom MJ, et al. Risks of breast, ovarian, and contralateral breast cancer for BRCA1 and BRCA2 mutation carriers. JAMA. 2017;317(23):2402–16. https://doi.org/10.1001/jama.2017.7112.
Dean M, Scherr CL, Clements M, Koruo R, Martinez J, Ross A. “When information is not enough”: a model for understanding BRCA-positive previvors’ information needs regarding hereditary breast and ovarian cancer risk. Patient Educ Couns. 2017;100(9):1738–43. https://doi.org/10.1016/j.pec.2017.03.013.
World Cancer Research Fund/American Institute for Cancer Research. Continuous update project expert report 2018. Diet, nutrition, physical activity and breast cancer survivors. http://www.wcrf.org/sites/default/files/Summary-of-Third-Expert-Report-2018.pdf. Accessed 20 Sept 2020.
Underhill ML, Crotser CB. Seeking balance: decision support needs of women without cancer and a deleterious BRCA1 or BRCA2 mutation. J Genet Couns. 2014;23(3):350–62. https://doi.org/10.1007/s10897-013-9667-2.
Paluch-Shimon F, Cardoso C, Sessa J, Balmana MJ, Cardoso F, Senkus G, E on behalf of the ESMO Guidelines Committee. Prevention and screening in BRCA mutation carriers and their breast/ovarian hereditary cancer syndromes ESMO Clinical Practice Guidelines for cancer prevention and screening. Ann Oncol. 2016;27(Suppl5):v103–10. https://doi.org/10.1093/annonc/mdw327.
National Institute for Health and Care Excellence (NICE). Familial breast cancer: Classification, care and managing breast cancer and related risks in people with a family history of breast cancer. Clinical guideline (CG164). 2013, updated 2019. http://www.nice.org.uk/guidance/cg164. Accessed 17 Jan 2021.
Collins JM, Isaacs C. Management of breast cancer risk in BRCA1/2 mutation carriers who are unaffected with cancer. Breast J. 2020;26:1520–7. https://doi.org/10.1111/tbj.13970.
Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF. Leitlinienprogramm Onkologie: S3-Leitlinie Früherkennung, Diagnostik, Therapie und Nachsorge des Mammakarzinoms, Langversion 4.1, AWMF-Registernummer: 32-045OL [Guidelines Programme Oncology: S3-guideline screening, diagnosis, therapy and aftercare of breast carcinoma, long version 4.1, AWMF registry number: 32-045OL] 2019. http://www.leitlinienprogramm-onkologie.de/leitlinien/mammakarzinom/. Accessed 9 Oktober 2019.
AGO Breast Committee. Diagnosis and Treatment of Patients with early and advanced Breast Cancer. Guidelines Breast Version 2019.1 2019. http://www.agoonline.de/fileadmin/downloads/leitlinien/mamma/2019-03/EN/Updated_Guidelines_2019.pdf. Accessed 22 April 2019.
Bick U, Engel C, Krug B, Heindel W, Fallenberg EM, Rhiem K, et al. High-risk breast cancer surveillance with MRI: 10-year experience from the German consortium for hereditary breast and ovarian cancer. Breast Cancer Res Treat. 2019;175(1):217–28. https://doi.org/10.1007/s10549-019-05152-9.
De Felice F, Marchetti C, Musella A, Palaia I, Perniola G, Musio D, et al. Bilateral risk-reduction mastectomy in BRCA1 and BRCA2 mutation carriers: a meta-analysis. Ann Surg Oncol. 2015;22(9):2876–80. https://doi.org/10.1245/s10434-015-4532-1.
Heemskerk-Gerritsen BAM, Jager A, Koppert LB, Obdeijn AI, Collee M, Meijers-Heijboer HEJ, et al. Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat. 2019;177(3):723–33. https://doi.org/10.1007/s10549-019-05345-2.
Li X, You R, Wang X, Liu C, Xu Z, Zhou J, et al. Effectiveness of prophylactic surgeries in BRCA1 or BRCA2 mutation carriers: a meta-analysis and systematic Review. Clin Cancer Res. 2016;22(15):3971–81. https://doi.org/10.1158/1078-0432.CCR-15-1465.
Deutsche Krebsgesellschaft, Deutsche Krebshilfe, AWMF. Leitlinienprogramm Onkologie: S3-Leitlinie Diagnostik, Therapie und Nachsorge maligner Ovarialtumoren, Langversion 3.01, AWMF-Registernummer: 032/035OL. [Guidelines Programme Oncology: S3-guideline diagnosis, therapy and aftercare of malignant ovarian tumours, long version 3.01, AWMF registry number 032/035OL] 2018. http://leitlinienprogramm-onkologie.de/Ovarialkarzinom.61.0.html. Accessed 4 Feb 2019.
Buys SS, Partridge E, Black A, Johnson CC, Lamerato L, Isaacs C, et al. Effect of screening on ovarian cancer mortality: the prostate, lung, colorectal and ovarian (PLCO) cancer screening randomized controlled trial. JAMA. 2011;305(22):2295–303. https://doi.org/10.1001/jama.2011.766.
Henderson JT, Webber EM, Sawaya GF. Screening for ovarian cancer: updated evidence report and systematic review for the US preventive services task force. JAMA. 2018;319(6):595–606. https://doi.org/10.1001/jama.2017.21421.
Gronwald J, Lubinski J, Huzarski T, Cybulski C, Menkiszak J, Siolek M, et al. A comparison of ovarian cancer mortality in women with BRCA1 mutations undergoing annual ultrasound screening or preventive oophorectomy. Gynecol Oncol. 2019;155(2):270–4. https://doi.org/10.1016/j.ygyno.2019.08.034.
Heemskerk-Gerritsen BA, Rookus MA, Aalfs CM, Ausems MG, Collee JM, Jansen L, et al. Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysis. Int J Cancer. 2015;136(3):668–77. https://doi.org/10.1002/ijc.29032.
Manchanda R, Burnell M, Abdelraheim A, Johnson M, Sharma A, Benjamin E, et al. Factors influencing uptake and timing of risk reducing salpingo-oophorectomy in women at risk of familial ovarian cancer: a competing risk time to event analysis. BJOG. 2012;119(5):527–36. https://doi.org/10.1111/j.1471-0528.2011.03257.x.
Rini C, O’Neill SC, Valdimarsdottir H, Goldsmith RE, Jandorf L, Brown K, et al. Cognitive and emotional factors predicting decisional conflict among high-risk breast cancer survivors who receive uninformative BRCA1/2 results. Health Psychol. 2009;28(5):569–78. https://doi.org/10.1037/a0015205.
Schwartz MD, Valdimarsdottir HB, DeMarco TA, Peshkin BN, Lawrence W, Rispoli J, et al. Randomized trial of a decision aid for BRCA1/BRCA2 mutation carriers: impact on measures of decision making and satisfaction. Health Psychol. 2009;28(1):11–9. https://doi.org/10.1037/a0013147.
Stacey D, Murray MA, Legare F, Sandy D, Menard P, O’Connor A. Decision coaching to support shared decision making: a framework, evidence, and implications for nursing practice, education, and policy. Worldviews Evid Based Nurs. 2008;5(1):25–35. https://doi.org/10.1111/j.1741-6787.2007.00108.x.
Sun Q. Predicting downstream effects of high decisional confict: meta-analysis of the decisional conflict scale [Doctor of Philosophy]. Ottawa: University of Ottawa; 2005.
Wennberg JE, Fisher ES, Skinner JS. Geography and the debate over Medicare reform. Health Aff (Millwood). 2002;Suppl Web Exclusives:W96-114. https://doi.org/10.1377/hlthaff.w2.96.
Elwyn G, Frosch D, Thomson R, Joseph-Williams N, Lloyd A, Kinnersley P, et al. Shared decision making: a model for clinical practice. J Gen Intern Med. 2012;27(10):1361–7. https://doi.org/10.1007/s11606-012-2077-6.
Julian-Reynier C, Bouhnik AD, Mouret-Fourme E, Gauthier-Villars M, Berthet P, Lasset C, et al. Time to prophylactic surgery in BRCA1/2 carriers depends on psychological and other characteristics. Genet Med. 2010;12(12):801–7. https://doi.org/10.1097/GIM.0b013e3181f48d1c.
O’Neill SC, Mays D, Patenaude AF, Garber JE, DeMarco TA, Peshkin BN, et al. Women’s concerns about the emotional impact of awareness of heritable breast cancer risk and its implications for their children. J Community Genet. 2015;6(1):55–62. https://doi.org/10.1007/s12687-014-0201-5.
Stacey D, Legare F, Lewis K, Barry MJ, Bennett CL, Eden KB, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. 2017;4:001431. https://doi.org/10.1002/14651858.CD001431.pub5.
Krassuski L, Vennedey V, Stock S, Kautz-Freimuth S. Effectiveness of decision aids for female BRCA1 and BRCA2 mutation carriers: a systematic review. BMC Med Inform Decis Mak. 2019;19(1):154. https://doi.org/10.1186/s12911-019-0872-2.
Robert Koch Institute (Centre for Cancer Registry Data). Brustkrebs (Mammakarzinom) ICD-10 C50 (Daten für 2016) [Breast Cancer ICD-10 C50 (data for 2016)] Berlin, Germany. 2019. http://www.krebsdaten.de/Krebs/DE/Content/Krebsarten/Brustkrebs/brustkrebs.html. Accessed 17 Dec 2019.
Robert Koch Institute (Centre for Cancer Registry Data). Eierstockkrebs (Ovarialkarzinom) ICD-10 C56 (Daten für 2016) [Ovarian cancer ICD-10 C56 (data for 2016)] Berlin, Germany. 2019. http://www.krebsdaten.de/Krebs/DE/Content/Krebsarten/Eierstockkrebs/eierstockkrebs.html. Accessed 17 Dec 2019.
Rhiem K, Bucker-Nott HJ, Hellmich M, Fischer H, Ataseven B, Dittmer-Grabowski C, et al. Benchmarking of a checklist for the identification of familial risk for breast and ovarian cancers in a prospective cohort. Breast J. 2019;25(3):455–60. https://doi.org/10.1111/tbj.13257.
Kast K, Rhiem K, Wappenschmidt B, Hahnen E, Haukeet J, et al. German consortium for hereditary breast and ovarian cancer (GC-HBOC). Prevalence of BRCA1/2 germline mutations in 21 401 families with breast and ovarian cancer. J Med Genet. 2016;53(7):465–71. https://doi.org/10.1136/jmedgenet-2015-103672.
Deutsches Konsortium Familiärer Brust- und Eierstockkrebs. 2020. http://www.konsortium-familiaerer-brustkrebs.de/informationen/familiaerer-brust-und-eierstockkrebs/. Accessed 6 March 2020.
International Patient Decision Aid Standards (IPDAS) Collaboration. IPDAS 2005: Criteria for judging the quality of patient decision aids. 2005. http://ipdas.ohri.ca/IPDAS_checklist.pdf. Accessed 27 March 2017.
Elwyn G, O’Connor A, Stacey D, Volk R, Edwards A, Coulter A, et al. Developing a quality criteria framework for patient decision aids: online international Delphi consensus process. BMJ. 2006;333(7565):417. https://doi.org/10.1136/bmj.38926.629329.AE.
Coulter A, Stilwell D, Kryworuchko J, Mullen PD, Ng CJ, van der Weijden T. A systematic development process for patient decision aids. BMC Med Inform Decis Mak. 2013;13(Suppl 2):S2. https://doi.org/10.1186/1472-6947-13-S2-S2.
O'Connor AM, Jacobsen MJ. Workbook on developing and evaluating patient decision aids Ottawa, Canada. 2003. http://decisionaid.ohri.ca/docs/develop/Develop_DA.pdf. Accessed 29 April 2020.
O'Connor AM. Ottawa Decision support framework to address decisional conflict. 2006. http://decisionaid.ohri.ca/docs/develop/ODSF.pdf. Accessed 14 Sept 2020.
Joseph-Williams N, Newcombe R, Politi M, Durand MA, Sivell S, Stacey D, et al. Toward minimum standards for certifying patient decision aids: a modified Delphi consensus process. Med Decis Mak. 2014;34(6):699–710. https://doi.org/10.1177/0272989X13501721.
Elwyn G, O’Connor AM, Bennett C, Newcombe RG, Politi M, Durand MA, et al. Assessing the quality of decision support technologies using the international patient decision aid standards instrument (IPDASi). PLoS ONE. 2009;4(3):e4705. https://doi.org/10.1371/journal.pone.0004705.
Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JP, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6(7):e1000100. https://doi.org/10.1371/journal.pmed.1000100.
Stacey D, Kryworuchko J, Belkora J, Davison BJ, Durand MA, Eden KB, et al. Coaching and guidance with patient decision aids: a review of theoretical and empirical evidence. BMC Med Inform Decis Mak. 2013;13(Suppl 2):S11. https://doi.org/10.1186/1472-6947-13-S2-S11.
Sänger S, Lang B, Klemperer D, Thomeczek C, Dierks M-L. Manual Patienteninformation - Empfehlungen zur Erstellung evidenzbasierter Patienteninformationen [Manual patient information - Recommendations for preparation of evidence-based patient information] Berlin. 2006. http://www.aezq.de/mdb/edocs/pdf/schriftenreihe/schriftenreihe25.pdf. Accessed 3 Sept 2019.
Steckelberg A, Berger B, Köpke S, Heesen C, Mühlhauser I. Kriterien für evidenzbasierte Patienteninformationen [Criteria of evidence-based patient information]. Z ärztl Fortbild Qual Gesundhwes. 2005;99:343–51.
Härter ME. Methodenpapier zur Erstellung evidenzbasierter Gesundheitsinformationen und Entscheidungshilfen [Methods paper for preparation of evidence-based health information and decision aids] [Methodenpapier]. Universitätsklinikum Hamburg-Eppendorf, Germany. 2019, updated 17.05.2020. http://psychenet.de/images/20191204__Methodenpapier_psychenet---final.pdf. Accessed 17 May 2020.
Arbeitsgruppe GPGI. Gute Praxis Gesundheitsinformationen [Good practice guidelines for health information]. Z Evid Fortbild Qual Gesundhwes. 2016;110–111:85–92. https://doi.org/10.1016/j.zefq.2015.11.005.
Glaser BG, Strauss AL. Grounded theory. Strategien qualitativer Forschung [Grounded theory. Strategies for qualitative research]. Bern: Huber Verlag; 2008.
Liamputtong P. Qualitative data analysis: conceptual and practical considerations. Health Promot J Austr. 2009;20(2):133–9. https://doi.org/10.1071/he09133.
Tong A, Sainsbury P, Craig J. Consolidated criteria for reporting qualitative research (COREQ): a 32-item checklist for interviews and focus groups. Int J Qual Health Care. 2007;19(6):349–57. https://doi.org/10.1093/intqhc/mzm042.
Ayres L. Qualitative research proposals–part III: sampling and data collection. J Wound Ostomy Cont Nurs. 2007;34(3):242–4. https://doi.org/10.1097/01.WON.0000270816.99318.3b.
Dresing T, Pehl TH. Praxisbuch Interview. Transkription & Analyse: Anleitungen und Regelsysteme für qualitativ Forschende. 6. Auflage [Manual (on) Transcription. Transcription Conventions, Software Guides and Practical Hints for Qualitative Researchers. 6th edition] Marburg: Dr. Dresing und Pehl GmbH. 2015. http://www.audiotranskription.de/Praxisbuch-Transkription.pdf. Accessed 17 May 2020.
Mayring P. Qualitative inhaltsanalyse. Grundlagen und techniken [Qualitative content analysis. Background and procedures]. Weinheim, Basel: Beltz; 2015.
Witzel A. Das problemzentrierte interview [the problem-centered interview]. Qual Soc Res. 2000;1(1):22.
O’Connor AM, Cranney A. User manual—acceptability. 1996, updated 2002. Ottawa Hospital Research Institute, Ottawa, Canada. https://decisionaid.ohri.ca/docs/develop/User_Manuals/UM_Acceptability.pdf. Accessed 7 March 2017.
Metcalfe KA, Poll A, O’Connor A, Gershman S, Armel S, Finch A, Demsky R, Rosen B, Narod SA. Development and testing of a decision aid for breast cancer prevention for women with a BRCA1 or BRCA2 mutation. Clin Genet. 2007;72:208–17. https://doi.org/10.1111/j.1399-0004.2007.00859.x.
Metcalfe K, Narod S, Poll A, O’Connor A. What are my options for breast cancer prevention? Facts and decision aid for women with a BRCA1 or BRCA2 mutation. 2006.
Kurian AW, Plevritis SK. Decision tool for women with BRCA mutations. Stanford. 2011, updated 11 Januar 2012. http://brcatool.stanford.edu/brca.html. Accessed 19 July 2017.
Mayo Clinic Staff. Preventive (prophylactic) mastectomy: surgery to reduce breast cancer risk. 2016, updated 2 April 2019. http://www.mayoclinic.org/tests-procedures/mastectomy/in-depth/prophylactic-mastectomy/art-20047221?pg=1. Accessed 7 March 2017.
Mayo Clinic Staff. Prophylactic oophorectomy: preventing cancer by surgically removing your ovaries. 2014, updated 15 July 2019. http://www.mayoclinic.org/tests-procedures/oophorectomy/in-depth/breast-cancer/art-20047337?pg=1. Accessed 7 March 2017.
Healthwise Staff. Breast cancer: What should I do if I'm at high risk? 2016, updated 22 August 2019. http://www.stlukesonline.org/health-services/health-information/healthwise/2015/05/15/14/23/breast-cancer-what-should-i-do-if-im-at-high-risk. Accessed 7 March 2017.
Cardiff University. OvDex oophorectomy decision explorer. Cardiff, Wales, United Kingdom. 2014. http://decisionaid.ohri.ca/AZsumm.php?ID=1530. Accessed 12 Jan 2017.
Witt J. The oophorectomy decision explorer: a decision support intervention to facilitate deliberation and coping efforts in women at increased risk of ovarian cancer [Doctor of Philosophy]. Cardiff, Wales: Cardiff University. 2013. http://orca.cf.ac.uk/56817/1/2014WITTJPhD.pdf. Accessed 7 Aug 2020.
Hereditary Cancer Clinic, Prince of Wales Hospital, Centre for Genetics Education, NSW Health, Royal North Shore Hospital. Information for women considering preventive mastectomy because of a strong family history of breast cancer Sydney, NSW, Australia. 2012. http://www.genetics.edu.au/publications-and-resources/booklets-and-pamphlets/information-for-women-considering-preventive-mastectomy-because-of-a-strong-family-history-of-breast-cancer. Accessed 7 March 2017.
Nicolai K. Qualitative Inhaltsanalyse von Fokusgruppendiskussionen im Rahmen eines Projektes zur„ ntwicklung einer Entscheidungshilfe für Frauen mit einer BRCA1/2-Mutation“ Informationsbedarfe krebsgesunder Mutationsträgerinnen [Qualitative content analysis of focus group discussions as part of the project 'Development of a decision aid to support women with BRCA1/2 mutations"—Information needs of mutation carriers without cancer] [M.Sc.]. Cologne, Germany: University of Cologne; 2018.
Lühnen J, Albrecht M, Mühlhauser I, Steckelberg A. Leitlinie evidenzbasierte Gesundheitsinformation [Guideline evidence-based health information] Hamburg. 2017. http://www.leitlinie-gesundheitsinformation.de/wp-content/uploads/2017/07/Leitlinie-evidenzbasierte-Gesundheitsinformation.pdf. Accessed 26 March 2018.
Schnepper MJ. Informationsbedarfe von BRCA1/2-Mutationsträgerinnen mit der Diagnose Brustkrebs—Inhaltsanalyse von Fokusgruppen im Rahmen der Entwicklung einer Entscheidungshilfe [Information needs of female BRCA1/2 mutation carriers with the diagnosis of breast cancer - Content analysis of focus groups as part of the development of a decision aid] [M.Sc.]. Cologne, Germany: University of Cologne; 2018.
Lenz M, Buhse S, Kasper J, Kupfer R, Richter T, Muhlhauser I. Decision aids for patients. Dtsch Arztebl Int. 2012;109(22–23):401–8. https://doi.org/10.3238/arztebl.2012.0401.
Scheibler F, Moreno B. Der praktische Einsatz von Entscheidungshilfen für Patienten. Reine Informationsvermittlung reicht nicht aus [The practical use of patient decision aids. Pure Information transfer is not enough]. Klinikarzt. 2007;36(1):27–31. https://doi.org/10.1055/s-2007-970172.
Krassuski L, Kautz-Freimuth S, Vennedey V, Rhiem K, Schmutzler R, Stock S. Entscheidungshilfen zu präventiven Handlungsalternativen für BRCA1/2-Mutationsträgerinnen. Eine systematische Übersicht. [Decision aids on preventive options for BRCA1/2 mutation carriers. A systematic review.] Accepted for publication in Geburtshilfe Frauenheilk. 2021;81(6), currently in press.
Rhiem K, Engel C, Graeser M, Zachariae S, Kast K, Kiechle M, et al. The risk of contralateral breast cancer in patients from BRCA1/2 negative high risk families as compared to patients from BRCA1 or BRCA2 positive families: a retrospective cohort study. Breast Cancer Res. 2012;14(6):R156. https://doi.org/10.1186/bcr3369.
Kaufman EM, Peshkin BN, Lawrence WF, Shelby R, Isaacs C, Brown K, et al. Development of an interactive decision aid for female BRCA1/BRCA2 carriers. J Genet Couns. 2003;12(2):109–29. https://doi.org/10.1023/A:1022698112236.
van Roosmalen MS, Stalmeier PF, Verhoef LC, Hoekstra-Weebers JE, Oosterwijk JC, Hoogerbrugge N, et al. Randomized trial of a shared decision-making intervention consisting of trade-offs and individualized treatment information for BRCA1/2 mutation carriers. J Clin Oncol. 2004;22(16):3293–301. https://doi.org/10.1200/JCO.2004.05.066.
Centre for Genetics Education, NSW Health. Surgery to reduce the risk of ovarian cancer—information for women at increased risk St Leonards, NSW, Australia. 2017. http://www.genetics.edu.au/publications-and-resources/booklets-and-pamphlets/SurgeryToReduceTheRiskOfOvarianCancer.pdf. Accessed 7 August 2020.
Healthwise Staff. Ovarian cancer: Should I have my ovaries removed to prevent ovarian cancer? 2020. http://www.healthwise.net/ohridecisionaid/Print/PrintTableOfContents.aspx?docId=zx3060§ionId=zx3688. Accessed 5 Aug 2020.
Harmsen MG, Steenbeek MP, Hoogerbrugge N, et al. A patient decision aid for risk-reducing surgery in premenopausal BRCA1/2 mutation carriers. Dev Process Pilot Test Health Expect. 2018;21:659–67. https://doi.org/10.1111/hex.12661.
Culver JO, MacDonald DJ, Thornton AA, Sand SR, Grant M, Bowen DJ, et al. Development and evaluation of a decision aid for BRCA carriers with breast cancer. J Genet Couns. 2011;20(3):294–307. https://doi.org/10.1007/s10897-011-9350-4.
Bieber C, Gschwendtner K, Müller N, Eich W. Partizipative entscheidungsfindung (PEF)—patient und arzt als team [Shared decision making (SDM)—patient and physician as a team]. Psychother Psych Med. 2016;66:195–207. https://doi.org/10.1055/s-0042-105277.
Nickel S, Haack M, von dem Knesebeck O, Dierks ML, Seidel G, Werner S, et al. Teilnahme an Selbsthilfegruppen: Wirkungen auf Selbstmanagement und Wissenserwerb [Participation in self-help groups: impact on self-management and knowledge]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2019;62(1):10–6. https://doi.org/10.1007/s00103-018-2850-8.
We would like to thank all the women with BRCA1/2 mutations that supported the development process by actively participating in the focus group discussions and user tests. Special thanks also go to the German self-help organisation ‘BRCA-Netzwerk e.V.—Hilfe bei familiären Krebserkrankungen’, which supported this project at various levels. Self-help experts reviewed both DA alpha versions from a self-help perspective. Additionally, the organisation helped to acquire volunteer participants for user tests of the DA beta versions. We would also like to thank all the external medical specialists that intensively reviewed and amended both DA alpha versions and thus playing an important role in quality assurance for this project. We also thank Laura Lorenz for useful discussions regarding methodological questions on the qualitative content analysis and Claudia Stracke for supporting the work on the revision processes of the DA prototypes.
Open Access funding enabled and organized by Projekt DEAL. This work was supported by the Landeszentrum Gesundheit Nordrhein-Westfalen (LZG.NRW), Bochum, Germany. The source of funding was not involved in the study design, data collection, analysis and interpretation, report writing or publication.
Ethics approval and consent to participate
This project was approved by the Ethics Committee of the Faculty of Medicine of the University of Cologne [ethics votes of 26 April 2017, reference number 17-128]. Written informed consent was obtained from all participants in the focus group discussions. No personal data was collected from the participants in the user tests. To ensure the anonymity of these participants, only verbal informed consent was obtained and recorded in anonymised form.
Consent for publication
The authors declare that they have no competing interests.
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Method details Step 1–6. Table: Development of decision aids for women with BRCA1 and BRCA2 mutations - Methodological approach Steps 1–6.
Identified decision aids. Table S1 Systematic literature research: List of identified decision aids. Table S2 Systematic literature research: Evaluation of the identified decision aids with regard to the given target definitions.
Focus group discussions. Table S1 Characteristics of the focus group participants. Table S2 Basic results of the focus group discussions with previvors and survivors.
User tests. Table S1 Basic results of the user tests with previvors (n = 6) for DA A. Table S2 Basic results of the user tests with survivors (n = 5) for DA B. Table S3 Interview guideline for the user test of the beta version of decision aid A for previvors and decision aid B for survivors..
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Kautz-Freimuth, S., Redaèlli, M., Rhiem, K. et al. Development of decision aids for female BRCA1 and BRCA2 mutation carriers in Germany to support preference-sensitive decision-making. BMC Med Inform Decis Mak 21, 180 (2021). https://doi.org/10.1186/s12911-021-01528-4
- BRCA1/2 mutation carriers
- Decision aids
- Development process
- Hereditary breast and ovarian cancer
- Preference-sensitive decisions
- Preventive options