We aimed to systematically review the literature to identify primary-care providers’ perceived barriers against provision of genetics services.
We systematically searched PubMed and ERIC using key and Boolean term combinations for articles published from 2001 to 2012 that met inclusion/exclusion criteria. Specific barriers were identified and aggregated into categories based on topic similarity. These categories were then grouped into themes.
Of the 4,174 citations identified by the search, 38 publications met inclusion criteria. There were 311 unique barriers that were classified into 38 categories across 4 themes: knowledge and skills; ethical, legal, and social implications; health-care systems; and scientific evidence. Barriers most frequently mentioned by primary-care providers included a lack of knowledge about genetics and genetic risk assessment, concern for patient anxiety, a lack of access to genetics, and a lack of time.
Although studies reported that primary-care providers perceive genetics as being important, barriers to the integration of genetics medicine into routine patient care were identified. The promotion of practical guidelines, point-of-care risk assessment tools, tailored educational tools, and other systems-level strategies will assist primary-care providers in providing genetics services for their patients.
Genet Med 17 3, 169–176.
Although historically concerned with the identification and diagnosis of rare diseases, the field of medical genetics has expanded its scope in the past decade to include the identification of patients at risk for genetically based conditions and the provision of preventive health interventions. Because the practice of preventive medicine for common conditions is the mainstay of primary care, primary-care providers (PCPs) are critical to the success of this expansion of medical genetics. PCPs are responsible for gathering family history (FH), performing risk assessments, ordering tests, and specialist referrals. Yet barriers may interfere with PCPs’ willingness to embrace and perform these tasks, which are vital to the integration of genetics into primary-care practice. In fact, shortly after the completion of the Human Genome Project (HGP),1 Suther and Goodson2 conducted a systematic review of the literature and identified numerous barriers to the successful integration of genetics into primary-care medicine practice, including inadequate PCP knowledge of basic genetics, lack of detailed or updated FHs, lack of PCP confidence, and lack of referral guidelines.
More than a decade after the completion of the HGP, our understanding of the relationship between genetics and common disease, as well as our technological capabilities to identify genetic abnormalities, has advanced significantly. Yet our understanding of the barriers to the integration of genetics into primary-care medicine has not been revisited. Therefore, we sought to reassess our understanding of the barriers to the integration of genetics services into primary care by conducting a systematic review of the medical literature.
Materials and Methods
Study selection criteria
We conducted a systematic review of research studies in which new data were gathered and that examined PCP-identified barriers to the integration of genetics services into primary care. We chose a priori to include studies that addressed barriers related to the following areas of genetics services: genetic testing and screening, pharmacogenomics, and the evaluation, diagnosis, and management of genetic conditions.
For this review, we used the definition of primary care provided by the Institute of Medicine Committee on the Future of Primary Care, which defines primary care as “the provision of integrated, accessible health care services by clinicians who are accountable for addressing a large majority of personal health care needs, developing a sustained partnership with patients, and practicing in the context of family and community.”3 Therefore, we included the following types of nonstudent/nonresident clinicians in our definition of PCPs: pediatricians, family physicians or general practitioners, obstetricians and gynecologists, and primary-care advanced-practice registered nurses and physician assistants. Finally, we selected published research studies in which the subjects of the study were PCPs and barriers were explicitly identified by the PCPs. We did so to avoid identifying barriers based on assumptions made by non-PCPs.
We queried PubMed and ERIC using key terms to identify articles published from 2001 through 2012. We chose 2001 as the beginning of our time period because this was the last publication year for articles included in the review by Suther and Goodson.2 We searched using key terms “genetics,” “genetic testing,” or “genetic screening” combined (through the Boolean term “and”) with “primary care providers,” “primary care physicians,” “primary care,” “physicians,” “family practice,” “general practitioners,” “pediatricians,” “pediatric providers,” or “pediatric practitioners.” This search generated 4,174 citations, which were reviewed independently by three reviewers. Articles were excluded if review of title indicated that they did not meet selection criteria. Review of remaining abstracts (n = 350) identified 98 articles that required a full review to determine whether they met inclusion/exclusion criteria. Of these, 60 were excluded based on the above exclusion criteria, yielding a final sample of 38 studies for analysis (Figure 1). At every step in the review process, any disagreement regarding exclusion was discussed among the three reviewers.
Data abstraction and analysis
The first step in analysis of the studies was to extract data on PCPs’ self-reported barriers to delivering genetics services. Each study was reviewed by two authors (one of whom was the lead author), and specific barriers within each study were identified. Of note, an individual study could contain data on more than one barrier. We recorded the number of times a specific barrier appeared across studies. Next, the barriers from all studies were aggregated into categories based on similarity of topic. For example, a lack of genetic knowledge was one barrier category. Within this category we grouped general genetic knowledge barriers as well as more specific knowledge barriers. Finally, we organized the barrier categories into the following themes: (i) knowledge/skills (i.e., described self-reported deficiencies in understanding concepts or performing tasks); (ii) ethical, legal, and social implications (ELSI) (also included barriers that addressed psychosocial aspects of genetics); (iii) health-care systems (i.e., related to practical challenges, procedures, and policies); and (iv) scientific evidence (i.e., professional guidelines and strength of scientific evidence related to genetic evaluation and testing). The barriers were organized through an iterative process, and we did not use a previously published framework. Rather, we considered the context in which the barrier could be targeted (i.e., a competency deficit versus a clinic workflow issue) to organize the results. Additional data extracted from the studies included sample size, country of study, study methodology, subject demographics and response rate, study objective, and additional conclusions, such as overall attitudes and perceptions regarding the integration of genetics into primary-care practice (Supplementary Table S1 online).
We also assessed the quality of the studies. We were unaware of any validated tools that assess the quality of cross-sectional surveys or qualitative studies for systematic reviews. Therefore, we created our own metric for assessing the quality of a quantitative survey, which was the study design for all but one of the quantitative studies (Hindorff et al.4 was a case–control study). We used a checklist tool used in a previous systematic review for qualitative studies.5
In survey research, minimizing bias is critical to the collection of valid data. Therefore we constructed a simple assessment tool based on this concept. The most significant sources of bias during data collection in survey research include sample bias due to the use of a nonrepresentative sample (e.g., a nonrandom subsample of the population or a convenience sample) and attrition bias due to low response rates (we set a 50% cutoff). Because we have no evidence as to the relative contribution to or weight of each of these elements in the measure of bias, we assigned them equal weight. We calculated a bias risk score that gives 1 point for each source of bias (highest total score = 2). We feel that this addresses potential limitations regarding assessment of the relationship between the sample size of the study and the validity of the findings. Generalization of the findings depends more on the representativeness of a sample than its absolute size.
For qualitative studies, we used the nonvalidated, 28-item checklist tool used by Tong et al.5 in a recent systematic review of qualitative studies. Similarly, because we have no evidence as to the relative contribution to or weight of each of the individual elements in this checklist, we assigned them equal weight (highest total score = 28).
A total of 38 published research studies met the criteria for inclusion in this review (Figure 1). Of these, 24 studies used quantitative methods and 13 used qualitative methods (Table 1). We identified 311 barriers (nonunique) across all 38 studies, which were aggregated into 38 unique categories within 4 thematic areas, which are described below (Supplementary Table S2 online).
The majority of articles (n = 19) included in this review evaluated the perceptions of mixed cohorts of PCPs, whereas 17 studies included only general practitioners or family physicians. One study assessed only pediatricians and another included only obstetrics/gynecology providers. Because of the inability to identify PCP types in the majority of studies, we did not attempt to stratify our results by provider type. Seventeen studies were from the United States, 6 were from the United Kingdom, 4 were from Canada, and 11 were from other countries. It was difficult to compare studies across countries because of the wide array of countries represented and the small number of studies (Supplementary Table S1 online).
We found a range of biases across the quantitative studies. Using our bias score, 9 studies had a score of 0, 9 had a score of 1, and 6 had a score of 2 (the highest). The qualitative studies varied in quality, with a range in quality score between 9 and 23 of 28 possible and an average score of 13. All 13 qualitative studies received points for describing methods of sampling and sample size, providing a description of the sample, using an interview guide, deriving themes in data analysis, and providing respondent quotations.
Knowledge and skills
In total, 22 different knowledge and skills barriers were cited 84 times in the included studies; these barriers related to deficits in PCPs’ knowledge and skills, confidence, comfort, and ability to perform specific genetic tasks (Supplementary Figure S1 online). The most commonly cited barrier category within this theme was a general lack of genetic knowledge (n = 24 cited in 20/38 studies); this included specific barriers around PCPs’ self-reported lack of confidence in their own knowledge about genetics in general (n = 7)6,7,8,9,10,11,12 and about clinical genetics,13 an interest in gaining insight regarding the genetic background of a disease,14 and a lack of confidence in their ability to perform core competencies such as taking an FH,15 including a lack of knowledge about what FH information to collect.16
Among the several skill-related barriers identified, the most commonly cited (n = 16 citations in 16/38 studies) was a lack of confidence their ability to counsel patients about genetic risk and to manage them. Specifically, providers expressed concerns about feeling unqualified to provide genetic counseling to patients and making the correct management decisions. Freedman and colleagues17 surveyed 1,763 US physicians and found that only 28.8% of PCPs felt qualified to provide genetic counseling to their patients. Several studies mentioned insufficient knowledge to counsel patients18 or a lack in confidence or comfort in doing so.9,13,19,20 In regard to FH, PCPs reported a lack of awareness of guidelines or recommendations for interpreting FH; some knew guidelines existed but did not know the content21 or what to do with the results.14 Iredale et al.22 reported that PCPs were unsure how to address consanguinity with their patients.
Fourteen of the 38 studies described the barriers of a lack of confidence or ability to order a genetic test and the interpretation of genetic test results (Supplementary Table S2 online). Specifically, PCPs reported difficulty explaining the limitations of screening tests to patients, and issues with false-negative and false-positive test results, as well as with general interpretation of genetic tests results, which they often found ambiguous. For example, Bonter et al.11 surveyed 341 Canadian physicians; less than 10% of family physicians surveyed reported that they were sufficiently informed about genetic testing, and only 15% of respondents reported feeling able to interpret genetic test results.
Ten studies identified barriers related to providers’ ability to conduct genetic risk assessment. Specifically, PCPs cited a lack of knowledge and skills in assessing patient risk21 and testing for cancer susceptibility,15,17 as well as citing a lack of overall confidence in assessing patient risk.7,23 In their assessment of 860 US PCPs, Vig et al.24 found that 38.3% were uncomfortable with making screening and prevention recommendations and were uncertain about which patients are medically appropriate to refer.
PCPs reported that it was hard to keep up to date with evidence, specifically updated and revised professional guidelines (n = 9, citations of barrier in 9/38 studies).16,21,25,26,27,28,29,30 A lack of access to current information about genetics and being unaware of existing educational resources were also identified as barriers.10,12,25,31 When general practitioners in Australia were asked to nominate resources that would be valuable to them, they requested point-of-care resources to guide risk assessment.
Finally, barriers regarding the knowledge/skills for seeking referrals for medical genetics were cited on seven occasions. These encompassed a lack of understanding and confidence in how and when to make a referral to a genetic professional.14,24
Ethical, legal, and social implications
The majority of the studies reported at least one barrier related to the ELSI of genetics for both providers and patients. These were classified into 10 categories (Supplementary Figure S2 online). The most frequently cited ELSI barrier (n = 18 citations in 16/38 studies) was the potential for patient anxiety and psychological distress around genetic risk.7,11,32 PCPs mentioned the potential for a patient to react with anxiety to genetic test results33 and that these results would put a burden on people who do not want to know about it, make carriers feel less healthy,34 and potentially make patients feel “inadequate.”35 PCPs also mentioned that genetic testing may have unanticipated findings that are secondary to the intent of ordering testing and that may cause distress among adults and minors regarding adult-onset disorders.35,36
The second most common ELSI barrier (n = 15 citations in 15/38 studies) was the fear of social or insurance discrimination for their patients as a result of their genetic information.37 Freedman et al.17 found that more than 80% of 1,251 US PCPs surveyed thought that patients with positive genetic testing results were at risk for insurance discrimination. Another survey identified 70% of PCPs with this concern.38 In addition, Lowstuter et al.38 found that 75% of a sample of 1,222 California physicians thought that patients will decline testing for fear of health insurance discrimination. Of note, both of these studies were conducted before the enactment of the Genetic Information Nondiscrimination Act in 2008.
The concern over lack of confidentiality of genetic information, specifically the risk of harm resulting from a breach of privacy and disclosure of information, was cited as a barrier on 10 occasions. Examples of disclosure concerns included revelations of nonpaternity, as well as the implications of uncovering genetic risk for family members of the primary patient. In a national survey, 53% of PCPs felt it difficult to ensure that patients’ test results will remain confidential.17 In another study, 61% of Swiss physicians feared that confidentiality could be breached because the breast cancer test result had implications for other family members.39 Several issues related to prenatal ethics arose, including the perception that prenatal genetic testing dampens the natural excitement of pregnancy or could medicalize pregnancy and a fear that prenatal and preconception genetic testing would motivate individuals to want to create a “perfect child,” which might create additional disparities in society regarding individuals with genetic conditions or disabilities.26,39 The concept that genetics has the ability to cause “more harm than good” was also expressed as a concern.25,26,32,37,39
A total of 40 individual barriers related to health-care systems (Supplementary Figure S3 online). The largest category of systems barriers was lack of access to genetics services (n = 23 citations in 17/38 studies). This encompassed specific barriers related to lack of access to genetics services in general9,15,19,33 and a specific lack of access to genetic counselors or geneticists.2,15,22,24,25,37,40,41 PCPs reported an inability to obtain a consultation with clinicians in four studies, noting that the location of the nearest genetics center was too inconvenient for patients to be able to access.22,24,29,40 Chen et al.29 found that 24% of Alabama pediatricians surveyed were unable to obtain genetics consultations for their patients, 67% said it was difficult or not possible to obtain a face-to-face genetics evaluation, and 58% reported it was difficult or impossible to obtain a remote genetics evaluation. Iredale et al.22 found that rural location played a major role in access issues because of isolation, lack of social networks, poor transport, decreased accessibility, and lack of referral patterns to secondary and tertiary facilities. In several studies, PCPs reported that genetic testing was not readily available to them.4,11,17,33,40
The second most frequently cited systems barriers related to time (n = 21 cited in 18/38 studies). This included time needed to collect detailed FHs as part of the primary-care visit22,27 and having insufficient time to explain the results of genetic tests to patients.11,21,29 In the case of genetic medicine in prenatal care, the time to obtain results was reported as being too long to inform any treatment decisions.11,15
PCPs also reported being unclear about their role in providing genetics services (n = 15 cited in 15/38 studies). In some instances, PCPs felt that it was not their role to deliver genetics services8,36,39 or they simply were unclear about their role.9,12,13,14,32,37 Additional studies described PCPs’ perceptions that “genetics is for specialists”19,27,29,40 and that the management of genetic conditions requires complex high-level knowledge available only from a specialist. Furthermore, the perception that genetics was less prevalent or significant than other issues was identified as a barrier in eight studies. This included the notion that genetics was not perceived to have an impact on primary-care practice.7,12,23,25,27,33,42
Cost to both patients and providers was expressed as a barrier to integration of genetics services into primary care. This included a barrier in regard to the lack of insurance coverage for genetic tests (n = 6 citations), as well as the cost to the patient (n = 10 citations). Costs for PCPs also were cited as a barrier, particularly regarding unreimbursed time spent counseling and ordering genetic tests.11,12,18,42
Several practical barriers regarding the integration of genetics into the system of primary-care practice were mentioned. Among the most common was the notion that it is difficult to incorporate additional genetics tasks into practice/clinic flow (n = 8 cited in 5/38 studies).4,9,10,28,30 In addition, PCPs reported having insufficient tools to assess cancer risk and that it was difficult to enter FH information into the electronic health record.14,31 PCPs reported that their patients’ accuracy when providing FH information was a barrier,16,21,27,28 as were language and culture barriers when discussing FH and genetics with patients.14,21,22,27
A total of nine barriers related to current scientific evidence behind use of genetics services were identified in the studies (Supplementary Figure S4 online); the most commonly cited barrier was a perceived lack of therapeutic interventions available after the identification of increased risk (n = 11 cited in 11/38 studies)24,27,28,36,39 and the notion that patient management would not change as a result of genetic assessment.4,7,11,23,25,27 The second most frequently cited evidence barrier reported was the lack of guidelines and insufficient evidence to support risk assessment (n = 10 cited in 10/38 studies).
A lack of guidelines for when to order a genetic test was mentioned as a barrier (n = 6). Furthermore, PCPs reported that limitations of current genetic screening tests deterred them from utilizing them in practice (n = 10 cited in 7/38 studies). Specific limitations of genetic tests were inaccurate or unambiguous results,9,17,29 a high rate of false positives (in cancer risk testing),17,33 and concern over the validity of genetic testing.9,33 In a study of more than 1,200 US physicians, 45% believed patients’ risk of cancer is unclear after genetic testing.17
Most significant barriers
Among quantitative studies, sample size is likely to contribute to a more representative assessment of the study population. Because the barriers identified in each study were given equal weight, we also assessed the barriers from the largest studies (those that had a sample size of ≥400; n = 7) in an attempt to ascertain the relative priority of the barriers identified. We found that the barriers in the largest studies reflect the distribution of barriers across the four categories. Of the seven largest studies, four studies were conducted in the United States and discussed a lack of genetic knowledge and challenges with access to genetics services; three studies discussed a perceived lack of therapeutic interventions and fear of insurance discrimination; two studies mentioned lack of clear or accessible guidelines to support risk assessment, lack of confidence in genetic referrals, lack of confidence and ability to order genetic tests, and a lack of time. Thirteen other barriers were mentioned once across the largest studies.
This systematic review found that numerous challenges to the integration of genetics services into the routine provision of primary care remain a decade after completion of the HGP. Although four major barrier themes (knowledge/skills, systems, ELSI, and evidence) were identified, barriers related to insufficient knowledge and skills were the most frequently cited across the literature. A similar systematic review by Suther and Goodson2 conducted 12 years ago reached the same conclusion.
Why does knowledge still loom larger as a barrier? What does it mean for the successful integration of genetics into primary care? One reason may be that before PCPs even set foot in the clinic, they are already behind. Time has not stood still for the field of genetics since the completion of the HGP. On the contrary, advances in genetic technology and the discovery of new genetic mechanisms seem to occur almost daily. Meanwhile, PCPs’ genetics training is likely decades old and rusty from lack of use. Until only recently, the field of genetics has focused on rare diseases that are not frequently seen in a primary-care clinic. Yet the real challenge for providers is when and how to apply this information in their practice. A “train-the-trainer” model might be a helpful practical approach to addressing knowledge and competency barriers to the integration of genetics into primary care.
Although a lack of professional guidelines was cited as a barrier, we were unable to determine from the data whether this was because of an actual lack or the lack of awareness of the same. For example, Vig et al.24 found that 16.7% of physicians use professional guidelines to guide referral for cancer genetics evaluation. It is possible that dissemination and uptake of guidelines is incomplete given their recent development at the time of data collection. In the past 10 years, professional societies such as the American Academy of Pediatrics,43,44 the American College of Obstetricians and Gynecologists,45 the American Society of Clinical Oncology,46 and the American College of Medical Genetics and Genomics47,48 have published numerous guidelines on topics that could potentially be useful for PCPs.
Systems-level barriers collectively were noted as the most significant impediment to PCPs integrating genetics into their practice, particularly time constraints and lack of access to services. A solution might be the use of quality improvement strategies and process mapping to examine patient and clinician workflow in order to facilitate the integration of FH collection and genetic assessment. Barriers related to health information technology were largely not addressed in the studies reviewed, likely because the use of electronic health records in the primary-care setting over the past decade has increased significantly.49,50 Recent interventions aimed at improving the integration of genetics medicine into primary care have demonstrated significant barriers toward collecting and updating FH information in electronic health records. Patient-entered FH data, including the use of electronic risk assessment models, has been demonstrated to reduce the time required by health-care professionals to collect information and has not resulted in poorer quality of data.51,52 Point-of-care FH tools provide actionable clinical decision support for PCPs and have been developed for prenatal care,53,54 family medicine,55 and pediatrics. The exponential increase of genetic and genomic information is quickly exceeding the ability of humans to remember and process. PCPs in particular should be equipped to use existing resources, as opposed to learning endless facts.63 This model has been effective for pharmacogenomics.64 Finally, medical decision support systems must continue to be designed—current applications in progress relate to pharmacogenomics56—so that health professionals can access up-to-the-minute relevant information and respond appropriately to the concerns they hear when interacting with their patients.57
With the advancement of genetic technologies and continued workforce shortages of geneticists and genetic counselors,58 PCPs will need to assume a greater responsibility in genetics medicine related to the anticipatory guidance and disease prevention that lie within their purview. In the endeavor to improve systems to access genetic providers, alternative options for sharing and maximizing resources should be considered, particularly the use of telehealth and virtual consults. Moreover, streamlining activities among PCPs may result in an overall improvement in access to genetics. As care and management of patients with genetic conditions, as well as the initial evaluation and ordering of genetic tests, becomes integrated into primary care, the specialist’s role can be reserved for interpreting genetic test results. As genetic medicine becomes a mainstay of primary care, ensuring an equitable allocation of genetics services is necessary to avoid increased health disparities.
Not surprisingly, there were a number of ELSI barriers identified in the studies reviewed. The two most significant barriers related to the concern for patient anxiety and a fear of health insurance or social discrimination. Additional research regarding the burden and impact of patient anxiety is needed. As for discrimination, in 2008, the Genetic Information Nondiscrimination Act was passed to ensure that a person’s genetic information could not be used against him or her in health insurance and employment decisions. Interestingly, 12 of the 14 studies that reported the insurance concerns were published before the enactment of the legislation. However, there remains a gap in awareness of the Genetic Information Nondiscrimination Act,59 and in some cases PCPs remain skeptical about the potential of personal genetic information to affect negatively patients’ insurability or future coverage. There is a need to educate physicians further about the existence of the Genetic Information Nondiscrimination Act and the protections it offers, as well as the ever-changing legislation regarding genetic medicine.
One of the barriers identified in this study concerned the potential for loss of privacy in the breach of confidentiality for other family members. However, because one of the benefits of genetic medicine is the ability to identify other family members at risk for disease and assist in disease prevention, this barrier should be targeted as part of an effort to deconstruct myths about genetics. Although Acheson et al.37 found that 18% of PCPs surveyed reported social or ethical dilemmas such as the potential to disclose nonpaternity as a barrier, only 1% reported that their patients refused to disclose the risk of a serious condition to relatives.
This study reinforces findings from previous research that was conducted before the completion of the HGP regarding the hesitations, knowledge gaps, and systems-level challenges in the adoption of genetic medicine into primary-care practice.2 The review conducted by Suther and Goodson2 assessed PCPs’ perceived barriers as well as the quality of 18 studies from an original pool of 68 studies. In addition to identifying similar barriers, Suther and Goodson reported that PCPs cited a need for educational programs in genetics, informational resources, and referral guidelines, which is reflective of our findings as well. This review differs from Suther and Goodson’s in that we specifically chose to include only those barriers that were directly reported by PCPs, rather than those based on knowledge models, as a way to evaluate perceptions and attitudes. A major shift in the perceptions regarding genetics medicine in primary care over the past decade is reflected in Supplementary Table S1 online; the majority of studies reviewed concluded that PCPs have positive views of genetics medicine and feel an increasing need to integrate genetic risk assessment and services into routine primary care.
This study’s main strength lies in assessing research articles that were primarily designed to assess the available empirical evidence regarding PCPs’ perceived barriers to genetic medicine. However, this review contains limitations that should be acknowledged. Barriers in this study were grouped according to the type of barrier as opposed to the theme of the study to which they related, thereby combining barriers that were noted under different contexts (e.g., oncology versus prenatal). However, the assessment of barriers in this manner allows the development of interventions that encompass needs across various settings of genetics in primary care and is not limited to only FH or genetic testing. Another limitation is that this review contains studies of variable quality, size, and type. Qualitative data contributed to the richness of data, but the comment of one focus group participant holds the same weight as the majority of a national sample reporting another barrier. Also, as with any research, the issues addressed in the published medical literature may be biased toward those of interest to and pursued by the researchers and not the PCPs.
Interventions to address perceived barriers—practical barriers as well as misperceptions and knowledge deficits—must be tailored according to the patient population served and be adapted to the role and identity of the PCP. PCPs who care for patients prenatally, in childhood, and across the life span must understand the implications of genetics medicine for the patients and families they care for as well as their role in providing the services incumbent to them. Advances in genetics, genomics, pharmacogenomics, and other “genomic” sciences continue at a rapid rate; to stay abreast of ever-changing guidelines and tests, PCPs must have access to relevant information at the point of care.
Examples of recent efforts to enhance PCP knowledge regarding genetics include the American Academy of Pediatrics Genetics in Primary Care Institute website,60 the National Institutes of Health Genetic/Genomic Competency Center,61 and the Jackson Laboratory cancer risk assessment tools.62 However, development of educational resources alone is unlikely to effect widespread change in attitudes and behavior of PCPs. Existing resources should be promoted and marketing strategies should be aimed at making genetics less intimidating and integrating it into the accepted role of generalists. Payment models must support the integration of new genetic technologies into routine preventive and health supervision models of care. Professional societies should continue to develop specific guidelines, communicate messages to members that dispel existing myths regarding genetics, and provide direction regarding their respective roles in genetic medicine.
PCPs have varying levels of comfort regarding the application of genetics in primary care. Whether they chose to order genetic tests themselves or refer their patients to genetics services, they need to be able to tier patient risk and be prepared to counsel their patients on the implications of test results. Increasingly, PCPs will need to assume a greater responsibility in genetics medicine for the anticipatory guidance and disease prevention that lie within their purview. Addressing the barriers discussed herein is a first step toward realizing this goal.
The authors declare no conflict of interest.
The authors thank the Genetics in Primary Care Institute (GPCI) Project Advisory Committee for its helpful contributions to the manuscript. Support for this research was provided from the Health Resources and Services Administration Maternal and Child Health Bureau (UC7MC21713) for the GPCI, a cooperative agreement awarded to the American Academy of Pediatrics. In addition, B.A.T. was supported by the Clinical Sciences Scholars Program at the University of Michigan and a K23 Mentored Patient-Oriented Research Career Development Award from the National Institute for Child Health and Human Development (K23HD057994).
About this article
A comparative study of patients’ perceptions of genetic and genomic medicine services in California and Malaysia
Journal of Community Genetics (2018)